LP64868-0
SMN2 gene
Active
Description
The SMN2 gene (survival of motor neuron 2, centromeric) [HGNC Gene ID:11118] is located on chromosome 5q13.2. This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Sep 2008] [NCBI Gene ID:6607] Source: National Center for Biotechnology Information (NCBI) Gene
Reference Information
| Type | Source | Reference |
|---|---|---|
| Webcontent | Online Mendelian Inheritance in Man®Copyright OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University. | Link to OMIM |
Basic Part Properties
- Part Name
- SMN2 gene
- Part Display Name
- SMN2 gene
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2007-08-17
- Construct for LOINC Short Name
- SMN2 gene
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | SMN2 基因 Synonyms: BCD541; |
| et-EE | Estonian (Estonia) | SMN2 geen |
| es-ES | Spanish (Spain) | Gen SMN2 |
| it-IT | Italian (Italy) | SMN2, gene Synonyms: Gene SMN2 |
| tr-TR | Turkish (Turkey) | SMN2 geni |
| ru-RU | Russian (Russian Federation) | SMN2 ген |
| nl-NL | Dutch (Netherlands) | SMN2-gen Synonyms: SMN2 gen |
| fr-FR | French (France) | SMN2 gène |
| pl-PL | Polish (Poland) | SMN2 gen Synonyms: Gen SMN2 |
| el-GR | Greek (Greece) | Γονίδιο SMN2 Synonyms: Γονίδιο SMN2 |
LOINC Copyright
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