EYA1/EYA4 Polyclonal Antibody, 20ul Custom Peptide Synthesis Because of their central role

Because of their central role in linking amino acids with nucleotide triplets contained in tRNAS

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

™ Human IL-2 One-Step ELISA Kit-48 Tests

Two protein-coding transcripts and one non-protein coding transcript have been found for this gene

Alternate transcriptional splice variants of this gene

EYA1/EYA4 Polyclonal Antibody, 20ul Custom Peptide Synthesis Because of their central roleThis 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. Alternatively spliced transcript