Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
T |
A |
13: 81,652,097 (GRCm39) |
|
probably null |
Het |
Adh7 |
A |
C |
3: 137,929,716 (GRCm39) |
T131P |
possibly damaging |
Het |
Agxt |
G |
A |
1: 93,065,701 (GRCm39) |
G190D |
probably damaging |
Het |
AI182371 |
A |
G |
2: 34,978,815 (GRCm39) |
I193T |
probably damaging |
Het |
Akna |
T |
A |
4: 63,297,547 (GRCm39) |
T836S |
probably benign |
Het |
Alox12 |
T |
C |
11: 70,144,069 (GRCm39) |
|
probably null |
Het |
Anapc2 |
C |
A |
2: 25,163,075 (GRCm39) |
T104K |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,583,935 (GRCm39) |
L346P |
probably damaging |
Het |
Ankfn1 |
A |
T |
11: 89,332,217 (GRCm39) |
I443N |
probably damaging |
Het |
Arhgef17 |
G |
A |
7: 100,539,680 (GRCm39) |
T1066I |
probably damaging |
Het |
Bpifb5 |
T |
A |
2: 154,065,776 (GRCm39) |
H24Q |
probably benign |
Het |
Brd9 |
A |
G |
13: 74,092,862 (GRCm39) |
E283G |
probably damaging |
Het |
Cadm2 |
C |
A |
16: 66,581,727 (GRCm39) |
V184F |
probably damaging |
Het |
Casr |
A |
G |
16: 36,315,499 (GRCm39) |
V857A |
probably benign |
Het |
Ccdc18 |
A |
T |
5: 108,339,843 (GRCm39) |
Q796L |
probably damaging |
Het |
Cep290 |
T |
C |
10: 100,332,690 (GRCm39) |
V263A |
probably benign |
Het |
Clec10a |
A |
T |
11: 70,060,645 (GRCm39) |
N167Y |
probably damaging |
Het |
Cog1 |
A |
G |
11: 113,543,058 (GRCm39) |
I189V |
possibly damaging |
Het |
Commd2 |
A |
G |
3: 57,554,269 (GRCm39) |
I144T |
probably benign |
Het |
Cse1l |
A |
G |
2: 166,768,292 (GRCm39) |
T197A |
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,683,794 (GRCm39) |
S1783R |
probably benign |
Het |
Cxxc1 |
T |
C |
18: 74,352,278 (GRCm39) |
V334A |
possibly damaging |
Het |
Dennd2d |
A |
G |
3: 106,394,236 (GRCm39) |
I39V |
probably benign |
Het |
Dgkz |
G |
A |
2: 91,768,405 (GRCm39) |
P734S |
probably damaging |
Het |
Diaph3 |
T |
C |
14: 86,893,916 (GRCm39) |
D31G |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,956,518 (GRCm39) |
S731P |
probably benign |
Het |
Dmac2l |
G |
A |
12: 69,787,845 (GRCm39) |
D94N |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,894,991 (GRCm39) |
R3619G |
probably benign |
Het |
Doc2b |
A |
G |
11: 75,662,783 (GRCm39) |
L405P |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,829,563 (GRCm39) |
I1117N |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,874,112 (GRCm39) |
A453V |
probably benign |
Het |
Ece2 |
T |
A |
16: 20,461,263 (GRCm39) |
I474N |
probably damaging |
Het |
Etv4 |
A |
T |
11: 101,662,513 (GRCm39) |
|
probably null |
Het |
Fam171b |
A |
T |
2: 83,710,442 (GRCm39) |
M705L |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,561,631 (GRCm39) |
K959E |
probably benign |
Het |
Fyn |
T |
C |
10: 39,408,066 (GRCm39) |
M251T |
possibly damaging |
Het |
Galnt13 |
G |
A |
2: 54,747,869 (GRCm39) |
G250E |
probably damaging |
Het |
Ggh |
T |
C |
4: 20,054,204 (GRCm39) |
|
probably null |
Het |
Glcci1 |
A |
G |
6: 8,591,620 (GRCm39) |
E222G |
probably damaging |
Het |
Gm1968 |
G |
A |
16: 29,777,659 (GRCm39) |
|
noncoding transcript |
Het |
Gm3604 |
T |
A |
13: 62,519,414 (GRCm39) |
I52F |
possibly damaging |
Het |
Gm43302 |
T |
C |
5: 105,422,635 (GRCm39) |
I466V |
probably benign |
Het |
Gm9789 |
T |
C |
16: 88,955,034 (GRCm39) |
S48P |
unknown |
Het |
Gpat3 |
A |
T |
5: 101,031,254 (GRCm39) |
Y136F |
probably benign |
Het |
Gpr171 |
T |
C |
3: 59,005,142 (GRCm39) |
D211G |
possibly damaging |
Het |
Grep1 |
T |
A |
17: 23,936,118 (GRCm39) |
|
probably benign |
Het |
Hs3st1 |
T |
C |
5: 39,771,791 (GRCm39) |
K284R |
probably benign |
Het |
Htr2a |
C |
T |
14: 74,882,608 (GRCm39) |
A198V |
possibly damaging |
Het |
Ice1 |
C |
A |
13: 70,754,023 (GRCm39) |
D688Y |
probably damaging |
Het |
Jade1 |
T |
C |
3: 41,559,431 (GRCm39) |
M504T |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,420,250 (GRCm39) |
|
probably null |
Het |
Lsr |
A |
T |
7: 30,671,517 (GRCm39) |
I72N |
possibly damaging |
Het |
Magel2 |
G |
A |
7: 62,028,557 (GRCm39) |
R487H |
possibly damaging |
Het |
Mertk |
A |
G |
2: 128,624,446 (GRCm39) |
D619G |
probably benign |
Het |
Myo1b |
A |
T |
1: 51,838,722 (GRCm39) |
V245E |
probably damaging |
Het |
Myrip |
T |
A |
9: 120,253,689 (GRCm39) |
L254Q |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,603,031 (GRCm39) |
S1173P |
probably damaging |
Het |
Ncoa7 |
T |
C |
10: 30,647,725 (GRCm39) |
Y17C |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,187,003 (GRCm39) |
E7G |
probably benign |
Het |
Ninl |
A |
G |
2: 150,817,867 (GRCm39) |
V99A |
probably damaging |
Het |
Noct |
G |
T |
3: 51,155,333 (GRCm39) |
E34* |
probably null |
Het |
Notch1 |
A |
T |
2: 26,362,125 (GRCm39) |
Y1043* |
probably null |
Het |
Or10v1 |
T |
C |
19: 11,873,855 (GRCm39) |
S157P |
possibly damaging |
Het |
Or13a21 |
T |
A |
7: 139,999,326 (GRCm39) |
Y120F |
probably benign |
Het |
Or2d3 |
A |
G |
7: 106,490,483 (GRCm39) |
Y278H |
probably damaging |
Het |
Or6c88 |
G |
A |
10: 129,406,640 (GRCm39) |
G39R |
probably damaging |
Het |
Pde7b |
C |
A |
10: 20,355,432 (GRCm39) |
R104L |
possibly damaging |
Het |
Pkn1 |
C |
A |
8: 84,396,966 (GRCm39) |
R890L |
possibly damaging |
Het |
Podn |
A |
T |
4: 107,878,764 (GRCm39) |
Y368N |
probably damaging |
Het |
Polr1b |
G |
A |
2: 128,960,019 (GRCm39) |
|
probably null |
Het |
Ppp1r3c |
A |
T |
19: 36,711,361 (GRCm39) |
F136L |
probably benign |
Het |
Ppp2ca |
T |
A |
11: 52,011,800 (GRCm39) |
F260Y |
probably damaging |
Het |
Prss39 |
A |
G |
1: 34,537,616 (GRCm39) |
S27G |
possibly damaging |
Het |
Ptch1 |
A |
G |
13: 63,689,101 (GRCm39) |
V340A |
probably benign |
Het |
Ranbp17 |
T |
C |
11: 33,247,394 (GRCm39) |
I246V |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,653,618 (GRCm39) |
D181V |
probably damaging |
Het |
Sdk1 |
T |
A |
5: 142,080,354 (GRCm39) |
V1282D |
probably damaging |
Het |
Sh3rf2 |
T |
C |
18: 42,282,887 (GRCm39) |
S514P |
probably damaging |
Het |
Slc35f2 |
A |
T |
9: 53,716,992 (GRCm39) |
I252F |
possibly damaging |
Het |
Slc7a1 |
A |
G |
5: 148,272,403 (GRCm39) |
Y425H |
possibly damaging |
Het |
Spaca4 |
G |
T |
7: 45,374,984 (GRCm39) |
|
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,863,733 (GRCm39) |
S294P |
possibly damaging |
Het |
Ssh1 |
T |
G |
5: 114,090,064 (GRCm39) |
T342P |
probably damaging |
Het |
Stk10 |
T |
A |
11: 32,483,440 (GRCm39) |
S13T |
possibly damaging |
Het |
Tbx1 |
G |
T |
16: 18,402,843 (GRCm39) |
D214E |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,878,571 (GRCm39) |
E453G |
probably damaging |
Het |
Tlr1 |
T |
C |
5: 65,084,319 (GRCm39) |
Y86C |
probably damaging |
Het |
Tmem241 |
A |
T |
18: 12,176,297 (GRCm39) |
C124S |
possibly damaging |
Het |
Trp63 |
A |
G |
16: 25,703,599 (GRCm39) |
M516V |
probably benign |
Het |
Ttc28 |
T |
C |
5: 111,248,677 (GRCm39) |
V210A |
possibly damaging |
Het |
Tut1 |
C |
T |
19: 8,942,850 (GRCm39) |
R646W |
probably benign |
Het |
Ubald1 |
C |
T |
16: 4,694,261 (GRCm39) |
E49K |
possibly damaging |
Het |
Usp28 |
T |
C |
9: 48,949,096 (GRCm39) |
Y897H |
probably benign |
Het |
Vmn2r27 |
A |
C |
6: 124,168,730 (GRCm39) |
F800C |
probably damaging |
Het |
Vmn2r83 |
T |
A |
10: 79,327,759 (GRCm39) |
M789K |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,300,002 (GRCm39) |
D945G |
probably benign |
Het |
Wdhd1 |
T |
A |
14: 47,482,507 (GRCm39) |
K947N |
possibly damaging |
Het |
Wdr12 |
A |
T |
1: 60,123,007 (GRCm39) |
|
probably null |
Het |
Xrra1 |
A |
T |
7: 99,520,564 (GRCm39) |
E57V |
probably damaging |
Het |
|
Other mutations in Atg2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Atg2a
|
APN |
19 |
6,304,629 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01612:Atg2a
|
APN |
19 |
6,302,514 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02105:Atg2a
|
APN |
19 |
6,300,433 (GRCm39) |
splice site |
probably benign |
|
IGL02151:Atg2a
|
APN |
19 |
6,305,787 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02228:Atg2a
|
APN |
19 |
6,296,830 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02329:Atg2a
|
APN |
19 |
6,299,959 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02408:Atg2a
|
APN |
19 |
6,291,858 (GRCm39) |
nonsense |
probably null |
|
IGL02538:Atg2a
|
APN |
19 |
6,307,658 (GRCm39) |
missense |
probably benign |
|
IGL02830:Atg2a
|
APN |
19 |
6,297,711 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03349:Atg2a
|
APN |
19 |
6,308,054 (GRCm39) |
missense |
possibly damaging |
0.77 |
PIT4515001:Atg2a
|
UTSW |
19 |
6,303,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0099:Atg2a
|
UTSW |
19 |
6,302,819 (GRCm39) |
missense |
probably damaging |
0.97 |
R0212:Atg2a
|
UTSW |
19 |
6,296,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Atg2a
|
UTSW |
19 |
6,297,713 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0398:Atg2a
|
UTSW |
19 |
6,296,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Atg2a
|
UTSW |
19 |
6,306,632 (GRCm39) |
missense |
probably benign |
0.01 |
R0483:Atg2a
|
UTSW |
19 |
6,306,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R0494:Atg2a
|
UTSW |
19 |
6,303,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Atg2a
|
UTSW |
19 |
6,302,569 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0590:Atg2a
|
UTSW |
19 |
6,295,037 (GRCm39) |
unclassified |
probably benign |
|
R0592:Atg2a
|
UTSW |
19 |
6,295,037 (GRCm39) |
unclassified |
probably benign |
|
R0593:Atg2a
|
UTSW |
19 |
6,295,037 (GRCm39) |
unclassified |
probably benign |
|
R0630:Atg2a
|
UTSW |
19 |
6,294,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R1306:Atg2a
|
UTSW |
19 |
6,303,051 (GRCm39) |
missense |
probably benign |
0.31 |
R1437:Atg2a
|
UTSW |
19 |
6,300,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Atg2a
|
UTSW |
19 |
6,300,628 (GRCm39) |
missense |
probably benign |
0.01 |
R1781:Atg2a
|
UTSW |
19 |
6,306,243 (GRCm39) |
missense |
probably damaging |
0.96 |
R1854:Atg2a
|
UTSW |
19 |
6,302,461 (GRCm39) |
missense |
probably benign |
0.11 |
R1884:Atg2a
|
UTSW |
19 |
6,304,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Atg2a
|
UTSW |
19 |
6,295,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Atg2a
|
UTSW |
19 |
6,302,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Atg2a
|
UTSW |
19 |
6,300,299 (GRCm39) |
critical splice donor site |
probably null |
|
R2071:Atg2a
|
UTSW |
19 |
6,307,488 (GRCm39) |
missense |
probably benign |
0.00 |
R2513:Atg2a
|
UTSW |
19 |
6,308,076 (GRCm39) |
critical splice donor site |
probably null |
|
R3808:Atg2a
|
UTSW |
19 |
6,302,846 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4065:Atg2a
|
UTSW |
19 |
6,308,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4109:Atg2a
|
UTSW |
19 |
6,308,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4352:Atg2a
|
UTSW |
19 |
6,307,487 (GRCm39) |
missense |
probably benign |
0.04 |
R4440:Atg2a
|
UTSW |
19 |
6,305,859 (GRCm39) |
critical splice donor site |
probably null |
|
R4472:Atg2a
|
UTSW |
19 |
6,308,985 (GRCm39) |
missense |
probably damaging |
0.98 |
R4669:Atg2a
|
UTSW |
19 |
6,309,017 (GRCm39) |
critical splice donor site |
probably null |
|
R4878:Atg2a
|
UTSW |
19 |
6,300,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4926:Atg2a
|
UTSW |
19 |
6,307,563 (GRCm39) |
missense |
probably damaging |
0.96 |
R5237:Atg2a
|
UTSW |
19 |
6,296,844 (GRCm39) |
missense |
probably benign |
|
R5350:Atg2a
|
UTSW |
19 |
6,301,368 (GRCm39) |
missense |
probably damaging |
0.99 |
R5507:Atg2a
|
UTSW |
19 |
6,295,100 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5732:Atg2a
|
UTSW |
19 |
6,307,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R5784:Atg2a
|
UTSW |
19 |
6,311,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5960:Atg2a
|
UTSW |
19 |
6,304,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R5985:Atg2a
|
UTSW |
19 |
6,304,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Atg2a
|
UTSW |
19 |
6,291,759 (GRCm39) |
unclassified |
probably benign |
|
R6572:Atg2a
|
UTSW |
19 |
6,304,695 (GRCm39) |
missense |
probably damaging |
0.98 |
R6878:Atg2a
|
UTSW |
19 |
6,300,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R6879:Atg2a
|
UTSW |
19 |
6,301,882 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6983:Atg2a
|
UTSW |
19 |
6,310,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R7024:Atg2a
|
UTSW |
19 |
6,300,249 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7217:Atg2a
|
UTSW |
19 |
6,303,471 (GRCm39) |
critical splice donor site |
probably null |
|
R7384:Atg2a
|
UTSW |
19 |
6,311,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R7387:Atg2a
|
UTSW |
19 |
6,305,198 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7425:Atg2a
|
UTSW |
19 |
6,305,682 (GRCm39) |
missense |
probably benign |
0.02 |
R7512:Atg2a
|
UTSW |
19 |
6,310,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7658:Atg2a
|
UTSW |
19 |
6,301,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7893:Atg2a
|
UTSW |
19 |
6,301,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R8062:Atg2a
|
UTSW |
19 |
6,302,609 (GRCm39) |
critical splice donor site |
probably null |
|
R8258:Atg2a
|
UTSW |
19 |
6,299,859 (GRCm39) |
missense |
probably damaging |
0.98 |
R8259:Atg2a
|
UTSW |
19 |
6,299,859 (GRCm39) |
missense |
probably damaging |
0.98 |
R8350:Atg2a
|
UTSW |
19 |
6,296,841 (GRCm39) |
missense |
probably benign |
0.03 |
R8412:Atg2a
|
UTSW |
19 |
6,294,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R8450:Atg2a
|
UTSW |
19 |
6,296,841 (GRCm39) |
missense |
probably benign |
0.03 |
R8474:Atg2a
|
UTSW |
19 |
6,301,433 (GRCm39) |
critical splice donor site |
probably null |
|
R8501:Atg2a
|
UTSW |
19 |
6,304,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Atg2a
|
UTSW |
19 |
6,306,674 (GRCm39) |
missense |
probably benign |
0.00 |
R8786:Atg2a
|
UTSW |
19 |
6,294,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Atg2a
|
UTSW |
19 |
6,300,651 (GRCm39) |
missense |
probably benign |
0.01 |
R8898:Atg2a
|
UTSW |
19 |
6,306,721 (GRCm39) |
splice site |
probably benign |
|
R9016:Atg2a
|
UTSW |
19 |
6,300,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R9111:Atg2a
|
UTSW |
19 |
6,311,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Atg2a
|
UTSW |
19 |
6,291,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R9184:Atg2a
|
UTSW |
19 |
6,291,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9268:Atg2a
|
UTSW |
19 |
6,291,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R9496:Atg2a
|
UTSW |
19 |
6,310,022 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9570:Atg2a
|
UTSW |
19 |
6,305,749 (GRCm39) |
missense |
probably benign |
0.03 |
R9642:Atg2a
|
UTSW |
19 |
6,300,198 (GRCm39) |
nonsense |
probably null |
|
X0065:Atg2a
|
UTSW |
19 |
6,308,226 (GRCm39) |
missense |
possibly damaging |
0.89 |
|