Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930567H17Rik |
G |
A |
X: 69,437,994 (GRCm39) |
R100W |
possibly damaging |
Het |
Adamts10 |
G |
A |
17: 33,768,270 (GRCm39) |
R814H |
probably damaging |
Het |
Akr1a1 |
A |
G |
4: 116,498,260 (GRCm39) |
L95P |
probably damaging |
Het |
Amigo2 |
G |
T |
15: 97,143,389 (GRCm39) |
N344K |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,621,014 (GRCm39) |
D946G |
possibly damaging |
Het |
Arb2a |
T |
A |
13: 78,147,773 (GRCm39) |
N280K |
probably damaging |
Het |
Btnl6 |
T |
G |
17: 34,734,391 (GRCm39) |
I124L |
probably benign |
Het |
Bzw2 |
A |
T |
12: 36,173,982 (GRCm39) |
C97* |
probably null |
Het |
Celsr2 |
G |
A |
3: 108,320,880 (GRCm39) |
T644I |
possibly damaging |
Het |
Cep85l |
A |
T |
10: 53,224,911 (GRCm39) |
L226Q |
possibly damaging |
Het |
Ces1g |
T |
C |
8: 94,046,512 (GRCm39) |
K338E |
possibly damaging |
Het |
Cldn10 |
G |
A |
14: 119,092,507 (GRCm39) |
D36N |
probably damaging |
Het |
Cntnap4 |
T |
A |
8: 113,479,598 (GRCm39) |
I261N |
probably benign |
Het |
Csnk1g1 |
T |
C |
9: 65,915,109 (GRCm39) |
|
probably null |
Het |
Cyp2c69 |
T |
C |
19: 39,869,910 (GRCm39) |
D104G |
possibly damaging |
Het |
Cyp3a11 |
T |
C |
5: 145,797,330 (GRCm39) |
T350A |
probably benign |
Het |
Daw1 |
T |
A |
1: 83,187,011 (GRCm39) |
C274S |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,850,144 (GRCm39) |
T267A |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,055,112 (GRCm39) |
Y585H |
possibly damaging |
Het |
Dsg2 |
T |
G |
18: 20,723,126 (GRCm39) |
V384G |
probably damaging |
Het |
Elmo1 |
C |
T |
13: 20,748,630 (GRCm39) |
L492F |
probably damaging |
Het |
Fmo1 |
T |
C |
1: 162,657,827 (GRCm39) |
D438G |
probably benign |
Het |
Folr2 |
C |
T |
7: 101,489,408 (GRCm39) |
V244M |
unknown |
Het |
Galnt18 |
T |
C |
7: 111,378,709 (GRCm39) |
I16V |
possibly damaging |
Het |
Gm10036 |
C |
A |
18: 15,966,207 (GRCm39) |
Y119* |
probably null |
Het |
Gria4 |
A |
G |
9: 4,664,951 (GRCm39) |
S102P |
probably damaging |
Het |
Hc |
A |
T |
2: 34,890,861 (GRCm39) |
N1318K |
probably benign |
Het |
Ifitm1 |
T |
C |
7: 140,549,499 (GRCm39) |
L94P |
probably damaging |
Het |
Iqca1l |
T |
C |
5: 24,755,628 (GRCm39) |
D298G |
probably benign |
Het |
Itga9 |
G |
A |
9: 118,510,835 (GRCm39) |
V455M |
probably damaging |
Het |
Kank4 |
C |
T |
4: 98,653,747 (GRCm39) |
V894I |
possibly damaging |
Het |
Kcnip2 |
T |
A |
19: 45,785,100 (GRCm39) |
|
probably benign |
Het |
Lamb1 |
A |
G |
12: 31,352,953 (GRCm39) |
T885A |
possibly damaging |
Het |
Lamp5 |
A |
G |
2: 135,902,874 (GRCm39) |
T198A |
probably benign |
Het |
Ldc1 |
T |
C |
4: 130,105,223 (GRCm39) |
K316E |
probably benign |
Het |
Lipi |
A |
T |
16: 75,352,710 (GRCm39) |
L376I |
probably benign |
Het |
Lrrc37 |
T |
A |
11: 103,509,656 (GRCm39) |
T771S |
unknown |
Het |
Luc7l |
T |
C |
17: 26,472,978 (GRCm39) |
I31T |
possibly damaging |
Het |
Malrd1 |
A |
T |
2: 15,850,038 (GRCm39) |
N1219I |
unknown |
Het |
Mcf2l |
C |
T |
8: 13,034,330 (GRCm39) |
|
probably benign |
Het |
Mrpl35 |
C |
T |
6: 71,793,271 (GRCm39) |
A127T |
possibly damaging |
Het |
Myom2 |
T |
A |
8: 15,152,589 (GRCm39) |
Y645* |
probably null |
Het |
Naip2 |
T |
C |
13: 100,325,644 (GRCm39) |
H88R |
probably benign |
Het |
Noc3l |
T |
A |
19: 38,798,751 (GRCm39) |
K282N |
probably damaging |
Het |
Nwd2 |
T |
C |
5: 63,963,241 (GRCm39) |
Y942H |
probably damaging |
Het |
Or10ag2 |
T |
C |
2: 87,248,659 (GRCm39) |
V87A |
probably benign |
Het |
Or52d1 |
T |
A |
7: 103,756,302 (GRCm39) |
I272N |
probably damaging |
Het |
Osbpl9 |
C |
A |
4: 108,930,333 (GRCm39) |
A221S |
probably benign |
Het |
Paip1 |
T |
C |
13: 119,566,801 (GRCm39) |
L45S |
probably benign |
Het |
Peak1 |
T |
C |
9: 56,113,938 (GRCm39) |
T1668A |
probably benign |
Het |
Pgap3 |
A |
G |
11: 98,281,602 (GRCm39) |
F199L |
possibly damaging |
Het |
Ppip5k2 |
T |
C |
1: 97,639,544 (GRCm39) |
M1061V |
probably benign |
Het |
Ppp6r3 |
A |
T |
19: 3,544,017 (GRCm39) |
W333R |
probably damaging |
Het |
Ptk2b |
T |
A |
14: 66,412,242 (GRCm39) |
N383I |
probably benign |
Het |
Rab21 |
G |
C |
10: 115,151,080 (GRCm39) |
R58G |
probably benign |
Het |
Rabif |
C |
T |
1: 134,433,935 (GRCm39) |
T83I |
probably damaging |
Het |
Rdh7 |
A |
T |
10: 127,724,430 (GRCm39) |
F18Y |
probably benign |
Het |
Scart2 |
C |
T |
7: 139,841,532 (GRCm39) |
P279S |
possibly damaging |
Het |
Septin5 |
A |
G |
16: 18,441,861 (GRCm39) |
M315T |
possibly damaging |
Het |
Slc27a6 |
A |
G |
18: 58,715,306 (GRCm39) |
Y303C |
probably damaging |
Het |
Slc7a7 |
T |
A |
14: 54,607,293 (GRCm39) |
M495L |
probably benign |
Het |
Sntg1 |
T |
A |
1: 8,748,074 (GRCm39) |
|
probably null |
Het |
Spred2 |
T |
A |
11: 19,951,019 (GRCm39) |
I72N |
probably benign |
Het |
St3gal1 |
A |
T |
15: 66,980,086 (GRCm39) |
I271N |
possibly damaging |
Het |
Stox1 |
A |
T |
10: 62,495,386 (GRCm39) |
H962Q |
probably benign |
Het |
Supt6 |
A |
T |
11: 78,103,664 (GRCm39) |
M1347K |
probably damaging |
Het |
Susd2 |
G |
T |
10: 75,475,452 (GRCm39) |
A484D |
possibly damaging |
Het |
Tmem260 |
A |
G |
14: 48,737,845 (GRCm39) |
|
probably benign |
Het |
Tpbg |
C |
A |
9: 85,726,520 (GRCm39) |
A163E |
possibly damaging |
Het |
Tpx2 |
T |
C |
2: 152,724,255 (GRCm39) |
Y344H |
probably damaging |
Het |
Ttf2 |
A |
T |
3: 100,870,028 (GRCm39) |
F348L |
probably benign |
Het |
Ttn |
A |
T |
2: 76,663,650 (GRCm39) |
V11675E |
unknown |
Het |
Txnl4b |
T |
A |
8: 110,299,467 (GRCm39) |
Y142* |
probably null |
Het |
Vmn2r18 |
G |
A |
5: 151,485,140 (GRCm39) |
R785C |
possibly damaging |
Het |
Zbtb18 |
T |
A |
1: 177,276,044 (GRCm39) |
V459E |
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 |
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 |
|