Species: Hu, Mu, Rt, Bv, Pm-Or, Xp
Applications: WB, IP
Host: Rabbit Polyclonal
Species: Hu, Mu, Rt
Applications: WB, ICC/IF
Host: Mouse Polyclonal
Species: Hu, Mu, Rt, Po, Bv, RM
Applications: WB, ICC/IF, IHC
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Species: Hu
Applications: PAGE
Species: Hu
Applications: AC
Species: Hu
Applications: AC
Description
SMNDC1 is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq]
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
Human
Human
Human
|
| Product By Gene ID |
10285 |
| Alternate Names |
- SMNRSMN-related protein
- SPF30splicing factor 30, survival of motor neuron-related
- survival motor neuron domain containing 1,30 kDa splicing factor SMNrp
- Survival motor neuron domain-containing protein 1
- survival of motor neuron-related-splicing factor 30
|
Research Areas for SMNDC1
Find related products by research area and learn more about each of the different research areas below.
Apoptosis
