Entry |
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Symbol |
CLCN3_4_5
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Name |
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Pathway |
map04613 | Neutrophil extracellular trap formation |
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Disease |
H00214 | Hypophosphatemic rickets |
H00658 | X-linked syndromic intellectual developmental disorder |
H02142 | X-linked recessive hypophosphatemic rickets |
H02147 | X-linked recessive nephrolithiasis with renal failure |
H02148 | Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis |
H02149 | X-linked hypercalciuric nephrolithiasis |
H02397 | Neurodevelopmental disorder with movement abnormalities or hypotonia |
|
Brite |
KEGG Orthology (KO) [BR:ko00001]
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
K05012 CLCN3_4_5; chloride channel 3/4/5
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels
K05012 CLCN3_4_5; chloride channel 3/4/5
Ion channels [BR:ko04040]
Chloride channels
Chloride channel (CLC)
K05012 CLCN3_4_5; chloride channel 3/4/5
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Other DBs |
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Genes |
» show all
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Reference |
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Authors |
Borsani G, Rugarli EI, Taglialatela M, Wong C, Ballabio A |
Title |
Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein. |
Journal |
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Sequence |
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Reference |
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Authors |
Kawasaki M, Fukuma T, Yamauchi K, Sakamoto H, Marumo F, Sasaki S |
Title |
Identification of an acid-activated Cl(-) channel from human skeletal muscles. |
Journal |
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Sequence |
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Reference |
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Authors |
Fisher SE, van Bakel I, Lloyd SE, Pearce SH, Thakker RV, Craig IW |
Title |
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). |
Journal |
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Sequence |
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LinkDB |
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