Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730409E04Rik |
T |
A |
4: 126,505,475 (GRCm39) |
M1K |
probably null |
Het |
5730507C01Rik |
A |
C |
12: 18,581,967 (GRCm39) |
R119S |
possibly damaging |
Het |
Abca1 |
T |
A |
4: 53,090,251 (GRCm39) |
|
probably null |
Het |
Aff1 |
G |
A |
5: 103,988,923 (GRCm39) |
G830D |
probably damaging |
Het |
AI987944 |
T |
C |
7: 41,023,873 (GRCm39) |
T369A |
possibly damaging |
Het |
Aoah |
A |
G |
13: 21,184,283 (GRCm39) |
|
probably null |
Het |
Arhgap40 |
C |
G |
2: 158,381,190 (GRCm39) |
C349W |
probably damaging |
Het |
Atic |
T |
A |
1: 71,615,286 (GRCm39) |
D438E |
probably benign |
Het |
Barhl2 |
A |
T |
5: 106,601,365 (GRCm39) |
M338K |
probably benign |
Het |
Btd |
T |
C |
14: 31,388,747 (GRCm39) |
V156A |
probably damaging |
Het |
Catspere2 |
A |
G |
1: 177,874,552 (GRCm39) |
K140E |
unknown |
Het |
Ccdc82 |
T |
C |
9: 13,262,397 (GRCm39) |
V319A |
probably damaging |
Het |
Celsr1 |
G |
T |
15: 85,915,263 (GRCm39) |
N903K |
probably damaging |
Het |
Cenpf |
T |
A |
1: 189,389,968 (GRCm39) |
N1288I |
probably damaging |
Het |
Ciao1 |
G |
A |
2: 127,086,857 (GRCm39) |
T252I |
probably benign |
Het |
Cma2 |
T |
C |
14: 56,210,573 (GRCm39) |
C87R |
probably damaging |
Het |
Cops7a |
T |
A |
6: 124,939,401 (GRCm39) |
R83W |
probably damaging |
Het |
Cxcr6 |
A |
T |
9: 123,639,613 (GRCm39) |
M205L |
possibly damaging |
Het |
Dcc |
A |
G |
18: 71,553,409 (GRCm39) |
L749P |
probably benign |
Het |
Dync1i2 |
C |
T |
2: 71,081,323 (GRCm39) |
T484I |
possibly damaging |
Het |
Epas1 |
A |
T |
17: 87,136,455 (GRCm39) |
K742N |
probably damaging |
Het |
Evc2 |
A |
G |
5: 37,506,094 (GRCm39) |
T138A |
probably benign |
Het |
F5 |
T |
C |
1: 164,035,457 (GRCm39) |
I1877T |
probably damaging |
Het |
Fat1 |
T |
G |
8: 45,406,201 (GRCm39) |
V984G |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,034,928 (GRCm39) |
V2860D |
probably damaging |
Het |
Foxn4 |
C |
T |
5: 114,394,955 (GRCm39) |
R324Q |
probably benign |
Het |
Gapdhs |
C |
T |
7: 30,436,427 (GRCm39) |
R120H |
probably damaging |
Het |
Gcnt3 |
T |
C |
9: 69,941,659 (GRCm39) |
D303G |
probably benign |
Het |
Gng11 |
A |
T |
6: 4,008,066 (GRCm39) |
Y43F |
probably benign |
Het |
Hectd4 |
A |
C |
5: 121,455,308 (GRCm39) |
M651L |
probably benign |
Het |
Ifngr2 |
T |
A |
16: 91,357,484 (GRCm39) |
Y200N |
probably benign |
Het |
Iqgap3 |
T |
C |
3: 88,005,708 (GRCm39) |
V512A |
probably benign |
Het |
Kdm2a |
A |
C |
19: 4,378,240 (GRCm39) |
D187E |
probably damaging |
Het |
Klhl8 |
A |
G |
5: 104,019,911 (GRCm39) |
V370A |
probably damaging |
Het |
Kmt2a |
G |
A |
9: 44,747,967 (GRCm39) |
|
probably benign |
Het |
Krt12 |
C |
A |
11: 99,311,650 (GRCm39) |
V184F |
probably benign |
Het |
Lrrc8c |
A |
T |
5: 105,754,623 (GRCm39) |
I133F |
probably benign |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Map1a |
C |
G |
2: 121,136,889 (GRCm39) |
S2568R |
possibly damaging |
Het |
Mbnl1 |
C |
A |
3: 60,532,593 (GRCm39) |
Q301K |
probably damaging |
Het |
Med12l |
A |
T |
3: 59,001,038 (GRCm39) |
K724N |
probably damaging |
Het |
Mroh2a |
A |
C |
1: 88,169,340 (GRCm39) |
I672L |
probably benign |
Het |
Mybph |
C |
T |
1: 134,121,374 (GRCm39) |
P45S |
probably benign |
Het |
Myo15a |
T |
A |
11: 60,392,527 (GRCm39) |
S2157T |
probably damaging |
Het |
Or14j2 |
G |
T |
17: 37,886,164 (GRCm39) |
T50K |
probably damaging |
Het |
Or1ab2 |
T |
C |
8: 72,863,623 (GRCm39) |
V71A |
probably benign |
Het |
Or2t35 |
T |
A |
14: 14,407,880 (GRCm38) |
Y217* |
probably null |
Het |
Or5h25 |
T |
C |
16: 58,930,967 (GRCm39) |
E2G |
probably benign |
Het |
Otogl |
A |
G |
10: 107,634,218 (GRCm39) |
I1419T |
possibly damaging |
Het |
Ovol1 |
A |
T |
19: 5,601,667 (GRCm39) |
F118L |
probably damaging |
Het |
Pak5 |
T |
C |
2: 135,958,680 (GRCm39) |
D136G |
probably damaging |
Het |
Pik3r2 |
T |
C |
8: 71,223,250 (GRCm39) |
Y417C |
probably damaging |
Het |
Ppp2r2a |
T |
C |
14: 67,254,052 (GRCm39) |
N372S |
probably benign |
Het |
Prss30 |
G |
T |
17: 24,191,806 (GRCm39) |
N238K |
possibly damaging |
Het |
Prss33 |
C |
A |
17: 24,053,785 (GRCm39) |
|
probably null |
Het |
Ptpn4 |
T |
C |
1: 119,692,788 (GRCm39) |
E187G |
probably damaging |
Het |
Ptprg |
A |
T |
14: 12,207,357 (GRCm38) |
N100I |
probably damaging |
Het |
Rbpms2 |
T |
C |
9: 65,558,324 (GRCm39) |
V130A |
probably benign |
Het |
Rdh7 |
A |
T |
10: 127,724,481 (GRCm39) |
M1K |
probably null |
Het |
Rtp3 |
A |
C |
9: 110,815,751 (GRCm39) |
S205A |
probably benign |
Het |
Ryr3 |
G |
T |
2: 112,539,618 (GRCm39) |
D3207E |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,313,803 (GRCm39) |
T1972S |
probably benign |
Het |
Scnn1b |
T |
C |
7: 121,501,551 (GRCm39) |
V122A |
probably benign |
Het |
Slc15a4 |
A |
G |
5: 127,686,043 (GRCm39) |
L213S |
probably damaging |
Het |
Slc27a5 |
T |
A |
7: 12,725,173 (GRCm39) |
I425F |
probably damaging |
Het |
Tcf25 |
T |
A |
8: 124,108,289 (GRCm39) |
S115T |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,172,613 (GRCm39) |
L1883P |
possibly damaging |
Het |
Trim21 |
T |
A |
7: 102,211,105 (GRCm39) |
R205* |
probably null |
Het |
Ttc23 |
G |
T |
7: 67,375,069 (GRCm39) |
|
probably null |
Het |
Tut7 |
T |
C |
13: 59,947,717 (GRCm39) |
E466G |
possibly damaging |
Het |
Unc13d |
T |
C |
11: 115,959,499 (GRCm39) |
K658R |
probably null |
Het |
Vmn1r43 |
A |
G |
6: 89,846,572 (GRCm39) |
F305L |
possibly damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,024,551 (GRCm39) |
C677S |
probably benign |
Het |
Wnt5a |
T |
C |
14: 28,240,300 (GRCm39) |
M150T |
probably benign |
Het |
Ythdc1 |
G |
A |
5: 86,975,981 (GRCm39) |
|
probably null |
Het |
Zdbf2 |
A |
T |
1: 63,343,408 (GRCm39) |
R596* |
probably null |
Het |
|
Other mutations in Spata31d1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01525:Spata31d1b
|
APN |
13 |
59,860,280 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02317:Spata31d1b
|
APN |
13 |
59,865,854 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02885:Spata31d1b
|
APN |
13 |
59,866,941 (GRCm39) |
utr 3 prime |
probably benign |
|
R0017:Spata31d1b
|
UTSW |
13 |
59,863,883 (GRCm39) |
missense |
probably benign |
|
R0071:Spata31d1b
|
UTSW |
13 |
59,863,163 (GRCm39) |
missense |
probably benign |
0.26 |
R0071:Spata31d1b
|
UTSW |
13 |
59,863,163 (GRCm39) |
missense |
probably benign |
0.26 |
R0595:Spata31d1b
|
UTSW |
13 |
59,864,091 (GRCm39) |
missense |
probably benign |
0.09 |
R0961:Spata31d1b
|
UTSW |
13 |
59,865,618 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1054:Spata31d1b
|
UTSW |
13 |
59,865,332 (GRCm39) |
missense |
probably damaging |
0.96 |
R1124:Spata31d1b
|
UTSW |
13 |
59,864,468 (GRCm39) |
missense |
probably benign |
|
R1338:Spata31d1b
|
UTSW |
13 |
59,865,975 (GRCm39) |
frame shift |
probably null |
|
R1539:Spata31d1b
|
UTSW |
13 |
59,863,733 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1688:Spata31d1b
|
UTSW |
13 |
59,863,274 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1776:Spata31d1b
|
UTSW |
13 |
59,864,381 (GRCm39) |
missense |
probably benign |
|
R1793:Spata31d1b
|
UTSW |
13 |
59,863,779 (GRCm39) |
missense |
probably benign |
|
R1838:Spata31d1b
|
UTSW |
13 |
59,865,279 (GRCm39) |
missense |
probably benign |
0.00 |
R1838:Spata31d1b
|
UTSW |
13 |
59,863,671 (GRCm39) |
missense |
probably benign |
|
R1861:Spata31d1b
|
UTSW |
13 |
59,865,150 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1903:Spata31d1b
|
UTSW |
13 |
59,865,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R1940:Spata31d1b
|
UTSW |
13 |
59,865,835 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1994:Spata31d1b
|
UTSW |
13 |
59,864,194 (GRCm39) |
missense |
probably benign |
|
R1995:Spata31d1b
|
UTSW |
13 |
59,864,194 (GRCm39) |
missense |
probably benign |
|
R2407:Spata31d1b
|
UTSW |
13 |
59,864,660 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3692:Spata31d1b
|
UTSW |
13 |
59,865,705 (GRCm39) |
missense |
probably benign |
0.03 |
R4576:Spata31d1b
|
UTSW |
13 |
59,864,675 (GRCm39) |
missense |
probably damaging |
0.98 |
R4734:Spata31d1b
|
UTSW |
13 |
59,866,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Spata31d1b
|
UTSW |
13 |
59,864,426 (GRCm39) |
missense |
probably damaging |
0.98 |
R4749:Spata31d1b
|
UTSW |
13 |
59,866,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Spata31d1b
|
UTSW |
13 |
59,863,535 (GRCm39) |
missense |
probably benign |
0.32 |
R4808:Spata31d1b
|
UTSW |
13 |
59,863,535 (GRCm39) |
missense |
probably benign |
0.32 |
R4844:Spata31d1b
|
UTSW |
13 |
59,866,169 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4942:Spata31d1b
|
UTSW |
13 |
59,864,917 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4953:Spata31d1b
|
UTSW |
13 |
59,864,097 (GRCm39) |
missense |
probably damaging |
0.96 |
R5093:Spata31d1b
|
UTSW |
13 |
59,863,838 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5169:Spata31d1b
|
UTSW |
13 |
59,864,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Spata31d1b
|
UTSW |
13 |
59,866,032 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5386:Spata31d1b
|
UTSW |
13 |
59,866,866 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5502:Spata31d1b
|
UTSW |
13 |
59,864,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R5751:Spata31d1b
|
UTSW |
13 |
59,866,787 (GRCm39) |
missense |
probably benign |
0.03 |
R6054:Spata31d1b
|
UTSW |
13 |
59,863,464 (GRCm39) |
missense |
probably benign |
|
R6433:Spata31d1b
|
UTSW |
13 |
59,864,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R6571:Spata31d1b
|
UTSW |
13 |
59,865,269 (GRCm39) |
missense |
probably benign |
|
R6980:Spata31d1b
|
UTSW |
13 |
59,863,236 (GRCm39) |
missense |
probably benign |
0.26 |
R7047:Spata31d1b
|
UTSW |
13 |
59,860,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Spata31d1b
|
UTSW |
13 |
59,863,955 (GRCm39) |
missense |
probably benign |
|
R7147:Spata31d1b
|
UTSW |
13 |
59,866,028 (GRCm39) |
missense |
probably benign |
0.28 |
R7273:Spata31d1b
|
UTSW |
13 |
59,865,446 (GRCm39) |
missense |
probably benign |
|
R7359:Spata31d1b
|
UTSW |
13 |
59,860,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R7457:Spata31d1b
|
UTSW |
13 |
59,864,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R7469:Spata31d1b
|
UTSW |
13 |
59,863,278 (GRCm39) |
missense |
probably benign |
0.04 |
R7519:Spata31d1b
|
UTSW |
13 |
59,864,726 (GRCm39) |
missense |
probably benign |
0.43 |
R7548:Spata31d1b
|
UTSW |
13 |
59,864,468 (GRCm39) |
missense |
probably benign |
|
R7586:Spata31d1b
|
UTSW |
13 |
59,866,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7657:Spata31d1b
|
UTSW |
13 |
59,863,577 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7778:Spata31d1b
|
UTSW |
13 |
59,865,047 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7824:Spata31d1b
|
UTSW |
13 |
59,865,047 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7989:Spata31d1b
|
UTSW |
13 |
59,866,182 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8078:Spata31d1b
|
UTSW |
13 |
59,863,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R8176:Spata31d1b
|
UTSW |
13 |
59,865,117 (GRCm39) |
missense |
probably benign |
|
R8530:Spata31d1b
|
UTSW |
13 |
59,864,964 (GRCm39) |
missense |
unknown |
|
R8776:Spata31d1b
|
UTSW |
13 |
59,863,283 (GRCm39) |
missense |
probably benign |
0.00 |
R8776-TAIL:Spata31d1b
|
UTSW |
13 |
59,863,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9385:Spata31d1b
|
UTSW |
13 |
59,863,403 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Spata31d1b
|
UTSW |
13 |
59,863,467 (GRCm39) |
missense |
probably benign |
0.08 |
R9522:Spata31d1b
|
UTSW |
13 |
59,864,780 (GRCm39) |
missense |
probably benign |
0.00 |
R9786:Spata31d1b
|
UTSW |
13 |
59,866,155 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9789:Spata31d1b
|
UTSW |
13 |
59,860,196 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Spata31d1b
|
UTSW |
13 |
59,866,674 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Spata31d1b
|
UTSW |
13 |
59,863,265 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Spata31d1b
|
UTSW |
13 |
59,860,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|