Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aff3 |
T |
A |
1: 38,308,810 (GRCm39) |
D375V |
probably damaging |
Het |
Agfg1 |
C |
G |
1: 82,871,243 (GRCm39) |
P492A |
probably benign |
Het |
Asb13 |
T |
C |
13: 3,692,089 (GRCm39) |
V23A |
probably damaging |
Het |
Atxn1l |
A |
T |
8: 110,460,230 (GRCm39) |
C11S |
probably damaging |
Het |
Bbs9 |
T |
G |
9: 22,590,244 (GRCm39) |
S661A |
probably benign |
Het |
Btrc |
T |
C |
19: 45,496,198 (GRCm39) |
V211A |
probably damaging |
Het |
Camk1g |
T |
C |
1: 193,030,794 (GRCm39) |
|
probably null |
Het |
Capn11 |
A |
T |
17: 45,943,801 (GRCm39) |
L578I |
probably benign |
Het |
Cd82 |
A |
T |
2: 93,252,239 (GRCm39) |
I124N |
probably damaging |
Het |
Cdkl4 |
G |
T |
17: 80,858,258 (GRCm39) |
H120Q |
probably benign |
Het |
Cftr |
T |
C |
6: 18,319,728 (GRCm39) |
V1393A |
probably damaging |
Het |
Col14a1 |
A |
T |
15: 55,318,706 (GRCm39) |
R1402* |
probably null |
Het |
Col6a3 |
T |
G |
1: 90,727,747 (GRCm39) |
Y1960S |
probably benign |
Het |
Col9a1 |
A |
T |
1: 24,224,127 (GRCm39) |
Y103F |
unknown |
Het |
Cux1 |
A |
G |
5: 136,311,796 (GRCm39) |
V1180A |
probably damaging |
Het |
Cyp17a1 |
A |
T |
19: 46,658,166 (GRCm39) |
C249S |
probably benign |
Het |
Derl1 |
A |
T |
15: 57,755,568 (GRCm39) |
W42R |
probably benign |
Het |
Dhx36 |
C |
A |
3: 62,386,747 (GRCm39) |
M668I |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,044,428 (GRCm39) |
K3228E |
possibly damaging |
Het |
Dst |
C |
T |
1: 34,267,750 (GRCm39) |
A3050V |
probably benign |
Het |
Efr3b |
A |
G |
12: 4,049,594 (GRCm39) |
Y70H |
probably damaging |
Het |
Epb42 |
T |
A |
2: 120,856,324 (GRCm39) |
T407S |
possibly damaging |
Het |
Fads2b |
T |
A |
2: 85,324,387 (GRCm39) |
|
probably benign |
Het |
Fap |
T |
A |
2: 62,342,777 (GRCm39) |
I608L |
probably benign |
Het |
Fblim1 |
A |
G |
4: 141,310,387 (GRCm39) |
Y292H |
probably benign |
Het |
Fmod |
A |
G |
1: 133,968,043 (GRCm39) |
I28V |
probably benign |
Het |
Gad2 |
T |
A |
2: 22,524,985 (GRCm39) |
Y256* |
probably null |
Het |
Gapdh |
G |
A |
6: 125,139,017 (GRCm39) |
A353V |
probably benign |
Het |
Gm5460 |
T |
G |
14: 33,739,149 (GRCm39) |
W44G |
unknown |
Het |
Ino80e |
A |
T |
7: 126,460,974 (GRCm39) |
V91D |
probably benign |
Het |
Iqgap2 |
G |
A |
13: 95,802,258 (GRCm39) |
P896S |
probably damaging |
Het |
Kif26b |
T |
A |
1: 178,692,430 (GRCm39) |
I457N |
probably damaging |
Het |
Klc2 |
T |
A |
19: 5,168,477 (GRCm39) |
|
probably benign |
Het |
Ldlrap1 |
C |
A |
4: 134,495,147 (GRCm39) |
W22L |
probably benign |
Het |
Matn3 |
A |
G |
12: 9,017,665 (GRCm39) |
D439G |
possibly damaging |
Het |
Met |
T |
C |
6: 17,540,510 (GRCm39) |
L812P |
probably benign |
Het |
Mki67 |
A |
T |
7: 135,315,504 (GRCm39) |
I90N |
probably damaging |
Het |
Mptx2 |
A |
C |
1: 173,105,256 (GRCm39) |
S12A |
probably benign |
Het |
Nbeal2 |
G |
A |
9: 110,456,949 (GRCm39) |
R2350C |
probably damaging |
Het |
Nsmaf |
A |
G |
4: 6,396,748 (GRCm39) |
I913T |
probably benign |
Het |
Nuggc |
G |
T |
14: 65,882,535 (GRCm39) |
C760F |
probably benign |
Het |
Or10a3m |
T |
A |
7: 108,312,964 (GRCm39) |
F135I |
probably damaging |
Het |
Or1j13 |
T |
A |
2: 36,369,629 (GRCm39) |
N171I |
probably benign |
Het |
Or2y1f |
T |
A |
11: 49,184,965 (GRCm39) |
F272L |
probably damaging |
Het |
Or4c110 |
C |
A |
2: 88,832,351 (GRCm39) |
E94* |
probably null |
Het |
Or51b6 |
A |
G |
7: 103,555,913 (GRCm39) |
N86S |
|
Het |
Pdgfrb |
C |
T |
18: 61,214,073 (GRCm39) |
P953S |
probably damaging |
Het |
Pemt |
T |
G |
11: 59,874,285 (GRCm39) |
I102L |
probably benign |
Het |
Pla2g4c |
G |
T |
7: 13,069,154 (GRCm39) |
M109I |
probably benign |
Het |
Pla2g4d |
T |
A |
2: 120,100,466 (GRCm39) |
Y622F |
probably damaging |
Het |
Pmpca |
T |
A |
2: 26,283,531 (GRCm39) |
V400D |
probably damaging |
Het |
Pnpt1 |
G |
C |
11: 29,104,815 (GRCm39) |
|
probably null |
Het |
Pramel29 |
A |
C |
4: 143,935,192 (GRCm39) |
L183R |
probably damaging |
Het |
Prrc1 |
T |
A |
18: 57,496,408 (GRCm39) |
S120T |
possibly damaging |
Het |
Prrx2 |
T |
G |
2: 30,768,578 (GRCm39) |
V135G |
probably damaging |
Het |
Qrfprl |
A |
G |
6: 65,433,260 (GRCm39) |
K360R |
probably benign |
Het |
Recql4 |
T |
C |
15: 76,593,054 (GRCm39) |
N352S |
probably benign |
Het |
Sftpa1 |
T |
C |
14: 40,856,044 (GRCm39) |
S130P |
probably damaging |
Het |
Slc35e2 |
T |
C |
4: 155,695,042 (GRCm39) |
L136P |
probably benign |
Het |
Tarbp2 |
T |
A |
15: 102,430,202 (GRCm39) |
S155T |
probably benign |
Het |
Tenm4 |
C |
T |
7: 96,555,148 (GRCm39) |
P2618S |
probably benign |
Het |
Tmem116 |
A |
T |
5: 121,620,433 (GRCm39) |
Y146F |
|
Het |
Ttc17 |
C |
T |
2: 94,206,374 (GRCm39) |
|
probably null |
Het |
Vmn2r114 |
G |
A |
17: 23,529,142 (GRCm39) |
T320I |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,055,783 (GRCm39) |
V785D |
probably damaging |
Het |
Vmn2r89 |
T |
A |
14: 51,693,722 (GRCm39) |
N357K |
probably damaging |
Het |
Zfp811 |
A |
T |
17: 33,017,197 (GRCm39) |
L281Q |
possibly damaging |
Het |
|
Other mutations in Mrgpra9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Mrgpra9
|
APN |
7 |
46,884,839 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL00575:Mrgpra9
|
APN |
7 |
46,885,053 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01649:Mrgpra9
|
APN |
7 |
46,884,900 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03207:Mrgpra9
|
APN |
7 |
46,885,385 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0388:Mrgpra9
|
UTSW |
7 |
46,902,542 (GRCm39) |
start codon destroyed |
probably null |
0.08 |
R0972:Mrgpra9
|
UTSW |
7 |
46,885,203 (GRCm39) |
missense |
probably damaging |
0.99 |
R1270:Mrgpra9
|
UTSW |
7 |
46,902,531 (GRCm39) |
critical splice donor site |
probably null |
|
R1381:Mrgpra9
|
UTSW |
7 |
46,885,050 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1403:Mrgpra9
|
UTSW |
7 |
46,885,386 (GRCm39) |
missense |
probably benign |
0.24 |
R1403:Mrgpra9
|
UTSW |
7 |
46,885,386 (GRCm39) |
missense |
probably benign |
0.24 |
R1448:Mrgpra9
|
UTSW |
7 |
46,885,561 (GRCm39) |
missense |
probably benign |
0.02 |
R2045:Mrgpra9
|
UTSW |
7 |
46,885,583 (GRCm39) |
missense |
probably benign |
|
R2144:Mrgpra9
|
UTSW |
7 |
46,885,211 (GRCm39) |
missense |
probably benign |
0.31 |
R2187:Mrgpra9
|
UTSW |
7 |
46,884,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R2507:Mrgpra9
|
UTSW |
7 |
46,885,242 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2913:Mrgpra9
|
UTSW |
7 |
46,884,828 (GRCm39) |
missense |
probably benign |
|
R3810:Mrgpra9
|
UTSW |
7 |
46,885,527 (GRCm39) |
missense |
probably damaging |
0.98 |
R4177:Mrgpra9
|
UTSW |
7 |
46,885,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R4521:Mrgpra9
|
UTSW |
7 |
46,884,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R4781:Mrgpra9
|
UTSW |
7 |
46,884,795 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4926:Mrgpra9
|
UTSW |
7 |
46,884,759 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6469:Mrgpra9
|
UTSW |
7 |
46,884,854 (GRCm39) |
missense |
probably benign |
0.02 |
R6505:Mrgpra9
|
UTSW |
7 |
46,884,884 (GRCm39) |
missense |
probably benign |
0.00 |
R6724:Mrgpra9
|
UTSW |
7 |
46,884,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R7398:Mrgpra9
|
UTSW |
7 |
46,885,385 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8824:Mrgpra9
|
UTSW |
7 |
46,885,041 (GRCm39) |
missense |
probably benign |
0.06 |
R8881:Mrgpra9
|
UTSW |
7 |
46,885,242 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9320:Mrgpra9
|
UTSW |
7 |
46,885,392 (GRCm39) |
missense |
probably benign |
0.00 |
|