Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55863
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 126B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM126B
Synonyms (NCBI Gene) Gene synonyms aliases
HT007, MC1DN29
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MC1DN29
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q14.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a mitochondrial transmembrane protein which is a component of the mitochondrial complex I assembly complex. The encoded protein serves as an assembly factor that is required for formation of the membrane arm of the complex. It interacts
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs141542003 G>T Uncertain-significance, pathogenic Coding sequence variant, genic downstream transcript variant, non coding transcript variant, missense variant
rs573006534 G>A Pathogenic Coding sequence variant, missense variant, intron variant
rs886037835 A>- Pathogenic Downstream transcript variant, genic downstream transcript variant, frameshift variant, non coding transcript variant, coding sequence variant
rs886037857 C>T Pathogenic Stop gained, missense variant, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT039977 hsa-miR-615-3p CLASH 23622248
MIRT039977 hsa-miR-615-3p CLASH 23622248
MIRT482764 hsa-miR-34b-3p PAR-CLIP 23592263
MIRT482765 hsa-miR-6800-3p PAR-CLIP 23592263
MIRT482763 hsa-miR-1306-5p PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 25416956
GO:0005739 Component Mitochondrion IBA 21873635
GO:0005739 Component Mitochondrion IDA
GO:0005743 Component Mitochondrial inner membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615533 30883 ENSG00000171204
Protein
UniProt ID Q8IUX1
Protein name Complex I assembly factor TMEM126B, mitochondrial (Transmembrane protein 126B)
Protein function As part of the MCIA complex, involved in the assembly of the mitochondrial complex I (PubMed:27374773, PubMed:27374774, PubMed:32320651). Participates in constructing the membrane arm of complex I (PubMed:24191001). {ECO:0000269|PubMed:24191001,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07114 TMEM126 51 228 Transmembrane protein 126 Family
Sequence
Sequence length 230
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Complex I biogenesis
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Diabetes mellitus Diabetes Mellitus rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
Epileptic encephalopathy Encephalopathies rs587776508, rs121918334, rs121918317, rs121918321, rs74315390, rs28939684, rs74315391, rs74315392, rs118192244, rs121918622, rs121918623, rs121917953, rs121917955, rs121918624, rs121918625
View all (860 more)
Hearing loss Sensorineural Hearing Loss (disorder) rs267607135, rs267606855, rs779841884, rs267606854, rs28942097, rs121908073, rs121908076, rs74315289, rs121908144, rs111033313, rs74315437, rs121908348, rs121908349, rs121908350, rs397515359
View all (184 more)
Unknown
Disease term Disease name Evidence References Source
Ptosis Blepharoptosis, Ptosis ClinVar
Mitochondrial Complex Deficiency mitochondrial complex 1 deficiency, nuclear type 29, mitochondrial complex I deficiency GenCC
Mitochondrial Diseases mitochondrial disease GenCC
Associations from Text Mining
Disease Name Relationship Type References
Cardiomyopathies Associate 27374774
Hypoxia Associate 29464284
Kidney Failure Chronic Associate 27374774
Leigh Disease Associate 36482121
Mitochondrial complex I deficiency Associate 27374773, 27374774, 36482121
Mitochondrial Diseases Associate 27290639, 27374774, 36482121
Muscle Weakness Associate 27374773
Muscular Diseases Associate 27374774
Prostatic Neoplasms Associate 38052461