Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029I15Rik |
C |
A |
2: 92,383,472 |
P68Q |
probably damaging |
Het |
Abcg3 |
A |
G |
5: 104,968,215 |
L251S |
probably damaging |
Het |
Acsbg1 |
C |
T |
9: 54,628,559 |
S53N |
unknown |
Het |
Adamts18 |
A |
G |
8: 113,713,223 |
C913R |
probably damaging |
Het |
Adck5 |
C |
A |
15: 76,595,388 |
Y524* |
probably null |
Het |
Adgrv1 |
G |
T |
13: 81,103,324 |
Q6225K |
possibly damaging |
Het |
Ahr |
T |
C |
12: 35,504,017 |
N701S |
probably damaging |
Het |
Apc |
T |
C |
18: 34,314,208 |
C1386R |
probably damaging |
Het |
Bbs1 |
A |
G |
19: 4,906,154 |
S38P |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,978,732 |
C1366* |
probably null |
Het |
Cep290 |
A |
C |
10: 100,540,057 |
H1424P |
probably benign |
Het |
Clcn3 |
C |
T |
8: 60,933,085 |
R311K |
possibly damaging |
Het |
Crat |
C |
T |
2: 30,404,565 |
R497Q |
probably benign |
Het |
Dhx9 |
A |
G |
1: 153,458,406 |
Y1002H |
probably damaging |
Het |
Ermard |
T |
C |
17: 15,059,462 |
S505P |
probably benign |
Het |
Fbxw17 |
G |
A |
13: 50,425,644 |
D166N |
probably damaging |
Het |
Fmo3 |
T |
C |
1: 162,958,332 |
K363R |
possibly damaging |
Het |
Gadd45gip1 |
A |
T |
8: 84,832,351 |
R21W |
probably damaging |
Het |
Galnt4 |
A |
G |
10: 99,109,964 |
N517S |
probably benign |
Het |
Ganc |
T |
A |
2: 120,433,792 |
W409R |
probably damaging |
Het |
Glrx3 |
T |
C |
7: 137,459,191 |
S185P |
probably damaging |
Het |
Gm49368 |
T |
C |
7: 128,113,242 |
S853P |
probably damaging |
Het |
Gtf3c2 |
A |
C |
5: 31,168,267 |
L443V |
probably damaging |
Het |
Gxylt2 |
A |
T |
6: 100,804,528 |
Q388L |
probably benign |
Het |
Hcar2 |
C |
T |
5: 123,865,333 |
V36M |
possibly damaging |
Het |
Ifit3b |
A |
T |
19: 34,612,555 |
D377V |
possibly damaging |
Het |
Ints5 |
A |
G |
19: 8,896,804 |
D709G |
probably benign |
Het |
Lyst |
A |
G |
13: 13,669,865 |
E1880G |
probably benign |
Het |
Mep1a |
C |
T |
17: 43,479,174 |
S428N |
probably benign |
Het |
Mllt6 |
T |
C |
11: 97,676,964 |
L739P |
probably damaging |
Het |
Mlst8 |
T |
C |
17: 24,476,057 |
Y284C |
probably damaging |
Het |
Mmel1 |
T |
C |
4: 154,871,654 |
M1T |
probably null |
Het |
Muc5ac |
C |
T |
7: 141,809,383 |
P2144S |
unknown |
Het |
Myh4 |
T |
C |
11: 67,240,930 |
V72A |
probably benign |
Het |
Naa15 |
T |
A |
3: 51,469,974 |
|
probably null |
Het |
Nlrc5 |
A |
G |
8: 94,521,400 |
|
probably null |
Het |
Nme8 |
T |
A |
13: 19,650,975 |
M514L |
probably benign |
Het |
Nudt9 |
C |
A |
5: 104,047,080 |
S14* |
probably null |
Het |
Olfr538 |
T |
C |
7: 140,574,246 |
F31S |
probably damaging |
Het |
Olfr748 |
A |
T |
14: 50,710,758 |
I143F |
possibly damaging |
Het |
Optn |
G |
A |
2: 5,054,650 |
T19I |
probably benign |
Het |
Osbpl8 |
T |
A |
10: 111,276,509 |
L495* |
probably null |
Het |
Panx2 |
T |
C |
15: 89,067,770 |
S147P |
possibly damaging |
Het |
Pclo |
T |
A |
5: 14,680,616 |
V3044D |
unknown |
Het |
Pcnt |
T |
C |
10: 76,422,808 |
K608E |
probably benign |
Het |
Pde7a |
T |
A |
3: 19,227,745 |
N447I |
probably damaging |
Het |
Peli2 |
G |
T |
14: 48,280,034 |
C186F |
not run |
Het |
Pgm5 |
A |
G |
19: 24,727,851 |
F433L |
probably benign |
Het |
Plce1 |
G |
A |
19: 38,748,433 |
V1588I |
probably benign |
Het |
Plin4 |
T |
A |
17: 56,102,413 |
H1295L |
probably benign |
Het |
Poli |
T |
C |
18: 70,525,519 |
E134G |
probably benign |
Het |
Pramef6 |
T |
A |
4: 143,897,801 |
D42V |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,643,978 |
I1144F |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,024,978 |
T1738S |
probably damaging |
Het |
Pxdc1 |
A |
G |
13: 34,652,284 |
L51P |
probably damaging |
Het |
Rabepk |
C |
T |
2: 34,779,296 |
G362S |
probably damaging |
Het |
Rftn1 |
G |
T |
17: 50,047,380 |
A318D |
probably damaging |
Het |
Rhd |
T |
A |
4: 134,884,509 |
|
probably null |
Het |
Rpp14 |
T |
C |
14: 8,090,453 |
S126P |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,676,192 |
C1451Y |
probably damaging |
Het |
Sdr39u1 |
G |
A |
14: 55,897,734 |
R251* |
probably null |
Het |
Sephs2 |
G |
T |
7: 127,273,334 |
P196T |
possibly damaging |
Het |
Slc22a16 |
T |
C |
10: 40,574,089 |
Y195H |
possibly damaging |
Het |
Spg11 |
C |
A |
2: 122,068,880 |
V1575F |
probably damaging |
Het |
Sqle |
C |
T |
15: 59,316,041 |
S66L |
probably benign |
Het |
Tas2r124 |
T |
G |
6: 132,755,093 |
W122G |
probably damaging |
Het |
Tex52 |
A |
T |
6: 128,384,958 |
|
probably null |
Het |
Thoc1 |
T |
A |
18: 9,993,454 |
C604* |
probably null |
Het |
Tmc3 |
T |
C |
7: 83,597,458 |
S136P |
probably damaging |
Het |
Tmem212 |
T |
A |
3: 27,896,313 |
T11S |
probably benign |
Het |
Ubn2 |
A |
G |
6: 38,491,792 |
N1147S |
probably benign |
Het |
Uggt2 |
A |
G |
14: 119,075,347 |
I350T |
probably damaging |
Het |
Ust |
A |
T |
10: 8,207,575 |
Y346N |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,098,300 |
T1399A |
probably benign |
Het |
Zc3h18 |
G |
A |
8: 122,413,876 |
R850Q |
unknown |
Het |
Zfp800 |
C |
A |
6: 28,244,194 |
K257N |
probably damaging |
Het |
Zfp985 |
T |
A |
4: 147,582,874 |
D66E |
probably benign |
Het |
|