TRBV28 (T cell receptor beta variable 28) - Rat Genome Database

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Gene: TRBV28 (T cell receptor beta variable 28) Homo sapiens
Analyze
Symbol: TRBV28
Name: T cell receptor beta variable 28
RGD ID: 1352321
HGNC Page HGNC:12209
Description: Predicted to enable peptide antigen binding activity. Predicted to be involved in cell surface receptor signaling pathway. Predicted to be located in membrane. Predicted to be part of T cell receptor complex. Predicted to be active in plasma membrane.
Type: gene (Ensembl: TR_V_gene)
RefSeq Status: VALIDATED
Previously known as: TCRBV28S1; TCRBV3S1
RGD Orthologs
Mouse
Dog
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Annotation category: partial on reference assembly
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387142,720,680 - 142,721,160 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7142,720,660 - 142,721,160 (+)EnsemblGRCh38hg38GRCh38
GRCh377142,428,504 - 142,428,984 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367142,108,085 - 142,108,565 (+)NCBINCBI36Build 36hg18NCBI36
Celera7137,235,275 - 137,235,755 (+)NCBICelera
Cytogenetic Map7q34NCBI
HuRef7136,756,999 - 136,757,479 (+)NCBIHuRef
CHM1_17142,354,652 - 142,355,132 (+)NCBICHM1_1
T2T-CHM13v2.07144,076,387 - 144,076,867 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References
Additional References at PubMed
PMID:1660526   PMID:8163948   PMID:8650574   PMID:21873635  


Genomics

Comparative Map Data
TRBV28
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387142,720,680 - 142,721,160 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7142,720,660 - 142,721,160 (+)EnsemblGRCh38hg38GRCh38
GRCh377142,428,504 - 142,428,984 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367142,108,085 - 142,108,565 (+)NCBINCBI36Build 36hg18NCBI36
Celera7137,235,275 - 137,235,755 (+)NCBICelera
Cytogenetic Map7q34NCBI
HuRef7136,756,999 - 136,757,479 (+)NCBIHuRef
CHM1_17142,354,652 - 142,355,132 (+)NCBICHM1_1
T2T-CHM13v2.07144,076,387 - 144,076,867 (+)NCBIT2T-CHM13v2.0
Trbv29
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39641,248,337 - 41,248,815 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl641,248,328 - 41,248,815 (+)EnsemblGRCm39 Ensembl
GRCm38641,271,403 - 41,271,881 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl641,271,394 - 41,271,881 (+)EnsemblGRCm38mm10GRCm38
MGSCv37641,221,402 - 41,221,880 (+)NCBIGRCm37MGSCv37mm9NCBIm37
Celera641,226,046 - 41,226,524 (+)NCBICelera
Cytogenetic Map6B1NCBI
cM Map619.38NCBI
TRBV28
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1166,794,932 - 6,796,547 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl166,767,154 - 6,795,545 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha167,653,100 - 7,654,191 (-)NCBIDog10K_Boxer_Tasha


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q34-35(chr7:141126407-145652221)x3 copy number gain See cases [RCV000133645] Chr7:141126407..145652221 [GRCh38]
Chr7:140826207..145349314 [GRCh37]
Chr7:140472676..144980247 [NCBI36]
Chr7:7q34-35		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q34(chr7:142620494-142732123)x1 copy number loss See cases [RCV000135131] Chr7:142620494..142732123 [GRCh38]
Chr7:142328008..142455543 [GRCh37]
Chr7:142009000..142135117 [NCBI36]
Chr7:7q34		 benign
GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3 copy number gain See cases [RCV000136592] Chr7:137751200..154815582 [GRCh38]
Chr7:137435946..154607292 [GRCh37]
Chr7:137086486..154238225 [NCBI36]
Chr7:7q33-36.2		 pathogenic
GRCh38/hg38 7q34(chr7:142699919-142764809)x1 copy number loss See cases [RCV000136164] Chr7:142699919..142764809 [GRCh38]
Chr7:142087312..142152233 [NCBI36]
Chr7:7q34		 benign
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3		 pathogenic
GRCh38/hg38 7q34(chr7:142237788-142779344)x3 copy number gain See cases [RCV000137716] Chr7:142237788..142779344 [GRCh38]
Chr7:141584064..142187156 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1 copy number loss See cases [RCV000137256] Chr7:141960861..159335866 [GRCh38]
Chr7:142528609..159128556 [GRCh37]
Chr7:141307130..158821317 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 copy number loss See cases [RCV000138120] Chr7:134666829..158591882 [GRCh38]
Chr7:134351581..158384574 [GRCh37]
Chr7:134002121..158077335 [NCBI36]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q34(chr7:142620632-142753000)x1 copy number loss See cases [RCV000138687] Chr7:142620632..142753000 [GRCh38]
Chr7:142009138..142140425 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3		 pathogenic
GRCh38/hg38 7q34(chr7:142578930-142753745)x1 copy number loss See cases [RCV000138582] Chr7:142578930..142753745 [GRCh38]
Chr7:141967536..142141170 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q34(chr7:142503036-142753076)x1 copy number loss See cases [RCV000139181] Chr7:142503036..142753076 [GRCh38]
Chr7:141871507..142140501 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q33-36.1(chr7:135017687-148807400)x1 copy number loss See cases [RCV000138903] Chr7:135017687..148807400 [GRCh38]
Chr7:134702438..148504492 [GRCh37]
Chr7:134352978..148135425 [NCBI36]
Chr7:7q33-36.1		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 copy number gain See cases [RCV000139654] Chr7:132444095..159335866 [GRCh38]
Chr7:132128854..159128556 [GRCh37]
Chr7:131779394..158821317 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q34(chr7:142620632-142753076)x1 copy number loss See cases [RCV000139708] Chr7:142620632..142753076 [GRCh38]
Chr7:142009138..142140501 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q34(chr7:142578930-142752607)x3 copy number gain See cases [RCV000139475] Chr7:142578930..142752607 [GRCh38]
Chr7:141967536..142140032 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3		 pathogenic
GRCh38/hg38 7q34(chr7:142503036-142753745)x1 copy number loss See cases [RCV000142812] Chr7:142503036..142753745 [GRCh38]
Chr7:141871507..142141170 [NCBI36]
Chr7:7q34		 likely benign
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 copy number gain See cases [RCV000142802] Chr7:131228764..159335866 [GRCh38]
Chr7:130913523..159128556 [GRCh37]
Chr7:130564063..158821317 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 copy number gain See cases [RCV000143754] Chr7:131171478..159327017 [GRCh38]
Chr7:130856237..159119707 [GRCh37]
Chr7:130506777..158812468 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q34-35(chr7:140061285-144622893)x3 copy number gain See cases [RCV000143724] Chr7:140061285..144622893 [GRCh38]
Chr7:139761085..144319986 [GRCh37]
Chr7:139407554..143950919 [NCBI36]
Chr7:7q34-35		 uncertain significance
GRCh37/hg19 7q34(chr7:141937588-142486548)x3 copy number gain See cases [RCV000143759] Chr7:141937588..142486548 [GRCh37]
Chr7:141584062..142186550 [NCBI36]
Chr7:7q34		 uncertain significance
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 copy number gain See cases [RCV000143707] Chr7:132438072..159327017 [GRCh38]
Chr7:132122831..159119707 [GRCh37]
Chr7:131773371..158812468 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 copy number gain See cases [RCV000050876] Chr7:129310166..159282390 [GRCh38]
Chr7:128950007..159075079 [GRCh37]
Chr7:128737243..158767840 [NCBI36]
Chr7:7q32.1-36.3		 pathogenic
GRCh38/hg38 7q34-35(chr7:142578948-144254897)x1 copy number loss See cases [RCV000050639] Chr7:142578948..144254897 [GRCh38]
Chr7:142528609..143951990 [GRCh37]
Chr7:141967554..143582923 [NCBI36]
Chr7:7q34-35		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 copy number gain See cases [RCV000051101] Chr7:132850196..159325876 [GRCh38]
Chr7:132534956..159118566 [GRCh37]
Chr7:132185496..158811327 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 copy number gain See cases [RCV000053576] Chr7:136309982..159307523 [GRCh38]
Chr7:135994730..159100212 [GRCh37]
Chr7:135645270..158792973 [NCBI36]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:142021716-159325876)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|See cases [RCV000053577] Chr7:142021716..159325876 [GRCh38]
Chr7:142528609..159118566 [GRCh37]
Chr7:141367985..158811327 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.1(chr7:132023155-149309794)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|See cases [RCV000054172] Chr7:132023155..149309794 [GRCh38]
Chr7:131707914..149006885 [GRCh37]
Chr7:131358454..148637818 [NCBI36]
Chr7:7q32.3-36.1		 pathogenic
GRCh38/hg38 7q33-35(chr7:135414108-144140219)x1 copy number loss See cases [RCV000054173] Chr7:135414108..144140219 [GRCh38]
Chr7:135098857..143837312 [GRCh37]
Chr7:134749397..143468245 [NCBI36]
Chr7:7q33-35		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] Chr7:139365967..159282531 [GRCh38]
Chr7:139050713..159075220 [GRCh37]
Chr7:138701253..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1 copy number loss See cases [RCV000054176] Chr7:140754198..159307523 [GRCh38]
Chr7:140453998..159100212 [GRCh37]
Chr7:140100467..158792973 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:142358524-159282531)x1 copy number loss See cases [RCV000054177] Chr7:142358524..159282531 [GRCh38]
Chr7:142528609..159075220 [GRCh37]
Chr7:141726947..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3 copy number gain Neurodevelopmental disorder [RCV003327609] Chr7:137463392..159345973 [GRCh38]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3 copy number gain Neurodevelopmental disorder [RCV003327610] Chr7:138620939..159233475 [GRCh38]
Chr7:7q34-36.3		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:264
Count of miRNA genes:249
Interacting mature miRNAs:264
Transcripts:ENST00000390400
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH69087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,428,609 - 142,428,719UniSTSGRCh37
Build 367142,108,190 - 142,108,300RGDNCBI36
Celera7137,235,380 - 137,235,490RGD
Cytogenetic Map7q34UniSTS
HuRef7136,757,104 - 136,757,214UniSTS
CRA_TCAGchr7v27141,799,920 - 141,800,030UniSTS
GeneMap99-GB4 RH Map7653.5UniSTS
STS-K02545  
Human AssemblyChrPosition (strand)SourceJBrowse
Build 367142,194,761 - 142,194,981RGDNCBI36
Celera7137,321,936 - 137,322,156RGD
Cytogenetic Map7q34UniSTS
HuRef7136,823,290 - 136,823,510UniSTS
CRA_TCAGchr7v27141,886,491 - 141,886,711UniSTS
GeneMap99-GB4 RH Map7654.85UniSTS
SHGC-58840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,441,284 - 142,441,372UniSTSGRCh37
GRCh37933,778,934 - 33,779,025UniSTSGRCh37
Build 367142,120,866 - 142,120,954RGDNCBI36
Celera7137,248,043 - 137,248,131RGD
Celera933,710,791 - 33,710,882UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9p11.2UniSTS
HuRef7136,769,767 - 136,769,855UniSTS
HuRef933,736,879 - 33,736,970UniSTS
CRA_TCAGchr7v27141,812,596 - 141,812,684UniSTS
TNG Radiation Hybrid Map917825.0UniSTS
D7S2277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,460,728 - 142,460,897UniSTSGRCh37
Build 367142,140,302 - 142,140,471RGDNCBI36
Celera7137,267,480 - 137,267,649RGD
Cytogenetic Map7q34UniSTS
HuRef7136,789,213 - 136,789,382UniSTS
CRA_TCAGchr7v27141,832,032 - 141,832,201UniSTS
GDB:374188  
Human AssemblyChrPosition (strand)SourceJBrowse
Build 367142,193,953 - 142,195,518RGDNCBI36
Celera7137,321,128 - 137,322,693RGD
Cytogenetic Map7q34UniSTS
HuRef7136,822,482 - 136,824,047UniSTS
CRA_TCAGchr7v27141,885,683 - 141,887,248UniSTS
G65748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,451,176 - 142,451,473UniSTSGRCh37
GRCh37933,789,295 - 33,789,592UniSTSGRCh37
Build 367142,130,751 - 142,131,049RGDNCBI36
Celera7137,257,929 - 137,258,227RGD
Celera933,721,146 - 33,721,443UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9p11.2UniSTS
HuRef7136,779,660 - 136,779,958UniSTS
HuRef933,747,220 - 33,747,517UniSTS
CRA_TCAGchr7v27141,822,481 - 141,822,779UniSTS
GDB:1318702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,469,220 - 142,469,364UniSTSGRCh37
Build 367142,148,795 - 142,148,939RGDNCBI36
Celera7137,275,974 - 137,276,118RGD
Cytogenetic Map7q34UniSTS
HuRef7136,797,707 - 136,797,851UniSTS
CRA_TCAGchr7v27141,840,525 - 141,840,669UniSTS
RH69072  
Human AssemblyChrPosition (strand)SourceJBrowse
Build 367142,195,543 - 142,195,678RGDNCBI36
Celera7137,322,718 - 137,322,853RGD
Cytogenetic Map7q34UniSTS
HuRef7136,824,072 - 136,824,207UniSTS
CRA_TCAGchr7v27141,887,273 - 141,887,408UniSTS
GeneMap99-GB4 RH Map7653.5UniSTS
RH46953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,448,226 - 142,448,358UniSTSGRCh37
Build 367142,127,801 - 142,127,933RGDNCBI36
Celera7137,254,979 - 137,255,111RGD
Cytogenetic Map7q34UniSTS
HuRef7136,776,710 - 136,776,842UniSTS
CRA_TCAGchr7v27141,819,531 - 141,819,663UniSTS
GeneMap99-GB4 RH Map7654.79UniSTS
NCBI RH Map71357.2UniSTS
STS-M14158  
Human AssemblyChrPosition (strand)SourceJBrowse
Build 367142,196,367 - 142,196,606RGDNCBI36
Celera7137,323,542 - 137,323,781RGD
Cytogenetic Map7q34UniSTS
HuRef7136,824,896 - 136,825,135UniSTS
CRA_TCAGchr7v27141,888,097 - 141,888,336UniSTS
GeneMap99-GB4 RH Map7654.23UniSTS
PRSS1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,460,824 - 142,460,917UniSTSGRCh37
Build 367142,140,398 - 142,140,491RGDNCBI36
Celera7137,267,576 - 137,267,669RGD
Cytogenetic Map7q34UniSTS
HuRef7136,789,309 - 136,789,402UniSTS
CRA_TCAGchr7v27141,832,128 - 141,832,221UniSTS
D7S2928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377142,460,732 - 142,460,861UniSTSGRCh37
GRCh377142,482,225 - 142,482,354UniSTSGRCh37
Celera7137,267,484 - 137,267,613UniSTS
Celera7137,288,980 - 137,289,109UniSTS
Celera7137,309,351 - 137,309,480UniSTS
Cytogenetic Map7q34UniSTS
HuRef7136,810,705 - 136,810,834UniSTS
HuRef7136,789,217 - 136,789,346UniSTS
CRA_TCAGchr7v27141,873,902 - 141,874,031UniSTS
CRA_TCAGchr7v27141,853,531 - 141,853,660UniSTS
CRA_TCAGchr7v27141,832,036 - 141,832,165UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1
Medium 41 291 22 6 448 7 6 1 1 15 13 48
Low 569 780 506 212 903 174 527 72 205 166 591 776 36 429 253 1 2
Below cutoff 627 653 520 188 118 120 1250 487 874 96 390 333 72 1 430 741 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000390400   ⟹   ENSP00000374923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7142,720,660 - 142,721,160 (+)Ensembl
Protein Sequences
GenBank Protein A0A5B6 (Get FASTA)   NCBI Sequence Viewer  
  AAB60326 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000374923.2
  ENSP00000480928.2
Reference Protein Sequences
RefSeq Acc Id: ENSP00000374923   ⟸   ENST00000390400
Protein Domains
Ig-like

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A0A5B6-F1-model_v2 AlphaFold A0A5B6 1-114 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12209 AgrOrtholog
COSMIC TRBV28 COSMIC
Ensembl Genes ENSG00000211753 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000282812 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000390400.2 UniProtKB/Swiss-Prot
  ENST00000619125.2 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot
GTEx ENSG00000211753 GTEx
  ENSG00000282812 GTEx
HGNC ID HGNC:12209 ENTREZGENE
Human Proteome Map TRBV28 Human Proteome Map
InterPro Ig-like_dom UniProtKB/Swiss-Prot
  Ig-like_dom_sf UniProtKB/Swiss-Prot
  Ig-like_fold UniProtKB/Swiss-Prot
  Ig_V-set UniProtKB/Swiss-Prot
NCBI Gene TRBV28 ENTREZGENE
PANTHER T CELL RECEPTOR BETA VARIABLE 28 UniProtKB/Swiss-Prot
  T-CELL RECEPTOR BETA CHAIN UniProtKB/Swiss-Prot
Pfam V-set UniProtKB/Swiss-Prot
PharmGKB PA36889 PharmGKB
PROSITE IG_LIKE UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot
UniProt A0A5B6 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A0A0G2JN94 UniProtKB/Swiss-Prot