Gene Gene information from NCBI Gene database.
Entrez ID 134288
Gene name Transmembrane protein 174
Gene symbol TMEM174
Synonyms (NCBI Gene)
-
Chromosome 5
Chromosome location 5q13.2
miRNA miRNA information provided by mirtarbase database.
63
miRTarBase ID miRNA Experiments Reference
MIRT724005 hsa-miR-3184-3p HITS-CLIP 19536157
MIRT724004 hsa-miR-186-3p HITS-CLIP 19536157
MIRT724003 hsa-miR-4330 HITS-CLIP 19536157
MIRT724002 hsa-miR-150-5p HITS-CLIP 19536157
MIRT724001 hsa-miR-4261 HITS-CLIP 19536157
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 25416956, 32296183, 32814053
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IDA 20331980
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614909 28187 ENSG00000164325
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8WUU8
Protein name Transmembrane protein 174
Protein function Regulator of plasma phosphate homeostasis. Decreases serum inorganic phosphate (Pi) uptake by regulating the sodium-phosphate cotransporter SLC34A1 trafficking by PTH and FGF23 in the kidney.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15029 TMEM174 9 241 Transmembrane protein 174 Family
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in kidney (PubMed:20331980). Selectively localized in the apical membrane of renal proximal tubule epithelial cells (PubMed:35459732). {ECO:0000269|PubMed:20331980, ECO:0000269|PubMed:35459732}.
Sequence
Sequence length 243
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
10
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
ANKYLOSING SPONDYLITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHRONIC GRAFT VERSUS HOST DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CROHN'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations