Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
A |
G |
6: 86,963,321 (GRCm39) |
D917G |
unknown |
Het |
Adad1 |
T |
C |
3: 37,134,050 (GRCm39) |
S322P |
probably damaging |
Het |
Agbl4 |
C |
T |
4: 110,976,224 (GRCm39) |
L194F |
probably damaging |
Het |
Ahr |
C |
T |
12: 35,558,271 (GRCm39) |
G250R |
probably damaging |
Het |
AI987944 |
A |
T |
7: 41,024,310 (GRCm39) |
I226N |
probably benign |
Het |
Ankar |
A |
G |
1: 72,691,619 (GRCm39) |
V1114A |
probably damaging |
Het |
Ankrd49 |
C |
A |
9: 14,692,823 (GRCm39) |
A114S |
probably damaging |
Het |
Arl6 |
C |
T |
16: 59,442,802 (GRCm39) |
G140D |
unknown |
Het |
Arrdc3 |
A |
G |
13: 81,031,790 (GRCm39) |
S8G |
probably benign |
Het |
Ate1 |
A |
T |
7: 130,105,495 (GRCm39) |
V298E |
probably benign |
Het |
Atp6v1b2 |
A |
G |
8: 69,554,035 (GRCm39) |
I71V |
probably benign |
Het |
Bin1 |
A |
G |
18: 32,546,166 (GRCm39) |
M112V |
probably benign |
Het |
Camk2b |
C |
T |
11: 5,940,383 (GRCm39) |
A152T |
probably benign |
Het |
Cars2 |
A |
C |
8: 11,579,706 (GRCm39) |
F251V |
probably damaging |
Het |
Cdkl1 |
A |
T |
12: 69,800,952 (GRCm39) |
F229I |
probably damaging |
Het |
Ceacam5 |
A |
T |
7: 17,486,171 (GRCm39) |
Y556F |
possibly damaging |
Het |
Chst15 |
T |
C |
7: 131,849,615 (GRCm39) |
N442S |
probably benign |
Het |
Ckap5 |
T |
A |
2: 91,436,707 (GRCm39) |
D1602E |
possibly damaging |
Het |
Col9a3 |
A |
T |
2: 180,245,183 (GRCm39) |
I131F |
unknown |
Het |
Cyp4f15 |
A |
T |
17: 32,909,733 (GRCm39) |
D110V |
possibly damaging |
Het |
Dlec1 |
A |
G |
9: 118,968,457 (GRCm39) |
I1258V |
probably benign |
Het |
Dpyd |
A |
G |
3: 119,108,452 (GRCm39) |
T832A |
possibly damaging |
Het |
Eno1 |
A |
G |
4: 150,329,693 (GRCm39) |
Y189C |
probably damaging |
Het |
Gnat3 |
A |
G |
5: 18,208,838 (GRCm39) |
T181A |
|
Het |
Kif1b |
T |
C |
4: 149,306,805 (GRCm39) |
M852V |
probably damaging |
Het |
Klk1b26 |
A |
T |
7: 43,665,508 (GRCm39) |
I139F |
probably damaging |
Het |
Loxhd1 |
G |
A |
18: 77,493,681 (GRCm39) |
V1547M |
possibly damaging |
Het |
Lrp4 |
A |
G |
2: 91,318,790 (GRCm39) |
T876A |
probably damaging |
Het |
Malrd1 |
G |
T |
2: 15,638,035 (GRCm39) |
W451L |
unknown |
Het |
Marchf6 |
A |
T |
15: 31,494,262 (GRCm39) |
N261K |
possibly damaging |
Het |
Mcpt2 |
T |
C |
14: 56,280,250 (GRCm39) |
C50R |
probably damaging |
Het |
Muc16 |
A |
G |
9: 18,569,981 (GRCm39) |
V846A |
unknown |
Het |
Muc5b |
A |
T |
7: 141,414,602 (GRCm39) |
D2516V |
unknown |
Het |
Myh15 |
T |
C |
16: 48,913,120 (GRCm39) |
L359P |
probably benign |
Het |
Nemp1 |
G |
A |
10: 127,528,898 (GRCm39) |
V201I |
probably benign |
Het |
Nr2e1 |
A |
T |
10: 42,444,425 (GRCm39) |
L228Q |
probably damaging |
Het |
Nrg1 |
C |
A |
8: 32,312,334 (GRCm39) |
V388L |
probably benign |
Het |
Nrg3 |
T |
A |
14: 38,734,053 (GRCm39) |
T278S |
probably damaging |
Het |
Numb |
T |
C |
12: 83,854,990 (GRCm39) |
E112G |
probably benign |
Het |
Or1l4b |
T |
C |
2: 37,036,778 (GRCm39) |
S185P |
probably damaging |
Het |
Or8g2b |
A |
C |
9: 39,751,612 (GRCm39) |
N294T |
probably damaging |
Het |
Pdlim2 |
C |
A |
14: 70,403,563 (GRCm39) |
C283F |
probably damaging |
Het |
Potegl |
T |
A |
2: 23,147,017 (GRCm39) |
|
probably null |
Het |
Ppm1a |
G |
A |
12: 72,830,909 (GRCm39) |
G145R |
probably damaging |
Het |
Pramel14 |
T |
A |
4: 143,720,809 (GRCm39) |
D44V |
probably benign |
Het |
Pramel18 |
A |
T |
4: 101,767,581 (GRCm39) |
M277L |
probably benign |
Het |
Prune2 |
C |
A |
19: 17,103,027 (GRCm39) |
Q2729K |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Scn9a |
G |
T |
2: 66,366,626 (GRCm39) |
T719K |
probably benign |
Het |
Slc12a7 |
T |
C |
13: 73,933,281 (GRCm39) |
V113A |
probably benign |
Het |
Slc23a1 |
C |
T |
18: 35,755,588 (GRCm39) |
G436E |
probably damaging |
Het |
Slc37a2 |
A |
T |
9: 37,149,510 (GRCm39) |
|
probably null |
Het |
Sucnr1 |
C |
T |
3: 59,994,155 (GRCm39) |
R228C |
probably damaging |
Het |
Sult3a1 |
G |
A |
10: 33,742,517 (GRCm39) |
G48D |
probably damaging |
Het |
Syn3 |
A |
T |
10: 86,302,891 (GRCm39) |
V88D |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,058,622 (GRCm39) |
D7297G |
probably benign |
Het |
Tmco5 |
T |
C |
2: 116,710,734 (GRCm39) |
I18T |
probably damaging |
Het |
Trpc1 |
A |
G |
9: 95,608,601 (GRCm39) |
L230P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,719,785 (GRCm39) |
N7108S |
unknown |
Het |
Ubr5 |
A |
G |
15: 38,025,081 (GRCm39) |
V559A |
|
Het |
Ugt1a7c |
T |
C |
1: 88,022,973 (GRCm39) |
V44A |
possibly damaging |
Het |
Vmn2r60 |
A |
T |
7: 41,790,494 (GRCm39) |
S494C |
possibly damaging |
Het |
|
Other mutations in Steap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02492:Steap1
|
APN |
5 |
5,790,561 (GRCm39) |
missense |
possibly damaging |
0.87 |
E0370:Steap1
|
UTSW |
5 |
5,790,673 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4468001:Steap1
|
UTSW |
5 |
5,786,642 (GRCm39) |
missense |
probably damaging |
0.98 |
R0087:Steap1
|
UTSW |
5 |
5,786,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Steap1
|
UTSW |
5 |
5,786,431 (GRCm39) |
missense |
probably benign |
|
R0525:Steap1
|
UTSW |
5 |
5,792,903 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0834:Steap1
|
UTSW |
5 |
5,790,357 (GRCm39) |
missense |
probably damaging |
0.98 |
R1665:Steap1
|
UTSW |
5 |
5,786,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1941:Steap1
|
UTSW |
5 |
5,790,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R4808:Steap1
|
UTSW |
5 |
5,788,829 (GRCm39) |
intron |
probably benign |
|
R4860:Steap1
|
UTSW |
5 |
5,786,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Steap1
|
UTSW |
5 |
5,786,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Steap1
|
UTSW |
5 |
5,792,829 (GRCm39) |
nonsense |
probably null |
|
R5138:Steap1
|
UTSW |
5 |
5,786,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R5330:Steap1
|
UTSW |
5 |
5,790,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Steap1
|
UTSW |
5 |
5,790,579 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6273:Steap1
|
UTSW |
5 |
5,790,827 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8478:Steap1
|
UTSW |
5 |
5,786,432 (GRCm39) |
missense |
probably benign |
0.30 |
R8850:Steap1
|
UTSW |
5 |
5,790,838 (GRCm39) |
missense |
probably benign |
0.01 |
R8949:Steap1
|
UTSW |
5 |
5,789,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R9036:Steap1
|
UTSW |
5 |
5,790,708 (GRCm39) |
missense |
probably benign |
0.19 |
R9344:Steap1
|
UTSW |
5 |
5,786,459 (GRCm39) |
missense |
probably damaging |
0.99 |
R9402:Steap1
|
UTSW |
5 |
5,790,664 (GRCm39) |
missense |
|
|
R9473:Steap1
|
UTSW |
5 |
5,790,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R9495:Steap1
|
UTSW |
5 |
5,786,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R9548:Steap1
|
UTSW |
5 |
5,790,700 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9777:Steap1
|
UTSW |
5 |
5,786,517 (GRCm39) |
missense |
probably benign |
0.13 |
Z1177:Steap1
|
UTSW |
5 |
5,790,580 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1177:Steap1
|
UTSW |
5 |
5,789,882 (GRCm39) |
missense |
probably damaging |
0.98 |
|