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 |
Actr10 |
T |
A |
12: 70,987,575 (GRCm39) |
C27* |
probably null |
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 |
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 Rad51ap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01879:Rad51ap2
|
APN |
12 |
11,508,139 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01908:Rad51ap2
|
APN |
12 |
11,508,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02415:Rad51ap2
|
APN |
12 |
11,506,930 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02731:Rad51ap2
|
APN |
12 |
11,506,897 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03407:Rad51ap2
|
APN |
12 |
11,507,198 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0190:Rad51ap2
|
UTSW |
12 |
11,508,540 (GRCm39) |
missense |
probably benign |
0.01 |
R0281:Rad51ap2
|
UTSW |
12 |
11,507,043 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0564:Rad51ap2
|
UTSW |
12 |
11,507,897 (GRCm39) |
missense |
probably benign |
0.20 |
R0674:Rad51ap2
|
UTSW |
12 |
11,508,818 (GRCm39) |
critical splice donor site |
probably null |
|
R0699:Rad51ap2
|
UTSW |
12 |
11,507,601 (GRCm39) |
missense |
probably benign |
0.03 |
R1033:Rad51ap2
|
UTSW |
12 |
11,506,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R1255:Rad51ap2
|
UTSW |
12 |
11,508,095 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1572:Rad51ap2
|
UTSW |
12 |
11,507,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R1746:Rad51ap2
|
UTSW |
12 |
11,507,776 (GRCm39) |
missense |
probably benign |
|
R1882:Rad51ap2
|
UTSW |
12 |
11,506,251 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2038:Rad51ap2
|
UTSW |
12 |
11,507,025 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2152:Rad51ap2
|
UTSW |
12 |
11,507,986 (GRCm39) |
missense |
probably benign |
0.02 |
R2154:Rad51ap2
|
UTSW |
12 |
11,507,986 (GRCm39) |
missense |
probably benign |
0.02 |
R2159:Rad51ap2
|
UTSW |
12 |
11,507,752 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2321:Rad51ap2
|
UTSW |
12 |
11,507,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R2355:Rad51ap2
|
UTSW |
12 |
11,507,109 (GRCm39) |
missense |
probably benign |
|
R2393:Rad51ap2
|
UTSW |
12 |
11,507,798 (GRCm39) |
missense |
probably damaging |
0.98 |
R2407:Rad51ap2
|
UTSW |
12 |
11,508,502 (GRCm39) |
missense |
probably damaging |
0.99 |
R2518:Rad51ap2
|
UTSW |
12 |
11,507,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R2929:Rad51ap2
|
UTSW |
12 |
11,507,185 (GRCm39) |
missense |
probably benign |
0.07 |
R3085:Rad51ap2
|
UTSW |
12 |
11,506,758 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4009:Rad51ap2
|
UTSW |
12 |
11,507,052 (GRCm39) |
missense |
probably benign |
0.33 |
R4108:Rad51ap2
|
UTSW |
12 |
11,508,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Rad51ap2
|
UTSW |
12 |
11,506,465 (GRCm39) |
missense |
probably benign |
0.01 |
R4536:Rad51ap2
|
UTSW |
12 |
11,507,850 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4594:Rad51ap2
|
UTSW |
12 |
11,507,881 (GRCm39) |
missense |
probably benign |
0.01 |
R4678:Rad51ap2
|
UTSW |
12 |
11,506,552 (GRCm39) |
missense |
probably damaging |
0.96 |
R4679:Rad51ap2
|
UTSW |
12 |
11,506,552 (GRCm39) |
missense |
probably damaging |
0.96 |
R4810:Rad51ap2
|
UTSW |
12 |
11,507,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Rad51ap2
|
UTSW |
12 |
11,507,516 (GRCm39) |
missense |
probably benign |
0.09 |
R5421:Rad51ap2
|
UTSW |
12 |
11,509,368 (GRCm39) |
nonsense |
probably null |
|
R5517:Rad51ap2
|
UTSW |
12 |
11,508,313 (GRCm39) |
missense |
probably benign |
0.19 |
R5786:Rad51ap2
|
UTSW |
12 |
11,506,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R5884:Rad51ap2
|
UTSW |
12 |
11,507,534 (GRCm39) |
small deletion |
probably benign |
|
R5932:Rad51ap2
|
UTSW |
12 |
11,508,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R6022:Rad51ap2
|
UTSW |
12 |
11,508,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R6064:Rad51ap2
|
UTSW |
12 |
11,507,418 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6112:Rad51ap2
|
UTSW |
12 |
11,507,290 (GRCm39) |
missense |
probably benign |
0.01 |
R6235:Rad51ap2
|
UTSW |
12 |
11,507,517 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6282:Rad51ap2
|
UTSW |
12 |
11,507,560 (GRCm39) |
missense |
probably benign |
0.12 |
R6488:Rad51ap2
|
UTSW |
12 |
11,508,161 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6668:Rad51ap2
|
UTSW |
12 |
11,507,647 (GRCm39) |
missense |
probably benign |
0.17 |
R6759:Rad51ap2
|
UTSW |
12 |
11,507,145 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7030:Rad51ap2
|
UTSW |
12 |
11,507,432 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7080:Rad51ap2
|
UTSW |
12 |
11,506,366 (GRCm39) |
missense |
probably benign |
|
R7105:Rad51ap2
|
UTSW |
12 |
11,508,278 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7269:Rad51ap2
|
UTSW |
12 |
11,506,807 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7286:Rad51ap2
|
UTSW |
12 |
11,507,692 (GRCm39) |
missense |
probably benign |
0.19 |
R7305:Rad51ap2
|
UTSW |
12 |
11,507,344 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7451:Rad51ap2
|
UTSW |
12 |
11,507,982 (GRCm39) |
missense |
probably benign |
0.05 |
R7632:Rad51ap2
|
UTSW |
12 |
11,507,116 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7833:Rad51ap2
|
UTSW |
12 |
11,506,656 (GRCm39) |
missense |
probably benign |
|
R7839:Rad51ap2
|
UTSW |
12 |
11,507,238 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7953:Rad51ap2
|
UTSW |
12 |
11,512,593 (GRCm39) |
nonsense |
probably null |
|
R8040:Rad51ap2
|
UTSW |
12 |
11,508,792 (GRCm39) |
missense |
probably benign |
0.03 |
R8879:Rad51ap2
|
UTSW |
12 |
11,507,401 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8963:Rad51ap2
|
UTSW |
12 |
11,506,255 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9010:Rad51ap2
|
UTSW |
12 |
11,508,675 (GRCm39) |
missense |
probably benign |
0.01 |
R9328:Rad51ap2
|
UTSW |
12 |
11,507,772 (GRCm39) |
missense |
probably benign |
0.03 |
R9691:Rad51ap2
|
UTSW |
12 |
11,509,413 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9712:Rad51ap2
|
UTSW |
12 |
11,507,593 (GRCm39) |
missense |
possibly damaging |
0.95 |
RF023:Rad51ap2
|
UTSW |
12 |
11,508,076 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0026:Rad51ap2
|
UTSW |
12 |
11,508,097 (GRCm39) |
missense |
possibly damaging |
0.93 |
|