Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
A |
G |
16: 88,556,260 (GRCm39) |
Y158C |
probably damaging |
Het |
Abhd18 |
T |
A |
3: 40,885,331 (GRCm39) |
S239T |
possibly damaging |
Het |
Ankrd13b |
G |
A |
11: 77,368,552 (GRCm39) |
T56I |
probably benign |
Het |
Arhgef10l |
T |
A |
4: 140,291,582 (GRCm39) |
Q454L |
possibly damaging |
Het |
Atp1a2 |
T |
C |
1: 172,112,179 (GRCm39) |
E572G |
probably benign |
Het |
Cdk5rap2 |
T |
C |
4: 70,282,257 (GRCm39) |
H164R |
probably benign |
Het |
Clca4b |
A |
G |
3: 144,631,917 (GRCm39) |
M196T |
probably benign |
Het |
Cnbd1 |
T |
G |
4: 19,055,045 (GRCm39) |
K127T |
probably benign |
Het |
Cog3 |
A |
T |
14: 75,979,836 (GRCm39) |
V165E |
probably damaging |
Het |
Crim1 |
G |
A |
17: 78,654,686 (GRCm39) |
R654H |
probably benign |
Het |
Ctnnb1 |
G |
A |
9: 120,786,628 (GRCm39) |
V617I |
possibly damaging |
Het |
Dach1 |
T |
A |
14: 98,406,129 (GRCm39) |
Q206L |
probably damaging |
Het |
Dhx30 |
C |
T |
9: 109,929,974 (GRCm39) |
V41I |
probably benign |
Het |
Dnase2a |
T |
C |
8: 85,636,410 (GRCm39) |
L176P |
probably damaging |
Het |
Dpp10 |
T |
C |
1: 123,360,739 (GRCm39) |
D262G |
probably damaging |
Het |
Dsel |
T |
A |
1: 111,789,385 (GRCm39) |
E383D |
probably damaging |
Het |
Flt1 |
T |
A |
5: 147,576,253 (GRCm39) |
Y585F |
probably damaging |
Het |
Fubp1 |
T |
A |
3: 151,926,190 (GRCm39) |
I304N |
probably damaging |
Het |
Gab2 |
A |
G |
7: 96,948,337 (GRCm39) |
D309G |
probably damaging |
Het |
Gon4l |
T |
C |
3: 88,762,086 (GRCm39) |
V291A |
probably damaging |
Het |
Gpam |
C |
T |
19: 55,070,063 (GRCm39) |
V398M |
possibly damaging |
Het |
Grin3b |
C |
T |
10: 79,810,422 (GRCm39) |
R643C |
probably damaging |
Het |
Hdac3 |
T |
A |
18: 38,074,475 (GRCm39) |
H339L |
possibly damaging |
Het |
Hsdl2 |
A |
T |
4: 59,610,621 (GRCm39) |
Q326L |
unknown |
Het |
Insr |
T |
C |
8: 3,215,514 (GRCm39) |
|
probably benign |
Het |
Ivl |
T |
A |
3: 92,479,943 (GRCm39) |
T41S |
probably benign |
Het |
Lama4 |
C |
T |
10: 38,902,703 (GRCm39) |
P226S |
possibly damaging |
Het |
Lpin1 |
A |
G |
12: 16,613,621 (GRCm39) |
|
probably null |
Het |
Lrrc42 |
A |
T |
4: 107,104,721 (GRCm39) |
N81K |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,897,900 (GRCm39) |
H838Q |
probably damaging |
Het |
Mcmdc2 |
A |
G |
1: 9,990,806 (GRCm39) |
M314V |
possibly damaging |
Het |
Me3 |
A |
G |
7: 89,389,086 (GRCm39) |
E130G |
probably damaging |
Het |
Mpnd |
A |
G |
17: 56,316,405 (GRCm39) |
D28G |
possibly damaging |
Het |
Mtch2 |
G |
T |
2: 90,683,208 (GRCm39) |
E102* |
probably null |
Het |
Myh13 |
A |
T |
11: 67,254,011 (GRCm39) |
|
probably null |
Het |
Or10ag55-ps1 |
G |
A |
2: 87,114,978 (GRCm39) |
V115I |
probably benign |
Het |
Or5ae2 |
C |
A |
7: 84,506,497 (GRCm39) |
H309N |
probably benign |
Het |
Plch2 |
T |
A |
4: 155,074,192 (GRCm39) |
D891V |
probably damaging |
Het |
Ppfibp2 |
T |
C |
7: 107,327,957 (GRCm39) |
|
probably null |
Het |
Rag1 |
A |
G |
2: 101,473,009 (GRCm39) |
L711P |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,450,636 (GRCm39) |
Y4227* |
probably null |
Het |
Sec23ip |
C |
T |
7: 128,352,151 (GRCm39) |
H176Y |
probably benign |
Het |
Sema3a |
T |
C |
5: 13,523,487 (GRCm39) |
|
probably null |
Het |
Serpina10 |
C |
T |
12: 103,594,563 (GRCm39) |
G219R |
probably damaging |
Het |
Sp1 |
C |
T |
15: 102,318,118 (GRCm39) |
L546F |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,073,057 (GRCm39) |
N1256S |
probably benign |
Het |
Tbc1d5 |
G |
T |
17: 51,089,455 (GRCm39) |
|
probably benign |
Het |
Tns1 |
T |
C |
1: 73,964,765 (GRCm39) |
S33G |
probably benign |
Het |
Tpsab1 |
A |
G |
17: 25,564,445 (GRCm39) |
L3P |
possibly damaging |
Het |
Trgv3 |
A |
G |
13: 19,427,036 (GRCm39) |
T8A |
probably benign |
Het |
Vav2 |
A |
T |
2: 27,159,050 (GRCm39) |
|
probably benign |
Het |
Vmn1r44 |
T |
C |
6: 89,870,610 (GRCm39) |
S119P |
possibly damaging |
Het |
Vmn2r31 |
A |
G |
7: 7,387,699 (GRCm39) |
L624P |
probably damaging |
Het |
Vps33a |
A |
T |
5: 123,671,944 (GRCm39) |
W475R |
possibly damaging |
Het |
Xpnpep3 |
G |
T |
15: 81,311,795 (GRCm39) |
R167L |
possibly damaging |
Het |
Zfhx4 |
T |
A |
3: 5,463,918 (GRCm39) |
S1384T |
probably damaging |
Het |
Zfp3 |
G |
A |
11: 70,663,384 (GRCm39) |
E448K |
probably benign |
Het |
Zfp362 |
T |
A |
4: 128,679,769 (GRCm39) |
H299L |
probably damaging |
Het |
Zfp664 |
C |
T |
5: 124,962,827 (GRCm39) |
L74F |
possibly damaging |
Het |
Zfp808 |
A |
G |
13: 62,319,926 (GRCm39) |
Y385C |
probably damaging |
Het |
|
Other mutations in 1110002E22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0026:1110002E22Rik
|
UTSW |
3 |
137,772,566 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0047:1110002E22Rik
|
UTSW |
3 |
137,772,025 (GRCm39) |
missense |
probably damaging |
0.97 |
R0047:1110002E22Rik
|
UTSW |
3 |
137,772,025 (GRCm39) |
missense |
probably damaging |
0.97 |
R0102:1110002E22Rik
|
UTSW |
3 |
137,773,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:1110002E22Rik
|
UTSW |
3 |
137,773,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:1110002E22Rik
|
UTSW |
3 |
137,775,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:1110002E22Rik
|
UTSW |
3 |
137,771,595 (GRCm39) |
small deletion |
probably benign |
|
R0394:1110002E22Rik
|
UTSW |
3 |
137,773,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R0401:1110002E22Rik
|
UTSW |
3 |
137,776,067 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0496:1110002E22Rik
|
UTSW |
3 |
137,774,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:1110002E22Rik
|
UTSW |
3 |
137,774,704 (GRCm39) |
nonsense |
probably null |
|
R0711:1110002E22Rik
|
UTSW |
3 |
137,773,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R0883:1110002E22Rik
|
UTSW |
3 |
137,775,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:1110002E22Rik
|
UTSW |
3 |
137,775,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R0968:1110002E22Rik
|
UTSW |
3 |
137,772,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R1023:1110002E22Rik
|
UTSW |
3 |
137,772,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:1110002E22Rik
|
UTSW |
3 |
137,773,661 (GRCm39) |
missense |
probably benign |
0.20 |
R1472:1110002E22Rik
|
UTSW |
3 |
137,773,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1538:1110002E22Rik
|
UTSW |
3 |
137,771,162 (GRCm39) |
missense |
probably benign |
0.02 |
R1648:1110002E22Rik
|
UTSW |
3 |
137,775,181 (GRCm39) |
missense |
probably benign |
0.18 |
R1800:1110002E22Rik
|
UTSW |
3 |
137,772,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:1110002E22Rik
|
UTSW |
3 |
137,773,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R1974:1110002E22Rik
|
UTSW |
3 |
137,773,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:1110002E22Rik
|
UTSW |
3 |
137,771,419 (GRCm39) |
nonsense |
probably null |
|
R1991:1110002E22Rik
|
UTSW |
3 |
137,771,419 (GRCm39) |
nonsense |
probably null |
|
R2102:1110002E22Rik
|
UTSW |
3 |
137,770,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R2761:1110002E22Rik
|
UTSW |
3 |
137,773,541 (GRCm39) |
missense |
probably damaging |
0.99 |
R2899:1110002E22Rik
|
UTSW |
3 |
137,771,443 (GRCm39) |
missense |
probably benign |
0.00 |
R3618:1110002E22Rik
|
UTSW |
3 |
137,774,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R3904:1110002E22Rik
|
UTSW |
3 |
137,772,400 (GRCm39) |
missense |
probably benign |
0.15 |
R3955:1110002E22Rik
|
UTSW |
3 |
137,773,834 (GRCm39) |
missense |
probably benign |
0.00 |
R4520:1110002E22Rik
|
UTSW |
3 |
137,776,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R4619:1110002E22Rik
|
UTSW |
3 |
137,775,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R4736:1110002E22Rik
|
UTSW |
3 |
137,774,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R4752:1110002E22Rik
|
UTSW |
3 |
137,775,751 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4777:1110002E22Rik
|
UTSW |
3 |
137,771,503 (GRCm39) |
missense |
probably benign |
0.09 |
R4780:1110002E22Rik
|
UTSW |
3 |
137,771,131 (GRCm39) |
missense |
probably benign |
0.02 |
R4824:1110002E22Rik
|
UTSW |
3 |
137,771,437 (GRCm39) |
missense |
probably benign |
0.00 |
R4829:1110002E22Rik
|
UTSW |
3 |
137,774,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R4965:1110002E22Rik
|
UTSW |
3 |
137,775,433 (GRCm39) |
missense |
probably benign |
|
R5206:1110002E22Rik
|
UTSW |
3 |
137,772,272 (GRCm39) |
missense |
probably benign |
0.00 |
R5212:1110002E22Rik
|
UTSW |
3 |
137,771,611 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5373:1110002E22Rik
|
UTSW |
3 |
137,773,396 (GRCm39) |
missense |
probably benign |
|
R5374:1110002E22Rik
|
UTSW |
3 |
137,773,396 (GRCm39) |
missense |
probably benign |
|
R5506:1110002E22Rik
|
UTSW |
3 |
137,773,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R5528:1110002E22Rik
|
UTSW |
3 |
137,772,260 (GRCm39) |
missense |
probably benign |
|
R5536:1110002E22Rik
|
UTSW |
3 |
137,772,149 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5587:1110002E22Rik
|
UTSW |
3 |
137,771,170 (GRCm39) |
missense |
probably benign |
|
R5759:1110002E22Rik
|
UTSW |
3 |
137,774,419 (GRCm39) |
missense |
probably benign |
|
R5933:1110002E22Rik
|
UTSW |
3 |
137,776,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5957:1110002E22Rik
|
UTSW |
3 |
137,775,922 (GRCm39) |
missense |
probably benign |
|
R6092:1110002E22Rik
|
UTSW |
3 |
137,774,701 (GRCm39) |
missense |
probably benign |
0.02 |
R6305:1110002E22Rik
|
UTSW |
3 |
137,773,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R6457:1110002E22Rik
|
UTSW |
3 |
137,772,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R6469:1110002E22Rik
|
UTSW |
3 |
137,772,736 (GRCm39) |
missense |
probably damaging |
0.97 |
R6499:1110002E22Rik
|
UTSW |
3 |
137,774,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:1110002E22Rik
|
UTSW |
3 |
137,773,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R6580:1110002E22Rik
|
UTSW |
3 |
137,772,386 (GRCm39) |
missense |
probably benign |
0.00 |
R6693:1110002E22Rik
|
UTSW |
3 |
137,774,915 (GRCm39) |
missense |
probably benign |
0.00 |
R6751:1110002E22Rik
|
UTSW |
3 |
137,771,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:1110002E22Rik
|
UTSW |
3 |
137,770,930 (GRCm39) |
nonsense |
probably null |
|
R6920:1110002E22Rik
|
UTSW |
3 |
137,773,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:1110002E22Rik
|
UTSW |
3 |
137,771,272 (GRCm39) |
missense |
probably benign |
|
R7145:1110002E22Rik
|
UTSW |
3 |
137,775,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:1110002E22Rik
|
UTSW |
3 |
137,775,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:1110002E22Rik
|
UTSW |
3 |
137,771,237 (GRCm39) |
missense |
probably benign |
|
R7425:1110002E22Rik
|
UTSW |
3 |
137,771,456 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:1110002E22Rik
|
UTSW |
3 |
137,772,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:1110002E22Rik
|
UTSW |
3 |
137,774,044 (GRCm39) |
nonsense |
probably null |
|
R7663:1110002E22Rik
|
UTSW |
3 |
137,771,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R7743:1110002E22Rik
|
UTSW |
3 |
137,774,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:1110002E22Rik
|
UTSW |
3 |
137,775,362 (GRCm39) |
missense |
probably benign |
0.33 |
R8181:1110002E22Rik
|
UTSW |
3 |
137,774,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R8264:1110002E22Rik
|
UTSW |
3 |
137,773,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R8273:1110002E22Rik
|
UTSW |
3 |
137,772,211 (GRCm39) |
missense |
probably benign |
|
R8530:1110002E22Rik
|
UTSW |
3 |
137,774,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R8754:1110002E22Rik
|
UTSW |
3 |
137,771,798 (GRCm39) |
missense |
probably benign |
|
R8808:1110002E22Rik
|
UTSW |
3 |
137,775,874 (GRCm39) |
missense |
probably benign |
0.01 |
R8891:1110002E22Rik
|
UTSW |
3 |
137,772,520 (GRCm39) |
nonsense |
probably null |
|
R9026:1110002E22Rik
|
UTSW |
3 |
137,770,909 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9177:1110002E22Rik
|
UTSW |
3 |
137,775,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:1110002E22Rik
|
UTSW |
3 |
137,772,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:1110002E22Rik
|
UTSW |
3 |
137,772,464 (GRCm39) |
missense |
probably benign |
0.02 |
R9293:1110002E22Rik
|
UTSW |
3 |
137,771,839 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9307:1110002E22Rik
|
UTSW |
3 |
137,771,183 (GRCm39) |
missense |
probably benign |
0.04 |
R9439:1110002E22Rik
|
UTSW |
3 |
137,772,048 (GRCm39) |
missense |
probably benign |
0.00 |
R9509:1110002E22Rik
|
UTSW |
3 |
137,771,595 (GRCm39) |
small deletion |
probably benign |
|
R9582:1110002E22Rik
|
UTSW |
3 |
137,772,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R9599:1110002E22Rik
|
UTSW |
3 |
137,774,267 (GRCm39) |
missense |
probably benign |
0.16 |
R9613:1110002E22Rik
|
UTSW |
3 |
137,771,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R9670:1110002E22Rik
|
UTSW |
3 |
137,770,894 (GRCm39) |
missense |
probably benign |
|
X0003:1110002E22Rik
|
UTSW |
3 |
137,774,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|