Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405L10Rik |
C |
T |
8: 105,708,974 |
T88M |
probably damaging |
Het |
9130011E15Rik |
A |
C |
19: 45,975,252 |
S42R |
probably benign |
Het |
9430038I01Rik |
A |
G |
7: 137,377,066 |
|
probably benign |
Het |
Adgra3 |
A |
C |
5: 49,961,492 |
S905A |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,544,533 |
Y1618H |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,673,314 |
T26A |
probably benign |
Het |
Ankrd13d |
T |
C |
19: 4,271,595 |
K360E |
probably damaging |
Het |
Anks1b |
T |
A |
10: 90,512,889 |
|
probably null |
Het |
Apob |
T |
C |
12: 8,007,602 |
F2028S |
possibly damaging |
Het |
Arap3 |
G |
A |
18: 37,975,583 |
R1265W |
probably damaging |
Het |
Arhgef37 |
A |
G |
18: 61,518,050 |
Y135H |
probably damaging |
Het |
Atp1a1 |
T |
C |
3: 101,582,017 |
T760A |
probably benign |
Het |
Cdc42bpb |
T |
A |
12: 111,322,821 |
M497L |
probably benign |
Het |
Ces5a |
C |
T |
8: 93,514,231 |
V413M |
probably damaging |
Het |
Chd5 |
A |
T |
4: 152,385,806 |
Y1903F |
probably damaging |
Het |
Chd9 |
T |
A |
8: 91,010,794 |
N1500K |
probably benign |
Het |
Chmp7 |
G |
T |
14: 69,719,799 |
D303E |
probably benign |
Het |
Chrnb4 |
A |
T |
9: 55,034,818 |
Y391N |
possibly damaging |
Het |
Crtc1 |
T |
C |
8: 70,388,152 |
T475A |
probably benign |
Het |
Cyp2c69 |
A |
G |
19: 39,877,528 |
I207T |
probably benign |
Het |
Dcp1a |
A |
G |
14: 30,518,983 |
E250G |
probably damaging |
Het |
Ddx20 |
T |
C |
3: 105,679,082 |
Q649R |
probably benign |
Het |
Defb12 |
T |
A |
8: 19,112,738 |
K59N |
probably damaging |
Het |
Dpy19l3 |
A |
T |
7: 35,729,760 |
I85N |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,292,258 |
|
probably null |
Het |
E430018J23Rik |
A |
C |
7: 127,391,488 |
D442E |
probably benign |
Het |
Ebi3 |
T |
A |
17: 55,956,679 |
Y197N |
probably damaging |
Het |
Emc1 |
G |
A |
4: 139,375,512 |
R994Q |
probably benign |
Het |
Ercc6 |
G |
T |
14: 32,546,820 |
M530I |
probably damaging |
Het |
Evl |
T |
A |
12: 108,652,996 |
D70E |
probably damaging |
Het |
Fam35a |
A |
G |
14: 34,267,803 |
I382T |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,265,775 |
N819S |
probably damaging |
Het |
Foxk2 |
A |
G |
11: 121,285,537 |
I170V |
probably benign |
Het |
Gfm1 |
T |
C |
3: 67,435,610 |
V159A |
probably damaging |
Het |
Gm10837 |
A |
G |
14: 122,490,765 |
T18A |
unknown |
Het |
Gm12887 |
A |
T |
4: 121,622,030 |
V25E |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,297,180 |
H985R |
possibly damaging |
Het |
Hsfy2 |
A |
G |
1: 56,636,632 |
Y249H |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,545,567 |
V2639A |
probably damaging |
Het |
Igf2r |
A |
G |
17: 12,704,270 |
|
probably null |
Het |
Invs |
T |
A |
4: 48,422,035 |
I889N |
probably damaging |
Het |
Kcnq1 |
A |
T |
7: 143,183,120 |
M209L |
probably benign |
Het |
Klra7 |
A |
G |
6: 130,229,994 |
I48T |
possibly damaging |
Het |
Krt26 |
CTAGTA |
CTA |
11: 99,333,526 |
|
probably benign |
Het |
Lrif1 |
T |
A |
3: 106,732,811 |
V404D |
probably damaging |
Het |
Lrriq1 |
T |
A |
10: 103,227,173 |
|
probably null |
Het |
Lypd6 |
T |
A |
2: 50,188,762 |
I90N |
possibly damaging |
Het |
Mbp |
A |
G |
18: 82,584,122 |
D174G |
probably damaging |
Het |
Megf9 |
G |
T |
4: 70,534,785 |
P13Q |
probably damaging |
Het |
Myo15b |
A |
T |
11: 115,869,586 |
T1155S |
probably benign |
Het |
Nlrp6 |
T |
A |
7: 140,923,093 |
C371S |
probably damaging |
Het |
Nosip |
T |
A |
7: 45,077,309 |
|
probably null |
Het |
Nox3 |
G |
T |
17: 3,669,878 |
P344H |
probably damaging |
Het |
Nup210l |
T |
C |
3: 90,172,086 |
V959A |
probably damaging |
Het |
Olfr1360 |
C |
A |
13: 21,674,672 |
V91L |
probably benign |
Het |
Olfr1475 |
A |
G |
19: 13,479,931 |
I89T |
probably benign |
Het |
Olfr175-ps1 |
T |
A |
16: 58,824,077 |
I211F |
probably damaging |
Het |
Olfr267 |
T |
C |
4: 58,785,384 |
I113V |
probably benign |
Het |
Olfr959 |
A |
G |
9: 39,572,735 |
Y175H |
possibly damaging |
Het |
Osbpl3 |
A |
C |
6: 50,370,143 |
S25A |
probably damaging |
Het |
Otog |
G |
A |
7: 46,246,283 |
C107Y |
probably damaging |
Het |
Pax7 |
G |
A |
4: 139,784,491 |
R260C |
probably damaging |
Het |
Pbrm1 |
A |
T |
14: 31,038,957 |
I224F |
probably damaging |
Het |
Pcdh1 |
T |
A |
18: 38,192,225 |
|
probably null |
Het |
Pcnx |
T |
C |
12: 81,980,935 |
L1585P |
probably damaging |
Het |
Pde4c |
C |
T |
8: 70,747,950 |
H362Y |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,164,779 |
R296H |
probably damaging |
Het |
Pgm2 |
A |
T |
4: 99,961,478 |
Q90L |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,343,505 |
H814R |
probably benign |
Het |
Pknox2 |
A |
T |
9: 36,954,831 |
M5K |
possibly damaging |
Het |
Pole |
G |
A |
5: 110,330,835 |
|
probably null |
Het |
Polr1b |
A |
G |
2: 129,102,966 |
I61V |
probably benign |
Het |
Prelp |
T |
C |
1: 133,914,757 |
K217E |
probably damaging |
Het |
Prkce |
C |
T |
17: 86,475,546 |
Q202* |
probably null |
Het |
Psmd2 |
T |
G |
16: 20,656,582 |
M370R |
probably benign |
Het |
Rimklb |
A |
T |
6: 122,464,009 |
H68Q |
probably damaging |
Het |
Rnasel |
A |
G |
1: 153,754,674 |
D312G |
possibly damaging |
Het |
Rxrg |
A |
T |
1: 167,598,752 |
M1L |
probably benign |
Het |
Scrn1 |
A |
G |
6: 54,522,841 |
F220L |
possibly damaging |
Het |
Scyl3 |
A |
G |
1: 163,950,675 |
S461G |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,895,023 |
T411S |
probably benign |
Het |
Serpinb6d |
C |
T |
13: 33,671,381 |
P346L |
probably benign |
Het |
Slc9a3r2 |
C |
T |
17: 24,641,719 |
S150N |
possibly damaging |
Het |
Spg21 |
G |
T |
9: 65,465,336 |
V17F |
probably damaging |
Het |
Spink5 |
A |
T |
18: 43,999,891 |
M525L |
probably benign |
Het |
Sun2 |
T |
C |
15: 79,737,563 |
T155A |
probably benign |
Het |
Tchh |
T |
A |
3: 93,446,780 |
F1176I |
unknown |
Het |
Tex15 |
T |
A |
8: 33,576,654 |
D2037E |
probably benign |
Het |
Tfdp2 |
T |
C |
9: 96,317,804 |
C392R |
possibly damaging |
Het |
Tmem30c |
T |
C |
16: 57,276,780 |
N139S |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,113,133 |
|
probably null |
Het |
Trim66 |
T |
C |
7: 109,475,839 |
E405G |
probably damaging |
Het |
Tspo2 |
T |
C |
17: 48,448,790 |
D108G |
possibly damaging |
Het |
Tyk2 |
A |
T |
9: 21,121,554 |
C304* |
probably null |
Het |
Vgll4 |
A |
T |
6: 114,862,795 |
S185T |
probably benign |
Het |
Vmn2r94 |
A |
C |
17: 18,244,470 |
S519R |
probably benign |
Het |
Vmn2r96 |
T |
G |
17: 18,597,921 |
S587A |
probably benign |
Het |
Vps4b |
C |
A |
1: 106,778,982 |
A287S |
possibly damaging |
Het |
Yeats2 |
C |
T |
16: 20,229,564 |
P1332S |
probably benign |
Het |
Zfp462 |
T |
G |
4: 55,010,010 |
S659A |
possibly damaging |
Het |
Zfp507 |
C |
T |
7: 35,793,725 |
R631Q |
probably damaging |
Het |
Zswim5 |
G |
T |
4: 116,877,699 |
E80D |
unknown |
Het |
|
Other mutations in Trpc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Trpc4
|
APN |
3 |
54,302,175 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01067:Trpc4
|
APN |
3 |
54,222,562 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01475:Trpc4
|
APN |
3 |
54,266,407 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL01544:Trpc4
|
APN |
3 |
54,302,146 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01688:Trpc4
|
APN |
3 |
54,266,074 (GRCm38) |
splice site |
probably benign |
|
IGL02134:Trpc4
|
APN |
3 |
54,315,654 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02237:Trpc4
|
APN |
3 |
54,222,362 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02301:Trpc4
|
APN |
3 |
54,291,232 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02549:Trpc4
|
APN |
3 |
54,222,349 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02742:Trpc4
|
APN |
3 |
54,299,246 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02815:Trpc4
|
APN |
3 |
54,299,274 (GRCm38) |
splice site |
probably benign |
|
R0498:Trpc4
|
UTSW |
3 |
54,291,211 (GRCm38) |
missense |
probably damaging |
1.00 |
R0555:Trpc4
|
UTSW |
3 |
54,302,090 (GRCm38) |
splice site |
probably benign |
|
R0609:Trpc4
|
UTSW |
3 |
54,194,768 (GRCm38) |
missense |
probably damaging |
1.00 |
R1351:Trpc4
|
UTSW |
3 |
54,195,002 (GRCm38) |
missense |
probably damaging |
1.00 |
R1595:Trpc4
|
UTSW |
3 |
54,315,815 (GRCm38) |
missense |
probably benign |
0.02 |
R1623:Trpc4
|
UTSW |
3 |
54,299,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R1763:Trpc4
|
UTSW |
3 |
54,194,822 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1856:Trpc4
|
UTSW |
3 |
54,279,989 (GRCm38) |
missense |
probably damaging |
1.00 |
R1936:Trpc4
|
UTSW |
3 |
54,279,890 (GRCm38) |
missense |
probably damaging |
1.00 |
R2196:Trpc4
|
UTSW |
3 |
54,302,193 (GRCm38) |
missense |
probably benign |
0.03 |
R2441:Trpc4
|
UTSW |
3 |
54,222,283 (GRCm38) |
missense |
probably damaging |
0.96 |
R2877:Trpc4
|
UTSW |
3 |
54,291,340 (GRCm38) |
missense |
probably damaging |
1.00 |
R3846:Trpc4
|
UTSW |
3 |
54,318,012 (GRCm38) |
missense |
probably benign |
0.22 |
R3931:Trpc4
|
UTSW |
3 |
54,318,095 (GRCm38) |
missense |
probably damaging |
1.00 |
R4854:Trpc4
|
UTSW |
3 |
54,302,218 (GRCm38) |
missense |
probably damaging |
1.00 |
R5024:Trpc4
|
UTSW |
3 |
54,194,796 (GRCm38) |
missense |
probably benign |
0.11 |
R5284:Trpc4
|
UTSW |
3 |
54,279,947 (GRCm38) |
missense |
probably damaging |
0.99 |
R5320:Trpc4
|
UTSW |
3 |
54,299,178 (GRCm38) |
missense |
probably damaging |
0.99 |
R5973:Trpc4
|
UTSW |
3 |
54,315,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R6276:Trpc4
|
UTSW |
3 |
54,318,020 (GRCm38) |
missense |
probably benign |
0.25 |
R6335:Trpc4
|
UTSW |
3 |
54,317,574 (GRCm38) |
critical splice donor site |
probably null |
|
R7082:Trpc4
|
UTSW |
3 |
54,299,098 (GRCm38) |
nonsense |
probably null |
|
R7215:Trpc4
|
UTSW |
3 |
54,194,896 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7299:Trpc4
|
UTSW |
3 |
54,317,627 (GRCm38) |
missense |
possibly damaging |
0.87 |
R7423:Trpc4
|
UTSW |
3 |
54,318,029 (GRCm38) |
missense |
probably benign |
|
R7459:Trpc4
|
UTSW |
3 |
54,291,232 (GRCm38) |
missense |
probably damaging |
0.97 |
R7538:Trpc4
|
UTSW |
3 |
54,318,095 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7542:Trpc4
|
UTSW |
3 |
54,315,654 (GRCm38) |
missense |
probably damaging |
1.00 |
R7823:Trpc4
|
UTSW |
3 |
54,302,219 (GRCm38) |
nonsense |
probably null |
|
R7868:Trpc4
|
UTSW |
3 |
54,302,286 (GRCm38) |
missense |
probably benign |
0.00 |
R8046:Trpc4
|
UTSW |
3 |
54,194,914 (GRCm38) |
missense |
probably damaging |
1.00 |
R8164:Trpc4
|
UTSW |
3 |
54,315,805 (GRCm38) |
missense |
probably benign |
0.31 |
R8235:Trpc4
|
UTSW |
3 |
54,302,248 (GRCm38) |
missense |
probably benign |
0.01 |
R8263:Trpc4
|
UTSW |
3 |
54,222,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R8438:Trpc4
|
UTSW |
3 |
54,222,253 (GRCm38) |
missense |
possibly damaging |
0.90 |
R8854:Trpc4
|
UTSW |
3 |
54,194,701 (GRCm38) |
nonsense |
probably null |
|
R8987:Trpc4
|
UTSW |
3 |
54,194,711 (GRCm38) |
missense |
probably benign |
0.09 |
R9023:Trpc4
|
UTSW |
3 |
54,194,833 (GRCm38) |
missense |
possibly damaging |
0.52 |
R9196:Trpc4
|
UTSW |
3 |
54,222,451 (GRCm38) |
missense |
probably damaging |
1.00 |
R9210:Trpc4
|
UTSW |
3 |
54,266,320 (GRCm38) |
missense |
probably benign |
0.07 |
R9350:Trpc4
|
UTSW |
3 |
54,302,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R9600:Trpc4
|
UTSW |
3 |
54,194,827 (GRCm38) |
nonsense |
probably null |
|
R9605:Trpc4
|
UTSW |
3 |
54,318,129 (GRCm38) |
missense |
probably benign |
|
R9644:Trpc4
|
UTSW |
3 |
54,222,278 (GRCm38) |
missense |
probably damaging |
1.00 |
R9749:Trpc4
|
UTSW |
3 |
54,194,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R9755:Trpc4
|
UTSW |
3 |
54,315,794 (GRCm38) |
missense |
probably damaging |
1.00 |
X0066:Trpc4
|
UTSW |
3 |
54,194,750 (GRCm38) |
missense |
probably damaging |
1.00 |
|