Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat3 |
A |
G |
17: 13,147,402 (GRCm39) |
V205A |
probably damaging |
Het |
Acp7 |
A |
G |
7: 28,316,616 (GRCm39) |
F120L |
possibly damaging |
Het |
Adh4 |
T |
C |
3: 138,128,045 (GRCm39) |
V157A |
probably damaging |
Het |
Ahsa2 |
T |
C |
11: 23,443,314 (GRCm39) |
E146G |
probably benign |
Het |
Ank3 |
T |
C |
10: 69,822,389 (GRCm39) |
S353P |
|
Het |
Apob |
T |
C |
12: 8,058,954 (GRCm39) |
S2479P |
possibly damaging |
Het |
Arhgef37 |
A |
G |
18: 61,641,760 (GRCm39) |
L203P |
probably damaging |
Het |
Arpp21 |
T |
A |
9: 111,984,583 (GRCm39) |
N265I |
possibly damaging |
Het |
Cfap20dc |
T |
C |
14: 8,518,768 (GRCm38) |
|
probably null |
Het |
Dagla |
G |
A |
19: 10,246,615 (GRCm39) |
R162C |
probably damaging |
Het |
Ddx18 |
T |
C |
1: 121,489,135 (GRCm39) |
D304G |
probably damaging |
Het |
Dnah3 |
A |
T |
7: 119,618,987 (GRCm39) |
L1638Q |
possibly damaging |
Het |
Dnah6 |
T |
A |
6: 73,061,640 (GRCm39) |
N2815I |
possibly damaging |
Het |
Dnajc16 |
T |
C |
4: 141,510,371 (GRCm39) |
D94G |
probably benign |
Het |
Epor |
G |
T |
9: 21,870,655 (GRCm39) |
D408E |
probably benign |
Het |
Etaa1 |
A |
G |
11: 17,895,798 (GRCm39) |
I773T |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,941,324 (GRCm39) |
Y72* |
probably null |
Het |
Fbxw18 |
T |
G |
9: 109,517,491 (GRCm39) |
D404A |
probably benign |
Het |
Flot1 |
T |
A |
17: 36,140,859 (GRCm39) |
V283E |
probably damaging |
Het |
Gm5145 |
G |
T |
17: 20,791,194 (GRCm39) |
G191W |
probably damaging |
Het |
Gpr161 |
G |
A |
1: 165,134,166 (GRCm39) |
|
probably benign |
Het |
Helz |
C |
A |
11: 107,563,761 (GRCm39) |
Q1734K |
unknown |
Het |
Hycc1 |
A |
G |
5: 24,184,579 (GRCm39) |
C300R |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,747,822 (GRCm39) |
V1195A |
possibly damaging |
Het |
Khdc4 |
T |
A |
3: 88,596,582 (GRCm39) |
L121Q |
probably damaging |
Het |
Kmt2a |
T |
A |
9: 44,732,716 (GRCm39) |
T2534S |
unknown |
Het |
Lingo3 |
T |
C |
10: 80,670,821 (GRCm39) |
N370D |
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,748,501 (GRCm39) |
V3113A |
|
Het |
Mthfs |
C |
T |
9: 89,097,454 (GRCm39) |
L104F |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,488,607 (GRCm39) |
V576D |
probably damaging |
Het |
Nlrc5 |
A |
G |
8: 95,217,013 (GRCm39) |
R1001G |
probably benign |
Het |
Obscn |
C |
T |
11: 58,972,636 (GRCm39) |
A2137T |
probably benign |
Het |
Ociad1 |
T |
A |
5: 73,460,951 (GRCm39) |
H70Q |
probably damaging |
Het |
Opa1 |
T |
A |
16: 29,404,836 (GRCm39) |
C11* |
probably null |
Het |
Or4a76 |
A |
G |
2: 89,461,161 (GRCm39) |
V27A |
probably benign |
Het |
Parp10 |
T |
C |
15: 76,125,964 (GRCm39) |
E408G |
possibly damaging |
Het |
Pcdhb19 |
G |
A |
18: 37,631,143 (GRCm39) |
E313K |
probably benign |
Het |
Pmel |
G |
T |
10: 128,551,918 (GRCm39) |
A251S |
probably benign |
Het |
Polr3d |
G |
T |
14: 70,678,153 (GRCm39) |
P181T |
probably damaging |
Het |
Prmt3 |
A |
T |
7: 49,430,104 (GRCm39) |
H69L |
probably damaging |
Het |
Rc3h2 |
A |
T |
2: 37,289,628 (GRCm39) |
Y395N |
possibly damaging |
Het |
Rubcnl |
A |
T |
14: 75,269,717 (GRCm39) |
N125I |
possibly damaging |
Het |
Shprh |
T |
C |
10: 11,030,446 (GRCm39) |
F221S |
probably benign |
Het |
Skint5 |
A |
T |
4: 113,403,684 (GRCm39) |
S1179R |
unknown |
Het |
Skint6 |
C |
A |
4: 113,095,347 (GRCm39) |
G104V |
probably damaging |
Het |
Slc44a3 |
T |
C |
3: 121,320,839 (GRCm39) |
Y54C |
probably damaging |
Het |
Sp140 |
TTTTTTTTTTTTT |
TTTTTTTTTTTTTTTTTT |
1: 85,572,290 (GRCm39) |
|
probably benign |
Het |
Spag5 |
A |
T |
11: 78,212,575 (GRCm39) |
I1137F |
probably benign |
Het |
Tchp |
A |
T |
5: 114,853,916 (GRCm39) |
Y277F |
probably benign |
Het |
Tdrd12 |
A |
C |
7: 35,204,468 (GRCm39) |
L267W |
probably damaging |
Het |
Tfcp2 |
A |
T |
15: 100,396,092 (GRCm39) |
I107N |
|
Het |
Vmn1r9 |
T |
C |
6: 57,048,513 (GRCm39) |
V196A |
probably benign |
Het |
Vmn2r62 |
T |
A |
7: 42,413,920 (GRCm39) |
D841V |
|
Het |
Zzef1 |
G |
T |
11: 72,813,302 (GRCm39) |
R2901L |
probably benign |
Het |
|
Other mutations in Erbb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Erbb4
|
APN |
1 |
68,110,789 (GRCm39) |
nonsense |
probably null |
|
IGL01020:Erbb4
|
APN |
1 |
68,337,608 (GRCm39) |
splice site |
probably benign |
|
IGL01349:Erbb4
|
APN |
1 |
68,385,752 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01386:Erbb4
|
APN |
1 |
68,383,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Erbb4
|
APN |
1 |
68,367,404 (GRCm39) |
nonsense |
probably null |
|
IGL01536:Erbb4
|
APN |
1 |
68,329,441 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01721:Erbb4
|
APN |
1 |
68,293,722 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01832:Erbb4
|
APN |
1 |
68,293,725 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02002:Erbb4
|
APN |
1 |
68,119,885 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02040:Erbb4
|
APN |
1 |
68,081,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02371:Erbb4
|
APN |
1 |
68,329,453 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02399:Erbb4
|
APN |
1 |
68,081,596 (GRCm39) |
splice site |
probably benign |
|
IGL02553:Erbb4
|
APN |
1 |
68,345,023 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03118:Erbb4
|
APN |
1 |
68,081,878 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03329:Erbb4
|
APN |
1 |
68,367,281 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03405:Erbb4
|
APN |
1 |
68,369,397 (GRCm39) |
missense |
probably benign |
0.02 |
earthworm
|
UTSW |
1 |
68,289,739 (GRCm39) |
missense |
possibly damaging |
0.67 |
excrescence
|
UTSW |
1 |
68,369,405 (GRCm39) |
missense |
probably damaging |
1.00 |
Mole
|
UTSW |
1 |
68,599,735 (GRCm39) |
missense |
probably damaging |
1.00 |
P0018:Erbb4
|
UTSW |
1 |
68,110,835 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4480001:Erbb4
|
UTSW |
1 |
68,114,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Erbb4
|
UTSW |
1 |
68,083,119 (GRCm39) |
intron |
probably benign |
|
R0329:Erbb4
|
UTSW |
1 |
68,337,439 (GRCm39) |
splice site |
probably benign |
|
R0335:Erbb4
|
UTSW |
1 |
68,298,418 (GRCm39) |
missense |
probably benign |
|
R0362:Erbb4
|
UTSW |
1 |
68,369,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R0579:Erbb4
|
UTSW |
1 |
68,081,621 (GRCm39) |
missense |
probably benign |
0.17 |
R0730:Erbb4
|
UTSW |
1 |
68,298,449 (GRCm39) |
missense |
probably damaging |
0.98 |
R1029:Erbb4
|
UTSW |
1 |
68,348,773 (GRCm39) |
missense |
probably damaging |
0.96 |
R1444:Erbb4
|
UTSW |
1 |
68,293,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Erbb4
|
UTSW |
1 |
68,599,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1469:Erbb4
|
UTSW |
1 |
68,599,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1503:Erbb4
|
UTSW |
1 |
68,385,705 (GRCm39) |
missense |
probably benign |
0.00 |
R1523:Erbb4
|
UTSW |
1 |
68,435,411 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1528:Erbb4
|
UTSW |
1 |
68,117,741 (GRCm39) |
nonsense |
probably null |
|
R1604:Erbb4
|
UTSW |
1 |
68,385,728 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1611:Erbb4
|
UTSW |
1 |
68,079,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Erbb4
|
UTSW |
1 |
68,370,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Erbb4
|
UTSW |
1 |
68,114,569 (GRCm39) |
splice site |
probably benign |
|
R1929:Erbb4
|
UTSW |
1 |
68,238,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R2046:Erbb4
|
UTSW |
1 |
68,337,482 (GRCm39) |
missense |
probably benign |
0.02 |
R2139:Erbb4
|
UTSW |
1 |
68,385,788 (GRCm39) |
missense |
probably damaging |
0.96 |
R2271:Erbb4
|
UTSW |
1 |
68,238,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R2298:Erbb4
|
UTSW |
1 |
68,081,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Erbb4
|
UTSW |
1 |
68,117,755 (GRCm39) |
missense |
probably benign |
0.00 |
R3821:Erbb4
|
UTSW |
1 |
68,345,072 (GRCm39) |
missense |
probably damaging |
0.97 |
R4007:Erbb4
|
UTSW |
1 |
68,779,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4012:Erbb4
|
UTSW |
1 |
68,599,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Erbb4
|
UTSW |
1 |
68,079,496 (GRCm39) |
missense |
probably benign |
0.07 |
R4196:Erbb4
|
UTSW |
1 |
68,383,014 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4536:Erbb4
|
UTSW |
1 |
68,385,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4561:Erbb4
|
UTSW |
1 |
68,383,080 (GRCm39) |
nonsense |
probably null |
|
R4642:Erbb4
|
UTSW |
1 |
68,289,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4737:Erbb4
|
UTSW |
1 |
68,383,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R4739:Erbb4
|
UTSW |
1 |
68,383,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R4780:Erbb4
|
UTSW |
1 |
68,337,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Erbb4
|
UTSW |
1 |
68,369,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Erbb4
|
UTSW |
1 |
68,369,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Erbb4
|
UTSW |
1 |
68,293,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Erbb4
|
UTSW |
1 |
68,369,397 (GRCm39) |
missense |
probably benign |
0.02 |
R5068:Erbb4
|
UTSW |
1 |
68,083,061 (GRCm39) |
splice site |
probably null |
|
R5546:Erbb4
|
UTSW |
1 |
68,337,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R5755:Erbb4
|
UTSW |
1 |
68,599,678 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6189:Erbb4
|
UTSW |
1 |
68,083,075 (GRCm39) |
missense |
probably benign |
|
R6257:Erbb4
|
UTSW |
1 |
68,435,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Erbb4
|
UTSW |
1 |
68,599,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6521:Erbb4
|
UTSW |
1 |
68,081,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6602:Erbb4
|
UTSW |
1 |
68,409,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R6808:Erbb4
|
UTSW |
1 |
68,079,462 (GRCm39) |
missense |
probably benign |
0.00 |
R7087:Erbb4
|
UTSW |
1 |
68,779,650 (GRCm39) |
missense |
probably null |
1.00 |
R7215:Erbb4
|
UTSW |
1 |
68,378,619 (GRCm39) |
missense |
probably benign |
|
R7356:Erbb4
|
UTSW |
1 |
68,378,514 (GRCm39) |
critical splice donor site |
probably null |
|
R7509:Erbb4
|
UTSW |
1 |
68,289,739 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7593:Erbb4
|
UTSW |
1 |
68,293,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R7743:Erbb4
|
UTSW |
1 |
68,367,278 (GRCm39) |
missense |
probably benign |
0.00 |
R7784:Erbb4
|
UTSW |
1 |
68,114,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Erbb4
|
UTSW |
1 |
68,081,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R7923:Erbb4
|
UTSW |
1 |
68,298,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Erbb4
|
UTSW |
1 |
68,435,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R8288:Erbb4
|
UTSW |
1 |
68,337,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Erbb4
|
UTSW |
1 |
68,110,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R8456:Erbb4
|
UTSW |
1 |
68,110,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Erbb4
|
UTSW |
1 |
68,348,785 (GRCm39) |
missense |
probably benign |
|
R8783:Erbb4
|
UTSW |
1 |
68,079,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8830:Erbb4
|
UTSW |
1 |
68,114,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Erbb4
|
UTSW |
1 |
68,382,997 (GRCm39) |
critical splice donor site |
probably null |
|
R9142:Erbb4
|
UTSW |
1 |
68,388,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R9237:Erbb4
|
UTSW |
1 |
68,081,601 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9350:Erbb4
|
UTSW |
1 |
68,329,638 (GRCm39) |
missense |
probably benign |
0.00 |
R9374:Erbb4
|
UTSW |
1 |
68,779,642 (GRCm39) |
nonsense |
probably null |
|
R9434:Erbb4
|
UTSW |
1 |
68,081,773 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9499:Erbb4
|
UTSW |
1 |
68,779,642 (GRCm39) |
nonsense |
probably null |
|
R9551:Erbb4
|
UTSW |
1 |
68,779,642 (GRCm39) |
nonsense |
probably null |
|
R9753:Erbb4
|
UTSW |
1 |
68,238,062 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Erbb4
|
UTSW |
1 |
68,112,304 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Erbb4
|
UTSW |
1 |
68,367,418 (GRCm39) |
nonsense |
probably null |
|
Z1176:Erbb4
|
UTSW |
1 |
68,337,561 (GRCm39) |
frame shift |
probably null |
|
Z1177:Erbb4
|
UTSW |
1 |
68,348,802 (GRCm39) |
missense |
probably benign |
0.06 |
Z1177:Erbb4
|
UTSW |
1 |
68,329,635 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Erbb4
|
UTSW |
1 |
68,298,342 (GRCm39) |
frame shift |
probably null |
|
|