Gene Gene information from NCBI Gene database.
Entrez ID 7104
Gene name Transmembrane 4 L six family member 4
Gene symbol TM4SF4
Synonyms (NCBI Gene)
ILTMPil-TMP
Chromosome 3
Chromosome location 3q25.1
Summary The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate
miRNA miRNA information provided by mirtarbase database.
12
miRTarBase ID miRNA Experiments Reference
MIRT2461538 hsa-miR-1298 CLIP-seq
MIRT2461539 hsa-miR-219-1-3p CLIP-seq
MIRT2461540 hsa-miR-4272 CLIP-seq
MIRT2461541 hsa-miR-571 CLIP-seq
MIRT2461542 hsa-miR-664 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0016020 Component Membrane IBA
GO:0016020 Component Membrane IEA
GO:0042246 Process Tissue regeneration IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606567 11856 ENSG00000169903
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P48230
Protein name Transmembrane 4 L6 family member 4 (Intestine and liver tetraspan membrane protein) (IL-TMP)
Protein function Regulates the adhesive and proliferative status of intestinal epithelial cells. Can mediate density-dependent cell proliferation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05805 L6_membrane 1 191 L6 membrane protein Family
Tissue specificity TISSUE SPECIFICITY: Jejunum and liver.
Sequence
Sequence length 202
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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
CHOLELITHIASIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GALLSTONES GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 32972043
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Stimulate 22236579
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 22236579, 39999090
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 22011044, 28687755, 37535601
★☆☆☆☆
Found in Text Mining only
Liver Failure Stimulate 22236579
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Stimulate 32972043
★☆☆☆☆
Found in Text Mining only
Neoplasm Metastasis Associate 22011044
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 22011044
★☆☆☆☆
Found in Text Mining only