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Result Filters

Homo sapiens mRNA; cDNA DKFZp434A139 (from clone DKFZp434A139)

GenBank: AL133649.1

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Articles about the RAI1 gene

Allele-Specific Regulation of the Candidate Autism Liability Gene RAI1 by the Enhancer Variant rs4925102 (C/G). [Genes (Basel). 2024]
Allele-Specific Regulation of the Candidate Autism Liability Gene RAI1 by the Enhancer Variant rs4925102 (C/G).
Yuan X, Chen L, Saffen D. Genes (Basel). 2024 Apr 6; 15(4). Epub 2024 Apr 6.
Interaction network of human early embryonic transcription factors. [EMBO Rep. 2024]
Interaction network of human early embryonic transcription factors.
Gawriyski L, Tan Z, Liu X, Chowdhury I, Malaymar Pinar D, Zhang Q, Weltner J, Jouhilahti EM, Wei GH, Kere J, et al. EMBO Rep. 2024 Mar; 25(3):1589-1622. Epub 2024 Jan 31.
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8. [Mov Disord. 2024]
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Yeetong P, Dembélé ME, Pongpanich M, Cissé L, Srichomthong C, Maiga AB, Dembélé K, Assawapitaksakul A, Bamba S, Yalcouyé A, et al. Mov Disord. 2024 Jan; 39(1):164-172. Epub 2023 Nov 22.

Reference sequence information

RefSeq alternative splicing
See 15 reference mRNA sequence splice variants for the RAI1 gene.

More about the RAI1 gene

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is express...
Also Known As: SMCR, SMS

Related information

Protein
Protein sequence from Nucleotide coding region
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Taxonomy sequences associated with Nucleotide record
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