GlyCosmos Portal

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GO Term	Evidence Code	PMID
endoplasmic reticulum	IDA	21527675
mitochondrial inner membrane	IDA TAS	21527675 29915090
mitochondrial outer membrane	IDA	21527675
mitochondrial envelope		1550553
mitochondrion	IBA IDA NAS	7958339

GO Hierarchy

cellular component

protein-containing complex [inference]

mitochondrial protein-containing complex [inference]

mitochondrial fatty acid beta-oxidation multienzyme complex

catalytic complex [inference]

fatty acid beta-oxidation multienzyme complex [inference]

mitochondrial fatty acid beta-oxidation multienzyme complex

cellular anatomical entity [inference]

nucleoid [inference]

mitochondrial nucleoid

membrane [inference]

outer membrane [inference]

organelle outer membrane [inference]

mitochondrial outer membrane

organelle membrane [inference]

organelle inner membrane [inference]

mitochondrial inner membrane

mitochondrial membrane [inference]

bounding membrane of organelle [inference]

organelle outer membrane [inference]

mitochondrial outer membrane

envelope [inference]

organelle envelope [inference]

mitochondrial envelope

organelle [inference]

membrane-bounded organelle [inference]

intracellular membrane-bounded organelle [inference]

non-membrane-bounded organelle [inference]

intracellular non-membrane-bounded organelle [inference]

mitochondrial nucleoid

intracellular organelle [inference]

intracellular membrane-bounded organelle [inference]

intracellular non-membrane-bounded organelle [inference]

mitochondrial nucleoid

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GO Term	Evidence Code	PMID
lncRNA binding	IEA
acetyl-CoA C-acyltransferase activity		8135828
acetyl-CoA C-myristoyltransferase activity	IEA
enoyl-CoA hydratase activity		1550553
acetyl-CoA C-acetyltransferase activity	IEA

GO Hierarchy

molecular function

catalytic activity [inference]

oxidoreductase activity [inference]

oxidoreductase activity, acting on CH-OH group of donors [inference]

oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor [inference]

3-hydroxyacyl-CoA dehydrogenase activity

transferase activity [inference]

acyltransferase activity [inference]

acyltransferase activity, transferring groups other than amino-acyl groups [inference]

acetyltransferase activity [inference]

C-acetyltransferase activity [inference]

acetyl-CoA C-acetyltransferase activity

C-acyltransferase activity [inference]

acetyl-CoA C-acyltransferase activity

acetyl-CoA C-acetyltransferase activity

C-acetyltransferase activity [inference]

acetyl-CoA C-acetyltransferase activity

acetyl-CoA C-myristoyltransferase activity

myristoyltransferase activity [inference]

acetyl-CoA C-myristoyltransferase activity

lyase activity [inference]

carbon-oxygen lyase activity [inference]

hydro-lyase activity [inference]

enoyl-CoA hydratase activity

binding [inference]

protein binding

organic cyclic compound binding [inference]

nucleic acid binding [inference]

RNA binding

lncRNA binding

Gene Ontology information from NCBI Gene and UniProt.

Human Protein Atlas

ENSG00000138029

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

Data available from v23.0.proteinatlas.org. Image credit: Human Protein Atlas

KEGG BRITE Database

Orthology

K07509

Name

acetyl-CoA acyltransferase [EC:2.3.1.16]

References

8135828

Rhea

RHEA:18161

acetyl-CoA + tetradecanoyl-CoA

CoA + 3-oxohexadecanoyl-CoA

Enzyme

2.3.1.155

PMID

RHEA:21564

acetyl-CoA + an acyl-CoA

CoA + a 3-oxoacyl-CoA

Enzyme

2.3.1.16

PMID

Disease

Disease Ontology

Displaying entries **41 - 50** of **168** in total

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DO ID	Disease Name	Source
DOID:0110184	Charcot-Marie-Tooth disease type 4J	DisGeNET
DOID:0110185	Charcot-Marie-Tooth disease type 4A	DisGeNET
DOID:0110186	Charcot-Marie-Tooth disease type 4D	DisGeNET
DOID:0110187	Charcot-Marie-Tooth disease type 4K	DisGeNET
DOID:0110190	Charcot-Marie-Tooth disease type 4B2	DisGeNET
DOID:0110191	Charcot-Marie-Tooth disease type 4B1	DisGeNET
DOID:0110192	Charcot-Marie-Tooth disease type 4H	DisGeNET
DOID:0110193	Charcot-Marie-Tooth disease type 4F	DisGeNET
DOID:0110194	Charcot-Marie-Tooth disease type 4B3	DisGeNET
DOID:0110195	Charcot-Marie-Tooth disease type 4E	DisGeNET

The Human Phenotype Ontology

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HPO ID	HPO Term
HP:0000007	Autosomal recessive inheritance
HP:0000580	Pigmentary retinopathy
HP:0000829	Hypoparathyroidism
HP:0001250	Seizure
HP:0001252	Hypotonia
HP:0001254	Lethargy
HP:0001259	Coma
HP:0001263	Global developmental delay
HP:0001270	Motor delay
HP:0001284	Areflexia

Displaying **all 2** entries
Disease ID	Disease Name
OMIM:620300	mitochondrial trifunctional protein deficiency 2
ORPHA:746	mitochondrial trifunctional protein deficiency

PubChem Disease

GHR Health Conditions

Mitochondrial trifunctional protein deficiency

MedGen Diseases

Mitochondrial trifunctional protein deficiency 2

OMIM Phenotypes

MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY 2; MTPD2

KEGG Diseases

Gene-Disease-Co-Occurrences-in-Literature (PubChem)

LIPID MAPS Gene / Proteome Database

LMPD ID: LMP001640
Gene Name: hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit

Ortholog

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Caenorhabditis elegans	176216	WB:WBGene00015125
Drosophila melanogaster	37784	FB:FBgn0025352
Callorhinchus milii	103183148		CALMI26668
Danio rerio	336606	ZFIN:ZDB-GENE-030131-8550	DANRE20284
Astyanax mexicanus	103046325		ASTMX13017
Ictalurus punctatus	108257741		ICTPU25960
Salmo trutta	115207341		SALTR23416
Gadus morhua	115534529		GADMO31840
Oreochromis niloticus	100709781		ORENI18205
Sparus aurata	115574192		SPAAU61660

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

LIPID MAPS Gene / Proteome Database

International Collaboration

Acknowledgements