131 phenotypes from 3 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Csf1Mhdabap25/Csf1Mhdabap25 C3HeB/FeJ-Csf1Mhdabap25	decreased circulating alkaline phosphatase level	J:183993
Csf1op/Csf1op B6;C3Fe a/a-Csf1op/J	abnormal auditory brainstem response waveform shape	J:35818
	abnormal microglial cell morphology	J:170081
	abnormal neurite morphology	J:35818
	abnormal ovarian folliculogenesis	J:30863
	abnormal ovulation	J:30863
	abnormal postnatal growth	J:170081
	abnormal visual evoked potential	J:35818
	normal behavior/neurological phenotype	J:170081
	decreased macrophage cell number	J:30863, J:147697
	decreased mature ovarian follicle number	J:30863
	decreased physiological sensitivity to xenobiotic	J:147697
	decreased tertiary ovarian follicle number	J:30863
	impaired granulosa cell differentiation	J:30863
	impaired macrophage chemotaxis	J:147697
Csf1op/Csf1op B6C3Fe a/a-Csf1op/J	abnormal auditory brainstem response	J:19549
	abnormal bone marrow cavity morphology	J:19549, J:26978
	abnormal bone marrow cell morphology/development	J:19549
	abnormal bone marrow morphology	J:73663
	abnormal bone remodeling	J:19549
	abnormal branching of the mammary ductal tree	J:20519
	abnormal femur morphology	J:18356
	abnormal hematopoietic stem cell morphology	J:19549
	abnormal Kupffer cell morphology	J:26978
	abnormal lactation	J:20519
	abnormal Langerhans cell morphology	J:112594
	abnormal Langerhans cell physiology	J:112594
	abnormal long bone hypertrophic chondrocyte zone	J:26978
	abnormal mammary gland alveolus morphology	J:20519
	abnormal mammary gland development	J:20519
	abnormal mammary gland growth during pregnancy	J:20519
	abnormal masseter muscle morphology	J:20589
	abnormal microglial cell morphology	J:49613
	abnormal osteoclast differentiation	J:4732, J:19549
	abnormal osteoclast morphology	J:26978
	abnormal parietal bone morphology	J:18356
	abnormal perivascular macrophage morphology	J:49613
	abnormal spleen red pulp morphology	J:26978
	abnormal splenic cell ratio	J:104139
	abnormal splenocyte physiology	J:19549
	abnormal tibia morphology	J:26978
	abnormal uterine epithelium development	J:26978
	abnormal vestibular system physiology	J:19549
	abnormal visual evoked potential	J:19549
	absent Langerhans cell	J:112594
	amyloid beta deposits	J:87261
	decreased body weight	J:73663, J:104139
	decreased bone marrow cell number	J:104139
	decreased circulating testosterone level	J:34371
	decreased hippocampus pyramidal cell number	J:87261
	decreased leukocyte cell number	J:104139
	decreased macrophage cell number	J:26978, J:104139
	decreased monocyte cell number	J:104139
	decreased osteoclast cell number	J:73663
	domed cranium	J:18356
	endometrium hypoplasia	J:26978
	extramedullary hematopoiesis	J:26978
	increased bone trabecula number	J:26978, J:73663
	increased testis weight	J:34371
	myometrium hypoplasia	J:26978
	necrospermia	J:34371
	oligozoospermia	J:34371
	postnatal growth retardation	J:73663
	postnatal lethality, incomplete penetrance	J:73663
	reduced male fertility	J:34371
	thymus cortex hypoplasia	J:26978
	thymus medulla atrophy	J:26978
Csf1op/Csf1op C57BL/6J-Csf1op	abnormal autopod morphology	J:5634
	abnormal bone marrow cavity morphology	J:5634
	abnormal bone structure	J:5634
	abnormal osteoblast physiology	J:5634
	abnormal osteoclast morphology	J:5634
	abnormal skeleton morphology	J:110981
	abnormal spleen red pulp morphology	J:5634
	abnormal thyroid parafollicular C-cell morphology	J:5634
	abnormal trabecular bone morphology	J:5634
	absent incisors	J:5634
	absent teeth	J:110981
	decreased circulating phosphate level	J:5634
	decreased macrophage cell number	J:110981
	decreased osteoclast cell number	J:5634
	domed cranium	J:5634
	osteopetrosis	J:5634
	osteoporosis	J:110981
	premature death	J:5634
	reduced fertility	J:5634
	round snout	J:110981
	short limbs	J:5634
	short tail	J:5634
	slow postnatal weight gain	J:5634
Csf1op/Csf1op involves: C3HeB/FeJ * C57BL/6J	abnormal bone marrow cavity morphology	J:5634
	abnormal bone remodeling	J:5634
	abnormal branching of the mammary ductal tree	J:20519
	abnormal circulating calcium level	J:5634
	abnormal eating behavior	J:40136
	abnormal lactation	J:20519
	abnormal mammary gland development	J:20519
	abnormal mammary gland growth during lactation	J:20519
	abnormal mammary gland lobule morphology	J:20519
	abnormal mating frequency	J:38039
	abnormal osteoclast cell number	J:33189
	abnormal osteoclast differentiation	J:38039
	abnormal ovary morphology	J:38039
	abnormal ovulation	J:38039
	abnormal proestrus	J:38039
	abnormal sperm number	J:34371
	abnormal testis physiology	J:34371
	abnormal thyroid parafollicular C-cell morphology	J:5634
	absent teeth	J:5634
	decreased body weight	J:40136
	decreased circulating phosphate level	J:5634
	decreased circulating testosterone level	J:34371
	decreased corpora lutea number	J:38039
	decreased fertilization frequency	J:38039
	decreased litter size	J:38039
	decreased osteoclast cell number	J:33189
	decreased ovulation rate	J:38039
	decreased susceptibility to atherosclerosis	J:40136
	domed cranium	J:5634
	impaired embryo implantation	J:38039
	prolonged estrous cycle	J:38039
	reduced female fertility	J:38039
	reduced male mating frequency	J:34371
Csf1tm1.2Sabw/Csf1tm1.2Sabw involves: 129S4/SvJaeSor * C57BL/6	abnormal bone marrow cavity morphology	J:180199
	abnormal bone structure	J:180199
	abnormal compact bone morphology	J:180199
	abnormal dental follicle morphology	J:180199
	abnormal dentin mineralization	J:180199
	abnormal Kupffer cell morphology	J:180199
	abnormal myeloid leukocyte morphology	J:180199
	abnormal osteoblast morphology	J:180199
	abnormal osteocyte dendritic process morphology	J:180199
	abnormal osteocyte lacuna morphology	J:180199
	abnormal osteocyte morphology	J:180199
	abnormal predentin morphology	J:180199
	abnormal tooth root development	J:180199
	abnormal trabecular bone morphology	J:180199
	decreased B cell number	J:180199
	decreased body weight	J:180199
	decreased bone marrow cell number	J:180199
	decreased bone mineralization	J:180199
	decreased bone resorption	J:180199
	decreased compact bone thickness	J:180199
	decreased length of long bones	J:180199
	decreased lymphocyte cell number	J:180199
	decreased macrophage cell number	J:180199
	decreased monocyte cell number	J:180199
	decreased osteoclast cell number	J:180199
	decreased spleen weight	J:180199
	decreased trabecular bone thickness	J:180199
	domed cranium	J:180199
	failure of tooth eruption	J:180199
	fragile skeleton	J:180199
	impaired osteoblast differentiation	J:180199
	increased bone mass	J:180199
	increased bone trabecula number	J:180199
	increased granulocyte number	J:180199
	increased long bone epiphyseal plate size	J:180199
	increased osteocyte apoptosis	J:180199
	increased T cell number	J:180199
	increased trabecular bone mass	J:180199
	increased trabecular bone volume	J:180199
	increased width of hypertrophic chondrocyte zone	J:180199
	osteopetrosis	J:180199
	osteosclerosis	J:180199
	postnatal growth retardation	J:180199
	small spleen	J:180199