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HADHB information


HADHB
Identifiers
AliasesHADHB, ECHB, MSTP029, MTPB, TP-BETA, hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit, hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
External IDsOMIM: 143450; MGI: 2136381; HomoloGene: 153; GeneCards: HADHB; OMA:HADHB - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000183
NM_001281512
NM_001281513

NM_145558
NM_001289798
NM_001289799

RefSeq (protein)

NP_000174
NP_001268441
NP_001268442

NP_001276727
NP_001276728
NP_663533

Location (UCSC)Chr 2: 26.24 – 26.29 MbChr 5: 30.36 – 30.39 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Trifunctional enzyme subunit beta, mitochondrial (TP-beta) also known as 3-ketoacyl-CoA thiolase, acetyl-CoA acyltransferase, or beta-ketothiolase is an enzyme that in humans is encoded by the HADHB gene.[5]

HADHB is a subunit of the mitochondrial trifunctional protein and has thiolase activity.

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000138029 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000059447 – 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. ^ "Entrez Gene: hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme A hydratase (trifunctional protein)".

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HADHB

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humans is encoded by the HADHB gene. HADHB is a subunit of the mitochondrial trifunctional protein and has thiolase activity. The HADHB gene is located on chromosome...

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Renin

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ATP6AP2. The level of renin mRNA appears to be modulated by the binding of HADHB, HuR and CP1 to a regulatory region in the 3' UTR. The gene for renin, REN...

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Chromosome 2

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thiolase/enoyl-Coenzyme A hydratase (trifunctional protein), alpha subunit HADHB: hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme...

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Thiolase

Last Update:

3-Ketoacyl-CoA thiolase; β-Ketothiolase 3-KAT ACAA1 peroxisomal ACAA2 mitochondrial HADHB mitochondrial EC 2.3.1.154 Propionyl-CoA C2-trimethyltridecanoyltransferase...

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Mitochondrial trifunctional protein

Last Update:

is a hetero-octamer composed of four alpha and four beta subunits: HADHA HADHB The three functions are 2-enoyl coenzyme A (CoA) hydratase, long-chain 3-hydroxy...

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Mitochondrial trifunctional protein deficiency

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trifunctional protein deficiency is based on mutations in the HADHA and HADHB genes which cause this disorder. These genes each provide instructions for...

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HADHA

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present. The alpha subunit catalyzes this reaction, and is attached to HADHB, which catalyzes the last step of the reaction. Mutations in this gene result...

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FASTKD3

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FASTKD2; Fatty acid beta oxidation pathway proteins (ACADVL, ECHS1, HADHA, HADHB, ACAA2); Amino acid catabolic pathways proteins (MCCC1, MCCC2, GLUD1, HIBADH...

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PCBP1

Last Update:

PMID 12890803. Adams DJ, Beveridge DJ, van der Weyden L, et al. (2004). "HADHB, HuR, and CP1 bind to the distal 3'-untranslated region of human renin mRNA...

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List of OMIM disorder codes

Last Update:

protein deficiency; 609015; HADHA Trifunctional protein deficiency; 609015; HADHB Trigonocephaly; 190440; FGFR1 Trimethylaminuria; 602079; FMO3 Triphalangeal...

Word Count : 18877

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