Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acod1 |
T |
G |
14: 103,288,776 (GRCm39) |
D95E |
probably damaging |
Het |
Agpat4 |
A |
G |
17: 12,429,209 (GRCm39) |
T154A |
possibly damaging |
Het |
Ahnak2 |
A |
T |
12: 112,742,114 (GRCm39) |
S653T |
probably benign |
Het |
Aoc1l2 |
G |
A |
6: 48,909,620 (GRCm39) |
V622I |
probably benign |
Het |
Aox1 |
C |
T |
1: 58,388,263 (GRCm39) |
P1124S |
probably damaging |
Het |
Armh3 |
A |
G |
19: 45,928,882 (GRCm39) |
|
probably null |
Het |
Atp4a |
T |
C |
7: 30,419,461 (GRCm39) |
I637T |
probably damaging |
Het |
Atxn7 |
T |
A |
14: 14,100,467 (GRCm38) |
C718S |
probably damaging |
Het |
Btbd2 |
T |
A |
10: 80,479,390 (GRCm39) |
I516F |
probably damaging |
Het |
Card6 |
A |
G |
15: 5,134,820 (GRCm39) |
S128P |
probably benign |
Het |
Cat |
T |
C |
2: 103,287,203 (GRCm39) |
K476E |
probably benign |
Het |
Ccr9 |
A |
T |
9: 123,609,022 (GRCm39) |
T235S |
probably benign |
Het |
Cep55 |
T |
G |
19: 38,057,517 (GRCm39) |
|
probably null |
Het |
Clec2e |
A |
G |
6: 129,072,091 (GRCm39) |
F96S |
possibly damaging |
Het |
Clk2 |
G |
A |
3: 89,074,498 (GRCm39) |
V53I |
probably benign |
Het |
Clnk |
T |
C |
5: 38,925,484 (GRCm39) |
M106V |
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,808,523 (GRCm39) |
I842V |
unknown |
Het |
Csf1r |
A |
T |
18: 61,243,572 (GRCm39) |
N196I |
probably benign |
Het |
Dnaja4 |
A |
G |
9: 54,616,494 (GRCm39) |
I166V |
probably benign |
Het |
Dqx1 |
A |
G |
6: 83,038,013 (GRCm39) |
E467G |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,129,719 (GRCm39) |
T1760A |
probably benign |
Het |
Eea1 |
T |
C |
10: 95,864,301 (GRCm39) |
V940A |
probably benign |
Het |
Egr1 |
T |
A |
18: 34,996,598 (GRCm39) |
V460E |
probably damaging |
Het |
Eral1 |
A |
G |
11: 77,965,359 (GRCm39) |
I352T |
possibly damaging |
Het |
F2 |
T |
C |
2: 91,459,041 (GRCm39) |
H476R |
possibly damaging |
Het |
Fam83b |
A |
G |
9: 76,399,714 (GRCm39) |
V463A |
possibly damaging |
Het |
Fat1 |
T |
A |
8: 45,490,374 (GRCm39) |
L3762H |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,476,359 (GRCm39) |
S1802P |
probably damaging |
Het |
Fibp |
A |
T |
19: 5,514,202 (GRCm39) |
N296Y |
probably benign |
Het |
Figla |
A |
G |
6: 85,994,308 (GRCm39) |
M28V |
probably benign |
Het |
Foxd3 |
C |
A |
4: 99,545,362 (GRCm39) |
Y167* |
probably null |
Het |
Gm17019 |
T |
A |
5: 15,081,006 (GRCm39) |
H145L |
probably benign |
Het |
Gm48552 |
C |
T |
10: 81,226,269 (GRCm39) |
P18L |
probably damaging |
Het |
H2-Q6 |
A |
G |
17: 35,647,077 (GRCm39) |
N283S |
probably benign |
Het |
Hrh2 |
T |
A |
13: 54,368,058 (GRCm39) |
C11* |
probably null |
Het |
Hrnr |
G |
T |
3: 93,239,506 (GRCm39) |
G3248V |
unknown |
Het |
Iapp |
C |
A |
6: 142,249,122 (GRCm39) |
N58K |
possibly damaging |
Het |
Itga5 |
T |
C |
15: 103,258,184 (GRCm39) |
N837S |
probably benign |
Het |
Klhl35 |
C |
A |
7: 99,117,647 (GRCm39) |
H64N |
probably benign |
Het |
Lcor |
T |
C |
19: 41,572,106 (GRCm39) |
L287S |
probably benign |
Het |
Lrba |
T |
A |
3: 86,439,508 (GRCm39) |
V2015E |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,734,421 (GRCm39) |
I3276T |
probably benign |
Het |
Mlh3 |
G |
T |
12: 85,315,058 (GRCm39) |
T376K |
possibly damaging |
Het |
Muc21 |
G |
A |
17: 35,932,977 (GRCm39) |
T403I |
unknown |
Het |
Nbea |
A |
T |
3: 55,557,126 (GRCm39) |
H2550Q |
probably damaging |
Het |
Nid1 |
G |
A |
13: 13,663,630 (GRCm39) |
G763D |
probably damaging |
Het |
Ntf5 |
C |
A |
7: 45,065,243 (GRCm39) |
A125E |
probably damaging |
Het |
Obsl1 |
A |
T |
1: 75,480,167 (GRCm39) |
C460S |
probably benign |
Het |
Or1j19 |
A |
T |
2: 36,677,022 (GRCm39) |
I162F |
probably benign |
Het |
Or1s2 |
A |
T |
19: 13,758,650 (GRCm39) |
R223W |
probably damaging |
Het |
Or2g7 |
G |
A |
17: 38,378,566 (GRCm39) |
C168Y |
probably damaging |
Het |
Or2y10 |
T |
A |
11: 49,455,588 (GRCm39) |
I280N |
possibly damaging |
Het |
Or4b1b |
T |
A |
2: 90,126,975 (GRCm39) |
K77* |
probably null |
Het |
Or6c33 |
A |
G |
10: 129,853,050 (GRCm39) |
|
probably benign |
Het |
Or8d1b |
G |
A |
9: 38,887,490 (GRCm39) |
V173I |
probably benign |
Het |
Orai3 |
G |
A |
7: 127,372,743 (GRCm39) |
G130S |
unknown |
Het |
Pcdhb12 |
T |
G |
18: 37,568,977 (GRCm39) |
V41G |
probably damaging |
Het |
Plec |
A |
T |
15: 76,067,823 (GRCm39) |
L1194Q |
unknown |
Het |
Pml |
C |
A |
9: 58,127,456 (GRCm39) |
C763F |
probably damaging |
Het |
Prdm15 |
T |
A |
16: 97,619,473 (GRCm39) |
I318F |
probably benign |
Het |
Rcbtb2 |
C |
A |
14: 73,415,906 (GRCm39) |
T473N |
probably benign |
Het |
Sbno1 |
T |
A |
5: 124,512,729 (GRCm39) |
I1347F |
probably benign |
Het |
Secisbp2l |
C |
T |
2: 125,610,113 (GRCm39) |
D269N |
probably damaging |
Het |
Serpina9 |
A |
T |
12: 103,967,575 (GRCm39) |
F273L |
probably damaging |
Het |
Sgms2 |
T |
A |
3: 131,116,898 (GRCm39) |
Y319F |
probably benign |
Het |
Sgo2b |
A |
T |
8: 64,379,531 (GRCm39) |
H1100Q |
probably benign |
Het |
Sh3bp5l |
A |
T |
11: 58,236,754 (GRCm39) |
|
probably null |
Het |
Shh |
T |
G |
5: 28,671,664 (GRCm39) |
K33T |
probably benign |
Het |
Slc5a9 |
A |
G |
4: 111,747,371 (GRCm39) |
Y339H |
probably damaging |
Het |
Spice1 |
T |
A |
16: 44,190,864 (GRCm39) |
|
probably null |
Het |
Tbx2 |
A |
G |
11: 85,726,727 (GRCm39) |
E257G |
probably damaging |
Het |
Tenm2 |
G |
A |
11: 35,914,133 (GRCm39) |
T2468I |
possibly damaging |
Het |
Tmeff2 |
A |
T |
1: 51,018,575 (GRCm39) |
N186Y |
probably benign |
Het |
Tmem132c |
T |
C |
5: 127,631,760 (GRCm39) |
V673A |
possibly damaging |
Het |
Trappc11 |
G |
T |
8: 47,975,411 (GRCm39) |
T269K |
probably damaging |
Het |
Trpc6 |
T |
C |
9: 8,653,150 (GRCm39) |
F652S |
possibly damaging |
Het |
Trpv1 |
G |
T |
11: 73,145,048 (GRCm39) |
K711N |
probably benign |
Het |
Vcan |
G |
T |
13: 89,841,056 (GRCm39) |
P1496Q |
probably damaging |
Het |
Vmn1r192 |
G |
T |
13: 22,371,845 (GRCm39) |
A125E |
probably damaging |
Het |
Vti1b |
A |
T |
12: 79,211,720 (GRCm39) |
|
probably null |
Het |
Vwa3b |
A |
C |
1: 37,163,126 (GRCm39) |
D583A |
probably damaging |
Het |
Zfp638 |
T |
C |
6: 83,953,254 (GRCm39) |
S1120P |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,315,409 (GRCm39) |
F1356I |
probably benign |
Het |
|
Other mutations in D5Ertd579e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01433:D5Ertd579e
|
APN |
5 |
36,776,098 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01925:D5Ertd579e
|
APN |
5 |
36,771,628 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01933:D5Ertd579e
|
APN |
5 |
36,773,100 (GRCm39) |
missense |
probably benign |
|
IGL02164:D5Ertd579e
|
APN |
5 |
36,772,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02399:D5Ertd579e
|
APN |
5 |
36,773,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02896:D5Ertd579e
|
APN |
5 |
36,771,326 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03141:D5Ertd579e
|
APN |
5 |
36,770,621 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03235:D5Ertd579e
|
APN |
5 |
36,776,172 (GRCm39) |
splice site |
probably benign |
|
R0201:D5Ertd579e
|
UTSW |
5 |
36,773,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:D5Ertd579e
|
UTSW |
5 |
36,761,911 (GRCm39) |
missense |
probably benign |
0.12 |
R0830:D5Ertd579e
|
UTSW |
5 |
36,771,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R0926:D5Ertd579e
|
UTSW |
5 |
36,830,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1350:D5Ertd579e
|
UTSW |
5 |
36,771,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:D5Ertd579e
|
UTSW |
5 |
36,760,083 (GRCm39) |
missense |
probably benign |
|
R1672:D5Ertd579e
|
UTSW |
5 |
36,770,621 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1676:D5Ertd579e
|
UTSW |
5 |
36,773,453 (GRCm39) |
missense |
probably benign |
0.01 |
R1693:D5Ertd579e
|
UTSW |
5 |
36,771,441 (GRCm39) |
missense |
probably damaging |
0.98 |
R1698:D5Ertd579e
|
UTSW |
5 |
36,761,874 (GRCm39) |
missense |
probably benign |
|
R1868:D5Ertd579e
|
UTSW |
5 |
36,773,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R1909:D5Ertd579e
|
UTSW |
5 |
36,771,402 (GRCm39) |
missense |
probably benign |
0.21 |
R2034:D5Ertd579e
|
UTSW |
5 |
36,770,882 (GRCm39) |
nonsense |
probably null |
|
R2080:D5Ertd579e
|
UTSW |
5 |
36,773,550 (GRCm39) |
missense |
probably benign |
0.01 |
R2105:D5Ertd579e
|
UTSW |
5 |
36,770,793 (GRCm39) |
missense |
probably benign |
0.12 |
R2197:D5Ertd579e
|
UTSW |
5 |
36,772,137 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4212:D5Ertd579e
|
UTSW |
5 |
36,771,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R4452:D5Ertd579e
|
UTSW |
5 |
36,773,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4626:D5Ertd579e
|
UTSW |
5 |
36,771,903 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4804:D5Ertd579e
|
UTSW |
5 |
36,786,996 (GRCm39) |
splice site |
probably null |
|
R4898:D5Ertd579e
|
UTSW |
5 |
36,772,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R4917:D5Ertd579e
|
UTSW |
5 |
36,773,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:D5Ertd579e
|
UTSW |
5 |
36,773,571 (GRCm39) |
nonsense |
probably null |
|
R4973:D5Ertd579e
|
UTSW |
5 |
36,830,249 (GRCm39) |
missense |
probably benign |
|
R5092:D5Ertd579e
|
UTSW |
5 |
36,760,047 (GRCm39) |
missense |
probably benign |
0.18 |
R5474:D5Ertd579e
|
UTSW |
5 |
36,772,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5475:D5Ertd579e
|
UTSW |
5 |
36,772,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5476:D5Ertd579e
|
UTSW |
5 |
36,772,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5477:D5Ertd579e
|
UTSW |
5 |
36,772,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:D5Ertd579e
|
UTSW |
5 |
36,761,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:D5Ertd579e
|
UTSW |
5 |
36,787,036 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6184:D5Ertd579e
|
UTSW |
5 |
36,787,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R6213:D5Ertd579e
|
UTSW |
5 |
36,759,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:D5Ertd579e
|
UTSW |
5 |
36,772,620 (GRCm39) |
missense |
probably damaging |
0.98 |
R6276:D5Ertd579e
|
UTSW |
5 |
36,761,858 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6285:D5Ertd579e
|
UTSW |
5 |
36,772,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R6358:D5Ertd579e
|
UTSW |
5 |
36,773,580 (GRCm39) |
splice site |
probably null |
|
R6875:D5Ertd579e
|
UTSW |
5 |
36,762,001 (GRCm39) |
splice site |
probably null |
|
R6967:D5Ertd579e
|
UTSW |
5 |
36,773,100 (GRCm39) |
missense |
probably benign |
|
R7139:D5Ertd579e
|
UTSW |
5 |
36,771,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7329:D5Ertd579e
|
UTSW |
5 |
36,773,739 (GRCm39) |
missense |
probably benign |
0.21 |
R7464:D5Ertd579e
|
UTSW |
5 |
36,771,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R7664:D5Ertd579e
|
UTSW |
5 |
36,771,961 (GRCm39) |
missense |
probably benign |
0.00 |
R7951:D5Ertd579e
|
UTSW |
5 |
36,772,517 (GRCm39) |
missense |
probably benign |
|
R8175:D5Ertd579e
|
UTSW |
5 |
36,772,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R8217:D5Ertd579e
|
UTSW |
5 |
36,771,402 (GRCm39) |
missense |
probably benign |
0.00 |
R8233:D5Ertd579e
|
UTSW |
5 |
36,772,588 (GRCm39) |
missense |
probably damaging |
0.99 |
R8281:D5Ertd579e
|
UTSW |
5 |
36,770,664 (GRCm39) |
missense |
|
|
R8398:D5Ertd579e
|
UTSW |
5 |
36,771,621 (GRCm39) |
nonsense |
probably null |
|
R8673:D5Ertd579e
|
UTSW |
5 |
36,830,151 (GRCm39) |
missense |
probably benign |
0.03 |
R8771:D5Ertd579e
|
UTSW |
5 |
36,761,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8853:D5Ertd579e
|
UTSW |
5 |
36,787,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R9106:D5Ertd579e
|
UTSW |
5 |
36,773,682 (GRCm39) |
missense |
probably benign |
0.39 |
R9121:D5Ertd579e
|
UTSW |
5 |
36,772,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9413:D5Ertd579e
|
UTSW |
5 |
36,772,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:D5Ertd579e
|
UTSW |
5 |
36,759,979 (GRCm39) |
missense |
probably damaging |
0.97 |
R9715:D5Ertd579e
|
UTSW |
5 |
36,787,029 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9723:D5Ertd579e
|
UTSW |
5 |
36,772,284 (GRCm39) |
missense |
probably damaging |
0.99 |
RF022:D5Ertd579e
|
UTSW |
5 |
36,772,006 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:D5Ertd579e
|
UTSW |
5 |
36,771,302 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:D5Ertd579e
|
UTSW |
5 |
36,773,106 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:D5Ertd579e
|
UTSW |
5 |
36,772,250 (GRCm39) |
missense |
probably damaging |
1.00 |
|