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1.C.123.1.7 Pejvakin (DFNB59; PJVK) of 357 aas. It is a constituent of the afferent auditory pathway, causing DFNB59 auditory neuropathy (Delmaghani et al. 2006), autosomal recessive nosyndromic hearing impairment (Collin et al. 2007). It is also called the diaphanous homologue 3 (DIAPH3).
Accession Number:	Q0ZLH3
Protein Name:	Pejvakin
Length:	352
Molecular Weight:	39913.00
Species:	Homo sapiens (Human) [9606]
Number of TMSs:	1
Substrate	orobol

UniProt (Universal Protein Resource)
CDD Search (Conserved Domain Database)

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FASTA formatted sequence

1:	MFAAATKSFV KQVGDGGRLV PVPSLSEADK YQPLSLVVKK KRCFLFPRYK FTSTPFTLKD 
61:	ILLGDREISA GISSYQLLNY EDESDVSLYG RRGNHIVNDV GINVAGSDSI AVKASFGIVT 
121:	KHEVEVSTLL KEITTRKINF DHSLIRQSRS SRKAVLCVVM ESIRTTRQCS LSVHAGIRGE 
181:	AMRFHFMDEQ NPKGRDKAIV FPAHTTIAFS VFELFIYLDG AFDLCVTSVS KGGFEREETA 
241:	TFALLYRLRN ILFERNRRVM DVISRSQLYL DDLFSDYYDK PLSMTDISLK EGTHIRVNLL 
301:	NHNIPKGPCI LCGMGNFKRE TVYGCFQCSV DGQKYVRLHA VPCFDIWHKR MK

1.C.123.1.7
Pejvakin (DFNB59; PJVK) of 357 aas. It is a constituent of the afferent auditory pathway, causing DFNB59 auditory neuropathy (Delmaghani et al. 2006), autosomal recessive nosyndromic hearing impairment (Collin et al. 2007). It is also called the diaphanous homologue 3 (DIAPH3).

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1.C.123.1.7Pejvakin (DFNB59; PJVK) of 357 aas. It is a constituent of the afferent auditory pathway, causing DFNB59 auditory neuropathy (Delmaghani et al. 2006), autosomal recessive nosyndromic hearing impairment (Collin et al. 2007). It is also called the diaphanous homologue 3 (DIAPH3).

Cross database links:

External Searches:

Analyze:

1.C.123.1.7
Pejvakin (DFNB59; PJVK) of 357 aas. It is a constituent of the afferent auditory pathway, causing DFNB59 auditory neuropathy (Delmaghani et al. 2006), autosomal recessive nosyndromic hearing impairment (Collin et al. 2007). It is also called the diaphanous homologue 3 (DIAPH3).