Fancd2 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fancd2
Fanconi anemia, complementation group D2
MGI:2448480

46 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Aldh2^{tm1a(EUCOMM)Wtsi}/Aldh2⁺ Fancd2^tm1Hou/Fancd2^tm1Hou involves: 129S4/SvJae * C57BL/6J * C57BL/6N	abnormal eye morphology	J:193232
	exencephaly	J:193232
Aldh2^{tm1a(EUCOMM)Wtsi}/Aldh2^{tm1a(EUCOMM)Wtsi} Fancd2^tm1Hou/Fancd2⁺ involves: 129S4/SvJae * C57BL/6J * C57BL/6N	maternal effect	J:193232
Aldh2^{tm1a(EUCOMM)Wtsi}/Aldh2^{tm1a(EUCOMM)Wtsi} Fancd2^tm1Hou/Fancd2^tm1Hou involves: 129S4/SvJae * C57BL/6J * C57BL/6N	abnormal bone marrow cell morphology/development	J:193232
	abnormal chest morphology	J:193232
	abnormal eye morphology	J:193232
	abnormal hematopoietic stem cell physiology	J:188123
	abnormal lymphopoiesis	J:193232
	abnormal spleen morphology	J:188123
	abnormal thymus morphology	J:188123
	anemia	J:188123, J:193232
	anophthalmia	J:193232
	decreased body weight	J:193232
	decreased bone marrow cell number	J:188123, J:193232
	decreased erythrocyte cell number	J:188123, J:193232
	decreased hematocrit	J:188123
	decreased hematopoietic stem cell number	J:188123
	decreased hemoglobin content	J:188123, J:193232
	decreased leukocyte cell number	J:188123
	embryonic lethality during organogenesis	J:193232
	enlarged spleen	J:193232
	exencephaly	J:193232
	extramedullary hematopoiesis	J:188123
	impaired hematopoiesis	J:193232
	increased acute lymphoblastic leukemia incidence	J:193232
	increased CD8-positive, alpha-beta T cell number	J:193232
	increased double-positive T cell number	J:193232
	increased lymphoma incidence	J:193232
	increased mean corpuscular volume	J:188123
	increased physiological sensitivity to xenobiotic	J:188123
	increased sensitivity to induced cell death	J:188123
	increased susceptibility to xenobiotic induced morbidity/mortality	J:193232
	increased T cell derived lymphoma incidence	J:193232
	kinked tail	J:193232
	lethargy	J:193232
	pancytopenia	J:188123
	premature death	J:193232
	thrombocytopenia	J:188123
	weight loss	J:193232
Brip1^{Gt(RRI409)Byg}/Brip1^{Gt(RRI409)Byg} Fancd2^tm1Hou/Fancd2^tm1Hou involves: 129P2/OlaHsd * 129S4/SvJae	abnormal seminiferous tubule morphology	J:227115
	increased cellular sensitivity to DNA damaging agents	J:227115
	small testis	J:227115
Dclre1a^tm1Remo/Dclre1a^tm1Remo Fancd2^tm1Hou/Fancd2^tm1Hou involves: 129S4/SvJae * 129X1/SvJ * C57BL/6J	perinatal lethality, incomplete penetrance	J:134461
Fan1^tm1.1Jrou/Fan1^tm1.1Jrou Fancd2^{Gt(OST57859)Lex}/Fancd2^{Gt(OST57859)Lex} involves: 129P2/OlaHsd * 129S5/SvEvBrd	increased physiological sensitivity to xenobiotic	J:232403
Fan1^{tm1d(KOMP)Wtsi}/Fan1^{tm1d(KOMP)Wtsi} Fancd2^tm1Hou/Fancd2^tm1Hou involves: 129S4/SvJae * C57BL/6N * FVB/N	abnormal hematopoietic stem cell morphology	J:232402
	increased physiological sensitivity to xenobiotic	J:232402
Fancd2^{Gt(OST57859)Lex}/Fancd2^{Gt(OST57859)Lex} Fanci^tm1.1Itl/Fanci^tm1.1Itl involves: 129S5/SvEvBrd * C57BL/6J * CBA	abnormal bone marrow cell morphology/development	J:285384
	decreased hematopoietic stem cell number	J:285384
	prenatal lethality, incomplete penetrance	J:285384
	thrombocytopenia	J:285384
Fancd2^{Gt(OST57859)Lex}/Fancd2^{Gt(OST57859)Lex} Usp1^tm1.1Ada/Usp1^tm1.1Ada involves: 129S5/SvEvBrd * C57BL/6	increased cellular sensitivity to ionizing radiation	J:146616
	induced chromosome breakage	J:146616
	ovary atrophy	J:146616

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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