跳转至内容
Merck
CN

CLDN19

claudin 19

别名:
HOMG5
物种:
UniProtKB ID:
基因ID:
  • Human(149461) Summary: The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]
  • Mouse(242653) claudin 19
  • Rat(298487) claudin 19
  • sheep(101102362) claudin 19
  • domestic guinea pig(100714164) claudin 19
  • cow(513034) claudin 19
  • dog(607005) claudin 19
  • naked mole-rat(101725162) claudin 19
  • Horse(100053591) claudin 19
  • Zebrafish(550431) claudin 19
  • domestic cat(101093875) claudin 19

Custom & Knockdown Gene Products

Antibodies

产品编号
说明
物种反应性
应用
Anti-Cldn19 Antibody Produced In Rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
物种反应性
human
应用
immunofluorescence

esiRNA

产品编号
说明
物种
MISSION® esiRNA, targeting mouse Cldn19,
物种
mouse