Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,629,449 (GRCm39) |
V1293M |
probably damaging |
Het |
Agt |
A |
G |
8: 125,290,537 (GRCm39) |
W257R |
possibly damaging |
Het |
Arhgef11 |
T |
A |
3: 87,620,406 (GRCm39) |
N457K |
probably benign |
Het |
Bcl3 |
G |
T |
7: 19,554,082 (GRCm39) |
H95Q |
probably benign |
Het |
C1d |
T |
A |
11: 17,213,662 (GRCm39) |
N64K |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,607 (GRCm39) |
R280C |
probably damaging |
Het |
Cd300c2 |
C |
T |
11: 114,891,466 (GRCm39) |
S136N |
probably benign |
Het |
Cdh8 |
A |
G |
8: 99,757,672 (GRCm39) |
V642A |
possibly damaging |
Het |
Cep290 |
A |
T |
10: 100,331,706 (GRCm39) |
I180F |
possibly damaging |
Het |
Copz2 |
A |
G |
11: 96,744,887 (GRCm39) |
E86G |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,230,635 (GRCm39) |
I971V |
probably benign |
Het |
Cracdl |
A |
G |
1: 37,652,537 (GRCm39) |
V1090A |
probably benign |
Het |
Csf3r |
A |
T |
4: 125,923,712 (GRCm39) |
D74V |
possibly damaging |
Het |
Cyp11b1 |
T |
G |
15: 74,710,789 (GRCm39) |
E257A |
possibly damaging |
Het |
Dlg2 |
A |
G |
7: 92,024,875 (GRCm39) |
Q580R |
probably damaging |
Het |
Dnai2 |
A |
T |
11: 114,645,275 (GRCm39) |
K570M |
unknown |
Het |
Dock8 |
A |
G |
19: 25,133,281 (GRCm39) |
K1143E |
probably benign |
Het |
Dxo |
T |
C |
17: 35,058,099 (GRCm39) |
S394P |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,810,977 (GRCm39) |
D1388G |
probably benign |
Het |
F13a1 |
C |
A |
13: 37,209,692 (GRCm39) |
R91L |
probably damaging |
Het |
Fam50b |
C |
T |
13: 34,930,856 (GRCm39) |
R111* |
probably null |
Het |
Fat2 |
T |
G |
11: 55,202,535 (GRCm39) |
N180H |
probably damaging |
Het |
Fitm2 |
A |
T |
2: 163,311,768 (GRCm39) |
H148Q |
probably benign |
Het |
Fjx1 |
A |
T |
2: 102,281,156 (GRCm39) |
S260T |
possibly damaging |
Het |
Fos |
T |
C |
12: 85,522,466 (GRCm39) |
L165P |
probably damaging |
Het |
Gm39115 |
C |
A |
7: 141,689,710 (GRCm39) |
C21F |
unknown |
Het |
Gucy1a1 |
C |
T |
3: 82,005,000 (GRCm39) |
C595Y |
probably damaging |
Het |
Hectd4 |
G |
T |
5: 121,467,172 (GRCm39) |
W2478L |
possibly damaging |
Het |
I830077J02Rik |
T |
A |
3: 105,836,060 (GRCm39) |
K9N |
probably damaging |
Het |
Ift70a1 |
T |
C |
2: 75,811,519 (GRCm39) |
D188G |
probably benign |
Het |
Ireb2 |
T |
C |
9: 54,811,265 (GRCm39) |
F723L |
possibly damaging |
Het |
Itpr1 |
G |
A |
6: 108,496,309 (GRCm39) |
V2580I |
probably damaging |
Het |
Kcnu1 |
G |
A |
8: 26,382,092 (GRCm39) |
G481R |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,926,129 (GRCm39) |
A90S |
probably benign |
Het |
Klra8 |
A |
G |
6: 130,105,056 (GRCm39) |
V23A |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,023,777 (GRCm39) |
M1T |
probably null |
Het |
Lpin3 |
C |
T |
2: 160,737,273 (GRCm39) |
P107S |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,265,867 (GRCm39) |
K1100* |
probably null |
Het |
Obscn |
G |
A |
11: 58,929,700 (GRCm39) |
H5172Y |
probably damaging |
Het |
Or10a3m |
T |
A |
7: 108,313,418 (GRCm39) |
M286K |
possibly damaging |
Het |
Or4p20 |
A |
G |
2: 88,253,745 (GRCm39) |
I208T |
probably benign |
Het |
Or5ae1 |
C |
T |
7: 84,565,787 (GRCm39) |
H267Y |
probably benign |
Het |
Or6z1 |
T |
A |
7: 6,504,734 (GRCm39) |
T170S |
probably damaging |
Het |
Or8c14-ps1 |
A |
T |
9: 38,101,498 (GRCm39) |
H159L |
possibly damaging |
Het |
Orc3 |
A |
G |
4: 34,593,173 (GRCm39) |
L298P |
probably damaging |
Het |
Otub1 |
A |
G |
19: 7,177,360 (GRCm39) |
F96L |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,736,670 (GRCm39) |
S156P |
probably benign |
Het |
Pde3b |
A |
G |
7: 114,126,129 (GRCm39) |
M788V |
probably damaging |
Het |
Pias4 |
A |
G |
10: 80,992,844 (GRCm39) |
|
probably null |
Het |
Polg |
A |
G |
7: 79,114,743 (GRCm39) |
C73R |
probably benign |
Het |
Ptbp2 |
T |
C |
3: 119,541,467 (GRCm39) |
Y190C |
probably damaging |
Het |
Rab33b |
T |
A |
3: 51,401,050 (GRCm39) |
F175I |
probably damaging |
Het |
Rfx1 |
A |
G |
8: 84,806,515 (GRCm39) |
T108A |
probably benign |
Het |
Ribc2 |
A |
G |
15: 85,019,461 (GRCm39) |
D81G |
probably benign |
Het |
Rnf213 |
T |
G |
11: 119,340,149 (GRCm39) |
M3460R |
|
Het |
Rsf1 |
T |
A |
7: 97,266,103 (GRCm39) |
S86T |
|
Het |
Rxfp2 |
C |
A |
5: 149,973,068 (GRCm39) |
T181N |
possibly damaging |
Het |
Samm50 |
G |
A |
15: 84,094,702 (GRCm39) |
E365K |
possibly damaging |
Het |
Shld2 |
A |
C |
14: 33,989,942 (GRCm39) |
N321K |
probably benign |
Het |
Slc22a18 |
T |
C |
7: 143,051,123 (GRCm39) |
V334A |
probably damaging |
Het |
Slc23a3 |
A |
T |
1: 75,110,085 (GRCm39) |
C97S |
probably benign |
Het |
Smchd1 |
T |
A |
17: 71,714,244 (GRCm39) |
H873L |
probably benign |
Het |
Snrpa1 |
G |
A |
7: 65,720,381 (GRCm39) |
G195R |
probably benign |
Het |
Sphkap |
T |
A |
1: 83,255,953 (GRCm39) |
I599F |
probably benign |
Het |
Stox1 |
A |
G |
10: 62,501,543 (GRCm39) |
V339A |
probably damaging |
Het |
Tlx1 |
A |
G |
19: 45,142,036 (GRCm39) |
E220G |
probably damaging |
Het |
Tmem71 |
C |
A |
15: 66,413,421 (GRCm39) |
|
probably null |
Het |
Tmprss3 |
T |
C |
17: 31,413,976 (GRCm39) |
D56G |
possibly damaging |
Het |
Trabd |
A |
G |
15: 88,970,107 (GRCm39) |
R368G |
probably benign |
Het |
Trf |
A |
G |
9: 103,094,675 (GRCm39) |
I461T |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,676,226 (GRCm39) |
T133A |
possibly damaging |
Het |
Trpv3 |
G |
A |
11: 73,186,209 (GRCm39) |
V667I |
possibly damaging |
Het |
Vps13b |
T |
A |
15: 35,455,246 (GRCm39) |
N718K |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,345,166 (GRCm39) |
S1182P |
possibly damaging |
Het |
Zfp13 |
T |
C |
17: 23,795,866 (GRCm39) |
D235G |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,227,987 (GRCm39) |
E1874G |
probably damaging |
Het |
Zfp503 |
T |
C |
14: 22,036,277 (GRCm39) |
K213R |
probably benign |
Het |
|
Other mutations in Zkscan2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Zkscan2
|
APN |
7 |
123,079,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02098:Zkscan2
|
APN |
7 |
123,099,064 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03093:Zkscan2
|
APN |
7 |
123,094,073 (GRCm39) |
missense |
probably benign |
0.01 |
R0016:Zkscan2
|
UTSW |
7 |
123,099,219 (GRCm39) |
start gained |
probably benign |
|
R0135:Zkscan2
|
UTSW |
7 |
123,079,864 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0541:Zkscan2
|
UTSW |
7 |
123,079,423 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0569:Zkscan2
|
UTSW |
7 |
123,097,898 (GRCm39) |
missense |
probably benign |
0.11 |
R1537:Zkscan2
|
UTSW |
7 |
123,099,064 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1726:Zkscan2
|
UTSW |
7 |
123,089,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Zkscan2
|
UTSW |
7 |
123,084,225 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3802:Zkscan2
|
UTSW |
7 |
123,094,365 (GRCm39) |
intron |
probably benign |
|
R3803:Zkscan2
|
UTSW |
7 |
123,094,365 (GRCm39) |
intron |
probably benign |
|
R3804:Zkscan2
|
UTSW |
7 |
123,094,365 (GRCm39) |
intron |
probably benign |
|
R4012:Zkscan2
|
UTSW |
7 |
123,097,883 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4111:Zkscan2
|
UTSW |
7 |
123,081,907 (GRCm39) |
intron |
probably benign |
|
R4605:Zkscan2
|
UTSW |
7 |
123,097,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4978:Zkscan2
|
UTSW |
7 |
123,094,542 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5004:Zkscan2
|
UTSW |
7 |
123,089,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Zkscan2
|
UTSW |
7 |
123,099,090 (GRCm39) |
missense |
probably benign |
0.01 |
R5753:Zkscan2
|
UTSW |
7 |
123,079,923 (GRCm39) |
missense |
probably benign |
|
R5830:Zkscan2
|
UTSW |
7 |
123,079,323 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6153:Zkscan2
|
UTSW |
7 |
123,088,993 (GRCm39) |
missense |
probably benign |
0.06 |
R6912:Zkscan2
|
UTSW |
7 |
123,099,196 (GRCm39) |
start gained |
probably benign |
|
R7170:Zkscan2
|
UTSW |
7 |
123,099,030 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7269:Zkscan2
|
UTSW |
7 |
123,088,994 (GRCm39) |
missense |
probably benign |
|
R7310:Zkscan2
|
UTSW |
7 |
123,089,276 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7399:Zkscan2
|
UTSW |
7 |
123,079,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R7624:Zkscan2
|
UTSW |
7 |
123,097,994 (GRCm39) |
missense |
probably damaging |
0.97 |
R7687:Zkscan2
|
UTSW |
7 |
123,099,085 (GRCm39) |
missense |
probably benign |
0.13 |
R8236:Zkscan2
|
UTSW |
7 |
123,079,135 (GRCm39) |
missense |
probably benign |
0.01 |
R9365:Zkscan2
|
UTSW |
7 |
123,079,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Zkscan2
|
UTSW |
7 |
123,084,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R9531:Zkscan2
|
UTSW |
7 |
123,088,837 (GRCm39) |
missense |
probably damaging |
0.97 |
R9757:Zkscan2
|
UTSW |
7 |
123,079,310 (GRCm39) |
nonsense |
probably null |
|
Z1177:Zkscan2
|
UTSW |
7 |
123,079,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|