72 phenotypes from 2 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gsctm1Bhr/Gsctm1Bhr 129S7/SvEvBrd-Gsctm1Bhr	abnormal craniofacial morphology	J:28702
	abnormal rib morphology	J:28702
Gsctm1Bhr/Gsctm1Bhr B6.129S7-Gsctm1Bhr	abnormal craniofacial morphology	J:28702
	abnormal rib morphology	J:28702
Gsctm1Bhr/Gsctm1Bhr involves: 129S7/SvEvBrd * C57BL/6	abnormal alisphenoid bone morphology	J:28702
	abnormal basicranium morphology	J:28702
	abnormal breathing pattern	J:28702
	abnormal craniofacial morphology	J:28702
	abnormal external auditory canal morphology	J:28702
	abnormal extrinsic tongue muscle morphology	J:28702
	abnormal frontal bone morphology	J:28702
	abnormal genioglossus muscle morphology	J:28702
	abnormal jaw morphology	J:28702
	abnormal malleus morphology	J:28702
	abnormal mandible morphology	J:28702
	abnormal maxilla morphology	J:28702
	abnormal Meckel's cartilage morphology	J:28702
	abnormal middle ear morphology	J:28702
	abnormal nasal cavity morphology	J:28702
	abnormal nasal mucosa morphology	J:28702
	abnormal nasal septum morphology	J:28702
	abnormal nose morphology	J:28702
	abnormal palatine bone morphology	J:28702
	abnormal pterygoid process morphology	J:28702
	abnormal rib morphology	J:28702
	abnormal sternocostal joint morphology	J:28702
	abnormal suckling behavior	J:28702
	absent turbinates	J:28702
	absent tympanic membrane	J:28702
	absent tympanic ring	J:28702
	normal endocrine/exocrine gland phenotype	J:28702
	normal limbs/digits/tail phenotype	J:28702
	neonatal lethality, complete penetrance	J:28702
	pallor	J:28702
	rib fusion	J:28702
	short mandible	J:28702
	small malleus manubrium	J:28702
	small malleus processus brevis	J:28702
Gsctm1Pgr/Gsctm1Pgr either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	abnormal acetabulum morphology	J:46948
	abnormal basicranium morphology	J:46948
	abnormal ethmoid bone morphology	J:46948
	abnormal femur head morphology	J:46948
	abnormal glenoid fossa morphology	J:46948
	abnormal hip joint morphology	J:46948
	abnormal humerus morphology	J:46948
	abnormal joint morphology	J:46948
	abnormal obturator foramen morphology	J:46948
	abnormal presphenoid bone morphology	J:46948
	abnormal pubic symphysis morphology	J:46948
	abnormal scapular coracoid process morphology	J:46948
	abnormal shoulder joint morphology	J:46948
	abnormal sternocostal joint morphology	J:46948
	abnormal trochanter morphology	J:46948
	abnormal vomer bone morphology	J:46948
	cervical vertebral transformation	J:46948
	increased rib number	J:46948
	presphenoid bone hypoplasia	J:46948
	rib fusion	J:46948
	small cribriform plate	J:46948
	small ischium	J:46948
	small vomer bone	J:46948
Gsctm1Pgr/Gsctm1Pgr involves: 129S1/Sv * 129X1/SvJ	abnormal epitympanic recess morphology	J:59750
	abnormal horizontal basal cell of olfactory epithelium morphology	J:29421
	abnormal intrinsic tongue muscle morphology	J:29421
	abnormal mandible morphology	J:29421
	abnormal mandibular angle morphology	J:29421
	abnormal masticatory muscle morphology	J:29421
	abnormal Meckel's cartilage morphology	J:29421
	abnormal nasal capsule morphology	J:29421
	abnormal nasal cavity morphology	J:29421
	abnormal nasal septum morphology	J:29421
	abnormal palatine bone morphology	J:29421
	abnormal tympanic membrane morphology	J:29421
	abnormal vomer bone morphology	J:29421
	absent ethmoturbinates	J:29421
	absent external auditory canal	J:29421, J:59750
	absent gastric milk in neonates	J:29421
	absent malleus processus brevis	J:29421
	absent tympanic membrane	J:59750
	absent tympanic ring	J:29421
	decreased birth body size	J:29421
	decreased tympanic ring size	J:59750
	mandible hypoplasia	J:29421
	neonatal lethality, complete penetrance	J:29421
	palatine bone hypoplasia	J:29421
	small alisphenoid bone	J:29421
	small malleus manubrium	J:29421
	small mandibular coronoid process	J:29421
	small pterygoid bone	J:29421
	small vomer bone	J:29421