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TRIM32

TRIM32

Protein-coding gene in the species Homo sapiens

protein 32 is a protein that in humans is encoded by the TRIM32 gene. Since its discovery in 1995, TRIM32 has been shown to be implicated in a number of diverse

TRIM32

Bardet–Biedl syndrome

Ciliopathic recessive genetic disorder

include: BBsome: BBS1, BBS2, ARL6/BBS3, BBS4, BBS5, BBS7, TTC8/BBS8, BBS10, TRIM32/BBS11 BBS12, CCDC28B, CEP290, TMEM67, MKS1, MKKS chaperone: BBS6[citation

Bardet–Biedl syndrome

Bardet–Biedl_syndrome

Vaginal atresia

Abnormal closure or absence of the vagina

ARL6 (BBS3), BBS4, BBS5, MKKS (BBS6), BBS7, TTC8 (BBS8), BBS9, BBS10, TRIM32 (BBS11), BBS12, MKS1 (BBS13), CEP290 (BBS14), WDPCP (BBS15), SDCCAG8 (BBS16)

Vaginal atresia

Vaginal_atresia

Limb–girdle muscular dystrophy

Muscular degenerative disorder primarily of the hip and shoulders

telethonin-related LGMD2G 601954 TCAP LGMD R8 TRIM 32-related LGMD2H 254110 TRIM32 LGMD R9 FKRP-related LGMD2I 607155 FKRP Congenital muscular dystrophy An

Limb–girdle muscular dystrophy

Limb–girdle_muscular_dystrophy

Stimulator of interferon genes

Protein-coding gene in the species Homo sapiens

PMC 3317237. PMID 22470840. Zhang J, Hu MM, Wang YY, Shu HB (Aug 2012). "TRIM32 protein modulates type I interferon induction and cellular antiviral response

Stimulator of interferon genes

Stimulator_of_interferon_genes

Rivka Carmi

Israeli pediatrician and geneticist (born 1948)

Kwang-Youn A. (18 April 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings

Rivka Carmi

Rivka_Carmi

RING finger domain

Protein family

TRIM21, TRIM22, TRIM23, TRIM24, TRIM25, TRIM26, TRIM27, TRIM28, TRIM31, TRIM32, TRIM33, TRIM34, TRIM35, TRIM36, TRIM38, TRIM39, TRIM40, TRIM41, TRIM42

RING finger domain

RING_finger_domain

Ciliopathy

Genetic disease resulting in abnormal formation or function of cilia

BBS4, BBS5, BBS7, BBS9, BBS10, BBS12, MKKS, MKS1, MKS3, SDCCAG8, TTC8, TRIM32, WDPCP Ellis–van Creveld syndrome 225500 EVC, EVC2 Joubert syndrome 213300

Ciliopathy

Tripartite motif family

TRIM14, TRIM16, TRIM18, TRIM19 21-30: TRIM23, TRIM25, TRIM29, TRIM30 31-40: TRIM32, TRIM36, TRIM37 41-50: TRIM42, TRIM44, TRIM45, TRIM46, TRIM47 51-60: TRIM51

Tripartite motif family

Tripartite_motif_family

List of human protein-coding genes 8

Q13263 17382 TRIM29 HGNC:17274; Q14134 17383 TRIM31 HGNC:16289; Q9BZY9 17384 TRIM32 HGNC:16380; Q13049 17385 TRIM33 HGNC:16290; Q9UPN9 17386 TRIM34 HGNC:10063;

List of human protein-coding genes 8

List_of_human_protein-coding_genes_8

ABI2

Protein-coding gene in the species Homo sapiens

by the ABI2 gene. ABI2 has been shown to interact with ABL1, ADAM19, and TRIM32. GRCh38: Ensembl release 89: ENSG00000138443 – Ensembl, May 2017 GRCm38:

ABI2

List of OMIM disorder codes

Bardet–Biedl syndrome 10; 209900; BBS10 Bardet–Biedl syndrome 11; 209900; TRIM32 Bardet–Biedl syndrome 12; 209900; BBS12 Bardet–Biedl syndrome 13; 209900;

List of OMIM disorder codes

List_of_OMIM_disorder_codes