Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anxa10 |
T |
A |
8: 62,545,543 (GRCm39) |
Y63F |
probably benign |
Het |
Atl2 |
T |
C |
17: 80,183,227 (GRCm39) |
|
probably null |
Het |
B3gnt4 |
A |
G |
5: 123,648,794 (GRCm39) |
N53S |
probably damaging |
Het |
Bpifb5 |
G |
A |
2: 154,067,042 (GRCm39) |
M98I |
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 28,786,232 (GRCm39) |
M585T |
probably damaging |
Het |
Cbarp |
T |
C |
10: 79,967,138 (GRCm39) |
D701G |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,244,794 (GRCm39) |
S1221P |
possibly damaging |
Het |
Cep350 |
T |
C |
1: 155,770,365 (GRCm39) |
S1842G |
probably benign |
Het |
Cntrl |
T |
A |
2: 35,060,546 (GRCm39) |
W1913R |
probably benign |
Het |
Creb5 |
C |
A |
6: 53,658,143 (GRCm39) |
Q158K |
unknown |
Het |
Crtam |
G |
C |
9: 40,892,478 (GRCm39) |
A266G |
probably benign |
Het |
Cry2 |
T |
C |
2: 92,243,392 (GRCm39) |
D483G |
possibly damaging |
Het |
Csmd1 |
A |
G |
8: 16,073,864 (GRCm39) |
F2044L |
possibly damaging |
Het |
Cxcr6 |
A |
T |
9: 123,639,305 (GRCm39) |
Y109F |
probably benign |
Het |
Cyb5b |
A |
G |
8: 107,897,048 (GRCm39) |
D106G |
probably benign |
Het |
D630036H23Rik |
T |
C |
12: 36,431,537 (GRCm39) |
R154G |
unknown |
Het |
Ddit4l |
A |
G |
3: 137,331,931 (GRCm39) |
E99G |
probably damaging |
Het |
Dmbt1 |
A |
T |
7: 130,710,192 (GRCm39) |
T1495S |
possibly damaging |
Het |
Gm21886 |
A |
T |
18: 80,132,867 (GRCm39) |
L97Q |
probably damaging |
Het |
Hlcs |
A |
G |
16: 94,068,758 (GRCm39) |
V154A |
probably benign |
Het |
Hpdl |
A |
T |
4: 116,678,062 (GRCm39) |
L133Q |
probably damaging |
Het |
Inpp5f |
A |
G |
7: 128,281,529 (GRCm39) |
D510G |
probably damaging |
Het |
Ism2 |
G |
T |
12: 87,333,769 (GRCm39) |
T92K |
possibly damaging |
Het |
Kif13b |
T |
C |
14: 65,025,909 (GRCm39) |
I1422T |
probably benign |
Het |
Leng8 |
C |
T |
7: 4,146,572 (GRCm39) |
R395W |
probably damaging |
Het |
Mocs2 |
A |
G |
13: 114,957,400 (GRCm39) |
I6V |
probably benign |
Het |
Mthfr |
A |
G |
4: 148,136,060 (GRCm39) |
M378V |
probably benign |
Het |
Myh13 |
A |
G |
11: 67,223,390 (GRCm39) |
T237A |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,204,494 (GRCm39) |
I1460N |
probably damaging |
Het |
Nup98 |
A |
T |
7: 101,784,208 (GRCm39) |
|
probably null |
Het |
Nxpe5 |
A |
C |
5: 138,238,022 (GRCm39) |
Y194S |
probably damaging |
Het |
Or12e9 |
G |
T |
2: 87,202,034 (GRCm39) |
V53L |
probably benign |
Het |
Or52m1 |
A |
G |
7: 102,289,533 (GRCm39) |
I27V |
probably benign |
Het |
Or5m12 |
T |
A |
2: 85,734,475 (GRCm39) |
R308* |
probably null |
Het |
Or5m3 |
A |
T |
2: 85,838,563 (GRCm39) |
I148L |
probably benign |
Het |
Or9s18 |
A |
G |
13: 65,300,866 (GRCm39) |
Y276C |
probably damaging |
Het |
Otof |
G |
T |
5: 30,547,169 (GRCm39) |
D383E |
probably damaging |
Het |
Pcdh9 |
G |
T |
14: 94,124,547 (GRCm39) |
T541K |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,800,531 (GRCm39) |
I1179F |
|
Het |
Pde6c |
T |
C |
19: 38,145,984 (GRCm39) |
|
probably null |
Het |
Pdia6 |
T |
C |
12: 17,328,546 (GRCm39) |
V167A |
probably damaging |
Het |
Phf7 |
C |
T |
14: 30,962,370 (GRCm39) |
R145Q |
possibly damaging |
Het |
Plxnb1 |
T |
C |
9: 108,937,236 (GRCm39) |
V1139A |
probably benign |
Het |
Prkg1 |
T |
C |
19: 30,556,235 (GRCm39) |
I585M |
probably damaging |
Het |
Prom2 |
A |
G |
2: 127,381,731 (GRCm39) |
L195P |
probably damaging |
Het |
Ptprd |
G |
A |
4: 76,004,705 (GRCm39) |
P17S |
probably benign |
Het |
Rfx4 |
C |
A |
10: 84,731,876 (GRCm39) |
Q618K |
probably benign |
Het |
Rhobtb1 |
T |
A |
10: 69,084,654 (GRCm39) |
I15N |
probably damaging |
Het |
Sap30 |
C |
T |
8: 57,940,546 (GRCm39) |
V19M |
possibly damaging |
Het |
Scrib |
G |
A |
15: 75,933,047 (GRCm39) |
T721M |
probably damaging |
Het |
Slc12a1 |
C |
A |
2: 125,056,052 (GRCm39) |
T861N |
probably benign |
Het |
Slc35f1 |
T |
A |
10: 52,965,510 (GRCm39) |
S308R |
probably damaging |
Het |
Slc35f4 |
T |
A |
14: 49,536,355 (GRCm39) |
I427F |
probably damaging |
Het |
Slco4c1 |
T |
C |
1: 96,765,245 (GRCm39) |
T402A |
possibly damaging |
Het |
Sprr2f |
G |
A |
3: 92,273,251 (GRCm39) |
V17M |
unknown |
Het |
Stab1 |
T |
C |
14: 30,881,216 (GRCm39) |
T605A |
probably benign |
Het |
Taar8c |
A |
C |
10: 23,977,446 (GRCm39) |
L122R |
probably damaging |
Het |
Tbc1d2 |
G |
A |
4: 46,649,965 (GRCm39) |
P24S |
probably benign |
Het |
Tex36 |
T |
C |
7: 133,196,866 (GRCm39) |
|
probably null |
Het |
Tmem145 |
T |
C |
7: 25,006,590 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
G |
2: 76,550,698 (GRCm39) |
D31528A |
probably damaging |
Het |
Vars2 |
A |
T |
17: 35,977,578 (GRCm39) |
V118E |
probably benign |
Het |
Vmn1r195 |
T |
C |
13: 22,463,022 (GRCm39) |
V164A |
probably benign |
Het |
Vmn2r69 |
T |
C |
7: 85,060,467 (GRCm39) |
I372M |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
Wnt9b |
T |
C |
11: 103,621,643 (GRCm39) |
Q338R |
probably benign |
Het |
Zfp128 |
A |
G |
7: 12,624,289 (GRCm39) |
D219G |
probably benign |
Het |
Zfp541 |
A |
T |
7: 15,826,793 (GRCm39) |
R1181W |
probably damaging |
Het |
Zfp867 |
C |
T |
11: 59,354,760 (GRCm39) |
G190S |
probably benign |
Het |
Zfp971 |
T |
A |
2: 177,674,967 (GRCm39) |
C189S |
probably damaging |
Het |
|
Other mutations in Nr1h4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01701:Nr1h4
|
APN |
10 |
89,314,669 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02628:Nr1h4
|
APN |
10 |
89,309,701 (GRCm39) |
missense |
probably damaging |
1.00 |
Aeronaut
|
UTSW |
10 |
89,334,091 (GRCm39) |
nonsense |
probably null |
|
I1329:Nr1h4
|
UTSW |
10 |
89,319,224 (GRCm39) |
splice site |
probably benign |
|
IGL02837:Nr1h4
|
UTSW |
10 |
89,352,342 (GRCm39) |
missense |
probably benign |
0.00 |
R0590:Nr1h4
|
UTSW |
10 |
89,292,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R0645:Nr1h4
|
UTSW |
10 |
89,342,390 (GRCm39) |
missense |
probably benign |
0.08 |
R1887:Nr1h4
|
UTSW |
10 |
89,290,729 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1905:Nr1h4
|
UTSW |
10 |
89,316,421 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2471:Nr1h4
|
UTSW |
10 |
89,309,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R2921:Nr1h4
|
UTSW |
10 |
89,334,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Nr1h4
|
UTSW |
10 |
89,314,650 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3277:Nr1h4
|
UTSW |
10 |
89,314,650 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4656:Nr1h4
|
UTSW |
10 |
89,334,115 (GRCm39) |
missense |
probably benign |
0.00 |
R4676:Nr1h4
|
UTSW |
10 |
89,309,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Nr1h4
|
UTSW |
10 |
89,314,659 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4993:Nr1h4
|
UTSW |
10 |
89,334,042 (GRCm39) |
missense |
probably benign |
0.01 |
R5117:Nr1h4
|
UTSW |
10 |
89,314,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R5131:Nr1h4
|
UTSW |
10 |
89,319,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R5176:Nr1h4
|
UTSW |
10 |
89,334,117 (GRCm39) |
missense |
probably benign |
0.02 |
R5241:Nr1h4
|
UTSW |
10 |
89,319,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Nr1h4
|
UTSW |
10 |
89,352,302 (GRCm39) |
missense |
probably benign |
0.16 |
R6114:Nr1h4
|
UTSW |
10 |
89,314,678 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6814:Nr1h4
|
UTSW |
10 |
89,290,607 (GRCm39) |
missense |
probably damaging |
0.98 |
R6888:Nr1h4
|
UTSW |
10 |
89,292,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R6990:Nr1h4
|
UTSW |
10 |
89,290,792 (GRCm39) |
missense |
probably benign |
0.18 |
R7141:Nr1h4
|
UTSW |
10 |
89,334,091 (GRCm39) |
nonsense |
probably null |
|
R7427:Nr1h4
|
UTSW |
10 |
89,334,267 (GRCm39) |
missense |
probably benign |
0.00 |
R7560:Nr1h4
|
UTSW |
10 |
89,334,123 (GRCm39) |
missense |
probably benign |
|
R7986:Nr1h4
|
UTSW |
10 |
89,290,634 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8881:Nr1h4
|
UTSW |
10 |
89,319,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R9365:Nr1h4
|
UTSW |
10 |
89,319,315 (GRCm39) |
missense |
probably damaging |
0.96 |
R9423:Nr1h4
|
UTSW |
10 |
89,309,688 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9659:Nr1h4
|
UTSW |
10 |
89,314,638 (GRCm39) |
critical splice donor site |
probably null |
|
R9776:Nr1h4
|
UTSW |
10 |
89,319,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R9788:Nr1h4
|
UTSW |
10 |
89,314,638 (GRCm39) |
critical splice donor site |
probably null |
|
R9792:Nr1h4
|
UTSW |
10 |
89,314,651 (GRCm39) |
missense |
probably benign |
0.02 |
R9795:Nr1h4
|
UTSW |
10 |
89,314,651 (GRCm39) |
missense |
probably benign |
0.02 |
R9800:Nr1h4
|
UTSW |
10 |
89,290,618 (GRCm39) |
missense |
probably benign |
0.03 |
X0023:Nr1h4
|
UTSW |
10 |
89,290,706 (GRCm39) |
missense |
possibly damaging |
0.45 |
Z1176:Nr1h4
|
UTSW |
10 |
89,334,212 (GRCm39) |
nonsense |
probably null |
|
|