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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc27a4
solute carrier family 27 (fatty acid transporter), member 4
MGI:1347347
47 phenotypes from 6 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc27a4Gt(OST329034)Lex/Slc27a4Gt(OST329034)Lex
involves: 129S5/SvEvBrd * C57BL/6J 		preweaning lethality, complete penetrance J:103485
Slc27a4pskn/Slc27a4pskn
involves: FVB 		abnormal epidermal layer morphology J:194779
abnormal epidermis stratum spinosum morphology J:194779
abnormal keratohyalin granule morphology J:194779
abnormal posture J:194779
abnormal skin appearance J:194779
absent gastric milk in neonates J:194779
epidermal necrosis J:194779
hyperkeratosis J:194779
increased keratinocyte proliferation J:194779
micrognathia J:194779
neonatal lethality, complete penetrance J:194779
protruding tongue J:194779
shiny skin J:194779
thick epidermis J:194779
tight skin J:194779
Slc27a4tm1.1Wsr/Slc27a4tm1.1Wsr
involves: 129P2/OlaHsd 		hyperkeratosis J:103206
impaired skin barrier function J:103206
parakeratosis J:103206
Slc27a4tm1.1Wsr/Slc27a4tm1.1Wsr
involves: 129P2/OlaHsd * BALB/cJ 		abnormal breathing pattern J:84096
abnormal dermal layer morphology J:84096
abnormal epidermal-dermal junction morphology J:84096
abnormal epidermis stratum corneum morphology J:84096
abnormal epidermis stratum spinosum morphology J:84096
abnormal facial morphology J:84096
abnormal locomotor activation J:84096
abnormal pulmonary alveolus morphology J:84096
abnormal skin condition J:84096
abnormal skin physiology J:84096
abnormal suckling behavior J:84096
cyanosis J:84096
decreased body weight J:84096
decreased keratohyalin granule size J:84096
herniated abdominal wall J:84096
hyperkeratosis J:84096
impaired skin barrier function J:84096
neonatal lethality, complete penetrance J:84096
parakeratosis J:84096
respiratory distress J:84096
scaly skin J:84096
thick pulmonary interalveolar septum J:84096
thick skin J:84096
tight skin J:84096
Slc27a4tm1Asta/Slc27a4tm1Asta
involves: 129S/SvEv * C57BL/6J 		embryonic lethality, complete penetrance J:86762
Slc27a4tm1Wsr/Slc27a4tm1Wsr
involves: 129P2/OlaHsd * C57BL/6 		abnormal epidermal layer morphology J:84096
abnormal epidermal-dermal junction morphology J:84096
abnormal epidermis stratum spinosum morphology J:84096
abnormal facial morphology J:84096
abnormal fluid regulation J:84096
abnormal pilosebaceous unit morphology J:84096
abnormal postnatal growth/weight/body size J:84096
abnormal pulmonary alveolus morphology J:84096
abnormal suckling behavior J:84096
decreased body weight J:84096
decreased keratohyalin granule size J:84096
hyperkeratosis J:84096
impaired skin barrier function J:84096
joint contracture J:84096
neonatal lethality, complete penetrance J:84096
protruding tongue J:84096
respiratory distress J:84096
thick skin J:84096
tight skin J:84096
Slc27a4wrfr/Slc27a4wrfr
involves: 129 * C57BL/6J 		abnormal digestive system morphology J:83282
abnormal respiratory system physiology J:83282
absent suckling reflex J:83282
decreased hair follicle number J:83282
decreased locomotor activity J:83282
neonatal lethality, complete penetrance J:83282
shiny skin J:83282
sparse hair J:83282
thick skin J:83282
tight skin J:83282
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory