Gene Gene information from NCBI Gene database.
Entrez ID 643641
Gene name Zinc finger protein 862
Gene symbol ZNF862
Synonyms (NCBI Gene)
GINGF6
Chromosome 7
Chromosome location 7q36.1
miRNA miRNA information provided by mirtarbase database.
184
miRTarBase ID miRNA Experiments Reference
MIRT018042 hsa-miR-335-5p Microarray 18185580
MIRT029574 hsa-miR-26b-5p Microarray 19088304
MIRT1542278 hsa-let-7a CLIP-seq
MIRT1542279 hsa-let-7b CLIP-seq
MIRT1542280 hsa-let-7c CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005575 Component Cellular_component ND
GO:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription IEA
GO:0008150 Process Biological_process ND
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620974 34519 ENSG00000106479
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60290
Protein name Zinc finger protein 862
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 10 38 KRAB box Family
PF01352 KRAB 332 373 KRAB box Family
PF14291 DUF4371 586 707 Domain of unknown function (DUF4371) Family
PF05699 Dimer_Tnp_hAT 989 1071 hAT family C-terminal dimerisation region Domain
Sequence
MEPRESGKAPVTFDDITVYLLQEEWVLLSQQQKELCGSNKLVAPLGPTVANPELFRKFGR
GPEPWLGSVQGQRSLLEHHPGKKQMGYMGEMEVQGPTRESGQSLPPQKKAYLSHLSTGSG
HIEGDWAGRNRKLLKPRSIQKSWFVQFPWLIMNEEQTALFCSACREYPSIRDKRSRLIEG
YTGPFKVETLKYHAKSKAHMFCVNALAARDPIWAARFRSIRDPPGDVLASPEPLFTADCP
IFYPPGPLGGFDSMAELLPSSRAELEDPGGDGAIPAMYLDCISDLRQKEITDGIHSSSDI
NILYNDAVESCIQDPSAEGLSEEVPVVFEELPVVFEDVAVYFTREEWGMLDKRQKELYRD
VMRMNYELLASLG
PAAAKPDLISKLERRAAPWIKDPNGPKWGKGRPPGNKKMVAVREADT
QASAADSALLPGSPVEARASCCSSSICEEGDGPRRIKRTYRPRSIQRSWFGQFPWLVIDP
KETKLFCSACIERPNLHDKSSRLVRGYTGPFKVETLKYHEVSKAHRLCVNTVEIKEDTPH
TALVPEISSDLMANMEHFFNAAYSIAYHSRPLNDFEKILQLLQSTGTVILGKYRNRTACT
QFIKYISETLKREILEDVRNSPCVSVLLDSSTDASEQACVGIYIRYFKQMEVKESYITLA
PLYSETADGYFETIVSALDELDIPFRKPGWVVGLGTDGSAMLSCRGG
LVEKFQEVIPQLL
PVHCVAHRLHLAVVDACGSIDLVKKCDRHIRTVFKFYQSSNKRLNELQEGAAPLEQEIIR
LKDLNAVRWVASRRRTLHALLVSWPALARHLQRVAEAGGQIGHRAKGMLKLMRGFHFVKF
CHFLLDFLSIYRPLSEVCQKEIVLITEVNATLGRAYVALESLRHQAGPKEEEFNASFKDG
RLHGICLDKLEVAEQRFQADRERTVLTGIEYLQQRFDADRPPQLKNMEVFDTMAWPSGIE
LASFGNDDILNLARYFECSLPTGYSEEALLEEWLGLKTIAQHLPFSMLCKNALAQHCRFP
LLSKLMAVVVCVPISTSCCERGFKAMNRIRTDERTKLSNEVLNMLMMTAVN
GVAVTEYDP
QPAIQHWYLTSSGRRFSHVYTCAQVPARSPASARLRKEEMGALYVEEPRTQKPPILPSRE
AAEVLKDCIMEPPERLLYPHTSQEAPGMS
Sequence length 1169
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Fibromatosis, gingival, 6 Likely pathogenic rs1444761945 RCV004776300
Gingival fibromatosis Likely pathogenic rs1444761945 RCV001090132
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Long QT syndrome Likely benign rs563616947 RCV000190199
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Asthma Associate 29692868
Fibromatosis Gingival Hereditary Associate 35142290