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FIGURE: 1 / 2
Sequence of this protein is as follows: MEGSNGFGID SILSHRAGSP ALPKGDPLLG DCRSPLELSP RSESSSDCSS PASPGRDCLE TGTPRPGGAS GPGLDSHLQP GQLSAPAQSR TVTSSFLIRD ILADCKPLAA CAPYSSSGQP AAPEPGGRLA AKAAEDFRDK LDKSGSNASS DSEYKVKEEG DREISSSRDS PPVRLKKPRK ARTAFTDHQL AQLERSFERQ KYLSVQDRME LAASLNLTDT QVKTWYQNRR TKWKRQTAVG LELLAEAGNY SALQRMFPSP YFYPQSLVSN LDPGAALYLY RGPSAPPPAL QRPLVPRILI HGLQGASEPP PPLPPLAGVL PRAAQPR
BARHL1 (BarH Like Homeobox 1) is a Protein Coding gene. Diseases associated with BARHL1 include Deafness, Autosomal Recessive 27 and Deafness, Autosomal Dominant 16. Gene Ontology (GO) annotations related to this gene include sequence-specific DNA binding and proximal promoter DNA-binding transcription activator activity, RNA polymerase II-specific. An important paralog of this gene is BARHL2.
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Protein Aliases: BarH-like 1 homeobox protein; BarH-like homeobox 1; PKCdeltaVIII
Gene Aliases: BARHL1; FKSG31
UniProt ID: (Human) Q9BZE3
Entrez Gene ID: (Human) 56751
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