SPTLC1

Source: Wikipedia, the free encyclopedia.
SPTLC1
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_001281303
NM_006415
NM_178324
NM_001368272
NM_001368273

NM_009269

RefSeq (protein)

NP_001268232
NP_006406
NP_847894
NP_001355201
NP_001355202

NP_033295

Location (UCSC)Chr 9: 92 – 92.12 MbChr 13: 53.49 – 53.53 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Serine palmitoyltransferase, long chain base subunit 1, also known as SPTLC1, is a protein which in humans is encoded by the SPTLC1 gene.[5][6]

hereditary sensory neuropathy type 1, macular disease,[7] and juvenile amyotrophic lateral sclerosis.[8][9] Alternatively spliced variants encoding different isoforms have been identified.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000090054 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000021468 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: SPTLC1 serine palmitoyltransferase, long chain base subunit 1".
  6. PMID 9363775
    .
  7. .
  8. .
  9. .

Further reading

External links


This page is based on the copyrighted Wikipedia article: SPTLC1. Articles is available under the CC BY-SA 3.0 license; additional terms may apply.Privacy Policy