Type | Description |
---|---|
Definition | metaxin 2 |
Date | Results | Publications |
---|---|---|
2020-10-03 12:59:00 | Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology. | 32917887 |
2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
2010-06-30 22:04:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2010-01-21 00:00:00 | The pathway of Voltage-dependent anion-selective channel biogenesis in human mitochondria involves the TOM complex, Sam50 and metaxins, and that it is evolutionarily conserved. | 17510655 |
2010-01-21 00:00:00 | mitofilin helps regulate mitochondrial morphology and at least four of the associated proteins (metaxins 1 and 2, SAM50 and CHCHD3) have been implicated in protein import | 17624330 |
Type | IDs |
---|---|
Gene |
UniProtKB-ID:
MTX2_HUMAN
UniprotKB:
O75431
UniParc:
UPI0000074170,
UPI000012F88B
EMBL:
AC073069,
AC016739,
BC067831,
AK289359,
AF053551,
AK303564,
BC017271,
BC088359,
CH471058
Ensembl:
ENSG00000128654
KO:
hsa:10651
|
Nucleutide sequences |
EMBL-CDS:
EAX11076.1,
AAY14795.1,
AAH17271.1,
BAF82048.1,
AAX93188.1,
EAX11078.1,
AAH67831.1,
BAG64587.1,
AAH88359.1,
AAC25105.1
Ensembl_TRS:
ENST00000249442
|
Protein sequencees |
Ensembl_PRO:
ENSP00000249442
RefSeq:
XP_011508799.1,
NP_001306027.1,
NP_001006636.1,
NP_006545.1,
NP_001306026.1
|
Others |
UniRef100:
UniRef100_O75431
UniRef90:
UniRef90_O75431
UniRef50:
UniRef50_O75431
UniGene:
Hs.470728
CCDS:
CCDS2272.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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