69 phenotypes from 1 allele in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ts(1716)65Dn/0 B6EiC3Sn a/A-Ts(1716)65Dn/J	abnormal dentate gyrus morphology	J:170195
	abnormal hippocampus granule cell layer	J:170195
	abnormal hippocampus morphology	J:170195
	abnormal learning/memory/conditioning	J:153579
	abnormal nervous system development	J:170195
	abnormal spatial learning	J:153579, J:170195
	decreased body length	J:153579
	decreased body weight	J:153579, J:170195
	decreased grip strength	J:153579
	decreased tumor growth/size	J:150286
	hyperactivity	J:153579
	impaired contextual conditioning behavior	J:153579
	impaired cued conditioning behavior	J:153579
	increased stereotypic behavior	J:153579
	increased vertical activity	J:153579
Ts(1716)65Dn/0 B6EiC3Sn.BLiA-Ts(1716)65Dn/DnJ	abnormal learning/memory/conditioning	J:153579
	abnormal spatial learning	J:153579
	decreased body length	J:153579
	decreased body weight	J:153579
	decreased grip strength	J:153579
	hyperactivity	J:153579
	impaired contextual conditioning behavior	J:153579
	impaired cued conditioning behavior	J:153579
	increased stereotypic behavior	J:153579
	increased vertical activity	J:153579
Ts(1716)65Dn/0 involves: BALB/c * C3H/He * C57BL/6JEiJ * DBA/2J	abnormal brain morphology	J:331897
	abnormal nest building behavior	J:331897
	abnormal response to novel object	J:331897
	abnormal spatial working memory	J:331897
	asthenozoospermia	J:331897
	hyperactivity	J:331897
	impaired contextual conditioning behavior	J:331897
	impaired spatial learning	J:331897
	increased thigmotaxis	J:331897
	increased vertical activity	J:331897
	oligozoospermia	J:331897
	reduced male fertility	J:331897
	small cranium	J:331897
Ts(1716)65Dn/0 involves: C3H * C57BL/6 * DBA/2J	abnormal incisor morphology	J:73800
	abnormal mandibular angle morphology	J:73800
	decreased cranium height	J:73800
	small mandible	J:73800
	small mandibular coronoid process	J:73800
Ts(1716)65Dn/0 involves: C3H/HeH * C3H/HeSn * C57BL/6Ei * C57BL/6J * DBA/2J	abnormal heart electrocardiography waveform feature	J:185269
	abnormal heart morphology	J:185269
	abnormal QRS complex	J:185269
	decreased heart rate	J:185269
	decreased P wave amplitude	J:185269
	decreased QRS amplitude	J:185269
	postnatal lethality, incomplete penetrance	J:185269
	prolonged PR interval	J:185269
	prolonged QRS complex duration	J:185269
	prolonged QT interval	J:185269
	prolonged RR interval	J:185269
	retroesophageal right subclavian artery	J:185269
	ventricular septal defect	J:185269
Ts(1716)65Dn/0 involves: C3H/HeJ * C57BL/6 * DBA/2J	abnormal cerebellar granule cell morphology	J:121764
	abnormal spatial learning	J:121764
	decreased body weight	J:121764
	decreased Purkinje cell number	J:121764
	increased brain size	J:121764
	small cerebellum	J:121764
Ts(1716)65Dn/0 involves: C3H/HeJ * C57BL/6J * DBA/2J	abnormal spleen B cell follicle morphology	J:174270
	abnormal spleen B cell follicle shape	J:174270
	abnormal spleen red pulp morphology	J:174270
	increased follicular lymphoma incidence	J:174270
	increased lymphoma incidence	J:174270
	increased malignant tumor incidence	J:174270
	increased spleen B cell follicle size	J:174270
Ts(1716)65Dn/0 involves: C3H/HeJ * C57BL/6JEi * DBA/2J	abnormal Purkinje cell morphology	J:91221
Ts(1716)65Dn/0 involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	abnormal cerebellar granule cell morphology	J:94569
	abnormal CNS synapse formation	J:94569
	abnormal dendrite morphology	J:94569
	abnormal male germ cell morphology	J:117029
	abnormal neuron morphology	J:96650
	abnormal Sertoli cell morphology	J:96650
	abnormal spermatogenesis	J:96650, J:117029
	abnormal testis morphology	J:96650
	arrest of male meiosis	J:117029
	decreased body size	J:96650
	decreased body weight	J:94569
	decreased sperm progressive motility	J:117029
	decreased testis weight	J:96650, J:117029
	male infertility	J:117029
	oligozoospermia	J:117029
Ts(1716)65Dn/0 involves: DBA/2J	enlarged neurocranium	J:93223
	short femur	J:93223
	small cranium	J:93223
	small mandible	J:93223