ZNF672 is a 452 amino acid nuclear protein that may be involved in transcriptional regulation. Belonging to the Krüppel C2H2-type zinc-finger protein family, ZNF672 contains 14 C2H2-type zinc fingers. ZNF672 exists as two alternatively spliced isoforms, and is encoded by a gene that maps to human chromosome 1q44. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes, comprises nearly 8% of the human genome, and houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome.
Function:
May be involved in transcriptional regulation.
Subcellular Location:
Nucleus.
Similarity:
Belongs to the krueppel C2H2-type zinc-finger protein family.
Contains 14 C2H2-type zinc fingers.
SWISS:
Q499Z4
Gene ID:
79894
Database links:
Entrez Gene: 79894 Human
Entrez Gene: 319475 Mouse
Entrez Gene: 303165 Rat
SwissProt: Q499Z4 Human
SwissProt: Q99LH4 Mouse
SwissProt: Q642B2 Rat
Unigene: 521151 Human
Unigene: 72124 Mouse
Unigene: 143913 Rat
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