Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Peptide sequence: AVGSIVYVLA GFQGVGRLGH ILEYNTETDK WVANSKVRAF PVTSCLICVV
Sequence homology: Cow: 93%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100%
Defects in KLHL7 are the cause of retinitis pigmentosa type 42 (RP42). The specific function of this protein remains unknown.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: kelch-like 6; kelch-like 7; kelch-like family member 7; Kelch-like protein 7; kelch/BTB
Gene Aliases: KLHL6; KLHL7; SBBI26
UniProt ID: (Human) Q8IXQ5
Entrez Gene ID: (Human) 55975
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