89 phenotypes from 4 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ttc7em1(IMPC)J/Ttc7+ C57BL/6NJ-Ttc7em1(IMPC)J/Mmjax	abnormal coat/ hair morphology	J:211773
	abnormal coat/hair pigmentation	J:211773
	abnormal vocalization	J:211773
	decreased grip strength	J:211773
	decreased lean body mass	J:211773
	increased total body fat amount	J:211773
Ttc7em1(IMPC)J/Ttc7em1(IMPC)J C57BL/6NJ-Ttc7em1(IMPC)J/Mmjax	preweaning lethality, complete penetrance	J:211773
Ttc7fsn-Jic/Ttc7fsn-Jic B6.INT-Ttc7fsn-Jic	abnormal tail pigmentation	J:115742
	anemia	J:115742
	increased fetal derived definitive erythrocyte cell number	J:115742
	normal integument phenotype	J:115742
	pallor	J:115742
	postnatal lethality, complete penetrance	J:115742
Ttc7fsn-Jic/Ttc7fsn-Jic C3.INT-Ttc7fsn-Jic	abnormal erythrocyte morphology	J:115742
	abnormal skin condition	J:115742
	acanthocytosis	J:115742
	acanthosis	J:115742
	anemia	J:115742
	dacryocytosis	J:115742
	decreased body weight	J:115742
	decreased heart weight	J:115742
	decreased hematocrit	J:115742
	decreased spleen white pulp amount	J:115742
	decreased thymus weight	J:115742
	extramedullary hematopoiesis	J:115742
	hyperkeratosis	J:115742
	increased nucleated erythrocyte cell number	J:115742
	increased spleen red pulp amount	J:115742
	increased spleen weight	J:115742
	liver hypoplasia	J:115742
	liver inflammation	J:115742
	low mean erythrocyte cell number	J:115742
	mixed cellular infiltration to dermis	J:115742
	pale kidney	J:115742
	pale liver	J:115742
	parakeratosis	J:115742
	postnatal lethality, complete penetrance	J:115742
	sparse hair	J:115742
	thrombocytosis	J:115742
Ttc7fsn-Jic/Ttc7fsn-Jic CBy.INT-Ttc7fsn-Jic	abnormal skin condition	J:115742
	anemia	J:115742
	postnatal lethality, complete penetrance	J:115742
	scaly skin	J:115742
Ttc7fsn/Ttc7fsn-Jic involves: A/J * BALB/c * C57BL/6 * INT	premature death	J:115742
Ttc7fsn/Ttc7fsn CByJ.A-Ttc7fsn	abnormal circulating iron level	J:92699
	abnormal dermal layer morphology	J:30519
	abnormal epidermal layer morphology	J:30519
	abnormal epidermis stratum granulosum morphology	J:30519
	abnormal erythropoiesis	J:92699
	abnormal iron level	J:92699
	abnormal mineral level	J:92699
	abnormal stomach epithelium morphology	J:30519
	acanthosis	J:30519
	alopecia	J:30519
	anemia	J:30519, J:92699
	decreased body weight	J:29200
	decreased hematocrit	J:92699
	decreased hemoglobin content	J:92699
	decreased mean corpuscular volume	J:92699
	enlarged heart	J:29200
	enlarged liver	J:29200
	enlarged spleen	J:29200, J:30519
	epidermal hyperplasia	J:30519
	extramedullary hematopoiesis	J:92699
	flaky skin	J:30519
	hyperkeratosis	J:30519
	low mean erythrocyte cell number	J:92699
	mixed cellular infiltration to dermis	J:30519
	orthokeratosis	J:30519
	pallor	J:30519
	parakeratosis	J:30519
	scaly skin	J:30519
	skin lesions	J:30519
	small thymus	J:29200
	thymus cortex hypoplasia	J:29200
Ttc7fsn/Ttc7fsn CByJ.A-Ttc7fsn/J	premature death	J:115742
Ttc7fsn/Ttc7fsn involves: A/J	abnormal forestomach morphology	J:2777
	abnormal stomach epithelium morphology	J:2777
	abnormal stomach mucosa morphology	J:2777
	abnormal stomach non-glandular epithelium morphology	J:2777
	anemia	J:2777
	increased papilloma incidence	J:2777
	stomach inflammation	J:2777
Ttc7fsn/Ttc7fsn involves: A/J * BALB/cByJ	abnormal epidermal layer morphology	J:29609
	abnormal hair cuticle	J:29609
	abnormal hair shaft morphology	J:29609
	abnormal keratinocyte morphology	J:29609
	abnormal keratohyalin granule morphology	J:29609
	abnormal nail morphology	J:29609
	deformed nails	J:29609
	hypergranulosis	J:29609
	increased dendritic epidermal T cell number	J:14506
	increased Langerhans cell number	J:14506
	thick epidermis	J:14506, J:29609
Ttc7hea/Ttc7hea CFO	abnormal definitive hematopoiesis	J:7515
	abnormal erythrocyte cell number	J:7515
	abnormal erythrocyte morphology	J:7515
	abnormal skin pigmentation	J:7515
	anemia	J:7515
	anisocytosis	J:7515
	colorless urine	J:7515
	decreased body weight	J:7515
	decreased hematocrit	J:7515
	decreased hemoglobin content	J:7515
	decreased megakaryocyte cell number	J:7515
	enlarged spleen	J:7515
	erythroblastosis	J:7515
	increased leukocyte cell number	J:7515
	low mean erythrocyte cell number	J:7515
	poikilocytosis	J:7515
	polychromatophilia	J:7515
	postnatal lethality, complete penetrance	J:7515
	reticulocytosis	J:7515
Ttc7hea/Ttc7hea WBB6F1	abnormal erythrocyte cell number	J:92699
	abnormal erythrocyte morphology	J:92699
	abnormal erythropoiesis	J:92699
	abnormal hepatocyte morphology	J:92699
	abnormal mineral level	J:92699
	anemia	J:92699
	anisocytosis	J:92699
	decreased body weight	J:92699
	decreased hematocrit	J:92699
	decreased hemoglobin content	J:92699
	epidermal hyperplasia	J:92699
	epidermal necrosis	J:92699
	erythroblastosis	J:92699
	extramedullary hematopoiesis	J:92699
	hyperkeratosis	J:92699
	increased circulating iron level	J:92699
	low mean erythrocyte cell number	J:92699
	pallor	J:92699
	poikilocytosis	J:92699
	polychromatophilia	J:92699
	postnatal lethality	J:92699