Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot6 |
T |
A |
12: 84,153,358 (GRCm39) |
L200Q |
possibly damaging |
Het |
Apbb1 |
A |
G |
7: 105,208,727 (GRCm39) |
S569P |
probably damaging |
Het |
C87436 |
A |
G |
6: 86,423,227 (GRCm39) |
D267G |
probably benign |
Het |
Ccdc7a |
T |
A |
8: 129,472,482 (GRCm39) |
I1617F |
possibly damaging |
Het |
Cic |
T |
C |
7: 24,987,502 (GRCm39) |
F1397L |
probably benign |
Het |
Cln6 |
T |
A |
9: 62,756,465 (GRCm39) |
M203K |
probably benign |
Het |
Clock |
A |
G |
5: 76,384,871 (GRCm39) |
S449P |
probably benign |
Het |
Cse1l |
C |
A |
2: 166,783,185 (GRCm39) |
N743K |
probably damaging |
Het |
Cyp1a2 |
A |
G |
9: 57,589,583 (GRCm39) |
I77T |
probably damaging |
Het |
D6Wsu163e |
A |
G |
6: 126,943,932 (GRCm39) |
I443V |
probably benign |
Het |
Dctn1 |
T |
C |
6: 83,176,684 (GRCm39) |
V1246A |
probably benign |
Het |
Dennd5b |
T |
C |
6: 149,002,698 (GRCm39) |
E37G |
probably benign |
Het |
Dnah11 |
C |
T |
12: 117,991,251 (GRCm39) |
E2372K |
probably damaging |
Het |
Ecpas |
A |
T |
4: 58,875,444 (GRCm39) |
D173E |
probably damaging |
Het |
Ercc5 |
T |
C |
1: 44,217,503 (GRCm39) |
W949R |
possibly damaging |
Het |
Fam13c |
A |
G |
10: 70,388,869 (GRCm39) |
E465G |
probably damaging |
Het |
Fam83d |
T |
A |
2: 158,610,466 (GRCm39) |
C145S |
probably damaging |
Het |
Fbln7 |
T |
A |
2: 128,737,343 (GRCm39) |
V386E |
probably damaging |
Het |
Fpr3 |
A |
T |
17: 18,191,131 (GRCm39) |
Q134L |
probably damaging |
Het |
Gm3636 |
T |
A |
14: 17,955,001 (GRCm39) |
R5S |
possibly damaging |
Het |
Gna15 |
A |
G |
10: 81,345,224 (GRCm39) |
S214P |
probably benign |
Het |
Hdac9 |
A |
G |
12: 34,220,101 (GRCm39) |
M897T |
probably benign |
Het |
Hdc |
T |
C |
2: 126,436,600 (GRCm39) |
N424D |
probably benign |
Het |
Krtap27-1 |
A |
G |
16: 88,468,316 (GRCm39) |
V76A |
possibly damaging |
Het |
Lrrd1 |
T |
A |
5: 3,900,995 (GRCm39) |
H433Q |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,197,298 (GRCm39) |
D1180G |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,577,925 (GRCm39) |
C20R |
unknown |
Het |
Mphosph9 |
T |
C |
5: 124,450,854 (GRCm39) |
N306D |
probably damaging |
Het |
Mpp7 |
T |
C |
18: 7,403,327 (GRCm39) |
R328G |
probably benign |
Het |
Mslnl |
C |
T |
17: 25,961,694 (GRCm39) |
P117S |
possibly damaging |
Het |
Muc16 |
T |
A |
9: 18,419,833 (GRCm39) |
K117M |
probably damaging |
Het |
Mycbp2 |
T |
C |
14: 103,532,664 (GRCm39) |
N430S |
probably benign |
Het |
Myl1 |
T |
C |
1: 66,973,683 (GRCm39) |
I8V |
probably benign |
Het |
Ncdn |
A |
T |
4: 126,644,041 (GRCm39) |
D260E |
probably benign |
Het |
Nkx3-2 |
T |
A |
5: 41,919,114 (GRCm39) |
R291S |
probably damaging |
Het |
Nr4a2 |
A |
G |
2: 56,999,093 (GRCm39) |
V448A |
probably damaging |
Het |
Nrip1 |
T |
C |
16: 76,089,616 (GRCm39) |
E647G |
possibly damaging |
Het |
Or4c12 |
C |
A |
2: 89,773,725 (GRCm39) |
V245L |
possibly damaging |
Het |
Or52a5b |
A |
G |
7: 103,417,478 (GRCm39) |
I42T |
probably benign |
Het |
Or8c14-ps1 |
T |
C |
9: 38,101,120 (GRCm39) |
M33T |
possibly damaging |
Het |
Or8s10 |
C |
A |
15: 98,335,614 (GRCm39) |
A88E |
probably benign |
Het |
Patj |
A |
T |
4: 98,427,310 (GRCm39) |
I172F |
unknown |
Het |
Per1 |
T |
C |
11: 68,995,636 (GRCm39) |
S739P |
possibly damaging |
Het |
Plekhn1 |
A |
C |
4: 156,306,859 (GRCm39) |
V510G |
possibly damaging |
Het |
Plxna4 |
A |
T |
6: 32,494,379 (GRCm39) |
V79D |
probably damaging |
Het |
Pram1 |
A |
G |
17: 33,859,801 (GRCm39) |
T123A |
probably benign |
Het |
Ptpn23 |
C |
A |
9: 110,237,101 (GRCm39) |
|
probably null |
Het |
Rcbtb2 |
C |
T |
14: 73,414,500 (GRCm39) |
S437L |
probably damaging |
Het |
Resf1 |
C |
T |
6: 149,228,027 (GRCm39) |
L358F |
probably damaging |
Het |
Rxfp4 |
T |
A |
3: 88,559,390 (GRCm39) |
R354* |
probably null |
Het |
Serpinb5 |
A |
G |
1: 106,803,853 (GRCm39) |
T180A |
probably damaging |
Het |
Slc7a14 |
T |
A |
3: 31,281,359 (GRCm39) |
D317V |
probably damaging |
Het |
Slco5a1 |
A |
G |
1: 13,059,802 (GRCm39) |
|
probably null |
Het |
Snx14 |
T |
A |
9: 88,265,832 (GRCm39) |
T768S |
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,353,462 (GRCm39) |
|
probably benign |
Het |
Stambp |
C |
T |
6: 83,528,954 (GRCm39) |
A364T |
probably damaging |
Het |
Tgm3 |
T |
A |
2: 129,865,618 (GRCm39) |
I6N |
possibly damaging |
Het |
Tmem106b |
A |
T |
6: 13,082,430 (GRCm39) |
T202S |
probably damaging |
Het |
Tnfsf8 |
A |
G |
4: 63,752,450 (GRCm39) |
V205A |
probably benign |
Het |
Treml2 |
A |
T |
17: 48,614,922 (GRCm39) |
R136* |
probably null |
Het |
Trim46 |
T |
C |
3: 89,142,466 (GRCm39) |
T674A |
possibly damaging |
Het |
Trmt13 |
T |
A |
3: 116,376,356 (GRCm39) |
Y345F |
possibly damaging |
Het |
Tspyl4 |
A |
G |
10: 34,173,568 (GRCm39) |
H20R |
probably benign |
Het |
Uvssa |
T |
C |
5: 33,571,419 (GRCm39) |
|
probably null |
Het |
Vmn1r192 |
A |
T |
13: 22,371,401 (GRCm39) |
F273Y |
probably damaging |
Het |
Vmn2r45 |
A |
T |
7: 8,486,298 (GRCm39) |
I330N |
probably damaging |
Het |
Zfp40 |
A |
G |
17: 23,394,551 (GRCm39) |
F679L |
probably damaging |
Het |
|
Other mutations in Atl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02667:Atl3
|
APN |
19 |
7,486,781 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0042:Atl3
|
UTSW |
19 |
7,506,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Atl3
|
UTSW |
19 |
7,507,031 (GRCm39) |
critical splice donor site |
probably null |
|
R0975:Atl3
|
UTSW |
19 |
7,498,500 (GRCm39) |
nonsense |
probably null |
|
R1582:Atl3
|
UTSW |
19 |
7,494,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R4195:Atl3
|
UTSW |
19 |
7,495,911 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4249:Atl3
|
UTSW |
19 |
7,509,703 (GRCm39) |
missense |
probably benign |
0.06 |
R4505:Atl3
|
UTSW |
19 |
7,498,184 (GRCm39) |
missense |
probably benign |
0.00 |
R4836:Atl3
|
UTSW |
19 |
7,486,910 (GRCm39) |
nonsense |
probably null |
|
R5649:Atl3
|
UTSW |
19 |
7,509,592 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5721:Atl3
|
UTSW |
19 |
7,506,376 (GRCm39) |
missense |
probably benign |
0.00 |
R6459:Atl3
|
UTSW |
19 |
7,498,163 (GRCm39) |
missense |
probably benign |
0.07 |
R6530:Atl3
|
UTSW |
19 |
7,499,499 (GRCm39) |
missense |
probably benign |
|
R6543:Atl3
|
UTSW |
19 |
7,487,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R6550:Atl3
|
UTSW |
19 |
7,499,503 (GRCm39) |
missense |
probably benign |
|
R7059:Atl3
|
UTSW |
19 |
7,511,334 (GRCm39) |
missense |
probably benign |
0.08 |
R7059:Atl3
|
UTSW |
19 |
7,511,333 (GRCm39) |
missense |
probably benign |
|
R7220:Atl3
|
UTSW |
19 |
7,506,433 (GRCm39) |
missense |
probably null |
0.02 |
R7666:Atl3
|
UTSW |
19 |
7,487,405 (GRCm39) |
missense |
probably benign |
0.19 |
R9143:Atl3
|
UTSW |
19 |
7,509,408 (GRCm39) |
missense |
probably benign |
0.01 |
R9206:Atl3
|
UTSW |
19 |
7,487,447 (GRCm39) |
missense |
probably benign |
0.09 |
R9631:Atl3
|
UTSW |
19 |
7,509,553 (GRCm39) |
missense |
probably benign |
0.00 |
R9709:Atl3
|
UTSW |
19 |
7,507,921 (GRCm39) |
missense |
probably benign |
0.00 |
R9733:Atl3
|
UTSW |
19 |
7,509,705 (GRCm39) |
missense |
probably damaging |
0.99 |
X0020:Atl3
|
UTSW |
19 |
7,507,934 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Atl3
|
UTSW |
19 |
7,487,402 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Atl3
|
UTSW |
19 |
7,507,918 (GRCm39) |
missense |
probably benign |
0.19 |
|