Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amz1 |
A |
G |
5: 140,733,921 (GRCm39) |
N166D |
probably benign |
Het |
Armh4 |
T |
A |
14: 50,011,497 (GRCm39) |
N70I |
probably damaging |
Het |
Asah2 |
A |
G |
19: 32,035,280 (GRCm39) |
F15S |
possibly damaging |
Het |
Axin2 |
A |
G |
11: 108,814,657 (GRCm39) |
M182V |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 136,002,881 (GRCm39) |
L326P |
probably damaging |
Het |
Ccdc169 |
T |
C |
3: 55,058,245 (GRCm39) |
|
probably null |
Het |
Cct8 |
A |
T |
16: 87,285,756 (GRCm39) |
V234D |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,817,844 (GRCm39) |
R633G |
probably benign |
Het |
Clca3a1 |
A |
T |
3: 144,714,939 (GRCm39) |
|
probably benign |
Het |
Crat |
G |
A |
2: 30,297,075 (GRCm39) |
P293S |
probably benign |
Het |
Crybg3 |
G |
A |
16: 59,375,696 (GRCm39) |
R139C |
probably benign |
Het |
Ctbs |
A |
G |
3: 146,165,588 (GRCm39) |
N301S |
possibly damaging |
Het |
Cyp4x1 |
T |
C |
4: 114,967,262 (GRCm39) |
H438R |
probably damaging |
Het |
Dglucy |
C |
A |
12: 100,837,706 (GRCm39) |
H616Q |
probably benign |
Het |
Dync1i1 |
T |
A |
6: 5,767,142 (GRCm39) |
L74Q |
possibly damaging |
Het |
Epn1 |
T |
C |
7: 5,095,860 (GRCm39) |
S167P |
possibly damaging |
Het |
Fbxw28 |
T |
C |
9: 109,155,749 (GRCm39) |
E341G |
probably benign |
Het |
Gk2 |
T |
A |
5: 97,604,110 (GRCm39) |
M243L |
probably benign |
Het |
Grhl3 |
T |
A |
4: 135,300,724 (GRCm39) |
E4D |
probably benign |
Het |
Hsd17b13 |
T |
C |
5: 104,125,009 (GRCm39) |
K58R |
probably benign |
Het |
Ighd5-7 |
G |
A |
12: 113,428,148 (GRCm39) |
Q9* |
probably null |
Het |
Izumo1 |
G |
A |
7: 45,276,496 (GRCm39) |
S353N |
probably benign |
Het |
Klhl31 |
T |
C |
9: 77,557,445 (GRCm39) |
S54P |
possibly damaging |
Het |
Lonp2 |
T |
C |
8: 87,363,198 (GRCm39) |
M272T |
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,603,250 (GRCm39) |
C682* |
probably null |
Het |
Magi2 |
A |
G |
5: 20,400,123 (GRCm39) |
K52E |
probably benign |
Het |
Nab2 |
C |
T |
10: 127,502,417 (GRCm39) |
|
probably benign |
Het |
Ncapg2 |
T |
A |
12: 116,390,356 (GRCm39) |
V435D |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,802,340 (GRCm39) |
D87G |
probably benign |
Het |
Or10a3 |
A |
G |
7: 108,480,453 (GRCm39) |
M120T |
probably benign |
Het |
Or9a7 |
T |
C |
6: 40,521,485 (GRCm39) |
M143V |
probably benign |
Het |
Pamr1 |
T |
C |
2: 102,380,538 (GRCm39) |
M1T |
probably null |
Het |
Pard3b |
T |
C |
1: 62,198,637 (GRCm39) |
C242R |
probably benign |
Het |
Pcif1 |
T |
A |
2: 164,727,346 (GRCm39) |
V106E |
probably benign |
Het |
Pitx2 |
T |
A |
3: 129,012,223 (GRCm39) |
F218I |
probably damaging |
Het |
Ppip5k1 |
G |
T |
2: 121,166,919 (GRCm39) |
Y877* |
probably null |
Het |
Prkch |
A |
G |
12: 73,749,312 (GRCm39) |
N354S |
probably benign |
Het |
Psen2 |
T |
A |
1: 180,073,201 (GRCm39) |
D40V |
probably benign |
Het |
Rfx7 |
T |
A |
9: 72,524,021 (GRCm39) |
S404T |
possibly damaging |
Het |
Ryr2 |
T |
A |
13: 11,683,855 (GRCm39) |
T3070S |
probably damaging |
Het |
Slc24a4 |
A |
G |
12: 102,196,711 (GRCm39) |
D263G |
probably benign |
Het |
Tox |
T |
C |
4: 6,823,047 (GRCm39) |
E90G |
probably damaging |
Het |
Unc13b |
C |
T |
4: 43,174,722 (GRCm39) |
S1850L |
unknown |
Het |
Vmn1r5 |
T |
A |
6: 56,963,100 (GRCm39) |
D258E |
possibly damaging |
Het |
Vmn2r84 |
C |
T |
10: 130,222,241 (GRCm39) |
V660M |
probably damaging |
Het |
Yju2b |
C |
T |
8: 84,988,423 (GRCm39) |
R68H |
probably damaging |
Het |
Zfp592 |
A |
T |
7: 80,674,353 (GRCm39) |
H439L |
probably benign |
Het |
Zfp775 |
A |
T |
6: 48,597,113 (GRCm39) |
H329L |
probably damaging |
Het |
Zswim5 |
T |
C |
4: 116,816,004 (GRCm39) |
L364P |
probably damaging |
Het |
|
Other mutations in Actr10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02084:Actr10
|
APN |
12 |
71,001,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Actr10
|
APN |
12 |
70,990,289 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02628:Actr10
|
APN |
12 |
71,001,430 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03202:Actr10
|
APN |
12 |
70,987,605 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03266:Actr10
|
APN |
12 |
71,003,440 (GRCm39) |
missense |
probably benign |
0.00 |
R0505:Actr10
|
UTSW |
12 |
71,006,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Actr10
|
UTSW |
12 |
71,008,770 (GRCm39) |
missense |
probably benign |
0.23 |
R1919:Actr10
|
UTSW |
12 |
70,989,104 (GRCm39) |
missense |
probably benign |
0.00 |
R2151:Actr10
|
UTSW |
12 |
70,987,575 (GRCm39) |
nonsense |
probably null |
|
R2201:Actr10
|
UTSW |
12 |
71,006,795 (GRCm39) |
missense |
probably damaging |
0.97 |
R4259:Actr10
|
UTSW |
12 |
70,999,759 (GRCm39) |
missense |
probably benign |
0.02 |
R4261:Actr10
|
UTSW |
12 |
70,999,759 (GRCm39) |
missense |
probably benign |
0.02 |
R5138:Actr10
|
UTSW |
12 |
71,008,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5326:Actr10
|
UTSW |
12 |
71,001,430 (GRCm39) |
unclassified |
probably benign |
|
R5542:Actr10
|
UTSW |
12 |
71,001,430 (GRCm39) |
unclassified |
probably benign |
|
R6248:Actr10
|
UTSW |
12 |
70,999,733 (GRCm39) |
missense |
probably benign |
0.00 |
R6882:Actr10
|
UTSW |
12 |
71,003,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7102:Actr10
|
UTSW |
12 |
70,999,805 (GRCm39) |
critical splice donor site |
probably null |
|
R7758:Actr10
|
UTSW |
12 |
70,989,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Actr10
|
UTSW |
12 |
70,990,283 (GRCm39) |
missense |
probably benign |
0.26 |
R8850:Actr10
|
UTSW |
12 |
70,989,032 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9011:Actr10
|
UTSW |
12 |
70,999,734 (GRCm39) |
missense |
probably benign |
0.01 |
R9068:Actr10
|
UTSW |
12 |
70,989,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Actr10
|
UTSW |
12 |
70,990,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Actr10
|
UTSW |
12 |
71,006,818 (GRCm39) |
critical splice donor site |
probably null |
|
X0012:Actr10
|
UTSW |
12 |
70,987,639 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Actr10
|
UTSW |
12 |
71,006,733 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Actr10
|
UTSW |
12 |
71,008,803 (GRCm39) |
missense |
probably damaging |
0.99 |
|