Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
22801
Gene name Gene Name - the full gene name approved by the HGNC.
Integrin subunit alpha 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ITGA11
Synonyms (NCBI Gene) Gene synonyms aliases
HsT18964
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q23
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes an alpha integrin. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This protein contains an I domain, is expressed in muscle tissue, dimerizes with beta 1 integrin in vitro, and appears
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005675 hsa-miR-29a-3p Luciferase reporter assay, Microarray, Northern blot, qRT-PCR 20971881
MIRT005675 hsa-miR-29a-3p Luciferase reporter assay, Microarray, Northern blot, qRT-PCR 20971881
MIRT608811 hsa-miR-2682-5p HITS-CLIP 23313552
MIRT608810 hsa-miR-34b-5p HITS-CLIP 23313552
MIRT608809 hsa-miR-449c-5p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001649 Process Osteoblast differentiation HDA 16210410
GO:0005518 Function Collagen binding IMP 11518510
GO:0005886 Component Plasma membrane TAS
GO:0005925 Component Focal adhesion HDA 21423176
GO:0005925 Component Focal adhesion IDA 11518510
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604789 6136 ENSG00000137809
Protein
UniProt ID Q9UKX5
Protein name Integrin alpha-11
Protein function Integrin alpha-11/beta-1 is a receptor for collagen.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00092 VWA 164 344 von Willebrand factor type A domain Domain
PF01839 FG-GAP 480 518 FG-GAP repeat Repeat
PF01839 FG-GAP 542 577 FG-GAP repeat Repeat
PF08441 Integrin_alpha2 635 1067 Integrin alpha Family
Tissue specificity TISSUE SPECIFICITY: According to PubMed:10464311, highest levels of expression in uterus and heart, intermediate levels in skeletal muscle and intermediate to low levels in pancreas, kidney and placenta. According to PubMed:10486209, also found in brain,
Sequence
MDLPRGLVVAWALSLWPGFTDTFNMDTRKPRVIPGSRTAFFGYTVQQHDISGNKWLVVGA
PLETNGYQKTGDVYKCPVIHGNCTKLNLGRVTLSNVSERKDNMRLGLSLATNPKDNSFLA
CSPLWSHECGSSYYTTGMCSRVNSNFRFSKTVAPALQRCQTYMDIVIVLDGSNSIYPWVE
VQHFLINILKKFYIGPGQIQVGVVQYGEDVVHEFHLNDYRSVKDVVEAASHIEQRGGTET
RTAFGIEFARSEAFQKGGRKGAKKVMIVITDGESHDSPDLEKVIQQSERDNVTRYAVAVL
GYYNRRGINPETFLNEIKYIASDPDDKHFFNVTDEAALKDIVDA
LGDRIFSLEGTNKNET
SFGLEMSQTGFSSHVVEDGVLLGAVGAYDWNGAVLKETSAGKVIPLRESYLKEFPEELKN
HGAYLGYTVTSVVSSRQGRVYVAGAPRFNHTGKVILFTMHNNRSLTIHQAMRGQQIGSYF
GSEITSVDIDGDGVTDVLLVGAPMYFNEGRERGKVYVY
ELRQNLFVYNGTLKDSHSYQNA
RFGSSIASVRDLNQDSYNDVVVGAPLEDNHAGAIYIFHGFRGSILKTPKQRITASELATG
LQYFGCSIHGQLDLNEDGLIDLAVGALGNAVILWSRPVVQINASLHFEPSKINIFHRDCK
RSGRDATCLAAFLCFTPIFLAPHFQTTTVGIRYNATMDERRYTPRAHLDEGGDRFTNRAV
LLSSGQELCERINFHVLDTADYVKPVTFSVEYSLEDPDHGPMLDDGWPTTLRVSVPFWNG
CNEDEHCVPDLVLDARSDLPTAMEYCQRVLRKPAQDCSAYTLSFDTTVFIIESTRQRVAV
EATLENRGENAYSTVLNISQSANLQFASLIQKEDSDGSIECVNEERRLQKQVCNVSYPFF
RAKAKVAFRLDFEFSKSIFLHHLEIELAAGSDSNERDSTKEDNVAPLRFHLKYEADVLFT
RSSSLSHYEVKPNSSLERYDGIGPPFSCIFRIQNLGLFPIHGMMMKITIPIATRSGNRLL
KLRDFLTDEANTSCNIWGNSTEYRPTPVEEDLRRAPQLNHSNSDVVS
INCNIRLVPNQEI
NFHLLGNLWLRSLKALKYKSMKIMVNAALQRQFHSPFIFREEDPSRQIVFEISKQEDWQV
PIWIIVGSTLGGLLLLALLVLALWKLGFFRSARRRREPGLDPTPKVLE
Sequence length 1188
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  PI3K-Akt signaling pathway
Focal adhesion
ECM-receptor interaction
Regulation of actin cytoskeleton
Cytoskeleton in muscle cells
Human papillomavirus infection
Hypertrophic cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy
Dilated cardiomyopathy
  Integrin cell surface interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs786205019 18839057
Unknown
Disease term Disease name Evidence References Source
Mental depression Major Depressive Disorder 23377640 ClinVar
Attention Deficit Hyperactivity Disorder Attention Deficit Hyperactivity Disorder GWAS
Mental Depression Mental Depression GWAS
Uterine Fibroids Uterine Fibroids GWAS
Associations from Text Mining
Disease Name Relationship Type References
Aortic Aneurysm Abdominal Associate 40275351
Bardet Biedl Syndrome Associate 10464311
Breast Neoplasms Associate 31605508
Carcinoma Non Small Cell Lung Associate 31778288, 33174014, 33682233
Carotid Artery Diseases Associate 29595698
Cognition Disorders Associate 36737481
Esophageal Neoplasms Associate 35813220
Gingival Overgrowth Associate 32455102
Intracranial Aneurysm Associate 40275351
Leiomyoma Associate 24520080