MLXIPL
Sign in to saveAlso known as MIO, CHREBP, MONDOB, WBSCR14, WS-bHLH, bHLHd14, MLX interacting protein like, MLX
protein-coding gene in the species Homo sapiens
Gene data
MLXIPL- Name
- MLX interacting protein like
- Type
- protein-coding
- Position
- 73,593,194–73,624,575 (−)
- Aliases
- CHREBP, MIO, MONDOB, WBSCR14, WS-bHLH, bHLHd14
- Ensembl
- ENSG00000009950
- RefSeq RNA
- NM_032951.3, NM_032952.3, NM_032953.3, NM_032954.3, NM_032994.2
- RefSeq protein
- NP_116569.1, NP_116570.1, NP_116571.1, NP_116572.1, XP_011514579.1
This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015].
Gene Ontology
Biological process
Molecular function
Cellular component
Pathways
via MyGene.info
Gene · Ensembl
MLX interacting protein like
- Symbol
- MLXIPL
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 7:73,593,194-73,624,575
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 32507
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/51085
- genetic association
- lipid metabolism disorder
- chromosome
- human chromosome 7
- genomic start
- 73007524
- genomic end
- 73038873
- cytogenetic location
- 7q11.23
Sources (8)
via Wikidata · CC0