Search Results: ATXN10

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Ataxin 10
Kamis, 2025-07-17 22:43:20

Ataxin-10 is a protein that in humans is encoded by the ATXN10 gene. The autosomal dominant cerebellar ataxias (ADCAs) are a clinically and genetically...

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22q13 deletion syndrome
Sabtu, 2026-08-01 15:23:38

(MPPED1, CYB5R3, FBLN1, NUP50, C22ORF9, KIAA1644, PARVB, TRMU, WNT7B and ATXN10), as well as microRNAs may all contribute to loss of language, a feature...

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Spinocerebellar ataxia
Sabtu, 2026-08-01 02:58:51

eyeball), dysphagia, lack of coordination/clumsiness   CTG repeat, 13q SCA10 (ATXN10) 36 years 9 years ataxia, seizures Mexico Chromosome 22q linked pentanucleotide...

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List of genetic disorders
Rabu, 2026-07-29 03:02:35

(types 1–29) ATXN1, ATXN2, ATXN3, PLEKHG4, SPTBN2, CACNA1A, ATXN7, ATXN8OS, ATXN10, TTBK2, PPP2R2B, KCNC3, PRKCG, ITPR1, TBP, KCND3, FGF14 dominant, recessive...

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List of OMIM disorder codes
Selasa, 2026-08-04 21:22:31

Spinocerebellar ataxia-1; 164400; ATXN1 Spinocerebellar ataxia-10; 603516; ATXN10 Spinocerebellar ataxia-11; 604432; TTBK2 Spinocerebellar ataxia-13; 605259;...

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Ciliopathy
Kamis, 2026-07-02 04:01:27

Ellis–van Creveld syndrome 225500 EVC, EVC2 Joubert syndrome 213300 AHI1, ATXN10, ARL13B, BRCC3, C5ORF42, CC2D2A, CEP41, CEP290, CORS2, INPP5E, JBTS1, JBTS3...

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Ataxin
Rabu, 2026-07-15 13:55:12

causes Spinocerebellar ataxia type 8 with CTG expansion. Ataxin 10, coded by ATXN10. It is associated with the pentanucleotide disorder, SCA10. Frataxin, follows...

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List of human protein-coding genes 1
Sabtu, 2026-08-15 12:55:46

Q14CW9 1329 ATXN7L3B HGNC:37931; Q96GX2 1330 ATXN8 HGNC:32925; Q156A1 1331 ATXN10 HGNC:10549; Q9UBB4 1332 AUH HGNC:890; Q13825 1333 AUNIP HGNC:28363; Q9H7T9...

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