Homo sapiens (human): 284654
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Entry
284654 CDS
T01001
Symbol
RSPO1, CRISTIN3, RSPO
Name
(RefSeq) R-spondin 1
KO
K19471
R-spondin 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04310
Wnt signaling pathway
Network
nt06505
WNT signaling
Element
N01440
Wnt signaling modulation, LGR/RSPO
Disease
H02318
Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
284654 (RSPO1)
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GFIT
Motif
Pfam:
Furin-like_2
TSP1_spondin
TSP_1
VSP
Motif
Other DBs
NCBI-GeneID:
284654
NCBI-ProteinID:
NP_001033722
OMIM:
609595
HGNC:
21679
Ensembl:
ENSG00000169218
UniProt:
Q2MKA7
Structure
PDB
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All DBs
Position
1:complement(37611350..37634892)
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AA seq
263 aa
AA seq
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MRLGLCVVALVLSWTHLTISSRGIKGKRQRRISAEGSQACAKGCELCSEVNGCLKCSPKL
FILLERNDIRQVGVCLPSCPPGYFDARNPDMNKCIKCKIEHCEACFSHNFCTKCKEGLYL
HKGRCYPACPEGSSAANGTMECSSPAQCEMSEWSPWGPCSKKQQLCGFRRGSEERTRRVL
HAPVGDHAACSDTKETRRCTVRRVPCPEGQKRRKGGQGRRENANRNLARKESKEAGAGSR
RRKGQQQQQQQGTVGPLTSAGPA
NT seq
792 nt
NT seq
+upstream
nt +downstream
nt
atgcggcttgggctgtgtgtggtggccctggttctgagctggacgcacctcaccatcagc
agccgggggatcaaggggaaaaggcagaggcggatcagtgccgaggggagccaggcctgt
gccaaaggctgtgagctctgctctgaagtcaacggctgcctcaagtgctcacccaagctg
ttcatcctgctggagaggaacgacatccgccaggtgggcgtctgcttgccgtcctgccca
cctggatacttcgacgcccgcaaccccgacatgaacaagtgcatcaaatgcaagatcgag
cactgtgaggcctgcttcagccataacttctgcaccaagtgtaaggagggcttgtacctg
cacaagggccgctgctatccagcttgtcccgagggctcctcagctgccaatggcaccatg
gagtgcagtagtcctgcgcaatgtgaaatgagcgagtggtctccgtgggggccctgctcc
aagaagcagcagctctgtggtttccggaggggctccgaggagcggacacgcagggtgcta
catgcccctgtgggggaccatgctgcctgctctgacaccaaggagacccggaggtgcaca
gtgaggagagtgccgtgtcctgaggggcagaagaggaggaagggaggccagggccggcgg
gagaatgccaacaggaacctggccaggaaggagagcaaggaggcgggtgctggctctcga
agacgcaaggggcagcaacagcagcagcagcaagggacagtggggccactcacatctgca
gggcctgcctag
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integrated database retrieval system