Homo sapiens (human): 255027
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Entry
255027 CDS
T01001
Symbol
MPV17L, M-LPH, M-LPH1, M-LPH2, MLPH1, MLPH2, MPV17L1
Name
(RefSeq) MPV17 mitochondrial inner membrane protein like
KO
K13349
Mpv17-like protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04146
Peroxisome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04146 Peroxisome
255027 (MPV17L)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Mpv17_PMP22
Motif
Other DBs
NCBI-GeneID:
255027
NCBI-ProteinID:
NP_001121895
OMIM:
618100
HGNC:
26827
Ensembl:
ENSG00000156968
Pharos:
Q2QL34
(Tbio)
UniProt:
Q2QL34
LinkDB
All DBs
Position
16:15395754..15413271
Genome browser
AA seq
196 aa
AA seq
DB search
MAGWWPALSRAARRHPWPTNVLLYGSLVSAGDALQQRLQGREANWRQTRRVATLVVTFHA
NFNYVWLRLLERALPGRAPHALLAKLLCDQVVGAPIAVSAFYVGMSILQGKDDIFLDLKQ
KFWNTYLSGLMYWPFVQLTNFSLVPVQWRTAYAGVCGFLWATFICFSQQSGDGTFKSAFT
ILYTKGTSATEGYPKK
NT seq
591 nt
NT seq
+upstream
nt +downstream
nt
atggcgggctggtggccggcgttgtcgcgcgcggcccggcgccacccgtggcccaccaac
gtgctgctttacggctcgctcgtctcggccggggacgcgctgcaacagcggctgcagggc
cgcgaggccaactggcgccagacgcggcgcgtggccacgttggtggtgaccttccacgcc
aacttcaactacgtgtggctgcgcctgctggagcgcgcgctcccgggccgagcgccgcac
gccctgctggccaagttgctgtgcgaccaggtggtcggtgcgcccatcgcggtctcggcc
ttctatgtcggtatgagcattctccaaggaaaggatgacatatttttggacctgaaacag
aaattctggaatacctatctgagtggactgatgtactggccctttgtacagctgaccaac
ttcagccttgttcctgttcaatggagaacagcttacgctggagtctgtggttttctctgg
gccaccttcatctgtttttcccagcagagtggtgacggcacattcaagtcagctttcacc
attttatatacaaaggggaccagtgccacagaagggtacccgaagaaatga
Homo sapiens (human): 4358
Help
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Mpv17_PMP22
Motif
Other DBs
NCBI-GeneID:
4358
NCBI-ProteinID:
NP_002428
OMIM:
137960
HGNC:
7224
Ensembl:
ENSG00000115204
Pharos:
P39210
(Tbio)
UniProt:
P39210
A0A0S2Z3Z9
LinkDB
All DBs
Position
2:complement(27309492..27323097)
Genome browser
AA seq
176 aa
AA seq
DB search
MALWRAYQRALAAHPWKVQVLTAGSLMGLGDIISQQLVERRGLQEHQRGRTLTMVSLGCG
FVGPVVGGWYKVLDRFIPGTTKVDALKKMLLDQGGFAPCFLGCFLPLVGALNGLSAQDNW
AKLQRDYPDALITNYYLWPAVQLANFYLVPLHYRLAVVQCVAVIWNSYLSWKAHRL
NT seq
531 nt
NT seq
+upstream
nt +downstream
nt
atggcactctggcgggcataccagcgggccctggccgctcacccgtggaaagtacaggtc
ctgacagctgggtccctgatgggcctgggtgacattatctcacagcagctggtggagagg
cggggtctgcaggaacaccagagaggccggactctgaccatggtgtccctgggctgtggc
tttgtgggccctgtggtaggaggctggtacaaggttttggatcggttcatccctggcacc
accaaagtggatgcactgaagaagatgttgttggatcaggggggctttgccccgtgtttt
ctaggctgctttctcccactggtaggggcacttaatggactgtcagcccaggacaactgg
gccaaactacagcgggattatcctgatgcccttatcaccaactactatctatggcctgct
gtgcagttagccaacttctacctggtcccccttcattacaggttggccgttgtccaatgt
gttgctgttatctggaactcctacctgtcctggaaggcacatcggctctaa
Homo sapiens (human): 84769
Help
Entry
84769 CDS
T01001
Symbol
MPV17L2, FKSG24
Name
(RefSeq) MPV17 mitochondrial inner membrane protein like 2
KO
K13348
protein Mpv17
Organism
hsa
Homo sapiens (human)
Pathway
hsa04146
Peroxisome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04146 Peroxisome
84769 (MPV17L2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Mpv17_PMP22
AhtL-like_1st
Motif
Other DBs
NCBI-GeneID:
84769
NCBI-ProteinID:
NP_116072
OMIM:
616133
HGNC:
28177
Ensembl:
ENSG00000254858
Pharos:
Q567V2
(Tbio)
UniProt:
Q567V2
LinkDB
All DBs
Position
19:18193218..18196948
Genome browser
AA seq
206 aa
AA seq
DB search
MARGGWRRLRRLLSAGQLLFQGRALLVTNTLGCGALMAAGDGVRQSWEIRARPGQVFDPR
RSASMFAVGCSMGPFLHYWYLSLDRLFPASGLRGFPNVLKKVLVDQLVASPLLGVWYFLG
LGCLEGQTVGESCQELREKFWEFYKADWCVWPAAQFVNFLFVPPQFRVTYINGLTLGWDT
YLSYLKYRSPVPLTPPGCVALDTRAD
NT seq
621 nt
NT seq
+upstream
nt +downstream
nt
atggcgcggggtggctggcgccggctacgccgcctgttatccgcggggcagcttctattc
cagggccgcgcgctgctcgtcactaacacgctgggctgcggcgcgctcatggcggccggt
gatggcgtgcgccagtcctgggagatccgcgcccggcccggccaggttttcgacccacgg
cgctccgcgagcatgtttgcggtgggctgcagcatgggtcccttcctgcactactggtac
ttgtcgctggaccgcctattccctgcgtctggcctccgaggcttcccaaatgtcctcaag
aaggtcctcgtggatcagctggtagcctctccattgctgggcgtctggtacttcttgggc
cttggctgcctggagggtcagacagtgggtgagagctgccaggagctgcgggagaagttc
tgggaattctacaaggcagactggtgcgtgtggcctgctgcgcagttcgtgaacttcctc
ttcgtgcccccccaatttcgagtcacctacatcaacggcctgacgctgggctgggacacg
tacctgtcctacttgaagtaccggagcccagttcctctgacacccccaggctgtgtggcc
ctggacacccgagcagactga
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