Gene Gene information from NCBI Gene database.
Entrez ID 54989
Gene name Zinc finger protein 770
Gene symbol ZNF770
Synonyms (NCBI Gene)
PRO1914
Chromosome 15
Chromosome location 15q14
miRNA miRNA information provided by mirtarbase database.
642
miRTarBase ID miRNA Experiments Reference
MIRT023429 hsa-miR-30b-5p Sequencing 20371350
MIRT051674 hsa-let-7e-5p CLASH 23622248
MIRT050686 hsa-miR-18a-5p CLASH 23622248
MIRT046694 hsa-miR-222-3p CLASH 23622248
MIRT044971 hsa-miR-186-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA
GO:0008270 Function Zinc 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.
Q6IQ21
Protein name Zinc finger protein 770
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 27 49 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 55 77 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 160 182 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 188 210 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 475 497 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 503 525 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 625 647 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 653 675 Zinc finger, C2H2 type Domain
Sequence
MMAENNLKMLKIQQCVVANKLPRNRPYVCNICFKHFETPSKLARHYLIHTGQKPFECDVC
HKTFRQLVHLERHQLTH
SLPFKCSICQRHFKNLKTFVKHQQLHNETYQNNVKQVRRLLEA
KQEKSMYGVYNTFTTEERWALHPCSKSDPMYSMKRRKNIHACTICGKMFPSQSKLDRHVL
IH
TGQRPFKCVLCTKSFRQSTHLKIHQLTHSEERPFQCCFCQKGFKIQSKLLKHKQIHTR
NKAFRALLLKKRRTESRPLPNKLNANQGGFENGEIGESEENNPLDVHSIYIVPFQCPKCE
KCFESEQILNEHSCFAARSGKIPSRFKRSYNYKTIVKKILAKLKRARSKKLDNFQSEKKV
FKKSFLRNCDLISGEQSSEQTQRTFVGSLGKHGTYKTIGNRKKKTLTLPFSWQNMGKNLK
GILTTENILSIDNSVNKKDLSICGSSGEEFFNNCEVLQCGFSVPRENIRTRHKICPCDKC
EKVFPSISKLKRHYLIH
TGQRPFGCNICGKSFRQSAHLKRHEQTHNEKSPYASLCQVEFG
NFNNLSNHSGNNVNYNASQQCQAPGVQKYEVSESDQMSGVKAESQDFIPGSTGQPCLPNV
LLESEQSNPFCSYSEHQEKNDVFLYRCSVCAKSFRSPSKLERHYLIHAGQKPFECSVCGK
TFRQAPHWKRHQLTH
FKERPQGKVVALDSVM
Sequence length 691
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
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 Evidence Score
BRONCHOPULMONARY DYSPLASIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations