SLC25A20 | ENSG00000178537 | NCBI 788

Details for: SLC25A20

Gene ID: 788

Symbol: SLC25A20

Ensembl ID: ENSG00000178537

Description: solute carrier family 25 member 20

Associated with

Carnitine metabolism
(R-HSA-200425)
Fatty acid metabolism
(R-HSA-8978868)
Metabolism
(R-HSA-1430728)
Metabolism of lipids
(R-HSA-556833)
Acyl carnitine transmembrane transport
(GO:1902616)
Acyl carnitine transmembrane transporter activity
(GO:0015227)
Carnitine shuttle
(GO:0006853)
Carnitine transmembrane transport
(GO:1902603)
Cytosol
(GO:0005829)
In utero embryonic development
(GO:0001701)
Mitochondrial envelope
(GO:0005740)
Mitochondrial inner membrane
(GO:0005743)
Mitochondrial transport
(GO:0006839)
Mitochondrion
(GO:0005739)
Protein binding
(GO:0005515)

Other Information

Proteins

Solute carrier family 25 member 20

Genular Protein ID: 229073912

Symbol: MCAT_HUMAN

Name: Solute carrier family 25 member 20

UniProtKB Accession Codes:

O43772 B2R7F4 Q9UIQ2

Database IDs:

Citations:

PubMed ID: 9399886

Title: Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient.

PubMed ID: 9399886

DOI: 10.1086/301628

PubMed ID: 9837782

Title: The structure and organization of the human carnitine/acylcarnitine translocase (CACT) gene.

PubMed ID: 9837782

DOI: 10.1006/bbrc.1998.9738

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 12892634

Title: Functional analysis of mutations in the human carnitine/acylcarnitine translocase in Aspergillus nidulans.

PubMed ID: 12892634

DOI: 10.1016/s1087-1845(03)00049-5

PubMed ID: 18307102

Title: Functional characterization of residues within the carnitine/acylcarnitine translocase RX2PANAAXF distinct motif.

PubMed ID: 18307102

DOI: 10.1080/09687680701697476

PubMed ID: 20347717

Title: Site-directed mutagenesis of charged amino acids of the human mitochondrial carnitine/acylcarnitine carrier: insight into the molecular mechanism of transport.

PubMed ID: 20347717

DOI: 10.1016/j.bbabio.2010.03.017

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 25944712

Title: N-terminome analysis of the human mitochondrial proteome.

PubMed ID: 25944712

DOI: 10.1002/pmic.201400617

PubMed ID: 12859414

Title: A novel molecular defect of the carnitine acylcarnitine translocase gene in a Saudi patient.

PubMed ID: 12859414

DOI: 10.1034/j.1399-0004.2003.00117.x

PubMed ID: 15057979

Title: Response to therapy in carnitine/acylcarnitine translocase (CACT) deficiency due to a novel missense mutation.

PubMed ID: 15057979

DOI: 10.1002/ajmg.a.20573

PubMed ID: 15365988

Title: Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency.

PubMed ID: 15365988

DOI: 10.1002/humu.20085

Sequence Information:

Length: 301
Mass: 32944
Checksum: AEB34E4E335102B0
Sequence:

MADQPKPISP LKNLLAGGFG GVCLVFVGHP LDTVKVRLQT QPPSLPGQPP MYSGTFDCFR 
KTLFREGITG LYRGMAAPII GVTPMFAVCF FGFGLGKKLQ QKHPEDVLSY PQLFAAGMLS 
GVFTTGIMTP GERIKCLLQI QASSGESKYT GTLDCAKKLY QEFGIRGIYK GTVLTLMRDV 
PASGMYFMTY EWLKNIFTPE GKRVSELSAP RILVAGGIAG IFNWAVAIPP DVLKSRFQTA 
PPGKYPNGFR DVLRELIRDE GVTSLYKGFN AVMIRAFPAN AACFLGFEVA MKFLNWATPN 
L

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: SLC25A20

Associated with

Other Information

Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient. PubMed ID: 9399886

The structure and organization of the human carnitine/acylcarnitine translocase (CACT) gene. PubMed ID: 9837782

Complete sequencing and characterization of 21,243 full-length human cDNAs. PubMed ID: 14702039

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Functional analysis of mutations in the human carnitine/acylcarnitine translocase in Aspergillus nidulans. PubMed ID: 12892634

Functional characterization of residues within the carnitine/acylcarnitine translocase RX2PANAAXF distinct motif. PubMed ID: 18307102

Site-directed mutagenesis of charged amino acids of the human mitochondrial carnitine/acylcarnitine carrier: insight into the molecular mechanism of transport. PubMed ID: 20347717

Initial characterization of the human central proteome. PubMed ID: 21269460

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome. PubMed ID: 24275569

N-terminome analysis of the human mitochondrial proteome. PubMed ID: 25944712

A novel molecular defect of the carnitine acylcarnitine translocase gene in a Saudi patient. PubMed ID: 12859414

Response to therapy in carnitine/acylcarnitine translocase (CACT) deficiency due to a novel missense mutation. PubMed ID: 15057979

Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency. PubMed ID: 15365988