Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,882,756 (GRCm39) |
Y233H |
possibly damaging |
Het |
Apaf1 |
A |
T |
10: 90,885,211 (GRCm39) |
|
probably benign |
Het |
Asah2 |
T |
C |
19: 31,964,342 (GRCm39) |
Y696C |
probably damaging |
Het |
Atp8b3 |
A |
T |
10: 80,370,292 (GRCm39) |
D112E |
probably damaging |
Het |
B3gat3 |
T |
C |
19: 8,903,215 (GRCm39) |
Y191H |
probably damaging |
Het |
Capns2 |
T |
C |
8: 93,628,738 (GRCm39) |
I209T |
probably damaging |
Het |
Ccnl2 |
T |
C |
4: 155,905,479 (GRCm39) |
I303T |
probably benign |
Het |
Cep57 |
A |
T |
9: 13,729,683 (GRCm39) |
L36* |
probably null |
Het |
Cers4 |
T |
A |
8: 4,566,878 (GRCm39) |
V60E |
probably damaging |
Het |
Ces2e |
T |
C |
8: 105,655,451 (GRCm39) |
Y125H |
probably benign |
Het |
Cyp4f18 |
T |
C |
8: 72,742,489 (GRCm39) |
E497G |
probably benign |
Het |
Ddx24 |
A |
T |
12: 103,383,864 (GRCm39) |
M575K |
possibly damaging |
Het |
Dmxl2 |
A |
T |
9: 54,323,655 (GRCm39) |
V1243E |
probably damaging |
Het |
Elf2 |
A |
T |
3: 51,165,193 (GRCm39) |
Y270* |
probably null |
Het |
Ep400 |
A |
G |
5: 110,875,429 (GRCm39) |
L844S |
unknown |
Het |
F13a1 |
A |
T |
13: 37,172,870 (GRCm39) |
I170N |
possibly damaging |
Het |
Gm16506 |
T |
A |
14: 43,961,603 (GRCm39) |
|
probably benign |
Het |
Grm4 |
A |
G |
17: 27,653,797 (GRCm39) |
F463L |
probably damaging |
Het |
H2-M10.2 |
A |
T |
17: 36,596,463 (GRCm39) |
N127K |
probably benign |
Het |
Lrrc49 |
T |
C |
9: 60,495,140 (GRCm39) |
Y691C |
probably damaging |
Het |
Mbip |
A |
C |
12: 56,384,547 (GRCm39) |
|
probably null |
Het |
Or9k2 |
T |
A |
10: 129,998,269 (GRCm39) |
K309* |
probably null |
Het |
Plod1 |
C |
T |
4: 148,007,580 (GRCm39) |
|
probably null |
Het |
Primpol |
A |
G |
8: 47,039,475 (GRCm39) |
W382R |
probably damaging |
Het |
Rufy2 |
A |
G |
10: 62,840,483 (GRCm39) |
E418G |
probably benign |
Het |
Samm50 |
T |
C |
15: 84,098,341 (GRCm39) |
V460A |
probably benign |
Het |
Senp2 |
T |
C |
16: 21,859,329 (GRCm39) |
V460A |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,698,442 (GRCm39) |
H453R |
probably benign |
Het |
Slc22a22 |
A |
G |
15: 57,112,948 (GRCm39) |
|
probably benign |
Het |
Spag1 |
A |
T |
15: 36,234,529 (GRCm39) |
D763V |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,504,167 (GRCm39) |
|
probably benign |
Het |
Tppp |
G |
T |
13: 74,169,535 (GRCm39) |
V92F |
possibly damaging |
Het |
Vmn1r32 |
G |
A |
6: 66,530,489 (GRCm39) |
L96F |
probably damaging |
Het |
Vmn2r53 |
C |
A |
7: 12,340,435 (GRCm39) |
A13S |
probably damaging |
Het |
Vmn2r75 |
G |
A |
7: 85,820,933 (GRCm39) |
|
probably benign |
Het |
Zfp750 |
C |
A |
11: 121,404,513 (GRCm39) |
G121* |
probably null |
Het |
|
Other mutations in Cdk5rap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Cdk5rap2
|
APN |
4 |
70,321,709 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01305:Cdk5rap2
|
APN |
4 |
70,298,472 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01987:Cdk5rap2
|
APN |
4 |
70,220,319 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02213:Cdk5rap2
|
APN |
4 |
70,235,839 (GRCm39) |
splice site |
probably benign |
|
IGL02732:Cdk5rap2
|
APN |
4 |
70,184,902 (GRCm39) |
nonsense |
probably null |
|
IGL03063:Cdk5rap2
|
APN |
4 |
70,273,114 (GRCm39) |
critical splice acceptor site |
probably null |
|
ANU22:Cdk5rap2
|
UTSW |
4 |
70,298,472 (GRCm39) |
missense |
possibly damaging |
0.52 |
F5426:Cdk5rap2
|
UTSW |
4 |
70,173,040 (GRCm39) |
missense |
probably benign |
|
R0010:Cdk5rap2
|
UTSW |
4 |
70,161,696 (GRCm39) |
missense |
probably benign |
0.01 |
R0010:Cdk5rap2
|
UTSW |
4 |
70,161,696 (GRCm39) |
missense |
probably benign |
0.01 |
R0044:Cdk5rap2
|
UTSW |
4 |
70,279,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Cdk5rap2
|
UTSW |
4 |
70,279,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Cdk5rap2
|
UTSW |
4 |
70,328,506 (GRCm39) |
start gained |
probably benign |
|
R0548:Cdk5rap2
|
UTSW |
4 |
70,267,379 (GRCm39) |
critical splice donor site |
probably null |
|
R0594:Cdk5rap2
|
UTSW |
4 |
70,273,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R0737:Cdk5rap2
|
UTSW |
4 |
70,255,612 (GRCm39) |
missense |
probably benign |
0.01 |
R0788:Cdk5rap2
|
UTSW |
4 |
70,225,468 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0960:Cdk5rap2
|
UTSW |
4 |
70,161,745 (GRCm39) |
missense |
probably benign |
0.03 |
R1682:Cdk5rap2
|
UTSW |
4 |
70,220,387 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1727:Cdk5rap2
|
UTSW |
4 |
70,208,209 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1727:Cdk5rap2
|
UTSW |
4 |
70,190,916 (GRCm39) |
missense |
probably benign |
|
R1768:Cdk5rap2
|
UTSW |
4 |
70,225,470 (GRCm39) |
missense |
probably benign |
0.09 |
R1903:Cdk5rap2
|
UTSW |
4 |
70,321,791 (GRCm39) |
splice site |
probably null |
|
R2270:Cdk5rap2
|
UTSW |
4 |
70,184,915 (GRCm39) |
missense |
probably benign |
0.01 |
R2271:Cdk5rap2
|
UTSW |
4 |
70,184,915 (GRCm39) |
missense |
probably benign |
0.01 |
R2272:Cdk5rap2
|
UTSW |
4 |
70,184,915 (GRCm39) |
missense |
probably benign |
0.01 |
R2364:Cdk5rap2
|
UTSW |
4 |
70,279,046 (GRCm39) |
critical splice donor site |
probably null |
|
R2763:Cdk5rap2
|
UTSW |
4 |
70,199,508 (GRCm39) |
missense |
probably benign |
|
R2893:Cdk5rap2
|
UTSW |
4 |
70,208,110 (GRCm39) |
missense |
probably benign |
|
R2894:Cdk5rap2
|
UTSW |
4 |
70,208,110 (GRCm39) |
missense |
probably benign |
|
R2958:Cdk5rap2
|
UTSW |
4 |
70,208,214 (GRCm39) |
frame shift |
probably null |
|
R2959:Cdk5rap2
|
UTSW |
4 |
70,208,214 (GRCm39) |
frame shift |
probably null |
|
R2961:Cdk5rap2
|
UTSW |
4 |
70,208,214 (GRCm39) |
frame shift |
probably null |
|
R2962:Cdk5rap2
|
UTSW |
4 |
70,208,214 (GRCm39) |
frame shift |
probably null |
|
R2963:Cdk5rap2
|
UTSW |
4 |
70,208,214 (GRCm39) |
frame shift |
probably null |
|
R3522:Cdk5rap2
|
UTSW |
4 |
70,168,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R3725:Cdk5rap2
|
UTSW |
4 |
70,153,674 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3726:Cdk5rap2
|
UTSW |
4 |
70,153,674 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3876:Cdk5rap2
|
UTSW |
4 |
70,208,214 (GRCm39) |
frame shift |
probably null |
|
R3919:Cdk5rap2
|
UTSW |
4 |
70,298,460 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4025:Cdk5rap2
|
UTSW |
4 |
70,168,624 (GRCm39) |
missense |
probably damaging |
0.98 |
R4324:Cdk5rap2
|
UTSW |
4 |
70,271,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R4485:Cdk5rap2
|
UTSW |
4 |
70,157,520 (GRCm39) |
critical splice donor site |
probably null |
|
R4516:Cdk5rap2
|
UTSW |
4 |
70,194,952 (GRCm39) |
splice site |
probably null |
|
R4556:Cdk5rap2
|
UTSW |
4 |
70,157,549 (GRCm39) |
missense |
probably damaging |
0.97 |
R4560:Cdk5rap2
|
UTSW |
4 |
70,233,568 (GRCm39) |
missense |
probably benign |
0.03 |
R4584:Cdk5rap2
|
UTSW |
4 |
70,184,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R4620:Cdk5rap2
|
UTSW |
4 |
70,184,943 (GRCm39) |
missense |
probably benign |
0.00 |
R4639:Cdk5rap2
|
UTSW |
4 |
70,220,413 (GRCm39) |
missense |
probably damaging |
0.97 |
R4755:Cdk5rap2
|
UTSW |
4 |
70,156,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Cdk5rap2
|
UTSW |
4 |
70,146,829 (GRCm39) |
splice site |
probably null |
|
R5116:Cdk5rap2
|
UTSW |
4 |
70,225,475 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5449:Cdk5rap2
|
UTSW |
4 |
70,194,888 (GRCm39) |
missense |
probably benign |
0.00 |
R5643:Cdk5rap2
|
UTSW |
4 |
70,184,970 (GRCm39) |
missense |
probably damaging |
0.99 |
R5899:Cdk5rap2
|
UTSW |
4 |
70,161,830 (GRCm39) |
splice site |
probably benign |
|
R6177:Cdk5rap2
|
UTSW |
4 |
70,199,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R6254:Cdk5rap2
|
UTSW |
4 |
70,282,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Cdk5rap2
|
UTSW |
4 |
70,153,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:Cdk5rap2
|
UTSW |
4 |
70,184,849 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6534:Cdk5rap2
|
UTSW |
4 |
70,273,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R6857:Cdk5rap2
|
UTSW |
4 |
70,163,633 (GRCm39) |
nonsense |
probably null |
|
R6959:Cdk5rap2
|
UTSW |
4 |
70,278,906 (GRCm39) |
splice site |
probably null |
|
R7104:Cdk5rap2
|
UTSW |
4 |
70,267,393 (GRCm39) |
missense |
probably benign |
0.00 |
R7145:Cdk5rap2
|
UTSW |
4 |
70,156,468 (GRCm39) |
missense |
probably benign |
0.13 |
R7223:Cdk5rap2
|
UTSW |
4 |
70,153,684 (GRCm39) |
missense |
probably benign |
0.02 |
R7234:Cdk5rap2
|
UTSW |
4 |
70,295,024 (GRCm39) |
splice site |
probably null |
|
R7240:Cdk5rap2
|
UTSW |
4 |
70,210,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Cdk5rap2
|
UTSW |
4 |
70,255,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Cdk5rap2
|
UTSW |
4 |
70,208,262 (GRCm39) |
missense |
probably benign |
0.19 |
R7413:Cdk5rap2
|
UTSW |
4 |
70,172,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Cdk5rap2
|
UTSW |
4 |
70,185,109 (GRCm39) |
missense |
probably benign |
0.01 |
R8236:Cdk5rap2
|
UTSW |
4 |
70,160,722 (GRCm39) |
missense |
probably benign |
|
R8434:Cdk5rap2
|
UTSW |
4 |
70,282,257 (GRCm39) |
missense |
probably benign |
0.00 |
R8688:Cdk5rap2
|
UTSW |
4 |
70,298,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8706:Cdk5rap2
|
UTSW |
4 |
70,157,562 (GRCm39) |
missense |
probably benign |
0.08 |
R8731:Cdk5rap2
|
UTSW |
4 |
70,163,747 (GRCm39) |
splice site |
probably benign |
|
R8782:Cdk5rap2
|
UTSW |
4 |
70,161,712 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8855:Cdk5rap2
|
UTSW |
4 |
70,218,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R8965:Cdk5rap2
|
UTSW |
4 |
70,185,042 (GRCm39) |
missense |
probably benign |
0.30 |
R9242:Cdk5rap2
|
UTSW |
4 |
70,255,583 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9308:Cdk5rap2
|
UTSW |
4 |
70,328,504 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R9396:Cdk5rap2
|
UTSW |
4 |
70,182,895 (GRCm39) |
missense |
probably damaging |
0.97 |
R9396:Cdk5rap2
|
UTSW |
4 |
70,172,903 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9507:Cdk5rap2
|
UTSW |
4 |
70,210,110 (GRCm39) |
missense |
probably benign |
|
Z1176:Cdk5rap2
|
UTSW |
4 |
70,184,980 (GRCm39) |
missense |
probably damaging |
0.99 |
|