anti-Ataxin 7-Like 2 Antibodies
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord.
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anti-Ataxin 7-Like 2 (ATXN7L2) (AA 555-584), (C-Term) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (N-Term) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (Middle Region) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (N-Term) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (Middle Region) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (Center) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (AA 562-593), (C-Term) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (AA 143-192) antibody Primary Antibody
anti-Ataxin 7-Like 2 (ATXN7L2) (AA 539-588) antibody Primary Antibody
Ataxin 7-Like 2 (ATXN7L2) Antigen Profile
Protein Summary
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the 'pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. This locus has been mapped to chromosome 3, and it has been determined that the diseased allele associated with spinocerebellar ataxia-7 contains 38-130 CAG repeats (near the N-terminus), compared to 7-17 in the normal allele. The encoded protein is a component of the SPT3/TAF9/GCN5 acetyltransferase (STAGA) and TBP-free TAF-containing (TFTC) chromatin remodeling complexes, and it thus plays a role in transcriptional regulation. Alternative splicing results in multiple transcript variants.
Gene names and symbols associated with ATXN7L2
- ataxin 7-like 2 (Atxn7l2) antibody
- ataxin 7 like 2 (ATXN7L2) antibody
- ataxin 7-like 2b (atxn7l2b) antibody
- ataxin 7-like 2a (atxn7l2a) antibody
- ataxin 7 like 2 (Atxn7l2) antibody
- 2610528J18Rik antibody
- atxn7l2 antibody
- RGD1307047 antibody
- wu:fi32b11 antibody
- wu:fi36e12 antibody
- zgc:92454 antibody
- zgc:136546 antibody
Protein level used designations for ATXN7L2
ataxin-7-like protein 2 , mFLJ00381 protein , ataxin 7-like 1 , ataxin 7-like 2 , fi32b11
GENE ID | SPECIES |
---|---|
72522 | Mus musculus |
127002 | Homo sapiens |
310781 | Rattus norvegicus |
436928 | Danio rerio |
457092 | Pan troglodytes |
490121 | Canis lupus familiaris |
541097 | Bos taurus |
701498 | Macaca mulatta |
692316 | Danio rerio |
100340504 | Oryctolagus cuniculus |
100581273 | Nomascus leucogenys |
100619233 | Monodelphis domestica |
100629633 | Equus caballus |
100718819 | Cavia porcellus |
100517342 | Sus scrofa |
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