Citing IMGT dynamic tools: Sanou G., Zeitoun G. et al. IMGT® at scale: FAIR, Dynamic and Automated Tools for Immune Locus Analysis, Nucleic Acids Research. 2025;,gkaf1024. doi: 10.1093/nar/gkaf1024 (Free Article) PMID: 41091930.
Program version: v. 

Add information about removed genes/alleles.
May 15th, 2025.

Add the possibility to obtain a gene table per strain (for mouse now and for other species later) and allotypes/isotypes for human.
September 25th, 2024.

Bibliographical references in alphabetic order, small design changes and addition of "NL" for non-localized gene.
June 14th, 2024.

Addition of 'Score for IMGT allele confirmation' as well as NCBI TPA accession numbers.
September 20th, 2023.

Implementation of the dynamic gene table.

Gene table legend:

"+" 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 in 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.

IMGT allele confirmation: A scoring system is employed to indicate the number of IMGT/LIGM-DB reference sequences and other sequences from the literature in which an IG or TR gene allele has been identified and annotated.

Removed genes/alleles
If a gene/allele existence or name has to be changed, the old name or gene/allele would be deleted and its name won't be reused. They are kept in the gene table for historical reasons.
A single star ()
indicates that an IG or TR gene allele is annotated in the reference sequence only.
Two stars ()
indicate that an IG or TR gene allele is annotated in its reference sequence and in one sequence from the literature.
Three stars ()
indicate that an IG or TR gene allele is annotated in its reference sequence and in at least two sequences from the literature.
In the Excel file, the stars are represented by the plus symbol (+).

Click on:
  • IMGT gene name to get the corresponding IMGT/GENE-DB entry (link).
  • IMGT allele name to see the corresponding Alignments of alleles (link).
  • Accession number to get the corresponding IMGT/LIGM-DB entry (link).
  • MAP: mapped sequences. Click to access GENE-DB «LOCALIZATION IN GENOME ASSEMBLIES» (link).
  • [number] to access the corresponding IMGT reference (popover).
  • (number) to see the corresponding IMGT note (popover).
Options:
  • You can show/hide columns (), download data () or put the table in fullscreen () using buttons.
See also (IMGT Scientific chart):
Select a species and a IMGT group to get the gene table:
Only IMGT available species/group are shown in the drop-down list.
The gene table can take several seconds to appear, please be patient.

TRBV genes are designated by a number for the subgroup followed, whenever there are several genes belonging to the same subgroup, by a dash and a number for their relative localisation in the locus at 6A-C. Numbers increase from 5' to 3' in the locus.

Gene table of house mouse (Mus musculus) TRBV IMGT group:
IMGT sub­groupIMGT gene nameIMGT allele nameScore for
IMGT allele
confirmation
FctChromosomosal
localization
R T PrIMGT/LIGM-DB reference sequencesIMGT/LIGM-DB sequences from the literature
Clone namesStrainAccession
numbers
Positions
in the sequence
(L-V-GENE-UNIT)
or V-REGION (*)
Secondary
accession
numbers
Clone namesStrainAccession
numbers
Positions
in the sequence
(L-V-GENE-UNIT)
or V-REGION (*)
TRBV1TRBV1 TRBV1*01 F 6B1 (20.5 cM)
RTPr
+++
V2S1 BALB/c AE000663 [7,26,27] MAP 13939-14225 * C57BL/6J IMGT000132 [10,11] 12503-13131
TRBV1TRBV1 TRBV1*02 (F) 6B1 (20.5 cM)
RTPr
+++
BALB/c X01642 [23] #c 129-412 *
TRBV2TRBV2 TRBV2*01 F 6B1 (20.5 cM)
RTPr
+++
V4S1 BALB/c AE000663 [7,26,27] MAP 169794-170272 C57BL/6J IMGT000132 [10,11] 168763-169241
TRBV3TRBV3 TRBV3*01 F 6B1 (20.5 cM)
RTPr
+++
V16S1 BALB/c AE000663 [7,26,27] MAP 170632-171101 C57BL/6J IMGT000132 [10,11] 169601-170070
TRBV3TRBV3 TRBV3*02 (F) (1) 6B1 (20.5 cM)
RTPr
+++
VbetaB10 B10.A (15) X03865 [13] #c 154-442 *
TRBV4TRBV4 TRBV4*01 (2) 6B1 (20.5 cM)
RTPr
+++
Vbeta10 C57BL/6 X56725 [15] MAP 17-499 V10S1 BALB/c AE000663 [7,26,27] 181842-182128 *
C57BL/6J IMGT000132 [10,11] 180650-181132
TRBV4TRBV4 TRBV4*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta10 SWR/J AJ249819 [30] #c 1-282 *
TRBV5TRBV5 TRBV5*01 F 6B1 (20.5 cM)
RTPr
+++
V1S1 BALB/c AE000663 [7,26,27] MAP 184601-185084 C57BL/6J IMGT000132 [10,11] 183566-184049
TRBV5TRBV5 TRBV5*02 (F) (1) 6B1 (20.5 cM)
RTPr
+++
BALB/c X00438 [14] #c 80-360 *
TRBV5TRBV5 TRBV5*03 (F) (1) 6B1 (20.5 cM)
RTPr
+++
Vbeta1 AKR X02779 [1] #c 58-338 *
TRBV5TRBV5 TRBV5*04 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta1 B10.S(9R) (15) M20878 [21] #c 7-288 *
TRBV5TRBV5 TRBV5*05 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta1 SWR/J AJ249820 [30] #c 1-279 *
TRBV6TRBV6 TRBV6*01 (3) 6B1 (20.5 cM) V26S1P BALB/c AE000663 [7,26,27] MAP 189111-189433 C57BL/6J IMGT000132 [10,11] 188086-188361 *
TRBV7TRBV7 TRBV7*01 (4) 6B1 (20.5 cM) V27S1P BALB/c AE000663 [7,26,27] MAP 202600-202890 * C57BL/6J IMGT000132 [10,11] 201571-201861 *
TRBV8TRBV8 TRBV8*01 (5) 6B1 (20.5 cM) V28S1P BALB/c AE000663 [7,26,27] MAP 206906-207378 C57BL/6J IMGT000132 [10,11] 205876-206348
TRBV9TRBV9 TRBV9*01 (6) 6B1 (20.5 cM) VbetaN8 BALB/c X16693 [19] MAP (16) 1-290 * V24S1P BALB/c AE000663 [7,26,27] 210236-210525 *
C57BL/6J IMGT000132 [10,11] 209206-209495 *
TRBV10TRBV10 TRBV10*01 (7) 6B1 (20.5 cM) VbetaN9 BALB/c X16694 [19] MAP (16) 1-289 * V25S1P BALB/c AE000663 [7,26,27] 214173-214504
C57BL/6J IMGT000132 [10,11] 213147-213435 *
TRBV11TRBV11 TRBV11*01 (8) 6B1 (20.5 cM) V29S1P BALB/c AE000663 [7,26,27] MAP 229282-229541 * C57BL/6J IMGT000132 [10,11] 228012-228547
TRBV12TRBV12-1 TRBV12-1*01 F 6B1 (20.5 cM)
RTPr
++
Vbeta5.2 C57BL/6 M15614 [9] MAP 13-552 V5S2 BALB/c AE000663 [7,26,27] 236021-236305 *
C57BL/6J IMGT000132 [10,11] 234774-235313
TRBV12TRBV12-1 TRBV12-1*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta5.2 NZW M30881 [3] #c 109-390 *
TRBV12TRBV12-2 TRBV12-2*01 F 6B1 (20.5 cM)
RTPr
++
Vbeta5.1 C57BL/6 M15613 [9] MAP 13-558 V5S1 BALB/c AE000663 [7,26,27] 241318-241602 *
C57BL/6J IMGT000132 [10,11] 240071-240610
TRBV12TRBV12-2 TRBV12-2*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta5.1 BALB/c X02782 [1] #c 3-284 *
TRBV12TRBV12-3 TRBV12-3*01 (9) 6B1 (20.5 cM) Vbeta5.3 C57BL/6 M15615 [9] MAP 13-538 V5S3P BALB/c AE000663 [7,26,27] 249827-250344
C57BL/6J IMGT000132 [10,11] 248999-249283 *
TRBV13TRBV13-1 TRBV13-1*01 F 6B1 (20.5 cM) Vbeta8.3 C57BL/6 M15618 [9] 158-443 *
TRBV13TRBV13-1 TRBV13-1*02 F 6B1 (20.5 cM)
RTPr
+++
V8S3 BALB/c AE000663 [7,26,27] MAP 238274-238745 C57BL/6J IMGT000132 [10,11] 237243-237714
TRBV13TRBV13-2 TRBV13-2*01 F 6B1 (20.5 cM)
RTPr
++
Vbeta8.2 C57BL/6 M15617 [9] MAP 11-484 V8S2 BALB/c AE000663 [7,26,27] 243632-244107
C57BL/6J IMGT000132 [10,11] 242603-243078
TRBV13TRBV13-2 TRBV13-2*02 (F) (1) 6B1 (20.5 cM)
RTPr
+++
Vbeta8.2 BALB/cnu/nu M27350 [18] (17) #c <1-274 *
TRBV13TRBV13-2 TRBV13-2*03 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta8.2 CBA/J M26417 [16] #c 61-342 *
TRBV13TRBV13-2 TRBV13-2*04 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta8.2 CI27 (18) AJ249823 [24] (19) #c <1-280 *
TRBV13TRBV13-2 TRBV13-2*05 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta8.2 ER34 (18) AJ250103 [24] (19) #c <1-279 *
TRBV13TRBV13-3 TRBV13-3*01 F 6B1 (20.5 cM)
RTPr
++
Vbeta8.1 C57BL/6 M15616 [9] MAP 11-488 V8S1 BALB/c AE000664 [7,26,27] 1829-2306
C57BL/6J IMGT000132 [10,11] 251354-251831
TRBV14TRBV14 TRBV14*01 F 6B1 (20.5 cM)
RTPr
+++
V13S1 BALB/c AE000664 [7,26,27] MAP 6845-7333 C57BL/6J IMGT000132 [10,11] 256374-256862
TRBV15TRBV15 TRBV15*01 F 6B1 (20.5 cM)
RTPr
++
V12S1 BALB/c AE000664 [7,26,27] MAP 12886-13372 C57BL/6J IMGT000132 [10,11] 262418-262904
TRBV16TRBV16 TRBV16*01 F 6B1 (20.5 cM)
RTPr
+++
C57BL/6 L29434 [12] MAP 694-1172 V11S1 BALB/c AE000664 [7,26,27] 23463-23941
C57BL/6J IMGT000132 [10,11] 272998-273476
TRBV16TRBV16 TRBV16*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta5 C57BL/6 M13670 [5] #c 97-381 *
TRBV16TRBV16 TRBV16*03 (F) 6B1 (20.5 cM)
RTPr
+++
C57BL/6 M15459 [25] #c 109-393 *
TRBV16TRBV16 TRBV16*04 (F) (1) 6B1 (20.5 cM)
RTPr
+++
Vbeta11 C57BL/6 X14388 [22] #c 58-343 *
TRBV17TRBV17 TRBV17*01 F 6B1 (20.5 cM)
RTPr
+++
V9S1 BALB/c AE000664 [7,26,27] MAP 34757-35260 C57BL/6J IMGT000132 [10,11] 284299-284802
TRBV18TRBV18 TRBV18*01 (10) 6B1 (20.5 cM) VbetaN5 BALB/c X16692 [19] MAP 1-294 * V23S1P BALB/c AE000664 [7,26,27] 46799-47309
C57BL/6J IMGT000132 [10,11] 296344-296854
TRBV19TRBV19 TRBV19*01 F 6B1 (20.5 cM)
RTPr
+++
V6S1 BALB/c AE000664 [7,26,27] MAP 50251-50749 C57BL/6J IMGT000132 [10,11] 299796-300294
TRBV19TRBV19 TRBV19*02 (F) (1) 6B1 (20.5 cM)
RTPr
+++
C57BL/6 X01643 [23] #c 233-517 *
TRBV19TRBV19 TRBV19*03 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta6 SWR/J AJ249821 [30] #c 1-282 *
TRBV20TRBV20 TRBV20*01 F 6B1 (20.5 cM)
RTPr
+++
V15S1 BALB/c AE000664 [7,26,27] MAP 59936-60679 C57BL/6J IMGT000132 [10,11] 309480-310223
TRBV20TRBV20 TRBV20*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta15 SJL M11859 [2,4] #c 40-327 *
TRBV21TRBV21 TRBV21*01 ORF 6B1 (20.5 cM) Vbeta19 BALB/c X16691 [19] MAP (20) 1-290 * V19S1P BALB/c AE000664 [7,26,27] 74250-74746
C57BL/6J IMGT000132 [10,11] 323794-324290
TRBV22TRBV22 TRBV22*01 (11) 6B1 (20.5 cM) Vbeta3.3P BALB/c X16690 [19] MAP (20) 1-291 * V22S1P BALB/c AE000664 [7,26,27] 83741-84239
C57BL/6J IMGT000132 [10,11] 333282-333780
TRBV23TRBV23 TRBV23*01 F 6B1 (20.5 cM) V20S1 BALB/c AE000664 [7,26,27] MAP 87903-88192 * Vbeta20 BALB/c X59150 [29] 235-524 *
C57BL/6J IMGT000132 [10,11] 337280-337771
TRBV24TRBV24 TRBV24*01 F 6B1 (20.5 cM) Vbeta17a2 PWK M61184 [6] 178-467 *
TRBV24TRBV24 TRBV24*02 (12) 6B1 (20.5 cM) V17S1 BALB/c AE000664 [7,26,27] MAP 89934-90223 * C57BL/6J IMGT000132 [10,11] 339298-339803
TRBV24TRBV24 TRBV24*03 (ORF) 6B1 (20.5 cM)
RTPr
++
Vbeta17a1 BALB/c M16203 [17] #g 184-471 *
TRBV24TRBV24 TRBV24*04 (F) 6B1 (20.5 cM)
RTPr
+
VB17a CzechII L48997 [31] #g 58-345 *
TRBV25TRBV25 TRBV25*01 (13) 6B1 (20.5 cM) VbetaN1 BALB/c X16689 [19] MAP 7-279 * V21S1P BALB/c AE000664 [7,26,27] <93594-93870 *
C57BL/6J IMGT000132 [10,11] 343138-343410 *
TRBV26TRBV26 TRBV26*01 F 6B1 (20.5 cM)
RTPr
+++
B10.A K02548 [8] MAP 2-291 * V3S1 BALB/c AE000664 [7,26,27] 99364-99653 *
C57BL/6J IMGT000132 [10,11] 348732-349239
TRBV26TRBV26 TRBV26*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta3 SWR/J AJ249822 [30] #c 1-285 *
TRBV27TRBV27 TRBV27*01 (14) 6B1 (20.5 cM) V30S1P BALB/c AE000664 [7,26,27] MAP 129825-130101 * C57BL/6J IMGT000132 [10,11] 379510-379786 *
TRBV28TRBV28 TRBV28*01 (14) 6B1 (20.5 cM) V31S1P BALB/c AE000664 [7,26,27] MAP 138214-138706 C57BL/6J IMGT000132 [10,11] 387904-388396
TRBV29TRBV29 TRBV29*01 F 6B1 (20.5 cM)
RTPr
+++
V7S1 BALB/c AE000664 [7,26,27] MAP 142920-143437 C57BL/6J IMGT000132 [10,11] 392610-393127
TRBV29TRBV29 TRBV29*02 (F) 6B1 (20.5 cM)
RTPr
+++
BALB/c X00696 [28] #c 36-311 *
TRBV30TRBV30 TRBV30*01 F 6B1 (20.5 cM)
RTPr
+++
Vbeta18 BALB/c X16695 [19] MAP (20) 1-290 * V18S1 BALB/c AE000664 [7,26,27] 153218-153507 *
C57BL/6J IMGT000132 [10,11] 402583-403236
TRBV31TRBV31 TRBV31*01 F 6B1 (20.5 cM)
RTPr
+++
Vbeta14 BALB/c X03277 [20] MAP 427-710 * V14S1 BALB/c AE000665 [7,26,27] (21) complement(177699-177982) *
C57BL/6J IMGT000132 [10,11] complement(678860-679577)
TRBV31TRBV31 TRBV31*02 (F) 6B1 (20.5 cM)
RTPr
+++
Vbeta14 B10.A M26418 [16] #c 1-281 *
IMGT notes:
  1. The position 3' end is determined by IMGT/JunctionAnalysis by comparison with the *01 allele. Note that the percentage of identity is evaluated by comparison with ethe closest allele identified by IMGT/V-QUEST
  2. The last codon of IMGT_CDR3 of the V-REGION is a STOP-CODON, which may disappear during rearrangement
  3. Pseudogene because of no L-PART1, frameshift in V-EXON
  4. Pseudogene because of STOP-CODON in L-PART1, gat instead of ggt in DONOR_SPLICE, Frameshift in V-EXON
  5. Pseudogene because of STOP-CODON in IMGT-FR2 of V-REGION
  6. STOP-CODON in V-REGION
  7. No L-PART1, no 1st-CYS, no 2nd-CYS
  8. Pseudogene because of frameshift in V-EXON
  9. Frameshift in IMGT-FR1 of V-REGION, STOP-CODON in IMGT-FR3 of V-REGION
  10. STOP-CODON in V-REGION, Frameshift in V-REGION
  11. STOP-CODON in V-REGION, frameshift in IMGT-FR3 of V-REGION
  12. Pseudogene because of STOP-CODON in IMGT-FR3
  13. STOP-CODON in V_REGION, frameshift in V-REGION
  14. pseudogene because of frameshift in V-REGION
  15. B10.A and B10.S[9R] are congenics strains, B10 is the abbreviated symbol of C57BL/10.
  16. V-EXON is partial: no L-PART2.
  17. V-REGION is partial: AA 1 to 3 are absent (partial FR1-IMGT).
  18. CI27 and ER34 are wild mice.
  19. V-REGION is partial: AA 1 and 2 are absent (partial FR1-IMGT).
  20. V-GENE is partial: no L-PART1, no L-PART2.
  21. In the TRB locus the TRBV14 gene is localised 3' from the TRBC2 gene and is in an inverted orientation of transcription.
IMGT references:
  1. Barth R.K. et al., The murine T-cell receptor uses a limited repertoire of expressed V beta gene segments, Nature, vol. 316, no. 6028, 1985, pp. 517-523. DOI: 10.1038/316517a0
  2. Behlke M.A, Unpublished.
  3. Behlke M.A. and Loh D.Y, Alternative splicing of murine T-cell receptor beta-chain transcripts, Nature, vol. 322, no. 6077, 1986, pp. 379-382. DOI: 10.1038/322379a0
  4. Behlke M.A. et al., Murine T-cell receptor mutants with deletions of beta-chain variable region genes, Proc. Natl. Acad. Sci. U.S.A, vol. 83, no. 3, 1986, pp. 767-771. PUBMED: 3456168
  5. Behlke M.A. et al., T-cell receptor beta-chain expression: dependence on relatively few variable region genes, Science, vol. 229, no. 4713, 1985, pp. 566-570. PUBMED: 3875151
  6. Cazenave P.-A. et al., V beta 17 gene polymorphism in wild-derived mouse strains: two amino acid substitutions in the V beta 17 region greatly alter T cell receptor specificity, Cell, vol. 63, no. 4, 1990, pp. 717-728. DOI: 10.1016/0092-8674(90)90138-5
  7. Chen F. et al., Differential transcriptional regulation of individual TCR V beta segments before gene rearrangement, J. Immunol, vol. 166, no. 3, 2001, pp. 1771-1780. PUBMED: 11160223
  8. Chien Y.-H. et al., Somatic recombination in a murine T-cell receptor gene, Nature, vol. 309, no. 5966, 1984, pp. 322-326. DOI: 10.1038/309322a0
  9. Chou H.S. et al., Tandem linkage and unusual RNA splicing of the T-cell receptor beta-chain variable-region genes, Proc. Natl. Acad. Sci. U.S.A, vol. 84, no. 7, 1987, pp. 1992-1996. PUBMED: 3470773
  10. Church,D.M. et al., Lineage-specific biology revealed by a finished genome assembly of the mouse, PLoS Biol (2009), PUBMED: 19468303
  11. Church,D.M. et al., Modernizing reference genome assemblies, PLoS Biol, vol. 9, no. 7, 2011, PUBMED: 21750661
  12. Epplen J.T. et al., Change in antigen specificity of cytotoxic T lymphocytes is associated with the rearrangement and expression of a T-cell receptor beta-chain gene, Proc. Natl. Acad. Sci. U.S.A, vol. 83, no. 12, 1986, pp. 4441-4445. PUBMED: 3487087
  13. Fink P.J. et al., Correlations between T-cell specificity and the structure of the antigen receptor, Nature, vol. 321, no. 6067, 1986, pp. 219-226. DOI: 10.1038/321219a0
  14. Hedrick S.M. et al., Sequence relationships between putative T-cell receptor polypeptides and immunoglobulins, Nature, vol. 308, no. 5955, 1984, pp. 153-158. DOI: 10.1038/308153a0
  15. Hirama T. et al., Conserved V(D)J junctional sequence of cross-reactive cytotoxic T cell receptor idiotype and the effect of a single amino acid substitution, Eur. J. Immunol, vol. 21, no. 2, 1991, pp. 483-488. PUBMED: 1705514
  16. Johnson N.A. et al., T cell receptor gene segment usage in a panel of hen-egg white lysozyme specific, I-Ak-restricted T helper hybridomas, J. Immunol, vol. 142, no. 9, 1989, pp. 3298-3304. PUBMED: 2468715
  17. Kappler J.W. et al., A T cell receptor V beta segment that imparts reactivity to a class II major histocompatibility complex product, Cell, vol. 49, no. 2, 1987, pp. 263-271. DOI: 10.1016/0092-8674(87)90567-8
  18. Kishihara K. et al., Functional alpha and beta T cell chain receptor messages can be detected in old but not in young athymic mice, Eur. J. Immunol, vol. 17, no. 4, 1987, pp. 477-482. PUBMED: 2883009
  19. Louie M.C. et al., Identification and Characterization of New Murine T-Cell Receptor beta-chain Variable-Region (V-beta) Genes, J. Exp. Med, vol. 170, no. 6, 1989, pp. 1987-1998. DOI: 10.1084/jem.170.6.1987
  20. Malissen M. et al., Direct evidence for chromosomal inversion during T-cell receptor beta-gene rearrangements, Nature, vol. 319, no. 6048, 1986, pp. 28-33. DOI: 10.1038/319028a0
  21. McElligott D.L. et al., Two distinct mechanisms account for the immune response (Ir) gene control of the T cell response to pigeon cytochrome c, J. Immunol, vol. 140, no. 12, 1988, pp. 4123-4131. PUBMED: 2453567
  22. Palmer M.S. et al., The T cell receptor from an influenza-A specific murine CTL clone, Nucleic Acids Res, vol. 17, no. 6, 1989, pp. 2353-2353. DOI: 10.1093/nar/17.6.2353
  23. Patten P. et al., Structure, expression and divergence of T-cell receptor beta-chain variable regions, Nature, vol. 312, no. 5989, 1984, pp. 40-46. DOI: 10.1038/312040a0
  24. Pullen A.M. et al., Surprisingly uneven distribution of the T cell receptor V beta repertoire in wild mice, J. Exp. Med, vol. 171, no. 1, 1990, pp. 49-62. DOI: 10.1084/jem.171.1.49
  25. Rinaldy A. et al., A highly homologous T-cell receptor beta-chain variable region is expressed in mouse and human T cells, Immunogenetics, vol. 21, no. 4, 1985, pp. 403-406. DOI: 10.1007/BF00430805
  26. Rowen L. et al., Comparison of the human and mouse T cell receptor beta and trypsinogen loci, Unpublished.
  27. Rowen L. et al., Sequence of the mouse T cell receptor locus, Unpublished.
  28. Saito H. et al., Complete primary structure of a heterodimeric T-cell receptor deduced from cDNA sequences, Nature, vol. 309, no. 5971, 1984, pp. 757-762. DOI: 10.1038/309757a0
  29. Six A. et al., Identification of a T cell receptor beta chain variable region, V beta 20, that is differentially expressed in various strains of mice, J. Exp. Med, vol. 174, no. 5, 1991, pp. 1263-1266. DOI: 10.1084/jem.174.5.1263
  30. Smith L.R. et al., Coding sequence polymorphisms among V beta T cell receptor genes, J. Immunol, vol. 144, no. 8, 1990, pp. 3234-3237. PUBMED: 2139080
  31. Tomonari K. et al., Influence fo allelic differences of VB17a on VB17a positive selection, Unpublished.