Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
A |
T |
8: 25,162,082 (GRCm39) |
|
probably benign |
Het |
Adgrf5 |
A |
G |
17: 43,739,477 (GRCm39) |
Y72C |
possibly damaging |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Ano1 |
A |
G |
7: 144,201,789 (GRCm39) |
V334A |
probably damaging |
Het |
Arhgap18 |
C |
T |
10: 26,730,904 (GRCm39) |
T122I |
probably benign |
Het |
Arhgef4 |
A |
G |
1: 34,761,458 (GRCm39) |
K238R |
unknown |
Het |
Atf6b |
A |
T |
17: 34,867,549 (GRCm39) |
|
probably null |
Het |
Atp2a1 |
G |
A |
7: 126,046,844 (GRCm39) |
A847V |
possibly damaging |
Het |
Baz1b |
T |
A |
5: 135,246,079 (GRCm39) |
N509K |
probably benign |
Het |
BC051076 |
A |
T |
5: 88,111,844 (GRCm39) |
|
noncoding transcript |
Het |
Cage1 |
A |
G |
13: 38,207,356 (GRCm39) |
V163A |
probably benign |
Het |
Canx |
T |
C |
11: 50,195,252 (GRCm39) |
N272S |
probably damaging |
Het |
Cd302 |
T |
A |
2: 60,082,767 (GRCm39) |
I186F |
possibly damaging |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cep112 |
T |
A |
11: 108,410,087 (GRCm39) |
|
probably null |
Het |
Cmtm4 |
A |
C |
8: 105,081,920 (GRCm39) |
F156V |
probably damaging |
Het |
Col4a1 |
T |
A |
8: 11,260,792 (GRCm39) |
D1330V |
probably damaging |
Het |
Ctsa |
T |
G |
2: 164,676,822 (GRCm39) |
M136R |
probably null |
Het |
Cyp2d10 |
T |
A |
15: 82,288,015 (GRCm39) |
I363F |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Dmwd |
T |
A |
7: 18,814,652 (GRCm39) |
L434Q |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Gcc2 |
T |
A |
10: 58,121,779 (GRCm39) |
S1102T |
probably benign |
Het |
Gcm2 |
T |
C |
13: 41,263,430 (GRCm39) |
M1V |
probably null |
Het |
Gna14 |
G |
C |
19: 16,585,505 (GRCm39) |
|
probably benign |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Gulo |
A |
G |
14: 66,228,608 (GRCm39) |
V270A |
possibly damaging |
Het |
Hps5 |
T |
A |
7: 46,417,475 (GRCm39) |
D904V |
probably damaging |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Jak3 |
A |
T |
8: 72,138,027 (GRCm39) |
|
probably null |
Het |
Klhl6 |
T |
G |
16: 19,801,681 (GRCm39) |
T25P |
probably benign |
Het |
Kremen2 |
T |
C |
17: 23,961,691 (GRCm39) |
E272G |
possibly damaging |
Het |
Map3k21 |
A |
G |
8: 126,665,461 (GRCm39) |
K550R |
probably benign |
Het |
Mphosph10 |
T |
A |
7: 64,026,499 (GRCm39) |
L650F |
probably damaging |
Het |
Mrpl48 |
T |
C |
7: 100,198,540 (GRCm39) |
E204G |
probably damaging |
Het |
Msh5 |
A |
C |
17: 35,248,732 (GRCm39) |
V738G |
probably damaging |
Het |
Mybph |
G |
A |
1: 134,127,857 (GRCm39) |
C473Y |
probably damaging |
Het |
Nid1 |
A |
C |
13: 13,675,058 (GRCm39) |
H926P |
probably benign |
Het |
Nlrp9a |
T |
A |
7: 26,256,787 (GRCm39) |
I46K |
possibly damaging |
Het |
Notch3 |
T |
C |
17: 32,362,618 (GRCm39) |
T1336A |
probably benign |
Het |
Nsun4 |
T |
C |
4: 115,910,877 (GRCm39) |
|
probably null |
Het |
Or1e30 |
A |
G |
11: 73,678,100 (GRCm39) |
N112S |
probably benign |
Het |
Or5m10 |
A |
T |
2: 85,717,296 (GRCm39) |
T51S |
possibly damaging |
Het |
Osgin1 |
A |
G |
8: 120,172,412 (GRCm39) |
D402G |
possibly damaging |
Het |
Patl1 |
A |
G |
19: 11,909,511 (GRCm39) |
E479G |
possibly damaging |
Het |
Pbsn |
T |
C |
X: 76,891,582 (GRCm39) |
K72E |
probably damaging |
Het |
Pcdhb13 |
A |
G |
18: 37,577,620 (GRCm39) |
Q666R |
possibly damaging |
Het |
Pi4k2b |
G |
A |
5: 52,908,022 (GRCm39) |
V131I |
probably benign |
Het |
Pkn2 |
G |
A |
3: 142,559,232 (GRCm39) |
H98Y |
possibly damaging |
Het |
Pms1 |
A |
G |
1: 53,314,327 (GRCm39) |
Y73H |
probably benign |
Het |
Ppt2 |
A |
T |
17: 34,841,818 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,545,469 (GRCm39) |
T1862A |
probably benign |
Het |
Prl6a1 |
T |
C |
13: 27,503,081 (GRCm39) |
Y231H |
probably benign |
Het |
Ranbp3l |
T |
A |
15: 9,029,641 (GRCm39) |
V41D |
probably damaging |
Het |
Rhobtb2 |
T |
C |
14: 70,031,488 (GRCm39) |
T546A |
possibly damaging |
Het |
Ripk4 |
A |
T |
16: 97,545,342 (GRCm39) |
L372* |
probably null |
Het |
Rnf126 |
A |
G |
10: 79,594,971 (GRCm39) |
|
probably benign |
Het |
S100pbp |
A |
G |
4: 129,075,893 (GRCm39) |
V144A |
probably benign |
Het |
Saal1 |
T |
C |
7: 46,348,880 (GRCm39) |
Q317R |
probably damaging |
Het |
Sap25 |
G |
A |
5: 137,641,034 (GRCm39) |
G277R |
probably damaging |
Het |
Senp2 |
C |
T |
16: 21,832,949 (GRCm39) |
T79I |
probably damaging |
Het |
Serpinb9c |
A |
T |
13: 33,340,854 (GRCm39) |
C81* |
probably null |
Het |
Set |
A |
G |
2: 29,959,048 (GRCm39) |
K70E |
possibly damaging |
Het |
Setd3 |
A |
G |
12: 108,073,600 (GRCm39) |
I559T |
probably benign |
Het |
Sik1 |
A |
G |
17: 32,067,771 (GRCm39) |
S435P |
probably benign |
Het |
Skint3 |
A |
T |
4: 112,112,980 (GRCm39) |
K197* |
probably null |
Het |
Skint5 |
T |
A |
4: 113,727,897 (GRCm39) |
I402F |
possibly damaging |
Het |
Slc19a3 |
A |
T |
1: 82,992,512 (GRCm39) |
I403K |
probably damaging |
Het |
Slc1a7 |
C |
T |
4: 107,861,636 (GRCm39) |
T225I |
probably benign |
Het |
Slc38a4 |
T |
C |
15: 96,906,606 (GRCm39) |
I336V |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 109,947,411 (GRCm39) |
|
probably benign |
Het |
St8sia5 |
A |
T |
18: 77,342,459 (GRCm39) |
I390F |
probably damaging |
Het |
Strc |
A |
T |
2: 121,209,368 (GRCm39) |
W290R |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,084,554 (GRCm39) |
D1858G |
possibly damaging |
Het |
Sympk |
G |
A |
7: 18,777,454 (GRCm39) |
R568Q |
probably damaging |
Het |
Tex44 |
A |
C |
1: 86,354,728 (GRCm39) |
K212N |
probably damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Thrap3 |
C |
T |
4: 126,073,967 (GRCm39) |
V260I |
probably damaging |
Het |
Thsd7a |
A |
T |
6: 12,318,105 (GRCm39) |
|
probably benign |
Het |
Trim12c |
A |
G |
7: 103,997,398 (GRCm39) |
F53L |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,938,683 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
G |
A |
17: 31,227,740 (GRCm39) |
|
probably null |
Het |
Usp17la |
A |
C |
7: 104,510,378 (GRCm39) |
T328P |
probably damaging |
Het |
Vmn2r113 |
T |
A |
17: 23,177,223 (GRCm39) |
L669* |
probably null |
Het |
Vps13b |
T |
A |
15: 35,841,593 (GRCm39) |
V2541E |
probably damaging |
Het |
Wnt3 |
T |
C |
11: 103,703,111 (GRCm39) |
I198T |
probably damaging |
Het |
Zfp316 |
T |
C |
5: 143,249,161 (GRCm39) |
E158G |
unknown |
Het |
Zfp362 |
T |
G |
4: 128,680,780 (GRCm39) |
I182L |
possibly damaging |
Het |
Zfp804a |
A |
G |
2: 82,087,710 (GRCm39) |
D513G |
probably benign |
Het |
Zfp879 |
C |
T |
11: 50,723,428 (GRCm39) |
E543K |
probably benign |
Het |
Zfp97 |
T |
A |
17: 17,365,018 (GRCm39) |
N172K |
possibly damaging |
Het |
Zmym6 |
A |
T |
4: 126,982,208 (GRCm39) |
K82* |
probably null |
Het |
|
Other mutations in Slc18a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Slc18a1
|
APN |
8 |
69,503,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00661:Slc18a1
|
APN |
8 |
69,526,383 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01568:Slc18a1
|
APN |
8 |
69,518,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02199:Slc18a1
|
APN |
8 |
69,496,632 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03011:Slc18a1
|
APN |
8 |
69,491,515 (GRCm39) |
missense |
probably benign |
|
IGL03260:Slc18a1
|
APN |
8 |
69,527,766 (GRCm39) |
missense |
probably benign |
0.24 |
R0349:Slc18a1
|
UTSW |
8 |
69,524,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R1019:Slc18a1
|
UTSW |
8 |
69,527,685 (GRCm39) |
critical splice donor site |
probably null |
|
R1759:Slc18a1
|
UTSW |
8 |
69,518,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1928:Slc18a1
|
UTSW |
8 |
69,526,464 (GRCm39) |
missense |
probably benign |
0.00 |
R4652:Slc18a1
|
UTSW |
8 |
69,496,583 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4724:Slc18a1
|
UTSW |
8 |
69,526,301 (GRCm39) |
nonsense |
probably null |
|
R4818:Slc18a1
|
UTSW |
8 |
69,492,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R6799:Slc18a1
|
UTSW |
8 |
69,493,633 (GRCm39) |
missense |
probably benign |
0.05 |
R6989:Slc18a1
|
UTSW |
8 |
69,491,514 (GRCm39) |
missense |
probably benign |
0.01 |
R7557:Slc18a1
|
UTSW |
8 |
69,518,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7736:Slc18a1
|
UTSW |
8 |
69,518,206 (GRCm39) |
critical splice donor site |
probably null |
|
R7956:Slc18a1
|
UTSW |
8 |
69,491,466 (GRCm39) |
missense |
probably benign |
0.00 |
R8024:Slc18a1
|
UTSW |
8 |
69,527,799 (GRCm39) |
missense |
probably benign |
0.00 |
R8146:Slc18a1
|
UTSW |
8 |
69,495,401 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8339:Slc18a1
|
UTSW |
8 |
69,518,273 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9055:Slc18a1
|
UTSW |
8 |
69,520,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9129:Slc18a1
|
UTSW |
8 |
69,491,533 (GRCm39) |
missense |
probably benign |
0.00 |
R9190:Slc18a1
|
UTSW |
8 |
69,519,790 (GRCm39) |
critical splice donor site |
probably null |
|
|