Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
T |
C |
2: 103,531,244 (GRCm39) |
L458P |
probably damaging |
Het |
Adgrl2 |
T |
C |
3: 148,526,068 (GRCm39) |
N130S |
|
Het |
Adgrv1 |
T |
C |
13: 81,732,234 (GRCm39) |
S161G |
probably benign |
Het |
Aldh1l1 |
A |
G |
6: 90,536,903 (GRCm39) |
D153G |
probably benign |
Het |
Arhgap20 |
G |
A |
9: 51,754,991 (GRCm39) |
S444N |
probably damaging |
Het |
Bpifc |
A |
G |
10: 85,812,129 (GRCm39) |
F360L |
probably benign |
Het |
Cacna1s |
A |
T |
1: 136,012,090 (GRCm39) |
I511F |
probably benign |
Het |
Chdh |
G |
A |
14: 29,758,806 (GRCm39) |
V584I |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,589,445 (GRCm39) |
R1037G |
probably benign |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,816,992 (GRCm39) |
N440D |
unknown |
Het |
Dsel |
A |
T |
1: 111,787,425 (GRCm39) |
Y1037N |
probably damaging |
Het |
Eloa |
A |
G |
4: 135,748,935 (GRCm39) |
M1T |
probably null |
Het |
Elp2 |
C |
G |
18: 24,755,560 (GRCm39) |
P436A |
probably damaging |
Het |
Etv5 |
A |
C |
16: 22,218,112 (GRCm39) |
S328A |
probably damaging |
Het |
Fat3 |
A |
T |
9: 16,288,691 (GRCm39) |
Y277* |
probably null |
Het |
Fbxo38 |
A |
T |
18: 62,644,160 (GRCm39) |
H899Q |
probably benign |
Het |
Fstl5 |
T |
C |
3: 76,229,583 (GRCm39) |
V128A |
|
Het |
Gm3371 |
T |
C |
14: 44,641,066 (GRCm39) |
E166G |
|
Het |
Herc6 |
T |
C |
6: 57,636,722 (GRCm39) |
S813P |
probably damaging |
Het |
Kbtbd2 |
A |
T |
6: 56,756,132 (GRCm39) |
C535S |
probably damaging |
Het |
Lgr5 |
A |
C |
10: 115,288,913 (GRCm39) |
L577W |
probably damaging |
Het |
Limk1 |
A |
T |
5: 134,686,358 (GRCm39) |
D590E |
probably benign |
Het |
Lnpep |
A |
T |
17: 17,795,609 (GRCm39) |
S301T |
probably benign |
Het |
Lrch1 |
A |
C |
14: 75,032,787 (GRCm39) |
V521G |
probably benign |
Het |
Lrrc71 |
T |
C |
3: 87,650,368 (GRCm39) |
H235R |
probably benign |
Het |
Mttp |
A |
G |
3: 137,820,962 (GRCm39) |
S282P |
probably benign |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Or2t1 |
G |
A |
14: 14,328,456 (GRCm38) |
G115D |
probably damaging |
Het |
Or55b10 |
T |
A |
7: 102,143,206 (GRCm39) |
T259S |
probably benign |
Het |
Or5a3 |
T |
C |
19: 12,399,889 (GRCm39) |
V72A |
|
Het |
Or5m13 |
T |
C |
2: 85,748,704 (GRCm39) |
V145A |
probably benign |
Het |
Or7a41 |
C |
T |
10: 78,871,395 (GRCm39) |
T255I |
probably damaging |
Het |
Or7c70 |
A |
G |
10: 78,682,906 (GRCm39) |
V281A |
probably damaging |
Het |
Pira12 |
T |
G |
7: 3,897,284 (GRCm39) |
|
probably null |
Het |
Ppfia3 |
T |
C |
7: 45,008,213 (GRCm39) |
Q219R |
possibly damaging |
Het |
Prdm5 |
T |
A |
6: 65,771,321 (GRCm39) |
M44K |
possibly damaging |
Het |
Psmc5 |
T |
C |
11: 106,153,303 (GRCm39) |
I315T |
probably damaging |
Het |
Ptprd |
T |
A |
4: 76,051,440 (GRCm39) |
E27V |
probably benign |
Het |
Rft1 |
T |
A |
14: 30,411,781 (GRCm39) |
I443N |
probably damaging |
Het |
Rsf1 |
G |
GACGGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Slco1a5 |
A |
G |
6: 142,214,001 (GRCm39) |
M40T |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,069,804 (GRCm39) |
T2661A |
possibly damaging |
Het |
Tigit |
T |
C |
16: 43,482,515 (GRCm39) |
D73G |
probably benign |
Het |
Tmem237 |
G |
A |
1: 59,159,213 (GRCm39) |
|
probably benign |
Het |
Trim42 |
T |
C |
9: 97,247,874 (GRCm39) |
D274G |
probably damaging |
Het |
Trmt61a |
C |
A |
12: 111,647,490 (GRCm39) |
L196I |
probably damaging |
Het |
Tspan8 |
T |
C |
10: 115,669,213 (GRCm39) |
C83R |
probably damaging |
Het |
Ttc7 |
CCTGCTGCTGCTGCTGCTG |
CCTGCTGCTGCTGCTG |
17: 87,678,147 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Unc80 |
G |
A |
1: 66,594,158 (GRCm39) |
G1179E |
probably damaging |
Het |
Vmn2r2 |
A |
G |
3: 64,041,945 (GRCm39) |
S257P |
probably damaging |
Het |
Xpo6 |
G |
T |
7: 125,748,418 (GRCm39) |
Y404* |
probably null |
Het |
|
Other mutations in Ifnlr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00817:Ifnlr1
|
APN |
4 |
135,431,596 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01637:Ifnlr1
|
APN |
4 |
135,413,856 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02090:Ifnlr1
|
APN |
4 |
135,432,578 (GRCm39) |
missense |
probably benign |
0.23 |
R0677:Ifnlr1
|
UTSW |
4 |
135,432,945 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0723:Ifnlr1
|
UTSW |
4 |
135,428,524 (GRCm39) |
splice site |
probably benign |
|
R0762:Ifnlr1
|
UTSW |
4 |
135,428,640 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1169:Ifnlr1
|
UTSW |
4 |
135,432,419 (GRCm39) |
missense |
probably benign |
0.00 |
R1303:Ifnlr1
|
UTSW |
4 |
135,431,528 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1819:Ifnlr1
|
UTSW |
4 |
135,413,834 (GRCm39) |
start gained |
probably benign |
|
R1957:Ifnlr1
|
UTSW |
4 |
135,413,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Ifnlr1
|
UTSW |
4 |
135,433,148 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2509:Ifnlr1
|
UTSW |
4 |
135,432,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Ifnlr1
|
UTSW |
4 |
135,432,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Ifnlr1
|
UTSW |
4 |
135,432,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R3020:Ifnlr1
|
UTSW |
4 |
135,433,041 (GRCm39) |
small deletion |
probably benign |
|
R3944:Ifnlr1
|
UTSW |
4 |
135,428,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Ifnlr1
|
UTSW |
4 |
135,433,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R4804:Ifnlr1
|
UTSW |
4 |
135,432,647 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4938:Ifnlr1
|
UTSW |
4 |
135,432,593 (GRCm39) |
missense |
probably benign |
0.35 |
R5070:Ifnlr1
|
UTSW |
4 |
135,431,509 (GRCm39) |
missense |
probably benign |
0.00 |
R5073:Ifnlr1
|
UTSW |
4 |
135,432,457 (GRCm39) |
missense |
probably benign |
0.06 |
R5493:Ifnlr1
|
UTSW |
4 |
135,432,877 (GRCm39) |
missense |
probably benign |
0.25 |
R5913:Ifnlr1
|
UTSW |
4 |
135,432,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5913:Ifnlr1
|
UTSW |
4 |
135,432,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5959:Ifnlr1
|
UTSW |
4 |
135,432,652 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6032:Ifnlr1
|
UTSW |
4 |
135,432,937 (GRCm39) |
missense |
probably benign |
0.03 |
R6032:Ifnlr1
|
UTSW |
4 |
135,432,937 (GRCm39) |
missense |
probably benign |
0.03 |
R6136:Ifnlr1
|
UTSW |
4 |
135,431,108 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7018:Ifnlr1
|
UTSW |
4 |
135,431,135 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7651:Ifnlr1
|
UTSW |
4 |
135,417,919 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8945:Ifnlr1
|
UTSW |
4 |
135,431,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Ifnlr1
|
UTSW |
4 |
135,428,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R9188:Ifnlr1
|
UTSW |
4 |
135,426,171 (GRCm39) |
missense |
probably damaging |
1.00 |
|