Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610030E20Rik |
A |
G |
6: 72,324,450 (GRCm39) |
D20G |
probably damaging |
Het |
Acbd3 |
T |
A |
1: 180,566,082 (GRCm39) |
Y258* |
probably null |
Het |
Adamts1 |
T |
A |
16: 85,599,498 (GRCm39) |
H34L |
|
Het |
Ankmy1 |
G |
T |
1: 92,813,882 (GRCm39) |
N432K |
possibly damaging |
Het |
Ano1 |
A |
G |
7: 144,143,893 (GRCm39) |
M966T |
possibly damaging |
Het |
Ark2n |
A |
T |
18: 77,722,989 (GRCm39) |
V349D |
possibly damaging |
Het |
C2cd3 |
A |
G |
7: 100,023,662 (GRCm39) |
T83A |
probably benign |
Het |
Cdk1 |
T |
A |
10: 69,178,449 (GRCm39) |
D137V |
possibly damaging |
Het |
Cfap299 |
T |
A |
5: 98,477,214 (GRCm39) |
M1K |
probably null |
Het |
Chia1 |
A |
G |
3: 106,037,996 (GRCm39) |
Y326C |
probably damaging |
Het |
Ciz1 |
A |
G |
2: 32,260,974 (GRCm39) |
D295G |
possibly damaging |
Het |
Clrn1 |
C |
T |
3: 58,792,251 (GRCm39) |
V71I |
probably benign |
Het |
Cr1l |
T |
C |
1: 194,800,149 (GRCm39) |
D175G |
probably damaging |
Het |
Crem |
A |
T |
18: 3,268,067 (GRCm39) |
V87E |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,125,679 (GRCm39) |
V243D |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,562,414 (GRCm39) |
V2658A |
possibly damaging |
Het |
Dnah3 |
T |
G |
7: 119,677,611 (GRCm39) |
M437L |
probably benign |
Het |
Flrt2 |
T |
A |
12: 95,745,425 (GRCm39) |
|
probably benign |
Het |
Gm10142 |
T |
A |
10: 77,551,880 (GRCm39) |
C80* |
probably null |
Het |
Gpr158 |
A |
G |
2: 21,831,315 (GRCm39) |
E805G |
probably damaging |
Het |
Grwd1 |
T |
C |
7: 45,479,473 (GRCm39) |
E134G |
probably benign |
Het |
Hdac11 |
T |
A |
6: 91,150,068 (GRCm39) |
V289D |
probably benign |
Het |
Hsdl1 |
T |
C |
8: 120,293,081 (GRCm39) |
E118G |
possibly damaging |
Het |
Igdcc4 |
T |
A |
9: 65,041,858 (GRCm39) |
L1095Q |
possibly damaging |
Het |
Ildr1 |
T |
A |
16: 36,528,749 (GRCm39) |
C65S |
probably damaging |
Het |
Itgal |
T |
C |
7: 126,929,422 (GRCm39) |
F1113S |
probably damaging |
Het |
Itsn2 |
G |
T |
12: 4,683,499 (GRCm39) |
V341F |
unknown |
Het |
Jak1 |
G |
A |
4: 101,019,085 (GRCm39) |
R723C |
probably damaging |
Het |
Limch1 |
A |
G |
5: 67,126,422 (GRCm39) |
T8A |
probably damaging |
Het |
Limd1 |
T |
A |
9: 123,345,903 (GRCm39) |
C561S |
possibly damaging |
Het |
Map3k19 |
A |
G |
1: 127,750,097 (GRCm39) |
F1085L |
possibly damaging |
Het |
Mcm7 |
A |
T |
5: 138,164,220 (GRCm39) |
Y600* |
probably null |
Het |
Mecom |
A |
T |
3: 30,033,803 (GRCm39) |
D300E |
probably benign |
Het |
Mfap4 |
T |
A |
11: 61,376,925 (GRCm39) |
Y51* |
probably null |
Het |
Mug1 |
T |
A |
6: 121,833,254 (GRCm39) |
N286K |
probably benign |
Het |
Myl2 |
A |
T |
5: 122,240,783 (GRCm39) |
R40* |
probably null |
Het |
Nom1 |
A |
G |
5: 29,642,623 (GRCm39) |
S375G |
probably damaging |
Het |
Nrcam |
C |
A |
12: 44,598,133 (GRCm39) |
P368Q |
probably null |
Het |
Oca2 |
G |
C |
7: 55,943,623 (GRCm39) |
Q265H |
probably null |
Het |
Or52a20 |
T |
A |
7: 103,366,475 (GRCm39) |
F225I |
probably damaging |
Het |
Or52n2c |
T |
C |
7: 104,574,075 (GRCm39) |
T299A |
probably damaging |
Het |
Or5k8 |
T |
A |
16: 58,644,176 (GRCm39) |
N299Y |
possibly damaging |
Het |
Or6c88 |
A |
T |
10: 129,406,664 (GRCm39) |
T47S |
probably damaging |
Het |
Or7a41 |
G |
A |
10: 78,871,577 (GRCm39) |
D316N |
probably benign |
Het |
Palmd |
T |
C |
3: 116,717,120 (GRCm39) |
E459G |
probably benign |
Het |
Pde1a |
G |
T |
2: 79,695,465 (GRCm39) |
A494D |
probably benign |
Het |
Pds5a |
T |
C |
5: 65,808,587 (GRCm39) |
Y428C |
probably damaging |
Het |
Pgm2 |
T |
C |
5: 64,254,391 (GRCm39) |
F59L |
probably benign |
Het |
Plekhm1 |
A |
G |
11: 103,258,950 (GRCm39) |
V980A |
possibly damaging |
Het |
Polb |
T |
C |
8: 23,118,346 (GRCm39) |
D318G |
possibly damaging |
Het |
Rasgef1c |
T |
A |
11: 49,861,040 (GRCm39) |
M335K |
probably damaging |
Het |
Rasgrp4 |
T |
C |
7: 28,849,687 (GRCm39) |
S651P |
probably benign |
Het |
Robo3 |
A |
C |
9: 37,334,558 (GRCm39) |
I624S |
possibly damaging |
Het |
Robo3 |
T |
A |
9: 37,339,087 (GRCm39) |
H290L |
probably benign |
Het |
Rps6kl1 |
T |
C |
12: 85,183,599 (GRCm39) |
H482R |
probably damaging |
Het |
Slc26a9 |
A |
T |
1: 131,681,691 (GRCm39) |
E168V |
probably benign |
Het |
Slc3a2 |
T |
C |
19: 8,691,226 (GRCm39) |
|
probably benign |
Het |
Slc4a4 |
A |
T |
5: 89,102,723 (GRCm39) |
K54* |
probably null |
Het |
Slitrk6 |
A |
G |
14: 110,988,258 (GRCm39) |
L483P |
probably damaging |
Het |
Svep1 |
T |
A |
4: 58,084,959 (GRCm39) |
N1793I |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,612,723 (GRCm39) |
I17119V |
possibly damaging |
Het |
Tulp4 |
T |
C |
17: 6,274,500 (GRCm39) |
L617P |
possibly damaging |
Het |
Uhrf1 |
A |
G |
17: 56,625,083 (GRCm39) |
N542S |
possibly damaging |
Het |
Vmn1r151 |
T |
A |
7: 22,198,368 (GRCm39) |
T246S |
probably damaging |
Het |
Vmn1r57 |
T |
A |
7: 5,224,069 (GRCm39) |
V198E |
probably damaging |
Het |
Vmn2r99 |
A |
T |
17: 19,598,889 (GRCm39) |
Q191L |
probably damaging |
Het |
Vrk3 |
C |
T |
7: 44,403,356 (GRCm39) |
T39M |
possibly damaging |
Het |
Zc3h3 |
C |
A |
15: 75,681,470 (GRCm39) |
R537L |
probably damaging |
Het |
Zfp64 |
A |
T |
2: 168,793,680 (GRCm39) |
V22E |
probably damaging |
Het |
Zwint |
T |
C |
10: 72,493,112 (GRCm39) |
L218P |
probably damaging |
Het |
|
Other mutations in Cyp2b19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00981:Cyp2b19
|
APN |
7 |
26,462,886 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01338:Cyp2b19
|
APN |
7 |
26,458,842 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01374:Cyp2b19
|
APN |
7 |
26,458,504 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01613:Cyp2b19
|
APN |
7 |
26,462,886 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01695:Cyp2b19
|
APN |
7 |
26,458,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02322:Cyp2b19
|
APN |
7 |
26,461,803 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03077:Cyp2b19
|
APN |
7 |
26,461,809 (GRCm39) |
missense |
probably benign |
|
R0047:Cyp2b19
|
UTSW |
7 |
26,466,251 (GRCm39) |
missense |
probably benign |
0.01 |
R0047:Cyp2b19
|
UTSW |
7 |
26,466,251 (GRCm39) |
missense |
probably benign |
0.01 |
R0452:Cyp2b19
|
UTSW |
7 |
26,466,187 (GRCm39) |
missense |
probably benign |
0.01 |
R0865:Cyp2b19
|
UTSW |
7 |
26,461,654 (GRCm39) |
splice site |
probably benign |
|
R1514:Cyp2b19
|
UTSW |
7 |
26,466,585 (GRCm39) |
missense |
probably benign |
0.00 |
R1681:Cyp2b19
|
UTSW |
7 |
26,462,765 (GRCm39) |
splice site |
probably null |
|
R2362:Cyp2b19
|
UTSW |
7 |
26,463,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Cyp2b19
|
UTSW |
7 |
26,461,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R4259:Cyp2b19
|
UTSW |
7 |
26,462,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R4592:Cyp2b19
|
UTSW |
7 |
26,470,819 (GRCm39) |
missense |
probably benign |
0.04 |
R4705:Cyp2b19
|
UTSW |
7 |
26,456,717 (GRCm39) |
missense |
probably benign |
0.03 |
R4789:Cyp2b19
|
UTSW |
7 |
26,463,801 (GRCm39) |
missense |
probably benign |
0.16 |
R5481:Cyp2b19
|
UTSW |
7 |
26,466,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R5749:Cyp2b19
|
UTSW |
7 |
26,462,844 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6041:Cyp2b19
|
UTSW |
7 |
26,458,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Cyp2b19
|
UTSW |
7 |
26,458,519 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6259:Cyp2b19
|
UTSW |
7 |
26,470,817 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6370:Cyp2b19
|
UTSW |
7 |
26,462,783 (GRCm39) |
missense |
probably benign |
0.07 |
R6519:Cyp2b19
|
UTSW |
7 |
26,458,536 (GRCm39) |
missense |
probably benign |
|
R6656:Cyp2b19
|
UTSW |
7 |
26,466,280 (GRCm39) |
missense |
probably benign |
|
R7283:Cyp2b19
|
UTSW |
7 |
26,466,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R7583:Cyp2b19
|
UTSW |
7 |
26,458,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Cyp2b19
|
UTSW |
7 |
26,461,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R7732:Cyp2b19
|
UTSW |
7 |
26,470,769 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7831:Cyp2b19
|
UTSW |
7 |
26,466,565 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8035:Cyp2b19
|
UTSW |
7 |
26,470,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8853:Cyp2b19
|
UTSW |
7 |
26,456,645 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9574:Cyp2b19
|
UTSW |
7 |
26,466,353 (GRCm39) |
missense |
probably null |
1.00 |
R9574:Cyp2b19
|
UTSW |
7 |
26,466,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Cyp2b19
|
UTSW |
7 |
26,466,208 (GRCm39) |
missense |
possibly damaging |
0.85 |
|