ZNF397 (zinc finger protein 397)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 84307 |
| Gene name | Zinc finger protein 397 |
| Gene symbol | ZNF397 |
| Synonyms (NCBI Gene) |
ZNF47ZSCAN15
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| Chromosome | 18 |
| Chromosome location | 18q12.2 |
| Summary | This gene encodes a protein with a N-terminal SCAN domain, and the longer isoform contains nine C2H2-type zinc finger repeats in the C-terminal domain. The protein localizes to centromeres during interphase and early prophase, and different isoforms can r |
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miRNA
miRNA information provided by mirtarbase database.
170
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q8NF99 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Protein name | Zinc finger protein 397 (Zinc finger and SCAN domain-containing protein 15) (Zinc finger protein 47) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Protein function | Isoform 3 acts as a DNA-dependent transcriptional repressor. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed strongly in testis, moderately in skeletal muscle, pancreas and prostate, and weakly in heart, placenta, liver, kidney, spleen, thymus and small intestine. {ECO:0000269|PubMed:12801647}. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sequence |
MAVESGVISTLIPQDPPEQELILVKVEDNFSWDEKFKQNGSTQSCQELFRQQFRKFCYQE |
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| Sequence length | 534 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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Related Genes
Genes most often co-reported with ZNF397 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to ZNF397 (see Related Genes above), that are NOT already directly curated for ZNF397 itself -- a lead worth checking, not a confirmed association.
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