LMPD Database

LMP013273

Gene Information

Gene Ontology (GO Annotations)

GO ID	Source	Type	Description
GO:0045177	IEA:Ensembl	C	apical part of cell
GO:0005615	IEA:Ensembl	C	extracellular space
GO:0070062	IEA:Ensembl	C	extracellular vesicular exosome
GO:0005730	IEA:Ensembl	C	nucleolus
GO:0043204	IEA:Ensembl	C	perikaryon
GO:0047708	IEA:UniProtKB-EC	F	biotinidase activity
GO:0006768	IEA:Ensembl	P	biotin metabolic process

KEGG Pathway Links

KEGG Pathway ID	Description
ko00780	Biotin metabolism
rno00780	Biotin metabolism
rno01100	Metabolic pathways
ko04977	Vitamin digestion and absorption
rno04977	Vitamin digestion and absorption

REACTOME Pathway Links

REACTOME Pathway ID	Description
5954011	Biotin transport and metabolism
5953298	Defective AMN causes hereditary megaloblastic anemia 1
5953308	Defective BTD causes biotidinase deficiency
5953307	Defective CD320 causes methylmalonic aciduria
5953299	Defective CUBN causes hereditary megaloblastic anemia 1
5953296	Defective GIF causes intrinsic factor deficiency
5953310	Defective HLCS causes multiple carboxylase deficiency
5953297	Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
5953305	Defective MMAA causes methylmalonic aciduria type cblA
5953302	Defective MMAB causes methylmalonic aciduria type cblB
5953304	Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
5953303	Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
5953301	Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
5953300	Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
5953306	Defective MUT causes methylmalonic aciduria mut type
5953293	Defective TCN2 causes hereditary megaloblastic anemia
5953309	Defects in biotin (Btn) metabolism
5953294	Defects in cobalamin (B12) metabolism
5953295	Defects in vitamin and cofactor metabolism
5953253	Disease
5953250	Metabolism
5953292	Metabolism of vitamins and cofactors
5953291	Metabolism of water-soluble vitamins and cofactors