Gene Gene information from NCBI Gene database.
Entrez ID 400746
Gene name Non-compact myelin associated protein
Gene symbol NCMAP
Synonyms (NCBI Gene)
C1orf130MP11
Chromosome 1
Chromosome location 1p36.11
miRNA miRNA information provided by mirtarbase database.
88
miRTarBase ID miRNA Experiments Reference
MIRT692589 hsa-miR-330-3p HITS-CLIP 23313552
MIRT692588 hsa-miR-383-3p HITS-CLIP 23313552
MIRT692587 hsa-miR-298 HITS-CLIP 23313552
MIRT692586 hsa-miR-214-5p HITS-CLIP 23313552
MIRT692585 hsa-miR-6811-3p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
GO:0016020 Component Membrane IEA
GO:0019911 Function Structural constituent of myelin sheath IBA
GO:0019911 Function Structural constituent of myelin sheath IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5T1S8
Protein name Noncompact myelin-associated protein (Myelin protein of 11 kDa) (MP11)
Protein function Plays a role in myelin formation.
Family and domains
Sequence
MTTATPLGDTTFFSLNMTTRGEDFLYKSSGAIVAAVVVVVIIIFTVVLILLKMYNRKMRT
RRELEPKGPKPTAPSAVGPNSNGSQHPATVTFSPVDVQVETR
Sequence length 102
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Hemorrhage Hemorrhage Pubtator 37203300 Associate
★☆☆☆☆
Found in Text Mining only