58 phenotypes from 6 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Trpm7Gt(XC765)Byg/Trpm7Gt(XC765)Byg involves: 129P2/OlaHsd * C57BL/6J	embryonic lethality between implantation and somite formation, complete penetrance	J:140630
Trpm7tm1.1Clph/Trpm7tm1.1Clph involves: 129S4/SvJae	embryonic lethality, complete penetrance	J:140630
Trpm7tm1.1Mkma/Trpm7tm1.1Mkma B6.129-Trpm7tm1.1Mkma	no abnormal phenotype detected	J:221252
Trpm7tm1Agry/Trpm7+ involves: 129	abnormal channel response	J:205665
	abnormal digestion	J:205665
	abnormal magnesium ion homeostasis	J:205665
	decreased circulating magnesium level	J:205665
	decreased erythrocyte magnesium level	J:205665
	decreased urine magnesium level	J:205665
	increased susceptibility to induced morbidity/mortality	J:205665
	increased susceptibility to type IV hypersensitivity reaction	J:205665
	limb grasping	J:205665
	seizures	J:205665
	tremors	J:205665
Trpm7tm1Agry/Trpm7tm1Agry involves: 129	abnormal cell physiology	J:205665
	decreased embryo size	J:205665
	embryonic growth arrest	J:205665
	prenatal lethality, complete penetrance	J:205665
Trpm7tm1b(KOMP)Wtsi/Trpm7+ C57BL/6N-Trpm7tm1b(KOMP)Wtsi/H	abnormal iris morphology	J:211773
	abnormal placement of pupils	J:211773
	cornea opacity	J:211773
	increased circulating alkaline phosphatase level	J:211773
	irregularly shaped pupil	J:211773
	thrombocytosis	J:211773
Trpm7tm1b(KOMP)Wtsi/Trpm7tm1b(KOMP)Wtsi C57BL/6N-Trpm7tm1b(KOMP)Wtsi/H	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Trpm7tm1Clph/Trpm7tm1.1Clph Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129S4/SvJae * C57BL/6 * CBA	embryonic lethality, complete penetrance	J:140630
Trpm7tm1Clph/Trpm7tm1.1Clph Tg(Gata1-cre)1Sho/0 involves: 129S4/SvJae * CD-1	embryonic lethality, complete penetrance	J:140630
Trpm7tm1Clph/Trpm7tm1.1Clph Tg(Lck-cre)548Jxm/0 involves: 129S4/SvJae * C57BL/6 * CBA	abnormal T cell differentiation	J:140630
	abnormal T cell physiology	J:140630
	abnormal thymus cell ratio	J:140630
	abnormal thymus corticomedullary boundary morphology	J:140630
	abnormal thymus medulla morphology	J:140630
	abnormal thymus morphology	J:140630
	decreased T cell number	J:140630
	decreased thymocyte number	J:140630
Trpm7tm1Clph/Trpm7tm1Clph Tg(CAG-cre/Esr1*)5Amc/0 involves: 129S4/SvJae * C57BL/6 * CBA	abnormal developmental patterning	J:181963
	abnormal embryo morphology	J:181963
	embryonic lethality, complete penetrance	J:181963
	no abnormal phenotype detected	J:181963
Trpm7tm1Clph/Trpm7tm1Clph Tg(Hoxb7-cre)5526Cmb/0 involves: 129S4/SvJae	normal renal/urinary system phenotype	J:181963
Trpm7tm1Clph/Trpm7tm1Clph Tg(Nes-cre)1Kln/0 involves: 129S4/SvJae * C57BL/6 * SJL	no abnormal phenotype detected	J:181963
Trpm7tm1Clph/Trpm7tm1Clph Tg(Pax3-cre)1Joe/0 involves: 129S4/SvJae * C57BL/6 * SJL	abnormal comma shaped body morphology	J:181963
	abnormal hair follicle melanocyte morphology	J:181963
	abnormal kidney development	J:181963
	abnormal nephron morphogenesis	J:181963
	abnormal renal tubule morphology	J:181963
	abnormal rostrocaudal coat patterning	J:181963
	abnormal S-shaped body morphology	J:181963
	absent hair follicle melanin granules	J:181963
	decreased melanocyte number	J:181963
	decreased renal glomerulus number	J:181963
	decreased sensory neuron number	J:181963
	dilated renal tubule	J:181963
	hindlimb paralysis	J:181963
	hypopigmentation	J:181963
	impaired limb coordination	J:181963
	kidney cortex cyst	J:181963
	kidney cyst	J:181963
	kidney failure	J:181963
	paresis	J:181963
	small dorsal root ganglion	J:181963
	small kidney	J:181963