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Gene entry

MLXIPL

MLX interacting protein like

Chromosome
7
Cytoband
7q11.23
Variants (rsID)
16

MLXIPL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q11.23). Its official name is “MLX interacting protein like”. The reference table lists 16 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

  • rs13235543Not classifiedsynonymous_variant
  • rs35332062Not classifiedmissense_variant&splice_region_variant
  • rs3812316Not classifiedmissense_variantHypertriglyceridemia 1|Hypertriglyceridemia, Transient Infantile|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Hypercholesterolemia, Familial, 1|Hypercholesterolemia, Familial, 3|Myocardial Infarction|Lipid Metabolism Disorder|Body Mass Index Quantitative Trait Locus 11|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10|Body Mass Index Quantitative Trait Locus 7|Body Mass Index Quantitative Trait Locus 4|Body Mass Index Quantitative Trait Locus 12|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.