Abca4 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Abca4
ATP-binding cassette, sub-family A member 4
MGI:109424

13 phenotypes from 4 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Abca4^tm1.1Rsmy/Abca4^tm1.1Rsmy involves: C57BL/6	abnormal eye physiology	J:255529
Abca4^tm1.1Rsmy/Abca4^tm1.1Rsmy involves: C57BL/6	abnormal retina pigment epithelium morphology	J:255529
Abca4^{tm1a(EUCOMM)Wtsi}/Abca4⁺ C57BL/6N-Abca4^{tm1a(EUCOMM)Wtsi}/Wtsi	increased mean corpuscular hemoglobin	J:175295
Abca4^{tm1a(EUCOMM)Wtsi}/Abca4^{tm1a(EUCOMM)Wtsi} C57BL/6N-Abca4^{tm1a(EUCOMM)Wtsi}/Wtsi	vertebral fusion	J:211773
Abca4^tm1Ght/Abca4^tm1Ght involves: 129S4/SvJae	abnormal eye physiology	J:117483
	abnormal retina pigment epithelium morphology	J:141801
	abnormal vitamin A level	J:141801
Abca4^tm1Ght/Abca4^tm1Ght involves: 129S4/SvJae * BALB/c	abnormal retina pigment epithelium morphology	J:141801
	photoreceptor outer segment degeneration	J:141801
	thin retina outer nuclear layer	J:141801
Abca4^tm1Ght/Abca4^tm1Ght involves: 129S4/SvJae * C57BL/6	abnormal Bruch membrane morphology	J:56317
	abnormal eye physiology	J:56317
	abnormal photoreceptor outer segment morphology	J:56317
	abnormal retina pigment epithelium morphology	J:56317
	delayed dark adaptation	J:56317
	retina photoreceptor degeneration	J:56317
Abca4^tm2.1Kpal/Abca4^tm2.1Kpal involves: 129 * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6N	lipofuscinosis	J:221141
	normal vision/eye phenotype	J:221141

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