TRAC (T cell receptor alpha constant)
|
Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
28755 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
T cell receptor alpha constant |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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TRAC |
SynonymsGene synonyms aliases
|
IMD7, TCRA, TRA, TRCA |
ChromosomeChromosome number
|
14 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
14q11.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha |
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
|
GO ID |
Ontology |
Definition |
Evidence |
Reference |
GO:0002250 |
Process |
Adaptive immune response |
IEA |
|
GO:0005886 |
Component |
Plasma membrane |
TAS |
|
GO:0009617 |
Process |
Response to bacterium |
IBA |
21873635 |
GO:0016021 |
Component |
Integral component of membrane |
IEA |
|
GO:0042101 |
Component |
T cell receptor complex |
IEA |
|
GO:0050776 |
Process |
Regulation of immune response |
TAS |
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GO:0050852 |
Process |
T cell receptor signaling pathway |
TAS |
|
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
P01848 |
Protein name |
T cell receptor alpha chain constant |
Protein function |
Constant region of T cell receptor (TR) alpha chain (PubMed:24600447). Alpha-beta T cell receptors are antigen specific receptors which are essential to the immune response and are present on the cell surface of T lymphocytes. Recognize peptide- |
PDB |
1AO7
,
1BD2
,
1FYT
,
1J8H
,
1KGC
,
1MI5
,
1OGA
,
1QRN
,
1QSF
,
1YMM
,
1ZGL
,
2AK4
,
2BNQ
,
2BNR
,
2BNU
,
2CDF
,
2CDG
,
2ESV
,
2EYR
,
2EYS
,
2EYT
,
2F53
,
2F54
,
2GJ6
,
2IAL
,
2IAM
,
2IAN
,
2NX5
,
2P5E
,
2P5W
,
2PO6
,
2PYE
,
2PYF
,
2VLJ
,
2VLK
,
2VLM
,
2VLR
,
2XN9
,
2XNA
,
3ARB
,
3ARD
,
3ARE
,
3ARF
,
3ARG
,
3D39
,
3DX9
,
3DXA
,
3FFC
,
3GSN
,
3HE7
,
3HG1
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF09291 |
DUF1968 |
6 → 90 |
|
Domain |
|
Sequence |
|
Sequence length |
140 |
Interactions |
View interactions |
Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Severe combined immunodeficiency disease |
Combined immunodeficiency |
rs886037607, rs118203993, rs121908714, rs121908739, rs121908740, rs121908735, rs121908721, rs121908722, rs121908156, rs1564414523, rs1564418254, rs1564446526, rs786205074, rs121908157, rs121908159, rs786200884, rs397515357, rs104894562, rs137852624, rs137852625, rs137852626, rs137852627, rs137852507, rs137852509, rs111033619, rs111033620, rs1569480018, rs111033621, rs137852510, rs587776729, rs111033622, rs111033617, rs111033618, rs121917894, rs121917896, rs2133313409, rs121917897, rs28933392, rs104894282, rs104894283, rs104894285, rs121918570, rs121918572, rs730880318, rs104893674, rs730880319, rs104894453, rs104894454, rs104894451, rs137853206, rs777503956, rs267606645, rs267606648, rs397515390, rs193922346, rs193922347, rs193922348, rs193922349, rs193922350, rs137852508, rs193922640, rs193922641, rs193922643, rs193922645, rs193922361, rs193922364, rs193922464, rs148508754, rs193922574, rs113994174, rs606231246, rs397514671, rs397514686, rs397514755, rs199474679, rs199474685, rs199474686, rs199474681, rs150739647, rs267605358, rs886041036, rs587777335, rs587778405, rs145092287, rs587777562, rs606231256, rs200296680, rs786205456, rs786205517, rs774202259, rs786205615, rs878853261, rs786205890, rs782753385, rs746052951, rs869025224, rs869312857, rs869320660, rs869320659, rs869320658, rs879253742, rs886037924, rs886037925, rs750610248, rs886039394, rs761242509, rs886039387, rs886041043, rs886041044, rs886042051, rs886041333, rs749481781, rs1057517747, rs1057519506, rs1057523762, rs1057521062, rs1057520644, rs761583890, rs751635016, rs55729925, rs1064793248, rs1064793347, rs1064794027, rs781410769, rs1555524788, rs1486760100, rs769633203, rs1556330713, rs1555322558, rs1556330234, rs1556330755, rs1556329779, rs1556330552, rs1556329822, rs1556330286, rs1556331272, rs2146178281, rs376610445, rs757797994, rs775704953, rs1555743321, rs1564995660, rs1564995662, rs1556330249, rs144104577, rs886041796, rs1026474882, rs570768621, rs1556330562, rs1556330568, rs780014431, rs778343059, rs1555844617, rs1567629968, rs1567628757, rs1567629943, rs1567632864, rs1567632829, rs1567626023, rs1559328006, rs1561423197, rs1452483770, rs1568400897, rs1569479913, rs1568404443, rs1569480047, rs1563340753, rs368303189, rs1568431262, rs1568431102, rs1561424886, rs1602289943, rs1241698978, rs1569479994, rs1569480082, rs1602289649, rs1573261820, rs770985198, rs1589050343, rs1340132582, rs1589064324, rs1589070600, rs1213680890, rs149316157, rs1599873591, rs755706305, rs1602288051, rs1602289411, rs1602289183, rs1583513256, rs1589136659, rs1380154594, rs1011307501, rs1599876167, rs1569967422, rs1602289631, rs1573262398, rs760191638, rs1592117677, rs1640406042, rs372597855, rs1839558393, rs1839622622, rs1839957089, rs777008519, rs1233957241, rs2092261618, rs1839255008, rs1677695565, rs936493226, rs1162344514, rs991089005 |
3464003 |
T-cell receptor alpha/beta deficiency |
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY, TCR-alpha-beta-positive T-cell deficiency |
rs397514259 |
3464003, 21206088 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Hypereosinophilia |
Hypereosinophilia |
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