KEGG   Homo sapiens (human): 343637
Entry
343637            CDS       T01001                                 
Symbol
RSPO4, C20orf182, CRISTIN4
Name
(RefSeq) R-spondin 4
  KO
K23099  R-spondin 4
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Network
nt06505  WNT signaling
  Element
N01440  Wnt signaling modulation, LGR/RSPO
Disease
H00683  Anonychia congenita
H01307  Nonsyndromic congenital nail disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    343637 (RSPO4)
SSDB
Motif
Pfam: Furin-like_2 TSP1_spondin
Other DBs
NCBI-GeneID: 343637
NCBI-ProteinID: NP_001025042
OMIM: 610573
HGNC: 16175
Ensembl: ENSG00000101282
UniProt: Q2I0M5
Position
20:complement(958452..1002311)
AA seq 234 aa
MRAPLCLLLLVAHAVDMLALNRRKKQVGTGLGGNCTGCIICSEENGCSTCQQRLFLFIRR
EGIRQYGKCLHDCPPGYFGIRGQEVNRCKKCGATCESCFSQDFCIRCKRQFYLYKGKCLP
TCPPGTLAHQNTRECQGECELGPWGGWSPCTHNGKTCGSAWGLESRVREAGRAGHEEAAT
CQVLSESRKCPIQRPCPGERSPGQKKGRKDRRPRKDRKLDRRLDVRPRQPGLQP
NT seq 705 nt   +upstreamnt  +downstreamnt
atgcgggcgccactctgcctgctcctgctcgtcgcccacgccgtggacatgctcgccctg
aaccgaaggaagaagcaagtgggcactggcctggggggcaactgcacaggctgtatcatc
tgctcagaggagaacggctgttccacctgccagcagaggctcttcctgttcatccgccgg
gaaggcatccgccagtacggcaagtgcctgcacgactgtccccctgggtacttcggcatc
cgcggccaggaggtcaacaggtgcaaaaaatgtggggccacttgtgagagctgcttcagc
caggacttctgcatccggtgcaagaggcagttttacttgtacaaggggaagtgtctgccc
acctgcccgccgggcactttggcccaccagaacacacgggagtgccagggggagtgtgaa
ctgggtccctggggcggctggagcccctgcacacacaatggaaagacctgcggctcggct
tggggcctggagagccgggtacgagaggctggccgggctgggcatgaggaggcagccacc
tgccaggtgctttctgagtcaaggaaatgtcccatccagaggccctgcccaggagagagg
agccccggccagaagaagggcaggaaggaccggcgcccacgcaaggacaggaagctggac
cgcaggctggacgtgaggccgcgccagcccggcctgcagccctga

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