Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 121,922,983 (GRCm39) |
S1181P |
probably benign |
Het |
Acvr1c |
C |
T |
2: 58,173,491 (GRCm39) |
C337Y |
probably damaging |
Het |
Adgrf5 |
A |
G |
17: 43,757,840 (GRCm39) |
E758G |
probably benign |
Het |
Akap3 |
T |
A |
6: 126,841,493 (GRCm39) |
D37E |
probably damaging |
Het |
Ano5 |
A |
T |
7: 51,222,776 (GRCm39) |
H445L |
probably benign |
Het |
Ap4b1 |
T |
A |
3: 103,720,116 (GRCm39) |
I121N |
probably damaging |
Het |
Arhgdia |
T |
C |
11: 120,470,354 (GRCm39) |
K135E |
probably benign |
Het |
Ass1 |
T |
C |
2: 31,391,544 (GRCm39) |
F273S |
possibly damaging |
Het |
Atp8a2 |
A |
C |
14: 59,885,366 (GRCm39) |
Y1119* |
probably null |
Het |
Birc6 |
T |
A |
17: 74,959,000 (GRCm39) |
M3839K |
probably damaging |
Het |
Cacna1a |
A |
G |
8: 85,365,370 (GRCm39) |
H2171R |
probably benign |
Het |
Ccdc90b |
T |
A |
7: 92,224,545 (GRCm39) |
D183E |
probably benign |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cdh23 |
T |
A |
10: 60,274,618 (GRCm39) |
T491S |
probably benign |
Het |
Cercam |
T |
C |
2: 29,771,829 (GRCm39) |
S550P |
possibly damaging |
Het |
Chd9 |
A |
G |
8: 91,723,472 (GRCm39) |
H1019R |
unknown |
Het |
Coil |
A |
T |
11: 88,871,980 (GRCm39) |
K114* |
probably null |
Het |
Csmd2 |
A |
C |
4: 128,440,483 (GRCm39) |
T3183P |
|
Het |
Cul9 |
T |
C |
17: 46,814,506 (GRCm39) |
Y2219C |
probably damaging |
Het |
Efhd2 |
G |
A |
4: 141,587,186 (GRCm39) |
Q199* |
probably null |
Het |
Elp3 |
A |
T |
14: 65,785,360 (GRCm39) |
S499R |
probably benign |
Het |
Exoc8 |
T |
G |
8: 125,622,709 (GRCm39) |
I553L |
probably benign |
Het |
Fyco1 |
C |
A |
9: 123,659,142 (GRCm39) |
V345L |
probably benign |
Het |
Galr3 |
T |
A |
15: 78,927,279 (GRCm39) |
V240E |
probably damaging |
Het |
Gm21190 |
A |
G |
5: 15,730,862 (GRCm39) |
S165P |
probably benign |
Het |
Gnal |
T |
A |
18: 67,350,255 (GRCm39) |
Y372* |
probably null |
Het |
H2-DMa |
A |
G |
17: 34,357,416 (GRCm39) |
N230D |
probably damaging |
Het |
Hk2 |
T |
C |
6: 82,721,847 (GRCm39) |
D164G |
possibly damaging |
Het |
Ighv3-4 |
T |
A |
12: 114,217,544 (GRCm39) |
I16F |
possibly damaging |
Het |
Ivl |
T |
C |
3: 92,480,078 (GRCm39) |
|
probably benign |
Het |
Lct |
A |
T |
1: 128,215,306 (GRCm39) |
S1757T |
probably damaging |
Het |
Lmbr1l |
T |
A |
15: 98,810,065 (GRCm39) |
Y132F |
probably damaging |
Het |
M6pr |
T |
C |
6: 122,293,029 (GRCm39) |
V203A |
possibly damaging |
Het |
Map9 |
T |
C |
3: 82,284,476 (GRCm39) |
|
probably null |
Het |
Muc5ac |
A |
T |
7: 141,360,892 (GRCm39) |
D1401V |
probably damaging |
Het |
Myh7 |
A |
G |
14: 55,227,786 (GRCm39) |
S291P |
probably damaging |
Het |
Nynrin |
G |
C |
14: 56,107,703 (GRCm39) |
V937L |
probably benign |
Het |
Or5d44 |
C |
T |
2: 88,141,825 (GRCm39) |
G105D |
probably benign |
Het |
Or5m3 |
T |
G |
2: 85,838,149 (GRCm39) |
F10V |
probably damaging |
Het |
Pank2 |
A |
G |
2: 131,135,320 (GRCm39) |
N386S |
probably benign |
Het |
Phkg2 |
G |
T |
7: 127,181,528 (GRCm39) |
R237L |
possibly damaging |
Het |
Pkhd1 |
C |
T |
1: 20,590,432 (GRCm39) |
V1772I |
probably benign |
Het |
Plch2 |
G |
T |
4: 155,068,852 (GRCm39) |
P1258Q |
probably benign |
Het |
Plekhm2 |
A |
T |
4: 141,369,764 (GRCm39) |
I77N |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,176,936 (GRCm39) |
T954A |
probably benign |
Het |
Ranbp3 |
T |
C |
17: 57,015,273 (GRCm39) |
V325A |
probably damaging |
Het |
Rgs10 |
A |
T |
7: 128,019,793 (GRCm39) |
S16T |
probably benign |
Het |
Scaper |
A |
T |
9: 55,771,722 (GRCm39) |
V398E |
probably benign |
Het |
Selenot |
A |
G |
3: 58,492,698 (GRCm39) |
I62V |
probably benign |
Het |
Serpinb9e |
T |
A |
13: 33,439,092 (GRCm39) |
C173S |
probably benign |
Het |
Slc13a3 |
G |
T |
2: 165,275,999 (GRCm39) |
T249K |
probably damaging |
Het |
Slc4a8 |
T |
A |
15: 100,701,171 (GRCm39) |
V741D |
possibly damaging |
Het |
Slco4a1 |
T |
C |
2: 180,106,592 (GRCm39) |
V258A |
probably damaging |
Het |
Sycp2l |
T |
G |
13: 41,291,390 (GRCm39) |
L256R |
probably damaging |
Het |
Tektl1 |
T |
C |
10: 78,585,038 (GRCm39) |
D266G |
probably benign |
Het |
Tektl1 |
T |
C |
10: 78,586,463 (GRCm39) |
D196G |
probably damaging |
Het |
Top2a |
C |
T |
11: 98,905,567 (GRCm39) |
V337I |
probably benign |
Het |
Tut4 |
T |
C |
4: 108,388,139 (GRCm39) |
L1160P |
probably damaging |
Het |
Unc13a |
A |
C |
8: 72,098,405 (GRCm39) |
F1127V |
possibly damaging |
Het |
Wdr25 |
C |
T |
12: 108,992,393 (GRCm39) |
Q435* |
probably null |
Het |
Zc3h7b |
T |
G |
15: 81,664,719 (GRCm39) |
L526R |
probably damaging |
Het |
Zeb1 |
C |
A |
18: 5,705,127 (GRCm39) |
T48K |
possibly damaging |
Het |
Zfhx2 |
A |
C |
14: 55,303,243 (GRCm39) |
S1580R |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,583,549 (GRCm39) |
I1139V |
possibly damaging |
Het |
Zfp536 |
C |
A |
7: 37,179,492 (GRCm39) |
V1038L |
probably benign |
Het |
Zfp759 |
T |
A |
13: 67,286,947 (GRCm39) |
V166E |
probably benign |
Het |
Zfp985 |
A |
T |
4: 147,667,883 (GRCm39) |
K250N |
possibly damaging |
Het |
|
Other mutations in Klhl8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0144:Klhl8
|
UTSW |
5 |
104,015,804 (GRCm39) |
missense |
probably benign |
0.45 |
R0718:Klhl8
|
UTSW |
5 |
104,024,159 (GRCm39) |
intron |
probably benign |
|
R1374:Klhl8
|
UTSW |
5 |
104,011,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Klhl8
|
UTSW |
5 |
104,019,911 (GRCm39) |
missense |
probably damaging |
0.96 |
R4440:Klhl8
|
UTSW |
5 |
104,015,433 (GRCm39) |
missense |
probably benign |
0.00 |
R6406:Klhl8
|
UTSW |
5 |
104,010,981 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6961:Klhl8
|
UTSW |
5 |
104,018,435 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7807:Klhl8
|
UTSW |
5 |
104,023,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7863:Klhl8
|
UTSW |
5 |
104,019,968 (GRCm39) |
missense |
probably benign |
|
R8217:Klhl8
|
UTSW |
5 |
104,015,466 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8240:Klhl8
|
UTSW |
5 |
104,015,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R8241:Klhl8
|
UTSW |
5 |
104,015,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R8278:Klhl8
|
UTSW |
5 |
104,022,107 (GRCm39) |
missense |
probably benign |
0.00 |
R8297:Klhl8
|
UTSW |
5 |
104,010,954 (GRCm39) |
missense |
probably benign |
0.23 |
R8539:Klhl8
|
UTSW |
5 |
104,015,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R8991:Klhl8
|
UTSW |
5 |
104,018,404 (GRCm39) |
missense |
probably benign |
0.03 |
R9051:Klhl8
|
UTSW |
5 |
104,015,709 (GRCm39) |
critical splice donor site |
probably null |
|
R9176:Klhl8
|
UTSW |
5 |
104,012,111 (GRCm39) |
missense |
probably benign |
0.00 |
R9183:Klhl8
|
UTSW |
5 |
104,012,111 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Klhl8
|
UTSW |
5 |
104,033,905 (GRCm39) |
missense |
probably benign |
0.00 |
|