Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
T |
7: 120,140,370 (GRCm39) |
I1557F |
probably damaging |
Het |
Acad10 |
A |
T |
5: 121,787,420 (GRCm39) |
D176E |
probably damaging |
Het |
Acta2 |
A |
T |
19: 34,229,922 (GRCm39) |
V11E |
probably damaging |
Het |
Ampd2 |
T |
C |
3: 107,986,609 (GRCm39) |
H225R |
probably damaging |
Het |
Arfgef3 |
A |
G |
10: 18,501,203 (GRCm39) |
Y1016H |
possibly damaging |
Het |
Atg7 |
C |
T |
6: 114,650,639 (GRCm39) |
T83M |
possibly damaging |
Het |
AU018091 |
A |
G |
7: 3,209,267 (GRCm39) |
|
probably null |
Het |
Birc2 |
A |
G |
9: 7,819,469 (GRCm39) |
V481A |
probably benign |
Het |
Cabp1 |
A |
T |
5: 115,310,960 (GRCm39) |
D295E |
probably damaging |
Het |
Cd180 |
A |
T |
13: 102,842,699 (GRCm39) |
T582S |
probably benign |
Het |
Ddx27 |
A |
G |
2: 166,857,297 (GRCm39) |
D15G |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,230,246 (GRCm39) |
Y353C |
probably benign |
Het |
Dsg1c |
C |
T |
18: 20,400,980 (GRCm39) |
T161I |
probably damaging |
Het |
Epm2a |
A |
G |
10: 11,266,829 (GRCm39) |
|
probably null |
Het |
Fat2 |
T |
C |
11: 55,152,914 (GRCm39) |
H3766R |
probably benign |
Het |
Fjx1 |
A |
G |
2: 102,280,903 (GRCm39) |
V344A |
probably benign |
Het |
Frmd3 |
A |
G |
4: 74,016,363 (GRCm39) |
I93V |
probably benign |
Het |
Gbe1 |
TAGTAAGAGT |
TAGT |
16: 70,230,444 (GRCm39) |
|
probably benign |
Het |
Gdf15 |
A |
G |
8: 71,082,794 (GRCm39) |
L104P |
possibly damaging |
Het |
Glra3 |
G |
A |
8: 56,393,961 (GRCm39) |
R24Q |
probably benign |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
Ighv1-9 |
A |
T |
12: 114,547,448 (GRCm39) |
M31K |
probably benign |
Het |
Ipmk |
G |
A |
10: 71,183,920 (GRCm39) |
G47S |
probably null |
Het |
Itsn2 |
T |
C |
12: 4,679,641 (GRCm39) |
I150T |
probably benign |
Het |
Kcnq5 |
T |
C |
1: 21,476,068 (GRCm39) |
Y545C |
probably damaging |
Het |
Klk1b8 |
C |
A |
7: 43,602,213 (GRCm39) |
H48Q |
possibly damaging |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrrc34 |
T |
C |
3: 30,678,969 (GRCm39) |
Y376C |
probably benign |
Het |
Mast4 |
A |
T |
13: 102,941,222 (GRCm39) |
D278E |
probably damaging |
Het |
Mtmr3 |
T |
C |
11: 4,437,505 (GRCm39) |
Y982C |
possibly damaging |
Het |
Ndst4 |
T |
G |
3: 125,403,160 (GRCm39) |
H422Q |
possibly damaging |
Het |
Nek7 |
T |
C |
1: 138,430,376 (GRCm39) |
E206G |
probably damaging |
Het |
Nufip2 |
CCAGCAGCAGCAGCAGCAGCAG |
CCAGCAGCAGCAGCAGCAG |
11: 77,577,122 (GRCm39) |
|
probably benign |
Het |
Or5b99 |
T |
A |
19: 12,976,861 (GRCm39) |
N170K |
possibly damaging |
Het |
Pglyrp2 |
T |
C |
17: 32,635,048 (GRCm39) |
Y438C |
probably damaging |
Het |
Pigr |
G |
T |
1: 130,775,064 (GRCm39) |
W497L |
probably damaging |
Het |
Pkd2l2 |
G |
T |
18: 34,549,936 (GRCm39) |
V194L |
probably benign |
Het |
Ppp1r16b |
A |
T |
2: 158,538,068 (GRCm39) |
K5M |
probably damaging |
Het |
Psat1 |
A |
T |
19: 15,898,307 (GRCm39) |
S35R |
probably damaging |
Het |
Qrfprl |
G |
A |
6: 65,424,385 (GRCm39) |
M126I |
probably damaging |
Het |
Rab11fip1 |
G |
A |
8: 27,646,303 (GRCm39) |
Q258* |
probably null |
Het |
Rad51d |
A |
G |
11: 82,780,623 (GRCm39) |
L53P |
probably damaging |
Het |
Rell2 |
G |
A |
18: 38,091,341 (GRCm39) |
A169T |
probably benign |
Het |
Rnf19b |
T |
C |
4: 128,976,572 (GRCm39) |
I545T |
probably benign |
Het |
Slc12a1 |
G |
T |
2: 125,055,999 (GRCm39) |
E843D |
possibly damaging |
Het |
Slc1a4 |
A |
G |
11: 20,254,346 (GRCm39) |
S507P |
probably damaging |
Het |
Slc6a1 |
G |
A |
6: 114,290,473 (GRCm39) |
W316* |
probably null |
Het |
Spesp1 |
A |
G |
9: 62,180,152 (GRCm39) |
L252P |
probably damaging |
Het |
Sphkap |
G |
A |
1: 83,385,811 (GRCm39) |
|
probably benign |
Het |
Srcap |
A |
G |
7: 127,141,769 (GRCm39) |
T1850A |
probably damaging |
Het |
Supv3l1 |
T |
C |
10: 62,266,365 (GRCm39) |
T604A |
possibly damaging |
Het |
Tacr1 |
A |
G |
6: 82,380,846 (GRCm39) |
T86A |
possibly damaging |
Het |
Tenm3 |
T |
C |
8: 49,127,451 (GRCm39) |
R76G |
probably damaging |
Het |
Tmprss6 |
C |
A |
15: 78,330,977 (GRCm39) |
A419S |
probably damaging |
Het |
Usp54 |
T |
G |
14: 20,612,177 (GRCm39) |
I880L |
probably benign |
Het |
Wwp2 |
T |
A |
8: 108,275,134 (GRCm39) |
V377D |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,581,159 (GRCm39) |
E65D |
probably benign |
Het |
Zfy2 |
T |
C |
Y: 2,121,491 (GRCm39) |
E134G |
probably benign |
Het |
|
Other mutations in Cnksr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01303:Cnksr3
|
APN |
10 |
7,104,281 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01583:Cnksr3
|
APN |
10 |
7,070,512 (GRCm39) |
missense |
probably benign |
|
IGL02374:Cnksr3
|
APN |
10 |
7,070,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02541:Cnksr3
|
APN |
10 |
7,085,073 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02551:Cnksr3
|
APN |
10 |
7,102,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02975:Cnksr3
|
APN |
10 |
7,088,354 (GRCm39) |
critical splice donor site |
probably null |
|
R0652:Cnksr3
|
UTSW |
10 |
7,070,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1451:Cnksr3
|
UTSW |
10 |
7,076,830 (GRCm39) |
missense |
probably null |
0.93 |
R1453:Cnksr3
|
UTSW |
10 |
7,079,132 (GRCm39) |
missense |
probably benign |
0.00 |
R1847:Cnksr3
|
UTSW |
10 |
7,104,324 (GRCm39) |
missense |
probably benign |
0.01 |
R1852:Cnksr3
|
UTSW |
10 |
7,070,539 (GRCm39) |
missense |
probably benign |
0.06 |
R3002:Cnksr3
|
UTSW |
10 |
7,102,856 (GRCm39) |
splice site |
probably benign |
|
R4621:Cnksr3
|
UTSW |
10 |
7,076,182 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4835:Cnksr3
|
UTSW |
10 |
7,110,757 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4941:Cnksr3
|
UTSW |
10 |
7,102,925 (GRCm39) |
missense |
probably benign |
0.07 |
R4981:Cnksr3
|
UTSW |
10 |
7,110,777 (GRCm39) |
missense |
probably benign |
0.00 |
R5000:Cnksr3
|
UTSW |
10 |
7,076,746 (GRCm39) |
nonsense |
probably null |
|
R5001:Cnksr3
|
UTSW |
10 |
7,076,746 (GRCm39) |
nonsense |
probably null |
|
R5267:Cnksr3
|
UTSW |
10 |
7,076,633 (GRCm39) |
critical splice donor site |
probably null |
|
R5322:Cnksr3
|
UTSW |
10 |
7,085,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5623:Cnksr3
|
UTSW |
10 |
7,070,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5853:Cnksr3
|
UTSW |
10 |
7,092,977 (GRCm39) |
missense |
probably benign |
0.09 |
R5930:Cnksr3
|
UTSW |
10 |
7,092,993 (GRCm39) |
missense |
probably benign |
|
R6459:Cnksr3
|
UTSW |
10 |
7,076,820 (GRCm39) |
missense |
probably benign |
0.00 |
R6893:Cnksr3
|
UTSW |
10 |
7,085,129 (GRCm39) |
splice site |
probably null |
|
R6949:Cnksr3
|
UTSW |
10 |
7,110,757 (GRCm39) |
missense |
probably benign |
0.02 |
R7075:Cnksr3
|
UTSW |
10 |
7,102,931 (GRCm39) |
missense |
probably benign |
0.33 |
R7487:Cnksr3
|
UTSW |
10 |
7,085,097 (GRCm39) |
missense |
probably benign |
0.01 |
R8165:Cnksr3
|
UTSW |
10 |
7,104,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R8181:Cnksr3
|
UTSW |
10 |
7,070,475 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8472:Cnksr3
|
UTSW |
10 |
7,084,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R8885:Cnksr3
|
UTSW |
10 |
7,090,201 (GRCm39) |
unclassified |
probably benign |
|
R8887:Cnksr3
|
UTSW |
10 |
7,104,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R8930:Cnksr3
|
UTSW |
10 |
7,110,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Cnksr3
|
UTSW |
10 |
7,110,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9195:Cnksr3
|
UTSW |
10 |
7,088,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R9617:Cnksr3
|
UTSW |
10 |
7,079,021 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Cnksr3
|
UTSW |
10 |
7,084,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|