Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9777
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane 9 superfamily member 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TM9SF4
Synonyms (NCBI Gene) Gene synonyms aliases
dJ836N17.2
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q11.21
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT036460 hsa-miR-1226-3p CLASH 23622248
MIRT652530 hsa-miR-4311 HITS-CLIP 23824327
MIRT652529 hsa-miR-216b-5p HITS-CLIP 23824327
MIRT652528 hsa-miR-3123 HITS-CLIP 23824327
MIRT652527 hsa-miR-5584-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001666 Process Response to hypoxia IDA 25961573
GO:0005515 Function Protein binding IPI 25659576
GO:0005769 Component Early endosome IDA 19893578
GO:0005794 Component Golgi apparatus IDA 25999474
GO:0006909 Process Phagocytosis IMP 19893578
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617727 30797 ENSG00000101337
Protein
UniProt ID Q92544
Protein name Transmembrane 9 superfamily member 4 (Tumor cannibalism associated protein 1)
Protein function Associates with proteins harboring glycine-rich transmembrane domains and ensures their efficient localization to the cell surface (PubMed:25999474). Regulates the assembly and activity of V-ATPase in colon cancer cells via its interaction with
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02990 EMP70 55 599 Endomembrane protein 70 Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in metastatic melanoma cells whereas it is undetectable in primary melanoma cells, healthy skin tissues and peripheral blood lymphocytes. Expressed in CD34(+) hematopoietic progenitor cells and during monocyte and gran
Sequence
Sequence length 642
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Inflammatory bowel disease Inflammatory Bowel Diseases rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 23128233
Unknown
Disease term Disease name Evidence References Source
Chronic obstructive pulmonary disease Chronic Obstructive Airway Disease 28166215 ClinVar
Autism Spectrum Disorder autism spectrum disorder GenCC
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Calcinosis Cutis Stimulate 25961573
Hypoxia Inhibit 25961573
Leukemia Associate 25961573
Leukemia Myeloid Acute Stimulate 25961573
Melanoma Associate 19893578
Melanoma Stimulate 25961573
Myelodysplastic Syndromes Stimulate 25961573
Neoplasm Metastasis Associate 35655258
Neoplasms Associate 19893578
Prostatic Neoplasms Associate 35655258