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TNNT1 information


TNNT1
Identifiers
AliasesTNNT1, ANM, NEM5, STNT, TNT, TNTS, troponin T1, slow skeletal type
External IDsOMIM: 191041 MGI: 1333868 HomoloGene: 20704 GeneCards: TNNT1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001126132
NM_001126133
NM_001291774
NM_003283

NM_001277903
NM_001277904
NM_011618
NM_001360154

RefSeq (protein)

NP_001119604
NP_001119605
NP_001278703
NP_003274

NP_001264832
NP_001264833
NP_035748
NP_001347083

Location (UCSC)Chr 19: 55.13 – 55.15 MbChr 7: 4.51 – 4.52 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Slow skeletal muscle troponin T (sTnT) is a protein that in humans is encoded by the TNNT1 gene.[5][6]

The TNNT1 gene is located at 19q13.4 in the human chromosomal genome, encoding the slow twitch skeletal muscle isoform of troponin T (ssTnT). ssTnT is an ~32-kDa protein consisting of 262 amino acids (including the first methionine) with an isoelectric point (pI) of 5.95. It is the tropomyosin binding and thin filament anchoring subunit of the troponin complex in the sarcomeres of slow twitch skeletal muscle fibers.[7][8][9] TNNT1 gene is specifically expressed in slow skeletal muscle of vertebrates, with one exception that dry land toad (Bufo) cardiac muscle expresses ssTnT other than cardiac TnT.[10]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000105048 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000064179 – 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. ^ Cite error: The named reference Samson_1992 was invoked but never defined (see the help page).
  6. ^ "Entrez Gene: TNNT1 troponin T type 1 (skeletal, slow)".
  7. ^ Cite error: The named reference Perry_1998 was invoked but never defined (see the help page).
  8. ^ Cite error: The named reference Jin_2008 was invoked but never defined (see the help page).
  9. ^ Cite error: The named reference Wei_2011 was invoked but never defined (see the help page).
  10. ^ Cite error: The named reference Feng_2012 was invoked but never defined (see the help page).

and 8 Related for: TNNT1 information

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TNNT1

Last Update:

troponin T (sTnT) is a protein that in humans is encoded by the TNNT1 gene. The TNNT1 gene is located at 19q13.4 in the human chromosomal genome, encoding...

Word Count : 1998

Troponin T

Last Update:

Heidelberg, who also developed the troponin T assay. Slow skeletal troponin T1, TNNT1 (19q13.4, 191041) Cardiac troponin T2, TNNT2 (1q32, 191045) Fast skeletal...

Word Count : 631

Nemaline myopathy

Last Update:

Deletion/duplication analysis TPM2 <1% Sequence analysis Deletion/duplication analysis TNNT1 Almost exclusively in Old Amish Sequence analysis Deletion/duplication analysis...

Word Count : 3561

TNNT2

Last Update:

published in Gene and can be cited as: Wei B, Jin JP (13 January 2016). "TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships"...

Word Count : 4857

TNNT3

Last Update:

significantly diverged from the slow skeletal muscle TnT (ssTnT encoded by TNNT1) and cardiac TnT (cTnT encoded by TNNT2), Structure of fsTnT is conserved...

Word Count : 1957

PRKG1

Last Update:

PRKG1 has been shown to interact with: GTF2I, ITPR1, MRVI1, RGS2, and TNNT1. GRCh38: Ensembl release 89: ENSG00000185532 – Ensembl, May 2017 GRCm38:...

Word Count : 1307

SBK3

Last Update:

interacts with SMAD3, MBD3L2, Q494R0, SNRNP35, A8MTQ0, AIMP2, DMAP1, EXOSC2, TNNT1, GATAD2B, and Q8WUT1. SMAD3 is a receptor-regulated subtype of SMAD, which...

Word Count : 2118

List of OMIM disorder codes

Last Update:

Nemaline myopathy; 609285; TPM2 Nemaline myopathy, Amish type; 605355; TNNT1 Nephrogenic syndrome of inappropriate antidiuresis; 300539; AVPR2 Nephrolithiasis...

Word Count : 18877

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