Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk1 |
C |
T |
3: 127,523,022 (GRCm39) |
V7M |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,926,663 (GRCm39) |
|
probably null |
Het |
Chil3 |
G |
A |
3: 106,067,815 (GRCm39) |
Q117* |
probably null |
Het |
Daglb |
T |
C |
5: 143,458,889 (GRCm39) |
|
probably benign |
Het |
Dnah11 |
G |
A |
12: 118,089,578 (GRCm39) |
R1163* |
probably null |
Het |
Ftsj3 |
G |
A |
11: 106,144,502 (GRCm39) |
A134V |
probably benign |
Het |
G530012D18Rik |
G |
C |
1: 85,504,923 (GRCm39) |
|
probably benign |
Het |
Gfod2 |
T |
C |
8: 106,444,177 (GRCm39) |
N122S |
possibly damaging |
Het |
Golga4 |
A |
G |
9: 118,380,946 (GRCm39) |
E507G |
probably benign |
Het |
Ids |
C |
A |
X: 69,389,950 (GRCm39) |
G506C |
probably damaging |
Het |
Ifna15 |
G |
T |
4: 88,476,079 (GRCm39) |
T135N |
probably benign |
Het |
Igsf9b |
G |
A |
9: 27,220,774 (GRCm39) |
V47I |
possibly damaging |
Het |
Kif24 |
A |
G |
4: 41,413,827 (GRCm39) |
|
probably null |
Het |
L3hypdh |
A |
T |
12: 72,124,198 (GRCm39) |
D247E |
probably damaging |
Het |
Lama2 |
A |
T |
10: 26,860,489 (GRCm39) |
N2999K |
probably damaging |
Het |
Lpcat2 |
C |
A |
8: 93,599,734 (GRCm39) |
P234Q |
probably benign |
Het |
Lrp10 |
C |
T |
14: 54,705,823 (GRCm39) |
R338C |
probably damaging |
Het |
Mcm9 |
A |
C |
10: 53,413,749 (GRCm39) |
C444G |
probably benign |
Het |
Mecom |
G |
A |
3: 30,033,934 (GRCm39) |
Q246* |
probably null |
Het |
Mib1 |
A |
G |
18: 10,751,844 (GRCm39) |
N242S |
probably benign |
Het |
Or2a7 |
T |
A |
6: 43,151,160 (GRCm39) |
M80K |
probably damaging |
Het |
Or8g26 |
G |
A |
9: 39,095,864 (GRCm39) |
C127Y |
probably damaging |
Het |
P3h4 |
A |
G |
11: 100,304,452 (GRCm39) |
F263S |
probably damaging |
Het |
Pcsk1 |
T |
C |
13: 75,260,838 (GRCm39) |
S354P |
possibly damaging |
Het |
Pms2 |
T |
A |
5: 143,862,744 (GRCm39) |
F617Y |
probably damaging |
Het |
Prps2 |
T |
A |
X: 166,146,545 (GRCm39) |
K176* |
probably null |
Het |
Psmd13 |
G |
T |
7: 140,469,418 (GRCm39) |
|
probably benign |
Het |
Pygl |
G |
A |
12: 70,242,464 (GRCm39) |
S573L |
probably damaging |
Het |
Rapgef3 |
A |
G |
15: 97,646,529 (GRCm39) |
V794A |
probably benign |
Het |
Rasgrf2 |
C |
A |
13: 92,038,796 (GRCm39) |
D1017Y |
probably damaging |
Het |
Rb1cc1 |
A |
G |
1: 6,315,861 (GRCm39) |
D555G |
probably damaging |
Het |
Rptor |
G |
T |
11: 119,562,171 (GRCm39) |
E111D |
probably damaging |
Het |
Sall4 |
T |
C |
2: 168,597,400 (GRCm39) |
E480G |
probably benign |
Het |
Scn4a |
G |
A |
11: 106,239,683 (GRCm39) |
|
probably null |
Het |
Scn8a |
G |
A |
15: 100,838,014 (GRCm39) |
A94T |
probably benign |
Het |
Slc26a6 |
T |
A |
9: 108,738,982 (GRCm39) |
C636S |
probably benign |
Het |
Slc38a11 |
T |
C |
2: 65,188,460 (GRCm39) |
K103R |
probably benign |
Het |
Sned1 |
T |
C |
1: 93,202,381 (GRCm39) |
L675P |
probably benign |
Het |
Spsb1 |
T |
C |
4: 149,991,232 (GRCm39) |
H112R |
probably damaging |
Het |
Tmem132d |
G |
A |
5: 128,061,405 (GRCm39) |
T399M |
possibly damaging |
Het |
Zfp939 |
A |
G |
7: 39,123,144 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Zfp951 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01897:Zfp951
|
APN |
5 |
104,963,149 (GRCm39) |
missense |
probably benign |
0.00 |
R0594:Zfp951
|
UTSW |
5 |
104,962,438 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1056:Zfp951
|
UTSW |
5 |
104,963,151 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1857:Zfp951
|
UTSW |
5 |
104,962,723 (GRCm39) |
missense |
probably damaging |
0.97 |
R1967:Zfp951
|
UTSW |
5 |
104,964,866 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2422:Zfp951
|
UTSW |
5 |
104,963,143 (GRCm39) |
missense |
probably benign |
0.14 |
R4671:Zfp951
|
UTSW |
5 |
104,962,567 (GRCm39) |
missense |
probably benign |
0.01 |
R5539:Zfp951
|
UTSW |
5 |
104,962,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R5634:Zfp951
|
UTSW |
5 |
104,963,155 (GRCm39) |
missense |
probably benign |
0.00 |
R7894:Zfp951
|
UTSW |
5 |
104,962,838 (GRCm39) |
missense |
probably benign |
0.00 |
R8058:Zfp951
|
UTSW |
5 |
104,962,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R8125:Zfp951
|
UTSW |
5 |
104,963,169 (GRCm39) |
nonsense |
probably null |
|
Z1177:Zfp951
|
UTSW |
5 |
104,976,821 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
|