87 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gas1tm1Fan/Gas1tm1Fan involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal anterior eye segment morphology	J:70735
	abnormal basicranium morphology	J:122159
	abnormal basisphenoid bone morphology	J:122159
	abnormal ciliary body morphology	J:70735
	abnormal cornea morphology	J:70735
	abnormal craniofacial bone morphology	J:122159
	abnormal external auditory canal morphology	J:122159
	abnormal eye development	J:70735, J:122159
	abnormal eye morphology	J:70735
	abnormal incisor morphology	J:122159
	abnormal iris morphology	J:70735
	abnormal malleus manubrium morphology	J:122159
	abnormal malleus morphology	J:122159
	abnormal malleus neck morphology	J:122159
	abnormal malleus processus brevis morphology	J:122159
	abnormal nasal capsule morphology	J:122159
	abnormal neurocranium morphology	J:122159
	abnormal otic capsule morphology	J:122159
	abnormal palatal mesenchymal cell proliferation	J:122159
	abnormal posterior eye segment morphology	J:70735
	abnormal premaxilla morphology	J:122159
	abnormal retina ganglion layer morphology	J:70735
	abnormal retina neuronal layer morphology	J:70735
	abnormal retina pigment epithelium morphology	J:70735
	abnormal secondary palate development	J:122159
	abnormal stapes morphology	J:122159
	abnormal styloid process morphology	J:122159
	abnormal synchondrosis	J:122159
	abnormal tegmen tympani morphology	J:122159
	abnormal temporal bone squamous part morphology	J:122159
	abnormal tympanic ring morphology	J:122159
	abnormal vitreous body morphology	J:70735
	absent gonial bone	J:122159
	absent hypoglossal canal	J:122159
	absent vomeronasal organ	J:122159
	cleft secondary palate	J:122159
	coloboma	J:70735
	decreased cornea size	J:70735
	gonial bone hypoplasia	J:122159
	holoprosencephaly	J:122159
	increased cornea thickness	J:70735
	microphthalmia	J:70735
	midface hypoplasia	J:122159
	narrow eye opening	J:70735
	palatal shelves fail to meet at midline	J:122159
	postnatal lethality, incomplete penetrance	J:70735
	premaxilla hypoplasia	J:122159
	small alisphenoid bone	J:122159
	small lens	J:70735
	styloid process hypoplasia	J:122159
	synostosis	J:122159
Gas1tm1Fan/Gas1tm1Fan involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal cerebellar foliation	J:70736
	abnormal cerebellar molecular layer	J:70736
	abnormal cerebellar Purkinje cell layer	J:70736
	abnormal cerebellum development	J:70736
	abnormal cerebellum external granule cell layer morphology	J:70736
	abnormal digit development	J:79482
	abnormal gait	J:70736
	abnormal limb bone morphology	J:79482
	abnormal limb bud morphology	J:79482
	abnormal limb mesenchyme morphology	J:79482
	abnormal phalanx morphology	J:79482
	abnormal Purkinje cell dendrite morphology	J:70736
	abnormal Purkinje cell morphology	J:70736
	brachydactyly	J:79482
	brachyphalangia	J:79482
	decreased autopod size	J:79482
	decreased eye pigmentation	J:70736
	decreased Purkinje cell size	J:70736
	impaired balance	J:70736
	normal mortality/aging	J:70736, J:79482
	short metacarpal bones	J:79482
	short metatarsal bones	J:79482
	small cerebellum	J:70736
	syndactyly	J:79482
	thin apical ectodermal ridge	J:79482
	thin cerebellar granule layer	J:70736
Gas1tm2Fan/Gas1tm2Fan involves: 129 * C57BL/6J	abnormal digit morphology	J:121554
	abnormal floor plate morphology	J:121554
	oligodactyly	J:121554
	short limbs	J:121554
Gas1tm2Fan/Gas1tm2Fan involves: C57BL/6J	abnormal floor plate morphology	J:121553
	abnormal medial nasal prominence morphology	J:121553
	abnormal tympanic ring morphology	J:121553
	abnormal vertebral body morphology	J:121553
	decreased neuronal precursor cell number	J:121553
	hindlimb oligodactyly	J:121553
	short maxilla	J:121553
	small parietal bone	J:121553
	syndactyly	J:121553