Gene Gene information from NCBI Gene database.
Entrez ID 148203
Gene name Zinc finger protein 738
Gene symbol ZNF738
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19p12
miRNA miRNA information provided by mirtarbase database.
54
miRTarBase ID miRNA Experiments Reference
MIRT681551 hsa-miR-6888-5p HITS-CLIP 23706177
MIRT681550 hsa-miR-3929 HITS-CLIP 23706177
MIRT681549 hsa-miR-4419b HITS-CLIP 23706177
MIRT681548 hsa-miR-4478 HITS-CLIP 23706177
MIRT681547 hsa-miR-6746-5p HITS-CLIP 23706177
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0000209 Process Protein polyubiquitination ISS
GO:0003677 Function DNA binding IEA
GO:0004842 Function Ubiquitin-protein transferase activity ISS
GO:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription 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.
Q8NE65
Protein name Zinc finger protein 738
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 34 75 KRAB box Family
Sequence
MDDLRYGVYPVKGASGYPGAERNLLEYSYFEKGPLTFRDVVIEFSQEEWQCLDTAQQDLY
RKVMLENFRNLVFLG
IDVSKPDLITCLEQGKDPWNMKRHSMVATPPESGVLKFPTIIILL
SRCFFQSVNICFIYLEP
Sequence length 137
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
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations