Gene/Proteome Database (LMPD)

LMPD ID
LMP004199
Gene ID
Species
Mus musculus (Mouse)
Gene Name
solute carrier family 27 (fatty acid transporter), member 4
Gene Symbol
Synonyms
BB144259; FATP4
Alternate Names
long-chain fatty acid transport protein 4; FATP-4; fatty acid transport protein 4; solute carrier family 27 member 4
Chromosome
2
Map Location
2 B|2 20.64 cM
EC Number
6.2.1.-

Proteins

long-chain fatty acid transport protein 4
Refseq ID NP_036119
Protein GI 45597453
UniProt ID Q91VE0
mRNA ID NM_011989
Length 643
RefSeq Status PROVISIONAL
MLLGASLVGALLFSKLVLKLPWTQVGFSLLLLYLGSGGWRFIRVFIKTVRRDIFGGMVLLKVKTKVRRYLQERKTVPLLFASMVQRHPDKTALIFEGTDTHWTFRQLDEYSSSVANFLQARGLASGNVVALFMENRNEFVGLWLGMAKLGVEAALINTNLRRDALRHCLDTSKARALIFGSEMASAICEIHASLEPTLSLFCSGSWEPSTVPVSTEHLDPLLEDAPKHLPSHPDKGFTDKLFYIYTSGTTGLPKAAIVVHSRYYRMASLVYYGFRMRPDDIVYDCLPLYHSAGNIVGIGQCLLHGMTVVIRKKFSASRFWDDCIKYNCTIVQYIGELCRYLLNQPPREAESRHKVRMALGNGLRQSIWTDFSSRFHIPQVAEFYGATECNCSLGNFDSRVGACGFNSRILSFVYPIRLVRVNEDTMELIRGPDGVCIPCQPGQPGQLVGRIIQQDPLRRFDGYLNQGANNKKIANDVFKKGDQAYLTGDVLVMDELGYLYFRDRTGDTFRWKGENVSTTEVEGTLSRLLHMADVAVYGVEVPGTEGRAGMAAVASPISNCDLESFAQTLKKELPLYARPIFLRFLPELHKTGTFKFQKTELRKEGFDPSVVKDPLFYLDARKGCYVALDQEAYTRIQAGEEKL

Gene Information

Entrez Gene ID
Gene Name
solute carrier family 27 (fatty acid transporter), member 4
Gene Symbol
Species
Mus musculus

Gene Ontology (GO Annotations)

GO ID Source Type Description
GO:0031526 IDA:MGI C brush border membrane
GO:0005783 IDA:MGI C endoplasmic reticulum
GO:0005789 IEA:Ensembl C endoplasmic reticulum membrane
GO:0016021 IEA:UniProtKB-KW C integral component of membrane
GO:0005902 IDA:MGI C microvillus
GO:0005886 IDA:MGI C plasma membrane
GO:0004467 IDA:MGI F long-chain fatty acid-CoA ligase activity
GO:0000166 IEA:UniProtKB-KW F nucleotide binding
GO:0031957 IDA:MGI F very long-chain fatty acid-CoA ligase activity
GO:0006631 IMP:MGI P fatty acid metabolic process
GO:0044539 IEA:Ensembl P long-chain fatty acid import
GO:0001676 IDA:MGI P long-chain fatty acid metabolic process
GO:0015909 IMP:MGI P long-chain fatty acid transport
GO:0001579 IDA:MGI P medium-chain fatty acid transport
GO:0007584 IEA:Ensembl P response to nutrient
GO:0043588 IMP:MGI P skin development
GO:0042760 IDA:MGI P very long-chain fatty acid catabolic process
GO:0000038 IDA:MGI P very long-chain fatty acid metabolic process

KEGG Pathway Links

KEGG Pathway ID Description
mmu04975 Fat digestion and absorption
mmu03320 PPAR signaling pathway

REACTOME Pathway Links

REACTOME Pathway ID Description
5893867 Transport of fatty acids

Domain Information

InterPro Annotations

Accession Description
IPR025110 AMP-binding enzyme C-terminal domain
IPR020845 AMP-binding, conserved site
IPR000873 AMP-dependent synthetase/ligase
IPR022272 Lipocalin family conserved site

UniProt Annotations

Entry Information

Gene Name
solute carrier family 27 (fatty acid transporter), member 4
Protein Entry
S27A4_MOUSE
UniProt ID
Species
Mouse

Comments

Comment Type Description
Disease Note=Defects in Slc27a4 are the cause of wrinkle-free (wrfr) phenotype. It is a spontaneous, autosomal recessive mutation resulting in very tight, thick skin and is secondary characterized by severe breathing difficulties. Mice die shortly after birth. This phenotype is similar to human restrictive dermopathy, a very rare human genetic disorder. {ECO:0000269|PubMed:12697906}.
Function Involved in translocation of long-chain fatty acids (LFCA) across the plasma membrane. Appears to be the principal fatty acid transporter in small intestinal enterocytes. Plays a role in the formation of the epidermal barrier. Required for fat absorption in early embryogenesis. Has acyl-CoA ligase activity for long-chain and very-long-chain fatty acids (VLCFAs). Indirectly inhibits RPE65 via substrate competition and via production of VLCFA derivatives like lignoceroyl-CoA. Prevents light-induced degeneration of rods and cones. {ECO:0000269|PubMed:10518211, ECO:0000269|PubMed:11404000, ECO:0000269|PubMed:12821645, ECO:0000269|PubMed:15653672, ECO:0000269|PubMed:15699031, ECO:0000269|PubMed:23407971}.
Miscellaneous Deletion of Slc27a4 results in embryonic lethality, which has been attributed to a requirement for fat absorption early in embryonic development across the visceral endoderm.
Miscellaneous Slc27a4 deficient mice display features of a neonatally lethal restrictive dermopathy. Their skin is characterized by hyperproliferative hyperkeratosis with a disturbed epidermal barrier, a flat dermal-epidermal junction, a reduced number of pilo-sebaceous structures, and a compact dermis. The rigid skin consistency results in an altered body shape with facial dysmorphia, generalized joint flexion contractures and impaired movement including suckling and breathing deficiencies. Lipid analysis demonstrates a disturbed fatty acid composition of epidermal ceramides, in particular a decrease in the C26:0 and C26:0-OH fatty acid substitutes.
Sequence Caution Sequence=AAC40188.1; Type=Frameshift; Positions=Several; Evidence={ECO:0000305}; Sequence=AAC40188.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Sequence of unknown origin in the N-terminal part.; Evidence={ECO:0000305};
Similarity Belongs to the ATP-dependent AMP-binding enzyme family. {ECO:0000305}.
Subcellular Location Membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}. Endoplasmic reticulum membrane.
Tissue Specificity Most abundantly expressed in small intestine, brain, kidney, liver, skin and heart. In small intestine, expressed at high levels on the apical side of mature enterocytes. Highly expressed by the epithelial cells of the visceral endoderm and localized to the brush-border membrane of extraembryonic endodermal cells (at protein level). Expressed in the retinal pigment epithelium and in the retina (at protein level). Expressed in the retinal pigment epithelium and in the retina. {ECO:0000269|PubMed:10518211, ECO:0000269|PubMed:11404000, ECO:0000269|PubMed:14512415, ECO:0000269|PubMed:23407971, ECO:0000269|PubMed:9671728}.

Identical and Related Proteins

Unique RefSeq proteins for LMP004199 (as displayed in Record Overview)

Protein GI Database Accession Length Protein Name
45597453 RefSeq NP_036119 643 long-chain fatty acid transport protein 4

Identical Sequences to LMP004199 proteins

Reference Database Accession Length Protein Name
GI:45597453 DBBJ BAC29639.1 643 unnamed protein product [Mus musculus]
GI:45597453 DBBJ BAE33236.1 643 unnamed protein product [Mus musculus]
GI:45597453 EMBL CAJ18520.1 643 Slc27a4 [Mus musculus]
GI:45597453 GenBank AAH23114.1 643 Solute carrier family 27 (fatty acid transporter), member 4 [Mus musculus]
GI:45597453 GenBank EDL08422.1 643 solute carrier family 27 (fatty acid transporter), member 4 [Mus musculus]
GI:45597453 SwissProt Q91VE0.1 643 RecName: Full=Long-chain fatty acid transport protein 4; Short=FATP-4; Short=Fatty acid transport protein 4; AltName: Full=Solute carrier family 27 member 4 [Mus musculus]

Related Sequences to LMP004199 proteins

Reference Database Accession Length Protein Name
GI:45597453 DBBJ BAE41756.1 643 unnamed protein product [Mus musculus]
GI:45597453 GenBank AAE81545.1 643 Sequence 45 from patent US 6288213
GI:45597453 GenBank AAE81558.1 643 Sequence 71 from patent US 6288213
GI:45597453 GenBank AAE92220.1 643 Sequence 45 from patent US 6348321
GI:45597453 GenBank AAQ80189.1 643 Sequence 45 from patent US 6300096
GI:45597453 GenBank ABH70740.1 643 Sequence 45 from patent US 7033772