Homo sapiens (human): 55812
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Entry
55812 CDS
T01001
Symbol
SPATA7, HEL-S-296, HSD-3.1, HSD3, LCA3, RP94
Name
(RefSeq) spermatogenesis associated 7
KO
K19655
spermatogenesis-associated protein 7
Organism
hsa
Homo sapiens (human)
Disease
H00527
Retinitis pigmentosa
H00837
Leber congenital amaurosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
55812 (SPATA7)
Cilium and associated proteins [BR:
hsa03037
]
Motile cilia and associated proteins
Sperm associated proteins
55812 (SPATA7)
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SSDB
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Gene cluster
GFIT
Motif
Pfam:
HSD3
YPEB_N
Motif
Other DBs
NCBI-GeneID:
55812
NCBI-ProteinID:
NP_060888
OMIM:
609868
HGNC:
20423
Ensembl:
ENSG00000042317
UniProt:
Q9P0W8
V9HVY9
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All DBs
Position
14:88385657..88470350
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AA seq
599 aa
AA seq
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MDGSRRVRATSVLPRYGPPCLFKGHLSTKSNAFCTDSSSLRLSTLQLVKNHMAVHYNKIL
SAKAAVDCSVPVSVSTSIKYADQQRREKLKKELAQCEKEFKLTKTAMRANYKNNSKSLFN
TLQKPSGEPQIEDDMLKEEMNGFSSFARSLVPSSERLHLSLHKSSKVITNGPEKNSSSSP
SSVDYAASGPRKLSSGALYGRRPRSTFPNSHRFQLVISKAPSGDLLDKHSELFSNKQLPF
TPRTLKTEAKSFLSQYRYYTPAKRKKDFTDQRIEAETQTELSFKSELGTAETKNMTDSEM
NIKQASNCVTYDAKEKIAPLPLEGHDSTWDEIKDDALQHSSPRAMCQYSLKPPSTRKIYS
DEEELLYLSFIEDVTDEILKLGLFSNRFLERLFERHIKQNKHLEEEKMRHLLHVLKVDLG
CTSEENSVKQNDVDMLNVFDFEKAGNSEPNELKNESEVTIQQERQQYQKALDMLLSAPKD
ENEIFPSPTEFFMPIYKSKHSEGVIIQQVNDETNLETSTLDENHPSISDSLTDRETSVNV
IEGDSDPEKVEISNGLCGLNTSPSQSVQFSSVKGDNNHDMELSTLKIMEMSIEDCPLDV
NT seq
1800 nt
NT seq
+upstream
nt +downstream
nt
atggatggcagccggagagtcagagcaacctctgtccttcccagatatggtccaccgtgc
ctatttaaaggacacttgagcaccaaaagtaatgctttttgcactgactcctcttctctc
agactaagcactctccagctggtcaagaatcacatggctgttcactataataaaatcctt
tcagccaaagctgcagtagactgctcggttccagtaagcgtgagtaccagcataaagtat
gcagaccaacaacgaagagagaaactcaaaaaggaattagcacaatgtgaaaaagagttc
aaattaactaaaactgcaatgcgagccaattataaaaataattccaagtcactttttaat
accttacaaaagccctcaggcgaaccgcaaattgaggatgacatgttaaaagaagaaatg
aatggattttcatcctttgcaaggtcactagtaccctcttcagagagactacacctaagt
ctacataaatccagtaaagtcatcacaaatggtcctgagaagaactccagttcctccccg
tccagtgtggattatgcagcctccgggccccggaaactgagctctggagccctgtatggc
agaaggcccagaagcacattcccaaattcccaccggtttcagttagtcatttcgaaagca
cccagtggggatcttttggataaacattctgaactcttttctaacaaacaattgccattc
actcctcgcactttaaaaacagaagcaaaatctttcctgtcacagtatcgctattataca
cctgccaaaagaaaaaaggattttacagatcaacggatagaagctgaaacccagactgaa
ttaagctttaaatctgagttggggacagctgagactaaaaacatgacagattcagaaatg
aacataaagcaggcatctaattgtgtgacatatgatgccaaagaaaaaatagctccttta
cctttagaagggcatgactcaacatgggatgagattaaggatgatgctcttcagcattcc
tcaccaagggcaatgtgtcagtattccctgaagcccccttcaactcgtaaaatctactct
gatgaagaagaactgttgtatctgagtttcattgaagatgtaacagatgaaattttgaaa
cttggtttattttcaaacaggtttttagaacgactgttcgagcgacatataaaacaaaat
aaacatttggaggaggaaaaaatgcgccacctgctgcatgtcctgaaagtagacttaggc
tgcacatcggaggaaaactcggtaaagcaaaatgatgttgatatgttgaatgtatttgat
tttgaaaaggctgggaattcagaaccaaatgaattaaaaaatgaaagtgaagtaacaatt
cagcaggaacgtcaacaataccaaaaggctttggatatgttattgtcggcaccaaaggat
gagaacgagatattcccttcaccaactgaatttttcatgcctatttataaatcaaagcat
tcagaaggggttataattcaacaggtgaatgatgaaacaaatcttgaaacttcaactttg
gatgaaaatcatccaagtatttcagacagtttaacagatcgggaaacttctgtgaatgtc
attgaaggtgatagtgaccctgaaaaggttgagatttcaaatggattatgtggtcttaac
acatcaccctcccaatctgttcagttctccagtgtcaaaggcgacaataatcatgacatg
gagttatcaactcttaaaatcatggaaatgagcattgaggactgccctttggatgtttaa
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