Gene table of LMBRD1 : LMBR1 domain containing 1

Gene-disease associations table

Disease IDDisease nameSource of annotation with LMBRD1OMIM linkNumber of associated genesgenes
277380METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPEOMIM link to OMIM 1LMBRD1

Download the gene annotation in CSV format

Annotation of the gene LMBRD1

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST
Associated KEGG pathways
KEGG pathwayKEGG IDKEGG IC
Vitamin digestion and absorptionhsa049778.24
Associated REACTOME pathways
REACTOME pathwayREACTOME IDREACTOME IC
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblFR-HSA-335945812.98
Metabolism of water-soluble vitamins and cofactorsR-HSA-1968496.54
Metabolism of vitamins and cofactorsR-HSA-1968546.54
Diseases of metabolismR-HSA-56689146.57
Defects in cobalamin (B12) metabolismR-HSA-32964699.28
MetabolismR-HSA-14307282.34
Defects in vitamin and cofactor metabolismR-HSA-32964828.52
Cobalamin (Cbl, vitamin B12) transport and metabolismR-HSA-1967418.73
DiseaseR-HSA-16436853.33
Associated GO terms for Molecular function
GO termGO IDGO IC
cobalamin bindingGO:00314197.54
cobalamin transporter activityGO:00152358.64
vitamin transporter activityGO:00511836.56
tetrapyrrole bindingGO:00469064.8
organic cyclic compound bindingGO:00971591.05
insulin receptor bindingGO:00051586.27
vitamin bindingGO:00198425.34
small molecule bindingGO:00360941.89
macromolecular complex bindingGO:00448772.61
bindingGO:00054880.18
protein bindingGO:00055150.46
transporter activityGO:00052152.57
protein complex bindingGO:00324033.09
receptor bindingGO:00051022.43
heterocyclic compound bindingGO:19013631.06