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TPM2 information


TPM2
Identifiers
AliasesTPM2, AMCD1, DA1, DA2B, HEL-S-273, NEM4, TMSB, tropomyosin 2 (beta), tropomyosin 2, DA2B4
External IDsOMIM: 190990; MGI: 98810; HomoloGene: 134045; GeneCards: TPM2; OMA:TPM2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145822
NM_001301226
NM_001301227
NM_003289
NM_213674

NM_001277875
NM_001277876
NM_009416

RefSeq (protein)

NP_001288155
NP_001288156
NP_003280
NP_998839

NP_001264804
NP_001264805
NP_033442

Location (UCSC)Chr 9: 35.68 – 35.69 MbChr 4: 43.51 – 43.52 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

β-Tropomyosin, also known as tropomyosin beta chain is a protein that in humans is encoded by the TPM2 gene.[5][6] β-tropomyosin is striated muscle-specific coiled coil dimer that functions to stabilize actin filaments and regulate muscle contraction.

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000198467 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028464 – 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. ^ Hunt CC, Eyre HJ, Akkari PA, Meredith C, Dorosz SM, Wilton SD, Callen DF, Laing NG, Baker E (Aug 1995). "Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation". Cytogenetics and Cell Genetics. 71 (1): 94–5. doi:10.1159/000134070. PMID 7606936.
  6. ^ "Entrez Gene: TPM2 tropomyosin 2 (beta)".

and 12 Related for: TPM2 information

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TPM2

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as tropomyosin beta chain is a protein that in humans is encoded by the TPM2 gene. β-tropomyosin is striated muscle-specific coiled coil dimer that functions...

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Trusted Platform Module

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Root Certificate ST Micro EK ECC Intermediate Certificate tpm2-software/tpm2-tss, Linux TPM2 & TSS2 Software, 2020-11-18, archived from the original on...

Word Count : 6479

Arthrogryposis

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in distal arthrogryposis. Mutations in at least five genes (TNN12, TNNT3, TPM2, MYH3 and MYH8) could cause distal arthrogryposis. There could be also connective...

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Nemaline myopathy

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Deletion/duplication analysis TPM3 2%-3% Sequence analysis Deletion/duplication analysis TPM2 <1% Sequence analysis Deletion/duplication analysis TNNT1 Almost exclusively...

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Tropomyosin

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dispersed. In humans, the α1-, β-, α3-, and α4-genes are formally known as TPM1, TPM2, TPM3, and TPM4 and are located at 15q22, 9p13, 1q22 and 19p13, respectively...

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Clubfoot

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clubfoot, specifically those encoding the muscle contractile complex (MYH3, TPM2, TNNT3, TNNI2 and MYH8). These can cause congenital contractures, including...

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Stress granule

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Beta Topoisomerase (DNA) III Beta TPM1 TPM1 Tropomyosin alpha-1 chain TPM2 TPM2 Tropomyosin beta chain TPR TPR Translocated Promoter Region, Nuclear Basket...

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FARS2

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TRIM54, FSD2, CYSRT1, HIGD1C, homez, SPRY1, ZNF500, KRT34, YIF1A, BAG4, TPM2, SYP, KRTAP10-8, KRTAP1-1, AP1B1, TRAF2, GRB10, MESD, TRIP6, CCDC152, BEX5...

Word Count : 1264

KHDRBS3

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troponin I3 (TNNI3), troponin T2 (TNNT2), tropomyosin 1 (TPM1), tropomyosin 2 (TPM2), and titin (TTN). In prostate cancer cell lines KHDRBS3 appears to be androgen...

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TPM1

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filaments. Human striated muscles express protein from the TPM1 (α-Tm), TPM2 (β-Tm) and TPM3 (γ-Tm) genes, with α-Tm being the predominant isoform in...

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List of OMIM disorder codes

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208050; SLC2A10 Arthrogryposis multiplex congenita, distal type 1; 108120; TPM2 Arthrogryposis multiplex congenita, distal type 2B; 601680; TNNI2 Arthrogryposis...

Word Count : 18877

PDLIM7

Last Update:

in multiple transcript variants. PDLIM7 has been shown to interact with TPM2. GRCh38: Ensembl release 89: ENSG00000196923 – Ensembl, May 2017 GRCm38:...

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