Gene Gene information from NCBI Gene database.
Entrez ID 90120
Gene name Transmembrane protein 250
Gene symbol TMEM250
Synonyms (NCBI Gene)
C9orf69
Chromosome 9
Chromosome location 9q34.3
miRNA miRNA information provided by mirtarbase database.
20
miRTarBase ID miRNA Experiments Reference
MIRT676038 hsa-miR-4797-5p HITS-CLIP 23824327
MIRT676037 hsa-miR-1911-3p HITS-CLIP 23824327
MIRT676036 hsa-miR-3664-5p HITS-CLIP 23824327
MIRT676035 hsa-miR-5007-5p HITS-CLIP 23824327
MIRT676034 hsa-miR-1226-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21667337
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 21667337
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
H0YL14
Protein name Transmembrane protein 250 (Herpes virus UL25-binding protein)
Protein function May play a role in cell proliferation by promoting progression into S phase. ; (Microbial infection) Promotes human herpes simplex virus 1/HHV-1 proliferation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17685 DUF5533 1 139 Family of unknown function (DUF5533) Family
Sequence
Sequence length 139
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CHRONIC KIDNEY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DIABETIC NEPHROPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LUNG ADENOCARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations