Homo sapiens (human): 199720
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Entry
199720 CDS
T01001
Symbol
GGN
Name
(RefSeq) gametogenetin
KO
K26807
gametogenetin
Organism
hsa
Homo sapiens (human)
Disease
H01208
Globozoospermia
H01282
Spermatogenic failure
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
199720 (GGN)
Cilium and associated proteins [BR:
hsa03037
]
Motile cilia and associated proteins
Sperm associated proteins
199720 (GGN)
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Ortholog
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Gene cluster
GFIT
Motif
Pfam:
GGN
Motif
Other DBs
NCBI-GeneID:
199720
NCBI-ProteinID:
NP_689870
OMIM:
609966
HGNC:
18869
Ensembl:
ENSG00000179168
UniProt:
Q86UU5
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Position
19:complement(38384267..38388384)
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AA seq
652 aa
AA seq
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MGNLQSEPSAGGGSRKVQPSDRAPDSRRTSLVEPEMTSQAMRLTRGLGVWFPGSATPPGL
MVPREPQASPSTLPLTLERPSPVMPPPEEAAAVSAPPPAPAGTLLPGPSKWQKPAGTPVP
RIRRLLEASHRGQGDPPSLRPLKPPPPPRQLSVKDTVPRAPSQFPPPLETWKPPPPLPSE
RQPADRRITPALATPASPPTESQAGPRNQGQTAGRARGGAPPHAGEGEMAQPADSESGLS
LLCKITFKSRPSLAPPAASSSLAAKASLGGGGGGGLFAASGAISYAEVLKQGPLPPGAAR
PLGEVSRGAQEAEGGDGDGEGCSGPPSAPASQARALPPPPYTTFPGSKPKFDWVSAPDGP
ERHFRFNGAGGGIGAPRRRAAALSGPWGSPPPPPEQIHSAPGPRRPAPALLAPPTFIFPA
PTNGEPMRPGPPGLQELPPLPPPTPPPTLQPPALQPTPLPVAPPLTPGLGHKESALAPTA
APALPPALAADQAPAPSPAPAPTVAEPSPPVSAPAPAAAPIKTRTRRNKGSRAARGATRK
DGLHGDGPRERATATVPDSSGGGGGGSGASQTGAANTRAARHWLPFQVLNSCPCKCYCHH
QPRHRRLPRNVSAWLSTSTNHLGEPPWVATIKLSGSLVAKLEHYDLQATHSN
NT seq
1959 nt
NT seq
+upstream
nt +downstream
nt
atggggaacttgcagtcggagccatccgcgggcgggggctcccgaaaagtgcagccctcg
gaccgcgcccccgactcccgccggacgtccctggtggagcccgagatgacctcccaggcc
atgcgcctgactcgtgggctgggtgtctggttccctggcagcgccacacccccgggactc
atggtaccccgggagccccaggcctcaccctcgaccctgcccctcaccttagaacggccc
tctccagtgatgccccctcctgaagaggcggccgcggtctctgcaccacccccggccccc
gcggggactctgctgcccggcccgtctaaatggcaaaagcccgcgggcactccagttccc
cggatccgccgcctgctggaggcgagccatcgcggccagggcgaccctccgagcctccgc
ccgctgaagccgccgccgccgccccggcaactatccgtgaaggacactgtcccgagggcc
ccatcccaatttccgccgcccctggagacttggaagccgccaccaccattaccttctgaa
cggcagccggcggaccgcagaatcactcctgctctggccacacccgcctcacccccgaca
gaaagccaggctgggccccgcaaccagggccagacggccggcagggctcgcggaggggcg
cctccccatgcgggcgaaggcgaaatggcccagcctgcggattccgagtccggtctgagc
ctgctgtgtaaaatcaccttcaagtcgaggccctctttggcccctccggcagcctcgagt
tccttagcagccaaagcttcgctggggggcggcggaggcggcggcctctttgctgcctca
ggtgccatctcttacgccgaggtcctgaagcaagggcccctgcctcctggagccgctcgc
cccttgggagaggtttctcgaggggcacaggaagccgagggaggtgatggagacggcgaa
gggtgctctggtcctccctcggcgcctgcgtcccaagcccgggccctaccgccgccaccc
tacaccaccttcccaggctcgaagcccaaattcgactgggttagcgctcccgacggccct
gaacgccacttccgcttcaacggggctggcggaggcatcggggcgccgcgacggcgtgcg
gccgcactctctgggccttggggctcccctccgccaccaccagagcagatacactcagct
cccgggccccggaggcccgcacctgccctgctggcgccgcctacgttcatcttcccagca
cccaccaatggcgagcccatgcgcccggggcctccaggcctgcaggagttaccaccgctg
ccaccgcccacaccgccgcccacactgcagccaccagcgctccagccaacgccgctgccg
gtggctcccccgctcaccccgggtctgggccacaaggagtcagccctggctcccaccgca
gcccctgctctgcccccagccttagccgccgaccaggccccggccccatccccggctcca
gctcccaccgtggctgagccctcgccgcctgtgtccgcgcccgcacccgcggctgcgccc
atcaagacccgcacgcgcaggaacaagggttcccgtgcagcccggggcgcgacccgtaag
gatggcttgcatggagatggtcctcgcgaacgagctacagctaccgtgcctgacagcagt
ggtggagggggtggtggcagcggggcctctcagactggggcagctaacacccgcgctgcg
cgccactggctgcccttccaggtgcttaactcctgtccctgcaagtgttactgccaccac
cagccacgccatcgccgcctgccacgcaacgtctctgcctggctgagcacatccaccaac
cacctgggcgagccaccctgggttgccaccatcaagctgtccggctctctggtggccaag
ctggagcactacgacttgcaggccacccattccaactga
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