Search
Search
Bioss
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
图: 1 / 3
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: BTB/POZ domain containing protein; kelch-like 6; kelch-like 7; kelch-like family member 7; Kelch-like protein 7; kelch/BTB
基因别名: 2700038B03Rik; D5Ertd363e; KLHL6; KLHL7; SBBI26
UniProt ID: (Human) Q8IXQ5, (Mouse) Q8BUL5, (Rat) Q5XHZ6
Entrez Gene ID: (Human) 55975, (Mouse) 52323, (Rat) 362303