All Phenotypes Dp(10Prmt2-Pdxk)2Yey MGI Mouse

Phenotypes associated with this allele

Allelic Composition	Dp(10Prmt2-Pdxk)2Yey/0 Dp(16Lipi-Zbtb21)1Yey/0
Genetic Background	B6.129S7-Dp(10Prmt2-Pdxk)2Yey Dp(16Lipi-Zbtb21)1Yey

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dp(10Prmt2-Pdxk)2Yey mutation (3 available); any Dp(10Prmt2-Pdxk)2Yey mutation (3 available)
Dp(16Lipi-Zbtb21)1Yey mutation (3 available); any Dp(16Lipi-Zbtb21)1Yey mutation (3 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality ( J:161325 )

• rate of neonatal lethality is similar to mice hemizygous for Dp(16Lipi-Zfp295)1Yey alone

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

decreased survivor rate ( J:161325 )

• mice with hydrocephaly die around 6 to 8 weeks of age

premature death ( J:161325 )

• mice with hydrocephaly die around 6 to 8 weeks of age

neonatal lethality, incomplete penetrance ( J:161325 )

• about 26% die soon after birth

behavior/neurological

impaired contextual conditioning behavior ( J:161325 )

• freeze significantly less when returned to the test chamber 24 h or 72 h after initial training and foot shock

abnormal spatial learning ( J:161325 )

• display a longer latency and a longer path length to reach the hidden platform in a Morris water maze

abnormal spatial reference memory ( J:161325 )

• in a Morris water maze probe test mice spend less time in the target quadrant

impaired swimming ( J:161325 )

• decrease in swimming speed

decreased grip strength ( J:161325 )

• in all limbs

nervous system

obstructive hydrocephaly ( J:161325 )

• seen in about 6.5% of mice, associated with aqueductal stenosis

cerebral aqueductal stenosis ( J:161325 )

dilated lateral ventricle ( J:161325 )

• in mice with hydrocephaly

reduced long-term potentiation ( J:161325 )

• in the hippocampus

cardiovascular system

abnormal heart morphology ( J:161325 )

• display heart defects at a similar frequency to mice hemizygous for Dp(16Lipi-Zfp295)1Yey alone

reproductive system

reproductive system phenotype ( J:161325 )

N	• unlike mice carrying Ts(17<16>)65Dn , no reproductive impairment is seen in mice even when put on an inbred background

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
Down syndrome		DOID:14250	OMIM:190685	J:161325

Allelic Composition	Dp(10Prmt2-Pdxk)2Yey/0 Dp(17Abcg1-Rrp1b)3Yey/0
Genetic Background	B6.129S7-Dp(10Prmt2-Pdxk)2Yey Dp(17Abcg1-Rrp1b)3Yey

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dp(10Prmt2-Pdxk)2Yey mutation (3 available); any Dp(10Prmt2-Pdxk)2Yey mutation (3 available)
Dp(17Abcg1-Rrp1b)3Yey mutation (3 available); any Dp(17Abcg1-Rrp1b)3Yey mutation (3 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

mortality/aging ( J:161325 )

N	• unlike mice carrying Dp(16Lipi-Zfp295)1Yey , no increase in neonatal lethality relative to wild-type controls is detected

Allelic Composition	Dp(10Prmt2-Pdxk)2Yey/0
Genetic Background	B6.129S7-Dp(10Prmt2-Pdxk)2Yey

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dp(10Prmt2-Pdxk)2Yey mutation (3 available); any Dp(10Prmt2-Pdxk)2Yey mutation (3 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

mortality/aging ( J:161325 )

N	• unlike mice carrying Dp(16Lipi-Zfp295)1Yey , no increase in neonatal lethality relative to wild-type controls is detected

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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