Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Organism Name
Psaptm1Suz/Psaptm1Suz
RRID:MGI:3711319 RRID Copied  
PDF Report How to cite
RRID:MGI:3711319
Copy Citation Copied
Organism Information

The record is no longer available at this source.

Proper Citation: RRID:MGI:3711319

Description: Allele Detail: Targeted This is a legacy resource.

Species: Mus musculus

Notes: Allele Detail: Targeted This is a legacy resource.

Phenotype: decreased spleen weight, slow postnatal weight gain, prenatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, abnormal lipid homeostasis, decreased seminal vesicle weight, head shaking, demyelination, decreased liver weight, abnormal head movements, small kidney, tonic seizures, abnormal brain white matter morphology, tremors, decreased testis weight, abnormal vascular endothelial cell morphology, abnormal Schwann cell morphology, abnormal corneal stroma morphology, abnormal enteric ganglia morphology, abnormal eye morphology, abnormal muscle fiber morphology, decreased kidney weight, decreased epididymis weight, lethality at weaning, complete penetrance, decreased male germ cell number, abnormal circulating testosterone level, abnormal epididymis morphology, ataxia, decreased body size, abnormal prostate gland epithelium morphology, abnormal choroid plexus morphology, abnormal macrophage morphology, abnormal hepatocyte morphology, decreased body weight, abnormal lipid level, axonal spheroids, abnormal dorsal root ganglion morphology, abnormal astrocyte morphology, abnormal renal tubule morphology, tremors, hindlimb paralysis, seizures, abnormal food intake, hyperactivity, hypoactivity, paraparesis, axon degeneration, astrocytosis, abnormal neuron morphology, abnormal nervous system morphology, decreased prostate gland weight, muscular atrophy, abnormal gait, abnormal prostate gland morphology, abnormal seminal vesicle morphology, progressive muscle weakness

Affected Gene: Psap

Expand All
Usage and Citation Metrics

We found {{ ctrl2.mentions.all_count }} mentions in open access literature.

We have not found any literature mentions for this resource.

We are searching literature mentions for this resource.

Most recent articles:

{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})

Checkfor all resource mentions.

Collaborator Network

A list of researchers who have used the resource and an author search tool

Find mentions based on location


{{ ctrl2.mentions.errors.location }}

A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.

Ratings and Alerts

No rating or validation information has been found for Psaptm1Suz/Psaptm1Suz.

No alerts have been found for Psaptm1Suz/Psaptm1Suz.

Data and Source Information

Source: Integrated Animals

Source Database: MGI, Mouse Genome Informatics MGI