Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anapc5 |
A |
G |
5: 122,938,664 (GRCm39) |
V362A |
probably benign |
Het |
Ash1l |
T |
A |
3: 88,973,722 (GRCm39) |
C2594S |
probably damaging |
Het |
Ccdc82 |
C |
A |
9: 13,253,043 (GRCm39) |
Q303K |
probably benign |
Het |
Cog1 |
A |
G |
11: 113,544,853 (GRCm39) |
Y345C |
probably damaging |
Het |
Fpgt |
T |
C |
3: 154,796,997 (GRCm39) |
|
probably benign |
Het |
Glrb |
A |
T |
3: 80,752,539 (GRCm39) |
V408D |
possibly damaging |
Het |
Gm7135 |
A |
G |
1: 97,328,123 (GRCm39) |
|
noncoding transcript |
Het |
Il1rn |
T |
C |
2: 24,239,557 (GRCm39) |
L151P |
probably damaging |
Het |
Itgav |
G |
T |
2: 83,555,184 (GRCm39) |
E36* |
probably null |
Het |
Kidins220 |
G |
A |
12: 25,106,845 (GRCm39) |
E1433K |
possibly damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Klra3 |
A |
G |
6: 130,311,265 (GRCm39) |
C39R |
probably benign |
Het |
Lce1i |
A |
G |
3: 92,684,742 (GRCm39) |
S145P |
unknown |
Het |
Memo1 |
T |
C |
17: 74,562,293 (GRCm39) |
|
probably null |
Het |
Mpp3 |
G |
A |
11: 101,914,289 (GRCm39) |
A102V |
probably damaging |
Het |
Mug2 |
T |
A |
6: 122,040,632 (GRCm39) |
D727E |
probably benign |
Het |
Ndufb8 |
T |
C |
19: 44,541,130 (GRCm39) |
I107V |
probably benign |
Het |
Or5h18 |
A |
T |
16: 58,847,976 (GRCm39) |
M98K |
probably benign |
Het |
Pnn |
C |
T |
12: 59,118,956 (GRCm39) |
T513I |
possibly damaging |
Het |
Ric8a |
A |
G |
7: 140,441,335 (GRCm39) |
Y210C |
probably damaging |
Het |
Ripor2 |
G |
A |
13: 24,908,992 (GRCm39) |
V1037M |
probably damaging |
Het |
Rreb1 |
A |
T |
13: 38,115,907 (GRCm39) |
T1089S |
probably benign |
Het |
Rrs1 |
C |
T |
1: 9,616,440 (GRCm39) |
S231L |
probably damaging |
Het |
Rrs1 |
C |
T |
1: 9,616,448 (GRCm39) |
R234C |
possibly damaging |
Het |
Sec23ip |
A |
G |
7: 128,379,057 (GRCm39) |
D838G |
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,902,276 (GRCm39) |
I464V |
probably benign |
Het |
Slc25a51 |
C |
T |
4: 45,399,768 (GRCm39) |
V141M |
probably benign |
Het |
Slc41a3 |
A |
T |
6: 90,617,904 (GRCm39) |
H310L |
probably benign |
Het |
Smurf1 |
A |
G |
5: 144,828,268 (GRCm39) |
S363P |
probably benign |
Het |
Tln1 |
C |
T |
4: 43,543,509 (GRCm39) |
R1269Q |
probably benign |
Het |
Tmed3 |
A |
G |
9: 89,586,951 (GRCm39) |
S10P |
probably benign |
Het |
Tomm70a |
T |
G |
16: 56,960,985 (GRCm39) |
Y313D |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,207,039 (GRCm39) |
E810G |
probably benign |
Het |
Unc5c |
T |
C |
3: 141,420,435 (GRCm39) |
I52T |
probably damaging |
Het |
Unc5d |
T |
A |
8: 29,209,824 (GRCm39) |
Y432F |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,168,337 (GRCm39) |
|
probably benign |
Het |
Zfp629 |
T |
C |
7: 127,211,110 (GRCm39) |
Y233C |
probably damaging |
Het |
|
Other mutations in Zfp986 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4548:Zfp986
|
UTSW |
4 |
145,625,928 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4142001:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R0126:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R1835:Zfp986
|
UTSW |
4 |
145,625,805 (GRCm39) |
missense |
probably benign |
0.00 |
R3926:Zfp986
|
UTSW |
4 |
145,619,090 (GRCm39) |
splice site |
probably benign |
|
R4401:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R6517:Zfp986
|
UTSW |
4 |
145,625,870 (GRCm39) |
missense |
probably benign |
0.30 |
R7836:Zfp986
|
UTSW |
4 |
145,625,691 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8108:Zfp986
|
UTSW |
4 |
145,625,875 (GRCm39) |
missense |
probably benign |
0.02 |
R8738:Zfp986
|
UTSW |
4 |
145,625,550 (GRCm39) |
missense |
probably benign |
0.04 |
R9153:Zfp986
|
UTSW |
4 |
145,626,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Zfp986
|
UTSW |
4 |
145,625,798 (GRCm39) |
missense |
probably benign |
0.01 |
R9212:Zfp986
|
UTSW |
4 |
145,625,798 (GRCm39) |
missense |
probably benign |
0.01 |
R9235:Zfp986
|
UTSW |
4 |
145,625,759 (GRCm39) |
missense |
probably benign |
0.09 |
R9326:Zfp986
|
UTSW |
4 |
145,626,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R9691:Zfp986
|
UTSW |
4 |
145,626,070 (GRCm39) |
missense |
probably benign |
0.25 |
|