EYA1 polyclonal, anti-human

Background:
This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Four transcript variants encoding three distinct isoforms have been identified for this gene.

Other Names:
Eyes absent homolog 1, 3.1.3.16, 3.1.3.48, EYA1

Antigen Types:
Synthetic Peptide

Gene Name:
EYA1
Gene ID:
2138
Primary Accession: Q99502
Other Accession: NP_742056;2138;14048 (mouse); 502935 (rat);