Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530021J07Rik |
G |
T |
7: 82,805,086 (GRCm39) |
|
noncoding transcript |
Het |
Aasdh |
T |
A |
5: 77,044,535 (GRCm39) |
K118N |
possibly damaging |
Het |
Abca14 |
A |
T |
7: 119,923,803 (GRCm39) |
N1620I |
possibly damaging |
Het |
Acap1 |
A |
T |
11: 69,776,641 (GRCm39) |
S149T |
possibly damaging |
Het |
Adgre1 |
T |
A |
17: 57,751,064 (GRCm39) |
Y579* |
probably null |
Het |
Aifm3 |
T |
C |
16: 17,318,296 (GRCm39) |
|
probably benign |
Het |
Aldh16a1 |
A |
G |
7: 44,791,385 (GRCm39) |
W107R |
probably damaging |
Het |
Amer2 |
A |
T |
14: 60,616,894 (GRCm39) |
H363L |
possibly damaging |
Het |
Arhgap10 |
A |
G |
8: 78,152,957 (GRCm39) |
|
probably null |
Het |
Arhgef6 |
A |
T |
X: 56,280,238 (GRCm39) |
D742E |
probably damaging |
Het |
Astn2 |
A |
T |
4: 65,647,644 (GRCm39) |
N731K |
probably damaging |
Het |
Atp1a2 |
T |
C |
1: 172,105,954 (GRCm39) |
T904A |
possibly damaging |
Het |
Atr |
C |
T |
9: 95,789,352 (GRCm39) |
R1503W |
probably damaging |
Het |
Cdh3 |
G |
T |
8: 107,263,242 (GRCm39) |
R97L |
probably benign |
Het |
Chst2 |
C |
T |
9: 95,288,059 (GRCm39) |
V96I |
probably benign |
Het |
Cit |
T |
A |
5: 116,123,856 (GRCm39) |
N1464K |
probably benign |
Het |
Col17a1 |
A |
T |
19: 47,658,897 (GRCm39) |
|
probably null |
Het |
Col4a3 |
G |
A |
1: 82,688,698 (GRCm39) |
|
probably benign |
Het |
Copz1 |
T |
A |
15: 103,199,757 (GRCm39) |
S57R |
probably damaging |
Het |
Cpped1 |
A |
T |
16: 11,646,143 (GRCm39) |
F227Y |
probably damaging |
Het |
Cyp2j12 |
A |
T |
4: 95,990,388 (GRCm39) |
|
probably null |
Het |
Dctn1 |
T |
A |
6: 83,166,189 (GRCm39) |
I195N |
possibly damaging |
Het |
Dhrs7b |
A |
G |
11: 60,742,751 (GRCm39) |
I148V |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,918,259 (GRCm39) |
D4096G |
probably damaging |
Het |
Dnajc13 |
T |
C |
9: 104,110,837 (GRCm39) |
N145D |
possibly damaging |
Het |
Ecpas |
A |
G |
4: 58,827,073 (GRCm39) |
V1020A |
probably damaging |
Het |
Entrep2 |
G |
T |
7: 64,409,116 (GRCm39) |
S426* |
probably null |
Het |
Ercc6l2 |
T |
C |
13: 64,042,627 (GRCm39) |
|
probably benign |
Het |
Fads6 |
T |
G |
11: 115,187,387 (GRCm39) |
I103L |
probably benign |
Het |
Fat4 |
T |
G |
3: 39,064,614 (GRCm39) |
Y4857D |
probably damaging |
Het |
Fbxl14 |
T |
A |
6: 119,457,671 (GRCm39) |
L284Q |
probably damaging |
Het |
Fkbp9 |
T |
C |
6: 56,826,655 (GRCm39) |
V85A |
possibly damaging |
Het |
Galnt13 |
T |
A |
2: 54,406,577 (GRCm39) |
V9E |
probably damaging |
Het |
Gm14412 |
A |
T |
2: 177,006,373 (GRCm39) |
S507R |
probably benign |
Het |
Gm15142 |
T |
A |
X: 153,421,415 (GRCm39) |
|
noncoding transcript |
Het |
Gm4787 |
T |
C |
12: 81,425,612 (GRCm39) |
E182G |
probably benign |
Het |
Gm6811 |
C |
A |
17: 21,314,893 (GRCm39) |
|
noncoding transcript |
Het |
Gm9791 |
A |
T |
3: 34,059,218 (GRCm39) |
|
noncoding transcript |
Het |
Hoxb7 |
A |
T |
11: 96,180,336 (GRCm39) |
|
probably null |
Het |
Ift122 |
T |
A |
6: 115,892,819 (GRCm39) |
|
probably benign |
Het |
Krt28 |
C |
T |
11: 99,265,458 (GRCm39) |
V70I |
probably benign |
Het |
Lig1 |
T |
C |
7: 13,032,664 (GRCm39) |
S459P |
probably damaging |
Het |
Lrfn3 |
C |
T |
7: 30,060,048 (GRCm39) |
R59H |
possibly damaging |
Het |
Mavs |
T |
C |
2: 131,088,663 (GRCm39) |
V489A |
probably benign |
Het |
Mcm8 |
C |
T |
2: 132,681,399 (GRCm39) |
P625L |
probably benign |
Het |
Megf10 |
G |
T |
18: 57,373,745 (GRCm39) |
R181L |
probably benign |
Het |
Mgrn1 |
G |
A |
16: 4,745,726 (GRCm39) |
G440D |
probably benign |
Het |
Mllt3 |
T |
C |
4: 87,700,642 (GRCm39) |
|
probably null |
Het |
Muc5ac |
T |
A |
7: 141,371,639 (GRCm39) |
Y2613* |
probably null |
Het |
Myh14 |
C |
T |
7: 44,284,926 (GRCm39) |
G662S |
probably benign |
Het |
Myod1 |
T |
A |
7: 46,026,474 (GRCm39) |
N126K |
probably damaging |
Het |
Nae1 |
A |
T |
8: 105,242,774 (GRCm39) |
H439Q |
possibly damaging |
Het |
Narf |
T |
A |
11: 121,135,765 (GRCm39) |
V136E |
possibly damaging |
Het |
Ncapd3 |
T |
A |
9: 26,983,031 (GRCm39) |
C926* |
probably null |
Het |
Ndufv2 |
C |
A |
17: 66,399,653 (GRCm39) |
|
probably null |
Het |
Neb |
T |
C |
2: 52,102,987 (GRCm39) |
S449G |
possibly damaging |
Het |
Nek10 |
C |
T |
14: 14,930,577 (GRCm38) |
P698L |
probably damaging |
Het |
Nox3 |
T |
A |
17: 3,685,550 (GRCm39) |
E566V |
probably null |
Het |
Oas1a |
C |
T |
5: 121,043,787 (GRCm39) |
R115H |
probably benign |
Het |
Or10ag60 |
C |
A |
2: 87,438,487 (GRCm39) |
L252I |
probably benign |
Het |
Or51b6 |
A |
G |
7: 103,555,879 (GRCm39) |
T78A |
probably damaging |
Het |
Or8k30 |
T |
A |
2: 86,339,469 (GRCm39) |
L222H |
probably damaging |
Het |
Pbld2 |
A |
G |
10: 62,883,778 (GRCm39) |
H142R |
probably damaging |
Het |
Pcdha4 |
C |
T |
18: 37,087,869 (GRCm39) |
T684M |
probably benign |
Het |
Phc3 |
G |
T |
3: 31,005,068 (GRCm39) |
T175N |
probably damaging |
Het |
Pigs |
G |
T |
11: 78,219,828 (GRCm39) |
V68L |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,913,528 (GRCm39) |
D857E |
possibly damaging |
Het |
Pitpnm3 |
G |
A |
11: 71,953,998 (GRCm39) |
P550S |
probably damaging |
Het |
Pla2g15 |
G |
A |
8: 106,889,850 (GRCm39) |
W374* |
probably null |
Het |
Ptpn14 |
G |
A |
1: 189,554,839 (GRCm39) |
C133Y |
probably damaging |
Het |
Ptpn20 |
A |
G |
14: 33,336,446 (GRCm39) |
N95S |
probably benign |
Het |
Ptrh2 |
G |
T |
11: 86,580,862 (GRCm39) |
V160F |
probably damaging |
Het |
Rapgef3 |
T |
C |
15: 97,655,256 (GRCm39) |
D486G |
probably damaging |
Het |
Rev3l |
T |
G |
10: 39,699,981 (GRCm39) |
S1493A |
probably benign |
Het |
Rgs9 |
T |
A |
11: 109,116,570 (GRCm39) |
D411V |
probably benign |
Het |
Rgsl1 |
A |
T |
1: 153,669,514 (GRCm39) |
Y291N |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,671,849 (GRCm39) |
Y1185H |
probably damaging |
Het |
Rpusd3 |
A |
G |
6: 113,393,167 (GRCm39) |
|
probably benign |
Het |
Scnn1a |
T |
C |
6: 125,299,136 (GRCm39) |
I72T |
probably damaging |
Het |
Sdk1 |
A |
T |
5: 141,842,758 (GRCm39) |
|
probably benign |
Het |
Sfmbt2 |
T |
C |
2: 10,450,556 (GRCm39) |
L277P |
probably benign |
Het |
Sgf29 |
A |
G |
7: 126,264,154 (GRCm39) |
E73G |
probably damaging |
Het |
Slc12a6 |
T |
A |
2: 112,183,306 (GRCm39) |
F764L |
probably damaging |
Het |
Slc4a2 |
T |
C |
5: 24,640,340 (GRCm39) |
|
probably null |
Het |
Slc9a3 |
T |
G |
13: 74,305,838 (GRCm39) |
V285G |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,395,772 (GRCm39) |
T608A |
probably benign |
Het |
Slfnl1 |
C |
T |
4: 120,392,882 (GRCm39) |
R325C |
probably damaging |
Het |
Smarcad1 |
T |
A |
6: 65,051,898 (GRCm39) |
F344I |
probably benign |
Het |
Snrnp70 |
A |
T |
7: 45,026,705 (GRCm39) |
|
probably null |
Het |
Sod2 |
C |
T |
17: 13,227,073 (GRCm39) |
T9M |
probably benign |
Het |
Spag5 |
T |
A |
11: 78,205,199 (GRCm39) |
S633T |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,018,622 (GRCm39) |
I531L |
probably benign |
Het |
Stra8 |
A |
G |
6: 34,910,091 (GRCm39) |
E60G |
probably benign |
Het |
Sult2a3 |
T |
A |
7: 13,845,482 (GRCm39) |
I126F |
probably benign |
Het |
Syt1 |
T |
C |
10: 108,340,373 (GRCm39) |
H315R |
possibly damaging |
Het |
Tanc2 |
T |
C |
11: 105,758,588 (GRCm39) |
L783P |
probably damaging |
Het |
Thbs2 |
C |
T |
17: 14,899,162 (GRCm39) |
C646Y |
probably damaging |
Het |
Ticam2 |
T |
A |
18: 46,693,989 (GRCm39) |
K33* |
probably null |
Het |
Trim17 |
T |
C |
11: 58,845,127 (GRCm39) |
|
probably benign |
Het |
Tsr1 |
G |
A |
11: 74,798,705 (GRCm39) |
M691I |
probably benign |
Het |
Ttn |
T |
A |
2: 76,592,763 (GRCm39) |
I20790F |
probably damaging |
Het |
Tubb2b |
A |
T |
13: 34,312,168 (GRCm39) |
Y208* |
probably null |
Het |
Ubr1 |
T |
A |
2: 120,745,419 (GRCm39) |
I890F |
probably damaging |
Het |
Usp54 |
T |
C |
14: 20,612,260 (GRCm39) |
E852G |
probably damaging |
Het |
Vmn2r78 |
T |
C |
7: 86,603,835 (GRCm39) |
V671A |
probably damaging |
Het |
Wipi1 |
T |
C |
11: 109,470,475 (GRCm39) |
K315E |
probably benign |
Het |
Xrn2 |
T |
C |
2: 146,893,638 (GRCm39) |
V735A |
possibly damaging |
Het |
Zdbf2 |
T |
A |
1: 63,347,973 (GRCm39) |
D2117E |
possibly damaging |
Het |
Zfp287 |
A |
T |
11: 62,604,962 (GRCm39) |
C648* |
probably null |
Het |
Zfp369 |
A |
G |
13: 65,444,614 (GRCm39) |
T586A |
possibly damaging |
Het |
|
Other mutations in Or5w19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01418:Or5w19
|
APN |
2 |
87,698,809 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01618:Or5w19
|
APN |
2 |
87,698,488 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02326:Or5w19
|
APN |
2 |
87,699,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03162:Or5w19
|
APN |
2 |
87,698,484 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03189:Or5w19
|
APN |
2 |
87,698,559 (GRCm39) |
missense |
possibly damaging |
0.76 |
I2288:Or5w19
|
UTSW |
2 |
87,698,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Or5w19
|
UTSW |
2 |
87,698,880 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1558:Or5w19
|
UTSW |
2 |
87,698,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Or5w19
|
UTSW |
2 |
87,698,805 (GRCm39) |
missense |
probably benign |
0.01 |
R3810:Or5w19
|
UTSW |
2 |
87,698,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R3812:Or5w19
|
UTSW |
2 |
87,698,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Or5w19
|
UTSW |
2 |
87,698,779 (GRCm39) |
missense |
probably benign |
0.13 |
R5172:Or5w19
|
UTSW |
2 |
87,699,171 (GRCm39) |
missense |
probably benign |
0.20 |
R5174:Or5w19
|
UTSW |
2 |
87,698,755 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6147:Or5w19
|
UTSW |
2 |
87,699,061 (GRCm39) |
missense |
probably benign |
0.03 |
R6195:Or5w19
|
UTSW |
2 |
87,698,904 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6233:Or5w19
|
UTSW |
2 |
87,698,904 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6541:Or5w19
|
UTSW |
2 |
87,698,638 (GRCm39) |
missense |
probably benign |
0.11 |
R7507:Or5w19
|
UTSW |
2 |
87,698,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R8068:Or5w19
|
UTSW |
2 |
87,698,995 (GRCm39) |
missense |
probably benign |
0.20 |
R8407:Or5w19
|
UTSW |
2 |
87,698,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R9110:Or5w19
|
UTSW |
2 |
87,698,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Or5w19
|
UTSW |
2 |
87,698,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R9797:Or5w19
|
UTSW |
2 |
87,698,478 (GRCm39) |
missense |
possibly damaging |
0.63 |
|