Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aoc1l2 |
G |
A |
6: 48,907,480 (GRCm39) |
S160N |
probably benign |
Het |
Arap3 |
A |
C |
18: 38,124,590 (GRCm39) |
|
probably null |
Het |
Arhgap10 |
A |
G |
8: 78,137,692 (GRCm39) |
F300L |
probably benign |
Het |
Ccdc116 |
T |
C |
16: 16,960,655 (GRCm39) |
E54G |
probably benign |
Het |
Cd53 |
T |
A |
3: 106,674,702 (GRCm39) |
I122F |
probably benign |
Het |
Ctnnd1 |
T |
C |
2: 84,454,849 (GRCm39) |
|
probably benign |
Het |
Ddx60 |
A |
G |
8: 62,490,104 (GRCm39) |
D1691G |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,150,617 (GRCm39) |
|
probably null |
Het |
Exoc1 |
T |
A |
5: 76,697,399 (GRCm39) |
M392K |
probably damaging |
Het |
Exoc3l |
G |
C |
8: 106,017,122 (GRCm39) |
R622G |
probably benign |
Het |
Grid2 |
C |
G |
6: 63,908,031 (GRCm39) |
R224G |
possibly damaging |
Het |
Kif20a |
A |
G |
18: 34,758,579 (GRCm39) |
E16G |
probably damaging |
Het |
Lhx4 |
T |
C |
1: 155,580,456 (GRCm39) |
S257G |
probably benign |
Het |
Med18 |
C |
T |
4: 132,187,293 (GRCm39) |
V114I |
probably benign |
Het |
Mrps30 |
C |
T |
13: 118,523,497 (GRCm39) |
V92M |
possibly damaging |
Het |
Mtrr |
C |
T |
13: 68,712,452 (GRCm39) |
V645I |
probably benign |
Het |
Nuak2 |
T |
G |
1: 132,260,048 (GRCm39) |
S609A |
probably damaging |
Het |
Or2y1g |
A |
T |
11: 49,171,379 (GRCm39) |
I135F |
probably benign |
Het |
Plk4 |
T |
C |
3: 40,756,263 (GRCm39) |
V58A |
probably damaging |
Het |
Polq |
T |
A |
16: 36,835,535 (GRCm39) |
F145L |
probably null |
Het |
Rab11fip2 |
T |
C |
19: 59,925,707 (GRCm39) |
K170R |
probably damaging |
Het |
Rapgef3 |
A |
G |
15: 97,657,865 (GRCm39) |
V246A |
probably benign |
Het |
Rc3h2 |
A |
G |
2: 37,290,555 (GRCm39) |
S316P |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Homo |
Rsf1 |
GCGGCGGC |
GCGGCGGCGACGGCGGC |
7: 97,229,135 (GRCm39) |
|
probably benign |
Het |
Sae1 |
G |
T |
7: 16,102,461 (GRCm39) |
A171E |
probably damaging |
Het |
Semp2l2b |
T |
C |
10: 21,943,620 (GRCm39) |
E120G |
probably damaging |
Het |
Setd5 |
T |
A |
6: 113,120,669 (GRCm39) |
N959K |
probably benign |
Het |
Siae |
T |
A |
9: 37,528,119 (GRCm39) |
Y31N |
probably damaging |
Het |
Sit1 |
C |
T |
4: 43,483,311 (GRCm39) |
G51D |
probably damaging |
Het |
Slc5a11 |
A |
G |
7: 122,867,012 (GRCm39) |
I436V |
possibly damaging |
Het |
Tcfl5 |
A |
G |
2: 180,264,447 (GRCm39) |
S470P |
probably damaging |
Het |
Timd2 |
A |
T |
11: 46,561,779 (GRCm39) |
C288* |
probably null |
Het |
Timeless |
T |
G |
10: 128,075,868 (GRCm39) |
|
probably null |
Het |
Ubxn8 |
G |
T |
8: 34,111,572 (GRCm39) |
Q274K |
possibly damaging |
Het |
Usp29 |
A |
G |
7: 6,965,276 (GRCm39) |
E373G |
probably benign |
Het |
Zap70 |
A |
G |
1: 36,821,598 (GRCm39) |
Y597C |
probably damaging |
Het |
Zfp523 |
T |
G |
17: 28,419,446 (GRCm39) |
Y195D |
probably damaging |
Het |
Zfp74 |
G |
A |
7: 29,634,559 (GRCm39) |
A383V |
probably damaging |
Het |
Zfp93 |
A |
T |
7: 23,975,338 (GRCm39) |
Q441L |
probably damaging |
Het |
Zfp976 |
A |
T |
7: 42,263,610 (GRCm39) |
Y76N |
probably damaging |
Het |
|
Other mutations in Kit |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00466:Kit
|
APN |
5 |
75,771,479 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00834:Kit
|
APN |
5 |
75,806,619 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00846:Kit
|
APN |
5 |
75,801,471 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01149:Kit
|
APN |
5 |
75,771,536 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01341:Kit
|
APN |
5 |
75,767,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02004:Kit
|
APN |
5 |
75,781,674 (GRCm39) |
missense |
probably benign |
|
IGL02281:Kit
|
APN |
5 |
75,815,194 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02424:Kit
|
APN |
5 |
75,799,766 (GRCm39) |
missense |
probably benign |
|
IGL02697:Kit
|
APN |
5 |
75,767,919 (GRCm39) |
missense |
probably benign |
|
IGL02929:Kit
|
APN |
5 |
75,801,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03053:Kit
|
APN |
5 |
75,771,574 (GRCm39) |
missense |
probably benign |
|
IGL03127:Kit
|
APN |
5 |
75,801,848 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03174:Kit
|
APN |
5 |
75,767,773 (GRCm39) |
missense |
probably benign |
|
IGL03381:Kit
|
APN |
5 |
75,767,788 (GRCm39) |
missense |
probably benign |
0.04 |
casper
|
UTSW |
5 |
75,806,535 (GRCm39) |
missense |
probably damaging |
1.00 |
Mooyah2
|
UTSW |
5 |
75,813,468 (GRCm39) |
missense |
probably damaging |
1.00 |
pretty2
|
UTSW |
5 |
75,810,210 (GRCm39) |
missense |
probably damaging |
1.00 |
slimmer
|
UTSW |
5 |
75,801,417 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02837:Kit
|
UTSW |
5 |
75,799,668 (GRCm39) |
missense |
probably benign |
0.00 |
R0022:Kit
|
UTSW |
5 |
75,783,657 (GRCm39) |
missense |
probably benign |
0.00 |
R0022:Kit
|
UTSW |
5 |
75,783,657 (GRCm39) |
missense |
probably benign |
0.00 |
R0092:Kit
|
UTSW |
5 |
75,808,414 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0254:Kit
|
UTSW |
5 |
75,781,581 (GRCm39) |
missense |
probably benign |
|
R0329:Kit
|
UTSW |
5 |
75,813,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Kit
|
UTSW |
5 |
75,771,539 (GRCm39) |
missense |
probably benign |
0.35 |
R1068:Kit
|
UTSW |
5 |
75,770,178 (GRCm39) |
missense |
probably benign |
|
R1115:Kit
|
UTSW |
5 |
75,810,192 (GRCm39) |
splice site |
probably benign |
|
R1480:Kit
|
UTSW |
5 |
75,797,977 (GRCm39) |
missense |
probably benign |
0.00 |
R1639:Kit
|
UTSW |
5 |
75,813,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Kit
|
UTSW |
5 |
75,809,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R1973:Kit
|
UTSW |
5 |
75,776,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R2033:Kit
|
UTSW |
5 |
75,797,977 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3125:Kit
|
UTSW |
5 |
75,808,488 (GRCm39) |
missense |
probably null |
0.00 |
R3125:Kit
|
UTSW |
5 |
75,808,487 (GRCm39) |
missense |
probably benign |
0.07 |
R3437:Kit
|
UTSW |
5 |
75,806,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R3791:Kit
|
UTSW |
5 |
75,799,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3939:Kit
|
UTSW |
5 |
75,769,978 (GRCm39) |
missense |
probably benign |
0.00 |
R3940:Kit
|
UTSW |
5 |
75,769,978 (GRCm39) |
missense |
probably benign |
0.00 |
R3941:Kit
|
UTSW |
5 |
75,769,978 (GRCm39) |
missense |
probably benign |
0.00 |
R3942:Kit
|
UTSW |
5 |
75,769,978 (GRCm39) |
missense |
probably benign |
0.00 |
R4092:Kit
|
UTSW |
5 |
75,771,470 (GRCm39) |
missense |
probably benign |
0.28 |
R4376:Kit
|
UTSW |
5 |
75,801,159 (GRCm39) |
missense |
probably benign |
0.00 |
R4377:Kit
|
UTSW |
5 |
75,801,159 (GRCm39) |
missense |
probably benign |
0.00 |
R4668:Kit
|
UTSW |
5 |
75,801,880 (GRCm39) |
splice site |
probably null |
|
R5104:Kit
|
UTSW |
5 |
75,776,138 (GRCm39) |
missense |
probably benign |
0.00 |
R5152:Kit
|
UTSW |
5 |
75,781,507 (GRCm39) |
missense |
probably benign |
0.00 |
R5154:Kit
|
UTSW |
5 |
75,801,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R5508:Kit
|
UTSW |
5 |
75,810,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5624:Kit
|
UTSW |
5 |
75,770,054 (GRCm39) |
missense |
probably benign |
0.40 |
R5731:Kit
|
UTSW |
5 |
75,815,075 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6270:Kit
|
UTSW |
5 |
75,770,169 (GRCm39) |
missense |
probably benign |
|
R6565:Kit
|
UTSW |
5 |
75,806,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Kit
|
UTSW |
5 |
75,813,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Kit
|
UTSW |
5 |
75,813,309 (GRCm39) |
missense |
probably benign |
0.01 |
R6848:Kit
|
UTSW |
5 |
75,767,872 (GRCm39) |
missense |
probably benign |
|
R7021:Kit
|
UTSW |
5 |
75,781,627 (GRCm39) |
missense |
probably benign |
0.00 |
R7080:Kit
|
UTSW |
5 |
75,767,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R7117:Kit
|
UTSW |
5 |
75,767,758 (GRCm39) |
missense |
probably benign |
0.18 |
R7156:Kit
|
UTSW |
5 |
75,776,034 (GRCm39) |
missense |
probably benign |
0.14 |
R7379:Kit
|
UTSW |
5 |
75,808,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7427:Kit
|
UTSW |
5 |
75,806,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7438:Kit
|
UTSW |
5 |
75,799,660 (GRCm39) |
missense |
probably benign |
0.01 |
R7531:Kit
|
UTSW |
5 |
75,767,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R7711:Kit
|
UTSW |
5 |
75,798,019 (GRCm39) |
missense |
probably damaging |
0.97 |
R7810:Kit
|
UTSW |
5 |
75,769,982 (GRCm39) |
missense |
probably benign |
0.11 |
R7819:Kit
|
UTSW |
5 |
75,806,592 (GRCm39) |
missense |
probably benign |
0.41 |
R8021:Kit
|
UTSW |
5 |
75,776,151 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8139:Kit
|
UTSW |
5 |
75,813,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R8165:Kit
|
UTSW |
5 |
75,781,540 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8249:Kit
|
UTSW |
5 |
75,802,068 (GRCm39) |
missense |
probably damaging |
0.97 |
R8288:Kit
|
UTSW |
5 |
75,815,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Kit
|
UTSW |
5 |
75,801,829 (GRCm39) |
missense |
probably benign |
|
R8829:Kit
|
UTSW |
5 |
75,799,791 (GRCm39) |
missense |
probably benign |
0.41 |
R8832:Kit
|
UTSW |
5 |
75,799,791 (GRCm39) |
missense |
probably benign |
0.41 |
R8969:Kit
|
UTSW |
5 |
75,799,722 (GRCm39) |
missense |
|
|
R9081:Kit
|
UTSW |
5 |
75,801,218 (GRCm39) |
missense |
probably benign |
|
R9146:Kit
|
UTSW |
5 |
75,810,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Kit
|
UTSW |
5 |
75,799,792 (GRCm39) |
missense |
probably benign |
0.00 |
R9631:Kit
|
UTSW |
5 |
75,767,689 (GRCm39) |
missense |
possibly damaging |
0.95 |
U24488:Kit
|
UTSW |
5 |
75,783,674 (GRCm39) |
nonsense |
probably null |
|
|