The following gene names and symbols are associated with antigen Bardet-Biedl Syndrome 1 across different species:

Bardet-Biedl syndrome 1 (BBS1), Bardet-Biedl syndrome 1 (human) (Bbs1), Bardet-Biedl syndrome 1 (bbs1), bardet-biedl syndrome 1 (BBS1)

Other aliases include:

BBS2L2, FLJ23590, MGC51114, MGC126183, MGC126184, AI451249, D19Ertd609e, BBS1, im:7144669, bbs2l2, DKFZp468B1612

On the protein level the following designations are being used for antigen Bardet-Biedl Syndrome 1:

Bardet-Biedl syndrome 1 – Bardet-Biedl syndrome 1 homolog – bardet-biedl syndrome 1

Bardet-Biedl Syndrome 1 fulfills a number of functions:

protein binding – molecular_function

Bardet-Biedl Syndrome 1 is relevant to the following processes:

adult behavior – brain morphogenesis – cellular lipid metabolic process – cerebral cortex development – cilium morphogenesis – dendrite development – fat cell differentiation – fertilization – flagellum assembly – hippocampus development – hormone metabolic process – microtubule cytoskeleton organization – multicellular organism growth – olfactory behavior – photoreceptor cell maintenance – photoreceptor cell morphogenesis – regulation of cilium beat frequency involved in ciliary motility – response to stimulus – retina homeostasis – sensory cilium assembly – sensory perception of smell – striatum development – cilium assembly – Kupffer's vesicle development – convergent extension – convergent extension involved in gastrulation – determination of left/right symmetry – melanosome transport – pectoral fin development

Locations for Bardet-Biedl Syndrome 1:

BBSome – cilium membrane – cytoplasm – motile secondary cilium – plasma membrane – cellular_component

Source: NCBI Entrez Gene, Gene Ontology