Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503B20Rik |
T |
C |
3: 146,356,716 (GRCm39) |
D64G |
possibly damaging |
Het |
Amtn |
T |
C |
5: 88,525,956 (GRCm39) |
L40P |
probably damaging |
Het |
Ano6 |
A |
G |
15: 95,792,342 (GRCm39) |
R90G |
probably damaging |
Het |
Arfgef3 |
A |
C |
10: 18,540,637 (GRCm39) |
|
probably null |
Het |
Asxl3 |
C |
T |
18: 22,658,445 (GRCm39) |
P2152S |
probably benign |
Het |
Atp7b |
A |
T |
8: 22,512,381 (GRCm39) |
V494E |
probably damaging |
Het |
Bik |
T |
A |
15: 83,428,409 (GRCm39) |
Y146N |
probably benign |
Het |
C1qtnf7 |
A |
T |
5: 43,766,436 (GRCm39) |
I12F |
possibly damaging |
Het |
Cacna1e |
A |
G |
1: 154,289,720 (GRCm39) |
|
probably null |
Het |
Ccdc168 |
A |
G |
1: 44,095,890 (GRCm39) |
V1736A |
probably benign |
Het |
Ccnj |
A |
G |
19: 40,833,636 (GRCm39) |
E231G |
probably damaging |
Het |
Cd101 |
T |
C |
3: 100,901,012 (GRCm39) |
K1020R |
probably benign |
Het |
Cdh6 |
C |
A |
15: 13,044,860 (GRCm39) |
V421L |
probably benign |
Het |
Cplane1 |
T |
C |
15: 8,205,668 (GRCm39) |
S135P |
probably benign |
Het |
Decr1 |
T |
C |
4: 15,924,355 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
C |
T |
18: 50,054,091 (GRCm39) |
P2566S |
probably damaging |
Het |
Dock9 |
G |
A |
14: 121,860,330 (GRCm39) |
P866L |
probably damaging |
Het |
Epx |
A |
G |
11: 87,759,452 (GRCm39) |
F546L |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,035,966 (GRCm39) |
M3206K |
probably benign |
Het |
Fgb |
T |
C |
3: 82,952,332 (GRCm39) |
D179G |
probably benign |
Het |
Gbgt1 |
A |
G |
2: 28,395,220 (GRCm39) |
D286G |
probably damaging |
Het |
Gpn1 |
T |
A |
5: 31,664,832 (GRCm39) |
S285R |
probably benign |
Het |
Htt |
T |
A |
5: 34,991,670 (GRCm39) |
Y1212N |
possibly damaging |
Het |
Kcnj13 |
T |
C |
1: 87,314,745 (GRCm39) |
K159R |
probably damaging |
Het |
Ldb2 |
T |
A |
5: 44,699,199 (GRCm39) |
I80F |
probably damaging |
Het |
Macrod2 |
T |
A |
2: 140,294,602 (GRCm39) |
N89K |
probably damaging |
Het |
Mdga2 |
G |
A |
12: 66,769,775 (GRCm39) |
R173C |
probably damaging |
Het |
Mroh9 |
A |
G |
1: 162,903,935 (GRCm39) |
F26L |
probably benign |
Het |
Nepro |
A |
G |
16: 44,551,720 (GRCm39) |
R193G |
probably damaging |
Het |
Or52d3 |
T |
A |
7: 104,229,447 (GRCm39) |
I198N |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,731,113 (GRCm39) |
Q3205L |
unknown |
Het |
Plekhm1 |
A |
T |
11: 103,267,715 (GRCm39) |
I752N |
probably damaging |
Het |
Podn |
T |
C |
4: 107,878,614 (GRCm39) |
T273A |
possibly damaging |
Het |
Prep |
T |
A |
10: 44,973,597 (GRCm39) |
M235K |
probably benign |
Het |
Ptprc |
A |
T |
1: 137,999,993 (GRCm39) |
|
probably null |
Het |
Reg2 |
A |
G |
6: 78,384,625 (GRCm39) |
H119R |
possibly damaging |
Het |
Rpe65 |
T |
C |
3: 159,319,805 (GRCm39) |
V225A |
probably benign |
Het |
Scn9a |
T |
C |
2: 66,398,373 (GRCm39) |
D79G |
probably damaging |
Het |
Slc25a23 |
G |
A |
17: 57,360,804 (GRCm39) |
R9* |
probably null |
Het |
Snai3 |
A |
G |
8: 123,183,212 (GRCm39) |
L111P |
probably damaging |
Het |
Stk38 |
A |
G |
17: 29,218,981 (GRCm39) |
|
probably null |
Het |
Stk38l |
A |
T |
6: 146,668,269 (GRCm39) |
I115F |
possibly damaging |
Het |
Tmco6 |
T |
A |
18: 36,871,406 (GRCm39) |
|
probably null |
Het |
Tollip |
A |
T |
7: 141,452,451 (GRCm39) |
M1K |
probably null |
Het |
Trim40 |
T |
C |
17: 37,199,742 (GRCm39) |
Y112C |
possibly damaging |
Het |
Ttc27 |
T |
A |
17: 75,163,550 (GRCm39) |
Y719* |
probably null |
Het |
Ubald1 |
T |
C |
16: 4,697,584 (GRCm39) |
D6G |
probably damaging |
Het |
Vmn2r59 |
A |
T |
7: 41,693,171 (GRCm39) |
S476R |
probably benign |
Het |
Wfdc3 |
C |
T |
2: 164,576,178 (GRCm39) |
G38R |
possibly damaging |
Het |
Zbtb21 |
C |
T |
16: 97,753,161 (GRCm39) |
G402D |
probably damaging |
Het |
Zfp84 |
A |
G |
7: 29,475,911 (GRCm39) |
Y201C |
probably benign |
Het |
Zswim2 |
T |
A |
2: 83,770,028 (GRCm39) |
H62L |
probably damaging |
Het |
|
Other mutations in Neil3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0426:Neil3
|
UTSW |
8 |
54,062,431 (GRCm39) |
unclassified |
probably benign |
|
R0533:Neil3
|
UTSW |
8 |
54,091,810 (GRCm39) |
splice site |
probably null |
|
R0943:Neil3
|
UTSW |
8 |
54,062,404 (GRCm39) |
unclassified |
probably benign |
|
R1688:Neil3
|
UTSW |
8 |
54,054,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Neil3
|
UTSW |
8 |
54,052,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R2238:Neil3
|
UTSW |
8 |
54,052,311 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3979:Neil3
|
UTSW |
8 |
54,076,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R4909:Neil3
|
UTSW |
8 |
54,091,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5069:Neil3
|
UTSW |
8 |
54,054,076 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5407:Neil3
|
UTSW |
8 |
54,054,054 (GRCm39) |
missense |
probably benign |
0.00 |
R6144:Neil3
|
UTSW |
8 |
54,052,447 (GRCm39) |
missense |
probably benign |
0.01 |
R6185:Neil3
|
UTSW |
8 |
54,052,182 (GRCm39) |
missense |
probably benign |
0.03 |
R6234:Neil3
|
UTSW |
8 |
54,061,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R6375:Neil3
|
UTSW |
8 |
54,040,311 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7003:Neil3
|
UTSW |
8 |
54,054,001 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8165:Neil3
|
UTSW |
8 |
54,042,129 (GRCm39) |
missense |
probably benign |
0.00 |
R8390:Neil3
|
UTSW |
8 |
54,062,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:Neil3
|
UTSW |
8 |
54,058,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Neil3
|
UTSW |
8 |
54,061,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|