Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
A |
G |
1: 120,099,216 (GRCm39) |
|
probably null |
Het |
4930550C14Rik |
G |
T |
9: 53,325,683 (GRCm39) |
R73S |
probably damaging |
Het |
Abca1 |
A |
G |
4: 53,085,261 (GRCm39) |
V517A |
probably benign |
Het |
Adck5 |
A |
T |
15: 76,478,887 (GRCm39) |
K370N |
possibly damaging |
Het |
Akap6 |
A |
C |
12: 53,072,575 (GRCm39) |
D981A |
probably damaging |
Het |
Apbb1 |
G |
A |
7: 105,223,459 (GRCm39) |
R51* |
probably null |
Het |
Arhgap23 |
A |
G |
11: 97,391,238 (GRCm39) |
M1252V |
probably benign |
Het |
Arhgef1 |
A |
G |
7: 24,617,367 (GRCm39) |
T354A |
probably benign |
Het |
Arid1a |
G |
T |
4: 133,412,287 (GRCm39) |
Q1636K |
unknown |
Het |
Asmt |
C |
T |
X: 169,110,202 (GRCm39) |
A237V |
possibly damaging |
Het |
Brat1 |
T |
A |
5: 140,691,716 (GRCm39) |
C43S |
probably benign |
Het |
Cd36 |
T |
C |
5: 18,000,593 (GRCm39) |
Y370C |
probably damaging |
Het |
Ceacam12 |
A |
T |
7: 17,803,030 (GRCm39) |
L145F |
probably benign |
Het |
Col24a1 |
C |
T |
3: 145,019,815 (GRCm39) |
T62I |
probably damaging |
Het |
Col6a3 |
G |
T |
1: 90,741,475 (GRCm39) |
N652K |
possibly damaging |
Het |
Dcbld1 |
T |
C |
10: 52,180,756 (GRCm39) |
L140P |
probably damaging |
Het |
Dhrs13 |
G |
A |
11: 77,927,808 (GRCm39) |
C218Y |
probably damaging |
Het |
Diaph1 |
T |
G |
18: 37,986,406 (GRCm39) |
E1158A |
probably damaging |
Het |
Emp2 |
A |
C |
16: 10,110,145 (GRCm39) |
F20C |
probably damaging |
Het |
Epha2 |
A |
G |
4: 141,045,791 (GRCm39) |
|
probably null |
Het |
Eprs1 |
G |
T |
1: 185,139,951 (GRCm39) |
|
probably null |
Het |
Etl4 |
T |
A |
2: 20,718,171 (GRCm39) |
I304N |
probably damaging |
Het |
Exoc3l2 |
C |
A |
7: 19,225,670 (GRCm39) |
S89* |
probably null |
Het |
F5 |
G |
A |
1: 164,017,756 (GRCm39) |
C611Y |
probably damaging |
Het |
F5 |
A |
T |
1: 164,009,204 (GRCm39) |
I325F |
probably damaging |
Het |
Fam133b |
A |
T |
5: 3,609,133 (GRCm39) |
S116C |
probably null |
Het |
Fam13b |
A |
T |
18: 34,627,330 (GRCm39) |
D190E |
probably damaging |
Het |
Fam169a |
T |
G |
13: 97,230,138 (GRCm39) |
Y58D |
probably damaging |
Het |
Far1 |
G |
A |
7: 113,160,603 (GRCm39) |
R383H |
possibly damaging |
Het |
Fnbp1l |
T |
C |
3: 122,364,579 (GRCm39) |
K52R |
possibly damaging |
Het |
Foxj3 |
C |
A |
4: 119,480,468 (GRCm39) |
Q469K |
unknown |
Het |
Frs3 |
A |
T |
17: 48,000,013 (GRCm39) |
|
probably benign |
Het |
Gdpd3 |
A |
G |
7: 126,374,674 (GRCm39) |
S290G |
probably benign |
Het |
Gmip |
T |
A |
8: 70,269,735 (GRCm39) |
L610Q |
probably damaging |
Het |
Gprc5c |
T |
A |
11: 114,754,851 (GRCm39) |
I176N |
probably damaging |
Het |
Grm3 |
A |
G |
5: 9,561,556 (GRCm39) |
F765L |
probably damaging |
Het |
Hhat |
A |
T |
1: 192,442,065 (GRCm39) |
L2Q |
probably damaging |
Het |
Hspbap1 |
T |
C |
16: 35,637,592 (GRCm39) |
S214P |
probably damaging |
Het |
Ighv1-62-3 |
C |
A |
12: 115,424,909 (GRCm39) |
V21F |
probably damaging |
Het |
Kcnj15 |
A |
T |
16: 95,096,527 (GRCm39) |
K50* |
probably null |
Het |
Kidins220 |
T |
C |
12: 25,106,908 (GRCm39) |
S1454P |
possibly damaging |
Het |
Kl |
T |
A |
5: 150,912,318 (GRCm39) |
M689K |
possibly damaging |
Het |
Klhl23 |
T |
G |
2: 69,655,198 (GRCm39) |
L356R |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,501,129 (GRCm39) |
D806V |
probably benign |
Het |
Krt26 |
T |
C |
11: 99,228,315 (GRCm39) |
E139G |
probably benign |
Het |
Lefty1 |
T |
C |
1: 180,762,681 (GRCm39) |
F3L |
unknown |
Het |
Madd |
A |
C |
2: 90,995,802 (GRCm39) |
Y853* |
probably null |
Het |
Map1a |
T |
A |
2: 121,120,304 (GRCm39) |
D63E |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,684,735 (GRCm39) |
V815E |
probably damaging |
Het |
Mettl3 |
A |
G |
14: 52,532,477 (GRCm39) |
Y569H |
probably damaging |
Het |
Mknk2 |
T |
C |
10: 80,504,859 (GRCm39) |
|
probably null |
Het |
Mpp3 |
C |
A |
11: 101,899,392 (GRCm39) |
R376S |
probably benign |
Het |
Ncoa4-ps |
T |
G |
12: 119,224,841 (GRCm39) |
|
noncoding transcript |
Het |
Nup160 |
T |
A |
2: 90,520,449 (GRCm39) |
Y293* |
probably null |
Het |
Nup58 |
A |
T |
14: 60,482,065 (GRCm39) |
F100I |
possibly damaging |
Het |
Nxpe2 |
A |
C |
9: 48,237,491 (GRCm39) |
L255V |
probably benign |
Het |
Or10ab4 |
A |
G |
7: 107,655,106 (GRCm39) |
I306V |
probably benign |
Het |
Or1e30 |
T |
A |
11: 73,678,521 (GRCm39) |
Y252* |
probably null |
Het |
Or2l5 |
A |
T |
16: 19,334,281 (GRCm39) |
L35Q |
probably damaging |
Het |
Or4d11 |
T |
C |
19: 12,014,100 (GRCm39) |
E2G |
probably benign |
Het |
Padi3 |
A |
T |
4: 140,523,705 (GRCm39) |
D248E |
probably damaging |
Het |
Paxip1 |
G |
T |
5: 27,966,616 (GRCm39) |
H637N |
probably damaging |
Het |
Pde4b |
T |
A |
4: 102,458,748 (GRCm39) |
M296K |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,794,580 (GRCm39) |
H2089R |
probably benign |
Het |
Plaat5 |
C |
T |
19: 7,596,656 (GRCm39) |
P148S |
probably damaging |
Het |
Prpf40a |
T |
C |
2: 53,047,927 (GRCm39) |
M197V |
probably benign |
Het |
Rhebl1 |
T |
C |
15: 98,776,160 (GRCm39) |
I165V |
probably benign |
Het |
Rock1 |
A |
T |
18: 10,106,426 (GRCm39) |
V481E |
possibly damaging |
Het |
Rtca |
T |
A |
3: 116,301,476 (GRCm39) |
T24S |
probably benign |
Het |
Serpina3c |
T |
A |
12: 104,118,327 (GRCm39) |
I4F |
possibly damaging |
Het |
Serpina3j |
C |
A |
12: 104,283,649 (GRCm39) |
A249E |
possibly damaging |
Het |
Slc38a9 |
A |
G |
13: 112,825,910 (GRCm39) |
N116S |
probably damaging |
Het |
Slco2b1 |
C |
T |
7: 99,339,770 (GRCm39) |
V58I |
possibly damaging |
Het |
Slfn8 |
T |
A |
11: 82,908,147 (GRCm39) |
Y132F |
probably damaging |
Het |
Smg6 |
T |
G |
11: 75,047,033 (GRCm39) |
I1242S |
probably damaging |
Het |
Tap2 |
G |
T |
17: 34,431,021 (GRCm39) |
V374L |
probably benign |
Het |
Tbc1d10b |
G |
A |
7: 126,807,168 (GRCm39) |
T123M |
probably damaging |
Het |
Tenm2 |
A |
C |
11: 35,899,610 (GRCm39) |
V2516G |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 48,848,608 (GRCm39) |
R12Q |
probably damaging |
Het |
Tmem130 |
T |
A |
5: 144,674,661 (GRCm39) |
M355L |
probably benign |
Het |
Tns4 |
C |
T |
11: 98,966,376 (GRCm39) |
S433N |
probably benign |
Het |
Traip |
G |
T |
9: 107,847,818 (GRCm39) |
|
probably null |
Het |
Trmo |
G |
A |
4: 46,389,390 (GRCm39) |
R2C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,774,504 (GRCm39) |
I2134N |
probably damaging |
Het |
Uba1y |
A |
G |
Y: 825,984 (GRCm39) |
D380G |
probably benign |
Het |
Ube2t |
T |
A |
1: 134,895,698 (GRCm39) |
|
probably null |
Het |
Ugdh |
A |
T |
5: 65,574,924 (GRCm39) |
Y367* |
probably null |
Het |
Usp45 |
A |
C |
4: 21,810,797 (GRCm39) |
D331A |
probably damaging |
Het |
Vmn1r84 |
G |
T |
7: 12,095,841 (GRCm39) |
T284K |
possibly damaging |
Het |
Vmn1r91 |
T |
A |
7: 19,835,360 (GRCm39) |
F93Y |
probably benign |
Het |
Vmn2r77 |
T |
A |
7: 86,450,878 (GRCm39) |
Y255N |
probably benign |
Het |
Vmn2r96 |
A |
T |
17: 18,804,221 (GRCm39) |
Q490H |
probably benign |
Het |
Vwa2 |
A |
G |
19: 56,891,897 (GRCm39) |
|
probably null |
Het |
Vwf |
A |
G |
6: 125,634,028 (GRCm39) |
K169E |
unknown |
Het |
Zc3h7b |
G |
C |
15: 81,662,911 (GRCm39) |
|
probably null |
Het |
Zfp458 |
T |
A |
13: 67,405,662 (GRCm39) |
H259L |
possibly damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,819,910 (GRCm39) |
V1051A |
probably benign |
Het |
Zfp998 |
A |
T |
13: 66,579,740 (GRCm39) |
C248S |
probably damaging |
Het |
|
Other mutations in Enpep |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00791:Enpep
|
APN |
3 |
129,125,731 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01895:Enpep
|
APN |
3 |
129,063,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02193:Enpep
|
APN |
3 |
129,075,336 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02215:Enpep
|
APN |
3 |
129,063,926 (GRCm39) |
splice site |
probably benign |
|
IGL02511:Enpep
|
APN |
3 |
129,115,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02579:Enpep
|
APN |
3 |
129,077,739 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02634:Enpep
|
APN |
3 |
129,103,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03034:Enpep
|
APN |
3 |
129,092,599 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03214:Enpep
|
APN |
3 |
129,086,896 (GRCm39) |
missense |
probably benign |
|
IGL03401:Enpep
|
APN |
3 |
129,106,269 (GRCm39) |
missense |
probably benign |
0.01 |
P0041:Enpep
|
UTSW |
3 |
129,125,847 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0371:Enpep
|
UTSW |
3 |
129,077,516 (GRCm39) |
critical splice donor site |
probably null |
|
R0479:Enpep
|
UTSW |
3 |
129,106,323 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1036:Enpep
|
UTSW |
3 |
129,077,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Enpep
|
UTSW |
3 |
129,113,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Enpep
|
UTSW |
3 |
129,113,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Enpep
|
UTSW |
3 |
129,113,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Enpep
|
UTSW |
3 |
129,074,172 (GRCm39) |
missense |
probably benign |
0.14 |
R2101:Enpep
|
UTSW |
3 |
129,092,587 (GRCm39) |
missense |
probably benign |
0.00 |
R2153:Enpep
|
UTSW |
3 |
129,074,231 (GRCm39) |
missense |
probably damaging |
0.99 |
R2474:Enpep
|
UTSW |
3 |
129,077,807 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3618:Enpep
|
UTSW |
3 |
129,077,807 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3619:Enpep
|
UTSW |
3 |
129,077,807 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4275:Enpep
|
UTSW |
3 |
129,125,927 (GRCm39) |
missense |
probably benign |
0.02 |
R4291:Enpep
|
UTSW |
3 |
129,063,966 (GRCm39) |
nonsense |
probably null |
|
R4438:Enpep
|
UTSW |
3 |
129,077,740 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4570:Enpep
|
UTSW |
3 |
129,075,197 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4678:Enpep
|
UTSW |
3 |
129,097,362 (GRCm39) |
critical splice donor site |
probably null |
|
R4679:Enpep
|
UTSW |
3 |
129,097,362 (GRCm39) |
critical splice donor site |
probably null |
|
R4748:Enpep
|
UTSW |
3 |
129,125,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Enpep
|
UTSW |
3 |
129,070,420 (GRCm39) |
missense |
probably benign |
0.17 |
R4954:Enpep
|
UTSW |
3 |
129,077,829 (GRCm39) |
missense |
probably damaging |
0.98 |
R5074:Enpep
|
UTSW |
3 |
129,097,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R5261:Enpep
|
UTSW |
3 |
129,099,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Enpep
|
UTSW |
3 |
129,074,159 (GRCm39) |
missense |
probably benign |
0.30 |
R5661:Enpep
|
UTSW |
3 |
129,070,406 (GRCm39) |
missense |
probably damaging |
0.98 |
R5687:Enpep
|
UTSW |
3 |
129,092,743 (GRCm39) |
splice site |
probably null |
|
R5695:Enpep
|
UTSW |
3 |
129,102,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5697:Enpep
|
UTSW |
3 |
129,102,772 (GRCm39) |
missense |
probably benign |
|
R5889:Enpep
|
UTSW |
3 |
129,106,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:Enpep
|
UTSW |
3 |
129,106,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5968:Enpep
|
UTSW |
3 |
129,074,587 (GRCm39) |
missense |
probably benign |
|
R5976:Enpep
|
UTSW |
3 |
129,092,773 (GRCm39) |
missense |
probably damaging |
0.97 |
R6367:Enpep
|
UTSW |
3 |
129,125,730 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6468:Enpep
|
UTSW |
3 |
129,125,509 (GRCm39) |
critical splice donor site |
probably null |
|
R6484:Enpep
|
UTSW |
3 |
129,115,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R6938:Enpep
|
UTSW |
3 |
129,092,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R6989:Enpep
|
UTSW |
3 |
129,074,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7073:Enpep
|
UTSW |
3 |
129,106,319 (GRCm39) |
nonsense |
probably null |
|
R7258:Enpep
|
UTSW |
3 |
129,125,724 (GRCm39) |
missense |
probably benign |
0.01 |
R7452:Enpep
|
UTSW |
3 |
129,065,052 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7576:Enpep
|
UTSW |
3 |
129,077,740 (GRCm39) |
missense |
probably benign |
0.03 |
R7684:Enpep
|
UTSW |
3 |
129,115,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7697:Enpep
|
UTSW |
3 |
129,102,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8050:Enpep
|
UTSW |
3 |
129,099,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8080:Enpep
|
UTSW |
3 |
129,092,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8318:Enpep
|
UTSW |
3 |
129,063,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Enpep
|
UTSW |
3 |
129,102,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8474:Enpep
|
UTSW |
3 |
129,113,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R8532:Enpep
|
UTSW |
3 |
129,070,302 (GRCm39) |
nonsense |
probably null |
|
R8826:Enpep
|
UTSW |
3 |
129,065,067 (GRCm39) |
missense |
probably damaging |
0.97 |
R8884:Enpep
|
UTSW |
3 |
129,115,052 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8936:Enpep
|
UTSW |
3 |
129,125,884 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8937:Enpep
|
UTSW |
3 |
129,115,007 (GRCm39) |
critical splice donor site |
probably null |
|
R8959:Enpep
|
UTSW |
3 |
129,113,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Enpep
|
UTSW |
3 |
129,102,772 (GRCm39) |
missense |
probably benign |
0.03 |
R9375:Enpep
|
UTSW |
3 |
129,125,529 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Enpep
|
UTSW |
3 |
129,070,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|