Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
G |
11: 84,151,505 (GRCm39) |
V801G |
possibly damaging |
Het |
Actbl2 |
T |
A |
13: 111,392,127 (GRCm39) |
M154K |
probably benign |
Het |
Adam7 |
A |
T |
14: 68,741,915 (GRCm39) |
|
probably null |
Het |
Arfgef1 |
T |
A |
1: 10,251,122 (GRCm39) |
T888S |
probably benign |
Het |
AW554918 |
C |
T |
18: 25,302,117 (GRCm39) |
P10L |
possibly damaging |
Het |
Bcap29 |
A |
G |
12: 31,680,881 (GRCm39) |
I35T |
probably damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Cby2 |
A |
G |
14: 75,830,077 (GRCm39) |
S39P |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,036,574 (GRCm39) |
D458G |
probably damaging |
Het |
Cdc42bpb |
T |
C |
12: 111,272,101 (GRCm39) |
K1104R |
probably benign |
Het |
Cep89 |
A |
G |
7: 35,137,803 (GRCm39) |
N729S |
probably damaging |
Het |
Clec4a4 |
T |
A |
6: 122,968,788 (GRCm39) |
M51K |
possibly damaging |
Het |
Dcdc2b |
A |
G |
4: 129,503,422 (GRCm39) |
L270P |
probably damaging |
Het |
Dennd5b |
G |
T |
6: 148,937,981 (GRCm39) |
H639N |
probably damaging |
Het |
Dnah11 |
T |
G |
12: 117,991,212 (GRCm39) |
T2385P |
probably benign |
Het |
Dnah11 |
T |
C |
12: 118,089,520 (GRCm39) |
E1182G |
probably damaging |
Het |
Dok7 |
T |
C |
5: 35,223,815 (GRCm39) |
V81A |
probably damaging |
Het |
Dtx1 |
T |
A |
5: 120,820,458 (GRCm39) |
M494L |
possibly damaging |
Het |
Foxj1 |
A |
T |
11: 116,223,080 (GRCm39) |
L241Q |
possibly damaging |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Hnmt |
T |
A |
2: 23,893,892 (GRCm39) |
T201S |
probably benign |
Het |
Jup |
G |
T |
11: 100,269,177 (GRCm39) |
T412K |
possibly damaging |
Het |
Kcnh2 |
G |
A |
5: 24,527,057 (GRCm39) |
S954F |
probably damaging |
Het |
Klk7 |
T |
A |
7: 43,461,424 (GRCm39) |
S14T |
probably benign |
Het |
Lama4 |
G |
A |
10: 38,923,944 (GRCm39) |
E451K |
probably damaging |
Het |
Ldhb |
A |
G |
6: 142,441,399 (GRCm39) |
C164R |
probably damaging |
Het |
Malrd1 |
G |
A |
2: 15,614,901 (GRCm39) |
D239N |
|
Het |
Mgam |
T |
A |
6: 40,643,788 (GRCm39) |
V572E |
probably damaging |
Het |
Mrgprb2 |
G |
T |
7: 48,201,890 (GRCm39) |
N278K |
probably damaging |
Het |
Msto1 |
A |
G |
3: 88,819,130 (GRCm39) |
Y206H |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,169,573 (GRCm39) |
S467G |
unknown |
Het |
Mysm1 |
T |
A |
4: 94,849,964 (GRCm39) |
I447L |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,688,795 (GRCm39) |
E494G |
possibly damaging |
Het |
Nol10 |
T |
G |
12: 17,452,174 (GRCm39) |
V376G |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,191,611 (GRCm39) |
I1032N |
probably damaging |
Het |
Oog2 |
A |
G |
4: 143,921,851 (GRCm39) |
K254E |
probably benign |
Het |
Or10ac1 |
A |
G |
6: 42,515,662 (GRCm39) |
F98S |
possibly damaging |
Het |
Or52z12 |
A |
T |
7: 103,233,588 (GRCm39) |
I120L |
possibly damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,811 (GRCm39) |
N286S |
probably damaging |
Het |
Or5d41 |
A |
T |
2: 88,055,366 (GRCm39) |
Y3* |
probably null |
Het |
Or5g25 |
T |
A |
2: 85,477,768 (GRCm39) |
D299V |
possibly damaging |
Het |
Or5g27 |
A |
G |
2: 85,409,640 (GRCm39) |
D19G |
probably benign |
Het |
Or6b1 |
T |
G |
6: 42,815,680 (GRCm39) |
Y288* |
probably null |
Het |
Or6c6 |
A |
T |
10: 129,186,426 (GRCm39) |
|
probably benign |
Het |
Or8h10 |
G |
A |
2: 86,808,501 (GRCm39) |
T213I |
probably benign |
Het |
Osbpl11 |
T |
A |
16: 33,056,649 (GRCm39) |
D694E |
probably benign |
Het |
Pcm1 |
T |
A |
8: 41,746,547 (GRCm39) |
Y1210N |
probably benign |
Het |
Pdxk |
T |
C |
10: 78,276,697 (GRCm39) |
M293V |
probably benign |
Het |
Plcb3 |
T |
C |
19: 6,940,235 (GRCm39) |
I451V |
probably benign |
Het |
Plekhm2 |
A |
G |
4: 141,361,687 (GRCm39) |
F272S |
probably damaging |
Het |
Pramel32 |
C |
A |
4: 88,546,202 (GRCm39) |
R380L |
probably benign |
Het |
Ptgdr |
A |
T |
14: 45,095,689 (GRCm39) |
|
probably null |
Het |
Ptprf |
C |
T |
4: 118,083,720 (GRCm39) |
V788I |
probably benign |
Het |
Ralbp1 |
C |
T |
17: 66,161,143 (GRCm39) |
V467I |
probably benign |
Het |
Ralgds |
A |
C |
2: 28,433,667 (GRCm39) |
Q229P |
possibly damaging |
Het |
Recql |
T |
C |
6: 142,320,610 (GRCm39) |
D146G |
probably damaging |
Het |
Reln |
T |
C |
5: 22,256,365 (GRCm39) |
N493S |
probably damaging |
Het |
Rfxank |
C |
T |
8: 70,587,936 (GRCm39) |
|
probably null |
Het |
Scn5a |
A |
T |
9: 119,315,596 (GRCm39) |
M1704K |
probably damaging |
Het |
Slc7a7 |
G |
T |
14: 54,611,725 (GRCm39) |
A316E |
possibly damaging |
Het |
Slco1a6 |
A |
T |
6: 142,036,794 (GRCm39) |
C538S |
probably benign |
Het |
Stard6 |
T |
C |
18: 70,631,718 (GRCm39) |
|
probably null |
Het |
Strip2 |
T |
A |
6: 29,927,612 (GRCm39) |
M219K |
possibly damaging |
Het |
Tcam1 |
T |
C |
11: 106,174,911 (GRCm39) |
V122A |
probably damaging |
Het |
Tha1 |
A |
G |
11: 117,760,516 (GRCm39) |
V236A |
possibly damaging |
Het |
Tmem201 |
A |
T |
4: 149,815,554 (GRCm39) |
I132N |
possibly damaging |
Het |
Tnc |
T |
C |
4: 63,938,894 (GRCm39) |
|
probably benign |
Het |
Vmn1r42 |
T |
C |
6: 89,822,495 (GRCm39) |
T25A |
probably benign |
Het |
Vmn2r94 |
T |
A |
17: 18,464,765 (GRCm39) |
|
probably null |
Het |
Wdfy4 |
A |
C |
14: 32,790,863 (GRCm39) |
V2188G |
|
Het |
Zfp623 |
T |
C |
15: 75,819,247 (GRCm39) |
S68P |
probably damaging |
Het |
Zfp950 |
A |
T |
19: 61,107,593 (GRCm39) |
C497S |
probably damaging |
Het |
Zkscan2 |
C |
T |
7: 123,079,327 (GRCm39) |
E877K |
probably damaging |
Het |
Zp3r |
C |
A |
1: 130,504,790 (GRCm39) |
V536L |
probably damaging |
Het |
|
Other mutations in Klhdc7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01574:Klhdc7b
|
APN |
15 |
89,271,572 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02711:Klhdc7b
|
APN |
15 |
89,272,246 (GRCm39) |
nonsense |
probably null |
|
R0115:Klhdc7b
|
UTSW |
15 |
89,272,724 (GRCm39) |
missense |
probably benign |
0.05 |
R0718:Klhdc7b
|
UTSW |
15 |
89,272,372 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0729:Klhdc7b
|
UTSW |
15 |
89,271,598 (GRCm39) |
nonsense |
probably null |
|
R0971:Klhdc7b
|
UTSW |
15 |
89,271,257 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1794:Klhdc7b
|
UTSW |
15 |
89,271,223 (GRCm39) |
missense |
probably benign |
0.00 |
R1815:Klhdc7b
|
UTSW |
15 |
89,271,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R1893:Klhdc7b
|
UTSW |
15 |
89,271,898 (GRCm39) |
splice site |
probably null |
|
R3508:Klhdc7b
|
UTSW |
15 |
89,271,095 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R3552:Klhdc7b
|
UTSW |
15 |
89,271,724 (GRCm39) |
missense |
probably benign |
0.02 |
R4001:Klhdc7b
|
UTSW |
15 |
89,272,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Klhdc7b
|
UTSW |
15 |
89,271,472 (GRCm39) |
missense |
probably benign |
0.01 |
R4727:Klhdc7b
|
UTSW |
15 |
89,271,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R5129:Klhdc7b
|
UTSW |
15 |
89,272,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Klhdc7b
|
UTSW |
15 |
89,271,562 (GRCm39) |
missense |
probably benign |
0.01 |
R5643:Klhdc7b
|
UTSW |
15 |
89,271,862 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5778:Klhdc7b
|
UTSW |
15 |
89,271,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Klhdc7b
|
UTSW |
15 |
89,271,359 (GRCm39) |
missense |
probably benign |
0.02 |
R5942:Klhdc7b
|
UTSW |
15 |
89,271,634 (GRCm39) |
missense |
probably benign |
0.03 |
R6020:Klhdc7b
|
UTSW |
15 |
89,272,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6653:Klhdc7b
|
UTSW |
15 |
89,271,292 (GRCm39) |
missense |
probably benign |
0.00 |
R6810:Klhdc7b
|
UTSW |
15 |
89,272,559 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7548:Klhdc7b
|
UTSW |
15 |
89,272,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R7640:Klhdc7b
|
UTSW |
15 |
89,271,463 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8461:Klhdc7b
|
UTSW |
15 |
89,271,824 (GRCm39) |
missense |
probably damaging |
0.97 |
R8712:Klhdc7b
|
UTSW |
15 |
89,271,025 (GRCm39) |
missense |
probably benign |
0.07 |
R8890:Klhdc7b
|
UTSW |
15 |
89,272,888 (GRCm39) |
missense |
probably benign |
0.03 |
R9497:Klhdc7b
|
UTSW |
15 |
89,272,463 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9785:Klhdc7b
|
UTSW |
15 |
89,272,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|