Gene Gene information from NCBI Gene database.
Entrez ID 128434
Gene name V-set and transmembrane domain containing 2 like
Gene symbol VSTM2L
Synonyms (NCBI Gene)
C20orf102dJ1118M15.2
Chromosome 20
Chromosome location 20q11.23
miRNA miRNA information provided by mirtarbase database.
84
miRTarBase ID miRNA Experiments Reference
MIRT017544 hsa-miR-335-5p Microarray 18185580
MIRT1487864 hsa-miR-1193 CLIP-seq
MIRT1487865 hsa-miR-1321 CLIP-seq
MIRT1487866 hsa-miR-1911 CLIP-seq
MIRT1487867 hsa-miR-3652 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16713569, 21393573, 25814554, 32814053
GO:0005576 Component Extracellular region IDA 21393573
GO:0005576 Component Extracellular region IEA
GO:0005737 Component Cytoplasm IDA 21393573
GO:0016020 Component Membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616537 16096 ENSG00000132821
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96N03
Protein name V-set and transmembrane domain-containing protein 2-like protein
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set 45 164 Immunoglobulin V-set domain Domain
Sequence
MGAPLAVALGALHYLALFLQLGGATRPAGHAPWDNHVSGHALFTETPHDMTARTGEDVEM
ACSFRGSGSPSYSLEIQWWYVRSHRDWTDKQAWASNQLKASQQEDAGKEATKISVVKVVG
SNISHKLRLSRVKPTDEGTYECRVIDFSDGKARHHKVKAYLRVQ
PGENSVLHLPEAPPAA
PAPPPPKPGKELRKRSVDQEACSL
Sequence length 204
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
RESTLESS LEGS SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TRIGEMINAL NERVE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Neoplasm Metastasis Associate 36790659
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 33506057
★☆☆☆☆
Found in Text Mining only
Ovarian Neoplasms Associate 35741755
★☆☆☆☆
Found in Text Mining only
Rectal Neoplasms Associate 33506057
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Associate 36790659
★☆☆☆☆
Found in Text Mining only