Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
G |
A |
7: 119,383,527 (GRCm39) |
V563I |
probably benign |
Het |
Amer3 |
T |
C |
1: 34,627,759 (GRCm39) |
V666A |
probably benign |
Het |
Ankrd16 |
A |
G |
2: 11,784,711 (GRCm39) |
|
probably benign |
Het |
Ankub1 |
G |
T |
3: 57,580,296 (GRCm39) |
C120* |
probably null |
Het |
Arhgap31 |
T |
C |
16: 38,445,941 (GRCm39) |
I135V |
probably benign |
Het |
Atp2c2 |
G |
A |
8: 120,476,584 (GRCm39) |
G633D |
probably benign |
Het |
Camta1 |
T |
A |
4: 151,537,751 (GRCm39) |
Q143L |
probably damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,644,727 (GRCm39) |
S1267P |
probably benign |
Het |
Ccn4 |
A |
G |
15: 66,791,176 (GRCm39) |
E326G |
probably benign |
Het |
Cdh1 |
T |
A |
8: 107,380,391 (GRCm39) |
|
probably benign |
Het |
Cdhr4 |
C |
A |
9: 107,873,460 (GRCm39) |
D397E |
probably damaging |
Het |
Cdk6 |
T |
G |
5: 3,394,387 (GRCm39) |
S7R |
probably benign |
Het |
Cert1 |
T |
A |
13: 96,771,394 (GRCm39) |
N550K |
probably damaging |
Het |
Cilp2 |
C |
A |
8: 70,335,442 (GRCm39) |
E519* |
probably null |
Het |
Clybl |
A |
G |
14: 122,548,718 (GRCm39) |
Y40C |
probably damaging |
Het |
Ctnnal1 |
T |
C |
4: 56,812,329 (GRCm39) |
*732W |
probably null |
Het |
Ctns |
A |
T |
11: 73,083,907 (GRCm39) |
S38R |
probably benign |
Het |
Cwh43 |
A |
T |
5: 73,578,873 (GRCm39) |
K293N |
possibly damaging |
Het |
Dcaf5 |
G |
T |
12: 80,385,635 (GRCm39) |
D830E |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,322,848 (GRCm39) |
V1512A |
probably damaging |
Het |
Dnah9 |
A |
T |
11: 65,951,950 (GRCm39) |
C1850S |
probably damaging |
Het |
Dpp8 |
C |
T |
9: 64,981,849 (GRCm39) |
|
probably null |
Het |
Enam |
A |
T |
5: 88,649,646 (GRCm39) |
Q385L |
probably damaging |
Het |
Etv3 |
A |
G |
3: 87,443,369 (GRCm39) |
T318A |
possibly damaging |
Het |
Exd2 |
T |
G |
12: 80,543,575 (GRCm39) |
I586S |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,909,813 (GRCm39) |
V2063A |
possibly damaging |
Het |
Fezf1 |
A |
G |
6: 23,247,331 (GRCm39) |
F248S |
possibly damaging |
Het |
Flnc |
T |
C |
6: 29,450,734 (GRCm39) |
|
probably null |
Het |
Foxc2 |
A |
G |
8: 121,844,819 (GRCm39) |
Y489C |
probably damaging |
Het |
Gfm2 |
A |
G |
13: 97,308,028 (GRCm39) |
E540G |
probably damaging |
Het |
Hrg |
T |
C |
16: 22,774,949 (GRCm39) |
I193T |
probably benign |
Het |
Ifih1 |
G |
A |
2: 62,440,889 (GRCm39) |
Q426* |
probably null |
Het |
Ifit1bl2 |
T |
A |
19: 34,596,920 (GRCm39) |
D232V |
probably benign |
Het |
Igf2bp1 |
A |
G |
11: 95,866,122 (GRCm39) |
V122A |
probably damaging |
Het |
Inpp1 |
T |
G |
1: 52,838,577 (GRCm39) |
Q24P |
probably damaging |
Het |
Kifc2 |
A |
G |
15: 76,545,454 (GRCm39) |
D67G |
probably damaging |
Het |
Lrrc43 |
G |
A |
5: 123,639,177 (GRCm39) |
G402D |
probably benign |
Het |
Lrrc8c |
C |
T |
5: 105,755,224 (GRCm39) |
T333M |
possibly damaging |
Het |
Mab21l3 |
G |
T |
3: 101,730,744 (GRCm39) |
A165D |
probably benign |
Het |
Mcub |
T |
A |
3: 129,712,337 (GRCm39) |
R179S |
probably benign |
Het |
Mdfi |
G |
C |
17: 48,135,562 (GRCm39) |
A56G |
possibly damaging |
Het |
Mdn1 |
A |
T |
4: 32,743,843 (GRCm39) |
|
probably null |
Het |
Meox2 |
A |
G |
12: 37,217,476 (GRCm39) |
T226A |
probably damaging |
Het |
Mipol1 |
A |
G |
12: 57,352,842 (GRCm39) |
|
probably null |
Het |
Mms22l |
T |
G |
4: 24,591,084 (GRCm39) |
N1018K |
probably benign |
Het |
Mn1 |
T |
C |
5: 111,602,617 (GRCm39) |
I1285T |
possibly damaging |
Het |
Muc20 |
T |
G |
16: 32,614,547 (GRCm39) |
S277R |
probably damaging |
Het |
Muc6 |
C |
A |
7: 141,213,991 (GRCm39) |
V2845L |
probably benign |
Het |
Mup5 |
C |
A |
4: 61,751,962 (GRCm39) |
G96C |
probably damaging |
Het |
Neb |
T |
A |
2: 52,146,826 (GRCm39) |
M2813L |
probably benign |
Het |
Neb |
C |
A |
2: 52,161,570 (GRCm39) |
R2074L |
probably damaging |
Het |
Oasl2 |
A |
T |
5: 115,049,063 (GRCm39) |
K168* |
probably null |
Het |
Or6c5 |
T |
C |
10: 129,074,368 (GRCm39) |
S117P |
probably damaging |
Het |
P2rx2 |
C |
T |
5: 110,489,007 (GRCm39) |
D203N |
probably damaging |
Het |
Ptprg |
T |
C |
14: 11,952,897 (GRCm38) |
|
probably null |
Het |
Rims4 |
C |
T |
2: 163,706,785 (GRCm39) |
|
probably null |
Het |
Rtn4ip1 |
T |
A |
10: 43,808,402 (GRCm39) |
W60R |
probably benign |
Het |
Sccpdh |
T |
C |
1: 179,498,162 (GRCm39) |
S69P |
probably benign |
Het |
Serpina3b |
T |
A |
12: 104,105,069 (GRCm39) |
I415N |
probably benign |
Het |
Slc4a5 |
G |
A |
6: 83,274,360 (GRCm39) |
A1076T |
probably benign |
Het |
Slit1 |
T |
C |
19: 41,590,686 (GRCm39) |
K1329E |
possibly damaging |
Het |
Synj2bp |
A |
C |
12: 81,548,826 (GRCm39) |
F138V |
probably benign |
Het |
Taar7a |
T |
C |
10: 23,868,959 (GRCm39) |
I141V |
probably damaging |
Het |
Tas1r3 |
T |
C |
4: 155,946,588 (GRCm39) |
E339G |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,088,037 (GRCm39) |
|
probably benign |
Het |
Tgds |
A |
T |
14: 118,359,149 (GRCm39) |
Y146* |
probably null |
Het |
Tgm3 |
G |
A |
2: 129,879,403 (GRCm39) |
V332I |
probably benign |
Het |
Tnnt2 |
A |
G |
1: 135,771,547 (GRCm39) |
|
probably benign |
Het |
Top1 |
T |
A |
2: 160,546,739 (GRCm39) |
Y340N |
probably damaging |
Het |
Topbp1 |
T |
C |
9: 103,195,181 (GRCm39) |
|
probably benign |
Het |
Tpst1 |
A |
G |
5: 130,131,202 (GRCm39) |
N224S |
probably benign |
Het |
Traf4 |
A |
G |
11: 78,050,840 (GRCm39) |
F439L |
probably damaging |
Het |
Trim58 |
A |
G |
11: 58,533,964 (GRCm39) |
|
probably benign |
Het |
Tspan31 |
T |
C |
10: 126,904,004 (GRCm39) |
N205S |
probably damaging |
Het |
Ube3a |
T |
A |
7: 58,926,225 (GRCm39) |
N334K |
possibly damaging |
Het |
Ugt2a3 |
A |
T |
5: 87,477,541 (GRCm39) |
|
probably null |
Het |
Vwf |
G |
A |
6: 125,623,293 (GRCm39) |
V1797I |
probably benign |
Het |
Wdr81 |
G |
T |
11: 75,343,809 (GRCm39) |
P486Q |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Yipf7 |
T |
A |
5: 69,678,462 (GRCm39) |
N56I |
possibly damaging |
Het |
Zfp523 |
A |
T |
17: 28,414,190 (GRCm39) |
T75S |
probably benign |
Het |
|
Other mutations in Slc22a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01459:Slc22a4
|
APN |
11 |
53,877,303 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01723:Slc22a4
|
APN |
11 |
53,879,671 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01839:Slc22a4
|
APN |
11 |
53,886,903 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02022:Slc22a4
|
APN |
11 |
53,874,435 (GRCm39) |
unclassified |
probably benign |
|
IGL02386:Slc22a4
|
APN |
11 |
53,879,598 (GRCm39) |
splice site |
probably benign |
|
PIT1430001:Slc22a4
|
UTSW |
11 |
53,918,783 (GRCm39) |
missense |
probably benign |
|
R0001:Slc22a4
|
UTSW |
11 |
53,918,829 (GRCm39) |
start gained |
probably benign |
|
R1111:Slc22a4
|
UTSW |
11 |
53,898,667 (GRCm39) |
missense |
probably benign |
|
R1710:Slc22a4
|
UTSW |
11 |
53,918,801 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R3081:Slc22a4
|
UTSW |
11 |
53,898,615 (GRCm39) |
missense |
probably benign |
0.38 |
R3498:Slc22a4
|
UTSW |
11 |
53,882,879 (GRCm39) |
missense |
probably benign |
0.00 |
R4014:Slc22a4
|
UTSW |
11 |
53,888,218 (GRCm39) |
missense |
probably benign |
0.04 |
R4658:Slc22a4
|
UTSW |
11 |
53,888,336 (GRCm39) |
missense |
probably benign |
0.05 |
R4720:Slc22a4
|
UTSW |
11 |
53,879,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R4727:Slc22a4
|
UTSW |
11 |
53,918,477 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5894:Slc22a4
|
UTSW |
11 |
53,888,341 (GRCm39) |
missense |
probably benign |
0.04 |
R5945:Slc22a4
|
UTSW |
11 |
53,886,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R6295:Slc22a4
|
UTSW |
11 |
53,898,634 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6848:Slc22a4
|
UTSW |
11 |
53,898,615 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6899:Slc22a4
|
UTSW |
11 |
53,879,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Slc22a4
|
UTSW |
11 |
53,877,364 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7414:Slc22a4
|
UTSW |
11 |
53,888,254 (GRCm39) |
missense |
probably benign |
0.00 |
R7806:Slc22a4
|
UTSW |
11 |
53,881,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R8068:Slc22a4
|
UTSW |
11 |
53,888,269 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8087:Slc22a4
|
UTSW |
11 |
53,886,887 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8218:Slc22a4
|
UTSW |
11 |
53,877,407 (GRCm39) |
missense |
probably benign |
0.00 |
R8971:Slc22a4
|
UTSW |
11 |
53,879,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R9008:Slc22a4
|
UTSW |
11 |
53,881,664 (GRCm39) |
nonsense |
probably null |
|
R9296:Slc22a4
|
UTSW |
11 |
53,888,217 (GRCm39) |
nonsense |
probably null |
|
R9484:Slc22a4
|
UTSW |
11 |
53,879,773 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9679:Slc22a4
|
UTSW |
11 |
53,881,599 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Slc22a4
|
UTSW |
11 |
53,918,544 (GRCm39) |
missense |
probably benign |
0.00 |
|