About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rhotm1.1Kpal
targeted mutation 1.1, Krzysztof Palczewski
MGI:4947230
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rhotm1.1Kpal/Rhotm1.1Kpal involves: 129S6/SvEvTac * C57BL/6 * FVB/N MGI:4947237
ht2
Rhotm1.1Kpal/Rho+ involves: 129S6/SvEvTac * C57BL/6 * FVB/N MGI:4947235
cx3
Lrattm1Kpal/Lrattm1Kpal
Rhotm1.1Kpal/Rho+
Rpe65450L/Rpe65450M
involves: 129S6/SvEvTac * C57BL/6 * FVB/N MGI:4947236


Genotype
MGI:4947237
hm1
Allelic
Composition
Rhotm1.1Kpal/Rhotm1.1Kpal
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rhotm1.1Kpal mutation (1 available); any Rho mutation (51 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Retinal degeneration in Rhotm1.1Kpal/Rho+ and Rhotm1.1Kpal/Rhotm1.1Kpal mice

vision/eye
• at P63, photoreceptor cells are almost gone unlike in wild-type mice

nervous system
• at P63, photoreceptor cells are almost gone unlike in wild-type mice




Genotype
MGI:4947235
ht2
Allelic
Composition
Rhotm1.1Kpal/Rho+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rhotm1.1Kpal mutation (1 available); any Rho mutation (51 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Retinal degeneration in Rhotm1.1Kpal/Rho+ and Rhotm1.1Kpal/Rhotm1.1Kpal mice

vision/eye
• the distance between retina pigmented epithelium and the outer limiting membrane is reduced compared to in wild-type mice
• half the number in wild-type mice
• shortened at P35 and P112
• due to necrosis
• continuous decline until P276
• mildly reduced at P70
• severely depressed at P170
• severely reduced at P41
• nearly undetectable by P170

nervous system
• half the number in wild-type mice
• shortened at P35 and P112
• due to necrosis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
retinitis pigmentosa 4 DOID:0110372 OMIM:613731
J:170648




Genotype
MGI:4947236
cx3
Allelic
Composition
Lrattm1Kpal/Lrattm1Kpal
Rhotm1.1Kpal/Rho+
Rpe65450L/Rpe65450M
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrattm1Kpal mutation (1 available); any Lrat mutation (26 available)
Rhotm1.1Kpal mutation (1 available); any Rho mutation (51 available)
Rpe65450L mutation (1 available); any Rpe65 mutation (52 available)
Rpe65450M mutation (2 available); any Rpe65 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Effect of genetic depletion of 11-cis-retinal production (Lrattm1Kpal/Lrattm1Kpal) on retinal degeneration in Rhotm1.1Kpal/Rho+ mice

vision/eye
• dramatically reduced at P36
• less than in Rhotm1.1Kpal heterozygotes
• due to increased apoptosis
• less than in Rhotm1.1Kpal heterozygotes

nervous system
• dramatically reduced at P36
• less than in Rhotm1.1Kpal heterozygotes
• due to increased apoptosis
• less than in Rhotm1.1Kpal heterozygotes





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
10/29/2024
MGI 6.24
The Jackson Laboratory