Gene Gene information from NCBI Gene database.
Entrez ID 387914
Gene name Shisa family member 2
Gene symbol SHISA2
Synonyms (NCBI Gene)
C13orf13PRO28631TMEM46WGAR9166bA398O19.2hShisa
Chromosome 13
Chromosome location 13q12.13
miRNA miRNA information provided by mirtarbase database.
239
miRTarBase ID miRNA Experiments Reference
MIRT047100 hsa-miR-183-5p CLASH 23622248
MIRT046670 hsa-miR-222-3p CLASH 23622248
MIRT044314 hsa-miR-106b-5p CLASH 23622248
MIRT571218 hsa-miR-138-1-3p HITS-CLIP 21572407
MIRT670557 hsa-miR-637 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005783 Component Endoplasmic reticulum IBA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617324 20366 ENSG00000180730
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UWI4
Protein name Protein shisa-2 homolog (Transmembrane protein 46)
Protein function Plays an essential role in the maturation of presomitic mesoderm cells by individual attenuation of both FGF and WNT signaling.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13908 Shisa 35 242 Wnt and FGF inhibitory regulator Family
Sequence
Sequence length 295
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
SCOLIOSIS 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
Malignant neoplasm of prostate Prostate cancer BEFREE 29344118
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 29344118
★☆☆☆☆
Found in Text Mining only
Prostate carcinoma Prostate cancer BEFREE 29344118
★☆☆☆☆
Found in Text Mining only