Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
G |
11: 119,912,277 (GRCm39) |
I56T |
probably benign |
Het |
Adissp |
T |
C |
2: 130,993,682 (GRCm39) |
|
probably null |
Het |
Akr1c12 |
A |
G |
13: 4,325,796 (GRCm39) |
L99S |
probably damaging |
Het |
Azin1 |
C |
A |
15: 38,493,871 (GRCm39) |
V251F |
possibly damaging |
Het |
Btbd16 |
C |
T |
7: 130,417,516 (GRCm39) |
R344C |
probably damaging |
Het |
C2cd3 |
A |
T |
7: 100,065,262 (GRCm39) |
M305L |
|
Het |
Casz1 |
A |
G |
4: 149,023,320 (GRCm39) |
T742A |
probably damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,352,426 (GRCm39) |
|
probably null |
Het |
Clec2e |
T |
A |
6: 129,071,420 (GRCm39) |
Y139F |
possibly damaging |
Het |
Crisp2 |
T |
A |
17: 41,094,724 (GRCm39) |
N117I |
possibly damaging |
Het |
Ddx52 |
A |
T |
11: 83,833,008 (GRCm39) |
D2V |
probably damaging |
Het |
Dmpk |
T |
A |
7: 18,824,946 (GRCm39) |
V442E |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,368,942 (GRCm39) |
M1654K |
probably benign |
Het |
Eln |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
5: 134,739,935 (GRCm39) |
|
probably benign |
Het |
Erlec1 |
A |
G |
11: 30,885,054 (GRCm39) |
V411A |
probably damaging |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Fry |
A |
G |
5: 150,356,994 (GRCm39) |
E1847G |
possibly damaging |
Het |
Gck |
A |
G |
11: 5,899,553 (GRCm39) |
|
probably null |
Het |
Gga2 |
T |
C |
7: 121,603,195 (GRCm39) |
D167G |
probably damaging |
Het |
Gprc6a |
A |
G |
10: 51,491,506 (GRCm39) |
S748P |
probably damaging |
Het |
H2-M10.2 |
T |
C |
17: 36,595,643 (GRCm39) |
R216G |
probably benign |
Het |
H2-M2 |
T |
A |
17: 37,792,215 (GRCm39) |
I312F |
probably benign |
Het |
Havcr2 |
A |
T |
11: 46,347,350 (GRCm39) |
Y109F |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,048,333 (GRCm39) |
V67A |
|
Het |
Ift70b |
T |
A |
2: 75,768,391 (GRCm39) |
I121F |
possibly damaging |
Het |
Kcnk12 |
C |
A |
17: 88,104,507 (GRCm39) |
V126L |
possibly damaging |
Het |
Klc1 |
A |
G |
12: 111,738,950 (GRCm39) |
E66G |
probably damaging |
Het |
Klhl2 |
A |
T |
8: 65,205,870 (GRCm39) |
Y350* |
probably null |
Het |
Letm1 |
T |
C |
5: 33,926,802 (GRCm39) |
H165R |
probably damaging |
Het |
Luc7l2 |
T |
C |
6: 38,547,489 (GRCm39) |
C36R |
probably damaging |
Het |
Mab21l1 |
A |
G |
3: 55,690,674 (GRCm39) |
N87S |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,678,414 (GRCm39) |
T681A |
probably damaging |
Het |
Mrpl38 |
A |
G |
11: 116,023,276 (GRCm39) |
S326P |
probably damaging |
Het |
Mtr |
T |
G |
13: 12,268,764 (GRCm39) |
K32N |
probably benign |
Het |
Mybpc3 |
T |
A |
2: 90,965,478 (GRCm39) |
C1128* |
probably null |
Het |
Ncdn |
T |
C |
4: 126,645,762 (GRCm39) |
D49G |
probably damaging |
Het |
Nfkbiz |
G |
A |
16: 55,642,337 (GRCm39) |
T27I |
probably damaging |
Het |
Npnt |
A |
T |
3: 132,653,866 (GRCm39) |
Y38* |
probably null |
Het |
Nrxn2 |
A |
G |
19: 6,581,931 (GRCm39) |
E1622G |
probably benign |
Het |
Nutm2 |
T |
C |
13: 50,626,964 (GRCm39) |
I373T |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,674,715 (GRCm39) |
I201V |
probably benign |
Het |
Or51m1 |
T |
C |
7: 103,578,980 (GRCm39) |
S317P |
possibly damaging |
Het |
Osbp2 |
A |
G |
11: 3,662,170 (GRCm39) |
S228P |
probably damaging |
Het |
Pbx3 |
C |
T |
2: 34,103,348 (GRCm39) |
R208Q |
probably damaging |
Het |
Pcdhgb5 |
T |
C |
18: 37,864,838 (GRCm39) |
V211A |
probably benign |
Het |
Pi16 |
C |
T |
17: 29,544,899 (GRCm39) |
T151M |
probably damaging |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Ptpro |
T |
C |
6: 137,420,933 (GRCm39) |
I1068T |
probably benign |
Het |
Rbl1 |
A |
T |
2: 157,035,154 (GRCm39) |
Y309N |
probably damaging |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,229,134 (GRCm39) |
|
probably benign |
Het |
Serpina3g |
G |
C |
12: 104,206,518 (GRCm39) |
E106D |
probably benign |
Het |
Slc4a11 |
C |
T |
2: 130,533,664 (GRCm39) |
A100T |
probably damaging |
Het |
Son |
G |
C |
16: 91,454,508 (GRCm39) |
R1085P |
probably damaging |
Het |
Tasor |
A |
T |
14: 27,163,927 (GRCm39) |
I238F |
probably damaging |
Het |
Tbx18 |
C |
A |
9: 87,612,675 (GRCm39) |
A75S |
probably benign |
Het |
Tmem232 |
C |
A |
17: 65,792,881 (GRCm39) |
Q105H |
probably damaging |
Het |
Ttc29 |
A |
G |
8: 79,060,390 (GRCm39) |
I437V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,621,887 (GRCm39) |
I15552L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,750,313 (GRCm39) |
T3579S |
probably benign |
Het |
Vps11 |
A |
G |
9: 44,267,719 (GRCm39) |
F298L |
probably benign |
Het |
Wbp11 |
T |
C |
6: 136,791,259 (GRCm39) |
T625A |
unknown |
Het |
Xylb |
T |
A |
9: 119,215,428 (GRCm39) |
N460K |
probably damaging |
Het |
Znrf4 |
C |
A |
17: 56,819,218 (GRCm39) |
V30F |
probably damaging |
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 |
R4897:Mrc1
|
UTSW |
2 |
14,323,952 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
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 |
|