Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438A13Rik |
T |
TTATTATGATTATTAC |
3: 37,050,760 |
|
probably benign |
Het |
A030005L19Rik |
TGTGGCTGC |
TGTGGCTGCGGTGGCTGC |
1: 82,913,580 |
|
probably benign |
Het |
Acap3 |
GCATCCTGGGCTGCT |
GCATCCTGGGCTGCTACATCCTGGGCTGCT |
4: 155,905,092 |
|
probably benign |
Het |
Alpk3 |
GAGAAGGCAC |
G |
7: 81,092,414 |
|
probably benign |
Het |
Cox7a2l |
GGA |
GGATGGGGA |
17: 83,502,722 |
|
probably benign |
Het |
Cpne1 |
TCCAC |
TC |
2: 156,073,510 |
|
probably benign |
Het |
Cyb5r4 |
GA |
GATGTGACAGACACACTGCCCAGGTA |
9: 87,040,447 |
|
probably null |
Het |
Cyb5r4 |
CCCAGGGATGTGACAGACACACTG |
CCCAGGGATGTGACAGACACACTGACCAGGGATGTGACAGACACACTG |
9: 87,040,417 |
|
probably benign |
Het |
Defb22 |
TGCGGCA |
TGCGGCAGGGCTGGCCTTTGCGGCA |
2: 152,485,832 |
|
probably benign |
Het |
Dnmt1 |
GGGCGGAGCACAGTTCCTACCTCGTT |
GGGCGGAGCACAGTTCCTACCTCGTTTTGGTGGCGGAGCACAGTTCCTACCTCGTT |
9: 20,910,120 |
|
probably null |
Het |
Fam71e1 |
GGGTCTGAGGGAGGA |
GGGTCTGAGGGAGGAAGGCTGGATCCTGGATACCTAGGTCTGAGGGAGGA |
7: 44,500,523 |
|
probably null |
Het |
Fbrsl1 |
GTG |
GTGCGTGTGCTGTTG |
5: 110,378,149 |
|
probably benign |
Het |
Frem3 |
GATC |
GATCATC |
8: 80,615,238 |
|
probably benign |
Het |
Gabre |
GCTC |
GCTCTGTCTC |
X: 72,270,762 |
|
probably benign |
Het |
Gm15155 |
CAA |
CAACAACAAA |
X: 156,345,640 |
|
probably null |
Het |
Krtap28-10 |
CACCACAGC |
CACCACAGCCACAGCGACCACAGC |
1: 83,042,282 |
|
probably benign |
Het |
Mamld1 |
AGC |
AGCGGC |
X: 71,118,835 |
|
probably benign |
Het |
Map1a |
GCTCCAGCTCCA |
GCTCCAGCTCCAGCTCCAGCTCCAGCTCCATCTCCAGCTCCA |
2: 121,306,307 |
|
probably benign |
Het |
Map1a |
CCAGCTCCAGCTCCA |
CCAGCTCCAGCTCCAGCTACAGCTCCAGATACAGCTCCAGCTCCA |
2: 121,306,304 |
|
probably benign |
Het |
Neu1 |
TCTTCTA |
T |
17: 34,932,558 |
|
probably benign |
Het |
Nolc1 |
CAGCAGC |
CAGCAGCAGAAGCAGC |
19: 46,081,371 |
|
probably benign |
Het |
Olfr850 |
G |
T |
9: 19,477,632 |
A206E |
possibly damaging |
Het |
Pdik1l |
TTTT |
TTTTGTTTTTGGTTT |
4: 134,279,374 |
|
probably null |
Het |
Rassf6 |
CACTCATGGTCCTGTAGAGCAATGGGGATTC |
CACTCATGGTCCTGTAGAGCAATGGGGATTCTGCCTGACTCATGGTCCTGTAGAGCAATGGGGATTC |
5: 90,608,912 |
|
probably benign |
Het |
Rassf6 |
ATGGTCCTGTAGAGCAATGGGGATTC |
ATGGTCCTGTAGAGCAATGGGGATTCTGCCTCACTCGTGGTCCTGTAGAGCAATGGGGATTC |
5: 90,608,917 |
|
probably benign |
Het |
Rassf6 |
CTGTAGAGCAATGGGGATTC |
CTGTAGAGCAATGGGGATTCTGCCTCACTCATGGTCATGTAGAGCAATGGGGATTC |
5: 90,608,923 |
|
probably benign |
Het |
Rpgrip1 |
AGAGGAGGA |
AGA |
14: 52,149,526 |
|
probably benign |
Het |
Rprd2 |
AGAGCCTGTGGTGCTCGCAGGGGAGGCTGTGGTGCTC |
AGAGGCTGTGGTGCTC |
3: 95,766,320 |
|
probably benign |
Het |
Rsf1 |
CG |
CGAGG |
7: 97,579,908 |
|
probably benign |
Het |
Rtbdn |
GCGGC |
GCGGCATCGGC |
8: 84,956,175 |
|
probably benign |
Het |
Smarca2 |
CA |
CACCAAGA |
19: 26,631,011 |
|
probably benign |
Het |
Tfeb |
GCA |
GCACCA |
17: 47,786,097 |
|
probably benign |
Het |
Tfeb |
CAG |
CAGTAG |
17: 47,786,098 |
|
probably null |
Het |
Tmed6 |
AGC |
AGCTGGC |
8: 107,061,596 |
|
probably null |
Het |
Tomm5 |
TCTTCCGC |
TCTTCCGCAGCTTCCGC |
4: 45,107,976 |
|
probably benign |
Het |
Trappc9 |
TG |
TGATGCTGCTGCTGCGG |
15: 72,801,298 |
|
probably benign |
Het |
|
Other mutations in Igf1r |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00742:Igf1r
|
APN |
7 |
68,190,023 (GRCm38) |
missense |
probably benign |
|
IGL00837:Igf1r
|
APN |
7 |
68,201,352 (GRCm38) |
splice site |
probably benign |
|
IGL01515:Igf1r
|
APN |
7 |
68,207,452 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01572:Igf1r
|
APN |
7 |
68,193,441 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02100:Igf1r
|
APN |
7 |
68,189,958 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02506:Igf1r
|
APN |
7 |
68,193,396 (GRCm38) |
missense |
probably benign |
|
IGL02672:Igf1r
|
APN |
7 |
68,190,033 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02701:Igf1r
|
APN |
7 |
68,201,249 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02742:Igf1r
|
APN |
7 |
68,189,991 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL03073:Igf1r
|
APN |
7 |
68,215,043 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03257:Igf1r
|
APN |
7 |
68,214,940 (GRCm38) |
missense |
probably damaging |
1.00 |
Frufru
|
UTSW |
7 |
68,004,163 (GRCm38) |
missense |
probably damaging |
1.00 |
Hungarian
|
UTSW |
7 |
68,214,997 (GRCm38) |
missense |
probably damaging |
1.00 |
Mimi
|
UTSW |
7 |
68,195,026 (GRCm38) |
missense |
possibly damaging |
0.67 |
Piroshka
|
UTSW |
7 |
68,207,336 (GRCm38) |
nonsense |
probably null |
|
Romanian
|
UTSW |
7 |
68,004,137 (GRCm38) |
missense |
possibly damaging |
0.94 |
Sublime
|
UTSW |
7 |
68,004,179 (GRCm38) |
missense |
probably damaging |
1.00 |
Toy
|
UTSW |
7 |
68,003,972 (GRCm38) |
missense |
probably damaging |
1.00 |
BB009:Igf1r
|
UTSW |
7 |
68,212,054 (GRCm38) |
missense |
possibly damaging |
0.88 |
BB019:Igf1r
|
UTSW |
7 |
68,212,054 (GRCm38) |
missense |
possibly damaging |
0.88 |
FR4548:Igf1r
|
UTSW |
7 |
68,226,186 (GRCm38) |
small insertion |
probably benign |
|
FR4737:Igf1r
|
UTSW |
7 |
68,226,181 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Igf1r
|
UTSW |
7 |
68,226,186 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Igf1r
|
UTSW |
7 |
68,226,181 (GRCm38) |
small insertion |
probably benign |
|
PIT4445001:Igf1r
|
UTSW |
7 |
68,207,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R0003:Igf1r
|
UTSW |
7 |
68,165,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R0184:Igf1r
|
UTSW |
7 |
68,226,193 (GRCm38) |
missense |
possibly damaging |
0.84 |
R0538:Igf1r
|
UTSW |
7 |
68,207,826 (GRCm38) |
missense |
probably damaging |
1.00 |
R0632:Igf1r
|
UTSW |
7 |
68,165,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R0727:Igf1r
|
UTSW |
7 |
68,212,158 (GRCm38) |
critical splice donor site |
probably null |
|
R0750:Igf1r
|
UTSW |
7 |
68,212,091 (GRCm38) |
missense |
probably damaging |
0.99 |
R1104:Igf1r
|
UTSW |
7 |
68,195,026 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1169:Igf1r
|
UTSW |
7 |
68,165,127 (GRCm38) |
missense |
probably benign |
0.00 |
R1348:Igf1r
|
UTSW |
7 |
68,218,468 (GRCm38) |
missense |
probably damaging |
1.00 |
R1471:Igf1r
|
UTSW |
7 |
68,003,837 (GRCm38) |
missense |
probably damaging |
0.98 |
R1580:Igf1r
|
UTSW |
7 |
68,207,869 (GRCm38) |
missense |
probably benign |
|
R1745:Igf1r
|
UTSW |
7 |
68,169,913 (GRCm38) |
missense |
probably damaging |
1.00 |
R1772:Igf1r
|
UTSW |
7 |
68,195,074 (GRCm38) |
missense |
probably benign |
0.03 |
R1789:Igf1r
|
UTSW |
7 |
68,214,933 (GRCm38) |
nonsense |
probably null |
|
R1823:Igf1r
|
UTSW |
7 |
68,194,981 (GRCm38) |
missense |
possibly damaging |
0.77 |
R1902:Igf1r
|
UTSW |
7 |
68,201,249 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1962:Igf1r
|
UTSW |
7 |
68,207,275 (GRCm38) |
missense |
probably damaging |
0.99 |
R2179:Igf1r
|
UTSW |
7 |
68,003,950 (GRCm38) |
missense |
probably damaging |
0.99 |
R2215:Igf1r
|
UTSW |
7 |
68,165,234 (GRCm38) |
missense |
probably benign |
|
R2221:Igf1r
|
UTSW |
7 |
68,201,962 (GRCm38) |
missense |
probably damaging |
1.00 |
R2233:Igf1r
|
UTSW |
7 |
68,212,080 (GRCm38) |
missense |
probably damaging |
1.00 |
R2234:Igf1r
|
UTSW |
7 |
68,212,080 (GRCm38) |
missense |
probably damaging |
1.00 |
R2235:Igf1r
|
UTSW |
7 |
68,212,080 (GRCm38) |
missense |
probably damaging |
1.00 |
R3023:Igf1r
|
UTSW |
7 |
68,183,399 (GRCm38) |
missense |
probably benign |
0.00 |
R4044:Igf1r
|
UTSW |
7 |
68,190,062 (GRCm38) |
missense |
possibly damaging |
0.83 |
R4226:Igf1r
|
UTSW |
7 |
68,195,078 (GRCm38) |
nonsense |
probably null |
|
R4387:Igf1r
|
UTSW |
7 |
68,170,009 (GRCm38) |
missense |
probably benign |
|
R4388:Igf1r
|
UTSW |
7 |
68,170,009 (GRCm38) |
missense |
probably benign |
|
R4728:Igf1r
|
UTSW |
7 |
68,189,624 (GRCm38) |
missense |
probably damaging |
1.00 |
R4781:Igf1r
|
UTSW |
7 |
68,165,199 (GRCm38) |
missense |
possibly damaging |
0.75 |
R5254:Igf1r
|
UTSW |
7 |
68,207,319 (GRCm38) |
missense |
probably damaging |
0.99 |
R5278:Igf1r
|
UTSW |
7 |
68,193,418 (GRCm38) |
missense |
possibly damaging |
0.78 |
R5510:Igf1r
|
UTSW |
7 |
68,193,359 (GRCm38) |
missense |
probably benign |
0.19 |
R5522:Igf1r
|
UTSW |
7 |
68,183,510 (GRCm38) |
missense |
probably damaging |
0.96 |
R5527:Igf1r
|
UTSW |
7 |
68,207,821 (GRCm38) |
missense |
probably damaging |
1.00 |
R5761:Igf1r
|
UTSW |
7 |
68,207,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R5849:Igf1r
|
UTSW |
7 |
68,190,033 (GRCm38) |
missense |
probably benign |
|
R6189:Igf1r
|
UTSW |
7 |
68,207,336 (GRCm38) |
nonsense |
probably null |
|
R6262:Igf1r
|
UTSW |
7 |
68,003,972 (GRCm38) |
missense |
probably damaging |
1.00 |
R6285:Igf1r
|
UTSW |
7 |
68,004,137 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6318:Igf1r
|
UTSW |
7 |
68,165,233 (GRCm38) |
missense |
probably benign |
0.02 |
R6365:Igf1r
|
UTSW |
7 |
68,190,050 (GRCm38) |
missense |
probably benign |
0.26 |
R6377:Igf1r
|
UTSW |
7 |
68,201,250 (GRCm38) |
missense |
probably benign |
0.00 |
R6831:Igf1r
|
UTSW |
7 |
68,207,319 (GRCm38) |
missense |
possibly damaging |
0.75 |
R6848:Igf1r
|
UTSW |
7 |
68,004,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R6902:Igf1r
|
UTSW |
7 |
68,004,163 (GRCm38) |
missense |
probably damaging |
1.00 |
R7193:Igf1r
|
UTSW |
7 |
68,187,157 (GRCm38) |
missense |
probably damaging |
1.00 |
R7373:Igf1r
|
UTSW |
7 |
68,195,078 (GRCm38) |
nonsense |
probably null |
|
R7442:Igf1r
|
UTSW |
7 |
68,173,278 (GRCm38) |
missense |
probably damaging |
1.00 |
R7903:Igf1r
|
UTSW |
7 |
68,184,752 (GRCm38) |
missense |
probably damaging |
1.00 |
R7923:Igf1r
|
UTSW |
7 |
68,190,101 (GRCm38) |
missense |
probably damaging |
1.00 |
R7932:Igf1r
|
UTSW |
7 |
68,212,054 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8368:Igf1r
|
UTSW |
7 |
68,187,048 (GRCm38) |
missense |
probably benign |
0.03 |
R8458:Igf1r
|
UTSW |
7 |
68,195,629 (GRCm38) |
missense |
probably benign |
|
R8539:Igf1r
|
UTSW |
7 |
68,003,848 (GRCm38) |
missense |
probably benign |
0.06 |
R8704:Igf1r
|
UTSW |
7 |
68,170,054 (GRCm38) |
splice site |
probably benign |
|
R8746:Igf1r
|
UTSW |
7 |
68,214,997 (GRCm38) |
missense |
probably damaging |
1.00 |
R8829:Igf1r
|
UTSW |
7 |
68,226,021 (GRCm38) |
missense |
probably damaging |
1.00 |
R8832:Igf1r
|
UTSW |
7 |
68,226,021 (GRCm38) |
missense |
probably damaging |
1.00 |
R8859:Igf1r
|
UTSW |
7 |
68,183,463 (GRCm38) |
missense |
possibly damaging |
0.75 |
R9057:Igf1r
|
UTSW |
7 |
68,183,438 (GRCm38) |
missense |
probably damaging |
1.00 |
R9243:Igf1r
|
UTSW |
7 |
68,212,027 (GRCm38) |
missense |
probably benign |
0.11 |
R9342:Igf1r
|
UTSW |
7 |
68,194,998 (GRCm38) |
missense |
probably benign |
0.00 |
R9412:Igf1r
|
UTSW |
7 |
68,207,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R9525:Igf1r
|
UTSW |
7 |
68,214,934 (GRCm38) |
missense |
probably damaging |
1.00 |
R9727:Igf1r
|
UTSW |
7 |
68,207,806 (GRCm38) |
missense |
probably damaging |
1.00 |
R9730:Igf1r
|
UTSW |
7 |
68,189,675 (GRCm38) |
missense |
probably damaging |
1.00 |
R9779:Igf1r
|
UTSW |
7 |
68,004,317 (GRCm38) |
missense |
probably damaging |
1.00 |
RF025:Igf1r
|
UTSW |
7 |
68,226,179 (GRCm38) |
small insertion |
probably benign |
|
RF032:Igf1r
|
UTSW |
7 |
68,226,179 (GRCm38) |
small insertion |
probably benign |
|
RF037:Igf1r
|
UTSW |
7 |
68,226,176 (GRCm38) |
small insertion |
probably benign |
|
RF039:Igf1r
|
UTSW |
7 |
68,226,176 (GRCm38) |
small insertion |
probably benign |
|
RF044:Igf1r
|
UTSW |
7 |
68,226,179 (GRCm38) |
small insertion |
probably benign |
|
Z1186:Igf1r
|
UTSW |
7 |
68,226,168 (GRCm38) |
small insertion |
probably benign |
|
Z1186:Igf1r
|
UTSW |
7 |
68,226,182 (GRCm38) |
small insertion |
probably benign |
|
Z1186:Igf1r
|
UTSW |
7 |
68,226,180 (GRCm38) |
small insertion |
probably benign |
|
Z1186:Igf1r
|
UTSW |
7 |
68,226,174 (GRCm38) |
small insertion |
probably benign |
|
Z1186:Igf1r
|
UTSW |
7 |
68,226,169 (GRCm38) |
small insertion |
probably benign |
|
Z1191:Igf1r
|
UTSW |
7 |
68,226,170 (GRCm38) |
small insertion |
probably benign |
|
Z1191:Igf1r
|
UTSW |
7 |
68,226,169 (GRCm38) |
small insertion |
probably benign |
|
Z1191:Igf1r
|
UTSW |
7 |
68,226,173 (GRCm38) |
small insertion |
probably benign |
|
|