Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap21 |
G |
A |
2: 20,885,524 (GRCm39) |
S551L |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,914,571 (GRCm39) |
S1734P |
probably benign |
Het |
Btnl2 |
T |
A |
17: 34,582,288 (GRCm39) |
S285T |
possibly damaging |
Het |
Cadm4 |
A |
G |
7: 24,202,970 (GRCm39) |
D364G |
possibly damaging |
Het |
Card6 |
T |
A |
15: 5,128,347 (GRCm39) |
K1016N |
possibly damaging |
Het |
Cdh2 |
G |
T |
18: 16,757,341 (GRCm39) |
N692K |
probably benign |
Het |
Cep76 |
G |
T |
18: 67,774,219 (GRCm39) |
S9* |
probably null |
Het |
Cklf |
T |
C |
8: 104,977,729 (GRCm39) |
|
probably null |
Het |
Ctsa |
T |
C |
2: 164,681,152 (GRCm39) |
*475R |
probably null |
Het |
Dapk1 |
A |
C |
13: 60,873,715 (GRCm39) |
D406A |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,748,647 (GRCm39) |
V443D |
probably damaging |
Het |
Dph5 |
C |
T |
3: 115,693,399 (GRCm39) |
Q106* |
probably null |
Het |
Drg2 |
C |
T |
11: 60,353,026 (GRCm39) |
R220* |
probably null |
Het |
Efcab8 |
A |
T |
2: 153,652,832 (GRCm39) |
Q509L |
unknown |
Het |
Efs |
C |
T |
14: 55,154,907 (GRCm39) |
S444N |
probably benign |
Het |
Evl |
T |
C |
12: 108,614,723 (GRCm39) |
V58A |
probably damaging |
Het |
Garin3 |
A |
G |
11: 46,295,730 (GRCm39) |
N34S |
|
Het |
Gbe1 |
G |
A |
16: 70,230,500 (GRCm39) |
R166H |
probably damaging |
Het |
Gcc1 |
T |
C |
6: 28,418,785 (GRCm39) |
E516G |
probably damaging |
Het |
Ghr |
T |
C |
15: 3,487,439 (GRCm39) |
T15A |
probably benign |
Het |
Gnb4 |
G |
A |
3: 32,650,480 (GRCm39) |
T50M |
probably damaging |
Het |
Grik3 |
T |
C |
4: 125,550,190 (GRCm39) |
|
probably null |
Het |
Gstk1 |
T |
C |
6: 42,224,686 (GRCm39) |
Y135H |
probably benign |
Het |
Gucy2c |
T |
A |
6: 136,685,404 (GRCm39) |
I846F |
probably damaging |
Het |
Itga7 |
A |
G |
10: 128,778,835 (GRCm39) |
T321A |
probably benign |
Het |
Jakmip1 |
A |
T |
5: 37,332,524 (GRCm39) |
N1068I |
probably damaging |
Het |
Krt36 |
A |
G |
11: 99,994,966 (GRCm39) |
I202T |
possibly damaging |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Mast2 |
A |
G |
4: 116,170,070 (GRCm39) |
L741P |
probably damaging |
Het |
Mctp2 |
T |
C |
7: 71,776,935 (GRCm39) |
N720S |
possibly damaging |
Het |
Mmp9 |
A |
T |
2: 164,790,956 (GRCm39) |
K115* |
probably null |
Het |
Mtf2 |
C |
T |
5: 108,228,743 (GRCm39) |
R20* |
probably null |
Het |
Mycbp2 |
T |
G |
14: 103,376,851 (GRCm39) |
Q3810P |
probably benign |
Het |
Myom2 |
A |
T |
8: 15,158,454 (GRCm39) |
H802L |
probably benign |
Het |
Naa25 |
A |
G |
5: 121,545,276 (GRCm39) |
N27D |
probably damaging |
Het |
Necab2 |
T |
C |
8: 120,181,103 (GRCm39) |
F126L |
probably damaging |
Het |
Nisch |
C |
G |
14: 30,896,608 (GRCm39) |
|
probably benign |
Het |
Nsd2 |
T |
A |
5: 34,000,938 (GRCm39) |
S152T |
probably damaging |
Het |
Ntsr1 |
T |
C |
2: 180,180,483 (GRCm39) |
L263P |
probably damaging |
Het |
Nup210 |
A |
G |
6: 90,995,759 (GRCm39) |
V922A |
possibly damaging |
Het |
Or12d17 |
T |
A |
17: 37,777,994 (GRCm39) |
M299K |
probably benign |
Het |
Or5b105 |
T |
A |
19: 13,080,417 (GRCm39) |
I84F |
probably benign |
Het |
Or5d45 |
A |
C |
2: 88,153,425 (GRCm39) |
I208S |
probably benign |
Het |
Pccb |
C |
A |
9: 100,909,137 (GRCm39) |
C144F |
probably damaging |
Het |
Pi16 |
C |
A |
17: 29,538,208 (GRCm39) |
P7Q |
possibly damaging |
Het |
Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
Prdm1 |
A |
G |
10: 44,334,478 (GRCm39) |
V16A |
probably benign |
Het |
Prr5 |
A |
C |
15: 84,649,933 (GRCm39) |
Y219S |
probably damaging |
Het |
Psme4 |
A |
G |
11: 30,824,245 (GRCm39) |
D1743G |
probably benign |
Het |
Rad21l |
G |
T |
2: 151,497,045 (GRCm39) |
D356E |
probably benign |
Het |
Retreg2 |
C |
A |
1: 75,123,185 (GRCm39) |
P319Q |
possibly damaging |
Het |
Robo2 |
T |
C |
16: 73,770,059 (GRCm39) |
Y559C |
probably damaging |
Het |
Ror1 |
T |
C |
4: 100,298,564 (GRCm39) |
Y646H |
probably damaging |
Het |
Rrp15 |
A |
G |
1: 186,481,373 (GRCm39) |
S45P |
probably benign |
Het |
Sacs |
G |
C |
14: 61,429,652 (GRCm39) |
K570N |
probably benign |
Het |
Serpinb8 |
C |
T |
1: 107,534,723 (GRCm39) |
Q265* |
probably null |
Het |
Sgo2b |
T |
C |
8: 64,380,318 (GRCm39) |
E838G |
probably damaging |
Het |
Slc2a12 |
G |
A |
10: 22,540,568 (GRCm39) |
R141K |
probably damaging |
Het |
Strc |
G |
T |
2: 121,208,219 (GRCm39) |
T384N |
probably benign |
Het |
Tcaf2 |
T |
C |
6: 42,606,033 (GRCm39) |
S547G |
possibly damaging |
Het |
Tekt5 |
T |
C |
16: 10,200,792 (GRCm39) |
N243S |
possibly damaging |
Het |
Tgm3 |
A |
G |
2: 129,883,819 (GRCm39) |
I492M |
probably benign |
Het |
Tgm7 |
G |
A |
2: 120,934,421 (GRCm39) |
T157I |
probably benign |
Het |
Trnp1 |
C |
A |
4: 133,225,350 (GRCm39) |
R140L |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,609,777 (GRCm39) |
V15797A |
probably damaging |
Het |
Ugp2 |
A |
T |
11: 21,283,762 (GRCm39) |
S102T |
probably benign |
Het |
Vav2 |
A |
T |
2: 27,172,299 (GRCm39) |
|
probably null |
Het |
Vmn1r202 |
T |
A |
13: 22,686,241 (GRCm39) |
I59F |
probably damaging |
Het |
Yju2b |
T |
C |
8: 84,988,411 (GRCm39) |
E72G |
probably damaging |
Het |
Zfp109 |
T |
C |
7: 23,928,570 (GRCm39) |
T288A |
probably benign |
Het |
Zscan12 |
T |
A |
13: 21,553,374 (GRCm39) |
H399Q |
probably damaging |
Het |
|
Other mutations in Rars1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01568:Rars1
|
APN |
11 |
35,716,808 (GRCm39) |
splice site |
probably benign |
|
IGL01672:Rars1
|
APN |
11 |
35,699,380 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01721:Rars1
|
APN |
11 |
35,719,491 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01887:Rars1
|
APN |
11 |
35,716,822 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02605:Rars1
|
APN |
11 |
35,715,353 (GRCm39) |
splice site |
probably benign |
|
IGL03296:Rars1
|
APN |
11 |
35,707,523 (GRCm39) |
nonsense |
probably null |
|
IGL03354:Rars1
|
APN |
11 |
35,715,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R0410:Rars1
|
UTSW |
11 |
35,716,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1193:Rars1
|
UTSW |
11 |
35,700,153 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1222:Rars1
|
UTSW |
11 |
35,700,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Rars1
|
UTSW |
11 |
35,700,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Rars1
|
UTSW |
11 |
35,711,921 (GRCm39) |
critical splice donor site |
probably null |
|
R1768:Rars1
|
UTSW |
11 |
35,700,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R1800:Rars1
|
UTSW |
11 |
35,716,822 (GRCm39) |
missense |
probably benign |
0.03 |
R2055:Rars1
|
UTSW |
11 |
35,717,410 (GRCm39) |
splice site |
probably benign |
|
R2294:Rars1
|
UTSW |
11 |
35,708,363 (GRCm39) |
splice site |
probably benign |
|
R4281:Rars1
|
UTSW |
11 |
35,712,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Rars1
|
UTSW |
11 |
35,699,973 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4898:Rars1
|
UTSW |
11 |
35,699,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R5522:Rars1
|
UTSW |
11 |
35,708,195 (GRCm39) |
nonsense |
probably null |
|
R5907:Rars1
|
UTSW |
11 |
35,719,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Rars1
|
UTSW |
11 |
35,717,374 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6289:Rars1
|
UTSW |
11 |
35,716,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6550:Rars1
|
UTSW |
11 |
35,724,010 (GRCm39) |
missense |
probably benign |
0.00 |
R6889:Rars1
|
UTSW |
11 |
35,699,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Rars1
|
UTSW |
11 |
35,725,281 (GRCm39) |
missense |
probably benign |
0.00 |
R7682:Rars1
|
UTSW |
11 |
35,719,579 (GRCm39) |
missense |
probably benign |
0.00 |
R7808:Rars1
|
UTSW |
11 |
35,719,534 (GRCm39) |
missense |
probably benign |
|
R7856:Rars1
|
UTSW |
11 |
35,699,412 (GRCm39) |
missense |
probably benign |
0.09 |
R8029:Rars1
|
UTSW |
11 |
35,711,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R9094:Rars1
|
UTSW |
11 |
35,718,182 (GRCm39) |
splice site |
probably benign |
|
R9096:Rars1
|
UTSW |
11 |
35,718,256 (GRCm39) |
missense |
probably benign |
0.00 |
R9300:Rars1
|
UTSW |
11 |
35,706,488 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rars1
|
UTSW |
11 |
35,716,936 (GRCm39) |
critical splice acceptor site |
probably null |
|
|