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SPTBN2

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
SPTBN2
Available structures
PDB Ortholog search: PDBe RCSB
List of PDB id codes

1WJM, 1WYQ

Identifiers
Aliases SPTBN2 , GTRAP41, SCA5, SCAR14, spectrin beta, non-erythrocytic 2
External IDsOMIM: 604985; MGI: 1313261; HomoloGene: 48482; GeneCards: SPTBN2; OMA:SPTBN2 - orthologs
Gene location (Human)
Chromosome 11 (human)
Chr. Chromosome 11 (human) [1]
Band 11q13.2Start66,682,497 bp [1]
End66,744,670 bp [1]
Gene location (Mouse)
Chromosome 19 (mouse)
Chr. Chromosome 19 (mouse)[2]
Band 19 A|19 4.1 cMStart4,761,195 bp [2]
End4,802,388 bp [2]
RNA expression pattern
Bgee
Human Mouse (ortholog)
  • right hemisphere of cerebellum

  • right frontal lobe

  • skin of leg

  • skin of abdomen

  • ganglionic eminence

  • prefrontal cortex

  • right testis

  • left testis

  • cingulate gyrus

  • anterior cingulate cortex
  • perirhinal cortex

  • CA3 field

  • entorhinal cortex

  • superior frontal gyrus

  • primary visual cortex

  • dentate gyrus of hippocampal formation granule cell

  • Region I of hippocampus proper

  • primary motor cortex

  • cerebellar cortex

  • prefrontal cortex
More reference expression data
BioGPS
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

6712

20743

Ensembl

ENSG00000173898

ENSMUSG00000067889

UniProt

O15020

Q68FG2

RefSeq (mRNA)

NM_006946

NM_021287

RefSeq (protein)

NP_008877

NP_067262

Location (UCSC)Chr 11: 66.68 – 66.74 Mb Chr 19: 4.76 – 4.8 Mb
PubMed search[3] [4]
Wikidata

Spectrin beta chain, brain 2 is a protein that in humans is encoded by the SPTBN2 gene.[5] [6] [7]

Clinical significance

[edit ]

Mutations in this gene is associated with Spinocerebellar ataxia type 5.

Interactions

[edit ]

SPTBN2 has been shown to interact with:

References

[edit ]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000173898Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000067889Ensembl, 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. ^ Stankewich MC, Tse WT, Peters LL, Ch'ng Y, John KM, Stabach PR, Devarajan P, Morrow JS, Lux SE (Dec 1998). "A widely expressed βIII spectrin associated with Golgi and cytoplasmic vesicles". Proc Natl Acad Sci U S A. 95 (24): 14158–63. Bibcode:1998PNAS...9514158S. doi:10.1073/pnas.95.24.14158 . PMC 24343 . PMID 9826670.
  6. ^ Ikeda Y, Dick KA, Weatherspoon MR, Gincel D, Armbrust KR, Dalton JC, Stevanin G, Dürr A, Zühlke C, Bürk K, Clark HB, Brice A, Rothstein JD, Schut LJ, Day JW, Ranum LP (January 2006). "Spectrin mutations cause spinocerebellar ataxia type 5". Nat Genet. 38 (2): 184–90. doi:10.1038/ng1728. PMID 16429157. S2CID 35280646.
  7. ^ "Entrez Gene: SPTBN2 spectrin, beta, non-erythrocytic 2".
  8. ^ a b Mao B, Wu W, Li Y, Hoppe D, Stannek P, Glinka A, Niehrs C (May 2001). "LDL-receptor-related protein 6 is a receptor for Dickkopf proteins". Nature. 411 (6835): 321–5. Bibcode:2001Natur.411..321M. doi:10.1038/35077108. PMID 11357136. S2CID 4323027.
  9. ^ a b Holleran EA, Ligon LA, Tokito M, Stankewich MC, Morrow JS, Holzbaur EL (September 2001). "beta III spectrin binds to the Arp1 subunit of dynactin". J. Biol. Chem. 276 (39): 36598–605. doi:10.1074/jbc.M104838200 . PMID 11461920.
  10. ^ Sakaguchi G, Orita S, Naito A, Maeda M, Igarashi H, Sasaki T, Takai Y (July 1998). "A novel brain-specific isoform of beta spectrin: isolation and its interaction with Munc13". Biochem. Biophys. Res. Commun. 248 (3): 846–51. doi:10.1006/bbrc.1998.9067. PMID 9704016.

Further reading

[edit ]
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