Gene Gene information from NCBI Gene database.
Entrez ID 7539
Gene name ZFP37 zinc finger protein
Gene symbol ZFP37
Synonyms (NCBI Gene)
ZNF906zfp-37
Chromosome 9
Chromosome location 9q32
Summary This gene encodes a transcription factor that belongs to a large family of zinc finger proteins. A similar protein in mouse is thought to play a role in regulating the structures of the nucleolus and centromere in neurons. Alternate splicing results in mu
miRNA miRNA information provided by mirtarbase database.
53
miRTarBase ID miRNA Experiments Reference
MIRT044388 hsa-miR-320a CLASH 23622248
MIRT036645 hsa-miR-935 CLASH 23622248
MIRT550663 hsa-miR-338-5p PAR-CLIP 21572407
MIRT550662 hsa-miR-383-5p PAR-CLIP 21572407
MIRT550661 hsa-miR-5694 PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0000977 Function RNA polymerase II transcription 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:0003700 Function DNA-binding transcription factor activity NAS 9585434
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602951 12863 ENSG00000136866
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y6Q3
Protein name Zinc finger protein 37 homolog (Zfp-37)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 41 72 KRAB box Family
PF00096 zf-C2H2 293 315 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 321 343 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 377 399 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 405 427 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 433 455 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 461 483 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 489 511 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 517 539 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 545 567 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 573 595 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 601 623 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Expressed at low level in several tissues including fetal cartilage.
Sequence
MSVSSGVQILTKPETVDRRRSAETTKEAGRPLEMAVSEPEASAAEWKQLDPAQSNLYNDV
MLENYCNQASMG
CQAPKPDMISKLEKGEAPWLGKGKRPSQGCPSKIARPKQKETDGKVQK
DDDQLENIQKSQNKLLREVAVKKKTQAKKNGSDCGSLGKKNNLHKKHVPSKKRLLKFESC
GKILKQNLDLPDHSRNCVKRKSDAAKEHKKSFNHSLSDTRKGKKQTGKKHEKLSSHSSSD
KCNKTGKKHDKLCCHSSSHIKQDKIQTGEKHEKSPSLSSSTKHEKPQACVKPYECNQCGK
VLSHKQGLIDHQRVH
TGEKPYECNECGIAFSQKSHLVVHQRTHTGEKPYECIQCGKAHGH
KHALTDHLRIHTGEKPYECAECGKTFRHSSNLIQHVRSHTGEKPYECKECGKSFRYNSSL
TEHVRTH
TGEIPYECNECGKAFKYSSSLTKHMRIHTGEKPFECNECGKAFSKKSHLIIHQ
RTH
TKEKPYKCNECGKAFGHSSSLTYHMRTHTGESPFECNQCGKGFKQIEGLTQHQRVHT
GEKPYECNECGKAFSQKSHLIVHQRTHTGEKPYECNECEKAFNAKSQLVIHQRSHTGEKP
YECNECGKTFKQNASLTKHVKTHSEDKSHE
Sequence length 630
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
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acrofacial Dysostosis Acrofacial Dysostosis BEFREE 9585434
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes mellitus Pubtator 36360783 Associate
★☆☆☆☆
Found in Text Mining only
Limb Deformities, Congenital Congenital anomaly of limb BEFREE 9585434
★☆☆☆☆
Found in Text Mining only
Nager syndrome Nager Syndrome BEFREE 9585434
★☆☆☆☆
Found in Text Mining only