Gene Gene information from NCBI Gene database.
Entrez ID 51333
Gene name Zinc finger protein 771
Gene symbol ZNF771
Synonyms (NCBI Gene)
DSC43
Chromosome 16
Chromosome location 16p11.2
miRNA miRNA information provided by mirtarbase database.
40
miRTarBase ID miRNA Experiments Reference
MIRT016930 hsa-miR-335-5p Microarray 18185580
MIRT1538987 hsa-miR-1 CLIP-seq
MIRT1538988 hsa-miR-1245 CLIP-seq
MIRT1538989 hsa-miR-142-3p CLIP-seq
MIRT1538990 hsa-miR-206 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm 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.
Q7L3S4
Protein name Zinc finger protein 771 (Mesenchymal stem cell protein DSC43)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 63 85 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 91 113 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 119 141 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 147 169 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 175 197 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 203 225 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 231 253 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 259 281 Zinc finger, C2H2 type Domain
Sequence
MPGEQQAEEEEEEEMQEEMVLLVKGEEDEGEEKYEVVKLKIPMDNKEVPGEAPAPSADPA
RPHACPDCGRAFARRSTLAKHARTHTGERPFGCTECGRRFSQKSALTKHGRTHTGERPYE
CPECDKRFSAASNLRQHRRRH
TGEKPYACAHCGRRFAQSSNYAQHLRVHTGEKPYACPDC
GRAFGGSSCLARHRRTH
TGERPYACADCGTRFAQSSALAKHRRVHTGEKPHRCAVCGRRF
GHRSNLAEHARTH
TGERPYPCAECGRRFRLSSHFIRHRRAHMRRRLYICAGCGRDFKLPP
GATAATATERCPECEGS
Sequence length 317
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
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Obesity Associate 27564309
★☆☆☆☆
Found in Text Mining only