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EIF2B2 information


EIF2B2
Identifiers
AliasesEIF2B2, EIF-2Bbeta, EIF2B, eukaryotic translation initiation factor 2B subunit beta, EIF2Bbeta
External IDsOMIM: 606454; MGI: 2145118; HomoloGene: 6507; GeneCards: EIF2B2; OMA:EIF2B2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014239

NM_145445

RefSeq (protein)

NP_055054

NP_663420

Location (UCSC)Chr 14: 75 – 75.01 MbChr 12: 85.27 – 85.27 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Translation initiation factor eIF-2B subunit beta is a protein that in humans is encoded by the EIF2B2 gene.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000119718 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000004788 – 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. ^ Yang W, Hinnebusch AG (December 1996). "Identification of a regulatory subcomplex in the guanine nucleotide exchange factor eIF2B that mediates inhibition by phosphorylated eIF2". Mol Cell Biol. 16 (11): 6603–16. doi:10.1128/MCB.16.11.6603. PMC 231662. PMID 8887689.
  6. ^ "Entrez Gene: EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa".

and 9 Related for: EIF2B2 information

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EIF2B2

Last Update:

factor eIF-2B subunit beta is a protein that in humans is encoded by the EIF2B2 gene. Eukaryotic initiation factor-2B (EIF2B) is a GTP exchange protein...

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Leukoencephalopathy with vanishing white matter

Last Update:

genes encoding subunits of the translation initiation factor eIF2B: EIF2B1, EIF2B2, EIF2B3, EIF2B4, or EIF2B5. The disease belongs to a family of conditions...

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EIF2B

Last Update:

genes which encode eIF-2B proteins include: EIF2B1 – alpha subunit (26kDa) EIF2B2 – beta subunit (39kDa) EIF2B3 – gamma subunit (58kDa) EIF2B4 – delta subunit...

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Housekeeping gene

Last Update:

arginine/serine-rich EIF1 aka SUI1 EIF1AD EIF1B EIF2A EIF2AK1 EIF2AK3 EIF2AK4 EIF2AK1 EIF2B2 EIF2B3 EIF2B4 EIF2S2 EIF3A EIF3B EIF3D formerly EIF3S4 EIF3G EIF3I EIF3H...

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EIF2

Last Update:

Leukoencephalopathy with vanishing white matter eIF2B consists of the sub-units EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 Kimball SR (1999). "Eukaryotic initiation factor...

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XX gonadal dysgenesis

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to signaling. Autosomal recessive. BMP15, associated with X-linked form. EIF2B2, EIF2B4, and EIF2B5, responsible for protein production (see eIF2). PSMC3IP...

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EIF2B5

Last Update:

humans is encoded by the EIF2B5 gene. EIF2B5 has been shown to interact with EIF2B2 and EIF2B1. GRCh38: Ensembl release 89: ENSG00000145191 – Ensembl, May 2017...

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List of OMIM disorder codes

Last Update:

603896; EIF2B1 Leukoencephalopathy with vanishing white matter; 603896; EIF2B2 Leukoencephalopathy with vanishing white matter; 603896; EIF2B3 Leukoencephalopathy...

Word Count : 18877

NCK1

Last Update:

induce motion. NCK1 has been shown to interact with: ABL1, CBL, DNM1, DAG1, EIF2B2, EPHB1, EGFR, KHDRBS1, LCP2, MAP4K1, MAP4K4, MINK1, NCKIPSD, NEDD9, PAK1...

Word Count : 3450

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