GRCR1 Rabbit Polyclonal Antibody, 20ul In vitro Transcription Defects in this gene are

Defects in this gene are a cause of congenital secretory sodium diarrhea

Cortactin is localized in the cytoplasm and in areas of the cell-substratum contacts

May be one regulator of transcriptional events during hemopoietic development

The protein encoded by this gene| in combination with autophagy protein 12| functions as an E1-like activating enzyme in a ubiquitin-like conjugating system

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GRCR1 Rabbit Polyclonal Antibody, 20ul In vitro Transcription Defects in this gene areThis gene is one of 60 loci associated with autosomal recessive nonsyndromic hearing impairment. This gene encodes a protein which contains GRX like domains; these domains play a role in the S glutathionylation of proteins and may be involved in actin organization in hair cells.