Alstrom syndrome 1 also known as ALMS1 is a protein which in humans is encoded by the ALMS1 gene. The gene is located on the short arm of chromosome 2...

gene ALMS1, which is involved in the formation of cellular cilia, making Alström syndrome a ciliopathy. At least 239 disease-causing mutations in ALMS1 have...

Ukawa, Hisashi; Matsumoto, Yuki (18 April 2023). "Presence of known feline ALMS1 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy...

encoding protein AF4/FMR2 family member 3 AFTPH: encoding protein Aftiphilin ALMS1: Alstrom syndrome 1 ABCG5 and ABCG8: ATP-binding cassette, subfamily A,...

hypothyroidism, hypogonadism, skeletal dysplasia, cardiomyopathy, pulmonary fibrosis ALMS1 hearing loss, vision loss, liver Bardet-Biedl syndrome 209900 Obesity, polydactyly...

HGNC:21306 Q9BT30 586 ALKBH8 HGNC:25189 Q96BT7 587 ALLC HGNC:17377 Q8N6M5 588 ALMS1 HGNC:428 Q8TCU4 589 ALOX5 HGNC:435 P09917 590 ALOX5AP HGNC:436 P20292 591...

phototransduction (converting light into electrical signals for the brain); ALMS1, CCT2, CEP290, CLUAP1, IFT140, IQCB1, LCA5, MYO7A, RD3, RPGRIP1, SPATA7...

Angel-shaped phalango-epiphyseal dysplasia GDF5 dominant Alström syndrome ALMS1 1:8,600,000 Alzheimer's disease PSEN1, PSEN2, APP, APOEε4 1:177 Amelogenesis...

genes. Orthologs of FAM149A include BRTD and its four isoforms, ECCHC11 and ALMS1. These genes are all found in humans and have conserved areas with FAM149A...

archives conference Search for "alms" on Wikipedia. Alm (disambiguation) ALMS1, a gene and protein All pages with titles beginning with ALMS All pages...

syndrome, autosomal recessive; 203780; COL4A4 Alström syndrome; 203800; ALMS1 Alternating hemiplegia of childhood; 104290; ATP1A2 Alveolar capillary dysplasia...