Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
C |
A |
2: 35,266,309 (GRCm39) |
M120I |
probably damaging |
Het |
4933427D14Rik |
A |
T |
11: 72,082,342 (GRCm39) |
L328Q |
probably damaging |
Het |
Adgrv1 |
A |
C |
13: 81,709,704 (GRCm39) |
|
probably null |
Het |
Ankrd46 |
A |
T |
15: 36,484,279 (GRCm39) |
|
probably benign |
Het |
Arhgef18 |
A |
T |
8: 3,494,979 (GRCm39) |
M413L |
probably benign |
Het |
Atp6v1e1 |
G |
A |
6: 120,781,044 (GRCm39) |
T87M |
probably null |
Het |
Bap1 |
T |
C |
14: 30,980,402 (GRCm39) |
|
probably benign |
Het |
Brf1 |
A |
G |
12: 112,929,507 (GRCm39) |
L385P |
probably benign |
Het |
C1qtnf1 |
A |
T |
11: 118,338,938 (GRCm39) |
N203Y |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,569,025 (GRCm39) |
N899I |
probably damaging |
Het |
Ccnjl |
A |
C |
11: 43,470,718 (GRCm39) |
D162A |
probably damaging |
Het |
Cd248 |
A |
C |
19: 5,119,195 (GRCm39) |
I348L |
probably benign |
Het |
Cdc20 |
T |
C |
4: 118,293,029 (GRCm39) |
T265A |
probably benign |
Het |
Cdca5 |
T |
A |
19: 6,140,427 (GRCm39) |
L196* |
probably null |
Het |
Cdk4 |
T |
A |
10: 126,900,444 (GRCm39) |
|
probably benign |
Het |
Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
Clec4b2 |
G |
T |
6: 123,177,999 (GRCm39) |
E105* |
probably null |
Het |
Dapk1 |
T |
A |
13: 60,909,600 (GRCm39) |
D1404E |
probably benign |
Het |
Dnah1 |
T |
C |
14: 30,989,496 (GRCm39) |
Y3308C |
probably damaging |
Het |
Dnah17 |
A |
C |
11: 117,969,419 (GRCm39) |
Y2260D |
probably damaging |
Het |
Dock8 |
T |
G |
19: 25,159,001 (GRCm39) |
S1720A |
probably benign |
Het |
Erc1 |
A |
G |
6: 119,754,947 (GRCm39) |
|
probably null |
Het |
Ergic1 |
A |
G |
17: 26,848,597 (GRCm39) |
I66V |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,843,158 (GRCm39) |
T1029A |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,034,781 (GRCm39) |
Y2811F |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,306,110 (GRCm39) |
M310T |
probably damaging |
Het |
Ganab |
T |
A |
19: 8,892,355 (GRCm39) |
C844S |
probably benign |
Het |
Gas2l2 |
C |
A |
11: 83,320,041 (GRCm39) |
V72F |
probably damaging |
Het |
Gm14401 |
T |
A |
2: 176,778,573 (GRCm39) |
C220S |
probably damaging |
Het |
Hmmr |
A |
T |
11: 40,619,261 (GRCm39) |
V73E |
probably benign |
Het |
Idi2l |
T |
G |
13: 8,990,637 (GRCm39) |
|
probably benign |
Het |
Ifih1 |
G |
T |
2: 62,465,358 (GRCm39) |
|
probably benign |
Het |
Jak3 |
A |
G |
8: 72,138,048 (GRCm39) |
E833G |
probably damaging |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Ldb1 |
G |
A |
19: 46,023,132 (GRCm39) |
A217V |
probably benign |
Het |
Lrrc8c |
A |
G |
5: 105,755,955 (GRCm39) |
T577A |
probably benign |
Het |
Mfn1 |
T |
A |
3: 32,600,711 (GRCm39) |
|
probably benign |
Het |
Mki67 |
G |
A |
7: 135,298,474 (GRCm39) |
P2187S |
probably damaging |
Het |
Msi1 |
A |
G |
5: 115,573,654 (GRCm39) |
|
probably benign |
Het |
Msto1 |
T |
A |
3: 88,819,559 (GRCm39) |
I152F |
probably benign |
Het |
Myo9a |
A |
G |
9: 59,803,800 (GRCm39) |
R2060G |
probably benign |
Het |
Nnt |
A |
T |
13: 119,541,107 (GRCm39) |
C44* |
probably null |
Het |
Nup210l |
A |
G |
3: 90,100,378 (GRCm39) |
D1468G |
probably damaging |
Het |
Or1j16 |
T |
C |
2: 36,530,906 (GRCm39) |
L285P |
probably damaging |
Het |
Or4c10b |
A |
G |
2: 89,711,476 (GRCm39) |
E102G |
probably benign |
Het |
Or5d46 |
C |
A |
2: 88,174,686 (GRCm39) |
C129F |
possibly damaging |
Het |
Or7a40 |
T |
C |
16: 16,491,482 (GRCm39) |
D121G |
probably damaging |
Het |
P2rx3 |
G |
A |
2: 84,855,270 (GRCm39) |
T62I |
probably damaging |
Het |
Pabpc4l |
G |
T |
3: 46,401,578 (GRCm39) |
T22K |
probably damaging |
Het |
Pcdha7 |
A |
G |
18: 37,108,646 (GRCm39) |
D557G |
probably damaging |
Het |
Pcdhb20 |
A |
G |
18: 37,639,298 (GRCm39) |
K608R |
possibly damaging |
Het |
Pcnx1 |
A |
G |
12: 81,964,939 (GRCm39) |
S369G |
probably damaging |
Het |
Plod1 |
T |
C |
4: 148,004,736 (GRCm39) |
I455V |
probably benign |
Het |
Prune2 |
A |
T |
19: 17,099,219 (GRCm39) |
E1574D |
probably benign |
Het |
Ptar1 |
T |
A |
19: 23,680,472 (GRCm39) |
L96H |
probably damaging |
Het |
Rabgap1 |
T |
C |
2: 37,450,583 (GRCm39) |
S904P |
probably benign |
Het |
Rps6ka4 |
C |
T |
19: 6,815,467 (GRCm39) |
V176I |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Runx1t1 |
T |
A |
4: 13,771,459 (GRCm39) |
M1K |
probably null |
Het |
Serinc4 |
T |
A |
2: 121,282,905 (GRCm39) |
Y419F |
probably damaging |
Het |
Serpina12 |
A |
T |
12: 104,004,056 (GRCm39) |
M192K |
possibly damaging |
Het |
Spata21 |
T |
A |
4: 140,832,261 (GRCm39) |
M474K |
probably damaging |
Het |
Stpg1 |
T |
C |
4: 135,246,676 (GRCm39) |
S135P |
possibly damaging |
Het |
Tdrkh |
A |
G |
3: 94,336,671 (GRCm39) |
D481G |
probably damaging |
Het |
Ube2e1 |
A |
C |
14: 18,285,268 (GRCm38) |
S68R |
probably damaging |
Het |
Vcpip1 |
A |
C |
1: 9,817,572 (GRCm39) |
N270K |
probably damaging |
Het |
Vmn2r79 |
T |
C |
7: 86,650,675 (GRCm39) |
F154L |
probably benign |
Het |
Vwa3b |
A |
G |
1: 37,153,684 (GRCm39) |
|
probably benign |
Het |
Xdh |
C |
A |
17: 74,207,703 (GRCm39) |
V885L |
probably benign |
Het |
Zfp141 |
A |
T |
7: 42,125,629 (GRCm39) |
V281D |
probably benign |
Het |
Zfp317 |
T |
A |
9: 19,558,143 (GRCm39) |
I119N |
probably benign |
Het |
Zfp345 |
G |
A |
2: 150,314,608 (GRCm39) |
R310C |
probably benign |
Het |
Zfp760 |
G |
A |
17: 21,942,229 (GRCm39) |
C468Y |
probably benign |
Het |
|
Other mutations in Mrc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01013:Mrc1
|
APN |
2 |
14,333,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Mrc1
|
APN |
2 |
14,271,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01340:Mrc1
|
APN |
2 |
14,314,895 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01758:Mrc1
|
APN |
2 |
14,243,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01799:Mrc1
|
APN |
2 |
14,243,187 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02280:Mrc1
|
APN |
2 |
14,249,024 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02435:Mrc1
|
APN |
2 |
14,253,671 (GRCm39) |
nonsense |
probably null |
|
IGL03073:Mrc1
|
APN |
2 |
14,310,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03110:Mrc1
|
APN |
2 |
14,298,289 (GRCm39) |
nonsense |
probably null |
|
IGL03155:Mrc1
|
APN |
2 |
14,335,912 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03289:Mrc1
|
APN |
2 |
14,313,634 (GRCm39) |
critical splice donor site |
probably null |
|
amlodipine
|
UTSW |
2 |
14,275,016 (GRCm39) |
missense |
probably damaging |
1.00 |
losartan
|
UTSW |
2 |
14,299,597 (GRCm39) |
splice site |
probably null |
|
Shug
|
UTSW |
2 |
14,275,017 (GRCm39) |
missense |
probably damaging |
1.00 |
sussigkeit
|
UTSW |
2 |
14,330,192 (GRCm39) |
splice site |
probably null |
|
R0011:Mrc1
|
UTSW |
2 |
14,266,148 (GRCm39) |
critical splice donor site |
probably null |
|
R0011:Mrc1
|
UTSW |
2 |
14,266,148 (GRCm39) |
critical splice donor site |
probably null |
|
R0066:Mrc1
|
UTSW |
2 |
14,266,011 (GRCm39) |
missense |
probably benign |
0.42 |
R0066:Mrc1
|
UTSW |
2 |
14,266,011 (GRCm39) |
missense |
probably benign |
0.42 |
R0110:Mrc1
|
UTSW |
2 |
14,243,353 (GRCm39) |
splice site |
probably benign |
|
R0234:Mrc1
|
UTSW |
2 |
14,284,705 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0234:Mrc1
|
UTSW |
2 |
14,284,705 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0381:Mrc1
|
UTSW |
2 |
14,312,720 (GRCm39) |
missense |
probably benign |
0.05 |
R0505:Mrc1
|
UTSW |
2 |
14,314,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Mrc1
|
UTSW |
2 |
14,274,937 (GRCm39) |
splice site |
probably benign |
|
R0613:Mrc1
|
UTSW |
2 |
14,299,630 (GRCm39) |
missense |
probably damaging |
0.96 |
R0626:Mrc1
|
UTSW |
2 |
14,333,382 (GRCm39) |
nonsense |
probably null |
|
R1122:Mrc1
|
UTSW |
2 |
14,266,147 (GRCm39) |
critical splice donor site |
probably null |
|
R1281:Mrc1
|
UTSW |
2 |
14,298,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R1399:Mrc1
|
UTSW |
2 |
14,284,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1428:Mrc1
|
UTSW |
2 |
14,320,074 (GRCm39) |
missense |
probably benign |
0.11 |
R1571:Mrc1
|
UTSW |
2 |
14,313,544 (GRCm39) |
missense |
probably damaging |
0.97 |
R1596:Mrc1
|
UTSW |
2 |
14,253,701 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1730:Mrc1
|
UTSW |
2 |
14,332,655 (GRCm39) |
missense |
probably benign |
0.01 |
R1733:Mrc1
|
UTSW |
2 |
14,261,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Mrc1
|
UTSW |
2 |
14,332,655 (GRCm39) |
missense |
probably benign |
0.01 |
R1860:Mrc1
|
UTSW |
2 |
14,333,390 (GRCm39) |
missense |
probably benign |
0.30 |
R1872:Mrc1
|
UTSW |
2 |
14,330,192 (GRCm39) |
splice site |
probably null |
|
R1889:Mrc1
|
UTSW |
2 |
14,313,488 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1938:Mrc1
|
UTSW |
2 |
14,324,052 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1971:Mrc1
|
UTSW |
2 |
14,249,103 (GRCm39) |
critical splice donor site |
probably null |
|
R2031:Mrc1
|
UTSW |
2 |
14,326,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Mrc1
|
UTSW |
2 |
14,275,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Mrc1
|
UTSW |
2 |
14,332,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2168:Mrc1
|
UTSW |
2 |
14,249,015 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2273:Mrc1
|
UTSW |
2 |
14,330,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R2901:Mrc1
|
UTSW |
2 |
14,333,354 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3767:Mrc1
|
UTSW |
2 |
14,323,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Mrc1
|
UTSW |
2 |
14,293,793 (GRCm39) |
splice site |
probably benign |
|
R4028:Mrc1
|
UTSW |
2 |
14,243,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4668:Mrc1
|
UTSW |
2 |
14,298,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Mrc1
|
UTSW |
2 |
14,275,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R4950:Mrc1
|
UTSW |
2 |
14,276,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Mrc1
|
UTSW |
2 |
14,249,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Mrc1
|
UTSW |
2 |
14,311,327 (GRCm39) |
missense |
probably benign |
0.00 |
R5279:Mrc1
|
UTSW |
2 |
14,314,869 (GRCm39) |
missense |
probably damaging |
0.99 |
R5366:Mrc1
|
UTSW |
2 |
14,326,725 (GRCm39) |
missense |
probably benign |
0.03 |
R5436:Mrc1
|
UTSW |
2 |
14,271,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R5552:Mrc1
|
UTSW |
2 |
14,284,768 (GRCm39) |
missense |
probably benign |
0.05 |
R5631:Mrc1
|
UTSW |
2 |
14,333,383 (GRCm39) |
nonsense |
probably null |
|
R5831:Mrc1
|
UTSW |
2 |
14,313,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R5978:Mrc1
|
UTSW |
2 |
14,320,204 (GRCm39) |
missense |
probably damaging |
0.97 |
R5993:Mrc1
|
UTSW |
2 |
14,310,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Mrc1
|
UTSW |
2 |
14,321,712 (GRCm39) |
missense |
probably benign |
0.04 |
R6030:Mrc1
|
UTSW |
2 |
14,321,712 (GRCm39) |
missense |
probably benign |
0.04 |
R6038:Mrc1
|
UTSW |
2 |
14,261,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R6038:Mrc1
|
UTSW |
2 |
14,261,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R6228:Mrc1
|
UTSW |
2 |
14,276,115 (GRCm39) |
missense |
probably benign |
0.08 |
R6344:Mrc1
|
UTSW |
2 |
14,248,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6457:Mrc1
|
UTSW |
2 |
14,275,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Mrc1
|
UTSW |
2 |
14,312,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6619:Mrc1
|
UTSW |
2 |
14,299,597 (GRCm39) |
splice site |
probably null |
|
R6631:Mrc1
|
UTSW |
2 |
14,243,296 (GRCm39) |
missense |
probably benign |
|
R6737:Mrc1
|
UTSW |
2 |
14,276,088 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6782:Mrc1
|
UTSW |
2 |
14,266,148 (GRCm39) |
critical splice donor site |
probably null |
|
R6887:Mrc1
|
UTSW |
2 |
14,330,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7108:Mrc1
|
UTSW |
2 |
14,308,957 (GRCm39) |
nonsense |
probably null |
|
R7120:Mrc1
|
UTSW |
2 |
14,313,508 (GRCm39) |
missense |
probably damaging |
0.97 |
R7460:Mrc1
|
UTSW |
2 |
14,253,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7567:Mrc1
|
UTSW |
2 |
14,330,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R7606:Mrc1
|
UTSW |
2 |
14,242,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Mrc1
|
UTSW |
2 |
14,284,788 (GRCm39) |
missense |
probably benign |
0.03 |
R7826:Mrc1
|
UTSW |
2 |
14,299,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Mrc1
|
UTSW |
2 |
14,253,771 (GRCm39) |
missense |
probably benign |
|
R8279:Mrc1
|
UTSW |
2 |
14,271,168 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8888:Mrc1
|
UTSW |
2 |
14,312,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8895:Mrc1
|
UTSW |
2 |
14,312,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8952:Mrc1
|
UTSW |
2 |
14,253,735 (GRCm39) |
missense |
probably damaging |
0.98 |
R9315:Mrc1
|
UTSW |
2 |
14,248,969 (GRCm39) |
nonsense |
probably null |
|
R9366:Mrc1
|
UTSW |
2 |
14,321,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R9373:Mrc1
|
UTSW |
2 |
14,274,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R9418:Mrc1
|
UTSW |
2 |
14,234,358 (GRCm39) |
missense |
probably benign |
0.12 |
R9420:Mrc1
|
UTSW |
2 |
14,312,790 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9489:Mrc1
|
UTSW |
2 |
14,324,110 (GRCm39) |
missense |
probably benign |
0.06 |
R9564:Mrc1
|
UTSW |
2 |
14,266,117 (GRCm39) |
missense |
probably benign |
0.00 |
R9572:Mrc1
|
UTSW |
2 |
14,234,334 (GRCm39) |
missense |
probably benign |
|
R9605:Mrc1
|
UTSW |
2 |
14,324,110 (GRCm39) |
missense |
probably benign |
0.06 |
R9606:Mrc1
|
UTSW |
2 |
14,313,517 (GRCm39) |
missense |
probably benign |
0.01 |
R9781:Mrc1
|
UTSW |
2 |
14,310,175 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9781:Mrc1
|
UTSW |
2 |
14,249,100 (GRCm39) |
missense |
probably benign |
|
Z1177:Mrc1
|
UTSW |
2 |
14,293,927 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mrc1
|
UTSW |
2 |
14,248,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|