ITGAM (integrin subunit alpha M)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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3684 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Integrin subunit alpha M |
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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ITGAM |
SynonymsGene synonyms aliases
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CD11B, CR3A, MAC-1, MAC1A, MO1A, SLEB6 |
ChromosomeChromosome number
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16 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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16p11.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes the integrin alpha M 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 a leukocyte-specific i |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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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
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UniProt ID |
P11215 |
Protein name |
Integrin alpha-M (CD11 antigen-like family member B) (CR-3 alpha chain) (Cell surface glycoprotein MAC-1 subunit alpha) (Leukocyte adhesion receptor MO1) (Neutrophil adherence receptor) (CD antigen CD11b) |
Protein function |
Integrin ITGAM/ITGB2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles and pathogens (PubMed:20008295, PubMed:9558116). It is identical wit |
PDB |
1BHO
,
1BHQ
,
1IDN
,
1IDO
,
1JLM
,
1M1U
,
1MF7
,
1N9Z
,
1NA5
,
2LKE
,
2LKJ
,
3Q3G
,
3QA3
,
4M76
,
4XW2
,
6RHW
,
7AKK
,
7P2D
,
7USL
,
7USM
,
8CE6
,
8CE9
,
8VOH
,
8VOI
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00092 |
VWA |
150 → 327 |
von Willebrand factor type A domain |
Domain |
PF01839 |
FG-GAP |
520 → 555 |
FG-GAP repeat |
Repeat |
PF08441 |
Integrin_alpha2 |
614 → 1005 |
Integrin alpha |
Family |
PF00357 |
Integrin_alpha |
1129 → 1143 |
Integrin alpha cytoplasmic region |
Family |
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Sequence |
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Sequence length |
1152 |
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
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Dermatitis |
Dermatitis, Allergic Contact |
rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 |
16033404 |
Hyperinsulinism |
Hyperinsulinism |
rs387906407, rs151344623, rs121913156, rs137853245, rs80356655, rs104894010, rs104894012, rs104894014, rs104894015, rs137852676, rs587783169, rs72559716, rs541269678, rs151344624, rs797045209, rs761749884, rs797045624, rs863225280, rs139964066, rs1057516281, rs1057516317, rs576684889, rs201682634, rs1350717554, rs768951263, rs1260178539, rs200670692, rs72559734, rs1400535021, rs372307320, rs1554923999, rs751279984, rs1008906426, rs367850779, rs1382448285, rs1564977373, rs750586210, rs1599937180 |
29035695 |
Multiple sclerosis |
Multiple Sclerosis |
rs104895219, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039, rs483353038, rs61731956, rs568165874, rs767480544 |
22190364 |
Obesity |
Obesity |
rs34911341, rs74315349, rs1474810899, rs2282440, rs2491132, rs121918111, rs796065034, rs753856820, rs796065035, rs121918112, rs104894023, rs137852821, rs1580764441, rs137852822, rs137852823, rs137852824, rs13447324, rs121913562, rs121913564, rs74315393, rs121913556, rs2989924, rs193922650, rs193922685, rs193922687, rs751160202, rs1421085, rs747681609, rs1553400259, rs13447339, rs370479598, rs1554394014, rs1553174844, rs756232889, rs369841551, rs1557670950, rs1571321748, rs148538980, rs1572820988, rs1591461970, rs1419374563, rs745921568, rs144159890, rs1570714352, rs779783209, rs1573250294, rs1573254045, rs1580744791, rs1580746829, rs6548238, rs7138803, rs7754840 |
29035695 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
23566496 |
Systemic lupus erythematosus |
Systemic lupus erythematosus |
rs77571059, rs10954213, rs2070197, rs72556554, rs3219018, rs121912990, rs1575496354, rs7574865, rs1307379746, rs758750492, rs1575497576 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Bipolar disorder |
Bipolar Disorder |
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19488045 |
Compensatory hyperinsulinemia |
Compensatory Hyperinsulinemia |
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29035695 |
Endogenous hyperinsulinism |
Endogenous Hyperinsulinism |
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29035695 |
Exogenous hyperinsulinism |
Exogenous Hyperinsulinism |
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29035695 |
Hyperglycemia |
Hyperglycemia |
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29035695 |
Ileitis |
Ileitis |
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10647630 |
Lupus erythematosus |
Lupus Erythematosus, Systemic |
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23943494, 18204446, 24871463, 19838195, 18204448, 23740937, 27399966, 26606652, 21408207, 19286673, 26502338, 23917156, 28714469 |
Lupus meningoencephalitis |
Lupus Meningoencephalitis |
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26773105 |
Central nervous system lupus |
Lupus Vasculitis, Central Nervous System |
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26773105 |
Neuropsychiatric systemic lupus erythematosus |
Neuropsychiatric Systemic Lupus Erythematosus |
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26773105 |
Nonbacterial verrucal endocardiosis |
Libman-Sacks Disease |
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18204448, 18204446 |
Promyelocytic leukemia |
Acute Promyelocytic Leukemia |
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16764927 |
Scleroderma |
Systemic Scleroderma |
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23740937 |
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