Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
A |
G |
10: 100,445,038 (GRCm39) |
I208V |
probably benign |
Het |
Abcb11 |
C |
T |
2: 69,130,211 (GRCm39) |
D282N |
probably damaging |
Het |
Aldh1l2 |
T |
A |
10: 83,338,321 (GRCm39) |
I646F |
probably damaging |
Het |
Alms1 |
C |
T |
6: 85,599,205 (GRCm39) |
P1344S |
possibly damaging |
Het |
Ank2 |
T |
A |
3: 126,730,302 (GRCm39) |
I711L |
possibly damaging |
Het |
Ankrd6 |
T |
C |
4: 32,821,298 (GRCm39) |
N251D |
probably damaging |
Het |
Ap3m1 |
T |
C |
14: 21,088,147 (GRCm39) |
T304A |
probably benign |
Het |
Arhgef39 |
T |
C |
4: 43,499,532 (GRCm39) |
T26A |
possibly damaging |
Het |
Carnmt1 |
G |
T |
19: 18,648,201 (GRCm39) |
|
probably benign |
Het |
Ccr4 |
C |
T |
9: 114,320,994 (GRCm39) |
R357H |
probably benign |
Het |
Cd4 |
T |
A |
6: 124,850,004 (GRCm39) |
M104L |
probably benign |
Het |
Cd74 |
A |
T |
18: 60,936,965 (GRCm39) |
|
probably benign |
Het |
Cdcp1 |
T |
C |
9: 123,002,878 (GRCm39) |
Y731C |
probably damaging |
Het |
Cdyl2 |
A |
G |
8: 117,350,790 (GRCm39) |
S114P |
not run |
Het |
Cenpv |
T |
C |
11: 62,427,114 (GRCm39) |
D148G |
probably damaging |
Het |
Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
Cfap57 |
T |
A |
4: 118,450,334 (GRCm39) |
Y596F |
probably benign |
Het |
Clec4a2 |
C |
A |
6: 123,116,079 (GRCm39) |
A122E |
unknown |
Het |
Col4a2 |
A |
G |
8: 11,496,184 (GRCm39) |
T1602A |
probably benign |
Het |
Cracd |
GCGCGAGGCCGAGAGGCAGGAGGAGGAAGCAAGACAACGCGAGGCCGAGAGGCAGG |
GCGCGAGGCCGAGAGGCAGG |
5: 77,004,801 (GRCm39) |
|
probably benign |
Het |
Cyp2j11 |
A |
T |
4: 96,204,677 (GRCm39) |
Y290N |
probably benign |
Het |
Dhx38 |
A |
T |
8: 110,283,155 (GRCm39) |
V554E |
probably damaging |
Het |
Ebf2 |
T |
C |
14: 67,474,975 (GRCm39) |
V70A |
probably damaging |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Fam217a |
A |
T |
13: 35,094,262 (GRCm39) |
I499K |
possibly damaging |
Het |
Fras1 |
C |
A |
5: 96,860,309 (GRCm39) |
Y2118* |
probably null |
Het |
Gm3248 |
A |
T |
14: 5,945,781 (GRCm38) |
|
probably null |
Het |
Gm5460 |
T |
G |
14: 33,765,879 (GRCm39) |
D165E |
possibly damaging |
Het |
Grk4 |
A |
T |
5: 34,908,962 (GRCm39) |
N490Y |
probably benign |
Het |
Iglc2 |
T |
A |
16: 19,013,886 (GRCm39) |
K59* |
probably null |
Het |
Iqsec3 |
T |
A |
6: 121,363,569 (GRCm39) |
H895L |
possibly damaging |
Het |
Itgb7 |
A |
G |
15: 102,127,689 (GRCm39) |
S410P |
probably damaging |
Het |
Kmt2d |
C |
A |
15: 98,754,265 (GRCm39) |
V1613F |
unknown |
Het |
Lama1 |
T |
C |
17: 68,024,256 (GRCm39) |
L118P |
|
Het |
Lrrc25 |
A |
T |
8: 71,070,830 (GRCm39) |
S204C |
possibly damaging |
Het |
Malrd1 |
A |
G |
2: 15,700,010 (GRCm39) |
D619G |
unknown |
Het |
Ms4a6d |
G |
A |
19: 11,567,437 (GRCm39) |
Q155* |
probably null |
Het |
Mup17 |
G |
A |
4: 61,512,635 (GRCm39) |
S86F |
probably benign |
Het |
Nbeal2 |
C |
T |
9: 110,459,257 (GRCm39) |
|
probably null |
Het |
Nfkb1 |
A |
C |
3: 135,319,458 (GRCm39) |
V291G |
possibly damaging |
Het |
Nomo1 |
G |
T |
7: 45,715,903 (GRCm39) |
V757F |
probably benign |
Het |
Nutm2 |
T |
A |
13: 50,624,043 (GRCm39) |
S247T |
probably damaging |
Het |
Or2at1 |
C |
A |
7: 99,416,553 (GRCm39) |
H61Q |
probably damaging |
Het |
Or4c120 |
C |
T |
2: 89,000,705 (GRCm39) |
V284I |
probably benign |
Het |
Or4f4-ps1 |
G |
T |
2: 111,330,241 (GRCm39) |
A215S |
probably damaging |
Het |
Or7g12 |
T |
A |
9: 18,900,006 (GRCm39) |
C241S |
probably damaging |
Het |
Or9k2b |
T |
A |
10: 130,016,123 (GRCm39) |
I209F |
probably damaging |
Het |
Pcdhb14 |
A |
G |
18: 37,581,961 (GRCm39) |
I356V |
probably benign |
Het |
Pnkp |
T |
A |
7: 44,508,102 (GRCm39) |
S142T |
probably damaging |
Het |
Ppia |
T |
C |
11: 6,369,218 (GRCm39) |
S99P |
possibly damaging |
Het |
Prss47 |
C |
T |
13: 65,192,807 (GRCm39) |
V325I |
probably benign |
Het |
Ptgr3 |
C |
T |
18: 84,106,315 (GRCm39) |
A9V |
probably benign |
Het |
Ptk7 |
T |
C |
17: 46,902,683 (GRCm39) |
D34G |
probably damaging |
Het |
Pwp2 |
C |
T |
10: 78,018,314 (GRCm39) |
G126R |
probably damaging |
Het |
Rasa3 |
G |
T |
8: 13,645,353 (GRCm39) |
D195E |
probably benign |
Het |
Sh2d1b2 |
T |
C |
1: 170,075,716 (GRCm39) |
V50A |
probably damaging |
Het |
Slc30a4 |
C |
T |
2: 122,527,224 (GRCm39) |
V390I |
possibly damaging |
Het |
Slc30a9 |
G |
T |
5: 67,510,109 (GRCm39) |
|
probably null |
Het |
Slc8a3 |
T |
A |
12: 81,260,832 (GRCm39) |
|
probably null |
Het |
Smpd3 |
G |
A |
8: 106,991,642 (GRCm39) |
R304W |
probably damaging |
Het |
Snta1 |
A |
G |
2: 154,218,780 (GRCm39) |
S490P |
probably damaging |
Het |
Srcap |
T |
G |
7: 127,134,000 (GRCm39) |
M887R |
probably damaging |
Het |
St3gal1 |
A |
G |
15: 66,983,195 (GRCm39) |
V187A |
possibly damaging |
Het |
Sult2a3 |
T |
C |
7: 13,845,449 (GRCm39) |
T137A |
probably benign |
Het |
Tspoap1 |
C |
T |
11: 87,656,945 (GRCm39) |
Q367* |
probably null |
Het |
Uroc1 |
C |
T |
6: 90,322,315 (GRCm39) |
R280C |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,643,613 (GRCm39) |
I4325T |
possibly damaging |
Het |
Vmn1r32 |
A |
G |
6: 66,530,173 (GRCm39) |
I201T |
probably benign |
Het |
Zbtb47 |
T |
A |
9: 121,596,411 (GRCm39) |
M626K |
probably damaging |
Het |
|
Other mutations in Rnf150 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02183:Rnf150
|
APN |
8 |
83,730,234 (GRCm39) |
missense |
probably damaging |
0.96 |
R0512:Rnf150
|
UTSW |
8 |
83,590,807 (GRCm39) |
missense |
probably benign |
0.01 |
R1848:Rnf150
|
UTSW |
8 |
83,590,639 (GRCm39) |
start codon destroyed |
possibly damaging |
0.67 |
R2078:Rnf150
|
UTSW |
8 |
83,730,234 (GRCm39) |
missense |
probably damaging |
0.96 |
R2192:Rnf150
|
UTSW |
8 |
83,591,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R3918:Rnf150
|
UTSW |
8 |
83,591,090 (GRCm39) |
missense |
probably benign |
0.25 |
R4365:Rnf150
|
UTSW |
8 |
83,590,744 (GRCm39) |
missense |
probably benign |
0.05 |
R4781:Rnf150
|
UTSW |
8 |
83,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Rnf150
|
UTSW |
8 |
83,716,991 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4859:Rnf150
|
UTSW |
8 |
83,590,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Rnf150
|
UTSW |
8 |
83,730,228 (GRCm39) |
nonsense |
probably null |
|
R6022:Rnf150
|
UTSW |
8 |
83,769,358 (GRCm39) |
missense |
probably benign |
0.00 |
R6241:Rnf150
|
UTSW |
8 |
83,591,093 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6283:Rnf150
|
UTSW |
8 |
83,717,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Rnf150
|
UTSW |
8 |
83,810,131 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7014:Rnf150
|
UTSW |
8 |
83,769,292 (GRCm39) |
missense |
probably benign |
|
R7023:Rnf150
|
UTSW |
8 |
83,590,706 (GRCm39) |
missense |
probably damaging |
0.97 |
R7710:Rnf150
|
UTSW |
8 |
83,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Rnf150
|
UTSW |
8 |
83,590,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8073:Rnf150
|
UTSW |
8 |
83,590,546 (GRCm39) |
start gained |
probably benign |
|
R8856:Rnf150
|
UTSW |
8 |
83,762,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R8980:Rnf150
|
UTSW |
8 |
83,717,087 (GRCm39) |
missense |
probably benign |
0.19 |
R9139:Rnf150
|
UTSW |
8 |
83,590,588 (GRCm39) |
start gained |
probably benign |
|
R9289:Rnf150
|
UTSW |
8 |
83,716,982 (GRCm39) |
missense |
probably benign |
|
R9410:Rnf150
|
UTSW |
8 |
83,762,722 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9594:Rnf150
|
UTSW |
8 |
83,717,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9603:Rnf150
|
UTSW |
8 |
83,717,208 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9763:Rnf150
|
UTSW |
8 |
83,732,968 (GRCm39) |
missense |
probably benign |
|
|