66 phenotypes from 8 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
HgsTg(Tyr)2400A-1Ove/HgsTg(Tyr)2400A-1Ove FVB/N-HgsTg(Tyr)2400A-1Ove	embryonic lethality between implantation and somite formation	J:175597
Hgstm1a(EUCOMM)Wtsi/Hgs+ Not Specified	abnormal coping response	J:165965
Hgstm1b(EUCOMM)Wtsi/Hgstm1b(EUCOMM)Wtsi C57BL/6N-Hgstm1b(EUCOMM)Wtsi/Ieg	preweaning lethality, complete penetrance	J:211773
Hgstm1Sor/Hgstm1Sor either: 129/Sv-Hgstm1Sor or B6.129-Hgstm1Sor or (involves: 129/Sv * 129S4/SvJae * C57BL/6J)	abnormal embryonic tissue morphology	J:55580
	abnormal extraembryonic tissue morphology	J:55580
	abnormal rostral-caudal axis patterning	J:55580
	abnormal somite development	J:55580
	absent foregut	J:55580
	cardia bifida	J:55580
	decreased embryo size	J:55580
	dilated allantois	J:55580
	embryonic lethality during organogenesis, complete penetrance	J:55580
	failure of chorioallantoic fusion	J:55580
	failure of initiation of embryo turning	J:55580
	open neural tube	J:55580
	wavy neural tube	J:55580
Hgstm1Sug/Hgstm1Sug involves: 129S4/SvJae * C57BL/6J	decreased embryo size	J:65990
	embryonic lethality, complete penetrance	J:65990
	failure of initiation of embryo turning	J:65990
Hgstm1Tkh/Hgstm1Tkh involves: 129S4/SvJae * C57BL/6	abnormal cell physiology	J:97764
	embryonic lethality during organogenesis, complete penetrance	J:97764
Hgstm2Tkh/Hgstm2Tkh Tg(Syn1-cre)671Jxm/0 involves: C57BL/6 * CBA * SJL	abnormal hippocampus pyramidal cell morphology	J:141391
	behavioral despair	J:141391
	decreased vertical activity	J:141391
	impaired passive avoidance behavior	J:141391
	increased neuron apoptosis	J:141391
	infertility	J:141391
	postnatal growth retardation	J:141391
	slow postnatal weight gain	J:141391
Hgstn/Hgstn B6.C3-Hgstn	abnormal axon morphology	J:5025
	abnormal brain development	J:5025
	abnormal cerebellar cortex morphology	J:5025
	abnormal CNS glial cell morphology	J:5025
	abnormal medulla oblongata morphology	J:5025
	abnormal motor coordination/balance	J:5025
	abnormal myelin sheath morphology	J:5025
	abnormal resting posture	J:5025
	abnormal spinal cord grey matter morphology	J:5025
	abnormal spinal cord white matter morphology	J:5025
	abnormal spinal nerve morphology	J:5025
	abnormal vertebral column morphology	J:5025
	abnormal vertebral spinous process morphology	J:5025
	axonal dystrophy	J:5025
	cachexia	J:5025
	decreased body height	J:5025
	decreased body size	J:5025
	decreased corticospinal tract size	J:5025
	decreased hindbrain size	J:5025
	decreased midbrain size	J:5025
	decreased neuron number	J:5025
	decreased pons size	J:5025
	decreased spinal cord size	J:5025
	decreased trabecular bone thickness	J:5025
	impaired balance	J:5025
	impaired swimming	J:5025
	increased stereotypic behavior	J:5025
	jerky movement	J:5025
	muscular atrophy	J:5025
	opisthotonus	J:5025
	paralysis	J:5025
	postnatal growth retardation	J:5025
	premature death	J:5025
	Purkinje cell degeneration	J:5025
	short vertebral body	J:5025
	small cerebellum	J:5025
	thin cerebellar granule layer	J:5025
Hgstn/Hgstn C3H/HeJ-Hgstn	abnormal posture	J:13411
	abnormal stationary movement	J:13411
	bradykinesia	J:13411
	normal hearing/vestibular/ear phenotype	J:13411
	premature death	J:13411