Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,433,890 (GRCm39) |
R4148S |
probably benign |
Het |
Acoxl |
T |
A |
2: 127,886,311 (GRCm39) |
L182Q |
possibly damaging |
Het |
Aldh7a1 |
T |
C |
18: 56,665,088 (GRCm39) |
T364A |
possibly damaging |
Het |
App |
T |
C |
16: 84,853,322 (GRCm39) |
D252G |
unknown |
Het |
Arid1a |
A |
G |
4: 133,408,672 (GRCm39) |
I1945T |
unknown |
Het |
Arsk |
C |
T |
13: 76,213,398 (GRCm39) |
|
probably null |
Het |
Atad2b |
G |
A |
12: 4,993,251 (GRCm39) |
G257S |
probably benign |
Het |
Best1 |
C |
A |
19: 9,969,062 (GRCm39) |
R218L |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,312,300 (GRCm39) |
|
probably null |
Het |
Cdh13 |
C |
T |
8: 119,484,129 (GRCm39) |
T130I |
possibly damaging |
Het |
Cela2a |
T |
C |
4: 141,552,902 (GRCm39) |
E25G |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,632,314 (GRCm39) |
I346F |
probably damaging |
Het |
Chil6 |
C |
T |
3: 106,297,244 (GRCm39) |
G299D |
possibly damaging |
Het |
Cic |
G |
A |
7: 24,972,327 (GRCm39) |
R686H |
probably damaging |
Het |
Cnpy1 |
T |
C |
5: 28,450,738 (GRCm39) |
I23V |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,707,011 (GRCm39) |
Y2034F |
unknown |
Het |
Coq10b |
T |
C |
1: 55,110,903 (GRCm39) |
Y224H |
probably benign |
Het |
Cryge |
G |
T |
1: 65,090,211 (GRCm39) |
|
probably benign |
Het |
Cyb5rl |
T |
G |
4: 106,941,510 (GRCm39) |
S252A |
probably benign |
Het |
Cyp2ab1 |
T |
A |
16: 20,133,814 (GRCm39) |
R125S |
probably damaging |
Het |
Dclk1 |
G |
A |
3: 55,387,811 (GRCm39) |
G86R |
probably damaging |
Het |
Dmtn |
A |
G |
14: 70,842,254 (GRCm39) |
M382T |
probably damaging |
Het |
Dnaaf8 |
A |
G |
16: 4,794,138 (GRCm39) |
|
noncoding transcript |
Het |
Dnah12 |
T |
A |
14: 26,437,784 (GRCm39) |
L471* |
probably null |
Het |
Dock10 |
A |
T |
1: 80,526,874 (GRCm39) |
S782T |
probably benign |
Het |
Ephb6 |
T |
A |
6: 41,595,079 (GRCm39) |
W698R |
probably benign |
Het |
Exoc4 |
T |
A |
6: 33,895,343 (GRCm39) |
C787S |
probably damaging |
Het |
Exosc8 |
A |
T |
3: 54,639,523 (GRCm39) |
|
probably benign |
Het |
Galc |
T |
A |
12: 98,193,533 (GRCm39) |
Q352L |
probably benign |
Het |
Galns |
A |
G |
8: 123,327,272 (GRCm39) |
Y167H |
probably damaging |
Het |
Glb1l |
T |
C |
1: 75,185,528 (GRCm39) |
|
probably benign |
Het |
Gm6185 |
A |
T |
1: 161,033,750 (GRCm39) |
|
noncoding transcript |
Het |
Gm7694 |
T |
C |
1: 170,128,794 (GRCm39) |
N245S |
probably benign |
Het |
Gmcl1 |
T |
G |
6: 86,681,538 (GRCm39) |
K385N |
possibly damaging |
Het |
Gramd1c |
A |
T |
16: 43,810,200 (GRCm39) |
W463R |
probably damaging |
Het |
Gtpbp8 |
C |
G |
16: 44,566,433 (GRCm39) |
A90P |
probably benign |
Het |
H2bc11 |
G |
T |
13: 22,227,421 (GRCm39) |
|
probably benign |
Het |
Hcar1 |
T |
C |
5: 124,016,731 (GRCm39) |
E320G |
probably benign |
Het |
Hhatl |
T |
C |
9: 121,618,077 (GRCm39) |
D226G |
probably damaging |
Het |
Hoxc5 |
T |
A |
15: 102,923,801 (GRCm39) |
I199N |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,059,845 (GRCm39) |
D121G |
probably damaging |
Het |
Il5ra |
T |
A |
6: 106,715,432 (GRCm39) |
H134L |
probably benign |
Het |
Isl2 |
T |
A |
9: 55,452,271 (GRCm39) |
I281N |
possibly damaging |
Het |
Kcnk13 |
T |
C |
12: 99,932,383 (GRCm39) |
F60L |
probably damaging |
Het |
Kdelr3 |
C |
T |
15: 79,409,066 (GRCm39) |
T85M |
possibly damaging |
Het |
Kdf1 |
A |
T |
4: 133,255,676 (GRCm39) |
H131L |
probably damaging |
Het |
Mipol1 |
T |
A |
12: 57,379,087 (GRCm39) |
L182I |
probably damaging |
Het |
Morc1 |
T |
G |
16: 48,381,980 (GRCm39) |
S513R |
probably benign |
Het |
Moxd2 |
A |
T |
6: 40,855,756 (GRCm39) |
L611H |
probably damaging |
Het |
Mpped2 |
T |
C |
2: 106,529,724 (GRCm39) |
|
probably benign |
Het |
Mrpl51 |
T |
C |
6: 125,170,270 (GRCm39) |
V92A |
probably benign |
Het |
Mrps26 |
G |
A |
2: 130,405,681 (GRCm39) |
|
probably benign |
Het |
Mrps5 |
A |
G |
2: 127,432,665 (GRCm39) |
T29A |
probably benign |
Het |
Mustn1 |
A |
G |
14: 30,601,517 (GRCm39) |
|
probably benign |
Het |
Ncor2 |
G |
A |
5: 125,110,431 (GRCm39) |
P858S |
possibly damaging |
Het |
Nfasc |
A |
G |
1: 132,529,759 (GRCm39) |
F807S |
probably damaging |
Het |
Nup50 |
G |
A |
15: 84,823,912 (GRCm39) |
V422I |
probably benign |
Het |
Or10x1 |
T |
A |
1: 174,196,562 (GRCm39) |
F26L |
probably benign |
Het |
Or13a25 |
A |
T |
7: 140,247,226 (GRCm39) |
M2L |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,493,883 (GRCm39) |
H159L |
probably damaging |
Het |
Or2ag13 |
A |
T |
7: 106,473,221 (GRCm39) |
V77D |
probably damaging |
Het |
Or3a1d |
C |
A |
11: 74,237,769 (GRCm39) |
V214L |
probably benign |
Het |
Or4c107 |
A |
G |
2: 88,788,930 (GRCm39) |
N40S |
probably damaging |
Het |
Or8b44 |
T |
A |
9: 38,410,319 (GRCm39) |
M118K |
probably damaging |
Het |
Or8u9 |
T |
A |
2: 86,002,015 (GRCm39) |
I49F |
probably damaging |
Het |
Osbpl8 |
T |
A |
10: 111,040,661 (GRCm39) |
M1K |
probably null |
Het |
Pcdhb22 |
A |
C |
18: 37,652,087 (GRCm39) |
D185A |
possibly damaging |
Het |
Pcdhga8 |
G |
T |
18: 37,949,457 (GRCm39) |
R291L |
probably damaging |
Het |
Saysd1 |
A |
T |
14: 20,127,672 (GRCm39) |
L84Q |
possibly damaging |
Het |
Slc41a1 |
T |
C |
1: 131,758,508 (GRCm39) |
I50T |
probably benign |
Het |
Smg7 |
G |
A |
1: 152,720,020 (GRCm39) |
P834S |
probably benign |
Het |
Speer4a1 |
C |
T |
5: 26,243,210 (GRCm39) |
V92M |
probably damaging |
Het |
Srf |
T |
C |
17: 46,860,400 (GRCm39) |
T461A |
probably benign |
Het |
Ssu72 |
A |
G |
4: 155,800,053 (GRCm39) |
D72G |
possibly damaging |
Het |
Suco |
T |
C |
1: 161,661,761 (GRCm39) |
E890G |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,763,656 (GRCm39) |
|
probably null |
Het |
Tm6sf1 |
A |
G |
7: 81,515,091 (GRCm39) |
E7G |
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,378,616 (GRCm39) |
K240R |
probably benign |
Het |
Tmem52 |
T |
A |
4: 155,554,825 (GRCm39) |
Y149* |
probably null |
Het |
Tpgs2 |
A |
T |
18: 25,284,305 (GRCm39) |
Y68N |
possibly damaging |
Het |
Vmn1r205 |
T |
A |
13: 22,777,074 (GRCm39) |
E9D |
probably benign |
Het |
Vmn2r32 |
A |
G |
7: 7,482,953 (GRCm39) |
V7A |
possibly damaging |
Het |
Vmn2r80 |
T |
C |
10: 79,030,156 (GRCm39) |
Y661H |
possibly damaging |
Het |
Vps39 |
G |
A |
2: 120,152,312 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
T |
6: 13,196,047 (GRCm39) |
V326D |
possibly damaging |
Het |
Zfp641 |
T |
A |
15: 98,186,598 (GRCm39) |
S342C |
probably damaging |
Het |
Zfp961 |
T |
C |
8: 72,722,847 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Egfem1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00766:Egfem1
|
APN |
3 |
29,711,302 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02111:Egfem1
|
APN |
3 |
29,705,045 (GRCm39) |
splice site |
probably null |
|
IGL02325:Egfem1
|
APN |
3 |
29,206,066 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02450:Egfem1
|
APN |
3 |
29,711,417 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02543:Egfem1
|
APN |
3 |
29,722,529 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02835:Egfem1
|
UTSW |
3 |
29,711,390 (GRCm39) |
missense |
probably damaging |
1.00 |
P0033:Egfem1
|
UTSW |
3 |
29,744,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Egfem1
|
UTSW |
3 |
29,637,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R0294:Egfem1
|
UTSW |
3 |
29,744,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Egfem1
|
UTSW |
3 |
29,722,399 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1479:Egfem1
|
UTSW |
3 |
29,711,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Egfem1
|
UTSW |
3 |
29,702,420 (GRCm39) |
missense |
probably benign |
0.02 |
R1754:Egfem1
|
UTSW |
3 |
29,722,482 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2568:Egfem1
|
UTSW |
3 |
29,637,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Egfem1
|
UTSW |
3 |
29,724,825 (GRCm39) |
missense |
probably benign |
0.01 |
R3411:Egfem1
|
UTSW |
3 |
29,637,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Egfem1
|
UTSW |
3 |
29,206,075 (GRCm39) |
missense |
probably benign |
0.14 |
R4049:Egfem1
|
UTSW |
3 |
29,740,880 (GRCm39) |
missense |
probably benign |
0.01 |
R4917:Egfem1
|
UTSW |
3 |
29,206,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Egfem1
|
UTSW |
3 |
29,206,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Egfem1
|
UTSW |
3 |
29,637,145 (GRCm39) |
missense |
probably damaging |
0.98 |
R4997:Egfem1
|
UTSW |
3 |
29,207,739 (GRCm39) |
missense |
probably benign |
0.00 |
R5148:Egfem1
|
UTSW |
3 |
29,511,972 (GRCm39) |
intron |
probably benign |
|
R5194:Egfem1
|
UTSW |
3 |
29,411,345 (GRCm39) |
critical splice donor site |
probably null |
|
R5284:Egfem1
|
UTSW |
3 |
29,704,936 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5354:Egfem1
|
UTSW |
3 |
29,136,361 (GRCm39) |
critical splice donor site |
probably null |
|
R5627:Egfem1
|
UTSW |
3 |
29,722,548 (GRCm39) |
nonsense |
probably null |
|
R5677:Egfem1
|
UTSW |
3 |
29,744,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R5928:Egfem1
|
UTSW |
3 |
29,637,077 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5982:Egfem1
|
UTSW |
3 |
29,711,419 (GRCm39) |
splice site |
probably null |
|
R6419:Egfem1
|
UTSW |
3 |
29,711,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6475:Egfem1
|
UTSW |
3 |
29,711,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:Egfem1
|
UTSW |
3 |
29,716,560 (GRCm39) |
nonsense |
probably null |
|
R7046:Egfem1
|
UTSW |
3 |
29,136,364 (GRCm39) |
splice site |
probably null |
|
R7079:Egfem1
|
UTSW |
3 |
29,207,731 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Egfem1
|
UTSW |
3 |
29,206,015 (GRCm39) |
missense |
probably benign |
0.09 |
R7362:Egfem1
|
UTSW |
3 |
29,206,069 (GRCm39) |
missense |
probably benign |
0.01 |
R7684:Egfem1
|
UTSW |
3 |
29,744,334 (GRCm39) |
missense |
probably damaging |
0.97 |
R7697:Egfem1
|
UTSW |
3 |
29,744,346 (GRCm39) |
critical splice donor site |
probably null |
|
R7814:Egfem1
|
UTSW |
3 |
29,740,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8226:Egfem1
|
UTSW |
3 |
29,711,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Egfem1
|
UTSW |
3 |
29,711,417 (GRCm39) |
critical splice donor site |
probably null |
|
R8928:Egfem1
|
UTSW |
3 |
29,744,561 (GRCm39) |
makesense |
probably null |
|
R9210:Egfem1
|
UTSW |
3 |
29,207,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Egfem1
|
UTSW |
3 |
29,411,317 (GRCm39) |
missense |
probably benign |
0.03 |
R9230:Egfem1
|
UTSW |
3 |
29,411,317 (GRCm39) |
missense |
probably benign |
0.03 |
R9720:Egfem1
|
UTSW |
3 |
29,716,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9745:Egfem1
|
UTSW |
3 |
29,716,532 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Egfem1
|
UTSW |
3 |
29,711,295 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Egfem1
|
UTSW |
3 |
29,202,602 (GRCm39) |
missense |
probably benign |
0.44 |
|