Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Abcd2 |
G |
T |
15: 91,075,246 (GRCm39) |
A189E |
probably benign |
Het |
Ahcy |
T |
C |
2: 154,906,817 (GRCm39) |
T159A |
probably benign |
Het |
Arfgef2 |
T |
C |
2: 166,669,560 (GRCm39) |
V84A |
probably damaging |
Het |
Brwd1 |
G |
A |
16: 95,832,748 (GRCm39) |
T1036M |
probably benign |
Het |
Ccdc187 |
G |
T |
2: 26,166,133 (GRCm39) |
S765R |
probably damaging |
Het |
Cfap210 |
A |
G |
2: 69,617,553 (GRCm39) |
M76T |
possibly damaging |
Het |
Chd1l |
G |
A |
3: 97,469,941 (GRCm39) |
R862* |
probably null |
Het |
Crmp1 |
A |
G |
5: 37,430,778 (GRCm39) |
D71G |
probably damaging |
Het |
Ctif |
CTGTGTCCGGTGT |
CTGT |
18: 75,654,650 (GRCm39) |
|
probably benign |
Het |
Ctsb |
A |
C |
14: 63,379,189 (GRCm39) |
Y267S |
probably damaging |
Het |
Cyp4a12b |
T |
A |
4: 115,290,164 (GRCm39) |
I239N |
possibly damaging |
Het |
Dna2 |
T |
C |
10: 62,796,203 (GRCm39) |
V544A |
possibly damaging |
Het |
Dnhd1 |
T |
A |
7: 105,346,106 (GRCm39) |
F2364Y |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,811,355 (GRCm39) |
E2558V |
probably damaging |
Het |
Gm10061 |
A |
C |
16: 88,948,169 (GRCm39) |
Y48S |
unknown |
Het |
Herc1 |
T |
A |
9: 66,323,545 (GRCm39) |
M1353K |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lin7a |
T |
C |
10: 107,107,780 (GRCm39) |
V20A |
probably benign |
Het |
Lsr |
T |
A |
7: 30,671,308 (GRCm39) |
I142F |
probably damaging |
Het |
Mei1 |
C |
T |
15: 81,964,285 (GRCm39) |
T275I |
possibly damaging |
Het |
Mon2 |
A |
G |
10: 122,838,724 (GRCm39) |
V1593A |
probably benign |
Het |
Mrpl32 |
A |
G |
13: 14,786,096 (GRCm39) |
I74T |
probably benign |
Het |
Nek11 |
C |
T |
9: 105,270,091 (GRCm39) |
V44I |
probably damaging |
Het |
Noa1 |
A |
G |
5: 77,455,402 (GRCm39) |
V438A |
possibly damaging |
Het |
Or5an1c |
A |
C |
19: 12,218,950 (GRCm39) |
I25R |
probably benign |
Het |
Or7g16 |
C |
T |
9: 18,727,266 (GRCm39) |
C108Y |
probably benign |
Het |
Or8g18 |
G |
C |
9: 39,149,547 (GRCm39) |
P58A |
probably benign |
Het |
Pcdhb17 |
T |
C |
18: 37,620,313 (GRCm39) |
L701P |
probably damaging |
Het |
Pde11a |
G |
A |
2: 75,988,698 (GRCm39) |
S481L |
probably benign |
Het |
Prkdc |
T |
C |
16: 15,491,861 (GRCm39) |
I602T |
possibly damaging |
Het |
Ptprh |
T |
A |
7: 4,606,091 (GRCm39) |
R3* |
probably null |
Het |
Reln |
A |
G |
5: 22,115,864 (GRCm39) |
L3048P |
probably damaging |
Het |
Slc6a11 |
T |
A |
6: 114,171,624 (GRCm39) |
I265N |
possibly damaging |
Het |
Sorbs2 |
T |
C |
8: 46,248,656 (GRCm39) |
S636P |
probably damaging |
Het |
Supt5 |
T |
C |
7: 28,028,172 (GRCm39) |
I44V |
probably benign |
Het |
Tdrd6 |
T |
A |
17: 43,937,523 (GRCm39) |
E1175V |
possibly damaging |
Het |
Tnxb |
A |
C |
17: 34,907,903 (GRCm39) |
T1316P |
probably damaging |
Het |
Ufc1 |
A |
C |
1: 171,116,810 (GRCm39) |
D119E |
probably benign |
Het |
Vmn1r220 |
A |
G |
13: 23,368,294 (GRCm39) |
F134S |
probably damaging |
Het |
Zfp106 |
A |
G |
2: 120,354,560 (GRCm39) |
S1404P |
probably damaging |
Het |
Zfyve28 |
A |
T |
5: 34,374,408 (GRCm39) |
H535Q |
probably benign |
Het |
|
Other mutations in Zfp866 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02755:Zfp866
|
APN |
8 |
70,219,290 (GRCm39) |
critical splice donor site |
probably null |
|
R0238:Zfp866
|
UTSW |
8 |
70,219,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R1073:Zfp866
|
UTSW |
8 |
70,220,272 (GRCm39) |
splice site |
probably benign |
|
R1388:Zfp866
|
UTSW |
8 |
70,218,834 (GRCm39) |
missense |
probably benign |
0.16 |
R5129:Zfp866
|
UTSW |
8 |
70,220,359 (GRCm39) |
splice site |
probably null |
|
R5204:Zfp866
|
UTSW |
8 |
70,218,690 (GRCm39) |
missense |
probably damaging |
0.96 |
R5225:Zfp866
|
UTSW |
8 |
70,218,091 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5504:Zfp866
|
UTSW |
8 |
70,218,341 (GRCm39) |
missense |
probably benign |
0.07 |
R5912:Zfp866
|
UTSW |
8 |
70,218,934 (GRCm39) |
missense |
probably benign |
0.03 |
R6046:Zfp866
|
UTSW |
8 |
70,218,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6939:Zfp866
|
UTSW |
8 |
70,218,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R7033:Zfp866
|
UTSW |
8 |
70,218,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Zfp866
|
UTSW |
8 |
70,219,221 (GRCm39) |
missense |
probably benign |
0.05 |
R7351:Zfp866
|
UTSW |
8 |
70,218,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R7458:Zfp866
|
UTSW |
8 |
70,218,202 (GRCm39) |
nonsense |
probably null |
|
R8098:Zfp866
|
UTSW |
8 |
70,218,628 (GRCm39) |
missense |
probably benign |
0.02 |
R8755:Zfp866
|
UTSW |
8 |
70,219,381 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9575:Zfp866
|
UTSW |
8 |
70,219,288 (GRCm39) |
missense |
probably damaging |
0.98 |
|