Homo sapiens (human): 9081
Help
Entry
9081 ncRNA
T01001
Symbol
PRY, PRY1, PTPN13LY
Name
(RefSeq) PTPN13 like Y-linked
Organism
hsa
Homo sapiens (human)
Disease
H02534
Y-linked spermatogenic failure
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Other DBs
NCBI-GeneID:
9081
OMIM:
400019
HGNC:
14024
Ensembl:
ENSG00000235059
LinkDB
All DBs
Position
Y:22490397..22514637
Genome browser
NT seq
1238 nt
NT seq
+upstream
nt +downstream
nt
aagaagaggagcacaccacaccagaaacagacatcttgcagtgtttcactgtctcaacct
tatctgcacagtccgaggtcagtctgagagagcttctgagagacccaggatgaagggatg
cagtgaggtcaagagcccaaccttctttcactgacacccacctctaaggactcagagaga
catgaataaaatgggcctcaacaatcccaagagaccactcaaggacaatgggagccactg
ggcttggctttctactttcctggagacaagacaatttgaatggcactgactgccagggat
gcaatattttatacttctctgagactacggggagcatgtgttctgaactttccttgaaca
gaggtcttgaggccagaaggaagaaggatcttaaagactcatttctctggagatatggga
aggttggctgtatctcacttccacttcgtgagatgaccgcctggattaacccaccccaaa
tttcagagattttccaaggctaccaccagagggtgcacggagctgatgcactgagcctgc
aaaccaactctctgagaagcaggttatcttcacagtgcctcggacagagcttccttctca
ggacactcgagagaggccgtggtttcagggcacttggggacatctgtggccacgttcatg
aagaagactaagcctacttcatctcaggacccgcccaagagtggccgcggctttgggaca
cctggggtcgggtccaccatgaggataaaacctccttctcttctggacatgtccaggagt
ggccgttgctacaagtcacctggtgctacgaccagggtgagaataaagacgtctcctcag
gaccctcccaggagagtacatggcattgagacatctggcggccaagtgaggaaaagacac
cctgtctgcagcacccagaactgaggaggggcactgccctgggccttacttcccagccct
ggcctccaattctgaccttacaaaagtgtcccttgagtgaggcagtgaccacgcattgtc
acagctaccaaagtgtggtttgcagatgatctgggcttgtttctggcagagattctggta
cagagaaaggagaggcgctgagtggaaccacgatgggctgaggccaggggagacatcaca
acctccaacaacactttttttcatgctttaataactcatttttcttagagaactaaagta
gttgaaacaatatagaaacattttttaagtaggcatat
DBGET
integrated database retrieval system