Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
3683 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Integrin subunit alpha L |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
ITGAL |
SynonymsGene synonyms aliases
|
CD11A, LFA-1, LFA1A |
ChromosomeChromosome number
|
16 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
16p11.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
|
ITGAL encodes the integrin alpha L chain. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This I-domain containing alpha integrin combines with the beta 2 chain (ITGB2) to form the integrin lymphocyte fu |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
|
Transcription factor |
Regulation |
Reference |
RFX1 |
Unknown |
21192791 |
|
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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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 |
P20701 |
Protein name |
Integrin alpha-L (CD11 antigen-like family member A) (Leukocyte adhesion glycoprotein LFA-1 alpha chain) (LFA-1A) (Leukocyte function-associated molecule 1 alpha chain) (CD antigen CD11a) |
Protein function |
Integrin ITGAL/ITGB2 is a receptor for ICAM1, ICAM2, ICAM3 and ICAM4. Integrin ITGAL/ITGB2 is a receptor for F11R (PubMed:11812992, PubMed:15528364). Integrin ITGAL/ITGB2 is a receptor for the secreted form of ubiquitin-like protein ISG15; the i |
PDB |
1CQP
,
1DGQ
,
1LFA
,
1MJN
,
1MQ8
,
1MQ9
,
1MQA
,
1RD4
,
1T0P
,
1XDD
,
1XDG
,
1XUO
,
1ZON
,
1ZOO
,
1ZOP
,
2ICA
,
2K8O
,
2M3E
,
2O7N
,
3BN3
,
3BQM
,
3BQN
,
3E2M
,
3EOA
,
3EOB
,
3F74
,
3F78
,
3HI6
,
3M6F
,
3TCX
,
4IXD
,
5E6R
,
5E6S
,
5E6U
,
6BXB
,
6BXF
,
6BXJ
,
6CKB
,
7KC3
,
7KC5
,
7KC6
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00092 |
VWA |
156 → 326 |
von Willebrand factor type A domain |
Domain |
PF01839 |
FG-GAP |
521 → 554 |
FG-GAP repeat |
Repeat |
PF08441 |
Integrin_alpha2 |
612 → 1002 |
Integrin alpha |
Family |
PF00357 |
Integrin_alpha |
1113 → 1127 |
Integrin alpha cytoplasmic region |
Family |
|
Sequence |
|
Sequence length |
1170 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Behcet syndrome |
Behcet Syndrome |
rs886040969, rs886039866, rs746055479, rs752615209, rs774164456, rs751454741 |
8712863 |
Inflammatory bowel disease |
Inflammatory Bowel Diseases |
rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs139868987, rs750447828, rs368138379, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 |
28067908 |
Psoriasis |
Psoriasis |
rs281875215, rs587777763, rs281875213, rs281875212 |
26974007 |
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