Gene Gene information from NCBI Gene database.
Entrez ID 90321
Gene name Zinc finger protein 766
Gene symbol ZNF766
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.41
miRNA miRNA information provided by mirtarbase database.
455
miRTarBase ID miRNA Experiments Reference
MIRT043666 hsa-miR-342-3p CLASH 23622248
MIRT716388 hsa-miR-5701 HITS-CLIP 19536157
MIRT716387 hsa-miR-1305 HITS-CLIP 19536157
MIRT661868 hsa-miR-490-3p HITS-CLIP 23824327
MIRT661867 hsa-miR-34b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus HDA 21630459
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.
Q5HY98
Protein name Zinc finger protein 766
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 8 49 KRAB box Family
PF00096 zf-C2H2 216 236 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 243 265 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 271 293 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 299 321 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 327 349 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 355 377 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 383 405 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 411 433 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 439 462 Zinc finger, C2H2 type Domain
Sequence
MAQLRRGHLTFRDVAIEFSQEEWKCLDPVQKALYRDVMLENYRNLVSLGICLPDLSIISM
MKQRTEPWTVENEMKVAKNPDRWEGIKDINTGRSCAVRSKAGNKPITNQLGLTFQLPLPE
LEIFQGEGKIYECNQVQKFISHSSSVSPLQRIYSGVKTHIFNKHRNDFVDFPLLSQEQKA
HIRRKPYECNEQGKVFRVSSSLPNHQVIHTADKPNRCHECGKTVRDKSGLAEHWRIRTGE
KPYKCKECGKLFNRIAYLARHEKVHTGESPYKCNECGKVFSRITYLVRHQKIHTREKPHK
CNKCGKVYSSSSYLAQHWRIH
TGEKLYKCNKCGKEFSGHSSLTTHLLIHTGEKPYKCKEC
DKAFRHKFSLTVHQRNH
NGEKPYKCHECGKVFTQVSHLARHQKIHTGEKPYKCNECGKVF
TQNSHLANHQRIH
TGEKPYKCHVCGKVFRHSSWFVQHQRSVHERVLTN
Sequence length 468
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 Evidence Score
HYPERCALCEMIA, INFANTILE, 1 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations