Homo sapiens (human): 343637 Help 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) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Furin-like_2 TSP1_spondin Motif Other DBs NCBI-GeneID:  343637 NCBI-ProteinID:  NP_001025042 OMIM:  610573 HGNC:  16175 Ensembl:  ENSG00000101282 UniProt:  Q2I0M5 LinkDB All DBs Position 20:complement(958452..1002311) Genome browser AA seq 234 aa AA seqDB search MRAPLCLLLLVAHAVDMLALNRRKKQVGTGLGGNCTGCIICSEENGCSTCQQRLFLFIRR EGIRQYGKCLHDCPPGYFGIRGQEVNRCKKCGATCESCFSQDFCIRCKRQFYLYKGKCLP TCPPGTLAHQNTRECQGECELGPWGGWSPCTHNGKTCGSAWGLESRVREAGRAGHEEAAT CQVLSESRKCPIQRPCPGERSPGQKKGRKDRRPRKDRKLDRRLDVRPRQPGLQP NT seq 705 nt NT seq  +upstreamnt  +downstreamnt atgcgggcgccactctgcctgctcctgctcgtcgcccacgccgtggacatgctcgccctg aaccgaaggaagaagcaagtgggcactggcctggggggcaactgcacaggctgtatcatc tgctcagaggagaacggctgttccacctgccagcagaggctcttcctgttcatccgccgg gaaggcatccgccagtacggcaagtgcctgcacgactgtccccctgggtacttcggcatc cgcggccaggaggtcaacaggtgcaaaaaatgtggggccacttgtgagagctgcttcagc caggacttctgcatccggtgcaagaggcagttttacttgtacaaggggaagtgtctgccc acctgcccgccgggcactttggcccaccagaacacacgggagtgccagggggagtgtgaa ctgggtccctggggcggctggagcccctgcacacacaatggaaagacctgcggctcggct tggggcctggagagccgggtacgagaggctggccgggctgggcatgaggaggcagccacc tgccaggtgctttctgagtcaaggaaatgtcccatccagaggccctgcccaggagagagg agccccggccagaagaagggcaggaaggaccggcgcccacgcaaggacaggaagctggac cgcaggctggacgtgaggccgcgccagcccggcctgcagccctga

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