(Translated by
https://www.hiragana.jp/
)
KEGG T01001: 4358
Homo sapiens (human): 4358
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Entry
4358 CDS
T01001
Symbol
MPV17, CMT2EE, MTDPS6, SYM1
Name
(RefSeq) mitochondrial inner membrane protein MPV17
KO
K13348
protein Mpv17
Organism
hsa
Homo sapiens (human)
Pathway
hsa04146
Peroxisome
Disease
H00264
Charcot-Marie-Tooth disease
H00469
Mitochondrial DNA depletion syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04146 Peroxisome
4358 (MPV17)
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Gene cluster
GFIT
Motif
Pfam:
Mpv17_PMP22
Motif
Other DBs
NCBI-GeneID:
4358
NCBI-ProteinID:
NP_002428
OMIM:
137960
HGNC:
7224
Ensembl:
ENSG00000115204
UniProt:
P39210
A0A0S2Z3Z9
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All DBs
Position
2:complement(27309492..27323097)
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AA seq
176 aa
AA seq
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MALWRAYQRALAAHPWKVQVLTAGSLMGLGDIISQQLVERRGLQEHQRGRTLTMVSLGCG
FVGPVVGGWYKVLDRFIPGTTKVDALKKMLLDQGGFAPCFLGCFLPLVGALNGLSAQDNW
AKLQRDYPDALITNYYLWPAVQLANFYLVPLHYRLAVVQCVAVIWNSYLSWKAHRL
NT seq
531 nt
NT seq
+upstream
nt +downstream
nt
atggcactctggcgggcataccagcgggccctggccgctcacccgtggaaagtacaggtc
ctgacagctgggtccctgatgggcctgggtgacattatctcacagcagctggtggagagg
cggggtctgcaggaacaccagagaggccggactctgaccatggtgtccctgggctgtggc
tttgtgggccctgtggtaggaggctggtacaaggttttggatcggttcatccctggcacc
accaaagtggatgcactgaagaagatgttgttggatcaggggggctttgccccgtgtttt
ctaggctgctttctcccactggtaggggcacttaatggactgtcagcccaggacaactgg
gccaaactacagcgggattatcctgatgcccttatcaccaactactatctatggcctgct
gtgcagttagccaacttctacctggtcccccttcattacaggttggccgttgtccaatgt
gttgctgttatctggaactcctacctgtcctggaaggcacatcggctctaa
DBGET
integrated database retrieval system