Gene Gene information from NCBI Gene database.
Entrez ID 219654
Gene name Zinc finger CCHC-type containing 24
Gene symbol ZCCHC24
Synonyms (NCBI Gene)
C10orf56Z3CXXC8
Chromosome 10
Chromosome location 10q22.3
miRNA miRNA information provided by mirtarbase database.
827
miRTarBase ID miRNA Experiments Reference
MIRT004927 hsa-miR-124-3p Microarray 15685193
MIRT016865 hsa-miR-335-5p Microarray 18185580
MIRT004927 hsa-miR-124-3p Microarray 18668037
MIRT004927 hsa-miR-124-3p Microarray 15685193
MIRT042709 hsa-miR-346 CLASH 23622248
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:0003676 Function Nucleic acid binding IEA
GO:0003723 Function RNA binding HDA 22681889
GO:0008270 Function Zinc ion binding IEA
GO:0046872 Function Metal ion binding IEA
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.
Q8N2G6
Protein name Zinc finger CCHC domain-containing protein 24
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13696 zf-CCHC_2 129 149 Zinc knuckle Domain
PF17180 zf-3CxxC_2 163 230 Zinc-binding domain Family
Sequence
MSLLSAIDTSAASVYQPAQLLNWVYLSLQDTHQASAFDAFRPEPTAGAAPPELAFGKGRP
EQLGSPLHSSYLNSFFQLQRGEALSNSVYKGASPYGSLNNIADGLSSLTEHFSDLTLTSE
ARKPSKRPPPNYLCHLCFNKGHYIKDCPQARPKGEGLTPYQGKKRCFGEYKCPKCKRKWM
SGNSWANMGQECIKCHINVYPHKQRPLEKPDGLDVSDQSKEHPQHLCEKC
KVLGYYCRRV
Q
Sequence length 241
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ANDROGENETIC ALOPECIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
FRONTOTEMPORAL DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SELECTIVE IGA DEFICIENCY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations