Gene Gene information from NCBI Gene database.
Entrez ID 149466
Gene name Chromosome 1 open reading frame 210
Gene symbol C1orf210
Synonyms (NCBI Gene)
TEMP
Chromosome 1
Chromosome location 1p34.2
miRNA miRNA information provided by mirtarbase database.
421
miRTarBase ID miRNA Experiments Reference
MIRT716057 hsa-miR-4999-3p HITS-CLIP 19536157
MIRT716056 hsa-miR-6814-5p HITS-CLIP 19536157
MIRT716055 hsa-miR-130b-5p HITS-CLIP 19536157
MIRT716054 hsa-miR-3124-3p HITS-CLIP 19536157
MIRT716053 hsa-miR-2682-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005768 Component Endosome IEA
GO:0005769 Component Early endosome IEA
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0055037 Component Recycling endosome IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620582 28755 ENSG00000253313
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IVY1
Protein name Type III endosome membrane protein TEMP (TEMP)
Protein function May be involved in membrane trafficking between endosomes and plasma membrane.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15176 LRR19-TM 17 84 Domain
Sequence
Sequence length 113
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations