KEGG   Homo sapiens (human): 7259
Entry
7259              CDS       T01001                                 
Symbol
TSPYL1, TSPYL
Name
(RefSeq) TSPY like 1
  KO
K11284  TSPY-like 1
Organism
hsa  Homo sapiens (human)
Disease
H02174  Sudden infant death with dysgenesis of the testes syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    7259 (TSPYL1)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Nucleosome assembly factors
   Histone chaperones
    NAPs (Nucleosome assembly proteins)
     7259 (TSPYL1)
SSDB
Motif
Pfam: NAP
Other DBs
NCBI-GeneID: 7259
NCBI-ProteinID: NP_003300
OMIM: 604714
HGNC: 12382
Ensembl: ENSG00000189241
UniProt: Q9H0U9
Position
6:complement(116274858..116279930)
AA seq 437 aa
MSGLDGVKRTTPLQTHSIIISDQVPSDQDAHQYLRLRDQSEATQVMAEPGEGGSETVALP
PPPPSEEGGVPQDAAGRGGTPQIRVVGGRGHVAIKAGQEEGQPPAEGLAAASVVMAADRS
LKKGVQGGEKALEICGAQRSASELTAGAEAEAEEVKTGKCATVSAAVAERESAEVVKEGL
AEKEVMEEQMEVEEQPPEGEEIEVAEEDRLEEEAREEEGPWPLHEALRMDPLEAIQLELD
TVNAQADRAFQQLEHKFGRMRRHYLERRNYIIQNIPGFWMTAFRNHPQLSAMIRGQDAEM
LRYITNLEVKELRHPRTGCKFKFFFRRNPYFRNKLIVKEYEVRSSGRVVSLSTPIIWRRG
HEPQSFIRRNQDLICSFFTWFSDHSLPESDKIAEIIKEDLWPNPLQYYLLREGVRRARRR
PLREPVEIPRPFGFQSG
NT seq 1314 nt   +upstreamnt  +downstreamnt
atgagcggcctggatggggtcaagaggaccactcccctccaaacccacagcatcattatt
tctgaccaagtcccgagcgaccaggacgcacaccagtacctgaggctccgcgaccaaagc
gaggcgacacaggtgatggcggagccgggtgagggaggctcggagaccgtcgcgctcccg
cctccaccgccttcagaggaggggggcgtaccccaggatgccgcgggccgtggcggtact
ccccagatccgagttgttgggggtcgcggtcatgtggcgatcaaagccgggcaggaagag
ggccagcctcccgccgaaggcctggcagccgcttctgtggtgatggcagccgaccgcagc
ctgaaaaagggcgttcagggtggagagaaggccctagaaatctgtggcgcccagagatcc
gcgtctgagctgacggcgggggcggaggctgaggcggaggaggtgaagacaggaaagtgc
gccaccgtctcagcagccgtggctgagagggagagcgctgaggtggtgaaggaaggcctg
gcggagaaggaggtaatggaggagcagatggaggtagaggagcagccgccagaaggtgaa
gaaatagaagtggcggaggaggatagattggaggaggaggcgagggaggaagaagggccc
tggcctttgcatgaggctctccgcatggaccctctggaggccatccagctggaactggac
actgtgaatgctcaggccgacagggccttccaacagctggagcacaagtttgggcggatg
cgtcgacactacctggagcggaggaactacatcattcagaatatcccgggcttctggatg
actgcttttcgaaaccacccccagttgtccgccatgattaggggccaagatgcagagatg
ttaaggtacataaccaatttagaggtgaaggaactcagacaccctagaaccggttgcaag
ttcaagttcttctttagaagaaacccctacttcagaaacaagctgattgtcaaggaatat
gaggtaagatcctccggccgagtggtgtctctttctactccaattatatggcgcaggggg
catgaaccccagtccttcattcgcagaaaccaagacctcatctgcagcttcttcacttgg
ttttcagaccacagccttccagagtccgacaaaattgctgagattattaaagaggatctg
tggccaaatccactgcaatactacctgttgcgtgaaggagtccgtagagcccgacgtcgc
ccgctaagggagcctgtagagatccccaggccctttgggttccagtctggttaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (21)   
   RefSeq(nuc) (1)   
   GenBank (10)   
   EMBL (10)   
Protein domain (1)   
   Pfam (1)   
All databases (44)   

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