About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fa2h
fatty acid 2-hydroxylase
MGI:2443327
54 phenotypes from 5 alleles in 4 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Fa2hem1(IMPC)Mbp/Fa2hem1(IMPC)Mbp
C57BL/6NCrl-Fa2hem1(IMPC)Mbp/MbpMmucd 		abnormal coat/ hair morphology J:211773
abnormal eye morphology J:211773
abnormal kidney morphology J:211773
abnormal retina morphology J:211773
abnormal skin morphology J:211773
abnormal spleen morphology J:211773
abnormal testis morphology J:211773
abnormal vitreous body morphology J:211773
cataract J:211773
decreased circulating cholesterol level J:211773
decreased circulating HDL cholesterol level J:211773
decreased grip strength J:211773
enlarged kidney J:211773
enlarged spleen J:211773
enlarged testis J:211773
increased freezing behavior J:211773
Fa2hm1Btlr/Fa2hm1Btlr
C57BL/6J-Fa2hm1Btlr 		alopecia J:267484
Fa2htm1.1Hama/Fa2htm1.1Hama
involves: 129 * C57BL/6 		abnormal astrocyte morphology J:171655
abnormal axon morphology J:171655
abnormal cerebellum morphology J:171655
abnormal galactolipid level J:171655
abnormal learning/memory/conditioning J:171655
abnormal lipid level J:171655
abnormal motor learning J:171655
abnormal myelin sheath morphology J:171655
abnormal optic nerve morphology J:171655
abnormal Purkinje cell morphology J:171655
abnormal spatial learning J:171655
decreased cholesterol level J:171655
decreased locomotor activity J:171655
decreased Purkinje cell size J:171655
decreased vertical activity J:171655
demyelination J:171655
impaired coordination J:171655
normal nervous system phenotype J:171655
Fa2htm1Hama/Fa2htm1Hama
Cnptm1(cre)Kan/Cnp+
involves: 129 * C57BL/6 		abnormal cerebellum morphology J:171655
abnormal galactolipid level J:171655
abnormal lipid level J:171655
abnormal Purkinje cell morphology J:171655
normal behavior/neurological phenotype J:171655
decreased locomotor activity J:171655
decreased Purkinje cell size J:171655
decreased vertical activity J:171655
impaired coordination J:171655
Fa2htm1Meck/Fa2htm1Meck
involves: 129P2/OlaHsd * C57BL/6N 		abnormal axon morphology J:143373
abnormal coat appearance J:175386
abnormal epidermal layer morphology J:175386
abnormal hair follicle ostium morphology J:175386
abnormal hair shaft morphology J:175386
abnormal locomotor activation J:143373
abnormal myelin sheath morphology J:143373
abnormal sebaceous gland physiology J:175386
abnormal sebaceous lipid secretion J:175386
alopecia J:175386
decreased vertical activity J:143373
delayed exit from anagen phase J:175386
delayed hair appearance J:175386
delayed hair regrowth J:175386
dilated piliary canal J:175386
enlarged sebaceous gland J:175386
flaky skin J:175386
focal hair loss J:175386
hindlimb paralysis J:143373
increased sebocyte number J:175386
normal nervous system phenotype J:143373
sebaceous gland hyperplasia J:175386
sparse hair J:175386
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory