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Gene Gene information from NCBI Gene database.
Entrez ID 92092
Gene name ZC3HAV1 like
Gene symbol ZC3HAV1L
Synonyms (NCBI Gene)
C7orf39
Chromosome 7
Chromosome location 7q34
miRNA miRNA information provided by mirtarbase database.
640 Show/Hide all (640)
miRTarBase ID miRNA Experiments Reference
MIRT697451 hsa-miR-6771-3p HITS-CLIP 23313552
MIRT697450 hsa-miR-340-3p HITS-CLIP 23313552
MIRT697449 hsa-miR-6827-3p HITS-CLIP 23313552
MIRT620870 hsa-miR-181a-5p HITS-CLIP 23824327
MIRT620869 hsa-miR-181b-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005829 Component Cytosol 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.
Q96H79
Protein name Zinc finger CCCH-type antiviral protein 1-like
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF18606 HTH_53 5 → 66 Zap helix turn helix N-terminal domain Domain
Sequence
MAEPTVCSFLTKVLCAHGGRMFLKDLRGHVELSEARLRDVLQRAGPERFLLQEVETQEGL
GDAEAE
AAAGAVGGGGTSAWRVVAVSSVRLCARYQRGECQACDQLHFCRRHMLGKCPNRD
CWSTCTLSHDIHTPVNMQVLKSHGLFGLNENQLRILLLQNDPCLLPEVCLLYNKGEALYG
YCNLKDKCNKFHVCKSFVKGECKLQTCKRSHQLIHAASLKLLQDQGLNIPSVVNFQIIST
YKHMKLHKMLENTDNSSPSTEHSQGLEKQGVHAAGAAEAGPLASVPAQSAKKPCPVSCEK
Sequence length 300
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 Reference Evidence Score
OLIGODENDROGLIOMA — GWAS catalog 36810956
★★★★★
★★☆☆☆
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
Colorectal Neoplasms Colorectal neoplasm Pubtator 34938284 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only