ZNF335 Antibody, HRP conjugated

1. ZNF335 gene mutation is associated with extreme microcephaly with a severely simplified gyral pattern, decreased brain size, increased extra-axial space, enlarged ventricles, absence of the corpus callosum and delayed myelination PMID: 26479514
2. In this article, we describe another family harboring ZNF335 mutations. The mutations were individually transmitted by her parents, indicating that the proband was compound heterozygous for the mutations. We speculate that invisible basal ganglia may be the key feature of ZNF335 mutations. PMID: 27540107
3. we performed a meta-analysis of our data with the previous reports, identifying two further loci harbouring the ZNF335 and NIFA genes which now exceed genome-wide significance, taking the total number of CD susceptibility loci to 42. PMID: 25920553
4. NIF-1 expression is associated with tumor grade in bladder cancer. PMID: 23924207
5. Study identifies and characterizes a nuclear zinc finger protein, ZNF335/NIF-1, as a causative gene for severe microcephaly, small somatic size, and neonatal death. PMID: 23178126
6. NRC-interacting factor 1 is a novel cotransducer that interacts with and regulates the activity of the nuclear hormone receptor coactivator NRC PMID: 12215545

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HGNC: 15807

OMIM: 610827

KEGG: hsa:63925

STRING: 9606.ENSP00000325326

UniGene: Hs.174193