| Name |
|---|
ESCO1 Geneestablishment of sister chromatid cohesion N-acetyltransferase 1 Enables identical protein binding activity; peptide-lysine-N-acetyltransferase activity; and zinc ion binding activity. Involved in peptidyl-lysine acetylation; post-translational protein acetylation; and regulation of DNA replication. Located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ESCO2 Geneestablishment of sister chromatid cohesion N-acetyltransferase 2 This gene encodes a protein that may have acetyltransferase activity and may be required for the establishment of sister chromatid cohesion during the S phase of mitosis. Mutations in this gene have been associated with Roberts syndrome. [provided by RefSeq, Jul 2008] |
LOC105375109 Geneskin secretory protein xP2-like |
PI3 Genepeptidase inhibitor 3, skin-derived This gene encodes an elastase-specific inhibitor that functions as an antimicrobial peptide against Gram-positive and Gram-negative bacteria, and fungal pathogens. The protein contains a WAP-type four-disulfide core (WFDC) domain, and is thus a member of the WFDC domain family. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. Expression of this gene is upgulated by bacterial lipopolysaccharides and cytokines. [provided by RefSeq, Oct 2014] |
LOC105379200 Geneskin secretory protein xP2-like |
TST2 GeneTuberculin skin test reactivity QTL |
TST1 GeneTuberculin skin test reactivity, absence of |
LOC105374086 Geneskin secretory protein xP2-like |
SHEP8 GeneSkin/hair/eye pigmentation 8, freckling |
KWE Genekeratolytic winter erythema (Oudtshoorn skin disease) |
LOC105378948 Geneskin secretory protein xP2-like |