Expressed in head. Is an ortholog of human BLTP3A (bridge-like lipid transfer protein family member 3A) and BLTP3B (bridge-like lipid transfer protein family member 3B). Human BLTP3B enables GARP complex binding activity; lipid transfer activity; and protein homodimerization activity.
Enables Hsp70 protein binding activity. Located in cytosol; intercellular bridge; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Predicted to enable RNA binding activity. Located in cytosol; intercellular bridge; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Predicted to be located in cilium; intercellular bridge; and microtubule cytoskeleton. Orthologous to human KIAA1671 (KIAA1671); INTERACTS WITH (+)-schisandrin B; 2,3,7,8-tetrachlorodibenzodioxine; atrazine.
PHENOTYPE: Homozygotes for this spontaneous mutation have a short face with broad nasal bridge and short snout and a belly spot. [provided by MGI curators]