KEGG   Homo sapiens (human): 442862
Entry
442862            CDS       T01001                                 
Symbol
PRY2, PTPN13LY2
Name
(RefSeq) PTPN13 like Y-linked 2
  KO
K27449  PTPN13-like protein, Y-linked
Organism
hsa  Homo sapiens (human)
Disease
H02534  Y-linked spermatogenic failure
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    442862 (PRY2)
Cilium and associated proteins [BR:hsa03037]
 Motile cilia and associated proteins
  Sperm associated proteins
   442862 (PRY2)
SSDB
Other DBs
NCBI-GeneID: 442862
NCBI-ProteinID: NP_001002758
OMIM: 400041
HGNC: 21504
Ensembl: ENSG00000169807
UniProt: O14603 A0A384MTZ8
Position
Y:complement(22071756..22096007)
AA seq 147 aa
MGATGLGFLLSWRQDNLNGTDCQGCNILYFSETTGSMCSELSLNRGLEARRKKDLKDSFL
WRYGKVGCISLPLREMTAWINPPQISEIFQGYHQRVHGADALSLQTNSLRSRLSSQCLGQ
SFLLRTLERGRGFRALGDICGHVHEED
NT seq 444 nt   +upstreamnt  +downstreamnt
atgggagccactgggcttggctttctactttcctggagacaagacaatttgaatggcact
gactgccagggatgcaatattttatacttctctgagactacggggagcatgtgttctgaa
ctttccttgaacagaggtcttgaggccagaaggaagaaggatcttaaagactcatttctc
tggagatatgggaaggttggctgtatctcacttccacttcgtgagatgaccgcctggatt
aacccaccccaaatttcagagattttccaaggctaccaccagagggtgcacggagctgat
gcactgagcctgcaaaccaactctctgagaagcaggttatcttcacagtgcctcggacag
agcttccttctcaggacactcgagagaggccgtggtttcagggcacttggggacatctgt
ggccacgttcatgaagaagactaa

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