103 phenotypes from 3 alleles in 22 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rpl38Rbt/Rpl38+ involves: C3H * C57BL/6J	prenatal lethality, incomplete penetrance	J:37422
Rpl38Rbt/Rpl38+ involves: C57BL/6J	prenatal lethality, incomplete penetrance	J:37422
Rpl38Rbt/Rpl38+ involves: C57BL/6J * DBA	prenatal lethality, complete penetrance	J:37422
Rpl38Rbt/Rpl38+ involves: C57BL/6J * NMRI	abnormal cervical atlas morphology	J:37422
	abnormal cervical vertebrae morphology	J:37422
	abnormal cranium morphology	J:37422
	abnormal rib morphology	J:37422
	abnormal vertebral arch morphology	J:37422
	abnormal vertebral lamina morphology	J:37422
	abnormal vertebral pedicle morphology	J:37422
	abnormal vertebral spinous process morphology	J:37422
	abnormal vertebral transverse process morphology	J:37422
	asymmetric sternocostal joints	J:37422
	caudal vertebral transformation	J:37422
	cervical vertebral fusion	J:37422
	decreased body size	J:37422
	decreased body weight	J:37422
	increased rib number	J:37422
	kinked tail	J:37422
	lumbar vertebral transformation	J:37422
	normal mortality/aging	J:37422
	postnatal growth retardation	J:37422
	sacral vertebral transformation	J:37422
	short tail	J:37422
	vertebral transformation	J:37422
Rpl38Rbt/Rpl38Rbt involves: C57BL/6J	embryonic lethality between implantation and somite formation, complete penetrance	J:37422
Rpl38Ts/Rpl38+ (BALB/c x A)F1	embryonic lethality, complete penetrance	J:13063
Rpl38Ts/Rpl38+ (BALB/c x C3H)F1	abnormal digit morphology	J:13063
	abnormal forelimb morphology	J:13063
	abnormal nasal bone morphology	J:13063
	absent caudal vertebrae	J:13063
	absent tail	J:13063
	anemia	J:13063
	belly spot	J:13063
	decreased body length	J:13063
	decreased cranium height	J:13063
	incomplete rostral neuropore closure	J:13063
	increased cranium width	J:13063
	irregular coat pigmentation	J:13063
	oligodactyly	J:13063
	perinatal lethality, incomplete penetrance	J:13063
	polydactyly	J:13063
	reduced fertility	J:13063
	spina bifida	J:13063
Rpl38Ts/Rpl38+ (BALB/c x C57BL)F1	short tail	J:13063
Rpl38Ts/Rpl38+ (BALB/c x C57BR)F1	short tail	J:13063
Rpl38Ts/Rpl38+ (BALB/c x DBA)F1	absent tail	J:13063
Rpl38Ts/Rpl38+ (BALB/c x I)F1	short tail	J:13063
Rpl38Ts/Rpl38+ (BALB/c x L)F1	short tail	J:13063
Rpl38Ts/Rpl38+ (BALB/c x Y)F1	short tail	J:13063
Rpl38Ts/Rpl38+ (TSJ/Le x A/JSlc)F1	postnatal lethality, complete penetrance	J:47940
Rpl38Ts/Rpl38+ (TSJ/Le x AKR/J)F1	postnatal lethality, complete penetrance	J:47940
Rpl38Ts/Rpl38+ (TSJ/Le x C3.SW-H2b/SnJ)F1	postnatal lethality, complete penetrance	J:47940
Rpl38Ts/Rpl38+ (TSJ/Le x C57BL/6JJcl)F1	short tail	J:47940
Rpl38Ts/Rpl38+ (TSJ/Le x CBA/J)F1	postnatal lethality, complete penetrance	J:47940
Rpl38Ts/Rpl38+ BALB/c-Rpl38Ts	abnormal autopod morphology	J:13063, J:15012
	abnormal heart development	J:15012
	abnormal humerus morphology	J:15012
	abnormal metacarpal bone morphology	J:15012
	abnormal metatarsal bone morphology	J:15012
	abnormal nasal cavity morphology	J:15012
	abnormal neural tube morphology	J:15012
	abnormal neuromere morphology	J:15012
	abnormal notochord morphology	J:15012
	abnormal olfactory bulb morphology	J:15012
	abnormal placenta vasculature	J:15012
	abnormal sacral vertebrae morphology	J:15012
	abnormal sternebra morphology	J:15012
	abnormal vertebrae development	J:15012
	abnormal vitelline vasculature morphology	J:15012
	anemia	J:15012
	caudal vertebral fusion	J:13063, J:15012
	curly tail	J:15012
	decreased body length	J:13063
	decreased body size	J:15012
	decreased body weight	J:15012
	decreased caudal vertebrae number	J:13063, J:15012
	decreased cranium height	J:15012
	decreased length of long bones	J:15012
	embryonic growth retardation	J:15012
	increased cranium width	J:15012
	increased rib number	J:15012
	increased sternebra number	J:15012
	increased thoracic vertebrae number	J:15012
	kinked tail	J:13063, J:15012
	perinatal lethality, incomplete penetrance	J:15012
	rib fusion	J:15012
	short femur	J:15012
	short humerus	J:15012
	short radius	J:15012
	short snout	J:15012
	short tail	J:13063, J:15012
	short tibia	J:15012
	small caudal vertebrae	J:15012
	sternebra fusion	J:15012
	vertebral fusion	J:15012
	wavy neural tube	J:15012
Rpl38Ts/Rpl38+ involves: BALB/c	abnormal notochord morphology	J:803
Rpl38Ts/Rpl38+ TSJ/Le	abnormal auditory tube morphology	J:168509
	abnormal distortion product otoacoustic emission	J:168509
	abnormal embryonic erythropoiesis	J:6184
	abnormal hearing physiology	J:168509
	abnormal middle ear morphology	J:168509
	abnormal oval window morphology	J:168509
	abnormal round window morphology	J:168509
	anencephaly	J:6184
	conductive hearing loss	J:168509
	decreased body weight	J:168509
	embryonic growth retardation	J:6184
	normal hematopoietic system phenotype	J:6184
	increased circulating phosphate level	J:168509
	increased or absent threshold for auditory brainstem response	J:168509
	increased susceptibility to otitis media	J:168509
	omphalocele	J:6184
	short snout	J:168509
	short tail	J:6184, J:168509
Rpl38Ts/Rpl38Ts BALB/c-Rpl38Ts	abnormal blastocoele morphology	J:6315
	abnormal blastocyst morphology	J:6315
	abnormal nucleolus morphology	J:6315
	abnormal preimplantation embryo development	J:6315
	absent blastocoele	J:6315
	decreased embryo size	J:6315
	embryonic growth arrest	J:6315
	embryonic growth retardation	J:6315
	embryonic lethality at implantation, incomplete penetrance	J:6315, J:15012
	embryonic lethality, complete penetrance	J:13063
Rpl38Tss/Rpl38+ BALB/cMs-Rpl38Tss	abnormal tail morphology	J:62561
	curly tail	J:62561
	kinked tail	J:62561
	short tail	J:62561
Rpl38Tss/Rpl38+ either: (involves: A/J * BALB/cMs) or (involves: BALB/cMs * C57BL/6J)	cleft palate	J:62561
	cleft upper lip	J:62561
	exencephaly	J:62561
	herniated abdominal wall	J:62561
	oligodactyly	J:62561
	polydactyly	J:62561
Rpl38Tss/Rpl38Tss BALB/cMs-Rpl38Tss	embryonic lethality, complete penetrance	J:62561