Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610524H06Rik |
A |
G |
5: 114,961,372 (GRCm39) |
|
probably null |
Het |
Abcd3 |
T |
C |
3: 121,586,491 (GRCm39) |
I70V |
possibly damaging |
Het |
Acad10 |
T |
C |
5: 121,759,411 (GRCm39) |
Y1024C |
probably damaging |
Het |
Atp2b3 |
T |
G |
X: 72,588,712 (GRCm39) |
V701G |
probably damaging |
Het |
Cbfa2t2 |
T |
A |
2: 154,342,347 (GRCm39) |
M21K |
probably damaging |
Het |
Cdc25a |
C |
T |
9: 109,710,614 (GRCm39) |
T106I |
possibly damaging |
Het |
Cdhr5 |
T |
C |
7: 140,852,083 (GRCm39) |
T190A |
probably damaging |
Het |
Chl1 |
A |
G |
6: 103,685,445 (GRCm39) |
T829A |
probably benign |
Het |
Clcn6 |
T |
C |
4: 148,097,226 (GRCm39) |
T614A |
possibly damaging |
Het |
Cntln |
A |
T |
4: 84,865,823 (GRCm39) |
R160* |
probably null |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dock3 |
C |
A |
9: 106,815,158 (GRCm39) |
M1236I |
possibly damaging |
Het |
Eif4g3 |
T |
A |
4: 137,847,719 (GRCm39) |
H213Q |
probably damaging |
Het |
Eya1 |
T |
A |
1: 14,279,141 (GRCm39) |
H372L |
probably damaging |
Het |
Fam13b |
A |
G |
18: 34,630,485 (GRCm39) |
V91A |
possibly damaging |
Het |
Hat1 |
T |
A |
2: 71,264,519 (GRCm39) |
I319K |
probably benign |
Het |
Kcnf1 |
T |
C |
12: 17,225,853 (GRCm39) |
N123D |
probably benign |
Het |
Kcns3 |
C |
A |
12: 11,141,551 (GRCm39) |
G383W |
probably damaging |
Het |
Kprp |
A |
T |
3: 92,732,689 (GRCm39) |
C120* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,672,774 (GRCm39) |
C2456S |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,366,658 (GRCm39) |
D539E |
probably damaging |
Het |
Matn3 |
T |
C |
12: 9,005,466 (GRCm39) |
L292S |
probably damaging |
Het |
Mbd3l1 |
T |
A |
9: 18,395,947 (GRCm39) |
I24N |
probably damaging |
Het |
Med10 |
T |
C |
13: 69,958,159 (GRCm39) |
L37P |
probably damaging |
Het |
Myo15a |
T |
A |
11: 60,409,290 (GRCm39) |
I3219N |
probably damaging |
Het |
Nom1 |
C |
T |
5: 29,647,633 (GRCm39) |
Q623* |
probably null |
Het |
Nrm |
T |
A |
17: 36,175,079 (GRCm39) |
W136R |
probably damaging |
Het |
Or8h8 |
A |
C |
2: 86,753,789 (GRCm39) |
V29G |
probably benign |
Het |
Pde7b |
T |
C |
10: 20,288,836 (GRCm39) |
N298S |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,277,990 (GRCm39) |
A305T |
possibly damaging |
Het |
Pimreg |
T |
C |
11: 71,936,042 (GRCm39) |
L175P |
possibly damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,390,237 (GRCm39) |
D1451G |
probably benign |
Het |
Ptpro |
A |
G |
6: 137,355,128 (GRCm39) |
S212G |
probably benign |
Het |
Rhpn1 |
C |
T |
15: 75,585,967 (GRCm39) |
R627C |
possibly damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnase4 |
T |
G |
14: 51,342,497 (GRCm39) |
F74V |
probably damaging |
Het |
Sbno2 |
A |
G |
10: 79,896,226 (GRCm39) |
|
probably null |
Het |
Selp |
T |
C |
1: 163,954,176 (GRCm39) |
Y159H |
probably damaging |
Het |
Senp6 |
A |
G |
9: 80,000,853 (GRCm39) |
T21A |
probably damaging |
Het |
Slco1a7 |
A |
T |
6: 141,700,135 (GRCm39) |
C132* |
probably null |
Het |
Slco3a1 |
T |
C |
7: 74,154,128 (GRCm39) |
D148G |
possibly damaging |
Het |
Smtn |
G |
A |
11: 3,480,102 (GRCm39) |
P373L |
probably benign |
Het |
Snx20 |
A |
T |
8: 89,356,597 (GRCm39) |
L73Q |
probably damaging |
Het |
Sobp |
A |
G |
10: 43,033,942 (GRCm39) |
V128A |
possibly damaging |
Het |
Tcerg1 |
A |
G |
18: 42,657,357 (GRCm39) |
T280A |
unknown |
Het |
Tgfbrap1 |
A |
G |
1: 43,088,973 (GRCm39) |
V810A |
probably benign |
Het |
Thbs1 |
C |
A |
2: 117,949,678 (GRCm39) |
D589E |
probably damaging |
Het |
Tjp2 |
A |
G |
19: 24,078,239 (GRCm39) |
Y885H |
probably damaging |
Het |
Tmem109 |
A |
G |
19: 10,849,993 (GRCm39) |
S100P |
probably damaging |
Het |
Trim36 |
T |
C |
18: 46,305,562 (GRCm39) |
K462E |
probably benign |
Het |
Vmn1r226 |
A |
T |
17: 20,908,538 (GRCm39) |
I257F |
probably damaging |
Het |
Vmn2r92 |
A |
G |
17: 18,372,352 (GRCm39) |
Y54C |
probably damaging |
Het |
Wdcp |
T |
A |
12: 4,901,924 (GRCm39) |
Y593* |
probably null |
Het |
Wdr59 |
T |
C |
8: 112,177,682 (GRCm39) |
S907G |
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 |
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 |
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 |
|