KEGG   Homo sapiens (human): 284654
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)
SSDB
Motif
Pfam: Furin-like_2 TSP1_spondin TSP_1 VSP
Other DBs
NCBI-GeneID: 284654
NCBI-ProteinID: NP_001033722
OMIM: 609595
HGNC: 21679
Ensembl: ENSG00000169218
UniProt: Q2MKA7
Structure
LinkDB
Position
1:complement(37611350..37634892)
AA seq 263 aa
MRLGLCVVALVLSWTHLTISSRGIKGKRQRRISAEGSQACAKGCELCSEVNGCLKCSPKL
FILLERNDIRQVGVCLPSCPPGYFDARNPDMNKCIKCKIEHCEACFSHNFCTKCKEGLYL
HKGRCYPACPEGSSAANGTMECSSPAQCEMSEWSPWGPCSKKQQLCGFRRGSEERTRRVL
HAPVGDHAACSDTKETRRCTVRRVPCPEGQKRRKGGQGRRENANRNLARKESKEAGAGSR
RRKGQQQQQQQGTVGPLTSAGPA
NT seq 792 nt   +upstreamnt  +downstreamnt
atgcggcttgggctgtgtgtggtggccctggttctgagctggacgcacctcaccatcagc
agccgggggatcaaggggaaaaggcagaggcggatcagtgccgaggggagccaggcctgt
gccaaaggctgtgagctctgctctgaagtcaacggctgcctcaagtgctcacccaagctg
ttcatcctgctggagaggaacgacatccgccaggtgggcgtctgcttgccgtcctgccca
cctggatacttcgacgcccgcaaccccgacatgaacaagtgcatcaaatgcaagatcgag
cactgtgaggcctgcttcagccataacttctgcaccaagtgtaaggagggcttgtacctg
cacaagggccgctgctatccagcttgtcccgagggctcctcagctgccaatggcaccatg
gagtgcagtagtcctgcgcaatgtgaaatgagcgagtggtctccgtgggggccctgctcc
aagaagcagcagctctgtggtttccggaggggctccgaggagcggacacgcagggtgcta
catgcccctgtgggggaccatgctgcctgctctgacaccaaggagacccggaggtgcaca
gtgaggagagtgccgtgtcctgaggggcagaagaggaggaagggaggccagggccggcgg
gagaatgccaacaggaacctggccaggaaggagagcaaggaggcgggtgctggctctcga
agacgcaaggggcagcaacagcagcagcagcaagggacagtggggccactcacatctgca
gggcctgcctag

KEGG   Homo sapiens (human): 340419
Entry
340419            CDS       T01001                                 
Symbol
RSPO2, CRISTIN2, HHRRD, TETAMS2
Name
(RefSeq) R-spondin 2
  KO
K23097  R-spondin 2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Network
nt06505  WNT signaling
  Element
N01440  Wnt signaling modulation, LGR/RSPO
Disease
H00636  Tetra-amelia syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    340419 (RSPO2)
SSDB
Motif
Pfam: Furin-like_2 TSP1_spondin VSP
Other DBs
NCBI-GeneID: 340419
NCBI-ProteinID: NP_848660
OMIM: 610575
HGNC: 28583
Ensembl: ENSG00000147655
UniProt: Q6UXX9 B3KVP3
LinkDB
Position
8:complement(107899316..108083620)
AA seq 243 aa
MQFRLFSFALIILNCMDYSHCQGNRWRRSKRASYVSNPICKGCLSCSKDNGCSRCQQKLF
FFLRREGMRQYGECLHSCPSGYYGHRAPDMNRCARCRIENCDSCFSKDFCTKCKVGFYLH
RGRCFDECPDGFAPLEETMECVEGCEVGHWSEWGTCSRNNRTCGFKWGLETRTRQIVKKP
VKDTILCPTIAESRRCKMTMRHCPGGKRTPKAKEKRNKKKKRKLIERAQEQHSVFLATDR
ANQ
NT seq 732 nt   +upstreamnt  +downstreamnt
atgcagtttcgccttttctcctttgccctcatcattctgaactgcatggattacagccac
tgccaaggcaaccgatggagacgcagtaagcgagctagttatgtatcaaatcccatttgc
aagggttgtttgtcttgttcaaaggacaatgggtgtagccgatgtcaacagaagttgttc
ttcttccttcgaagagaagggatgcgccagtatggagagtgcctgcattcctgcccatcc
gggtactatggacaccgagccccagatatgaacagatgtgcaagatgcagaatagaaaac
tgtgattcttgctttagcaaagacttttgtaccaagtgcaaagtaggcttttatttgcat
agaggccgttgctttgatgaatgtccagatggttttgcaccattagaagaaaccatggaa
tgtgtggaaggatgtgaagttggtcattggagcgaatggggaacttgtagcagaaataat
cgcacatgtggatttaaatggggtctggaaaccagaacacggcaaattgttaaaaagcca
gtgaaagacacaatactgtgtccaaccattgctgaatccaggagatgcaagatgacaatg
aggcattgtccaggagggaagagaacaccaaaggcgaaggagaagaggaacaagaaaaag
aaaaggaagctgatagaaagggcccaggagcaacacagcgtcttcctagctacagacaga
gctaaccaataa

KEGG   Homo sapiens (human): 84870
Entry
84870             CDS       T01001                                 
Symbol
RSPO3, CRISTIN1, PWTSR, THSD2
Name
(RefSeq) R-spondin 3
  KO
K23098  R-spondin 3
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Network
nt06505  WNT signaling
  Element
N01440  Wnt signaling modulation, LGR/RSPO
Drug target
Rosmantuzumab: D11369
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    84870 (RSPO3)
SSDB
Motif
Pfam: Furin-like_2 TSP1_spondin
Other DBs
NCBI-GeneID: 84870
NCBI-ProteinID: NP_116173
OMIM: 610574
HGNC: 20866
Ensembl: ENSG00000146374
UniProt: Q9BXY4
LinkDB
Position
6:127118671..127199481
AA seq 272 aa
MHLRLISWLFIILNFMEYIGSQNASRGRRQRRMHPNVSQGCQGGCATCSDYNGCLSCKPR
LFFALERIGMKQIGVCLSSCPSGYYGTRYPDINKCTKCKADCDTCFNKNFCTKCKSGFYL
HLGKCLDNCPEGLEANNHTMECVSIVHCEVSEWNPWSPCTKKGKTCGFKRGTETRVREII
QHPSAKGNLCPPTNETRKCTVQRKKCQKGERGKKGRERKRKKPNKGESKEAIPDSKSLES
SKEIPEQRENKQQQKKRKVQDKQKSVSVSTVH
NT seq 819 nt   +upstreamnt  +downstreamnt
atgcacttgcgactgatttcttggctttttatcattttgaactttatggaatacatcggc
agccaaaacgcctcccggggaaggcgccagcgaagaatgcatcctaacgttagtcaaggc
tgccaaggaggctgtgcaacatgctcagattacaatggatgtttgtcatgtaagcccaga
ctattttttgctctggaaagaattggcatgaagcagattggagtatgtctctcttcatgt
ccaagtggatattatggaactcgatatccagatataaataagtgtacaaaatgcaaagct
gactgtgatacctgtttcaacaaaaatttctgcacaaaatgtaaaagtggattttactta
caccttggaaagtgccttgacaattgcccagaagggttggaagccaacaaccatactatg
gagtgtgtcagtattgtgcactgtgaggtcagtgaatggaatccttggagtccatgcacg
aagaagggaaaaacatgtggcttcaaaagagggactgaaacacgggtccgagaaataata
cagcatccttcagcaaagggtaacctgtgtcccccaacaaatgagacaagaaagtgtaca
gtgcaaaggaagaagtgtcagaagggagaacgaggaaaaaaaggaagggagaggaaaaga
aaaaaacctaataaaggagaaagtaaagaagcaatacctgacagcaaaagtctggaatcc
agcaaagaaatcccagagcaacgagaaaacaaacagcagcagaagaagcgaaaagtccaa
gataaacagaaatcggtatcagtcagcactgtacactag

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
LinkDB
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

KEGG   Homo sapiens (human): 55366
Entry
55366             CDS       T01001                                 
Symbol
LGR4, BNMD17, DPSL, GPR48
Name
(RefSeq) leucine rich repeat containing G protein-coupled receptor 4
  KO
K04309  leucine-rich repeat-containing G protein-coupled receptor 4
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Network
nt06505  WNT signaling
  Element
N01440  Wnt signaling modulation, LGR/RSPO
Disease
H01593  Osteoporosis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    55366 (LGR4)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04030 G protein-coupled receptors [BR:hsa04030]
    55366 (LGR4)
G protein-coupled receptors [BR:hsa04030]
 Rhodopsin family
  Others
   R-spondin
    55366 (LGR4)
SSDB
Motif
Pfam: LRR_8 LRR_4 LRR_5 LRR_1 LRR_9 7tm_1 LRRNT LRR_6
Other DBs
NCBI-GeneID: 55366
NCBI-ProteinID: NP_060960
OMIM: 606666
HGNC: 13299
Ensembl: ENSG00000205213
UniProt: Q9BXB1 Q59ER8
Structure
LinkDB
Position
11:complement(27365961..27472790)
AA seq 951 aa
MPGPLGLLCFLALGLLGSAGPSGAAPPLCAAPCSCDGDRRVDCSGKGLTAVPEGLSAFTQ
ALDISMNNITQLPEDAFKNFPFLEELQLAGNDLSFIHPKALSGLKELKVLTLQNNQLKTV
PSEAIRGLSALQSLRLDANHITSVPEDSFEGLVQLRHLWLDDNSLTEVPVHPLSNLPTLQ
ALTLALNKISSIPDFAFTNLSSLVVLHLHNNKIRSLSQHCFDGLDNLETLDLNYNNLGEF
PQAIKALPSLKELGFHSNSISVIPDGAFDGNPLLRTIHLYDNPLSFVGNSAFHNLSDLHS
LVIRGASMVQQFPNLTGTVHLESLTLTGTKISSIPNNLCQEQKMLRTLDLSYNNIRDLPS
FNGCHALEEISLQRNQIYQIKEGTFQGLISLRILDLSRNLIHEIHSRAFATLGPITNLDV
SFNELTSFPTEGLNGLNQLKLVGNFKLKEALAAKDFVNLRSLSVPYAYQCCAFWGCDSYA
NLNTEDNSLQDHSVAQEKGTADAANVTSTLENEEHSQIIIHCTPSTGAFKPCEYLLGSWM
IRLTVWFIFLVALFFNLLVILTTFASCTSLPSSKLFIGLISVSNLFMGIYTGILTFLDAV
SWGRFAEFGIWWETGSGCKVAGFLAVFSSESAIFLLMLATVERSLSAKDIMKNGKSNHLK
QFRVAALLAFLGATVAGCFPLFHRGEYSASPLCLPFPTGETPSLGFTVTLVLLNSLAFLL
MAVIYTKLYCNLEKEDLSENSQSSMIKHVAWLIFTNCIFFCPVAFFSFAPLITAISISPE
IMKSVTLIFFPLPACLNPVLYVFFNPKFKEDWKLLKRRVTKKSGSVSVSISSQGGCLEQD
FYYDCGMYSHLQGNLTVCDCCESFLLTKPVSCKHLIKSHSCPALAVASCQRPEGYWSDCG
TQSAHSDYADEEDSFVSDSSDQVQACGRACFYQSRGFPLVRYAYNLPRVKD
NT seq 2856 nt   +upstreamnt  +downstreamnt
atgccgggcccgctagggctgctctgcttcctcgccctggggctgctcggctcggccggg
cccagcggcgcggcgccgcctctctgcgcggcgccctgcagctgcgacggcgaccgtcgg
gtggactgctccgggaaggggctgacggccgtgcccgaggggctcagcgccttcacccaa
gcgctggatatcagtatgaacaacattactcagttgccagaagatgcatttaagaacttt
ccttttctagaagagctacaattggcgggcaacgacctttcttttatccacccaaaggcc
ttgtctgggttgaaagaactcaaagttctaacgctccagaataatcagttgaaaacagta
cccagtgaagccattcgagggctgagtgctttgcagtctttgcgtttagatgccaaccat
attacctcagtccccgaggacagttttgaaggacttgttcagttacggcatctgtggctg
gatgacaacagcttgacggaggtgcctgtgcaccccctcagcaatctgcccaccctacag
gcgctgaccctggctctcaacaagatctcaagcatccctgactttgcatttaccaacctt
tcaagcctggtagttctgcatcttcataacaataaaattagaagcctgagtcaacactgt
tttgatggactagataacctggagaccttagacttgaattataataacttgggggaattt
cctcaggctattaaagcccttcctagccttaaagagctaggatttcatagtaattctatt
tctgttatccctgatggagcatttgatggtaatccactcttaagaactatacatttgtat
gataatcctctgtcttttgtggggaactcagcatttcacaatttatctgatcttcattcc
ctagtcattcgtggtgcaagcatggtgcagcagttccccaatcttacaggaactgtccac
ctggaaagtctgactttgacaggtacaaagataagcagcatacctaataatttgtgtcaa
gaacaaaagatgcttaggactttggacttgtcttacaataatataagagaccttccaagt
tttaatggttgccatgctctggaagaaatttctttacagcgtaatcaaatctaccaaata
aaggaaggcacctttcaaggcctgatatctctaaggattctagatctgagtagaaacctg
atacatgaaattcacagtagagcttttgccacacttgggccaataactaacctagatgta
agtttcaatgaattaacttcctttcctacggaaggcctgaatgggctaaatcaactgaaa
cttgtgggcaacttcaagctgaaagaagccttagcagcaaaagactttgttaacctcagg
tctttatcagtaccatatgcttatcagtgctgtgcattttggggttgtgactcttatgca
aatttaaacacagaagataacagcctccaggaccacagtgtggcacaggagaaaggtact
gctgatgcagcaaatgtcacaagcactcttgaaaatgaagaacatagtcaaataattatc
cattgtacaccttcaacaggtgcttttaagccctgtgaatatttactgggaagctggatg
attcgtcttactgtgtggttcattttcttggttgcattatttttcaacctgcttgttatt
ttaacaacatttgcatcttgtacatcactgccttcgtccaaattgtttataggcttgatt
tctgtgtctaacttattcatgggaatctatactggcatcctaacttttcttgatgctgtg
tcctggggcagattcgctgaatttggcatttggtgggaaactggcagtggctgcaaagta
gctgggtttcttgcagttttctcctcagaaagtgccatatttttattaatgctagcaact
gtcgaaagaagcttatctgcaaaagatataatgaaaaatgggaagagcaatcatctcaaa
cagttccgggttgctgcccttttggctttcctaggtgctacagtagcaggctgttttccc
cttttccatagaggggaatattctgcatcacccctttgtttgccatttcctacaggtgaa
acgccatcattaggattcactgtaacgttagtgctattaaactcactagcatttttatta
atggccgttatctacactaaactatactgcaacttggaaaaagaggacctctcagaaaac
tcacaatctagcatgattaagcatgtcgcttggctaatcttcaccaattgcatctttttc
tgccctgtggcgtttttttcatttgcaccattgatcactgcaatctctatcagccccgaa
ataatgaagtctgttactctgatattttttccattgcctgcttgcctgaatccagtcctg
tatgttttcttcaacccaaagtttaaagaagactggaagttactgaagcgacgtgttacc
aagaaaagtggatcagtttcagtttccatcagtagccaaggtggttgtctggaacaggat
ttctactacgactgtggcatgtactcacatttgcagggcaacctgactgtttgcgactgc
tgcgaatcgtttcttttaacaaagccagtatcatgcaaacacttgataaaatcacacagc
tgtcctgcattggcagtggcttcttgccaaagacctgagggctactggtccgactgtggc
acacagtcggcccactctgattatgcagatgaagaagattcctttgtctcagacagttct
gaccaggtgcaggcctgtggacgagcctgcttctaccagagtagaggattccctttggtg
cgctatgcttacaatctaccaagagttaaagactga

KEGG   Homo sapiens (human): 8549
Entry
8549              CDS       T01001                                 
Symbol
LGR5, FEX, GPR49, GPR67, GRP49, HG38
Name
(RefSeq) leucine rich repeat containing G protein-coupled receptor 5
  KO
K04308  leucine-rich repeat-containing G protein-coupled receptor 5
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Network
nt06505  WNT signaling
  Element
N01440  Wnt signaling modulation, LGR/RSPO
Drug target
Petosemtamab: D12416
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    8549 (LGR5)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04030 G protein-coupled receptors [BR:hsa04030]
    8549 (LGR5)
G protein-coupled receptors [BR:hsa04030]
 Rhodopsin family
  Others
   R-spondin
    8549 (LGR5)
SSDB
Motif
Pfam: LRR_8 LRR_4 LRR_5 LRR_1 LRR_9 7tm_1 LRRNT
Other DBs
NCBI-GeneID: 8549
NCBI-ProteinID: NP_003658
OMIM: 606667
HGNC: 4504
Ensembl: ENSG00000139292
UniProt: O75473 A0A0A8K8C7
Structure
LinkDB
Position
12:71439129..71586310
AA seq 907 aa
MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSEL
PSNLSVFTSYLDLSMNNISQLLPNPLPSLRFLEELRLAGNALTYIPKGAFTGLYSLKVLM
LQNNQLRHVPTEALQNLRSLQSLRLDANHISYVPPSCFSGLHSLRHLWLDDNALTEIPVQ
AFRSLSALQAMTLALNKIHHIPDYAFGNLSSLVVLHLHNNRIHSLGKKCFDGLHSLETLD
LNYNNLDEFPTAIRTLSNLKELGFHSNNIRSIPEKAFVGNPSLITIHFYDNPIQFVGRSA
FQHLPELRTLTLNGASQITEFPDLTGTANLESLTLTGAQISSLPQTVCNQLPNLQVLDLS
YNLLEDLPSFSVCQKLQKIDLRHNEIYEIKVDTFQQLLSLRSLNLAWNKIAIIHPNAFST
LPSLIKLDLSSNLLSSFPITGLHGLTHLKLTGNHALQSLISSENFPELKVIEMPYAYQCC
AFGVCENAYKISNQWNKGDNSSMDDLHKKDAGMFQAQDERDLEDFLLDFEEDLKALHSVQ
CSPSPGPFKPCEHLLDGWLIRIGVWTIAVLALTCNALVTSTVFRSPLYISPIKLLIGVIA
AVNMLTGVSSAVLAGVDAFTFGSFARHGAWWENGVGCHVIGFLSIFASESSVFLLTLAAL
ERGFSVKYSAKFETKAPFSSLKVIILLCALLALTMAAVPLLGGSKYGASPLCLPLPFGEP
STMGYMVALILLNSLCFLMMTIAYTKLYCNLDKGDLENIWDCSMVKHIALLLFTNCILNC
PVAFLSFSSLINLTFISPEVIKFILLVVVPLPACLNPLLYILFNPHFKEDLVSLRKQTYV
WTRSKHPSLMSINSDDVEKQSCDSTQALVTFTSSSITYDLPPSSVPSPAYPVTESCHLSS
VAFVPCL
NT seq 2724 nt   +upstreamnt  +downstreamnt
atggacacctcccggctcggtgtgctcctgtccttgcctgtgctgctgcagctggcgacc
gggggcagctctcccaggtctggtgtgttgctgaggggctgccccacacactgtcattgc
gagcccgacggcaggatgttgctcagggtggactgctccgacctggggctctcggagctg
ccttccaacctcagcgtcttcacctcctacctagacctcagtatgaacaacatcagtcag
ctgctcccgaatcccctgcccagtctccgcttcctggaggagttacgtcttgcgggaaac
gctctgacatacattcccaagggagcattcactggcctttacagtcttaaagttcttatg
ctgcagaataatcagctaagacacgtacccacagaagctctgcagaatttgcgaagcctt
caatccctgcgtctggatgctaaccacatcagctatgtgcccccaagctgtttcagtggc
ctgcattccctgaggcacctgtggctggatgacaatgcgttaacagaaatccccgtccag
gcttttagaagtttatcggcattgcaagccatgaccttggccctgaacaaaatacaccac
ataccagactatgcctttggaaacctctccagcttggtagttctacatctccataacaat
agaatccactccctgggaaagaaatgctttgatgggctccacagcctagagactttagat
ttaaattacaataaccttgatgaattccccactgcaattaggacactctccaaccttaaa
gaactaggatttcatagcaacaatatcaggtcgatacctgagaaagcatttgtaggcaac
ccttctcttattacaatacatttctatgacaatcccatccagtttgttgggagatctgct
tttcaacatttacctgaactaagaacactgactctgaatggtgcctcacaaataactgaa
tttcctgatttaactggaactgcaaacctggagagtctgactttaactggagcacagatc
tcatctcttcctcaaaccgtctgcaatcagttacctaatctccaagtgctagatctgtct
tacaacctattagaagatttacccagtttttcagtctgccaaaagcttcagaaaattgac
ctaagacataatgaaatctacgaaattaaagttgacactttccagcagttgcttagcctc
cgatcgctgaatttggcttggaacaaaattgctattattcaccccaatgcattttccact
ttgccatccctaataaagctggacctatcgtccaacctcctgtcgtcttttcctataact
gggttacatggtttaactcacttaaaattaacaggaaatcatgccttacagagcttgata
tcatctgaaaactttccagaactcaaggttatagaaatgccttatgcttaccagtgctgt
gcatttggagtgtgtgagaatgcctataagatttctaatcaatggaataaaggtgacaac
agcagtatggacgaccttcataagaaagatgctggaatgtttcaggctcaagatgaacgt
gaccttgaagatttcctgcttgactttgaggaagacctgaaagcccttcattcagtgcag
tgttcaccttccccaggccccttcaaaccctgtgaacacctgcttgatggctggctgatc
agaattggagtgtggaccatagcagttctggcacttacttgtaatgctttggtgacttca
acagttttcagatcccctctgtacatttcccccattaaactgttaattggggtcatcgca
gcagtgaacatgctcacgggagtctccagtgccgtgctggctggtgtggatgcgttcact
tttggcagctttgcacgacatggtgcctggtgggagaatggggttggttgccatgtcatt
ggttttttgtccatttttgcttcagaatcatctgttttcctgcttactctggcagccctg
gagcgtgggttctctgtgaaatattctgcaaaatttgaaacgaaagctccattttctagc
ctgaaagtaatcattttgctctgtgccctgctggccttgaccatggccgcagttcccctg
ctgggtggcagcaagtatggcgcctcccctctctgcctgcctttgccttttggggagccc
agcaccatgggctacatggtcgctctcatcttgctcaattccctttgcttcctcatgatg
accattgcctacaccaagctctactgcaatttggacaagggagacctggagaatatttgg
gactgctctatggtaaaacacattgccctgttgctcttcaccaactgcatcctaaactgc
cctgtggctttcttgtccttctcctctttaataaaccttacatttatcagtcctgaagta
attaagtttatccttctggtggtagtcccacttcctgcatgtctcaatccccttctctac
atcttgttcaatcctcactttaaggaggatctggtgagcctgagaaagcaaacctacgtc
tggacaagatcaaaacacccaagcttgatgtcaattaactctgatgatgtcgaaaaacag
tcctgtgactcaactcaagccttggtaacctttaccagctccagcatcacttatgacctg
cctcccagttccgtgccatcaccagcttatccagtgactgagagctgccatctttcctct
gtggcatttgtcccatgtctctaa

KEGG   Homo sapiens (human): 59352
Entry
59352             CDS       T01001                                 
Symbol
LGR6, GPCR, VTS20631
Name
(RefSeq) leucine rich repeat containing G protein-coupled receptor 6
  KO
K08399  leucine-rich repeat-containing G protein-coupled receptor 6
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Network
nt06505  WNT signaling
  Element
N01440  Wnt signaling modulation, LGR/RSPO
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    59352 (LGR6)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04030 G protein-coupled receptors [BR:hsa04030]
    59352 (LGR6)
G protein-coupled receptors [BR:hsa04030]
 Rhodopsin family
  Others
   R-spondin
    59352 (LGR6)
SSDB
Motif
Pfam: LRR_8 LRR_4 LRR_5 LRR_1 LRR_9 7tm_1 LRRNT
Other DBs
NCBI-GeneID: 59352
NCBI-ProteinID: NP_001017403
OMIM: 606653
HGNC: 19719
Ensembl: ENSG00000133067
UniProt: Q9HBX8
LinkDB
Position
1:202193799..202319761
AA seq 967 aa
MPSPPGLRALWLCAALCASRRAGGAPQPGPGPTACPAPCHCQEDGIMLSADCSELGLSAV
PGDLDPLTAYLDLSMNNLTELQPGLFHHLRFLEELRLSGNHLSHIPGQAFSGLYSLKILM
LQNNQLGGIPAEALWELPSLQSLRLDANLISLVPERSFEGLSSLRHLWLDDNALTEIPVR
ALNNLPALQAMTLALNRISHIPDYAFQNLTSLVVLHLHNNRIQHLGTHSFEGLHNLETLD
LNYNKLQEFPVAIRTLGRLQELGFHNNNIKAIPEKAFMGNPLLQTIHFYDNPIQFVGRSA
FQYLPKLHTLSLNGAMDIQEFPDLKGTTSLEILTLTRAGIRLLPSGMCQQLPRLRVLELS
HNQIEELPSLHRCQKLEEIGLQHNRIWEIGADTFSQLSSLQALDLSWNAIRSIHPEAFST
LHSLVKLDLTDNQLTTLPLAGLGGLMHLKLKGNLALSQAFSKDSFPKLRILEVPYAYQCC
PYGMCASFFKASGQWEAEDLHLDDEESSKRPLGLLARQAENHYDQDLDELQLEMEDSKPH
PSVQCSPTPGPFKPCEYLFESWGIRLAVWAIVLLSVLCNGLVLLTVFAGGPVPLPPVKFV
VGAIAGANTLTGISCGLLASVDALTFGQFSEYGARWETGLGCRATGFLAVLGSEASVLLL
TLAAVQCSVSVSCVRAYGKSPSLGSVRAGVLGCLALAGLAAALPLASVGEYGASPLCLPY
APPEGQPAALGFTVALVMMNSFCFLVVAGAYIKLYCDLPRGDFEAVWDCAMVRHVAWLIF
ADGLLYCPVAFLSFASMLGLFPVTPEAVKSVLLVVLPLPACLNPLLYLLFNPHFRDDLRR
LRPRAGDSGPLAYAAAGELEKSSCDSTQALVAFSDVDLILEASEAGRPPGLETYGFPSVT
LISCQQPGAPRLEGSHCVEPEGNHFGNPQPSMDGELLLRAEGSTPAGGGLSGGGGFQPSG
LAFASHV
NT seq 2904 nt   +upstreamnt  +downstreamnt
atgcccagcccgccggggctccgggcgctatggctttgcgccgcgctgtgcgcttcccgg
agggccggcggcgccccccagcccggcccggggcccaccgcctgcccggccccctgccac
tgccaggaggacggcatcatgctgtctgccgactgctctgagctcgggctgtccgccgtt
ccgggggacctggaccccctgacggcttacctggacctcagcatgaacaacctcacagag
cttcagcctggcctcttccaccacctgcgcttcttggaggagctgcgtctctctgggaac
catctctcacacatcccaggacaagcattctctggtctctacagcctgaaaatcctgatg
ctgcagaacaatcagctgggaggaatccccgcagaggcgctgtgggagctgccgagcctg
cagtcgctgcgcctagatgccaacctcatctccctggtcccggagaggagctttgagggg
ctgtcctccctccgccacctctggctggacgacaatgcactcacggagatccctgtcagg
gccctcaacaacctccctgccctgcaggccatgaccctggccctcaaccgcatcagccac
atccccgactacgcgttccagaatctcaccagccttgtggtgctgcatttgcataacaac
cgcatccagcatctggggacccacagcttcgaggggctgcacaatctggagacactagac
ctgaattataacaagctgcaggagttccctgtggccatccggaccctgggcagactgcag
gaactggggttccataacaacaacatcaaggccatcccagaaaaggccttcatggggaac
cctctgctacagacgatacacttttatgataacccaatccagtttgtgggaagatcggca
ttccagtacctgcctaaactccacacactatctctgaatggtgccatggacatccaggag
tttccagatctcaaaggcaccaccagcctggagatcctgaccctgacccgcgcaggcatc
cggctgctcccatcggggatgtgccaacagctgcccaggctccgagtcctggaactgtct
cacaatcaaattgaggagctgcccagcctgcacaggtgtcagaaattggaggaaatcggc
ctccaacacaaccgcatctgggaaattggagctgacaccttcagccagctgagctccctg
caagccctggatcttagctggaacgccatccggtccatccaccccgaggccttctccacc
ctgcactccctggtcaagctggacctgacagacaaccagctgaccacactgcccctggct
ggacttgggggcttgatgcatctgaagctcaaagggaaccttgctctctcccaggccttc
tccaaggacagtttcccaaaactgaggatcctggaggtgccttatgcctaccagtgctgt
ccctatgggatgtgtgccagcttcttcaaggcctctgggcagtgggaggctgaagacctt
caccttgatgatgaggagtcttcaaaaaggcccctgggcctccttgccagacaagcagag
aaccactatgaccaggacctggatgagctccagctggagatggaggactcaaagccacac
cccagtgtccagtgtagccctactccaggccccttcaagccctgtgagtacctctttgaa
agctggggcatccgcctggccgtgtgggccatcgtgttgctctccgtgctctgcaatgga
ctggtgctgctgaccgtgttcgctggcgggcctgtccccctgcccccggtcaagtttgtg
gtaggtgcgattgcaggcgccaacaccttgactggcatttcctgtggccttctagcctca
gtcgatgccctgacctttggtcagttctctgagtacggagcccgctgggagacggggcta
ggctgccgggccactggcttcctggcagtacttgggtcggaggcatcggtgctgctgctc
actctggccgcagtgcagtgcagcgtctccgtctcctgtgtccgggcctatgggaagtcc
ccctccctgggcagcgttcgagcaggggtcctaggctgcctggcactggcagggctggcc
gccgcgctgcccctggcctcagtgggagaatacggggcctccccactctgcctgccctac
gcgccacctgagggtcagccagcagccctgggcttcaccgtggccctggtgatgatgaac
tccttctgtttcctggtcgtggccggtgcctacatcaaactgtactgtgacctgccgcgg
ggcgactttgaggccgtgtgggactgcgccatggtgaggcacgtggcctggctcatcttc
gcagacgggctcctctactgtcccgtggccttcctcagctttgcctccatgctgggcctc
ttccctgtcacgcccgaggccgtcaagtctgtcctgctggtggtgctgcccctgcctgcc
tgcctcaacccactgctgtacctgctcttcaacccccacttccgggatgaccttcggcgg
cttcggccccgcgcaggggactcagggcccctagcctatgctgcggccggggagctggag
aagagctcctgtgattctacccaggccctggtagccttctctgatgtggatctcattctg
gaagcttctgaagctgggcggccccctgggctggagacctatggcttcccctcagtgacc
ctcatctcctgtcagcagccaggggcccccaggctggagggcagccattgtgtagagcca
gaggggaaccactttgggaacccccaaccctccatggatggagaactgctgctgagggca
gagggatctacgccagcaggtggaggcttgtcagggggtggcggctttcagccctctggc
ttggcctttgcttcacacgtgtaa

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