Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,774,168 (GRCm39) |
E1119G |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,749,842 (GRCm39) |
I132T |
probably damaging |
Het |
Arhgap29 |
G |
A |
3: 121,782,176 (GRCm39) |
D63N |
possibly damaging |
Het |
Bsn |
T |
A |
9: 107,994,760 (GRCm39) |
|
probably null |
Het |
Cfap161 |
A |
C |
7: 83,429,390 (GRCm39) |
Y209* |
probably null |
Het |
Drp2 |
A |
C |
X: 133,340,717 (GRCm39) |
D458A |
probably benign |
Het |
Efcab6 |
T |
C |
15: 83,834,270 (GRCm39) |
H446R |
probably benign |
Het |
Enpep |
G |
C |
3: 129,077,807 (GRCm39) |
S603R |
possibly damaging |
Het |
F13a1 |
G |
A |
13: 37,127,967 (GRCm39) |
T337I |
probably damaging |
Het |
Fhod3 |
TGAGGAGGAGGAGGAGGA |
TGAGGAGGAGGAGGA |
18: 25,153,722 (GRCm39) |
|
probably benign |
Het |
Hcfc1 |
A |
T |
X: 72,993,694 (GRCm39) |
V1157D |
probably benign |
Het |
Inava |
A |
C |
1: 136,142,110 (GRCm39) |
V663G |
probably benign |
Het |
Ino80 |
T |
C |
2: 119,277,353 (GRCm39) |
D374G |
probably null |
Het |
Kif1a |
T |
C |
1: 93,004,765 (GRCm39) |
E143G |
probably null |
Het |
Larp1 |
A |
T |
11: 57,948,172 (GRCm39) |
E990D |
probably benign |
Het |
Larp7 |
C |
A |
3: 127,330,614 (GRCm39) |
E568* |
probably null |
Het |
Ltn1 |
A |
T |
16: 87,217,787 (GRCm39) |
S298R |
probably damaging |
Het |
Mcm10 |
A |
G |
2: 5,001,913 (GRCm39) |
|
probably null |
Het |
Mef2a |
G |
A |
7: 66,918,075 (GRCm39) |
S111L |
probably benign |
Het |
Mroh1 |
A |
G |
15: 76,336,546 (GRCm39) |
T1590A |
possibly damaging |
Het |
Ncoa6 |
A |
T |
2: 155,249,709 (GRCm39) |
H1198Q |
possibly damaging |
Het |
Ogg1 |
A |
G |
6: 113,305,334 (GRCm39) |
E49G |
probably damaging |
Het |
Palm3 |
T |
A |
8: 84,755,973 (GRCm39) |
V495E |
probably benign |
Het |
Pam |
A |
G |
1: 97,762,157 (GRCm39) |
F809L |
probably damaging |
Het |
Parp3 |
T |
C |
9: 106,352,262 (GRCm39) |
E88G |
possibly damaging |
Het |
Ptprs |
A |
G |
17: 56,735,965 (GRCm39) |
I156T |
probably benign |
Het |
Pus7l |
T |
A |
15: 94,425,788 (GRCm39) |
I538F |
probably damaging |
Het |
Rgs8 |
A |
G |
1: 153,566,742 (GRCm39) |
T98A |
probably null |
Het |
Ryr2 |
C |
T |
13: 11,787,466 (GRCm39) |
|
probably null |
Het |
Slc8a2 |
A |
G |
7: 15,886,824 (GRCm39) |
N656D |
possibly damaging |
Het |
Stard9 |
C |
T |
2: 120,529,500 (GRCm39) |
T1919I |
possibly damaging |
Het |
Tbcel |
T |
C |
9: 42,372,591 (GRCm39) |
|
probably benign |
Het |
Uba2 |
A |
G |
7: 33,853,907 (GRCm39) |
|
probably null |
Het |
Usp53 |
A |
C |
3: 122,728,061 (GRCm39) |
S840R |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,743,692 (GRCm39) |
I452F |
probably benign |
Het |
Zbtb48 |
A |
T |
4: 152,110,484 (GRCm39) |
|
probably null |
Het |
Zfp385b |
G |
A |
2: 77,246,233 (GRCm39) |
P177S |
probably benign |
Het |
Zfp42 |
T |
C |
8: 43,748,938 (GRCm39) |
R188G |
possibly damaging |
Het |
|
Other mutations in Trpv3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01084:Trpv3
|
APN |
11 |
73,184,826 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01161:Trpv3
|
APN |
11 |
73,187,544 (GRCm39) |
splice site |
probably benign |
|
IGL02130:Trpv3
|
APN |
11 |
73,170,596 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02957:Trpv3
|
APN |
11 |
73,176,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03334:Trpv3
|
APN |
11 |
73,172,491 (GRCm39) |
splice site |
probably benign |
|
R0103:Trpv3
|
UTSW |
11 |
73,184,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Trpv3
|
UTSW |
11 |
73,184,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Trpv3
|
UTSW |
11 |
73,188,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R0685:Trpv3
|
UTSW |
11 |
73,187,640 (GRCm39) |
splice site |
probably benign |
|
R0969:Trpv3
|
UTSW |
11 |
73,169,764 (GRCm39) |
nonsense |
probably null |
|
R1748:Trpv3
|
UTSW |
11 |
73,186,209 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1974:Trpv3
|
UTSW |
11 |
73,174,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R2015:Trpv3
|
UTSW |
11 |
73,170,653 (GRCm39) |
missense |
probably damaging |
0.97 |
R3426:Trpv3
|
UTSW |
11 |
73,176,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R3427:Trpv3
|
UTSW |
11 |
73,176,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Trpv3
|
UTSW |
11 |
73,176,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R3712:Trpv3
|
UTSW |
11 |
73,169,780 (GRCm39) |
missense |
probably benign |
|
R3916:Trpv3
|
UTSW |
11 |
73,174,560 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3917:Trpv3
|
UTSW |
11 |
73,174,560 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3961:Trpv3
|
UTSW |
11 |
73,178,246 (GRCm39) |
nonsense |
probably null |
|
R4242:Trpv3
|
UTSW |
11 |
73,168,649 (GRCm39) |
missense |
probably benign |
0.43 |
R4277:Trpv3
|
UTSW |
11 |
73,187,264 (GRCm39) |
missense |
probably damaging |
0.97 |
R4506:Trpv3
|
UTSW |
11 |
73,186,150 (GRCm39) |
missense |
probably benign |
0.40 |
R4629:Trpv3
|
UTSW |
11 |
73,172,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R4656:Trpv3
|
UTSW |
11 |
73,186,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5059:Trpv3
|
UTSW |
11 |
73,186,149 (GRCm39) |
missense |
probably benign |
0.00 |
R5121:Trpv3
|
UTSW |
11 |
73,168,660 (GRCm39) |
critical splice donor site |
probably null |
|
R6113:Trpv3
|
UTSW |
11 |
73,176,844 (GRCm39) |
missense |
probably benign |
0.10 |
R6130:Trpv3
|
UTSW |
11 |
73,187,309 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6342:Trpv3
|
UTSW |
11 |
73,174,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Trpv3
|
UTSW |
11 |
73,182,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Trpv3
|
UTSW |
11 |
73,168,818 (GRCm39) |
missense |
probably benign |
|
R7434:Trpv3
|
UTSW |
11 |
73,179,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R7440:Trpv3
|
UTSW |
11 |
73,168,800 (GRCm39) |
missense |
probably benign |
0.37 |
R7741:Trpv3
|
UTSW |
11 |
73,179,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R7750:Trpv3
|
UTSW |
11 |
73,176,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R7785:Trpv3
|
UTSW |
11 |
73,168,558 (GRCm39) |
missense |
probably benign |
0.43 |
R8309:Trpv3
|
UTSW |
11 |
73,170,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Trpv3
|
UTSW |
11 |
73,182,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R8383:Trpv3
|
UTSW |
11 |
73,180,127 (GRCm39) |
missense |
probably benign |
0.30 |
R8443:Trpv3
|
UTSW |
11 |
73,186,209 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8454:Trpv3
|
UTSW |
11 |
73,182,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Trpv3
|
UTSW |
11 |
73,179,035 (GRCm39) |
nonsense |
probably null |
|
R8556:Trpv3
|
UTSW |
11 |
73,178,291 (GRCm39) |
missense |
probably benign |
|
R8701:Trpv3
|
UTSW |
11 |
73,169,762 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9046:Trpv3
|
UTSW |
11 |
73,176,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R9431:Trpv3
|
UTSW |
11 |
73,178,225 (GRCm39) |
missense |
probably benign |
|
R9492:Trpv3
|
UTSW |
11 |
73,187,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R9748:Trpv3
|
UTSW |
11 |
73,174,499 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1186:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1186:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1186:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
Z1187:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1187:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1187:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
Z1188:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1188:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1188:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
Z1189:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1189:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
Z1189:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1190:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1190:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1190:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
Z1191:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1191:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
Z1191:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1192:Trpv3
|
UTSW |
11 |
73,174,502 (GRCm39) |
missense |
probably benign |
|
Z1192:Trpv3
|
UTSW |
11 |
73,169,803 (GRCm39) |
missense |
probably benign |
|
Z1192:Trpv3
|
UTSW |
11 |
73,160,513 (GRCm39) |
missense |
probably benign |
|
|