KEGG T01001: 55812

Homo sapiens (human): 55812

Entry

55812 CDS T01001

Gene name

SPATA7, HSD-3.1, HSD3, LCA3

Definition

spermatogenesis associated 7

Organism

hsa Homo sapiens (human)

Disease

H00527	Retinitis pigmentosa (RP)
H00837	Leber congenital amaurosis (LCR)

Class

SSDB

Motif

Pfam:

HSD3

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

Ensembl:

Vega:

UniProt:

Position

14q31.3

AA seq 567 aa
MDGSRRVRATSVLPRYGPPCLFKGHLSTKSNAAVDCSVPVSVSTSIKYADQQRREKLKKE
LAQCEKEFKLTKTAMRANYKNNSKSLFNTLQKPSGEPQIEDDMLKEEMNGFSSFARSLVP
SSERLHLSLHKSSKVITNGPEKNSSSSPSSVDYAASGPRKLSSGALYGRRPRSTFPNSHR
FQLVISKAPSGDLLDKHSELFSNKQLPFTPRTLKTEAKSFLSQYRYYTPAKRKKDFTDQR
IEAETQTELSFKSELGTAETKNMTDSEMNIKQASNCVTYDAKEKIAPLPLEGHDSTWDEI
KDDALQHSSPRAMCQYSLKPPSTRKIYSDEEELLYLSFIEDVTDEILKLGLFSNRFLERL
FERHIKQNKHLEEEKMRHLLHVLKVDLGCTSEENSVKQNDVDMLNVFDFEKAGNSEPNEL
KNESEVTIQQERQQYQKALDMLLSAPKDENEIFPSPTEFFMPIYKSKHSEGVIIQQVNDE
TNLETSTLDENHPSISDSLTDRETSVNVIEGDSDPEKVEISNGLCGLNTSPSQSVQFSSV
KGDNNHDMELSTLKIMEMSIEDCPLDV

NT seq 1704 nt +upstreamnt +downstreamnt
atggatggcagccggagagtcagagcaacctctgtccttcccagatatggtccaccgtgc
ctatttaaaggacacttgagcaccaaaagtaatgctgcagtagactgctcggttccagta
agcgtgagtaccagcataaagtatgcagaccaacaacgaagagagaaactcaaaaaggaa
ttagcacaatgtgaaaaagagttcaaattaactaaaactgcaatgcgagccaattataaa
aataattccaagtcactttttaataccttacaaaagccctcaggcgaaccgcaaattgag
gatgacatgttaaaagaagaaatgaatggattttcatcctttgcaaggtcactagtaccc
tcttcagagagactacacctaagtctacataaatccagtaaagtcatcacaaatggtcct
gagaagaactccagttcctccccgtccagtgtggattatgcagcctccgggccccggaaa
ctgagctctggagccctgtatggcagaaggcccagaagcacattcccaaattcccaccgg
tttcagttagtcatttcgaaagcacccagtggggatcttttggataaacattctgaactc
ttttctaacaaacaattgccattcactcctcgcactttaaaaacagaagcaaaatctttc
ctgtcacagtatcgctattatacacctgccaaaagaaaaaaggattttacagatcaacgg
atagaagctgaaacccagactgaattaagctttaaatctgagttggggacagctgagact
aaaaacatgacagattcagaaatgaacataaagcaggcatctaattgtgtgacatatgat
gccaaagaaaaaatagctcctttacctttagaagggcatgactcaacatgggatgagatt
aaggatgatgctcttcagcattcctcaccaagggcaatgtgtcagtattccctgaagccc
ccttcaactcgtaaaatctactctgatgaagaagaactgttgtatctgagtttcattgaa
gatgtaacagatgaaattttgaaacttggtttattttcaaacaggtttttagaacgactg
ttcgagcgacatataaaacaaaataaacatttggaggaggaaaaaatgcgccacctgctg
catgtcctgaaagtagacttaggctgcacatcggaggaaaactcggtaaagcaaaatgat
gttgatatgttgaatgtatttgattttgaaaaggctgggaattcagaaccaaatgaatta
aaaaatgaaagtgaagtaacaattcagcaggaacgtcaacaataccaaaaggctttggat
atgttattgtcggcaccaaaggatgagaacgagatattcccttcaccaactgaatttttc
atgcctatttataaatcaaagcattcagaaggggttataattcaacaggtgaatgatgaa
acaaatcttgaaacttcaactttggatgaaaatcatccaagtatttcagacagtttaaca
gatcgggaaacttctgtgaatgtcattgaaggtgatagtgaccctgaaaaggttgagatt
tcaaatggattatgtggtcttaacacatcaccctcccaatctgttcagttctccagtgtc
aaaggcgacaataatcatgacatggagttatcaactcttaaaatcatggaaatgagcatt
gaggactgccctttggatgtttaa

All links

Ontology (1)   
   KEGG BRITE (1)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (18)   
   NCBI-Gene (1)   
   NCBI-GI (11)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   ENSEMBL-HSA (1)   
   OC (1)   
   VEGA (1)   
Protein sequence (3)   
   UniProt (1)   
   RefSeq(pep) (2)   
DNA sequence (32)   
   RefSeq(nuc) (2)   
   GenBank (15)   
   EMBL (15)   
Protein domain (1)   
   Pfam (1)   
All databases (61)   

Download RDF

DBGET integrated database retrieval system