Results for "mineral metabolism disease": 14 genes

Name

COMMD1 Gene

copper metabolism (Murr1) domain containing 1

Enables several functions, including phosphatidylinositol-3,4-bisphosphate binding activity; phospholipid binding activity; and protein homodimerization activity. Involved in several processes, including Golgi to plasma membrane transport; negative regulation of protein localization to cell surface; and regulation of protein metabolic process. Acts upstream of or within negative regulation of NF-kappaB transcription factor activity. Located in cytosol; endosome; and nucleoplasm. Part of Cul2-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025]

CHROMR Gene

cholesterol induced regulator of metabolism RNA

BMND8 Gene

bone mineral density quantiative trait locus 8

BMND9 Gene

Bone mineral density QTL 9

BMND6 Gene

Bone mineral density QTL 6

BMND5 Gene

Bone mineral density variation QTL 5

BMND2 Gene

Bone mineral density variation 2

BMND3 Gene

Bone mineral density variability 3

BMND10 Gene

Bone mineral density QTL 10

BMND11 Gene

Bone mineral density QTL 11

BMND13 Gene

Bone mineral density QTL 13

BMND14 Gene

Bone mineral density QTL 14

BMND7 Gene

bone mineral density quantiative trait locus 7

BMND4 Gene

Bone mineral density variation QTL 4