Abca4 Phenotype Annotations

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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)
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