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Immunogen sequence: LSVSKASDSQ EDQEKRNCLG TSEAQSNLSG GENRVQVLKT VPVNLSLNQD HLENSKREQY SISFPESSAI IPVSGITVVK AEDFTPVFMA PPVHYPRGDG EEQRVVIFEQ TQYDVPSLAT HSAYLKDDQR STPDSTYSES FKDAATEKFR SASVGAEEYM YDQTSSGTFQ Y; Positive Samples: SH-SY5Y; Cellular Location: Membrane, Nucleus
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Brother of mammalian grainyhead; grainyhead-like 2; Grainyhead-like protein 2 homolog; grainyhead-like transcription factor 2; Transcription factor CP2-like 3
Gene Aliases: BOM; DFNA28; ECTDS; GRHL2; RGD1561191; TFCP2L3
UniProt ID: (Human) Q6NT03
Entrez Gene ID: (Human) 79977, (Rat) 299979
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