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

Preparing word cloud

×

Integrated Animals is a virtual database currently indexing available animal strains and mutants from: AGSC (Ambystoma), BCBC (mice), BDSC (flies), European Xenopus Resource Center (frog), The National Xenopus Resource (frog), Xenopus Express (frog), CWRU Cystic Fibrosis Mouse Models (mice), DGGR (flies), FlyBase (flies), IMSR (mice), MGI (mice), MMRRC (mice), NSRRC (pig), RGD (rats), Sperm Stem Cell Libraries for Biological Research (rats), Tetrahymena Stock Center (Tetrahymena), WormBase (worms), XGSC (Xiphophorus), ZFIN (zebrafish), and ZIRC (zebrafish). Note, the IMSR data is linked, but users may need to re-execute the search if the top mouse is not returned properly.
Note: BCBC is no longer in service, so the links may not be functional.

Suggested Search Criteria

Enter extra filters to help narrow your search

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Background:mutant (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

1,458 Results - per page

Show More Columns | Download Top 1000 Results

Organism Name Proper Citation Species Synonyms Notes Phenotype Affected Gene Genomic Alteration Catalog Number Background Database Database Abbreviation Availability Source References Alternate IDs Authority Record Last Update Mentions Count
SD-Vwfem1Mcwi-/-
 
Resource Report
Resource Website
RRID:RGD_39128242 Rattus norvegicus CRISPR/Cas9 mediated gene editing resulted a 130,938-bp deletion between 32-bp in front of the 5' end of Exon 1 and 122bp after the stop codon. Contact MCW rat distribution at [email protected] 39128242 mutant Rat Genome Database (RGD) RGD Cryopreserved Sperm (as of 2020-10-09) 39128242 RGD 2026-10-17 01:54:07 0
Wpk +/-
 
Resource Report
Resource Website
RRID:RGD_15017093 Rattus norvegicus The wpk mutation was first recognized in 1994 in a colony of outbred Wistar rats at Utrecht University (Utrecht, The Netherlands). In 1996, a breeding pair of test-proven heterozygotes were transferred to the University of Rotterdam (Rotterdam, The Netherlands), and a new subcolony was initiated. This colony has been maintained by brother-sister matings for more than five generations. Individuals heterozygous for the mutant allele were identified in each generation by test-crossing phenotypically normal offspring from known heterozygotes. A single C to T substitution in exon 12 was identified as the mutated allele in the Wpk rat. This mutation converts a proline to a leucine in the protein products(P394L). 15017093 mutant Rat Genome Database (RGD) RGD Unknown 15017093 RGD 2026-10-17 01:54:07 0
LE-Cntnap2em1Mcwi
 
Resource Report
Resource Website
1+ mentions
RRID:RGD_25330087 Rattus norvegicus The rat strain was produced by injecting CRISPR/Cas9 targeting rat Cntnap2 into Crl:LE embryos. The result is a 1-bp deletion in exon 6 of the gene. Autism Rat Model Resource. Contact MCW rat distribution at [email protected] 25330087 mutant Rat Genome Database (RGD) RGD Unknown 25330087 RGD 2026-10-17 01:54:08 1
LE-Chd8em1Mcwi
 
Resource Report
Resource Website
1+ mentions
RRID:RGD_25330088 Rattus norvegicus The rat strain was produced by injecting the CRISPR/Cas9 system targeting rat Chd8 gene of Crl:LE embryos. The result is a 5-bp deletion in exon 3 of rat Chd8 gene. Autism Rat Model Resource, Contact MCW rat distribution at [email protected] 25330088 mutant Rat Genome Database (RGD) RGD Live Animals; Cryopreserved Sperm (as of 2025-02-20) 25330088 RGD 2026-10-17 01:54:08 1
SD-Cftrem2Apb
 
Resource Report
Resource Website
RRID:RGD_151356959 Rattus norvegicus The CRISPR/Cas9 system was used to target exon 11 and create a deletion at codon F508, which was injected into Sprague-Dawley one-cell embryos (C076 line). A rat with an 8-bp deletion upstream of the TTT site (c.1514_1521delATATCATC) was used to establish the KO strain. 151356959 mutant Rat Genome Database (RGD) RGD Unknown 151356959 RGD 2026-10-17 01:54:08 0
F344-Nppcem2Kyo
 
Resource Report
Resource Website
1+ mentions
RRID:RGD_127284868 Rattus norvegicus This strain was established by injecting Zinc-finger nucleases (ZFNs) to F344/Stm pronuclear stage embryos. Selected ZFNs were designed to target exon 1 of rat Nppc, which encodes the N-terminus of natriuretic peptide precursor C (target sequence: CGAAGCCAAGCCCGGGACaccaccGAAGGTGGGTGCTGTCGCG; nucleotides 179 - 221, NC_005108.4). The injected F344/Stm embryos were transferred into the oviducts of pseudopregnant rats. Four lines of knockout strains were estaglished. This F344-Nppcem2Kyo strain ( delta 9) was deduced to generate one amino-acid substitution (a.a. 26, from Gly to Ala, NP_446202, at nucleotides 192 - 194, NM_053750.1) and a three amino-acid deletion (a.a. 27 - 29, Thr, Pro and Pro, NP_446202, at nucleotides 193 - 201, NM_053750.1), within the N-terminal portion of the full-length Nppc National BioResource Project for the Rat in Japan 127284868 mutant Rat Genome Database (RGD) RGD Unknown 127284868 RGD 2026-10-17 01:54:07 1
LE-Ckmtm1(cre)/Rrrc
 
Resource Report
Resource Website
RRID:RGD_151667414 Rattus norvegicus This model expresses cre-recombinase under the control of the endogenous Ckm (creatine kinase, M-type) promoter. Cre was targeted to the rat Ckm gene of LE embryos through CRISP/Cas9 system genome editing system. This strain will be deposited with RRRC Rat Resource and Research Center 151667414 mutant Rat Genome Database (RGD) RGD Unknown 151667414 RGD 2026-10-17 01:54:08 0
BN-Themism1Adej
 
Resource Report
Resource Website
RRID:RGD_38599155 Rattus norvegicus This autosomal recessive mutation occurred spontaneously in a Brown-Norway rat colony and was identified as causing marked T cell lymphopenia. The mutation was identified as a frameshift mutation caused by a four-nucleotide insertion in the Themis gene, leading to its disruption. 38599155 mutant Rat Genome Database (RGD) RGD Unknown 38599155 RGD 2026-10-17 01:54:07 0
SD-Pon1em1Lizh
 
Resource Report
Resource Website
RRID:RGD_45073133 Rattus norvegicus CRISPR/Cas9 system was used to introduce a 342-bp deletion in exon 4 of rat PON1 gene in Sprague- Dawley embryos. The destruction of Pon1 gene caused the absence of the the expression of Pon1 mRNA, protein in liver, spleen and thymus in the Pon1 homozygous knock-out rat. 45073133 mutant Rat Genome Database (RGD) RGD Unknown 45073133 RGD 2026-10-17 01:54:07 0
WI- Msh6m1Hubr
 
Resource Report
Resource Website
RRID:RGD_126848737 Rattus norvegicus The Msh6 knockout mutant rat line was generated by target-selected ENU-driven mutagenesis on Crl:WI rats. The founder rat carried an ENU-induced premature stop codon in exon 4 of the Msh6 gene was bred to obtain homozygous animals. 126848737 mutant Rat Genome Database (RGD) RGD Unknown 126848737 RGD 2026-10-17 01:54:07 0
SS-Tgfb1em3Mcwi+/+
 
Resource Report
Resource Website
RRID:RGD_150340629 Rattus norvegicus ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed to produce homozygous wild type and heterozygous mutant littermates. 150340629 mutant Rat Genome Database (RGD) RGD Unknown 150340629 RGD 2026-10-17 01:54:07 0
SD-Slc9a6 em1Moro
 
Resource Report
Resource Website
RRID:RGD_151664748 Rattus norvegicus CRISPR/Cas9 system was used to generate this mutant. Guide RNA sequence is the following: 5'-CGGCTGTGTAACCCTGATGA-3'. Cas9-mediated cleavage at exon 7 in the Slc9a6 locus resulted in the insertion of 2 bp (TT) generating frameshift and a premature stop codon. 151664748 mutant Rat Genome Database (RGD) RGD Unknown 151664748 RGD 2026-10-17 01:54:08 0
W-Mkxem1Asah
 
Resource Report
Resource Website
RRID:RGD_126777684 Rattus norvegicus The CRISPR/Cas9 genome editing system targeting exon 2 of rat Mkx gene was injected to the Wistar embryo to generate this knock out rat strain with 14- bp deletion causing frameshift mutation in the gene. 126777684 mutant Rat Genome Database (RGD) RGD Unknown 126777684 RGD 2026-10-17 01:54:07 0
SD-Ube3aem1Jue
 
Resource Report
Resource Website
RRID:RGD_126790464 Rattus norvegicus The CRISPR/Cas9 genome editing system was injected into fertilized Sprague-Dawley rat embryos and inserted into a surrogate. Two genomic RNAs (gRNAs) were designed to target the 5ʹ-end of the Ube3a gene (upstream of the Ube3a coding sequence) and two gRNAs target sequences downstream of Ube3a. gRNA pairs were used on each end of the deletion to maximize the probability of a complete deletion of the 90-kb region encompassing the Ube3a gene. The 90 kb deletion in Ube3a was confirmed by genome sequencing. Only pups with maternal inheritance of the deletion carried traits for model of Angleman Syndrome. 126790464 mutant Rat Genome Database (RGD) RGD Unknown 126790464 RGD 2026-10-17 01:54:07 0
SD-Tshrem1Mlit
 
Resource Report
Resource Website
RRID:RGD_150521599 Rattus norvegicus CRISPR/Cas9 system targeting exon 10 of the rat Tshr gene was injected into Sprague Dawley embryos to create this mutant strain. The strain was homozygous with 5 bp deletion (CACGC) which introduces frameshift at residue 449 and a stop codon at 478 (P449fsX478). 150521599 mutant Rat Genome Database (RGD) RGD Unknown 150521599 RGD 2026-10-17 01:54:08 0
SD-Nkx3-1em1Pjhak-/-
 
Resource Report
Resource Website
RRID:RGD_150573818 Rattus norvegicus A pair of TALENs targeting coding region of rat Nkx3-1gene was electroporated into SD zygotes to create NKx3-1 mutants. The resulting mutation was indel mutation with sequences loss beyond TALEN recognition resulting a premature termination codon of the protein. 150573818 mutant Rat Genome Database (RGD) RGD Unknown 150573818 RGD 2026-10-17 01:54:08 0
F344-Angptl8em1Kyo-/-
 
Resource Report
Resource Website
RRID:RGD_127345123 Rattus norvegicus This line #1 Angptl8 knock out (KO) rats were generated using the CRISPR/Cas9 system containing two guide RNAs (gRNAs) targeting exons 2 and 3 in the rat Angptl8 gene. A mixture of transcribed Cas9 and gRNAs was microinjected into F344/Stm rat zygotes [National BioResource Project rat number: 0140) provided by the National BioResource Project for the Rat in Japan. Two lines of rats heterozygous for Angptl8 (lines #1 and #2). Male and female Het rats were intercrossed to obtain homozygous Angptl8 KO rats. Rats were genotyped by PCR with the following primers, 5'-CATCTGTTGAGCAGGCAGAA-3' (sense) and 5'-GTTCAGTGGTGGCTTCCTTC-3' (antisense) for line #1. A 7-bp deletion mutation was identified in line #1. National BioResource Project for the Rat in Japan 127345123 mutant Rat Genome Database (RGD) RGD Unknown 127345123 RGD 2026-10-17 01:54:07 0
F344-Angptl8em1Kyo+/-
 
Resource Report
Resource Website
RRID:RGD_127345124 Rattus norvegicus This line #1 Angptl8 heterozygous rats were generated using the CRISPR/Cas9 system containing two guide RNAs (gRNAs) targeting exons 2 and 3 in the rat Angptl8 gene. A mixture of transcribed Cas9 and gRNAs was microinjected into F344/Stm rat zygotes [National BioResource Project rat number: 0140) provided by the National BioResource Project for the Rat in Japan. Two lines of rats heterozygous for Angptl8 (lines #1 and #2). Male and female Het rats were intercrossed to obtain homozygous Angptl8 KO rats. Rats were genotyped by PCR with the following primers, 5'-CATCTGTTGAGCAGGCAGAA-3'(sense) and 5'-GTTCAGTGGTGGCTTCCTTC-3' (antisense) for line #1. A 7-bp deletion mutation was identified in line #1. National BioResource Project for the Rat in Japan 127345124 mutant Rat Genome Database (RGD) RGD Unknown 127345124 RGD 2026-10-17 01:54:07 0
SD-Gnalem1Hpng+/+
 
Resource Report
Resource Website
RRID:RGD_150429815 Rattus norvegicus The homozygous wild type Gnal rats were littermates of SD-Gnalem1Hpng+/- (RGD:150429814) created by CRISPR/Cas9. The heterozygous mutants carried one copy of mutated allele contained a 13- bp deletion in exon1 that corresponded to position 34 to 46 downstream of the translation start point ATG of theGnal splicing variant 2 was detected resulting in an early stop at position150 and producing a truncated protein with 50 amino acids . 150429815 mutant Rat Genome Database (RGD) RGD Unknown 150429815 RGD 2026-10-17 01:54:08 0
HHSE/Hat
 
Resource Report
Resource Website
RRID:RGD_38676463 Rattus norvegicus HHSE/Hat was derived from Hirosaki hairless rat (HHR) and Hirosaki small-eye rat (HiSER), which are Sprague-Dawley rat (SDR)mutant lines. HHR was established in 1984 as a spontaneous mutant of SDR that has been inbred in Department of Biochemistry and Genome Biology Hirosaki University Graduate School of Medicine. Whole body shows hypotrichosis, abnormal differentiation of thymus, and regressed mammary gland in females. These mutations are autosomal recessive and are suggested to be due to deletion of the keratin gene cluster and the lectin-like receptor gene Ly49s3. HiSER was established in 2013 as a spontaneous mutant of Sprague-Dawley rat maintained in our course in the same way as HHR/Hat. This mutant strain has retinal detachment and the disease is progressively exacerbated. The muation is autosomal recessive and is suggested to be due to deletion of the crystallin gene Cryba1. The mutations in HHR and HiSER are on different chromosomes and do not affect each other. The mutations in HHR and HiSER are on different chromosomes and do not affect each other. National BioResource Project for the Rat in Japan ;Depart of Biochemistry and Genome Biology, Hirosaki Univer-sity School of Medicine 38676463 mutant Rat Genome Database (RGD) RGD Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-09-18) 38676463 RGD 2026-10-17 01:54:08 0

Can't find your Organism?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific organism, it's easier to enter an RRID or a Catalog Number to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.

If you still could not find your organism in the search results, please help us by registering it into the system — it's easy. Organisms identifiers are registered through multiple sources depending on the species:

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.