Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84769
Gene name Gene Name - the full gene name approved by the HGNC.
MPV17 mitochondrial inner membrane protein like 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MPV17L2
Synonyms (NCBI Gene) Gene synonyms aliases
FKSG24
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.11
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1157033 hsa-miR-1182 CLIP-seq
MIRT1157034 hsa-miR-1185 CLIP-seq
MIRT1157035 hsa-miR-1203 CLIP-seq
MIRT1157036 hsa-miR-1205 CLIP-seq
MIRT1157037 hsa-miR-1253 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005739 Component Mitochondrion IBA 21873635
GO:0005743 Component Mitochondrial inner membrane IDA 24948607
GO:0005762 Component Mitochondrial large ribosomal subunit IDA 24948607
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616133 28177 ENSG00000254858
Protein
UniProt ID Q567V2
Protein name Mpv17-like protein 2
Protein function Required for the assembly and stability of the mitochondrial ribosome (PubMed:24948607). Is a positive regulator of mitochondrial protein synthesis (PubMed:24948607).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04117 Mpv17_PMP22 122 183 Mpv17 / PMP22 family Family
Sequence
MARGGWRRLRRLLSAGQLLFQGRALLVTNTLGCGALMAAGDGVRQSWEIRARPGQVFDPR
RSASMFAVGCSMGPFLHYWYLSLDRLFPASGLRGFPNVLKKVLVDQLVASPLLGVWYFLG
LGCLEGQTVGESCQELREKFWEFYKADWCVWPAAQFVNFLFVPPQFRVTYINGLTLGWDT
YLS
YLKYRSPVPLTPPGCVALDTRAD
Sequence length 206
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Peroxisome  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Multiple sclerosis Multiple Sclerosis rs104895219, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039
View all (4 more)
21833088
Unknown
Disease term Disease name Evidence References Source
Multiple Sclerosis Multiple Sclerosis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Neoplasms Associate 35579419