Homo sapiens (human): 442862
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Entry
442862 ncRNA
T01001
Symbol
PRY2, PTPN13LY2
Name
(RefSeq) PTPN13 like Y-linked 2
Organism
hsa
Homo sapiens (human)
Disease
H02534
Y-linked spermatogenic failure
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Other DBs
NCBI-GeneID:
442862
OMIM:
400041
HGNC:
21504
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Position
Y:complement(22071706..22084875)
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NT seq
1097 nt
NT seq
+upstream
nt +downstream
nt
tgggcctcaacaatcccaagagaccactcaaggacaatgggagccactgggcttggcttt
ctactttcctggagacaagacaatttgaatggcactgactgccagggatgcaatatttta
tacttctctgagactacggggagcatgtgttctgaactttccttgaacagaggtcttgag
gccagaaggaagaaggatcttaaagactcatttctctggagatatgggaaggttggctgt
atctcacttccacttcgtgagatgaccgcctggattaacccaccccaaatttcagagatt
ttccaaggctaccaccagagggtgcacggagctgatgcactgagcctgcaaaccaactct
ctgagaagcaggttatcttcacagtgcctcggacagagcttccttctcaggacactcgag
agaggccgtggtttcagggcacttggggacatctgtggccacgttcatgaagaagactaa
gcctacttcatctcaggacccgcccaagagtggccgcggctttgggacacctggggtcgg
gtccaccatgaggataaaacctccttctcttctggacatgtccaggagtggccgttgcta
caagtcacctggtgctacgaccagggtgagaataaagacgtctcctcaggaccctcccag
gagagtacatggcattgagacatctggcggccaagtgaggaaaagacaccctgtctgcag
cacccagaactgaggaggggcactgccctgggccttacttcccagccctggcctccaatt
ctgaccttacaaaagtgtcccttgagtgaggcagtgaccacgcattgtcacagctaccaa
agtgtggtttgcagatgatctgggcttgtttctggcagagattctggtacagagaaagga
gaggcgctgagtggaaccacgatgggctgaggccaggggagacatcgcaacctccaacaa
cactttttttcatgctttaataactcatttttcttagagaactaaagtagttgaaacaat
atagaaacattttttaagtaggcatattagaacttgaattattatgtaagtttaaatata
tgatatatgcctggtta
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