KEGG   Homo sapiens (human): 1193
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)
SSDB
Motif
Pfam: GST_N_2 GST_C_2 GST_N_3 Glutaredoxin MKT1_C GST_N_4 GST_N GST_C
Other DBs
NCBI-GeneID: 1193
NCBI-ProteinID: NP_001280
OMIM: 300138
HGNC: 2063
Ensembl: ENSG00000155962
UniProt: O15247
Structure
Position
X:complement(155276211..155334614)
AA seq 247 aa
MSGLRPGTQVDPEIELFVKAGSDGESIGNCPFCQRLFMILWLKGVKFNVTTVDMTRKPEE
LKDLAPGTNPPFLVYNKELKTDFIKIEEFLEQTLAPPRYPHLSPKYKESFDVGCNLFAKF
SAYIKNTQKEANKNFEKSLLKEFKRLDDYLNTPLLDEIDPDSAEEPPVSRRLFLDGDQLT
LADCSLLPKLNIIKVAAKKYRDFDIPAEFSGVWRYLHNAYAREEFTHTCPEDKEIENTYA
NVAKQKS
NT seq 744 nt   +upstreamnt  +downstreamnt
atgtcaggcctgcggcccggcactcaagtggaccctgagattgagctttttgtaaaggct
ggaagtgatggagagagtattggaaactgtcccttttgccaacgccttttcatgatcctc
tggcttaaaggagttaaatttaatgtgacaactgttgacatgaccagaaagcctgaagaa
ctaaaggacttagccccaggtaccaatcctccgttcctggtgtataacaaggagttgaaa
acagacttcattaaaattgaggagtttttagaacaaaccctggctcctccaaggtaccct
cacctgagtcccaagtacaaggagtcttttgatgtgggctgtaacctctttgccaagttt
tctgcatacattaagaatacacaaaaggaggcaaataagaattttgaaaaatctctgctc
aaagaattcaagcgtctggatgactacttaaacaccccacttctggatgaaattgatcca
gacagtgctgaggaacccccagtttccagaagactattcttggatggggaccagctaaca
ctggctgattgtagcttgttacccaagctgaacattattaaagttgctgccaagaaatat
cgtgactttgacattccagcagaattctcaggagtctggcgttatctccacaatgcctat
gcccgtgaagaatttacccacacgtgtcctgaagacaaagaaattgaaaatacttacgca
aatgtggctaaacagaagagttag

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