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EYA1/EYA4 Polyclonal Antibody, 50ul Liquid Handling This gene was reported to

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EYA1/EYA4 Polyclonal Antibody, 50ul Liquid Handling This gene was reported toThis 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

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Description

This gene was reported to be deleted

also known as Dwarfism of Sindh

Dystrophin (as enc

this gene is similar to the Shaw subfamily

EYA1/EYA4 Polyclonal Antibody, 50ul Liquid Handling This gene was reported toThis 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

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