KEGG   Homo sapiens (human): 4358
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)
SSDB
Motif
Pfam: Mpv17_PMP22
Other DBs
NCBI-GeneID: 4358
NCBI-ProteinID: NP_002428
OMIM: 137960
HGNC: 7224
Ensembl: ENSG00000115204
UniProt: P39210 A0A0S2Z3Z9
Position
2:complement(27309492..27323097)
AA seq 176 aa
MALWRAYQRALAAHPWKVQVLTAGSLMGLGDIISQQLVERRGLQEHQRGRTLTMVSLGCG
FVGPVVGGWYKVLDRFIPGTTKVDALKKMLLDQGGFAPCFLGCFLPLVGALNGLSAQDNW
AKLQRDYPDALITNYYLWPAVQLANFYLVPLHYRLAVVQCVAVIWNSYLSWKAHRL
NT seq 531 nt   +upstreamnt  +downstreamnt
atggcactctggcgggcataccagcgggccctggccgctcacccgtggaaagtacaggtc
ctgacagctgggtccctgatgggcctgggtgacattatctcacagcagctggtggagagg
cggggtctgcaggaacaccagagaggccggactctgaccatggtgtccctgggctgtggc
tttgtgggccctgtggtaggaggctggtacaaggttttggatcggttcatccctggcacc
accaaagtggatgcactgaagaagatgttgttggatcaggggggctttgccccgtgtttt
ctaggctgctttctcccactggtaggggcacttaatggactgtcagcccaggacaactgg
gccaaactacagcgggattatcctgatgcccttatcaccaactactatctatggcctgct
gtgcagttagccaacttctacctggtcccccttcattacaggttggccgttgtccaatgt
gttgctgttatctggaactcctacctgtcctggaaggcacatcggctctaa

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