Synonyms: BSCL2 seipin gng3lg, mouse, homolog of bscl2 gene
Term information
http://www.ncbi.nlm.nih.gov/pubmed/14981520
http://www.ncbi.nlm.nih.gov/pubmed/18585921
http://www.ncbi.nlm.nih.gov/pubmed/23564749
http://www.ncbi.nlm.nih.gov/pubmed/11479539
http://www.ncbi.nlm.nih.gov/pubmed/13680364
http://www.ncbi.nlm.nih.gov/pubmed/24026679
http://www.ncbi.nlm.nih.gov/pubmed/19396477
http://www.ncbi.nlm.nih.gov/pubmed/18057387
http://www.ncbi.nlm.nih.gov/pubmed/12030893
http://www.ncbi.nlm.nih.gov/pubmed/23142943
http://www.ncbi.nlm.nih.gov/pubmed/18093937
http://www.ncbi.nlm.nih.gov/pubmed/23553728
http://www.ncbi.nlm.nih.gov/pubmed/21551454
http://www.ncbi.nlm.nih.gov/pubmed/15732094
http://www.ncbi.nlm.nih.gov/pubmed/15181077
http://www.ncbi.nlm.nih.gov/pubmed/16427281
http://www.ncbi.nlm.nih.gov/pubmed/24651066
http://www.ncbi.nlm.nih.gov/pubmed/20806400
http://www.ncbi.nlm.nih.gov/pubmed/10908191
http://www.ncbi.nlm.nih.gov/pubmed/19041432
http://www.ncbi.nlm.nih.gov/pubmed/5964029
http://www.ncbi.nlm.nih.gov/pubmed/1674639
http://www.ncbi.nlm.nih.gov/pubmed/15126564
http://www.ncbi.nlm.nih.gov/pubmed/17387721
http://www.ncbi.nlm.nih.gov/pubmed/20982387
http://www.ncbi.nlm.nih.gov/pubmed/18790819
http://www.ncbi.nlm.nih.gov/pubmed/16574104
http://www.ncbi.nlm.nih.gov/pubmed/15350896
http://linkedlifedata.com/resource/umls/id/C4016959
https://identifiers.org/hgnc/15832
https://www.ncbi.nlm.nih.gov/gene/26580
http://linkedlifedata.com/resource/umls/id/C1423761
http://linkedlifedata.com/resource/umls/id/C1720863
https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/BSCL2
http://linkedlifedata.com/resource/umls/id/C5436838
http://linkedlifedata.com/resource/umls/id/C4014700
http://linkedlifedata.com/resource/umls/id/C2931276
Term relations
- SO_0000704
- RO_0003302 some spastic paraplegia 17, autosomal dominant
- RO_0002525 some CHR_9606chr11q12.3
- RO_0003302 some lipodystrophy, congenital generalized, type 2
- RO_0003302 some encephalopathy, progressive, with or without lipodystrophy
- RO_0003302 some neuronopathy, distal hereditary motor, autosomal dominant 13