Homo sapiens (human): 64065
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Entry
64065 CDS
T01001
Symbol
PERP, EKVP7, KCP1, KRTCAP1, OLMS2, PIGPC1, THW, dJ496H19.1
Name
(RefSeq) p53 apoptosis effector related to PMP22
KO
K10136
TP53 apoptosis effector
Organism
hsa
Homo sapiens (human)
Pathway
hsa04115
p53 signaling pathway
Disease
H00710
Erythrokeratodermia variabilis
H02517
Olmsted syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04115 p53 signaling pathway
64065 (PERP)
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Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
IgaA
Motif
Other DBs
NCBI-GeneID:
64065
NCBI-ProteinID:
NP_071404
OMIM:
609301
HGNC:
17637
Ensembl:
ENSG00000112378
UniProt:
Q96FX8
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All DBs
Position
6:complement(138088505..138107419)
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AA seq
193 aa
AA seq
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MIRCGLACERCRWILPLLLLSAIAFDIIALAGRGWLQSSDHGQTSSLWWKCSQEGGGSGS
YEEGCQSLMEYAWGRAAAAMLFCGFIILVICFILSFFALCGPQMLVFLRVIGGLLALAAV
FQIISLVIYPVKYTQTFTLHANPAVTYIYNWAYGFGWAATIILIGCAFFFCCLPNYEDDL
LGNAKPRYFYTSA
NT seq
582 nt
NT seq
+upstream
nt +downstream
nt
atgatccgctgcggcctggcctgcgagcgctgccgctggatcctgcccctgctcctactc
agcgccatcgccttcgacatcatcgcgctggccggccgcggctggttgcagtctagcgac
cacggccagacgtcctcgctgtggtggaaatgctcccaagagggcggcggcagcgggtcc
tacgaggagggctgtcagagcctcatggagtacgcgtggggtagagcagcggctgccatg
ctcttctgtggcttcatcatcctggtgatctgtttcatcctctccttcttcgccctctgt
ggaccccagatgcttgtcttcctgagagtgattggaggtctccttgccttggctgctgtg
ttccagatcatctccctggtaatttaccccgtgaagtacacccagaccttcacccttcat
gccaaccctgctgtcacttacatctataactgggcctacggctttgggtgggcagccacg
attatcctgattggctgtgccttcttcttctgctgcctccccaactacgaagatgacctt
ctgggcaatgccaagcccaggtacttctacacatctgcctaa
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