Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10903
Gene name Gene Name - the full gene name approved by the HGNC.
Myotubularin related protein 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MTMR11
Synonyms (NCBI Gene) Gene synonyms aliases
CRA
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q21.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1163698 hsa-miR-320a CLIP-seq
MIRT1163699 hsa-miR-320b CLIP-seq
MIRT1163700 hsa-miR-320c CLIP-seq
MIRT1163701 hsa-miR-320d CLIP-seq
MIRT1163702 hsa-miR-3616-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004438 Function Phosphatidylinositol-3-phosphatase activity IBA 21873635
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005737 Component Cytoplasm IDA 16787938
GO:0016020 Component Membrane IBA 21873635
GO:0046856 Process Phosphatidylinositol dephosphorylation IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID A4FU01
Protein name Myotubularin-related protein 11 (Cisplatin resistance-associated protein) (hCRA) (Inactive phosphatidylinositol 3-phosphatase 11)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06602 Myotub-related 169 318 Myotubularin-like phosphatase domain Domain
PF06602 Myotub-related 302 483 Myotubularin-like phosphatase domain Domain
PF12578 3-PAP 548 678 Myotubularin-associated protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in bone marrow, spleen and thymus. {ECO:0000269|PubMed:17498563}.
Sequence
MWWGGRGQSFNIAPQKEEPEMGSVQENRMPEPRSRQPSSCLASRCLPGEQILAWAPGVRK
GLEPELSGTLICTNFRVTFQPCGWQWNQDTPLNSEYDFALVNIGRLEAVSGLSRVQLLRP
GSLHKFIPEEILIHGRDFRLLRVGFEAGGLEPQAFQVTMAIVQARAQSNQAQQYSGITLS
KAGQGSGSRKPPIPLMETAEDWETERKKQAARGWRVSTVNERFDVATSLPRYFWVPNRIL
DSEVRRAFGHFHQGRGPRLSWHHPGGSDLLRCGGFYTASDPNKEDIRAVELMLQAGHSDV
V
LVDTMDELPSLADVQLAHLRLRALCLPDSSVAEDKWLSALEGTRWLDYVRACLRKASDI
SVLVTSRVRSVILQERGDRDLNGLLSSLVQLLSAPEARTLFGFQSLVQREWVAAGHPFLT
RLGGTGASEEAPVFLLFLDCVWQLLQQFPADFEFSEFFLLALHDSVRVPDTLTFLRNTPW
ERG
KQSGQLNSYTQVYTPGYSQPPAGNSFNLQLSVWDWDLRYSNAQILQFQNPGYDPEHC
PDSWLPRPQPSFMVPGPPSSVWLFSRGALTPLNQLCPWRDSPSLLAVSSRWLPRPAISSE
SLADQEWGLPSHWGACPLPPGLLLPGYLGPQIRLWRRCYLRGRPEVQMGLSAPTISGLQD
ELSHLQELLRKWTPRISP
EDHSKKRDPHTILNPTEIAGILKGRAEGDLG
Sequence length 709
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
29059683
Unknown
Disease term Disease name Evidence References Source
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Carpal Tunnel Syndrome Carpal Tunnel Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Aortic Aneurysm Abdominal Associate 25993293
Breast Neoplasms Associate 20413845
Epilepsy Associate 11879359
FOR heavy chain disease protein human Associate 4100047
Neoplasms Associate 20413845