Gene Gene information from NCBI Gene database.
Entrez ID 132989
Gene name Chromosome 4 open reading frame 36
Gene symbol C4orf36
Synonyms (NCBI Gene)
-
Chromosome 4
Chromosome location 4q21.3
miRNA miRNA information provided by mirtarbase database.
70
miRTarBase ID miRNA Experiments Reference
MIRT669264 hsa-miR-454-3p HITS-CLIP 23824327
MIRT669263 hsa-miR-4295 HITS-CLIP 23824327
MIRT669262 hsa-miR-3666 HITS-CLIP 23824327
MIRT669261 hsa-miR-301b-3p HITS-CLIP 23824327
MIRT669260 hsa-miR-130b-3p HITS-CLIP 23824327
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621278 28386 ENSG00000163633
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96KX1
Protein name Uncharacterized protein C4orf36
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15022 DUF4522 1 117 Protein of unknown function (DUF4522) Family
Sequence
Sequence length 117
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
AMYOTROPHIC LATERAL SCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPOTHYROIDISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations