Name

ESCO1 Gene

establishment 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 Gene

establishment 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 Gene

skin secretory protein xP2-like

PI3 Gene

peptidase 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 Gene

skin secretory protein xP2-like

TST2 Gene

Tuberculin skin test reactivity QTL

TST1 Gene

Tuberculin skin test reactivity, absence of

LOC105374086 Gene

skin secretory protein xP2-like

SHEP8 Gene

Skin/hair/eye pigmentation 8, freckling

KWE Gene

keratolytic winter erythema (Oudtshoorn skin disease)

LOC105378948 Gene

skin secretory protein xP2-like