Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
T |
C |
12: 72,954,725 (GRCm39) |
|
probably null |
Het |
4930579F01Rik |
A |
G |
3: 137,882,217 (GRCm39) |
|
probably null |
Het |
Abhd17c |
G |
T |
7: 83,800,663 (GRCm39) |
H130Q |
probably damaging |
Het |
Als2 |
G |
A |
1: 59,246,948 (GRCm39) |
H564Y |
probably damaging |
Het |
Anxa2r1 |
C |
T |
13: 120,496,335 (GRCm39) |
C178Y |
unknown |
Het |
Art5 |
A |
G |
7: 101,747,407 (GRCm39) |
L124P |
possibly damaging |
Het |
Asap2 |
A |
T |
12: 21,162,084 (GRCm39) |
T14S |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,482,841 (GRCm39) |
N901S |
probably benign |
Het |
Bicd2 |
G |
T |
13: 49,533,052 (GRCm39) |
C546F |
probably damaging |
Het |
Ccn3 |
G |
A |
15: 54,615,854 (GRCm39) |
A340T |
probably benign |
Het |
Cnbp |
C |
T |
6: 87,822,281 (GRCm39) |
G81D |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,444,237 (GRCm39) |
Y4012H |
probably damaging |
Het |
Dok5 |
G |
A |
2: 170,642,816 (GRCm39) |
G38D |
probably damaging |
Het |
Drc3 |
A |
T |
11: 60,265,983 (GRCm39) |
E224V |
probably benign |
Het |
Ehd2 |
T |
C |
7: 15,686,128 (GRCm39) |
K315E |
probably damaging |
Het |
Eif6 |
A |
T |
2: 155,664,810 (GRCm39) |
N225K |
probably benign |
Het |
Epg5 |
T |
C |
18: 78,070,517 (GRCm39) |
V2264A |
probably benign |
Het |
Faf2 |
T |
C |
13: 54,796,220 (GRCm39) |
F126L |
probably damaging |
Het |
Fiz1 |
T |
C |
7: 5,015,880 (GRCm39) |
S37G |
possibly damaging |
Het |
Frs3 |
T |
C |
17: 48,013,987 (GRCm39) |
S227P |
probably benign |
Het |
Garin3 |
A |
T |
11: 46,296,158 (GRCm39) |
K177* |
probably null |
Het |
Gm4787 |
T |
A |
12: 81,423,993 (GRCm39) |
I722F |
probably benign |
Het |
Gm6370 |
T |
A |
5: 146,430,451 (GRCm39) |
L212Q |
probably damaging |
Het |
Gmnc |
G |
A |
16: 26,779,456 (GRCm39) |
H142Y |
possibly damaging |
Het |
Gna15 |
T |
C |
10: 81,338,738 (GRCm39) |
Y367C |
probably damaging |
Het |
Gpr158 |
G |
A |
2: 21,832,325 (GRCm39) |
V1142M |
possibly damaging |
Het |
Gpx6 |
A |
G |
13: 21,503,141 (GRCm39) |
K185R |
probably damaging |
Het |
Hc |
A |
C |
2: 34,881,115 (GRCm39) |
|
probably benign |
Het |
Hdac9 |
A |
G |
12: 34,440,255 (GRCm39) |
S375P |
probably damaging |
Het |
Kat6b |
A |
T |
14: 21,718,735 (GRCm39) |
H1138L |
probably benign |
Het |
Klre1 |
G |
A |
6: 129,556,996 (GRCm39) |
E33K |
possibly damaging |
Het |
Ldhb |
C |
A |
6: 142,444,396 (GRCm39) |
V86L |
possibly damaging |
Het |
Maco1 |
A |
G |
4: 134,538,534 (GRCm39) |
V470A |
probably benign |
Het |
Magi3 |
T |
A |
3: 103,954,198 (GRCm39) |
K713I |
probably damaging |
Het |
Magi3 |
T |
C |
3: 103,992,554 (GRCm39) |
Y306C |
probably damaging |
Het |
Minar1 |
T |
G |
9: 89,484,221 (GRCm39) |
K392T |
possibly damaging |
Het |
Mmp17 |
T |
C |
5: 129,682,725 (GRCm39) |
Y455H |
probably benign |
Het |
Mmp25 |
T |
A |
17: 23,850,048 (GRCm39) |
Y504F |
probably damaging |
Het |
Myo1a |
T |
C |
10: 127,556,050 (GRCm39) |
I969T |
probably benign |
Het |
Nedd4l |
T |
A |
18: 65,343,401 (GRCm39) |
H820Q |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,338,396 (GRCm39) |
M1136K |
possibly damaging |
Het |
Nmi |
T |
C |
2: 51,842,555 (GRCm39) |
E179G |
probably damaging |
Het |
Nrros |
A |
T |
16: 31,962,076 (GRCm39) |
M611K |
probably benign |
Het |
Nsd1 |
A |
T |
13: 55,439,049 (GRCm39) |
N1692I |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,245,509 (GRCm39) |
N112S |
probably benign |
Het |
Odf2l |
T |
C |
3: 144,854,785 (GRCm39) |
Y488H |
possibly damaging |
Het |
Or4c106 |
C |
A |
2: 88,683,128 (GRCm39) |
P278H |
probably damaging |
Het |
Or8g21 |
T |
A |
9: 38,906,012 (GRCm39) |
T240S |
probably damaging |
Het |
Or8g30 |
T |
A |
9: 39,230,413 (GRCm39) |
I166F |
probably damaging |
Het |
Otop2 |
A |
G |
11: 115,220,237 (GRCm39) |
D359G |
possibly damaging |
Het |
Pi4ka |
A |
T |
16: 17,185,371 (GRCm39) |
F243Y |
probably benign |
Het |
Pnma8b |
T |
C |
7: 16,679,837 (GRCm39) |
C274R |
probably benign |
Het |
Ppp1r42 |
A |
G |
1: 10,073,572 (GRCm39) |
V6A |
probably benign |
Het |
Prrg4 |
A |
G |
2: 104,669,733 (GRCm39) |
L128S |
probably damaging |
Het |
Prss33 |
C |
T |
17: 24,053,817 (GRCm39) |
V87M |
probably damaging |
Het |
Psen2 |
A |
G |
1: 180,061,229 (GRCm39) |
V278A |
probably damaging |
Het |
Ptpn13 |
C |
A |
5: 103,673,651 (GRCm39) |
T538K |
probably damaging |
Het |
Pttg1ip2 |
C |
T |
5: 5,528,875 (GRCm39) |
V47I |
possibly damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,986 (GRCm39) |
H636R |
probably benign |
Het |
Rbak |
A |
C |
5: 143,162,257 (GRCm39) |
D35E |
possibly damaging |
Het |
Rbms1 |
C |
A |
2: 60,592,392 (GRCm39) |
|
probably null |
Het |
Rgs7bp |
T |
A |
13: 105,100,597 (GRCm39) |
N226I |
probably damaging |
Het |
Rnf182 |
T |
A |
13: 43,821,899 (GRCm39) |
V150E |
probably benign |
Het |
Sacs |
A |
G |
14: 61,447,089 (GRCm39) |
Y3045C |
probably damaging |
Het |
Scp2 |
G |
T |
4: 107,921,141 (GRCm39) |
A23E |
probably benign |
Het |
Sec16a |
A |
T |
2: 26,303,757 (GRCm39) |
|
probably benign |
Het |
Slc30a5 |
A |
T |
13: 100,940,457 (GRCm39) |
H619Q |
probably damaging |
Het |
Slfn10-ps |
T |
A |
11: 82,926,511 (GRCm39) |
|
noncoding transcript |
Het |
Slmap |
A |
G |
14: 26,139,402 (GRCm39) |
Y771H |
probably damaging |
Het |
Slx |
T |
A |
X: 26,489,689 (GRCm39) |
|
probably benign |
Het |
Spns3 |
C |
A |
11: 72,436,787 (GRCm39) |
|
probably benign |
Het |
Stxbp1 |
T |
A |
2: 32,692,868 (GRCm39) |
I383F |
probably damaging |
Het |
Taf3 |
C |
T |
2: 9,956,377 (GRCm39) |
E597K |
possibly damaging |
Het |
Tbcd |
A |
G |
11: 121,494,457 (GRCm39) |
Q1006R |
possibly damaging |
Het |
Tenm4 |
G |
T |
7: 96,552,054 (GRCm39) |
V2498F |
probably damaging |
Het |
Tex2 |
T |
C |
11: 106,458,161 (GRCm39) |
|
probably benign |
Het |
Tkfc |
A |
T |
19: 10,576,421 (GRCm39) |
L154Q |
probably damaging |
Het |
Tmem62 |
A |
G |
2: 120,817,343 (GRCm39) |
H257R |
probably damaging |
Het |
Trpm2 |
T |
C |
10: 77,768,013 (GRCm39) |
I829V |
probably benign |
Het |
Ttc38 |
A |
G |
15: 85,735,802 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,548,757 (GRCm39) |
Y30135* |
probably null |
Het |
Ttn |
A |
G |
2: 76,810,477 (GRCm39) |
V17A |
probably benign |
Het |
Ubqlnl |
A |
T |
7: 103,797,890 (GRCm39) |
C536S |
probably benign |
Het |
Vmn1r230 |
T |
A |
17: 21,067,063 (GRCm39) |
M84K |
probably damaging |
Het |
Vmn1r235 |
G |
A |
17: 21,482,628 (GRCm39) |
V318I |
probably benign |
Het |
Vmn2r76 |
T |
C |
7: 85,879,692 (GRCm39) |
I203V |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,167,584 (GRCm39) |
R613* |
probably null |
Het |
Zfp180 |
A |
G |
7: 23,804,685 (GRCm39) |
H368R |
probably damaging |
Het |
Zfp407 |
T |
C |
18: 84,227,774 (GRCm39) |
D1945G |
possibly damaging |
Het |
Zfyve27 |
G |
T |
19: 42,160,170 (GRCm39) |
R62L |
probably benign |
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 |
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 |
R8766:Actr10
|
UTSW |
12 |
71,001,430 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|