Homo sapiens (human): 1193
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Entry
1193 CDS
T01001
Symbol
CLIC2, CLCNL2, CLIC2b, MRXS32, XAP121
Name
(RefSeq) chloride intracellular channel 2
KO
K05022
chloride intracellular channel protein 2
Organism
hsa
Homo sapiens (human)
Disease
H00658
X-linked syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
hsa04040
]
1193 (CLIC2)
Ion channels [BR:
hsa04040
]
Chloride channels
Chloride channel, intracellular (CLIC)
1193 (CLIC2)
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Gene cluster
GFIT
Motif
Pfam:
CLIC-like_N
GST_N_2
GST_C_2
GST_N_3
Glutaredoxin
MKT1_C
GST_N
GST_N_4
Motif
Other DBs
NCBI-GeneID:
1193
NCBI-ProteinID:
NP_001280
OMIM:
300138
HGNC:
2063
Ensembl:
ENSG00000155962
UniProt:
O15247
Structure
PDB
PDBj
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All DBs
Position
X:complement(155276211..155334614)
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AA seq
247 aa
AA seq
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MSGLRPGTQVDPEIELFVKAGSDGESIGNCPFCQRLFMILWLKGVKFNVTTVDMTRKPEE
LKDLAPGTNPPFLVYNKELKTDFIKIEEFLEQTLAPPRYPHLSPKYKESFDVGCNLFAKF
SAYIKNTQKEANKNFEKSLLKEFKRLDDYLNTPLLDEIDPDSAEEPPVSRRLFLDGDQLT
LADCSLLPKLNIIKVAAKKYRDFDIPAEFSGVWRYLHNAYAREEFTHTCPEDKEIENTYA
NVAKQKS
NT seq
744 nt
NT seq
+upstream
nt +downstream
nt
atgtcaggcctgcggcccggcactcaagtggaccctgagattgagctttttgtaaaggct
ggaagtgatggagagagtattggaaactgtcccttttgccaacgccttttcatgatcctc
tggcttaaaggagttaaatttaatgtgacaactgttgacatgaccagaaagcctgaagaa
ctaaaggacttagccccaggtaccaatcctccgttcctggtgtataacaaggagttgaaa
acagacttcattaaaattgaggagtttttagaacaaaccctggctcctccaaggtaccct
cacctgagtcccaagtacaaggagtcttttgatgtgggctgtaacctctttgccaagttt
tctgcatacattaagaatacacaaaaggaggcaaataagaattttgaaaaatctctgctc
aaagaattcaagcgtctggatgactacttaaacaccccacttctggatgaaattgatcca
gacagtgctgaggaacccccagtttccagaagactattcttggatggggaccagctaaca
ctggctgattgtagcttgttacccaagctgaacattattaaagttgctgccaagaaatat
cgtgactttgacattccagcagaattctcaggagtctggcgttatctccacaatgcctat
gcccgtgaagaatttacccacacgtgtcctgaagacaaagaaattgaaaatacttacgca
aatgtggctaaacagaagagttag
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integrated database retrieval system