89 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cd19tm1(cre)Cgn/Cd19+ Srsf3tm1Pjln/Srsf3tm1Pjln involves: 129P2/OlaHsd * BALB/c	decreased B cell number	J:113645
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Srsf3tm1Pjln/Srsf3tm1Pjln involves: BALB/c * C57BL/6J * CBA/J	abnormal cartilage morphology	J:308882
	abnormal face development	J:308882
	abnormal facial morphology	J:308882
	abnormal forebrain morphology	J:308882
	abnormal hyoid bone greater horn morphology	J:308882
	abnormal hyoid bone lesser horn morphology	J:308882
	abnormal hyoid bone morphology	J:308882
	abnormal maxillary frontal process morphology	J:308882
	abnormal nasal pit morphology	J:308882
	abnormal neurocranium morphology	J:308882
	abnormal palate bone morphology	J:308882
	abnormal retrotympanic process morphology	J:308882
	abnormal styloid process morphology	J:308882
	abnormal temporal bone zygomatic process morphology	J:308882
	abnormal tracheal cartilage morphology	J:308882
	absent frontal bone	J:308882
	absent maxillary shelf	J:308882
	absent nasal bone	J:308882
	absent palatine bone horizontal plate	J:308882
	absent tympanic ring	J:308882
	basisphenoid bone hypoplasia	J:308882
	cricoid cartilage hypoplasia	J:308882
	decreased midbrain size	J:308882
	enlarged lateral ventricles	J:308882
	exencephaly	J:308882
	facial bone hypoplasia	J:308882
	facial cleft	J:308882
	increased forebrain size	J:308882
	internal hemorrhage	J:308882
	interparietal bone hypoplasia	J:308882
	lethality throughout fetal growth and development	J:308882
	mandible hypoplasia	J:308882
	mandibular coronoid process hypoplasia	J:308882
	maxilla hypoplasia	J:308882
	maxillary zygomatic process hypoplasia	J:308882
	Meckel's cartilage hypoplasia	J:308882
	microcephaly	J:308882
	midbrain hypoplasia	J:308882
	palatal shelf hypoplasia	J:308882
	parietal bone hypoplasia	J:308882
	premaxilla hypoplasia	J:308882
	prenatal lethality, complete penetrance	J:308882
	pterygoid bone hypoplasia	J:308882
	small supraoccipital bone	J:308882
	temporal bone hypoplasia	J:308882
	thyroid cartilage hypoplasia	J:308882
	tongue hypoplasia	J:308882
	wavy neural tube	J:308882
	zygomatic bone hypoplasia	J:308882
Srsf3tm1.1Pjln/Srsf3tm1.1Pjln involves: BALB/c	abnormal preimplantation embryo development	J:57047
	embryonic lethality before implantation, complete penetrance	J:57047
	failure of blastocyst formation	J:57047
Srsf3tm1Pjln/Srsf3tm1Pjln involves: BALB/c	no abnormal phenotype detected	J:57047
Srsf3tm1Pjln/Srsf3tm1Pjln Cd79atm1(cre)Reth/Cd79a+ involves: 129P2/OlaHsd * BALB/c	decreased B cell number	J:113645
	decreased pre-B cell number	J:113645
	decreased pro-B cell number	J:113645
Srsf3tm1Pjln/Srsf3tm1Pjln Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ involves: BALB/c * C57BL/6 * DBA	abnormal bile canaliculus morphology	J:205756
	abnormal endoplasmic reticulum morphology	J:205756
	abnormal glucose tolerance	J:205756
	abnormal hepatobiliary system development	J:205756
	abnormal hepatocyte morphology	J:205756
	abnormal kidney development	J:205756
	abnormal liver morphology	J:205756
	abnormal liver sinusoid morphology	J:205756
	abnormal thymus development	J:205756
	decreased body size	J:205756
	decreased brown adipose tissue amount	J:205756
	decreased circulating cholesterol level	J:205756
	decreased circulating HDL cholesterol level	J:205756
	decreased circulating insulin-like growth factor I level	J:205756
	decreased circulating serum albumin level	J:205756
	decreased circulating triglyceride level	J:205756
	decreased fatty acid oxidation	J:205756
	decreased liver cholesterol level	J:205756
	decreased liver glycogen level	J:205756
	decreased liver triglyceride level	J:205756
	decreased susceptibility to diet-induced obesity	J:205756
	hypoglycemia	J:205756
	increased circulating alanine transaminase level	J:205756
	increased circulating alkaline phosphatase level	J:205756
	increased circulating aspartate transaminase level	J:205756
	increased circulating bilirubin level	J:205756
	increased circulating growth hormone level	J:205756
	increased hepatocyte apoptosis	J:205756
	increased insulin sensitivity	J:205756
	pale liver	J:205756
	perinatal lethality, incomplete penetrance	J:205756
	postnatal lethality, incomplete penetrance	J:205756
	small liver	J:205756