Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
G |
A |
5: 138,562,447 (GRCm39) |
T98M |
probably damaging |
Het |
4932414N04Rik |
G |
T |
2: 68,541,392 (GRCm39) |
K10N |
possibly damaging |
Het |
Aadat |
T |
A |
8: 60,960,173 (GRCm39) |
S40T |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,278,098 (GRCm39) |
I3093V |
probably benign |
Het |
Acacb |
A |
T |
5: 114,383,951 (GRCm39) |
Q2160L |
probably damaging |
Het |
Acp6 |
G |
T |
3: 97,075,333 (GRCm39) |
S189I |
probably benign |
Het |
Actr5 |
A |
T |
2: 158,474,213 (GRCm39) |
M339L |
probably benign |
Het |
Adcy1 |
A |
T |
11: 7,111,885 (GRCm39) |
K917* |
probably null |
Het |
Adgrg5 |
C |
T |
8: 95,668,695 (GRCm39) |
R504C |
probably benign |
Het |
Ago1 |
T |
C |
4: 126,354,246 (GRCm39) |
H188R |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,025,685 (GRCm39) |
C23* |
probably null |
Het |
Ank3 |
T |
C |
10: 69,733,920 (GRCm39) |
I728T |
probably damaging |
Het |
Ankrd50 |
A |
G |
3: 38,508,642 (GRCm39) |
S1242P |
probably benign |
Het |
Arhgap29 |
G |
A |
3: 121,775,509 (GRCm39) |
R84H |
probably benign |
Het |
Arhgef10 |
A |
G |
8: 14,995,320 (GRCm39) |
D7G |
probably null |
Het |
Arid4b |
A |
G |
13: 14,362,230 (GRCm39) |
E898G |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,680,281 (GRCm39) |
N727S |
probably benign |
Het |
Baalc |
G |
T |
15: 38,796,629 (GRCm39) |
|
probably benign |
Het |
Cdc25c |
G |
C |
18: 34,871,292 (GRCm39) |
L275V |
probably damaging |
Het |
Chpf2 |
G |
T |
5: 24,796,274 (GRCm39) |
V407L |
probably benign |
Het |
Chrnb3 |
C |
A |
8: 27,876,839 (GRCm39) |
N84K |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,451,221 (GRCm39) |
F2171L |
possibly damaging |
Het |
Csmd3 |
C |
T |
15: 48,485,389 (GRCm39) |
|
probably null |
Het |
Cux1 |
T |
A |
5: 136,361,512 (GRCm39) |
Q138L |
probably damaging |
Het |
Cyp2c65 |
A |
G |
19: 39,070,675 (GRCm39) |
N286S |
probably benign |
Het |
Dclre1b |
T |
C |
3: 103,716,356 (GRCm39) |
S17G |
possibly damaging |
Het |
Dlgap5 |
A |
G |
14: 47,648,941 (GRCm39) |
S221P |
probably benign |
Het |
Dnah1 |
T |
G |
14: 31,001,080 (GRCm39) |
T2422P |
probably damaging |
Het |
Enpp1 |
A |
G |
10: 24,587,702 (GRCm39) |
|
probably null |
Het |
Exoc8 |
A |
G |
8: 125,622,219 (GRCm39) |
V716A |
probably benign |
Het |
Fam193a |
T |
A |
5: 34,619,494 (GRCm39) |
D766E |
probably benign |
Het |
Fbxo43 |
C |
A |
15: 36,162,278 (GRCm39) |
G310W |
probably damaging |
Het |
Fcgbp |
C |
T |
7: 27,819,785 (GRCm39) |
T2504I |
probably damaging |
Het |
Fnbp4 |
C |
T |
2: 90,587,876 (GRCm39) |
P418L |
probably benign |
Het |
Gjd2 |
T |
C |
2: 113,841,539 (GRCm39) |
T313A |
probably damaging |
Het |
Gm12695 |
T |
A |
4: 96,658,008 (GRCm39) |
R54W |
probably damaging |
Het |
Gm128 |
T |
C |
3: 95,148,051 (GRCm39) |
D81G |
possibly damaging |
Het |
Gm21834 |
A |
G |
17: 58,048,763 (GRCm39) |
V151A |
possibly damaging |
Het |
Grhl1 |
T |
A |
12: 24,636,151 (GRCm39) |
|
probably null |
Het |
Hcn1 |
C |
T |
13: 118,112,619 (GRCm39) |
T861I |
probably damaging |
Het |
Herc6 |
C |
A |
6: 57,602,961 (GRCm39) |
Q547K |
probably benign |
Het |
Iqgap3 |
T |
C |
3: 88,027,474 (GRCm39) |
L699P |
probably damaging |
Het |
Kank4 |
T |
C |
4: 98,668,339 (GRCm39) |
D36G |
probably damaging |
Het |
Kcnk5 |
A |
T |
14: 20,192,277 (GRCm39) |
S295T |
probably damaging |
Het |
Krt18 |
T |
C |
15: 101,937,935 (GRCm39) |
V144A |
probably benign |
Het |
Krtap9-5 |
A |
G |
11: 99,840,030 (GRCm39) |
I244V |
unknown |
Het |
Leng1 |
T |
G |
7: 3,668,400 (GRCm39) |
N16T |
probably damaging |
Het |
Lss |
A |
G |
10: 76,367,712 (GRCm39) |
K15E |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,022,836 (GRCm39) |
A629E |
possibly damaging |
Het |
Mavs |
G |
C |
2: 131,082,370 (GRCm39) |
A85P |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,660,536 (GRCm39) |
D678G |
probably damaging |
Het |
Nsd3 |
T |
G |
8: 26,181,116 (GRCm39) |
S906A |
probably damaging |
Het |
Nsfl1c |
A |
G |
2: 151,345,002 (GRCm39) |
N118S |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,207,451 (GRCm39) |
M1501K |
probably benign |
Het |
Or4p7 |
C |
T |
2: 88,221,882 (GRCm39) |
T97M |
possibly damaging |
Het |
Or6n1 |
T |
A |
1: 173,916,785 (GRCm39) |
Y60N |
possibly damaging |
Het |
Pax8 |
A |
G |
2: 24,326,520 (GRCm39) |
S281P |
probably benign |
Het |
Pds5b |
T |
G |
5: 150,671,655 (GRCm39) |
I433R |
probably damaging |
Het |
Peg3 |
T |
C |
7: 6,715,720 (GRCm39) |
N117D |
probably damaging |
Het |
Pfkm |
A |
T |
15: 98,029,573 (GRCm39) |
D728V |
probably benign |
Het |
Phkb |
T |
C |
8: 86,776,450 (GRCm39) |
|
probably null |
Het |
Pkp4 |
T |
C |
2: 59,165,248 (GRCm39) |
V704A |
probably benign |
Het |
Ppfia2 |
T |
A |
10: 106,673,160 (GRCm39) |
S501T |
probably damaging |
Het |
Ptpru |
T |
C |
4: 131,546,398 (GRCm39) |
E284G |
possibly damaging |
Het |
Ror1 |
C |
T |
4: 100,265,065 (GRCm39) |
R180* |
probably null |
Het |
Ryr3 |
T |
A |
2: 112,586,986 (GRCm39) |
Y2666F |
probably damaging |
Het |
Sec23a |
C |
A |
12: 59,037,754 (GRCm39) |
|
probably null |
Het |
Sertad3 |
C |
T |
7: 27,175,694 (GRCm39) |
Q43* |
probably null |
Het |
Setd2 |
C |
T |
9: 110,379,958 (GRCm39) |
H1258Y |
probably benign |
Het |
Sharpin |
A |
G |
15: 76,232,407 (GRCm39) |
S177P |
probably benign |
Het |
Skap1 |
T |
C |
11: 96,432,289 (GRCm39) |
F86S |
possibly damaging |
Het |
Slc8a2 |
T |
C |
7: 15,874,940 (GRCm39) |
I396T |
probably damaging |
Het |
Slc9a2 |
T |
C |
1: 40,765,597 (GRCm39) |
F329S |
probably damaging |
Het |
Slx4ip |
C |
T |
2: 136,908,125 (GRCm39) |
L161F |
possibly damaging |
Het |
Sox4 |
A |
G |
13: 29,136,764 (GRCm39) |
S81P |
probably damaging |
Het |
Ssc4d |
G |
T |
5: 135,999,118 (GRCm39) |
S28R |
probably benign |
Het |
St8sia2 |
C |
T |
7: 73,592,950 (GRCm39) |
G369S |
possibly damaging |
Het |
Swt1 |
T |
C |
1: 151,248,081 (GRCm39) |
Y836C |
probably damaging |
Het |
Taar7d |
A |
G |
10: 23,903,904 (GRCm39) |
D262G |
probably benign |
Het |
Taar8b |
T |
A |
10: 23,967,212 (GRCm39) |
L327F |
probably benign |
Het |
Tars1 |
A |
T |
15: 11,393,280 (GRCm39) |
L138* |
probably null |
Het |
Tbcd |
A |
T |
11: 121,344,496 (GRCm39) |
D75V |
probably damaging |
Het |
Tesc |
A |
G |
5: 118,184,394 (GRCm39) |
I25V |
probably damaging |
Het |
Tmem132e |
G |
T |
11: 82,331,264 (GRCm39) |
S407I |
probably damaging |
Het |
Tmem50b |
C |
A |
16: 91,377,180 (GRCm39) |
A95S |
possibly damaging |
Het |
Tnr |
T |
C |
1: 159,719,603 (GRCm39) |
I960T |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tpcn1 |
G |
C |
5: 120,681,453 (GRCm39) |
P532A |
probably damaging |
Het |
Tpsb2 |
T |
C |
17: 25,585,539 (GRCm39) |
|
probably benign |
Het |
Triobp |
C |
A |
15: 78,888,740 (GRCm39) |
H1948Q |
probably damaging |
Het |
Tshb |
T |
C |
3: 102,684,857 (GRCm39) |
I116V |
probably benign |
Het |
Ttc13 |
A |
T |
8: 125,398,950 (GRCm39) |
|
probably null |
Het |
Usp34 |
A |
T |
11: 23,414,468 (GRCm39) |
T2804S |
probably damaging |
Het |
Vmn2r18 |
A |
T |
5: 151,486,016 (GRCm39) |
C493S |
possibly damaging |
Het |
Vmn2r2 |
T |
C |
3: 64,024,766 (GRCm39) |
K605R |
possibly damaging |
Het |
Vmn2r37 |
T |
C |
7: 9,220,792 (GRCm39) |
Y357C |
probably damaging |
Het |
Zc3h6 |
T |
G |
2: 128,857,538 (GRCm39) |
S686A |
possibly damaging |
Het |
Zfp608 |
G |
A |
18: 55,121,386 (GRCm39) |
P67L |
probably benign |
Het |
Zyg11a |
T |
C |
4: 108,049,244 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Erbb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00978:Erbb2
|
APN |
11 |
98,326,456 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01460:Erbb2
|
APN |
11 |
98,325,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01483:Erbb2
|
APN |
11 |
98,325,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01514:Erbb2
|
APN |
11 |
98,323,745 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01520:Erbb2
|
APN |
11 |
98,324,835 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03007:Erbb2
|
APN |
11 |
98,319,819 (GRCm39) |
splice site |
probably benign |
|
IGL03367:Erbb2
|
APN |
11 |
98,313,701 (GRCm39) |
splice site |
probably null |
|
Angular
|
UTSW |
11 |
98,313,596 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4544001:Erbb2
|
UTSW |
11 |
98,311,865 (GRCm39) |
missense |
probably benign |
|
R0234:Erbb2
|
UTSW |
11 |
98,327,265 (GRCm39) |
missense |
probably benign |
0.33 |
R0234:Erbb2
|
UTSW |
11 |
98,327,265 (GRCm39) |
missense |
probably benign |
0.33 |
R0388:Erbb2
|
UTSW |
11 |
98,318,177 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0602:Erbb2
|
UTSW |
11 |
98,325,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Erbb2
|
UTSW |
11 |
98,327,001 (GRCm39) |
nonsense |
probably null |
|
R1467:Erbb2
|
UTSW |
11 |
98,327,001 (GRCm39) |
nonsense |
probably null |
|
R1500:Erbb2
|
UTSW |
11 |
98,319,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Erbb2
|
UTSW |
11 |
98,324,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1748:Erbb2
|
UTSW |
11 |
98,326,161 (GRCm39) |
missense |
probably benign |
0.06 |
R1807:Erbb2
|
UTSW |
11 |
98,319,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Erbb2
|
UTSW |
11 |
98,303,563 (GRCm39) |
critical splice donor site |
probably null |
|
R1926:Erbb2
|
UTSW |
11 |
98,315,990 (GRCm39) |
missense |
probably benign |
|
R1998:Erbb2
|
UTSW |
11 |
98,319,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R3147:Erbb2
|
UTSW |
11 |
98,324,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R4022:Erbb2
|
UTSW |
11 |
98,326,123 (GRCm39) |
missense |
probably benign |
0.09 |
R4238:Erbb2
|
UTSW |
11 |
98,318,869 (GRCm39) |
missense |
probably benign |
0.01 |
R4239:Erbb2
|
UTSW |
11 |
98,318,869 (GRCm39) |
missense |
probably benign |
0.01 |
R4240:Erbb2
|
UTSW |
11 |
98,318,869 (GRCm39) |
missense |
probably benign |
0.01 |
R4633:Erbb2
|
UTSW |
11 |
98,323,814 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4725:Erbb2
|
UTSW |
11 |
98,315,970 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5093:Erbb2
|
UTSW |
11 |
98,318,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R5306:Erbb2
|
UTSW |
11 |
98,319,032 (GRCm39) |
missense |
probably benign |
0.44 |
R5375:Erbb2
|
UTSW |
11 |
98,324,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Erbb2
|
UTSW |
11 |
98,313,596 (GRCm39) |
missense |
probably damaging |
0.98 |
R5710:Erbb2
|
UTSW |
11 |
98,317,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R5938:Erbb2
|
UTSW |
11 |
98,326,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R6062:Erbb2
|
UTSW |
11 |
98,324,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6116:Erbb2
|
UTSW |
11 |
98,318,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6514:Erbb2
|
UTSW |
11 |
98,310,972 (GRCm39) |
missense |
probably benign |
0.03 |
R6556:Erbb2
|
UTSW |
11 |
98,326,908 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6570:Erbb2
|
UTSW |
11 |
98,313,873 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6578:Erbb2
|
UTSW |
11 |
98,319,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Erbb2
|
UTSW |
11 |
98,318,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Erbb2
|
UTSW |
11 |
98,326,399 (GRCm39) |
missense |
probably benign |
|
R8274:Erbb2
|
UTSW |
11 |
98,324,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Erbb2
|
UTSW |
11 |
98,319,798 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9142:Erbb2
|
UTSW |
11 |
98,312,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Erbb2
|
UTSW |
11 |
98,326,107 (GRCm39) |
missense |
probably damaging |
0.98 |
R9489:Erbb2
|
UTSW |
11 |
98,311,746 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9599:Erbb2
|
UTSW |
11 |
98,318,216 (GRCm39) |
missense |
probably benign |
0.04 |
R9605:Erbb2
|
UTSW |
11 |
98,311,746 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9652:Erbb2
|
UTSW |
11 |
98,326,812 (GRCm39) |
missense |
probably damaging |
0.96 |
X0028:Erbb2
|
UTSW |
11 |
98,325,127 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Erbb2
|
UTSW |
11 |
98,313,946 (GRCm39) |
nonsense |
probably null |
|
|