Homo sapiens (human): 7259
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
NAP
Motif
Other DBs
NCBI-GeneID:
7259
NCBI-ProteinID:
NP_003300
OMIM:
604714
HGNC:
12382
Ensembl:
ENSG00000189241
UniProt:
Q9H0U9
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Position
6:complement(116274858..116279930)
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AA seq
437 aa
AA seq
DB search
MSGLDGVKRTTPLQTHSIIISDQVPSDQDAHQYLRLRDQSEATQVMAEPGEGGSETVALP
PPPPSEEGGVPQDAAGRGGTPQIRVVGGRGHVAIKAGQEEGQPPAEGLAAASVVMAADRS
LKKGVQGGEKALEICGAQRSASELTAGAEAEAEEVKTGKCATVSAAVAERESAEVVKEGL
AEKEVMEEQMEVEEQPPEGEEIEVAEEDRLEEEAREEEGPWPLHEALRMDPLEAIQLELD
TVNAQADRAFQQLEHKFGRMRRHYLERRNYIIQNIPGFWMTAFRNHPQLSAMIRGQDAEM
LRYITNLEVKELRHPRTGCKFKFFFRRNPYFRNKLIVKEYEVRSSGRVVSLSTPIIWRRG
HEPQSFIRRNQDLICSFFTWFSDHSLPESDKIAEIIKEDLWPNPLQYYLLREGVRRARRR
PLREPVEIPRPFGFQSG
NT seq
1314 nt
NT seq
+upstream
nt +downstream
nt
atgagcggcctggatggggtcaagaggaccactcccctccaaacccacagcatcattatt
tctgaccaagtcccgagcgaccaggacgcacaccagtacctgaggctccgcgaccaaagc
gaggcgacacaggtgatggcggagccgggtgagggaggctcggagaccgtcgcgctcccg
cctccaccgccttcagaggaggggggcgtaccccaggatgccgcgggccgtggcggtact
ccccagatccgagttgttgggggtcgcggtcatgtggcgatcaaagccgggcaggaagag
ggccagcctcccgccgaaggcctggcagccgcttctgtggtgatggcagccgaccgcagc
ctgaaaaagggcgttcagggtggagagaaggccctagaaatctgtggcgcccagagatcc
gcgtctgagctgacggcgggggcggaggctgaggcggaggaggtgaagacaggaaagtgc
gccaccgtctcagcagccgtggctgagagggagagcgctgaggtggtgaaggaaggcctg
gcggagaaggaggtaatggaggagcagatggaggtagaggagcagccgccagaaggtgaa
gaaatagaagtggcggaggaggatagattggaggaggaggcgagggaggaagaagggccc
tggcctttgcatgaggctctccgcatggaccctctggaggccatccagctggaactggac
actgtgaatgctcaggccgacagggccttccaacagctggagcacaagtttgggcggatg
cgtcgacactacctggagcggaggaactacatcattcagaatatcccgggcttctggatg
actgcttttcgaaaccacccccagttgtccgccatgattaggggccaagatgcagagatg
ttaaggtacataaccaatttagaggtgaaggaactcagacaccctagaaccggttgcaag
ttcaagttcttctttagaagaaacccctacttcagaaacaagctgattgtcaaggaatat
gaggtaagatcctccggccgagtggtgtctctttctactccaattatatggcgcaggggg
catgaaccccagtccttcattcgcagaaaccaagacctcatctgcagcttcttcacttgg
ttttcagaccacagccttccagagtccgacaaaattgctgagattattaaagaggatctg
tggccaaatccactgcaatactacctgttgcgtgaaggagtccgtagagcccgacgtcgc
ccgctaagggagcctgtagagatccccaggccctttgggttccagtctggttaa
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