Gene Gene information from NCBI Gene database.
Entrez ID 54819
Gene name Zinc finger CCHC-type containing 10
Gene symbol ZCCHC10
Synonyms (NCBI Gene)
-
Chromosome 5
Chromosome location 5q31.1
miRNA miRNA information provided by mirtarbase database.
297
miRTarBase ID miRNA Experiments Reference
MIRT1506639 hsa-miR-101 CLIP-seq
MIRT1506640 hsa-miR-1179 CLIP-seq
MIRT1506641 hsa-miR-1226 CLIP-seq
MIRT1506642 hsa-miR-1256 CLIP-seq
MIRT1506643 hsa-miR-144 CLIP-seq
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:0005515 Function Protein binding IPI 16189514, 22365833, 25416956, 29433439, 29892012, 31515488, 32296183, 33961781
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.
Q8TBK6
Protein name Zinc finger CCHC domain-containing protein 10
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13917 zf-CCHC_3 39 77 Domain
Sequence
MATPMHRLIARRQAFDTELQPVKTFWILIQPSIVISEANKQHVRCQKCLEFGHWTYECTG
KRKYLHRPSRTAELKKA
LKEKENRLLLQQSIGETNVERKAKKKRSKSVTSSSSSSSDSSA
SDSSSESEETSTSSSSEDSDTDESSSSSSSSASSTTSSSSSDSDSDSSSSSSSSTSTDSS
SDDEPPKKKKKK
Sequence length 192
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 OBSTRUCTIVE PULMONARY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
METABOLIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 31138778
★☆☆☆☆
Found in Text Mining only
Carcinoma of lung Lung carcinoma BEFREE 31138778
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of lung Lung Cancer BEFREE 31138778
★☆☆☆☆
Found in Text Mining only
melanoma Melanoma BEFREE 31404068
★☆☆☆☆
Found in Text Mining only
Melanoma Melanoma Pubtator 31404068 Inhibit
★☆☆☆☆
Found in Text Mining only
Post-Traumatic Stress Disorder Stress Disorder BEFREE 31039430
★☆☆☆☆
Found in Text Mining only