MAMMALIAN PHENOTYPE - ANNOTATIONS |
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The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
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Term: | mammalian phenotype |
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Accession: | MP:0000001
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browse the term
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Definition: | the observable morphological, physiological, behavioral and other characteristics of mammalian organisms that are manifested through development and lifespan |
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Pax6 |
paired box 6 |
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IAGP |
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RGD |
PMID:9247338 |
RGD:731242 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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Pax6Sey2 |
paired box gene 6, small eye mutation 2 |
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IAGP |
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RGD |
PMID:9247338 |
RGD:731242 |
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Mecp2 |
methyl CpG binding protein 2 |
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IMP |
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RGD |
PMID:27313794 |
RGD:11568037 |
NCBI chr X:156,650,389...156,713,813
Ensembl chr X:156,655,960...156,705,233
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Mecp2em1Sage |
methyl CpG binding protein 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
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IMP |
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RGD |
PMID:27313794 |
RGD:11568037 |
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Cyp11b2 |
cytochrome P450, family 11, subfamily b, polypeptide 2 |
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IAGP |
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RGD |
PMID:11832364 |
RGD:727991 |
NCBI chr 7:116,248,759...116,255,205
Ensembl chr 7:116,156,219...116,255,167
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Dhh |
desert hedgehog signaling molecule |
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IMP |
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RGD |
PMID:21062903 |
RGD:38548923 |
NCBI chr 7:140,575,288...140,580,783
Ensembl chr 7:140,575,288...140,580,783
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Depdc5 |
DEP domain containing 5, GATOR1 subcomplex subunit |
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IMP |
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RGD |
PMID:26873552 |
RGD:11573213 |
NCBI chr14:83,089,000...83,219,576
Ensembl chr14:83,089,000...83,219,464
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Depdc5em1Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant1, Kyo |
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IMP |
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RGD |
PMID:26873552 |
RGD:11573213 |
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Depdc5em2Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant2, Kyo |
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IMP |
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RGD |
PMID:26873552 |
RGD:11573213 |
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Myc |
MYC proto-oncogene, bHLH transcription factor |
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IMP |
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RGD |
PMID:22842522 |
RGD:7207891 |
NCBI chr 7:102,586,313...102,591,240
Ensembl chr 7:102,586,313...102,591,240
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Crh |
corticotropin releasing hormone |
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IDA |
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RGD |
PMID:11908464 |
RGD:704423 |
NCBI chr 2:104,459,999...104,461,863
Ensembl chr 2:104,459,999...104,461,863
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Myo7a |
myosin VIIA |
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IAGP |
DNA:nonsense mutation:cds |
RGD |
PMID:15965244 |
RGD:1581470 |
NCBI chr 1:163,001,313...163,071,545
Ensembl chr 1:163,001,875...163,071,508
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Myo7atnd/Hubr |
myosin VIIA; ENU induced tornado mutant, Hubr |
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IAGP |
DNA:nonsense mutation:cds |
RGD |
PMID:15965244 |
RGD:1581470 |
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Edaradd |
EDAR-associated death domain |
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IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
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IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
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Atrn |
attractin |
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IAGP |
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RGD |
PMID:12379762 |
RGD:1299186 |
NCBI chr 3:123,434,409...123,567,922
Ensembl chr 3:123,434,409...123,567,918
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Atrnmv |
attractin; myelin vacuolation mutant |
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IAGP |
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RGD |
PMID:12379762 |
RGD:1299186 |
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Cacna1f |
calcium voltage-gated channel subunit alpha1 F |
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IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:18246026 |
RGD:13782370 |
NCBI chr X:15,712,709...15,741,135
Ensembl chr X:15,712,713...15,741,103
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Cacna1f csnb |
calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant |
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IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:18246026 |
RGD:13782370 |
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Drd2 |
dopamine receptor D2 |
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IAGP |
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RGD |
PMID:11814400 |
RGD:1581462 |
NCBI chr 8:53,678,777...53,743,643
Ensembl chr 8:53,678,777...53,743,642
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Grm2 |
glutamate metabotropic receptor 2 |
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IMP |
knock-out compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
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IMP |
KO compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
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Pax6 |
paired box 6 |
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IAGP |
DNA:frameshift mutation:cds: |
RGD |
PMID:21203536 |
RGD:8552339 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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Grm2 |
glutamate metabotropic receptor 2 |
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IMP |
knock-out compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
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IMP |
KO compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
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Grm2 |
glutamate metabotropic receptor 2 |
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IMP |
knock-out compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
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IMP |
KO compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
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Abcb1a |
ATP binding cassette subfamily B member 1A |
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IMP |
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RGD |
PMID:22049154 |
RGD:8657330 |
NCBI chr 4:22,339,829...22,517,642
Ensembl chr 4:22,133,521...22,425,515
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Abcb1aem2Sage |
ATP binding cassette subfamily B member 1A; ZFN induced mutant 2, Sage |
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IMP |
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RGD |
PMID:22049154 |
RGD:8657330 |
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Abcc2 |
ATP binding cassette subfamily C member 2 |
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IAGP |
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RGD |
PMID:12663688 |
RGD:704399 |
NCBI chr 1:263,554,426...263,612,556
Ensembl chr 1:263,554,453...263,613,252
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Crh |
corticotropin releasing hormone |
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IDA |
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RGD |
PMID:12663088 |
RGD:704425 |
NCBI chr 2:104,459,999...104,461,863
Ensembl chr 2:104,459,999...104,461,863
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Tmem67 |
transmembrane protein 67 |
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IAGP |
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RGD |
PMID:30705305 |
RGD:14995942 |
NCBI chr 5:25,666,138...25,721,056
Ensembl chr 5:25,666,137...25,721,072
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Tmem67wpk |
transmembrane protein 67; wpk mutant |
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IAGP |
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RGD |
PMID:30705305 |
RGD:14995942 |
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Esr1 |
estrogen receptor 1 |
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IMP |
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RGD |
PMID:24506075 |
RGD:8552987 |
NCBI chr 1:41,192,029...41,594,799
Ensembl chr 1:41,192,824...41,594,796
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Esr1em1Soar |
estrogen receptor 1; ZFN induced mutant 1, Soar |
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IMP |
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RGD |
PMID:24506075 |
RGD:8552987 |
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Cckar |
cholecystokinin A receptor |
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IAGP |
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RGD |
PMID:15178543 |
RGD:1625204 |
NCBI chr14:59,610,939...59,619,786
Ensembl chr14:59,611,434...59,619,783
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Csf1 |
colony stimulating factor 1 |
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IAGP |
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RGD |
PMID:12379742 |
RGD:628338 |
NCBI chr 2:210,522,370...210,550,546
Ensembl chr 2:210,522,375...210,550,560
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Csf1tl |
colony stimulating factor 1; tooth less mutant |
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IAGP |
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RGD |
PMID:12379742 |
RGD:628338 |
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Arsb |
arylsulfatase B |
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IAGP |
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RGD |
PMID:21887218 |
RGD:39131283 |
NCBI chr 2:23,385,154...23,543,028
Ensembl chr 2:23,385,183...23,544,963
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Dcx |
doublecortin |
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IMP |
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RGD |
PMID:14625554 |
RGD:1304461 |
NCBI chr X:115,098,675...115,175,515
Ensembl chr X:115,098,675...115,175,299
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Ar |
androgen receptor |
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IAGP |
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RGD |
PMID:17490813 |
RGD:10043338 |
NCBI chr X:67,656,253...67,828,998
Ensembl chr X:67,656,253...67,829,026
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Cyfip1 |
cytoplasmic FMR1 interacting protein 1 |
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IMP |
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RGD |
PMID:31371763 |
RGD:14981598 |
NCBI chr 1:114,258,773...114,347,138
Ensembl chr 1:114,258,719...114,347,137
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Cyfip1em1Sage |
cytoplasmic FMR1 interacting protein 1; CRISPR/Cas9 induced mutant 1, Sage |
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IMP |
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RGD |
PMID:31371763 |
RGD:14981598 |
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Ttn |
titin |
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IAGP |
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RGD |
PMID:27869827 |
RGD:11565821 |
NCBI chr 3:63,565,160...63,837,815
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Ttnem1Sage |
Titin; zinc finger nuclease induced mutant 1,Sigma Advanced Genetic Engineering Labs |
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IAGP |
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RGD |
PMID:27869827 |
RGD:11565821 |
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Ttnem2Sage |
Titin; zinc finger nuclease induced mutant 2,Sigma Advanced Genetic Engineering Labs |
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IAGP |
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RGD |
PMID:27869827 |
RGD:11565821 |
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Tnnt2 |
troponin T2, cardiac type |
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IDA |
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RGD |
PMID:10946062 |
RGD:1580434 |
NCBI chr13:52,662,974...52,680,992
Ensembl chr13:52,662,996...52,680,990
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Kcnq1 |
potassium voltage-gated channel subfamily Q member 1 |
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IAGP |
DNA:deletion:exon (rat) |
RGD |
PMID:16368876 |
RGD:1581602 |
NCBI chr 1:216,293,087...216,630,339
Ensembl chr 1:216,293,087...216,630,339
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Kcnq1dfk |
potassium voltage-gated channel subfamily Q member 1;deafness Kyoto |
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IAGP |
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RGD |
PMID:16368876 |
RGD:1581602 |
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Cyp27b1 |
cytochrome P450, family 27, subfamily b, polypeptide 1 |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:70,333,150...70,340,006
Ensembl chr 7:70,335,061...70,340,005
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Cyp27b1em1Thka |
cytochrome P450, family 27, subfamily b, polypeptide 1; CRISPR/Cas9 induced mutant 1, Thka |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
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Vdr |
vitamin D receptor |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:139,344,452...139,394,138
Ensembl chr 7:139,342,063...139,394,166
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Vdrem1Thka |
vitamin D receptor; CRISPR/Cas9 induced mutant 1, Thka |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
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Vdrem2Thka |
vitamin D receptor; CRISPR/Cas9 induced mutant 2, Thka |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
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Atp7b |
ATPase copper transporting beta |
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IAGP |
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RGD |
PMID:17434290 |
RGD:15036800 |
NCBI chr16:74,865,516...74,944,935
Ensembl chr16:74,865,516...74,945,286
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Atp7bhts |
ATPase copper transporting beta; hepatitis |
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IAGP |
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RGD |
PMID:17434290 |
RGD:15036800 |
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Ptprk |
protein tyrosine phosphatase, receptor type, K |
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IAGP |
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RGD |
PMID:17434290 |
RGD:15036800 |
NCBI chr 1:17,445,052...18,058,266
Ensembl chr 1:17,446,417...18,058,055
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Myc |
MYC proto-oncogene, bHLH transcription factor |
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IMP |
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RGD |
PMID:22842522 |
RGD:7207891 |
NCBI chr 7:102,586,313...102,591,240
Ensembl chr 7:102,586,313...102,591,240
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Pclo |
piccolo (presynaptic cytomatrix protein) |
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IMP |
compared to wild-type rat |
RGD |
PMID:31074746 |
RGD:41408338 |
NCBI chr 4:16,454,904...17,058,921
Ensembl chr 4:16,454,904...17,058,921
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PcloTn(sb-B-Geo)Fkh |
presynaptic cytomatrix protein; sleeping beauty transposon induced mutant, Fkh |
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IMP |
compared to wild-type rat |
RGD |
PMID:31074746 |
RGD:41408338 |
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Tmem67 |
transmembrane protein 67 |
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IAGP |
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RGD |
PMID:30705305 |
RGD:14995942 |
NCBI chr 5:25,666,138...25,721,056
Ensembl chr 5:25,666,137...25,721,072
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Tmem67wpk |
transmembrane protein 67; wpk mutant |
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IAGP |
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RGD |
PMID:30705305 |
RGD:14995942 |
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Cftr |
CF transmembrane conductance regulator |
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IMP |
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RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
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Cd36 |
CD36 molecule |
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IAGP |
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RGD |
PMID:18288886 |
RGD:2307226 |
NCBI chr 4:14,150,309...14,191,498
Ensembl chr 4:14,001,761...14,249,749
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Cryba1 |
crystallin, beta A1 |
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IAGP |
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RGD |
PMID:26303524 |
RGD:38676460 |
NCBI chr10:65,160,777...65,167,504
Ensembl chr10:65,161,152...65,167,494
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Cryba1Hiser |
crystallin, beta A1; HiSER mutant |
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IAGP |
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RGD |
PMID:26303524 |
RGD:38676460 |
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Tmem67 |
transmembrane protein 67 |
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IAGP |
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RGD |
PMID:30705305 |
RGD:14995942 |
NCBI chr 5:25,666,138...25,721,056
Ensembl chr 5:25,666,137...25,721,072
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Tmem67wpk |
transmembrane protein 67; wpk mutant |
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IAGP |
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RGD |
PMID:30705305 |
RGD:14995942 |
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Astn1 |
astrotactin 1 |
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IMP |
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RGD |
PMID:24714719 |
RGD:12792227 |
NCBI chr13:76,054,965...76,370,674
Ensembl chr13:76,055,410...76,370,674
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Brinp2 |
BMP/retinoic acid inducible neural specific 2 |
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IMP |
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RGD |
PMID:24714719 |
RGD:12792227 |
NCBI chr13:75,948,679...76,049,363
Ensembl chr13:75,948,679...76,049,363
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Cop1 |
COP1, E3 ubiquitin ligase |
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IMP |
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RGD |
PMID:24714719 |
RGD:12792227 |
NCBI chr13:76,942,883...77,076,015
Ensembl chr13:76,942,928...77,075,723
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Pappa2 |
pappalysin 2 |
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IMP |
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RGD |
PMID:24714719 |
RGD:12792227 |
NCBI chr13:76,389,150...76,660,248
Ensembl chr13:76,389,150...76,660,245
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Tnr |
tenascin R |
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IMP |
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RGD |
PMID:24714719 |
RGD:12792227 |
NCBI chr13:77,602,249...77,678,385
Ensembl chr13:77,485,113...77,678,437
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Esr2 |
estrogen receptor 2 |
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IMP |
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RGD |
PMID:29580824 |
RGD:38548925 |
NCBI chr 6:99,163,953...99,214,711
Ensembl chr 6:99,164,357...99,214,251
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G |
Esr2em1Soar |
estrogen receptor 2; ZFN induced mutant 1, Soar |
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IMP |
compared to wild type |
RGD |
PMID:29580824 |
RGD:38548925 |
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Lrrk2 |
leucine-rich repeat kinase 2 |
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IMP |
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RGD |
PMID:23799078 |
RGD:13462048 |
NCBI chr 7:132,857,311...133,018,549
Ensembl chr 7:132,857,628...133,018,584
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Lrrk2em1Sage |
leucine-rich repeat kinase 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
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IMP |
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RGD |
PMID:23799078 |
RGD:13462048 |
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Cftr |
CF transmembrane conductance regulator |
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IMP |
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RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
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Ednrb |
endothelin receptor type B |
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IAGP |
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RGD |
PMID:8570650 |
RGD:628515 |
NCBI chr15:88,004,775...88,036,354
Ensembl chr15:88,006,977...88,036,354
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Ednrbsl |
endothelin receptor type B, spotting lethal |
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IAGP |
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RGD |
PMID:8570650 |
RGD:628515 |
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G |
Rab38 |
RAB38, member RAS oncogene family |
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IAGP |
DNA:point mutation:exon:p.M1I |
RGD |
PMID:15112108 |
RGD:1300411 |
NCBI chr 1:152,072,716...152,153,449
Ensembl chr 1:152,072,665...152,153,449
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Rab38ru |
Rab38, member of RAS oncogene family, ruby allele |
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IAGP |
DNA:point mutation:exon:p.M1I (rat) |
RGD |
PMID:15112108 |
RGD:1300411 |
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Grm2 |
glutamate metabotropic receptor 2 |
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IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935 |
RGD:38501064 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
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IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935 |
RGD:38501064 |
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Myo7a |
myosin VIIA |
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IAGP |
DNA:nonsense mutation:cds |
RGD |
PMID:15965244 |
RGD:1581470 |
NCBI chr 1:163,001,313...163,071,545
Ensembl chr 1:163,001,875...163,071,508
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G |
Myo7atnd/Hubr |
myosin VIIA; ENU induced tornado mutant, Hubr |
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IAGP |
DNA:nonsense mutation:cds |
RGD |
PMID:15965244 |
RGD:1581470 |
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Drd2 |
dopamine receptor D2 |
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IDA |
decreased after administration of D2 antagonist |
RGD |
PMID:11311883 |
RGD:1581463 |
NCBI chr 8:53,678,777...53,743,643
Ensembl chr 8:53,678,777...53,743,642
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Prkcz |
protein kinase C, zeta |
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IDA |
inhibition eliminates long term memory of taste aversion stimulus |
RGD |
PMID:17702943 |
RGD:1642657 |
NCBI chr 5:172,658,071...172,769,492
Ensembl chr 5:172,658,748...172,769,421
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G |
Cacna1f |
calcium voltage-gated channel subunit alpha1 F |
|
IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:18246026 |
RGD:13782370 |
NCBI chr X:15,712,709...15,741,135
Ensembl chr X:15,712,713...15,741,103
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G |
Cacna1f csnb |
calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant |
|
IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:18246026 |
RGD:13782370 |
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G |
L1cam |
L1 cell adhesion molecule |
|
IMP |
|
RGD |
PMID:30738385 |
RGD:14695001 |
NCBI chr X:156,901,244...156,928,064
Ensembl chr X:156,909,913...156,928,057
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G |
Nell1 |
neural EGFL like 1 |
|
IMP |
|
RGD |
PMID:12235118 |
RGD:633405 |
NCBI chr 1:105,348,577...106,218,970
Ensembl chr 1:105,349,069...106,218,958
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G |
Lpar1 |
lysophosphatidic acid receptor 1 |
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IMP |
|
RGD |
PMID:20531371 |
RGD:13825198 |
NCBI chr 5:75,557,038...75,678,067
Ensembl chr 5:75,557,042...75,676,584
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G |
Cdh13 |
cadherin 13 |
|
IMP |
knock-out compared to wild-type rats |
RGD |
PMID:28387990 |
RGD:13503340 |
NCBI chr19:50,848,793...51,971,618
Ensembl chr19:50,848,736...51,972,103
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G |
Cdh13em1Mcwi |
cadherin 13; zinc finger nuclease induced mutant 1, Medical College of Wisconsin |
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IMP |
knock-out compared to wild-type rats |
RGD |
PMID:28387990 |
RGD:13503340 |
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G |
Grm2 |
glutamate metabotropic receptor 2 |
|
IMP |
knock-out compared to wild-type rats knockout compared to wild type |
RGD |
PMID:30283001, PMID:28700935 |
RGD:38501063, RGD:38501064 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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G |
Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
|
IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935, PMID:30283001 |
RGD:38501064, RGD:38501063 |
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G |
Ilk |
integrin-linked kinase |
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IMP |
inhibition in the nucleus accumbens decreases dendrite density of medium spiny neurons |
RGD |
PMID:18602949 |
RGD:2301736 |
NCBI chr 1:170,578,941...170,585,192
Ensembl chr 1:170,578,889...170,585,189
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G |
Kdr |
kinase insert domain receptor |
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IDA |
|
RGD |
PMID:17360578 |
RGD:2292006 |
NCBI chr14:34,727,677...34,787,127
Ensembl chr14:34,727,623...34,787,183
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G |
Plcb1 |
phospholipase C beta 1 |
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IDA |
|
RGD |
PMID:15536495 |
RGD:1582557 |
NCBI chr 3:127,721,244...128,419,565
Ensembl chr 3:128,155,069...128,419,545
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G |
Comt |
catechol-O-methyltransferase |
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IDA |
|
RGD |
PMID:12535946 |
RGD:704422 |
NCBI chr11:86,715,981...86,735,630
Ensembl chr11:86,715,981...86,735,622
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G |
Dpp4 |
dipeptidylpeptidase 4 |
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IAGP |
|
RGD |
PMID:14568317 |
RGD:1626460 |
NCBI chr 3:48,291,055...48,372,672
Ensembl chr 3:48,291,055...48,372,672
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G |
Themis |
thymocyte selection associated |
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IAGP |
DNA:frameshift mutation: |
RGD |
PMID:22275874 |
RGD:38599149 |
NCBI chr 1:17,152,973...17,378,225
Ensembl chr 1:17,171,631...17,378,047
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G |
Themism1Adej |
thymocyte selection associated; mutant1, Adej |
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IAGP |
compared to BN |
RGD |
PMID:22275874 |
RGD:38599149 |
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G |
Pax6 |
paired box 6 |
|
IAGP |
|
RGD |
PMID:17178107 |
RGD:12790972 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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G |
Ednrb |
endothelin receptor type B |
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IAGP |
|
RGD |
PMID:9739043, PMID:8570650 |
RGD:628516, RGD:628515 |
NCBI chr15:88,004,775...88,036,354
Ensembl chr15:88,006,977...88,036,354
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G |
Egfr |
epidermal growth factor receptor |
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IDA |
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RGD |
PMID:11796513 |
RGD:70386 |
NCBI chr14:99,919,485...100,104,136
Ensembl chr14:99,919,485...100,098,796
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G |
Inha |
inhibin subunit alpha |
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IDA |
rat transgene introduced into female mice |
RGD |
PMID:15359127 |
RGD:2290396 |
NCBI chr 9:82,700,482...82,703,383
Ensembl chr 9:82,700,468...82,703,400
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G |
P2ry2 |
purinergic receptor P2Y2 |
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IMP |
|
RGD |
PMID:19155635 |
RGD:2316657 |
NCBI chr 1:166,031,228...166,045,423
Ensembl chr 1:166,031,272...166,037,424
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G |
Grm2 |
glutamate metabotropic receptor 2 |
|
IMP |
knockout compared to wild type |
RGD |
PMID:28700935 |
RGD:38501064 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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G |
Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
|
IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935 |
RGD:38501064 |
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G |
Pax6 |
paired box 6 |
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QTM |
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RGD |
PMID:9247338 |
RGD:731242 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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G |
Pax6 |
paired box 6 |
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IAGP |
|
RGD |
PMID:7981749 |
RGD:1601213 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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G |
Pax6Sey |
paired box gene 6, small eye mutation |
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IAGP |
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RGD |
PMID:7981749 |
RGD:1601213 |
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G |
Frem2 |
FRAS1 related extracellular matrix 2 |
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IAGP |
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RGD |
PMID:21756877 |
RGD:13464328 |
NCBI chr 2:142,747,501...142,885,604
Ensembl chr 2:142,747,501...142,885,604
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G |
Frem2fpl |
Fras1 related extracellular matrix protein 2;fpl mutant |
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IAGP |
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RGD |
PMID:21756877 |
RGD:13464328 |
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G |
Htr1b |
5-hydroxytryptamine receptor 1B |
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IDA |
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RGD |
PMID:12040062 |
RGD:625756 |
NCBI chr 8:89,113,984...89,130,830
Ensembl chr 8:89,129,453...89,130,991
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G |
Esr1 |
estrogen receptor 1 |
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IMP |
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RGD |
PMID:24506075 |
RGD:8552987 |
NCBI chr 1:41,192,029...41,594,799
Ensembl chr 1:41,192,824...41,594,796
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G |
Esr1em1Soar |
estrogen receptor 1; ZFN induced mutant 1, Soar |
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IMP |
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RGD |
PMID:24506075 |
RGD:8552987 |
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G |
Cyp27b1 |
cytochrome P450, family 27, subfamily b, polypeptide 1 |
treatment |
IMP |
compared to Jcl:Wi and untreated |
RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:70,333,150...70,340,006
Ensembl chr 7:70,335,061...70,340,005
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G |
Cyp27b1em1Thka |
cytochrome P450, family 27, subfamily b, polypeptide 1; CRISPR/Cas9 induced mutant 1, Thka |
treatment |
IMP |
compared to Jcl:Wi and untreated |
RGD |
PMID:32231239 |
RGD:32716373 |
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G |
Lrp5 |
LDL receptor related protein 5 |
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IMP |
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RGD |
PMID:32833527 |
RGD:40902996 |
NCBI chr 1:218,816,833...218,920,147
Ensembl chr 1:218,816,841...218,920,094
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G |
Lrp5em1Vari |
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari |
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IMP |
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RGD |
PMID:32833527 |
RGD:40902996 |
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G |
Lrp5em2Vari |
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, Vari |
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IMP |
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RGD |
PMID:32833527 |
RGD:40902996 |
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G |
Lrp5em3Vari |
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari |
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IMP |
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RGD |
PMID:32833527 |
RGD:40902996 |
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G |
Vdr |
vitamin D receptor |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:139,344,452...139,394,138
Ensembl chr 7:139,342,063...139,394,166
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G |
Vdrem1Thka |
vitamin D receptor; CRISPR/Cas9 induced mutant 1, Thka |
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IMP |
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RGD |
PMID:32231239 |
RGD:32716373 |
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G |
Dhh |
desert hedgehog signaling molecule |
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IMP |
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RGD |
PMID:21062903 |
RGD:38548923 |
NCBI chr 7:140,575,288...140,580,783
Ensembl chr 7:140,575,288...140,580,783
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G |
Mc4r |
melanocortin 4 receptor |
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IMP |
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RGD |
PMID:21527895 |
RGD:6478803 |
NCBI chr18:62,612,838...62,614,725
Ensembl chr18:62,612,838...62,614,725
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G |
Bckdk |
branched chain ketoacid dehydrogenase kinase |
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IAGP |
DNA:missense mutation:cds:G369E (rat) |
RGD |
PMID:27472223 |
RGD:39131293 |
NCBI chr 1:199,351,628...199,356,299
Ensembl chr 1:199,351,628...199,356,881
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G |
Cacna1a |
calcium voltage-gated channel subunit alpha1 A |
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IAGP |
|
RGD |
PMID:17196942 |
RGD:1598976 |
NCBI chr19:25,453,236...25,749,550
Ensembl chr19:25,526,751...25,749,550
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G |
Cacna1agry |
calcium voltage-gated channel subunit alpha1 A; groggy mutant |
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IAGP |
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RGD |
PMID:17196942 |
RGD:1598976 |
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G |
Park7 |
Parkinsonism associated deglycase |
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IMP |
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RGD |
PMID:24969022 |
RGD:13210569 |
NCBI chr 5:167,982,438...168,004,724
Ensembl chr 5:167,982,439...168,004,724
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G |
Park7em1Sage |
parkinson protein 7; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
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IMP |
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RGD |
PMID:24969022 |
RGD:13210569 |
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G |
Pink1 |
PTEN induced kinase 1 |
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IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
NCBI chr 5:156,677,146...156,689,258
Ensembl chr 5:156,677,146...156,689,415
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G |
Pink1em1Sage |
PTEN induced putative kinase 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
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IMP |
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RGD |
PMID:24969022 |
RGD:13210569 |
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G |
Lepr |
leptin receptor |
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IMP |
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RGD |
PMID:27465994 |
RGD:12911217 |
NCBI chr 5:120,503,475...120,682,281
Ensembl chr 5:120,564,645...120,682,221
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G |
Leprem2Mcwi |
leptin receptor; zinc finger nuclease induced mutant 2, Medical College of Wisconsin |
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IMP |
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RGD |
PMID:27465994 |
RGD:12911217 |
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G |
Foxn1 |
forkhead box N1 |
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IAGP |
|
RGD |
PMID:8790387 |
RGD:1300512 |
NCBI chr10:65,621,142...65,634,666
Ensembl chr10:65,621,257...65,634,666
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G |
Kb23 |
type II keratin 23 |
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IAGP |
DNA:deletion |
RGD |
PMID:18420582 |
RGD:2316553 |
NCBI chr 7:143,134,980...143,141,659
Ensembl chr 7:143,135,074...143,141,589
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G |
Krt83 |
keratin 83 |
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IAGP |
DNA:deletion |
RGD |
PMID:18420582 |
RGD:2316553 |
NCBI chr 7:143,078,996...143,085,833
Ensembl chr 7:143,078,996...143,085,833
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G |
Edaradd |
EDAR-associated death domain |
|
IAGP |
compared to heterozygous animals |
RGD |
PMID:15829729 |
RGD:2304219 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
|
IAGP |
compared to heterozygous animals |
RGD |
PMID:15829729 |
RGD:2304219 |
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G |
Tmem67 |
transmembrane protein 67 |
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IAGP |
|
RGD |
PMID:30705305 |
RGD:14995942 |
NCBI chr 5:25,666,138...25,721,056
Ensembl chr 5:25,666,137...25,721,072
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G |
Tmem67wpk |
transmembrane protein 67; wpk mutant |
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IAGP |
|
RGD |
PMID:30705305 |
RGD:14995942 |
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G |
Tmem67 |
transmembrane protein 67 |
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IAGP |
|
RGD |
PMID:30705305 |
RGD:14995942 |
NCBI chr 5:25,666,138...25,721,056
Ensembl chr 5:25,666,137...25,721,072
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G |
Tmem67wpk |
transmembrane protein 67; wpk mutant |
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IAGP |
|
RGD |
PMID:30705305 |
RGD:14995942 |
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G |
Dmd |
dystrophin |
|
IMP |
|
RGD |
PMID:25310701 |
RGD:12880034 |
NCBI chr X:51,149,358...53,519,271
Ensembl chr X:51,286,737...53,519,259
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G |
Dmdem1Ang |
dystrophin; TALEN-induced mutant1, Ang |
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IMP |
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RGD |
PMID:25310701 |
RGD:12880034 |
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G |
Slc6a4 |
solute carrier family 6 member 4 |
|
IMP |
|
RGD |
PMID:19246633 |
RGD:4889487 |
NCBI chr10:63,153,656...63,188,377
Ensembl chr10:63,153,651...63,176,463
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G |
Bckdk |
branched chain ketoacid dehydrogenase kinase |
|
IAGP |
DNA:missense mutation:cds:G369E (rat) |
RGD |
PMID:27472223 |
RGD:39131293 |
NCBI chr 1:199,351,628...199,356,299
Ensembl chr 1:199,351,628...199,356,881
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G |
Pax6 |
paired box 6 |
|
IAGP |
|
RGD |
PMID:9247338 |
RGD:731242 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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G |
Pax6Sey2 |
paired box gene 6, small eye mutation 2 |
|
IAGP |
|
RGD |
PMID:9247338 |
RGD:731242 |
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G |
Themis |
thymocyte selection associated |
|
IAGP |
DNA:frameshift mutation: |
RGD |
PMID:22275874 |
RGD:38599149 |
NCBI chr 1:17,152,973...17,378,225
Ensembl chr 1:17,171,631...17,378,047
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G |
Themism1Adej |
thymocyte selection associated; mutant1, Adej |
|
IAGP |
compared to BN |
RGD |
PMID:22275874 |
RGD:38599149 |
|
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G |
Nfe2l2 |
nuclear factor, erythroid 2-like 2 |
|
IMP |
|
RGD |
PMID:27071940 |
RGD:12910550 |
NCBI chr 3:62,497,568...62,525,146
Ensembl chr 3:62,497,571...62,524,996
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G |
Nfe2l2em1Kyo |
nuclear factor, erythroid 2-like 2; zinc finger nuclease induced mutant 1, Kyoto University |
|
IMP |
|
RGD |
PMID:27071940 |
RGD:12910550 |
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G |
Nfe2l2em2Kyo |
nuclear factor, erythroid 2-like 2; zinc finger nuclease induced mutant 2, Kyoto University |
|
IMP |
|
RGD |
PMID:27071940 |
RGD:12910550 |
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G |
Lep |
leptin |
|
IMP |
|
RGD |
PMID:22948215 |
RGD:12904911 |
NCBI chr 4:56,337,695...56,351,818
Ensembl chr 4:56,337,695...56,351,818
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G |
Lepem1Sage |
leptin; zinc finger nuclease induced mutant1, Sage |
|
IMP |
|
RGD |
PMID:22948215 |
RGD:12904911 |
|
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G |
Kit |
KIT proto-oncogene receptor tyrosine kinase |
|
IMP |
|
RGD |
PMID:17322067 |
RGD:12910822 |
NCBI chr14:35,072,131...35,149,638
Ensembl chr14:35,072,108...35,149,610
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G |
KitWs |
KIT proto-oncogene receptor tyrosine kinase; mutant 1 |
|
IMP |
|
RGD |
PMID:17322067 |
RGD:12910822 |
|
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G |
Abcb1a |
ATP binding cassette subfamily B member 1A |
|
IMP |
|
RGD |
PMID:22049154 |
RGD:8657330 |
NCBI chr 4:22,339,829...22,517,642
Ensembl chr 4:22,133,521...22,425,515
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G |
Abcb1aem2Sage |
ATP binding cassette subfamily B member 1A; ZFN induced mutant 2, Sage |
|
IMP |
|
RGD |
PMID:22049154 |
RGD:8657330 |
|
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G |
Men1 |
menin 1 |
severity |
IMP |
|
RGD |
PMID:15054094 |
RGD:1304318 |
NCBI chr 1:221,704,394...221,710,343
Ensembl chr 1:221,704,493...221,710,331
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|
G |
Grk6 |
G protein-coupled receptor kinase 6 |
|
IMP |
associated with Parkinson Disease |
RGD |
PMID:20410529 |
RGD:5684919 |
NCBI chr17:9,705,917...9,721,921
Ensembl chr17:9,703,453...9,721,574
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G |
Nr4a1 |
nuclear receptor subfamily 4, group A, member 1 |
treatment |
IMP |
|
RGD |
PMID:29530712 |
RGD:40924655 |
NCBI chr 7:142,899,358...142,920,216
Ensembl chr 7:142,905,758...142,920,216
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G |
Nr4a1m1Mcwi |
nuclear receptor subfamily 4, group A, member 1; mutation 1, Medical College of Wisconsin |
treatment |
IMP |
|
RGD |
PMID:29530712 |
RGD:40924655 |
|
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G |
Slc11a2 |
solute carrier family 11 member 2 |
|
IAGP |
|
RGD |
PMID:9448300, PMID:14675167 |
RGD:729808, RGD:1580428 |
NCBI chr 7:142,025,812...142,062,892
Ensembl chr 7:142,025,815...142,063,212
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|
|
G |
Themis |
thymocyte selection associated |
|
IAGP |
DNA:frameshift mutation: |
RGD |
PMID:22275874 |
RGD:38599149 |
NCBI chr 1:17,152,973...17,378,225
Ensembl chr 1:17,171,631...17,378,047
|
|
G |
Themism1Adej |
thymocyte selection associated; mutant1, Adej |
|
IAGP |
compared to BN |
RGD |
PMID:22275874 |
RGD:38599149 |
|
|
|
G |
Fh |
fumarate hydratase |
|
IMP |
|
RGD |
PMID:27556703 |
RGD:13792708 |
NCBI chr13:93,651,486...93,677,371
Ensembl chr13:93,651,484...93,677,377
|
|
G |
Fhem1 |
fumarate hydratase; TALEN induced mutant 1 |
|
IMP |
|
RGD |
PMID:27556703 |
RGD:13792708 |
|
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G |
Depdc5 |
DEP domain containing 5, GATOR1 subcomplex subunit |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
NCBI chr14:83,089,000...83,219,576
Ensembl chr14:83,089,000...83,219,464
|
|
G |
Depdc5em1Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant1, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
|
|
G |
Depdc5em2Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant2, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
|
|
|
G |
Comt |
catechol-O-methyltransferase |
|
TAS |
|
RGD |
PMID:12535946 |
RGD:704422 |
NCBI chr11:86,715,981...86,735,630
Ensembl chr11:86,715,981...86,735,622
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G |
Lamp2 |
lysosomal-associated membrane protein 2 |
|
IMP |
in hemizygote mutant male (LAMP2y/-) |
RGD |
PMID:29720683 |
RGD:13703117 |
NCBI chr X:124,722,628...124,766,079
Ensembl chr X:124,722,628...124,766,044
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G |
Lamp2em1 |
lysosomal-associated membrane protein 2; TALEN induced mutant1 |
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IMP |
in hemizygote mutant male (LAMP2y/-) |
RGD |
PMID:29720683 |
RGD:13703117 |
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G |
Gja8 |
gap junction protein, alpha 8 |
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IAGP |
DNA:missense mutation:cds:p.L7Q(rat) |
RGD |
PMID:18470322 |
RGD:2293186 |
NCBI chr 2:199,050,854...199,052,470
Ensembl chr 2:199,050,854...199,052,470
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G |
Gja8m1Cub |
gap junction protein, alpha 8; mutant 1 Cub |
|
IAGP |
|
RGD |
PMID:18470322 |
RGD:2293186 |
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G |
Cryba1 |
crystallin, beta A1 |
|
IAGP |
|
RGD |
PMID:26303524 |
RGD:38676460 |
NCBI chr10:65,160,777...65,167,504
Ensembl chr10:65,161,152...65,167,494
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G |
Cryba1Hiser |
crystallin, beta A1; HiSER mutant |
|
IAGP |
|
RGD |
PMID:26303524 |
RGD:38676460 |
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G |
Cebpa |
CCAAT/enhancer binding protein alpha |
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IDA |
|
RGD |
PMID:12865412 |
RGD:704418 |
NCBI chr 1:91,363,492...91,366,164
Ensembl chr 1:91,363,492...91,366,164
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G |
Cd36 |
CD36 molecule |
|
IAGP |
|
RGD |
PMID:9916795 |
RGD:619666 |
NCBI chr 4:14,150,309...14,191,498
Ensembl chr 4:14,001,761...14,249,749
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G |
Plau |
plasminogen activator, urokinase |
treatment |
IMP |
|
RGD |
PMID:23018346 |
RGD:7241553 |
NCBI chr15:3,644,296...3,650,765
Ensembl chr15:3,644,769...3,650,819
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G |
Ccnd1 |
cyclin D1 |
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IDA |
|
RGD |
PMID:12668975 |
RGD:704417 |
NCBI chr 1:218,090,750...218,100,447
Ensembl chr 1:218,090,750...218,100,325
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G |
Dpp4 |
dipeptidylpeptidase 4 |
|
IAGP |
|
RGD |
PMID:14568317 |
RGD:1626460 |
NCBI chr 3:48,291,055...48,372,672
Ensembl chr 3:48,291,055...48,372,672
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G |
Grk6 |
G protein-coupled receptor kinase 6 |
|
IMP |
associated with Parkinson Disease |
RGD |
PMID:20410529 |
RGD:5684919 |
NCBI chr17:9,705,917...9,721,921
Ensembl chr17:9,703,453...9,721,574
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G |
Lamp2 |
lysosomal-associated membrane protein 2 |
|
IMP |
in hemizygote mutant male (LAMP2y/-) |
RGD |
PMID:29720683 |
RGD:13703117 |
NCBI chr X:124,722,628...124,766,079
Ensembl chr X:124,722,628...124,766,044
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G |
Lamp2em1 |
lysosomal-associated membrane protein 2; TALEN induced mutant1 |
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IMP |
in hemizygote mutant male (LAMP2y/-) |
RGD |
PMID:29720683 |
RGD:13703117 |
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G |
Reln |
reelin |
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IAGP |
|
RGD |
PMID:12820163 |
RGD:729917 |
NCBI chr 4:9,347,533...9,774,257
Ensembl chr 4:9,347,528...9,773,670
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G |
Csf1 |
colony stimulating factor 1 |
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IAGP |
|
RGD |
PMID:12379742 |
RGD:628338 |
NCBI chr 2:210,522,370...210,550,546
Ensembl chr 2:210,522,375...210,550,560
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G |
Csf1tl |
colony stimulating factor 1; tooth less mutant |
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IAGP |
|
RGD |
PMID:12379742 |
RGD:628338 |
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G |
Fh |
fumarate hydratase |
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IMP |
|
RGD |
PMID:27556703 |
RGD:13792708 |
NCBI chr13:93,651,486...93,677,371
Ensembl chr13:93,651,484...93,677,377
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G |
Fhem1 |
fumarate hydratase; TALEN induced mutant 1 |
|
IMP |
|
RGD |
PMID:27556703 |
RGD:13792708 |
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G |
Esr1 |
estrogen receptor 1 |
|
IMP |
|
RGD |
PMID:24506075 |
RGD:8552987 |
NCBI chr 1:41,192,029...41,594,799
Ensembl chr 1:41,192,824...41,594,796
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G |
Esr1em1Soar |
estrogen receptor 1; ZFN induced mutant 1, Soar |
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IMP |
|
RGD |
PMID:24506075 |
RGD:8552987 |
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G |
Edaradd |
EDAR-associated death domain |
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IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
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IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
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G |
Esr1 |
estrogen receptor 1 |
|
IMP |
|
RGD |
PMID:24506075 |
RGD:8552987 |
NCBI chr 1:41,192,029...41,594,799
Ensembl chr 1:41,192,824...41,594,796
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G |
Esr1em1Soar |
estrogen receptor 1; ZFN induced mutant 1, Soar |
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IMP |
|
RGD |
PMID:24506075 |
RGD:8552987 |
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G |
Cacna1f |
calcium voltage-gated channel subunit alpha1 F |
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IAGP |
DNA:mutation:cds: c.2941C>T |
RGD |
PMID:22800190 |
RGD:13792551 |
NCBI chr X:15,712,709...15,741,135
Ensembl chr X:15,712,713...15,741,103
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G |
Cacna1f csnb |
calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant |
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IAGP |
DNA:mutation:cds: c.2941C>T |
RGD |
PMID:22800190 |
RGD:13792551 |
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G |
Spata22 |
spermatogenesis associated 22 |
treatment |
IMP |
|
RGD |
PMID:23903057 |
RGD:38549346 |
NCBI chr10:59,893,064...59,910,769
Ensembl chr10:59,879,850...59,911,051
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G |
Atm |
ATM serine/threonine kinase |
|
IMP |
DNA:deletion:exon: |
RGD |
PMID:28007901 |
RGD:12879399 |
NCBI chr 8:58,015,938...58,119,973
Ensembl chr 8:58,015,940...58,120,045
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G |
Atmem1Kyo |
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo |
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IMP |
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RGD |
PMID:28007901 |
RGD:12879399 |
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G |
Myc |
MYC proto-oncogene, bHLH transcription factor |
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IMP |
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RGD |
PMID:22629444 |
RGD:7240532 |
NCBI chr 7:102,586,313...102,591,240
Ensembl chr 7:102,586,313...102,591,240
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G |
Mrs2 |
magnesium transporter MRS2 |
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IMP |
DNA:missense mutation:intron (Mrs2) |
RGD |
PMID:21253565 |
RGD:12793070 |
NCBI chr17:42,064,271...42,083,602
Ensembl chr17:42,064,376...42,082,300
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G |
Mrs2dmyKyo |
MRS2 magnesium transporter; demyelination mutant, Kyo |
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IMP |
DNA:missense mutation:intron (Mrs2) |
RGD |
PMID:21253565 |
RGD:12793070 |
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G |
Lamp2 |
lysosomal-associated membrane protein 2 |
|
IMP |
in hemizygote mutant male (LAMP2y/-) |
RGD |
PMID:28124283 |
RGD:13703118 |
NCBI chr X:124,722,628...124,766,079
Ensembl chr X:124,722,628...124,766,044
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G |
Lamp2em1 |
lysosomal-associated membrane protein 2; TALEN induced mutant1 |
|
IMP |
in hemizygote mutant male (LAMP2y/-) |
RGD |
PMID:28124283 |
RGD:13703118 |
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G |
Edaradd |
EDAR-associated death domain |
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IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
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IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
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G |
Cyp2d4 |
cytochrome P450, family 2, subfamily d, polypeptide 4 |
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IAGP |
|
RGD |
PMID:12629505 |
RGD:1358549 |
NCBI chr 7:123,599,264...123,608,436
Ensembl chr 7:123,599,266...123,608,436
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G |
Bace1 |
beta-secretase 1 |
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IMP |
|
RGD |
PMID:28281673 |
RGD:13782149 |
NCBI chr 8:50,140,092...50,162,388
Ensembl chr 8:50,139,997...50,162,361
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G |
Bace1em1Sage |
|
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IMP |
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RGD |
PMID:28281673 |
RGD:13782149 |
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G |
Mecp2 |
methyl CpG binding protein 2 |
|
IMP |
compared to SD wild-type |
RGD |
PMID:27329765 |
RGD:40924662 |
NCBI chr X:156,650,389...156,713,813
Ensembl chr X:156,655,960...156,705,233
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G |
Mecp2em1Sage |
methyl CpG binding protein 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
compared to SD wild-type |
RGD |
PMID:27329765 |
RGD:40924662 |
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G |
Park7 |
Parkinsonism associated deglycase |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
NCBI chr 5:167,982,438...168,004,724
Ensembl chr 5:167,982,439...168,004,724
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G |
Park7em1Sage |
parkinson protein 7; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
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G |
Pink1 |
PTEN induced kinase 1 |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
NCBI chr 5:156,677,146...156,689,258
Ensembl chr 5:156,677,146...156,689,415
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G |
Pink1em1Sage |
PTEN induced putative kinase 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
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G |
Crb1 |
crumbs cell polarity complex component 1 |
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IAGP |
|
RGD |
PMID:25878282 |
RGD:13451131 |
NCBI chr13:56,270,519...56,462,893
Ensembl chr13:56,270,781...56,462,834
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G |
Crb1m1 |
crumbs 1, cell polarity complex component;mutant 1 |
|
IAGP |
|
RGD |
PMID:25878282 |
RGD:13451131 |
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G |
Park7 |
Parkinsonism associated deglycase |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
NCBI chr 5:167,982,438...168,004,724
Ensembl chr 5:167,982,439...168,004,724
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G |
Park7em1Sage |
parkinson protein 7; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
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G |
Pink1 |
PTEN induced kinase 1 |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
NCBI chr 5:156,677,146...156,689,258
Ensembl chr 5:156,677,146...156,689,415
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G |
Pink1em1Sage |
PTEN induced putative kinase 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:24969022 |
RGD:13210569 |
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G |
Cftr |
CF transmembrane conductance regulator |
|
IMP |
|
RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
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G |
Depdc5 |
DEP domain containing 5, GATOR1 subcomplex subunit |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
NCBI chr14:83,089,000...83,219,576
Ensembl chr14:83,089,000...83,219,464
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G |
Depdc5em1Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant1, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
|
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G |
Depdc5em2Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant2, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
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G |
Depdc5 |
DEP domain containing 5, GATOR1 subcomplex subunit |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
NCBI chr14:83,089,000...83,219,576
Ensembl chr14:83,089,000...83,219,464
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G |
Depdc5em1Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant1, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
|
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G |
Depdc5em2Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant2, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
|
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G |
Depdc5 |
DEP domain containing 5, GATOR1 subcomplex subunit |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
NCBI chr14:83,089,000...83,219,576
Ensembl chr14:83,089,000...83,219,464
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G |
Depdc5em1Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant1, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
|
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G |
Depdc5em2Kyo |
DEP domain containing 5, GATOR1 subcomplex subunit; TALEN induced mutant2, Kyo |
|
IMP |
|
RGD |
PMID:26873552 |
RGD:11573213 |
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G |
Grm2 |
glutamate metabotropic receptor 2 |
|
IMP |
knock-out compared to wild-type rats knockout compared to wild type |
RGD |
PMID:30283001, PMID:28700935 |
RGD:38501063, RGD:38501064 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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G |
Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
|
IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935, PMID:30283001 |
RGD:38501064, RGD:38501063 |
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G |
Aire |
autoimmune regulator |
|
IMP |
|
RGD |
PMID:29959280 |
RGD:38599145 |
NCBI chr20:11,365,630...11,380,636
Ensembl chr20:11,365,697...11,380,631
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G |
Aireem1Ang |
autoimmune regulator; ZFN induced mutant1, Ang |
|
IMP |
|
RGD |
PMID:29959280 |
RGD:38599145 |
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G |
F2r |
coagulation factor II (thrombin) receptor |
|
IDA |
|
RGD |
PMID:12126749 |
RGD:1582348 |
NCBI chr 2:26,118,760...26,135,340
Ensembl chr 2:26,118,760...26,135,340
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|
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G |
Grm2 |
glutamate metabotropic receptor 2 |
|
IMP |
knock-out compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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G |
Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
|
IMP |
KO compared to wild-type rats |
RGD |
PMID:30283001 |
RGD:38501063 |
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G |
Pax6 |
paired box 6 |
|
IAGP |
|
RGD |
PMID:7981749 |
RGD:1601213 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
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G |
Pax6Sey |
paired box gene 6, small eye mutation |
|
IAGP |
|
RGD |
PMID:7981749 |
RGD:1601213 |
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G |
Adcy3 |
adenylate cyclase 3 |
|
IDA |
|
RGD |
PMID:2255909 |
RGD:70798 |
NCBI chr 6:28,570,941...28,648,848
Ensembl chr 6:28,571,351...28,650,148
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G |
Fmr1 |
FMRP translational regulator 1 |
|
IMP |
DNA:deletion:intron 7, exon 8: |
RGD |
PMID:30877790 |
RGD:38548928 |
NCBI chr X:154,684,924...154,722,369
Ensembl chr X:154,684,935...154,722,314
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|
G |
Fmr1em1Sage |
FMRP translational regulator 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
DNA:deletion:intron 7, exon 8: |
RGD |
PMID:30877790 |
RGD:38548928 |
|
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G |
Zbtb16 |
zinc finger and BTB domain containing 16 |
|
IAGP |
|
RGD |
PMID:27727328 |
RGD:40924666 |
NCBI chr 8:52,980,226...53,146,765
Ensembl chr 8:52,985,313...53,146,953
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|
|
G |
Atm |
ATM serine/threonine kinase |
|
IMP |
DNA:deletion:exon: |
RGD |
PMID:27895165, PMID:28007901 |
RGD:12879393, RGD:12879399 |
NCBI chr 8:58,015,938...58,119,973
Ensembl chr 8:58,015,940...58,120,045
|
|
G |
Atmem1Kyo |
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo |
|
IMP |
|
RGD |
PMID:28007901 |
RGD:12879399 |
|
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G |
Atmm1Kyo |
ATM serine/threonine kinase; ENU induced mutant 1, Kyo |
|
IMP |
|
RGD |
PMID:27895165 |
RGD:12879393 |
|
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|
G |
Dpp4 |
dipeptidylpeptidase 4 |
|
IAGP |
|
RGD |
PMID:14568317 |
RGD:1626460 |
NCBI chr 3:48,291,055...48,372,672
Ensembl chr 3:48,291,055...48,372,672
|
|
|
G |
Pax6 |
paired box 6 |
|
IAGP |
|
RGD |
PMID:17178107 |
RGD:12790972 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
|
|
|
G |
Dpp4 |
dipeptidylpeptidase 4 |
|
IAGP |
|
RGD |
PMID:14568317 |
RGD:1626460 |
NCBI chr 3:48,291,055...48,372,672
Ensembl chr 3:48,291,055...48,372,672
|
|
G |
Kdr |
kinase insert domain receptor |
|
IDA |
|
RGD |
PMID:15258583 |
RGD:1581594 |
NCBI chr14:34,727,677...34,787,127
Ensembl chr14:34,727,623...34,787,183
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|
|
G |
Il15 |
interleukin 15 |
|
IMP |
|
RGD |
PMID:28395334 |
RGD:12910490 |
NCBI chr19:23,542,606...23,624,366
Ensembl chr19:23,542,889...23,554,594
|
|
G |
Il15em1Soar |
interleukin 15; ZFN induced mutant 1, Soar |
|
IMP |
|
RGD |
PMID:28395334 |
RGD:12910490 |
|
|
|
G |
Rab38 |
RAB38, member RAS oncogene family |
|
IAGP |
|
RGD |
PMID:18983523 |
RGD:2324691 |
NCBI chr 1:152,072,716...152,153,449
Ensembl chr 1:152,072,665...152,153,449
|
|
G |
Rab38ru |
Rab38, member of RAS oncogene family, ruby allele |
|
IAGP |
|
RGD |
PMID:18983523 |
RGD:2324691 |
|
|
|
G |
P2ry2 |
purinergic receptor P2Y2 |
|
IMP |
|
RGD |
PMID:19155635 |
RGD:2316657 |
NCBI chr 1:166,031,228...166,045,423
Ensembl chr 1:166,031,272...166,037,424
|
|
|
G |
Esr2 |
estrogen receptor 2 |
|
IMP |
|
RGD |
PMID:28520870 |
RGD:38548924 |
NCBI chr 6:99,163,953...99,214,711
Ensembl chr 6:99,164,357...99,214,251
|
|
G |
Esr2em1Soar |
estrogen receptor 2; ZFN induced mutant 1, Soar |
|
IMP |
|
RGD |
PMID:28520870 |
RGD:38548924 |
|
|
|
G |
Mecp2 |
methyl CpG binding protein 2 |
|
IMP |
|
RGD |
PMID:27313794 |
RGD:11568037 |
NCBI chr X:156,650,389...156,713,813
Ensembl chr X:156,655,960...156,705,233
|
|
G |
Mecp2em1Sage |
methyl CpG binding protein 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:27313794 |
RGD:11568037 |
|
|
|
G |
P2rx7 |
purinergic receptor P2X 7 |
|
IMP |
|
RGD |
PMID:31630543 |
RGD:14995937 |
NCBI chr12:39,353,613...39,396,042
Ensembl chr12:39,353,613...39,396,042
|
|
|
G |
Nr4a1 |
nuclear receptor subfamily 4, group A, member 1 |
|
IMP |
|
RGD |
PMID:24722447 |
RGD:12910103 |
NCBI chr 7:142,899,358...142,920,216
Ensembl chr 7:142,905,758...142,920,216
|
|
|
G |
P2ry2 |
purinergic receptor P2Y2 |
|
IMP |
|
RGD |
PMID:19155635 |
RGD:2316657 |
NCBI chr 1:166,031,228...166,045,423
Ensembl chr 1:166,031,272...166,037,424
|
|
|
G |
Atp7b |
ATPase copper transporting beta |
|
IAGP |
|
RGD |
PMID:11509115 |
RGD:1302456 |
NCBI chr16:74,865,516...74,944,935
Ensembl chr16:74,865,516...74,945,286
|
|
G |
Atp7bhts |
ATPase copper transporting beta; hepatitis |
|
IAGP |
|
RGD |
PMID:11509115 |
RGD:1302456 |
|
|
|
G |
Ugt1a1 |
UDP glucuronosyltransferase family 1 member A1 |
treatment |
IAGP |
|
RGD |
PMID:1127102 |
RGD:1354700 |
NCBI chr 9:95,295,701...95,302,822
Ensembl chr 9:95,161,157...95,302,822
|
|
G |
Ugt1a1j |
UDP glucuronosyltransferase family 1 member A1, jaundice mutant |
treatment |
IAGP |
|
RGD |
PMID:1127102 |
RGD:1354700 |
|
|
|
G |
Esr1 |
estrogen receptor 1 |
|
IMP |
|
RGD |
PMID:24506075 |
RGD:8552987 |
NCBI chr 1:41,192,029...41,594,799
Ensembl chr 1:41,192,824...41,594,796
|
|
|
G |
Isca1 |
iron-sulfur cluster assembly 1 |
|
IMP |
|
RGD |
PMID:31016283 |
RGD:39131292 |
NCBI chr17:5,281,727...5,294,386
Ensembl chr17:5,281,727...5,294,384
|
|
|
G |
Grm2 |
glutamate metabotropic receptor 2 |
|
IMP |
knockout compared to wild type |
RGD |
PMID:28700935 |
RGD:38501064 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
|
|
G |
Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
|
IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935 |
RGD:38501064 |
|
|
|
G |
Fmr1 |
FMRP translational regulator 1 |
|
IMP |
|
RGD |
PMID:24773431, PMID:28894415 |
RGD:9831152, RGD:38501107 |
NCBI chr X:154,684,924...154,722,369
Ensembl chr X:154,684,935...154,722,314
|
|
G |
Fmr1em1Mzhe |
FMRP translational regulator 1; CRISPR/Cas9 induced mutant1, Mzhe |
|
IMP |
|
RGD |
PMID:28894415 |
RGD:38501107 |
|
|
G |
Mecp2 |
methyl CpG binding protein 2 |
|
IMP |
|
RGD |
PMID:27313794 |
RGD:11568037 |
NCBI chr X:156,650,389...156,713,813
Ensembl chr X:156,655,960...156,705,233
|
|
G |
Mecp2em1Sage |
methyl CpG binding protein 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:27313794 |
RGD:11568037 |
|
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G |
Lta |
lymphotoxin alpha |
|
IDA |
|
RGD |
PMID:9798700 |
RGD:1580413 |
NCBI chr20:4,851,889...4,854,677
Ensembl chr20:4,852,496...4,854,677
|
|
G |
Tnfsf4 |
TNF superfamily member 4 |
|
IDA |
|
RGD |
PMID:12626546 |
RGD:1580395 |
NCBI chr13:79,269,973...79,293,775
Ensembl chr13:79,269,973...79,293,778
|
|
|
G |
Pax6 |
paired box 6 |
|
IAGP |
|
RGD |
PMID:7981749 |
RGD:1601213 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
|
|
|
G |
Hras |
HRas proto-oncogene, GTPase |
|
IDA |
|
RGD |
PMID:14988264 |
RGD:1358731 |
NCBI chr 1:214,178,404...214,181,841
Ensembl chr 1:214,178,407...214,181,686
|
|
|
G |
Lrp5 |
LDL receptor related protein 5 |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
NCBI chr 1:218,816,833...218,920,147
Ensembl chr 1:218,816,841...218,920,094
|
|
G |
Lrp5em1Vari |
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
|
|
G |
Lrp5em2Vari |
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, Vari |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
|
|
G |
Lrp5em3Vari |
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
|
|
|
G |
Lrp5 |
LDL receptor related protein 5 |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
NCBI chr 1:218,816,833...218,920,147
Ensembl chr 1:218,816,841...218,920,094
|
|
G |
Lrp5em1Vari |
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
|
|
G |
Lrp5em2Vari |
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, Vari |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
|
|
G |
Lrp5em3Vari |
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari |
|
IMP |
|
RGD |
PMID:32833527 |
RGD:40902996 |
|
|
G |
Pde6b |
phosphodiesterase 6B |
|
IMP |
compared to wild-type |
RGD |
PMID:31009522 |
RGD:40924664 |
NCBI chr14:2,328,690...2,371,913
Ensembl chr14:2,328,750...2,371,883
|
|
G |
Pde6bem1Baek |
phosphodiesterase 6B; Cpf1-CRISPR induced mutant1, Baek |
|
IMP |
compared to wild-type |
RGD |
PMID:31009522 |
RGD:40924664 |
|
|
|
G |
Cryba1 |
crystallin, beta A1 |
|
IAGP |
|
RGD |
PMID:26303524 |
RGD:38676460 |
NCBI chr10:65,160,777...65,167,504
Ensembl chr10:65,161,152...65,167,494
|
|
G |
Cryba1Hiser |
crystallin, beta A1; HiSER mutant |
|
IAGP |
|
RGD |
PMID:26303524 |
RGD:38676460 |
|
|
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G |
Cacna1f |
calcium voltage-gated channel subunit alpha1 F |
|
IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:22634626 |
RGD:13782386 |
NCBI chr X:15,712,709...15,741,135
Ensembl chr X:15,712,713...15,741,103
|
|
G |
Cacna1f csnb |
calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant |
|
IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:22634626 |
RGD:13782386 |
|
|
|
G |
Mertk |
MER proto-oncogene, tyrosine kinase |
treatment |
IAGP |
|
RGD |
PMID:11592982 |
RGD:69668 |
NCBI chr 3:121,235,230...121,340,932
Ensembl chr 3:121,235,119...121,342,444
|
|
G |
Mertkrdy |
MER proto-oncogene, tyrosine kinase; retinal dystrophy mutant |
treatment |
IAGP |
|
RGD |
PMID:11592982 |
RGD:69668 |
|
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|
G |
Crb1 |
crumbs cell polarity complex component 1 |
|
IAGP |
|
RGD |
PMID:25878282 |
RGD:13451131 |
NCBI chr13:56,270,519...56,462,893
Ensembl chr13:56,270,781...56,462,834
|
|
G |
Crb1m1 |
crumbs 1, cell polarity complex component;mutant 1 |
|
IAGP |
|
RGD |
PMID:25878282 |
RGD:13451131 |
|
|
|
G |
Kdr |
kinase insert domain receptor |
|
IDA |
inhibition significantly reduces retinal neovascularization |
RGD |
PMID:15951738 |
RGD:1581593 |
NCBI chr14:34,727,677...34,787,127
Ensembl chr14:34,727,623...34,787,183
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|
|
G |
Bckdk |
branched chain ketoacid dehydrogenase kinase |
|
IAGP |
DNA:missense mutation:cds:G369E (rat) |
RGD |
PMID:27472223 |
RGD:39131293 |
NCBI chr 1:199,351,628...199,356,299
Ensembl chr 1:199,351,628...199,356,881
|
|
|
G |
Bckdk |
branched chain ketoacid dehydrogenase kinase |
|
IAGP |
DNA:missense mutation:cds:G369E (rat) |
RGD |
PMID:27472223 |
RGD:39131293 |
NCBI chr 1:199,351,628...199,356,299
Ensembl chr 1:199,351,628...199,356,881
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|
G |
Lpin1 |
lipin 1 |
|
IMP |
|
RGD |
PMID:21715287 |
RGD:38599010 |
NCBI chr 6:41,796,214...41,905,149
Ensembl chr 6:41,799,749...41,870,046
|
|
G |
Lpin1m1Hubr |
lipin 1; ENU induced mutant 1, Hubr |
|
IMP |
compared to Wild type |
RGD |
PMID:21715287 |
RGD:38599010 |
|
|
G |
Ngly1 |
N-glycanase 1 |
|
IMP |
|
RGD |
PMID:32259258 |
RGD:39457703 |
NCBI chr15:10,405,453...10,455,973
Ensembl chr15:10,405,164...10,455,956
|
|
|
G |
Mecp2 |
methyl CpG binding protein 2 |
|
IMP |
compared to SD wild-type male |
RGD |
PMID:27329765 |
RGD:40924662 |
NCBI chr X:156,650,389...156,713,813
Ensembl chr X:156,655,960...156,705,233
|
|
G |
Mecp2em1Sage |
methyl CpG binding protein 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
compared to SD wild-type male |
RGD |
PMID:27329765 |
RGD:40924662 |
|
|
|
G |
Atm |
ATM serine/threonine kinase |
|
IMP |
DNA:deletion:exon: |
RGD |
PMID:27895165, PMID:28007901 |
RGD:12879393, RGD:12879399 |
NCBI chr 8:58,015,938...58,119,973
Ensembl chr 8:58,015,940...58,120,045
|
|
G |
Atmem1Kyo |
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo |
|
IMP |
|
RGD |
PMID:28007901 |
RGD:12879399 |
|
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G |
Atmm1Kyo |
ATM serine/threonine kinase; ENU induced mutant 1, Kyo |
|
IMP |
|
RGD |
PMID:27895165 |
RGD:12879393 |
|
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G |
Vdr |
vitamin D receptor |
|
IMP |
|
RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:139,344,452...139,394,138
Ensembl chr 7:139,342,063...139,394,166
|
|
G |
Vdrem2Thka |
vitamin D receptor; CRISPR/Cas9 induced mutant 2, Thka |
|
IMP |
|
RGD |
PMID:32231239 |
RGD:32716373 |
|
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|
G |
Cntnap2 |
contactin associated protein 2 |
|
IMP |
|
RGD |
PMID:28364455 |
RGD:12880397 |
NCBI chr 4:74,700,539...77,025,463
|
|
G |
Cntnap2em1Sage |
contactin associated protein-like 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:28364455 |
RGD:12880397 |
|
|
G |
Ghrhr |
growth hormone releasing hormone receptor |
|
IDA |
|
RGD |
PMID:12161265 |
RGD:728477 |
NCBI chr 4:85,587,321...85,602,389
Ensembl chr 4:85,588,595...85,601,666
|
|
|
G |
Cftr |
CF transmembrane conductance regulator |
|
IMP |
|
RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
|
|
|
G |
Cacna1c |
calcium voltage-gated channel subunit alpha1 C |
|
IMP |
compared to wide-type male |
RGD |
PMID:29739816 |
RGD:42724471 |
NCBI chr 4:150,635,808...151,270,790
Ensembl chr 4:150,641,066...150,829,913
|
|
G |
Cacna1cem1Sage |
calcium voltage-gated channel subunit alpha1 C; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
compared to wide-type male |
RGD |
PMID:29739816 |
RGD:42724471 |
|
|
G |
Fmr1 |
FMRP translational regulator 1 |
|
IMP |
|
RGD |
PMID:24773431 |
RGD:9831152 |
NCBI chr X:154,684,924...154,722,369
Ensembl chr X:154,684,935...154,722,314
|
|
G |
Fmr1em1Sage |
FMRP translational regulator 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:24773431 |
RGD:9831152 |
|
|
G |
Nlgn3 |
neuroligin 3 |
|
IMP |
|
RGD |
PMID:24773431 |
RGD:9831152 |
NCBI chr X:71,199,390...71,227,460
Ensembl chr X:71,199,491...71,222,732
|
|
G |
Nlgn3em1Sage |
neuroligin 3; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
|
RGD |
PMID:24773431 |
RGD:9831152 |
|
|
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G |
Dpp4 |
dipeptidylpeptidase 4 |
|
IAGP |
|
RGD |
PMID:14568317 |
RGD:1626460 |
NCBI chr 3:48,291,055...48,372,672
Ensembl chr 3:48,291,055...48,372,672
|
|
G |
Pax6 |
paired box 6 |
|
IAGP |
DNA:frameshift mutation:cds: |
RGD |
PMID:21203536 |
RGD:8552339 |
NCBI chr 3:95,700,241...95,728,682
Ensembl chr 3:95,707,386...95,728,624
|
|
|
G |
Bckdk |
branched chain ketoacid dehydrogenase kinase |
|
IAGP |
DNA:missense mutation:cds:G369E (rat) |
RGD |
PMID:27472223 |
RGD:39131293 |
NCBI chr 1:199,351,628...199,356,299
Ensembl chr 1:199,351,628...199,356,881
|
|
|
G |
Kdr |
kinase insert domain receptor |
|
IDA |
|
RGD |
PMID:15258583 |
RGD:1581594 |
NCBI chr14:34,727,677...34,787,127
Ensembl chr14:34,727,623...34,787,183
|
|
|
G |
Nrg1 |
neuregulin 1 |
|
IMP |
DNA:transposon insertion |
RGD |
PMID:23098760 |
RGD:10449010 |
NCBI chr16:62,969,573...64,065,063
Ensembl chr16:63,837,216...64,057,434
|
|
|
G |
Bscl2 |
BSCL2 lipid droplet biogenesis associated, seipin |
|
IMP |
|
RGD |
PMID:25934999 |
RGD:11085488 |
NCBI chr 1:225,035,956...225,046,137
Ensembl chr 1:225,037,737...225,046,040
|
|
G |
Bscl2m1Kyo |
BSCL2, seipin lipid droplet biogenesis associated; ENU induced mutant1, Kyo |
|
IMP |
|
RGD |
PMID:25934999 |
RGD:11085488 |
|
|
G |
Nrg1 |
neuregulin 1 |
|
IMP |
DNA:transposon insertion |
RGD |
PMID:23098760 |
RGD:10449010 |
NCBI chr16:62,969,573...64,065,063
Ensembl chr16:63,837,216...64,057,434
|
|
|
G |
Brca2 |
BRCA2, DNA repair associated |
|
IAGP |
|
RGD |
PMID:16964288 |
RGD:1599505 |
NCBI chr12:503,660...544,754
Ensembl chr12:504,007...544,748
|
|
|
G |
Ednrb |
endothelin receptor type B |
|
IAGP |
|
RGD |
PMID:22975636 |
RGD:7207471 |
NCBI chr15:88,004,775...88,036,354
Ensembl chr15:88,006,977...88,036,354
|
|
G |
Ednrbsl |
endothelin receptor type B, spotting lethal |
|
IAGP |
|
RGD |
PMID:22975636 |
RGD:7207471 |
|
|
|
G |
Ednrb |
endothelin receptor type B |
|
IAGP |
|
RGD |
PMID:22975636 |
RGD:7207471 |
NCBI chr15:88,004,775...88,036,354
Ensembl chr15:88,006,977...88,036,354
|
|
G |
Ednrbsl |
endothelin receptor type B, spotting lethal |
|
IAGP |
|
RGD |
PMID:22975636 |
RGD:7207471 |
|
|
|
G |
Edaradd |
EDAR-associated death domain |
|
IAGP |
|
RGD |
PMID:31028034 |
RGD:14398763 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
|
|
G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
|
IAGP |
|
RGD |
PMID:31028034 |
RGD:14398763 |
|
|
|
G |
Nr4a1 |
nuclear receptor subfamily 4, group A, member 1 |
|
IMP |
compared to wild-type and untreated |
RGD |
PMID:29530712 |
RGD:40924655 |
NCBI chr 7:142,899,358...142,920,216
Ensembl chr 7:142,905,758...142,920,216
|
|
G |
Nr4a1m1Mcwi |
nuclear receptor subfamily 4, group A, member 1; mutation 1, Medical College of Wisconsin |
|
IMP |
compared to wild-type and untreated |
RGD |
PMID:29530712 |
RGD:40924655 |
|
|
|
G |
Rab38 |
RAB38, member RAS oncogene family |
|
IAGP |
|
RGD |
PMID:19897744 |
RGD:2324690 |
NCBI chr 1:152,072,716...152,153,449
Ensembl chr 1:152,072,665...152,153,449
|
|
G |
Rab38ru |
Rab38, member of RAS oncogene family, ruby allele |
|
IAGP |
|
RGD |
PMID:19897744 |
RGD:2324690 |
|
|
|
G |
Atm |
ATM serine/threonine kinase |
|
IMP |
|
RGD |
PMID:27895165 |
RGD:12879393 |
NCBI chr 8:58,015,938...58,119,973
Ensembl chr 8:58,015,940...58,120,045
|
|
G |
Atmm1Kyo |
ATM serine/threonine kinase; ENU induced mutant 1, Kyo |
|
IMP |
|
RGD |
PMID:27895165 |
RGD:12879393 |
|
|
G |
Cyp27b1 |
cytochrome P450, family 27, subfamily b, polypeptide 1 |
|
IMP |
compared to CE-2 diet containing 1.15% calcium fed Cyp27b1-KO rats |
RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:70,333,150...70,340,006
Ensembl chr 7:70,335,061...70,340,005
|
|
G |
Cyp27b1em1Thka |
cytochrome P450, family 27, subfamily b, polypeptide 1; CRISPR/Cas9 induced mutant 1, Thka |
|
IMP |
compared to CE-2 diet containing 1.15% calcium fed Cyp27b1-KO rats |
RGD |
PMID:32231239 |
RGD:32716373 |
|
|
|
G |
Pclo |
piccolo (presynaptic cytomatrix protein) |
|
IMP |
|
RGD |
PMID:31074746 |
RGD:41408338 |
NCBI chr 4:16,454,904...17,058,921
Ensembl chr 4:16,454,904...17,058,921
|
|
G |
PcloTn(sb-B-Geo)Fkh |
presynaptic cytomatrix protein; sleeping beauty transposon induced mutant, Fkh |
|
IMP |
|
RGD |
PMID:31074746 |
RGD:41408338 |
|
|
|
G |
Pclo |
piccolo (presynaptic cytomatrix protein) |
|
IMP |
|
RGD |
PMID:31074746 |
RGD:41408338 |
NCBI chr 4:16,454,904...17,058,921
Ensembl chr 4:16,454,904...17,058,921
|
|
G |
PcloTn(sb-B-Geo)Fkh |
presynaptic cytomatrix protein; sleeping beauty transposon induced mutant, Fkh |
|
IMP |
|
RGD |
PMID:31074746 |
RGD:41408338 |
|
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G |
Arsb |
arylsulfatase B |
|
IAGP |
|
RGD |
PMID:21887218 |
RGD:39131283 |
NCBI chr 2:23,385,154...23,543,028
Ensembl chr 2:23,385,183...23,544,963
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G |
Zbtb16 |
zinc finger and BTB domain containing 16 |
|
IAGP |
|
RGD |
PMID:27727328 |
RGD:40924666 |
NCBI chr 8:52,980,226...53,146,765
Ensembl chr 8:52,985,313...53,146,953
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|
G |
Cckar |
cholecystokinin A receptor |
|
IAGP |
|
RGD |
PMID:16081877 |
RGD:1625203 |
NCBI chr14:59,610,939...59,619,786
Ensembl chr14:59,611,434...59,619,783
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G |
Fmr1 |
FMRP translational regulator 1 |
|
IMP |
|
RGD |
PMID:28894415 |
RGD:38501107 |
NCBI chr X:154,684,924...154,722,369
Ensembl chr X:154,684,935...154,722,314
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|
G |
Fmr1em1Mzhe |
FMRP translational regulator 1; CRISPR/Cas9 induced mutant1, Mzhe |
|
IMP |
|
RGD |
PMID:28894415 |
RGD:38501107 |
|
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G |
Ngly1 |
N-glycanase 1 |
|
IMP |
|
RGD |
PMID:32259258 |
RGD:39457703 |
NCBI chr15:10,405,453...10,455,973
Ensembl chr15:10,405,164...10,455,956
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G |
Aire |
autoimmune regulator |
|
IMP |
|
RGD |
PMID:29959280 |
RGD:38599145 |
NCBI chr20:11,365,630...11,380,636
Ensembl chr20:11,365,697...11,380,631
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G |
Aireem1Ang |
autoimmune regulator; ZFN induced mutant1, Ang |
|
IMP |
|
RGD |
PMID:29959280 |
RGD:38599145 |
|
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G |
Arsb |
arylsulfatase B |
|
IAGP |
|
RGD |
PMID:21887218 |
RGD:39131283 |
NCBI chr 2:23,385,154...23,543,028
Ensembl chr 2:23,385,183...23,544,963
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G |
Edaradd |
EDAR-associated death domain |
|
IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
|
IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
|
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G |
Cftr |
CF transmembrane conductance regulator |
|
IMP |
|
RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
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G |
Arsb |
arylsulfatase B |
|
IAGP |
|
RGD |
PMID:21887218 |
RGD:39131283 |
NCBI chr 2:23,385,154...23,543,028
Ensembl chr 2:23,385,183...23,544,963
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G |
Vdr |
vitamin D receptor |
|
IMP |
|
RGD |
PMID:32231239 |
RGD:32716373 |
NCBI chr 7:139,344,452...139,394,138
Ensembl chr 7:139,342,063...139,394,166
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G |
Vdrem1Thka |
vitamin D receptor; CRISPR/Cas9 induced mutant 1, Thka |
|
IMP |
|
RGD |
PMID:32231239 |
RGD:32716373 |
|
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G |
Vdrem2Thka |
vitamin D receptor; CRISPR/Cas9 induced mutant 2, Thka |
|
IMP |
|
RGD |
PMID:32231239 |
RGD:32716373 |
|
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G |
Cftr |
CF transmembrane conductance regulator |
|
IMP |
|
RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
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G |
Arsb |
arylsulfatase B |
|
IAGP |
|
RGD |
PMID:21887218 |
RGD:39131283 |
NCBI chr 2:23,385,154...23,543,028
Ensembl chr 2:23,385,183...23,544,963
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G |
Cftr |
CF transmembrane conductance regulator |
|
IMP |
|
RGD |
PMID:24608905 |
RGD:11566051 |
NCBI chr 4:42,693,263...42,860,679
Ensembl chr 4:42,692,836...42,860,676
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G |
Il15 |
interleukin 15 |
|
IMP |
|
RGD |
PMID:28395334 |
RGD:12910490 |
NCBI chr19:23,542,606...23,624,366
Ensembl chr19:23,542,889...23,554,594
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G |
Il15em1Soar |
interleukin 15; ZFN induced mutant 1, Soar |
|
IMP |
|
RGD |
PMID:28395334 |
RGD:12910490 |
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G |
Mmp12 |
matrix metallopeptidase 12 |
|
IMP |
|
RGD |
PMID:27807143 |
RGD:12910498 |
NCBI chr 8:5,594,717...5,616,494
Ensembl chr 8:5,606,592...5,616,493
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G |
Cryba1 |
crystallin, beta A1 |
|
IAGP |
DNA:insertion:exon |
RGD |
PMID:17931883 |
RGD:2303652 |
NCBI chr10:65,160,777...65,167,504
Ensembl chr10:65,161,152...65,167,494
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G |
Gpr182 |
G protein-coupled receptor 182 |
|
IDA |
|
RGD |
PMID:7592696 |
RGD:61533 |
NCBI chr 7:71,044,786...71,048,713
Ensembl chr 7:71,045,543...71,048,383
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G |
Nfe2l2 |
nuclear factor, erythroid 2-like 2 |
|
IMP |
|
RGD |
PMID:26637559 |
RGD:11344212 |
NCBI chr 3:62,497,568...62,525,146
Ensembl chr 3:62,497,571...62,524,996
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G |
Nfe2l2em1Mcwi |
nuclear factor, erythroid 2-like 2; TALEN induced mutant 1, Medical College of Wisconsin |
|
IMP |
|
RGD |
PMID:26637559 |
RGD:11344212 |
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G |
Sod3 |
superoxide dismutase 3 |
|
IMP |
DNA:missense mutation:CDS:p.E124D |
RGD |
PMID:24322611 |
RGD:38548929 |
NCBI chr14:60,958,583...60,971,143
Ensembl chr14:60,958,592...60,964,324
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G |
Sod3m1Mcwi |
superoxide dismutase 3; mutation 1, Medical College of Wisconsin |
|
IMP |
|
RGD |
PMID:24322611 |
RGD:38548929 |
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G |
Myo7a |
myosin VIIA |
|
IAGP |
DNA:nonsense mutation:cds |
RGD |
PMID:15965244 |
RGD:1581470 |
NCBI chr 1:163,001,313...163,071,545
Ensembl chr 1:163,001,875...163,071,508
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G |
Myo7atnd/Hubr |
myosin VIIA; ENU induced tornado mutant, Hubr |
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IAGP |
DNA:nonsense mutation:cds |
RGD |
PMID:15965244 |
RGD:1581470 |
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G |
Fmr1 |
FMRP translational regulator 1 |
|
IMP |
DNA:deletion:intron 7, exon 8: |
RGD |
PMID:27465362 |
RGD:38548926 |
NCBI chr X:154,684,924...154,722,369
Ensembl chr X:154,684,935...154,722,314
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G |
Fmr1em1Sage |
FMRP translational regulator 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
DNA:deletion:intron 7, exon 8: |
RGD |
PMID:27465362 |
RGD:38548926 |
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G |
Cacna1c |
calcium voltage-gated channel subunit alpha1 C |
|
IMP |
compared to wild-type female compared to wide-type male |
RGD |
PMID:30902660, PMID:29739816 |
RGD:42724472, RGD:42724471 |
NCBI chr 4:150,635,808...151,270,790
Ensembl chr 4:150,641,066...150,829,913
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G |
Cacna1cem1Sage |
calcium voltage-gated channel subunit alpha1 C; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs |
|
IMP |
compared to wild-type female compared to wide-type male |
RGD |
PMID:30902660, PMID:29739816 |
RGD:42724472, RGD:42724471 |
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G |
Cd247 |
Cd247 molecule |
|
IMP |
|
RGD |
PMID:24343121 |
RGD:13442481 |
NCBI chr13:83,996,045...84,071,408
Ensembl chr13:83,996,080...84,071,400
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G |
Cd247em1Mcwi |
Cd247 molecule; zinc finger nuclease induced mutant 1, Medical College of Wisconsin |
|
IMP |
|
RGD |
PMID:24343121 |
RGD:13442481 |
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G |
Cacna1f |
calcium voltage-gated channel subunit alpha1 F |
|
IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:23425697 |
RGD:13782191 |
NCBI chr X:15,712,709...15,741,135
Ensembl chr X:15,712,713...15,741,103
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G |
Cacna1f csnb |
calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant |
|
IAGP |
DNA:mutation:cds: c.2941C>T (rat) |
RGD |
PMID:23425697 |
RGD:13782191 |
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G |
Unc5c |
unc-5 netrin receptor C |
|
IAGP |
|
RGD |
PMID:14993736 |
RGD:1302461 |
NCBI chr 2:247,045,813...247,397,483
Ensembl chr 2:247,248,407...247,397,483
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G |
Unc5ccvd |
unc-5 netrin receptor C; cerebellar vermis defect |
|
IAGP |
|
RGD |
PMID:14993736 |
RGD:1302461 |
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G |
Unc5chob |
unc-5 netrin receptor C; hobble mutant |
|
IAGP |
|
RGD |
PMID:14993736 |
RGD:1302461 |
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G |
Tyr |
tyrosinase |
|
IMP IAGP |
DNA:deletion:cds: DNA:missense mutation:exon:p.R299H |
RGD |
PMID:23409244, PMID:15760344 |
RGD:12792973, RGD:1599687 |
NCBI chr 1:151,012,598...151,106,802
Ensembl chr 1:151,012,598...151,106,802
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G |
Tyrem1Kyo |
tyrosinase; TALEN induced mutant1, Kyo |
|
IMP |
|
RGD |
PMID:23409244 |
RGD:12792973 |
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G |
Esr2 |
estrogen receptor 2 |
|
IMP |
|
RGD |
PMID:28520870, PMID:29580824 |
RGD:38548924, RGD:38548925 |
NCBI chr 6:99,163,953...99,214,711
Ensembl chr 6:99,164,357...99,214,251
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G |
Esr2em1Soar |
estrogen receptor 2; ZFN induced mutant 1, Soar |
|
IMP |
|
RGD |
PMID:28520870, PMID:29580824 |
RGD:38548924, RGD:38548925 |
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|
G |
Kit |
KIT proto-oncogene receptor tyrosine kinase |
|
IMP |
|
RGD |
PMID:1912576 |
RGD:5133424 |
NCBI chr14:35,072,131...35,149,638
Ensembl chr14:35,072,108...35,149,610
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G |
KitWs |
KIT proto-oncogene receptor tyrosine kinase; mutant 1 |
|
IMP |
|
RGD |
PMID:1912576 |
RGD:5133424 |
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G |
Rag2 |
recombination activating 2 |
|
IMP |
|
RGD |
PMID:30206106 |
RGD:38508903 |
NCBI chr 3:91,191,837...91,200,134
Ensembl chr 3:91,191,837...91,200,134
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G |
Edaradd |
EDAR-associated death domain |
|
IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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|
G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
|
IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
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G |
Esr2 |
estrogen receptor 2 |
|
IMP |
compared to wild type |
RGD |
PMID:28520870 |
RGD:38548924 |
NCBI chr 6:99,163,953...99,214,711
Ensembl chr 6:99,164,357...99,214,251
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|
G |
Esr2em1Soar |
estrogen receptor 2; ZFN induced mutant 1, Soar |
|
IMP |
compared to wild type |
RGD |
PMID:28520870 |
RGD:38548924 |
|
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|
G |
Cyba |
cytochrome b-245 alpha chain |
|
IAGP |
DNA:deletion:splice junction: |
RGD |
PMID:19406829 |
RGD:11040542 |
NCBI chr19:55,249,634...55,257,824
Ensembl chr19:55,249,616...55,257,876
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G |
Cybam1Sdi |
cytochrome b-245 alpha chain;mutant 1,Sdi |
|
IAGP |
DNA:deletion:splice junction: |
RGD |
PMID:19406829 |
RGD:11040542 |
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G |
Kiss1 |
KiSS-1 metastasis-suppressor |
|
IMP |
|
RGD |
PMID:25582792 |
RGD:10059342 |
NCBI chr13:50,529,506...50,537,603
Ensembl chr13:50,529,510...50,535,389
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|
G |
Kiss1tm1Nips |
KiSS-1 metastasis-suppressor; targeted mutant 1, Nips |
|
IMP |
|
RGD |
PMID:25582792 |
RGD:10059342 |
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G |
Edaradd |
EDAR-associated death domain |
|
IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
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G |
EdaraddswhKyo |
EDAR-associated death domain;swh Kyo mutant |
|
IAGP |
DNA:missense mutation:exon:p.Pro153Ser(rat) |
RGD |
PMID:22013926 |
RGD:14398762 |
|
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G |
Csf1 |
colony stimulating factor 1 |
|
IAGP |
|
RGD |
PMID:12379742 |
RGD:628338 |
NCBI chr 2:210,522,370...210,550,546
Ensembl chr 2:210,522,375...210,550,560
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G |
Csf1tl |
colony stimulating factor 1; tooth less mutant |
|
IAGP |
|
RGD |
PMID:12379742 |
RGD:628338 |
|
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|
G |
Bdnf |
brain-derived neurotrophic factor |
|
IMP |
WT compared to heterozygous rats |
RGD |
PMID:23583595 |
RGD:38501054 |
NCBI chr 3:100,768,637...100,819,216
Ensembl chr 3:100,768,637...100,819,210
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|
G |
Bdnfem1Sage |
brain-derived neurotrophic factor; ZFN induced mutant 1, Sage |
severity |
IMP |
|
RGD |
PMID:23583595 |
RGD:38501054 |
|
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G |
Grm2 |
glutamate metabotropic receptor 2 |
|
IMP |
knockout compared to wild type |
RGD |
PMID:28700935 |
RGD:38501064 |
NCBI chr 8:115,344,999...115,358,628
Ensembl chr 8:115,344,999...115,358,046
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|
G |
Grm2em1 |
glutamate metabotropic receptor 2; endonuclease induced mutant 1 |
|
IMP |
KO compared to wild-type rats |
RGD |
PMID:28700935 |
RGD:38501064 |
|
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G |
Ednrb |
endothelin receptor type B |
|
IAGP |
|
RGD |
PMID:21915282, PMID:22132166 |
RGD:6480217, RGD:6480215 |
NCBI chr15:88,004,775...88,036,354
Ensembl chr15:88,006,977...88,036,354
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G |
Ednrbsl |
endothelin receptor type B, spotting lethal |
|
IAGP |
|
RGD |
PMID:21915282, PMID:22132166 |
RGD:6480217, RGD:6480215 |
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G |
Btg2 |
BTG anti-proliferation factor 2 |
|
IAGP |
|
RGD |
PMID:23817491 |
RGD:12802368 |
NCBI chr13:50,913,185...50,916,944
Ensembl chr13:50,913,180...50,916,982
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G |
Chi3l1 |
chitinase 3 like 1 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:51,022,844...51,030,797
Ensembl chr13:51,022,681...51,030,802
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G |
Chit1 |
chitinase 1 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:50,947,020...50,994,644
Ensembl chr13:50,974,872...50,994,643
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G |
Etnk2 |
ethanolamine kinase 2 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:50,481,178...50,498,991
Ensembl chr13:50,481,163...50,499,140
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G |
Fmod |
fibromodulin |
|
IAGP |
|
RGD |
PMID:23817491 |
RGD:12802368 |
NCBI chr13:50,874,886...50,885,503
Ensembl chr13:50,873,605...50,885,563
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|
G |
Gpr37l1 |
G protein-coupled receptor 37-like 1 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:51,985,698...51,992,547
Ensembl chr13:51,985,684...51,992,693
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G |
Ipo9 |
importin 9 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:52,203,384...52,256,196
Ensembl chr13:52,207,435...52,256,196
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|
G |
Lepr |
leptin receptor |
sexual_dimorphism treatment |
IAGP |
compared to BN compared to ad lib fed rats |
RGD |
PMID:20159938, PMID:11500530 |
RGD:7365117, RGD:628581 |
NCBI chr 5:120,503,475...120,682,281
Ensembl chr 5:120,564,645...120,682,221
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|
G |
Leprfa |
leptin receptor; fa mutant |
sexual_dimorphism treatment |
IAGP |
compared to BN compared to ad lib fed rats |
RGD |
PMID:20159938, PMID:11500530 |
RGD:7365117, RGD:628581 |
|
|
G |
Lgr6 |
leucine-rich repeat-containing G protein-coupled receptor 6 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:51,811,904...51,931,193
Ensembl chr13:51,815,215...51,930,972
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G |
Mybph |
myosin binding protein H |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:51,034,228...51,041,903
Ensembl chr13:51,034,256...51,041,902
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|
G |
Nr4a1 |
nuclear receptor subfamily 4, group A, member 1 |
|
IMP |
|
RGD |
PMID:24722447 |
RGD:12910103 |
NCBI chr 7:142,899,358...142,920,216
Ensembl chr 7:142,905,758...142,920,216
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|
G |
Optc |
opticin |
|
IAGP |
|
RGD |
PMID:23817491 |
RGD:12802368 |
NCBI chr13:50,735,509...50,748,908
Ensembl chr13:50,735,599...50,746,354
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|
G |
Plekha6 |
pleckstrin homology domain containing A6 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:50,555,454...50,582,236
Ensembl chr13:50,555,454...50,578,720
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|
G |
Prelp |
proline and arginine rich end leucine rich repeat protein |
|
IAGP |
|
RGD |
PMID:23817491 |
RGD:12802368 |
NCBI chr13:50,749,526...50,773,934
Ensembl chr13:50,749,514...50,761,355
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G |
Ptprv |
protein tyrosine phosphatase, receptor type, V |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:51,935,239...51,956,262
Ensembl chr13:51,935,243...51,955,735
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|
G |
Ren |
renin |
|
IAGP |
|
RGD |
PMID:23817491 |
RGD:12802368 |
NCBI chr13:50,502,724...50,513,953
Ensembl chr13:50,502,724...50,514,151
|
|
G |
Rnpep |
arginyl aminopeptidase |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:52,092,863...52,124,006
Ensembl chr13:52,092,859...52,111,363
|
|
G |
Sox13 |
SRY-box transcription factor 13 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:50,434,702...50,479,118
Ensembl chr13:50,434,702...50,479,657
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|
G |
Syt2 |
synaptotagmin 2 |
|
IAGP |
|
RGD |
PMID:23460292 |
RGD:12802369 |
NCBI chr13:51,569,248...51,577,824
Ensembl chr13:51,534,025...51,578,052
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G |
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