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Invitrogen
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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: kelch-like 6; kelch-like 7; kelch-like family member 7; Kelch-like protein 7; kelch/BTB
基因别名: KLHL6; KLHL7; SBBI26
UniProt ID: (Human) Q8IXQ5
Entrez Gene ID: (Human) 55975