Homo sapiens (human): 1041
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Entry
1041 CDS
T01001
Symbol
CDSN, HTSS, HTSS1, HYPT2, PSS, PSS1
Name
(RefSeq) corneodesmosin
KO
K23457
corneodesmosin
Organism
hsa
Homo sapiens (human)
Disease
H00737
Peeling skin syndrome
H00786
Hypotrichosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99992 Structural proteins
1041 (CDSN)
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NCBI-GeneID:
1041
NCBI-ProteinID:
NP_001255
OMIM:
602593
HGNC:
1802
Ensembl:
ENSG00000204539
UniProt:
Q15517
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Position
6:complement(31115087..31120446)
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AA seq
529 aa
AA seq
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MGSSRAPWMGRVGGHGMMALLLAGLLLPGTLAKSIGTFSDPCKDPTRITSPNDPCLTGKG
DSSGFSSYSGSSSSGSSISSARSSGGGSSGSSSGSSIAQGGSAGSFKPGTGYSQVSYSSG
SGSSLQGASGSSQLGSSSSHSGNSGSHSGSSSSHSSSSSSFQFSSSSFQVGNGSALPTND
NSYRGILNPSQPGQSSSSSQTFGVSSSGQSVSSNQRPCSSDIPDSPCSGGPIVSHSGPYI
PSSHSVSGGQRPVVVVVDQHGSGAPGVVQGPPCSNGGLPGKPCPPITSVDKSYGGYEVVG
GSSDSYLVPGMTYSKGKIYPVGYFTKENPVKGSPGVPSFAAGPPISEGKYFSSNPIIPSQ
SAASSAIAFQPVGTGGVQLCGGGSTGSKGPCSPSSSRVPSSSSISSSSGLPYHPCGSASQ
SPCSPPGTGSFSSSSSSQSSGKIILQPCGSKSSSSGHPCMSVSSLTLTGGPDGSPHPDPS
AGAKPCGSSSAGKIPCRSIRDILAQVKPLGPQLADPEVFLPQGELLNSP
NT seq
1590 nt
NT seq
+upstream
nt +downstream
nt
atgggctcgtctcgggcaccctggatggggcgtgtgggtgggcacgggatgatggcactg
ctgctggctggtctcctcctgccagggaccttggctaagagcattggcaccttctcagac
ccttgtaaggaccccacgcgtatcacctcccctaacgacccctgcctcactgggaagggt
gactccagcggtttcagtagctacagtggctccagcagttctggcagctccatttccagt
gccagaagctctggtggtggctccagtggtagctccagcggatccagcattgcccagggt
ggttctgcaggatcttttaagccaggaacggggtattcccaggtcagctactcctccgga
tctggctctagtctacaaggtgcatccggttcctcccagctggggagcagcagctctcac
tcgggaaacagcggctctcactcgggaagcagcagctctcattcgagcagcagcagcagc
tttcagttcagcagcagcagcttccaagtagggaatggctctgctctgccaaccaatgac
aactcttaccgcggaatactaaacccttcccagcctggacaaagctcttcctcttcccag
acctttggggtatccagcagtggccaaagcgtcagctccaaccagcgtccctgtagttcg
gacatccccgactctccctgcagtggagggcccatcgtctcgcactccggcccctacatc
cccagctcccactctgtgtcagggggtcagaggcctgtggtggtggtggtggaccagcac
ggttctggtgcccctggagtggttcaaggtcccccctgtagcaatggtggccttccaggc
aagccctgtcccccaatcacctctgtagacaaatcctatggtggctacgaggtggtgggt
ggctcctctgacagttatctggttccaggcatgacctacagtaagggtaaaatctaccct
gtgggctacttcaccaaagagaaccctgtgaaaggctctccaggggtcccttcctttgca
gctgggccccccatctctgagggcaaatacttctccagcaaccccatcatccccagccag
tcggcagcttcctcggccattgcattccagccagtggggactggtggggtccagctctgt
ggaggcggctccacgggctccaagggaccctgctctccctccagttctcgagtccccagc
agttctagcatttccagcagctccggtttaccctaccatccctgcggcagtgcttcccag
agcccctgctccccaccaggcaccggctccttcagcagcagctccagttcccaatccagt
ggcaaaatcatccttcagccttgtggcagcaagtccagctcttctggtcacccttgcatg
tctgtctcctccttgacactgactgggggccccgatggctctccccatcctgatccctcc
gctggtgccaagccctgtggctccagcagtgctggaaagatcccctgccgctccatccgg
gatatcctagcccaagtgaagcctctggggccccagctagctgaccctgaagttttccta
ccccaaggagagttactcaacagtccataa
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