Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,203,369 (GRCm39) |
T403A |
probably damaging |
Het |
Acat3 |
T |
A |
17: 13,147,493 (GRCm39) |
R175* |
probably null |
Het |
Adam1b |
C |
A |
5: 121,639,104 (GRCm39) |
C647F |
probably damaging |
Het |
Adam28 |
T |
C |
14: 68,876,659 (GRCm39) |
N197S |
possibly damaging |
Het |
Adcy2 |
C |
T |
13: 68,837,380 (GRCm39) |
|
probably null |
Het |
Adcy5 |
A |
T |
16: 35,069,310 (GRCm39) |
N426I |
probably damaging |
Het |
Adgre1 |
T |
C |
17: 57,748,299 (GRCm39) |
S500P |
probably benign |
Het |
Aloxe3 |
A |
G |
11: 69,020,911 (GRCm39) |
Y212C |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,562,942 (GRCm39) |
S180P |
probably damaging |
Het |
Arhgap20 |
C |
T |
9: 51,760,626 (GRCm39) |
R790W |
probably damaging |
Het |
Atp8b4 |
C |
A |
2: 126,203,702 (GRCm39) |
A757S |
possibly damaging |
Het |
Begain |
G |
A |
12: 109,001,249 (GRCm39) |
|
probably benign |
Het |
Ccdc141 |
T |
C |
2: 76,842,009 (GRCm39) |
E1474G |
probably benign |
Het |
Ccdc88b |
A |
G |
19: 6,831,477 (GRCm39) |
|
probably benign |
Het |
Ccnk |
A |
G |
12: 108,161,333 (GRCm39) |
T195A |
probably damaging |
Het |
Cd55b |
C |
A |
1: 130,341,842 (GRCm39) |
C265F |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,707,105 (GRCm39) |
H1196R |
probably benign |
Het |
Cenpt |
T |
C |
8: 106,575,646 (GRCm39) |
S190G |
possibly damaging |
Het |
Chd8 |
T |
C |
14: 52,442,340 (GRCm39) |
S2077G |
probably benign |
Het |
Col6a5 |
G |
A |
9: 105,742,032 (GRCm39) |
H2296Y |
probably benign |
Het |
Cxxc4 |
C |
A |
3: 133,946,414 (GRCm39) |
H332N |
probably damaging |
Het |
Cyp24a1 |
T |
C |
2: 170,338,661 (GRCm39) |
I12V |
probably benign |
Het |
Cyp3a57 |
T |
A |
5: 145,318,111 (GRCm39) |
L364Q |
probably damaging |
Het |
Ddi2 |
T |
C |
4: 141,440,837 (GRCm39) |
I47V |
probably benign |
Het |
Ddx5 |
A |
T |
11: 106,675,723 (GRCm39) |
D322E |
probably benign |
Het |
Dhx40 |
A |
G |
11: 86,680,123 (GRCm39) |
C405R |
possibly damaging |
Het |
Emc1 |
T |
C |
4: 139,087,796 (GRCm39) |
F100S |
probably damaging |
Het |
Exoc2 |
T |
C |
13: 31,090,480 (GRCm39) |
|
probably benign |
Het |
Gm10110 |
A |
T |
14: 90,135,272 (GRCm39) |
|
noncoding transcript |
Het |
Gm17332 |
T |
C |
11: 31,132,386 (GRCm39) |
H26R |
possibly damaging |
Het |
Gna12 |
T |
C |
5: 140,748,367 (GRCm39) |
N183S |
probably benign |
Het |
Gpx6 |
A |
G |
13: 21,496,497 (GRCm39) |
N24D |
probably benign |
Het |
Gsdma3 |
C |
T |
11: 98,520,684 (GRCm39) |
A105V |
probably benign |
Het |
Hsd3b5 |
T |
C |
3: 98,527,044 (GRCm39) |
Y134C |
probably benign |
Het |
Ifi213 |
T |
C |
1: 173,417,166 (GRCm39) |
I415M |
probably damaging |
Het |
Ints9 |
C |
A |
14: 65,253,979 (GRCm39) |
P278T |
probably damaging |
Het |
Krt79 |
C |
T |
15: 101,846,373 (GRCm39) |
E192K |
possibly damaging |
Het |
Lrrk2 |
A |
G |
15: 91,567,337 (GRCm39) |
N132S |
probably benign |
Het |
Ltn1 |
T |
A |
16: 87,213,152 (GRCm39) |
K470* |
probably null |
Het |
Magi2 |
A |
T |
5: 20,670,825 (GRCm39) |
T163S |
probably damaging |
Het |
Mcm9 |
A |
G |
10: 53,417,649 (GRCm39) |
M18T |
probably damaging |
Het |
Med12l |
A |
G |
3: 58,975,740 (GRCm39) |
T212A |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,058,012 (GRCm39) |
L829P |
possibly damaging |
Het |
Mgme1 |
T |
A |
2: 144,121,407 (GRCm39) |
C288S |
probably benign |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Myh7 |
T |
C |
14: 55,210,637 (GRCm39) |
N1725S |
possibly damaging |
Het |
Naa80 |
G |
A |
9: 107,460,216 (GRCm39) |
R37H |
possibly damaging |
Het |
Nme4 |
A |
T |
17: 26,311,071 (GRCm39) |
W165R |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,196,649 (GRCm39) |
D1128E |
probably benign |
Het |
Or2t48 |
A |
T |
11: 58,420,199 (GRCm39) |
Y204* |
probably null |
Het |
Or5ae2 |
T |
C |
7: 84,505,756 (GRCm39) |
Y60H |
probably damaging |
Het |
Pcdh1 |
T |
C |
18: 38,332,538 (GRCm39) |
D155G |
possibly damaging |
Het |
Pex12 |
A |
T |
11: 83,188,648 (GRCm39) |
S116T |
probably damaging |
Het |
Plekhh1 |
C |
T |
12: 79,125,731 (GRCm39) |
|
probably benign |
Het |
Plekhh3 |
A |
G |
11: 101,054,426 (GRCm39) |
|
probably benign |
Het |
Pnpt1 |
T |
C |
11: 29,104,342 (GRCm39) |
M572T |
possibly damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,765,719 (GRCm39) |
R667G |
probably benign |
Het |
Rbpms2 |
ACTGCTGCTGCTGCTGC |
ACTGCTGCTGCTGCTGCTGC |
9: 65,558,948 (GRCm39) |
|
probably benign |
Het |
Rgs14 |
T |
C |
13: 55,530,651 (GRCm39) |
|
probably benign |
Het |
Rhbdf2 |
A |
T |
11: 116,491,017 (GRCm39) |
V645E |
possibly damaging |
Het |
Robo3 |
A |
G |
9: 37,333,623 (GRCm39) |
V696A |
probably benign |
Het |
Sall1 |
A |
G |
8: 89,755,344 (GRCm39) |
F1212L |
possibly damaging |
Het |
Sdc4 |
T |
C |
2: 164,270,932 (GRCm39) |
E109G |
probably benign |
Het |
Serpind1 |
G |
T |
16: 17,160,856 (GRCm39) |
R462L |
probably damaging |
Het |
Smad9 |
CTTT |
CTT |
3: 54,696,600 (GRCm39) |
|
probably benign |
Het |
Sstr4 |
C |
A |
2: 148,237,453 (GRCm39) |
N21K |
probably benign |
Het |
Tap1 |
C |
T |
17: 34,407,083 (GRCm39) |
A77V |
possibly damaging |
Het |
Thap4 |
T |
C |
1: 93,678,009 (GRCm39) |
E259G |
probably benign |
Het |
Thra |
A |
G |
11: 98,646,969 (GRCm39) |
N30S |
probably benign |
Het |
Tmem207 |
A |
T |
16: 26,343,571 (GRCm39) |
V27E |
possibly damaging |
Het |
Top3a |
A |
G |
11: 60,644,714 (GRCm39) |
V305A |
probably damaging |
Het |
Trim59 |
A |
T |
3: 68,944,971 (GRCm39) |
I123K |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,691,839 (GRCm39) |
|
probably benign |
Het |
Ubac1 |
T |
A |
2: 25,897,750 (GRCm39) |
E290V |
possibly damaging |
Het |
Unc13b |
T |
C |
4: 43,258,308 (GRCm39) |
|
probably benign |
Het |
Uri1 |
A |
T |
7: 37,666,814 (GRCm39) |
D206E |
probably benign |
Het |
Utp4 |
A |
G |
8: 107,640,086 (GRCm39) |
H465R |
probably benign |
Het |
Vmn1r39 |
T |
C |
6: 66,782,217 (GRCm39) |
|
probably null |
Het |
Vps39 |
A |
T |
2: 120,155,878 (GRCm39) |
L514H |
probably damaging |
Het |
Vps72 |
G |
A |
3: 95,026,529 (GRCm39) |
R158Q |
possibly damaging |
Het |
Wdr59 |
T |
C |
8: 112,211,972 (GRCm39) |
D366G |
probably benign |
Het |
Zfp366 |
C |
A |
13: 99,365,000 (GRCm39) |
Q54K |
probably damaging |
Het |
Zfp523 |
T |
A |
17: 28,413,967 (GRCm39) |
I34N |
probably damaging |
Het |
Zfp974 |
G |
A |
7: 27,609,781 (GRCm39) |
P648L |
possibly damaging |
Het |
|
Other mutations in Uvssa |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00849:Uvssa
|
APN |
5 |
33,566,192 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02136:Uvssa
|
APN |
5 |
33,549,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02339:Uvssa
|
APN |
5 |
33,572,193 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03096:Uvssa
|
APN |
5 |
33,568,268 (GRCm39) |
missense |
probably benign |
0.29 |
IGL03130:Uvssa
|
APN |
5 |
33,549,189 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL03248:Uvssa
|
APN |
5 |
33,549,160 (GRCm39) |
missense |
probably damaging |
1.00 |
blinkered
|
UTSW |
5 |
33,547,096 (GRCm39) |
missense |
probably benign |
0.04 |
lowbrow
|
UTSW |
5 |
33,571,228 (GRCm39) |
splice site |
probably benign |
|
BB001:Uvssa
|
UTSW |
5 |
33,568,295 (GRCm39) |
missense |
probably damaging |
1.00 |
BB011:Uvssa
|
UTSW |
5 |
33,568,295 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Uvssa
|
UTSW |
5 |
33,559,914 (GRCm39) |
missense |
possibly damaging |
0.50 |
PIT4142001:Uvssa
|
UTSW |
5 |
33,549,428 (GRCm39) |
missense |
probably benign |
0.05 |
R0326:Uvssa
|
UTSW |
5 |
33,566,191 (GRCm39) |
missense |
probably benign |
0.01 |
R0443:Uvssa
|
UTSW |
5 |
33,546,168 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1438:Uvssa
|
UTSW |
5 |
33,571,228 (GRCm39) |
splice site |
probably benign |
|
R1474:Uvssa
|
UTSW |
5 |
33,546,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Uvssa
|
UTSW |
5 |
33,571,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R1522:Uvssa
|
UTSW |
5 |
33,545,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Uvssa
|
UTSW |
5 |
33,549,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Uvssa
|
UTSW |
5 |
33,547,162 (GRCm39) |
missense |
probably damaging |
0.99 |
R3405:Uvssa
|
UTSW |
5 |
33,547,162 (GRCm39) |
missense |
probably damaging |
0.99 |
R3406:Uvssa
|
UTSW |
5 |
33,547,162 (GRCm39) |
missense |
probably damaging |
0.99 |
R3892:Uvssa
|
UTSW |
5 |
33,547,096 (GRCm39) |
missense |
probably benign |
0.04 |
R4624:Uvssa
|
UTSW |
5 |
33,547,300 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4898:Uvssa
|
UTSW |
5 |
33,571,257 (GRCm39) |
nonsense |
probably null |
|
R5413:Uvssa
|
UTSW |
5 |
33,568,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R5921:Uvssa
|
UTSW |
5 |
33,547,096 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Uvssa
|
UTSW |
5 |
33,547,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Uvssa
|
UTSW |
5 |
33,566,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R6566:Uvssa
|
UTSW |
5 |
33,549,520 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6884:Uvssa
|
UTSW |
5 |
33,566,461 (GRCm39) |
splice site |
probably null |
|
R7924:Uvssa
|
UTSW |
5 |
33,568,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Uvssa
|
UTSW |
5 |
33,566,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8196:Uvssa
|
UTSW |
5 |
33,568,311 (GRCm39) |
missense |
probably benign |
0.07 |
R8252:Uvssa
|
UTSW |
5 |
33,549,523 (GRCm39) |
missense |
probably benign |
0.00 |
R9104:Uvssa
|
UTSW |
5 |
33,571,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R9208:Uvssa
|
UTSW |
5 |
33,571,419 (GRCm39) |
critical splice donor site |
probably null |
|
R9276:Uvssa
|
UTSW |
5 |
33,572,180 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9320:Uvssa
|
UTSW |
5 |
33,547,365 (GRCm39) |
missense |
probably benign |
0.20 |
R9658:Uvssa
|
UTSW |
5 |
33,568,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R9723:Uvssa
|
UTSW |
5 |
33,547,382 (GRCm39) |
critical splice donor site |
probably null |
|
|