- Fct: FUNCTIONALITY
- R: Rearranged
- T: Transcribed
- Pr: Translated into protein
"+" or "-" indicates if the gene sequences have been found (+) or not been found (-)
rearranged (R),
transcribed (T) and/or translated into protein
(Pr). Arbitrarily that information is shown on the first line of each gene
when the data have been confirmed by several studies.
Functionality is shown between parentheses, (F) and (P), when the accession
number refers to rearranged genomic DNA or cDNA and the corresponding germline
gene has not yet been isolated.
Functionality is shown between brackets, [F] and [P], when the accession number
refers to genomic DNA, but not known as being germline or rearranged.
Click on:
- IMGT gene name to get the corresponding IMGT/GENE-DB entry,
- IMGT allele name to see the corresponding Alignments of alleles,
- accession number to get the corresponding IMGT/LIGM-DB entry.
The 7 human (Homo sapiens) IGKV subgroups belong to three clans
(Figure IGKV clans).
Clans comprise, respectively:
- clan I: IGKV1 subgroup genes
- clan II: IGKV2, IGKV3, IGKV4 and IGKV6 subgroup genes
- clan III: IGKV5 and IGKV7 subgroup genes
IGKV gene names are designated by a number for the subgroup, followed by a dash and a number for the localization from 3' to 5' in the locus.
The IGKV genes of the distal duplicated V-CLUSTER are designated by the same number as the corresponding genes in the proximal V-CLUSTER, with the letter D added.
°: DNA genomic sequence, but not known to be rearranged or germline.
NL: Not Localized in the locus.
MAP: Mapped reference sequences.
IMGT notes:
- (1) Based on a 21 bp DELETION starting at nucleotide 4 of DECAMER [11] (https://www.imgt.org/IMGTrepertoire/Regulation/promoters/human/IGK/IGKV/Hu_IGKVpromoters.html), the IGKV1-8 functionality was initially defined as "ORF". However the identification of several transcripts indicated that the IGKV1-8 gene is functional (Stamatopoulos K., Belessi C. and Lefranc M. P. 10/10/2007). As the deletion is not observed in KM455559, the 21 bp deletion in Z00014 may correspond to an artefact or to a promoter polymorphism of IGHV8*01.
- (2) TTTGCTT instead of TTTGCAT in the core sequence of the DECAMER element [11], but transcript found [8].
- (3) CONSERVED-TRP replaced by a STOP-CODON in FR2-IMGT, and non canonical V-HEPTAMER: CATAGTG instead of CACAGTG [11].
- (4) STOP-CODONs in FR2-IMGT, INSERTION of 4 bp at position 72 leading to a frameshift in FR3-IMGT [11].
- (5) Non canonical V-HEPTAMER: CACTGTG instead of CACAGTG [33], but rearrangement products and productive cDNA found ([8] and see IMGT/GENE-DB).
- (6) DELETION of 2 bp at position 17 and INSERTION of 1 bp at position 27/28, 1 bp at position 87/88, and 3 bp at position 85, leading to frameshifts [11]
- (7) DELETION of nucleotide 4, and INSERTION of 1 bp at position 15/16. Defective DONOR-SPLICE [11].
- (8) STOP-CODON in L-PART1 [11].
- (9) IGKV1D-13*01, initially considered as an ORF, due to a non canonical V-HEPTAMER: CATAGTG instead of CACAGTG [11], has been found rearranged and transcribed in a 'productive' sequence (DQ101035). The sequence was obtained from a CLL case expressing kappa light chain isotype (by flow); this case also carried a non-productive, non-transcribed rearranged of the IGKV2-29*01 pseudogene. On these grounds, the IGKV1D-13*01 rearrangement was considered as expressed. (message from K. Stamatopoulous and C. Belessi to M.-P. Lefranc, 07/04/2008).
- (10) INSERTION of 1 bp at position 57 in FR3-IMGT, leading to a frameshift [11].
- (11) DELETION of 2 bp at position 17, INSERTION of 1 bp between codons 27/28, INSERTION of 3 bp in codon 85, INSERTION of 1 bp between codons 87/88 [11].
- (12) TTTGCTT instead of TTTGCAT in the core sequence of the DECAMER, and altered V-HEPTAMER: CACAGGG instead of CACAGTG [11].
- (13) No INIT-CODON: ATG replaced by GTG [11].
- (14) DELETION of 1 bp at position 74 leading to a frameshift, no INIT-CODON: ATG replaced by GTG, and non canonical ACCEPTOR-SPLICE [11].
- (15) No INIT-CODON: ATG replaced by GTG , CT instead of GT in ACCEPTOR_SPLICE, and DELETION of 1 bp at position 4 leading to a frameshift, and non canonical V-HEPTAMER [11].
- (16) No INIT-CODON: ATG replaced by ATA [11].
- (17) No Vk-gene related sequence was found upstream of codon 12, 5' part of V-REGION truncated [11].
- (18) V-EXON consists of 2 parts, separated by 180 bp that show no homology to Ig genes. STOP-CODON at position 35, and no INIT-CODON: ATG replaced by GTG [11].
- (19) Frameshift in FR2-IMGT due to 1 bp INSERTION at position 39, and non canonical V-NONAMER [11].
- (20) STOP-CODON at position 88 in FR3-IMGT [11].
- (21) STOP-CODONs in V-REGION, V-REGION truncated: breakoff of homology before codon 15 and after codon 87 [11].
- (22) STOP-CODONs in V-REGION, and breakoff of homology before codon 21, and STOP-CODON in V-REGION [11].
- (23) No Vk-gene related sequence was found upstream of codon 12, 5' part of V-REGION truncated [11].
- (24) V-EXON consists of 2 parts, separated by 180 bp that show no homology to Ig genes, STOP-CODON in FR2-IMGT, and no INIT-CODON [11].
- (25) INSERTION of 1 bp in codon 45 (134^135>ins^a) and DELETION of 1 bp in codon 51 (g153>del) [11]. The insertion in codon 45 leads to a frameshift but the normal reading frame is reestablished by the deletion in codon 51. The resulting sequence shows six amino acid changes from codon 46 to 51 in the FR2-IMGT. The frameshift originally described in FR1-IMGT [13] has not been confirmed.
- (26) IGKV2D-29*02, initially considered as an ORF due to a non canonical V-HEPTAMER: CACAGAG instead of CACAGTG, has been found rearranged and transcribed in a 'productive' sequence (DQ101097).
- (27) GG instead of AG in the ACCEPTOR_SPLICE [11].
- (28) Heavily mutated, insertion of 1.2 kb in V-INTRON. INSERTION of: 3 bp in codon -14/13, 7 bp in codon 81, and DELETION of: 2 bp in codon 27A, 24 bp from codon 56 to 65, 1 bp in codon 83 [11].
- (29) STOP-CODON in L-PART1, and DELETION of 2 bp in codon 6 leading to a frameshift [11].
- (30) STOP-CODON in L-PART1, frameshift in V-REGION: deletion of 2 nt in FR1-IMGT [33].
- (31) DELETION of 2 bp at position 6, leading to a frameshift [11].
- (32) STOP-CODON in FR1-IMGT and FR2-IMGT at positions 23 and 38, INSERTION of 1 bp at position 85/86 [11].
- (33) STOP-CODON in CDR3 in codon 94 [11].
- (34) STOP-CODON in L-PART1, and 2 bp DELETION at position 6 leading to a frameshift [11].
- (35) STOP-CODON in FR1-IMGT and FR2-IMGT at positions 23 and 38, INSERTION of 1 bp at position 85/86 [11].
- (36) Non canonical V-HEPTAMER: CACTGTG instead of CACAGTG [11].
- (37) No INIT-CODON: ATG replaced by ATA[11].
- (38) IGKV2nd-CYS replaced by a Glycine in FR3-IMGT.
- (39) IGKV4-1 is in an inverted orientation of transcription.
- (40) IGKV5-2 is in an inverted orientation of transcription.
- (41) IGKV1st-CYS replaced by a Phenylalanine in FR1-IMGT.
- (42) IGKV1-13*02, initially considered as an ORF, has been found rearranged and expressed in a functional anti-TPO sequence (clone TR1.9) (L12099) [38] (N. Chapal, S. Roux, T. Chardes and M.-P. Lefranc, comment, 9/11/2000). The Fab of that clone has been crystallized and its 3D structure determined (PDB: 1vge). Note that the four first amino acids ELVM of the V-REGION in L12099 and PDB: 1vge are introduced by the primer. The IgA1 theoretical model (PDB: 1iga) uses the 1vge sequence and structure for the kappa chain (M.-P. Lefranc comments, 28/09/2001)
- (43) In EMBL, a new accession number M27751 was created, the original accession number X12688 becoming secondary accession number of M27751.
- (44) IGKV1-NL1 is most probably a polymorphic gene by insertion/deletion (found in 12 of 57 (21 %) healthy Caucasians) [40].
- (45) The most 3' nucleotide of L-PART2 of A18c is A instead of G. This allele is described as IGKV2-29*03 (L-PART2 g12>a) according to the IMGT numbering for coding regions.
- (46) It is not known if this sequence corresponds to that gene or to its duplicate. For that reason, the sequence appears twice in the IMGT/GENE-DB reference sequences.
- (47) In the absence of complete sequence the functionality ORF has been assigned based on the other alleles.
- (48) As the DPK sequences only contain the V-REGION, some of them could be assigned neither to a gene or its duplicate, nor to any allele of the gene.
- (49) Means that the rearrangement, transcript or protein could not be assigned to the gene in the proximal or distal cluster.
- (50) IGKV6-21*01, initially considered as an ORF, due to a non canonical V-HEPTAMER: CACTGTG instead of CACAGTG [11], has been found rearranged.
- (51) IGKV6D-21*01, initially considered as an ORF, due to a non canonical V-HEPTAMER: CACTGTG instead of CACAGTG [11], has been found rearranged.
- (52) The sequence FM164407 previously designated as IGKV1D-17*02 has been shown to correspond to allele IGKV1-17*03 (19/01/2015).
- (53) Chimeric sequence between IGKV3D-20 in 5', codons 1 to 106, and IGHV3D-11 in 3', codons 107 to 111, and absence of transcripts.
- (54) The sequence L19272 obtained by Polymerase Chain Reaction (PCR) has the features of a chimeric sequence between two different genes belonging to the Homo sapiens IGKV3 subgroup (IGKV3D-20 in 5', codons 1 to 106, and IGHV3D-11*02 in 3', codons 107 to 111). This sequence has been assigned to IGKV3D-20*02 allele with the functionality ORF (chimeric sequence and absence of identified transcripts). This assignment needs to be confirmed by analysis of other genomic and mapped germline clones. (M-P. Lefranc, IMGT-NC, 15/02/15)
- (55) Inferred allele: IMGT-NC_Report_2020-3-1120_Homsap_IGKV_IGLV.
- (56) IMGT-NC_Report_2021-1-0608_Homsap_IGKV_IGLV.
- (57) truncated pseudogene, no L-PART2, several STOP-CODON in V-REGION.
IMGT references:
- [1] Atkinson M.J. et al., Immunogenetics, 44, 115-120 (1996). PMID:8662073
- [2] Bentley D.L. and Rabbitts T.H., Nature, 288, 730-733 (1980). PMID:6779204
- [3] Bentley D.L. and Rabbitts T.H., Cell, 32, 181-189 (1983). PMID:6402305
- [4] Chen P.P. et al., Proc. Natl. Acad. Sci. USA, 83, 8318-8322 (1986). PMID:3095834
- [5] Chen P.P. et al., J. Exp. Med., 166, 1900-1905 (1987). PMID:3119763
- [6] Cox J.P. et al., Eur. J. Immunol., 24, 827-836 (1994). PMID:8149953
- [7] Fang Q. et al., Clin. Immunol. Immunopathol., 75, 159-167 (1995). PMID:7704974
- [8] Giachino C. et al., J. Exp. Med., 181, 1245-1250 (1995). PMID:7869042
- [9] Harada T. et al., J. Immunol., 153, 4806-4815 (1994). PMID:7963546
- [10] Huber C. et al., Eur. J. Immunol., 23, 2868-2875 (1993). PMID:8223863
- [11] Ichiyoshi Y. et al., J. Immunol., 154, 226-238 (1995). PMID:7995943
- [12] Jaenichen H.R. et al., Nucleic Acids Res., 12, 5249-5263 (1984). PMID:6087279
- [13] Kimberly V.D. et al., J. Clin. Invest., 87, 1603-1613 (1991). PMID:2022732
- [14] Klobeck H.G. et al., Nucleic Acids Res., 13, 6515-6529 (1985). PMID:2997712
- [15] Lautner-Rieske A. et al., Eur. J. Immunol., 22, 1023-1029 (1992). PMID:1551402
- [16] Liu M.F. et al., J. Immunol., 142, 688-694 (1989). PMID:2492051
- [17] Manheimer-Lory A. et al., J. Exp. Med., 174, 1639-1652 (1991). PMID:1660528
- [18] Pargent W. et al., Eur. J. Immunol., 21, 1821-1827 (1991). PMID:1907917
- [19] Pech M. and Zachau H.G., Nucleic Acids Res., 12, 9229-9236 (1984). PMID:6440122
- [20] Pech M. et al., J. Mol. Biol., 176, 189-204 (1984). PMID:6086934
- [21] Pech M. et al., J. Mol. Biol., 183, 291-299 (1985). PMID:3927006
- [22] Radoux V. et al., J. Exp. Med., 164, 2119-2124 (1986). PMID:3023521
- [23] Schäble K.F. and Zachau, H.G., Biol. Chem. Hoppe-Seyler, 374, 1001-1022 (1993). PMID:8292259
- [24] Schäble K.F. et al., Biol. Chem. Hoppe-Seyler, 375, 189-199 (1994). PMID:8011175
- [25] Scott M.G. et al., J. Immunol., 143, 4110-4116 (1989). PMID:2512350
- [26] Scott M.G. et al., J. Immunol., 147, 4007-4013 (1991). PMID:1940382
- [27] Stavnezer J. et al., Nucleic Acids Res., 13, 3495-3514 (1985). PMID:3925437
- [28] Straubinger B. et al., Biol. Chem. Hoppe-Seyler, 369, 601-607 (1988). PMID:2852016
- [29] Straubinger B. et al., J. Mol. Biol., 199, 23-34 (1988). PMID:3351922
- [30] Timmers E. et al., Eur. J. Immunol., 23, 619-624 (1993). PMID:8449210
- [31] van Es J.H. et al., J. Exp. Med., 173, 461-470 (1991). PMID:1899104
- [32] Youngblood K. et al., J. Clin. Invest., 93, 852-861 (1994). PMID:7509350
- [33] Chen P.P. et al., J. Immunol., 139, 1727-1733 (1987). PMID:3114376
- [34] Schäble K.F., Unpublished.
- [35] Straubinger B. et al., Nucleic Acids Res., 15, 9567-9575 (1987). PMID:2825139
- [36] Lorenz W. et al., Mol. Immunol., 25, 479-484 (1988). PMID:3137458
- [37] Brandt P., Unpublished.
- [38] Chazenbalk G.D. et al., J. Clin. Invest., 92, 62-74 (1993). PMID:7686925
- [39] Suzuki N. et al., J. Clin. Invest., 98, 1843-1850 (1996). PMID:8878436
- [40] Juul L. et al., Immunogenetics, 48, 40-46 (1998). PMID:9601942
- [41] Juul L. et al., Tissue Antigens, 49, 595-604 (1997). PMID:9234481
- [42] Collins A.M. et al., Unpublished.
- [43] Watson C.T. et al., Genes and Immunity, 16, 24-34 (2015). PMID:25338678
- [44] Vazquez Bernat N. et al., Front. Immunol., 10, 660-660(2019). PMID:31024532
- [45] Mikocziova I., Unpublished.
- [46] Ladeana W Hillier et al., Nature, 434(7034), 724-31 (2005). PMID:15815621
Chromosomal orphon set IGKV
IMGT subgroup |
IMGT gene name |
IMGT allele name |
Fct |
Chromosomal localization |
R |
T |
Pr |
Positions in the locus |
IMGT/LIGM-DB reference sequences |
IMGT/LIGM-DB sequences from the literature |
Clone names |
Accession numbers |
Positions in the sequence |
Secondary accession numbers |
Clone names |
Accession numbers |
Positions in the sequence |
IGKV1 |
|
|
|
IGKV1/OR-2 |
|
|
|
IGKV1/OR-2*01 |
|
|
|
P |
|
(2) |
|
Outside chr2 |
[7] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Z2 |
|
|
MAP |
|
|
|
|
X64640 |
[7] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
DPK34 |
|
|
|
X93650 |
[2] |
|
|
|
|
|
|
IGKV1/OR-3 |
|
|
|
IGKV1/OR-3*01 |
|
|
|
P |
|
(3) |
|
Outside chr2 |
[7] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Z3 |
|
|
MAP |
|
|
|
|
X64641 |
[7] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
DPK37 |
|
|
|
Z27501 |
[2] |
|
|
|
|
|
|
IGKV1/OR-4 |
|
|
|
IGKV1/OR-4*01 |
|
|
|
P |
|
(4) |
|
Outside chr2 |
[7] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Z4 |
|
|
MAP |
|
|
|
|
X64642 |
[7] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR1-1 |
|
|
|
IGKV1/OR1-1*01 |
|
|
|
P |
|
(5) |
|
Chr1 between 1p13 and 1q12 |
[5] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Chr1 |
|
|
MAP |
|
|
|
|
M20809 |
[11] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-0 |
|
|
|
IGKV1/OR2-0*01 |
|
|
|
ORF |
|
(21) |
|
2p11.2, at, at least, 140 kb in 5' of IGKV3D-7 |
[1] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Z0 |
|
|
MAP |
|
|
|
|
Y08392 |
[1] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-1 |
|
|
|
IGKV1/OR2-1*01 |
|
|
|
P |
|
(1) |
|
2p11.1 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Z1 |
|
|
MAP |
|
|
|
|
M20813 |
[13] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
RP11-389I13 |
|
|
|
AC127391 |
|
|
|
|
|
|
|
IGKV1/OR2-2 |
|
|
|
IGKV1/OR2-2*01 |
|
|
|
P |
|
(1) |
|
2p11.1 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
RP11-271A22 |
|
|
MAP |
|
|
|
|
AC128677 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-3 |
|
|
|
IGKV1/OR2-3*01 |
|
|
|
P |
|
(6) |
|
Long arm of chr2: 2q11.2 |
[9] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
W3 |
|
|
MAP |
|
|
|
|
X05102 |
[6] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-6 |
|
|
|
IGKV1/OR2-6*01 |
|
|
|
P |
|
(7) |
|
Long arm of chr2: 2q11.2 |
[9] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
W6 |
|
|
MAP |
|
|
|
|
X05103 |
[6] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-9 |
|
|
|
IGKV1/OR2-9*01 |
|
|
|
P |
|
(6) |
|
Long arm of chr2: 2q11.2 |
[9] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
W9 |
|
|
MAP |
|
|
|
|
X51879 |
[9] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-11 |
|
|
|
IGKV1/OR2-11*01 |
|
|
|
P |
|
(6) |
|
Long arm of chr2: 2q11.2 |
[9] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
W11 |
|
|
MAP |
|
|
|
|
X51885 |
[9] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-108 |
|
|
|
IGKV1/OR2-108*01 |
|
|
|
ORF |
|
|
|
Long arm of chr2: 2q12-14 |
[8,3] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
V108 |
|
|
MAP |
|
|
|
|
X51887 |
[3] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
IGKV1/OR2-118 |
|
|
|
IGKV1/OR2-118*01 |
|
|
|
P |
|
(28) |
|
2p11.1 |
|
(29) |
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MAP |
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AC018696 |
[16] |
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IGKV1/OR9-1 |
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IGKV1/OR9-1*01 |
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P |
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(1) |
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Chr9, at 9q21.11 |
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MAP |
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AL512605 |
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IGKV1/OR9-2 |
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IGKV1/OR9-2*01 |
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P |
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(1) |
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9p12 |
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RP11-1221G12 |
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MAP |
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AC129778 |
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IGKV1/OR10-1 |
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IGKV1/OR10-1*01 |
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P |
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(34) |
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Chr10, at 10q11.21 |
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Y237C10 |
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MAP |
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AL031601 |
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ABC16-2334G3 |
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AC238517 |
[18] |
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IGKV1/OR15-118 |
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IGKV1/OR15-118 |
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P |
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(9) |
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Chr15, 15 pter-15qter |
[4] |
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VkappaIcos118 |
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MAP |
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M20812 |
[11] |
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IGKV1/OR22-1 |
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IGKV1/OR22-1*01 |
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P |
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(10) |
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Chr22, at 22q11 |
[4,15] |
(22) |
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VkappaI, Chr22-1 |
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MAP |
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Z00040 |
[4] |
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IGKVP5 |
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AC006548 |
[10] |
(23) |
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IGKV1/OR22-5 |
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IGKV1/OR22-5*01 |
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P |
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(11) |
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Chr22, at 22q11 |
[5,15] |
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Chr22-5 |
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MAP |
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Z00003 |
[12] |
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V14 |
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V2b |
[8] |
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MAP |
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Z00003 |
[12] |
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IGKVP7 |
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AC006548 |
[10] |
(24) |
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IGKV1/OR22-5*02 |
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P |
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(11) |
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Chr22, at 22q11 |
[5,15] |
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Chr22-5a |
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MAP |
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Z00002 |
[12] |
(22) |
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M23849 |
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IGKV1/ORY-1 |
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IGKV1/ORY-1 |
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P |
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(31) |
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ChrY |
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RP11-295P22 |
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MAP |
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AC134879 |
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IGKV2 |
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IGKV2/OR2-1 |
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IGKV2/OR2-1*01 |
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P |
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(8) |
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Long arm of chr2: 2q11.2 |
[9] |
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W1 |
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MAP |
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X05101 |
[6] |
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W1a |
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X76074 |
[8] |
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IGKV2/OR2-2 |
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IGKV2/OR2-2*01 |
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P |
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(12) |
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Long arm of chr2: 2q11.2 |
[9] |
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W2 |
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MAP |
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X51884 |
[9] |
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DPK32 |
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X93648 |
[2] |
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IGKV2/OR2-4 |
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IGKV2/OR2-4*01 |
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P |
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(13) |
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Long arm of chr2: 2q11.2 |
[9] |
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W4 |
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MAP |
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X51883 |
[9] |
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IGKV2/OR2-7 |
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IGKV2/OR2-7*01 |
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P |
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(14) |
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Long arm of chr2: 2q11.2 |
[9] |
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W7 |
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MAP |
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X51881 |
[9] |
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IGKV2/OR2-7D |
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IGKV2/OR2-7D*01 |
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P |
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(33) |
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2q11.2 |
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(30) |
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MAP |
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AC092683 |
[17] |
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IGKV2/OR2-8 |
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IGKV2/OR2-8*01 |
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P |
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(15) |
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Long arm of chr2: 2q11.2 |
[9] |
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W8 |
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MAP |
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X51880 |
[9] |
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DPK33 |
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X93649 |
[2] |
(32) |
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IGKV2/OR2-10 |
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IGKV2/OR2-10*01 |
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P |
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(16) |
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Long arm of chr2: 2q11.2 |
[9] |
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W10 |
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MAP |
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X51886 |
[9] |
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DPK33 |
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(32) |
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IGKV2/OR22-3 |
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IGKV2/OR22-3*01 |
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P |
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(17) |
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Chr22, at 22q11 |
[4,15] |
(22) |
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VkappaII, Chr22-3 |
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MAP |
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Z00041 |
[4] |
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IGKVP4 |
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AC006548 |
[10] |
(25) |
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IGKV2/OR22-4 |
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IGKV2/OR22-4*01 |
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P |
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(18) |
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Chr22, at 22q11 |
[5,15] |
(22) |
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Chr22-4 |
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MAP |
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M20707 |
[11] |
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DPK36 |
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X93652 |
[2] |
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IGKVP6 |
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AC006548 |
[10] |
(26) |
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IGKV3 |
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IGKV3/OR2-5 |
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IGKV3/OR2-5*01 |
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P |
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(19) |
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Long arm of chr2: 2q11.2 |
[9] |
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W5 |
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MAP |
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X51882 |
[9] |
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IGKV3/OR2-268 |
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IGKV3/OR2-268*01 |
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ORF |
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2p12, 3' side of IGKC at 1.5Mb |
[8,14] |
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V268 |
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MAP |
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X74459 |
[14] |
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IGKV3/OR2-268*02 |
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ORF |
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2p12, 3' side of IGKC at 1.5Mb |
[8,14] |
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V268a |
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MAP |
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X74460 |
[14] |
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IGKV3/OR22-2 |
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IGKV3/OR22-2*01 |
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P |
|
(20) |
|
Chr22, at 22q11 |
[4,15] |
(22) |
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VkappaIII, Chr22-2 |
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MAP |
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Z00042 |
[4] |
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IGKVP3 |
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AC006548 |
[10] |
(27) |
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MAP: Mapped sequences.
IMGT notes:
- (1) No INIT-CODON: ATG replaced by ACG.
- (2) No INIT-CODON: ATG replaced by ACG [7].
- (3) No INIT-CODON: ATG replaced by AAG [7].
- (4) No INIT-CODON: ATG replaced by ACA [7].
- (5) No INIT-CODON: ATG replaced by ACA.
- (6) STOP-CODON at position 87.
- (7) STOP-CODONs at position -5 and 91, and 10 bp DELETION between codons 91/92 [6].
- (8) STOP-CODONs at positions 35 and 36, and INSERTION of 2 bp in codon 87, leading to a frameshift [6].
- (9) STOP-CODON at position 87, and no INIT-CODON: ATG replaced by ACA.
- (10) INSERTION of 7 bp at position 1093 leading to a frameshift [4].
- (11) STOP-CODON at position 71 (87 IMGT numbering), and no INIT-CODON: ATG replaced by ACG [seq].
- (12) 1 bp DELETION at position 740, 1 bp DELETION at position 935 leading to frameshifts, and STOP-CODON in L-PART1.
- (13) 1 bp DELETION in L-PART1, STOP-CODON at position 36, and 2 bp INSERTION between positions 1046/1047 leading to a frameshift.
- (14) STOP-CODON at position 36, INSERTION of 2 bp at position 957 leading to a frameshift.
- (15) STOP-CODON in L-PART1, 1 bp DELETION at positions 731 and 925 leading to frameshifts.
- (16) STOP-CODON in L-PART1, 1 bp DELETION at positions 744 and 938 leading to frameshifts.
- (17) INSERTION of 3 bp between codons 22 and 23, DELETION of 1 bp at position 315 leading to a frameshift, and STOP-CODONs.
- (18) STOP-CODON at position 81.
- (19) No INIT-CODON: ATG replaced by ACG, 2 bp DELETIONs at positions 727, 831 and 833, 1 bp DELETION at position 747, leading to frameshifts.
- (20) Breakoff of homology after codon 79, STOP-CODONs and DELETION [4].
- (21) Defective DECAMER, non canonical V-HEPTAMER and V-NONAMER [1].
- (22) The five IGKV/OR22-5 orphons are localized on a 30 kb DNA stretch at 1,3 Mb of the centromere sequences [10].The 5' end of the cluster is telomeric, whereas the 3' end is centromeric.
- (23) V-REGION is 100% identical to Z00040.
- (24) V-REGION is 100% identical to Z00002.
- (25) V-REGION is 99% identical to Z00041. 4 bp (ttgt) DELETION at the same position as the Z00041 1bp DELETION leading to a frameshift. Otherwise, identity with Z00041, with the same STOP-CODONs.
- (26) V-REGION is 100% identical to M20707. AC006548 has an one nucleotide insertion (g) in the V-INTRON.
- (27) V-REGION is 99% identical to Z00042. AC006548 has an one nucleotide deletion in the FR1-IMGT compared to Z00042.
- (28) no INIT-CODON: ATG replaced by ACA.
- (29) Gene identified on Genome assembly Built 37.1 at NCBI on AC018696 (plus/minus), 110698..111148 (M. Landrum, R. Seal, G. Folch and M.-P. lefranc, IMGT (26/10/2009)).
- (30) Gene identified on Genome assembly Built 37.1 at NCBI on AC092683, 103208..103976 (M. Landrum, R. Seal, G. Folch and M.-P. lefranc, IMGT (26/10/2009)).
- (31) No INIT-CODON due to a nucleotide substitution t>c and an amino acid change M>T'.
- (32) DPK33 could not be assigned to either IGKV2/OR2-8 or IGKV2/OR2-10 by the authors.
- (33) STOP-CODON in V-REGION.
- (34) No INIT-CODON: ATG replaced by GTG.
IMGT references:
- [1] Brensing-Küppers, J. et al., Gene, 191, 173-181 (1997). PMID:9218717
- [2] Cox, J.P. et al., Eur. J. Immunol., 24, 827-836 (1994). PMID:8149953
- [3] Huber, C. et al., Nucl. Acids Res., 18, 3475-3478 (1990). PMID:2114012
- [4] Lötscher, E. et al., Nature, 320, 456-458 (1986). PMID:3083265
- [5] Meindl, A. et al., Eur. J. Immunol., 20, 1855-1863 (1990). PMID:1976522
- [6] Pohlenz, H.D. et al., J. Mol. Biol., 193, 241-253 (1987). PMID:3037085
- [7] Röschenthaler, F. et al., Biol. Chem. Hoppe-Seyler, 373, 177-186 (1992). PMID:1596359
- [8] Schäble, K. F. and Zachau, H. G., Biol. Chem. Hoppe-Seyler, 374, 1001-1022 (1993). PMID:8292259
- [9] Zimmer, F.J. et al., Biol. Chem. Hoppe-Seyler, 371, 283-290 (1990). PMID:2111145
- [10] Dunham, I. et al., Nature, 402, 489-495 (1999). PMID:10591208
- [11] Lötscher, E. et al., Gene, 69, 215-223 (1988). PMID:2853099
- [12] Jaenichen, H.R. et al., Nucleic Acid. Res., 12, 5249-5263 (1984). PMID:6087279
- [13] Straubinger, B. et al., Gene, 69, 209-214 (1988). PMID:2853098
- [14] Huber, C. et al., Genomics, 22, 213-215 (1994). PMID:7959772
- [15] Adolph, S. et al., Nucl. Acids Res., 16, 6241 (1988). PMID:3135538
- [16] Ozersky P. et al., Unpublished.
- [17] Cotton M. et al., Unpublished.
- [18] Schatzkamer K. et al., Unpublished.
See also (IMGT Scientific chart):
- Created:
- 03/02/1997
- Last updated:
- 22/09/2023
- Authors:
- Valérie Barbié, Dominique Scaviner