Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730071L15Rik |
G |
A |
11: 6,150,439 (GRCm39) |
W137* |
probably null |
Het |
Acads |
G |
A |
5: 115,250,417 (GRCm39) |
T169I |
probably benign |
Het |
Adgrg7 |
T |
A |
16: 56,570,787 (GRCm39) |
N414Y |
probably damaging |
Het |
Ankrd35 |
T |
A |
3: 96,577,742 (GRCm39) |
S6T |
probably damaging |
Het |
Armc3 |
A |
G |
2: 19,206,630 (GRCm39) |
|
probably null |
Het |
Atp9a |
C |
A |
2: 168,496,140 (GRCm39) |
V555F |
possibly damaging |
Het |
Bltp1 |
A |
G |
3: 37,075,630 (GRCm39) |
Y3610C |
probably damaging |
Het |
Cars2 |
C |
T |
8: 11,566,198 (GRCm39) |
V443I |
probably benign |
Het |
Cblc |
A |
G |
7: 19,526,821 (GRCm39) |
L137P |
probably damaging |
Het |
Ccdc198 |
T |
C |
14: 49,481,270 (GRCm39) |
|
probably null |
Het |
Cdk5r1 |
T |
A |
11: 80,369,021 (GRCm39) |
C229* |
probably null |
Het |
Cep85 |
C |
G |
4: 133,883,167 (GRCm39) |
A241P |
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,710,877 (GRCm39) |
Y2728C |
unknown |
Het |
Ckap5 |
T |
A |
2: 91,400,597 (GRCm39) |
W650R |
probably damaging |
Het |
Cnot11 |
C |
T |
1: 39,579,148 (GRCm39) |
Q12* |
probably null |
Het |
Commd6 |
A |
T |
14: 101,874,534 (GRCm39) |
D19E |
probably damaging |
Het |
Crygc |
C |
T |
1: 65,112,361 (GRCm39) |
G71D |
possibly damaging |
Het |
Cstf3 |
A |
G |
2: 104,486,076 (GRCm39) |
K439E |
probably benign |
Het |
Cyp11b2 |
G |
T |
15: 74,727,340 (GRCm39) |
H114N |
probably benign |
Het |
Cyp2d40 |
T |
C |
15: 82,645,687 (GRCm39) |
D106G |
probably benign |
Het |
Dhx8 |
T |
A |
11: 101,655,618 (GRCm39) |
V1117E |
probably damaging |
Het |
Duoxa1 |
G |
T |
2: 122,134,462 (GRCm39) |
L219I |
probably damaging |
Het |
Dynap |
A |
T |
18: 70,374,253 (GRCm39) |
I91N |
probably damaging |
Het |
Elfn1 |
G |
T |
5: 139,958,900 (GRCm39) |
G635W |
probably damaging |
Het |
Fan1 |
A |
T |
7: 64,014,377 (GRCm39) |
I618N |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,876,410 (GRCm39) |
D2381G |
probably damaging |
Het |
Fxyd6 |
T |
A |
9: 45,302,851 (GRCm39) |
|
probably null |
Het |
Gpr137b |
A |
T |
13: 13,538,094 (GRCm39) |
W286R |
probably damaging |
Het |
Gpsm3 |
A |
T |
17: 34,809,536 (GRCm39) |
|
probably null |
Het |
Has1 |
C |
T |
17: 18,064,122 (GRCm39) |
V506I |
probably benign |
Het |
Hoxd10 |
T |
A |
2: 74,522,616 (GRCm39) |
V98D |
probably benign |
Het |
Htr2b |
T |
A |
1: 86,027,615 (GRCm39) |
D297V |
probably benign |
Het |
Hydin |
G |
C |
8: 111,265,007 (GRCm39) |
R2730P |
probably benign |
Het |
I830077J02Rik |
T |
C |
3: 105,833,830 (GRCm39) |
N109D |
possibly damaging |
Het |
Igf2r |
A |
T |
17: 12,922,263 (GRCm39) |
F1284I |
probably damaging |
Het |
Ildr2 |
C |
G |
1: 166,098,144 (GRCm39) |
D167E |
probably damaging |
Het |
Ipo9 |
T |
C |
1: 135,314,046 (GRCm39) |
D949G |
probably benign |
Het |
Itga10 |
T |
C |
3: 96,564,030 (GRCm39) |
F895L |
probably damaging |
Het |
Itpr1 |
A |
G |
6: 108,365,153 (GRCm39) |
N27S |
probably damaging |
Het |
Klra4 |
C |
A |
6: 130,042,162 (GRCm39) |
R35L |
probably benign |
Het |
Map3k2 |
T |
A |
18: 32,359,682 (GRCm39) |
C512S |
probably benign |
Het |
Mertk |
A |
G |
2: 128,601,150 (GRCm39) |
|
probably null |
Het |
Mgat2 |
T |
A |
12: 69,232,407 (GRCm39) |
I327N |
probably damaging |
Het |
Mogat1 |
T |
C |
1: 78,499,496 (GRCm39) |
I59T |
probably damaging |
Het |
Mrpl2 |
A |
T |
17: 46,958,382 (GRCm39) |
M55L |
probably benign |
Het |
Nxpe3 |
T |
C |
16: 55,664,685 (GRCm39) |
M512V |
possibly damaging |
Het |
Pcdh15 |
T |
C |
10: 74,286,052 (GRCm39) |
L769P |
probably damaging |
Het |
Pcmtd2 |
T |
G |
2: 181,486,231 (GRCm39) |
V117G |
probably damaging |
Het |
Pdia2 |
A |
T |
17: 26,415,578 (GRCm39) |
|
probably null |
Het |
Repin1 |
A |
T |
6: 48,574,859 (GRCm39) |
Q593L |
possibly damaging |
Het |
Rnf213 |
C |
T |
11: 119,340,692 (GRCm39) |
T3517I |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,942,210 (GRCm39) |
|
probably benign |
Het |
Skint8 |
T |
C |
4: 111,785,968 (GRCm39) |
L138P |
probably damaging |
Het |
Slc35a3 |
T |
A |
3: 116,506,417 (GRCm39) |
Q5L |
probably null |
Het |
Stab2 |
T |
A |
10: 86,778,054 (GRCm39) |
N758I |
probably damaging |
Het |
Sulf1 |
T |
A |
1: 12,908,658 (GRCm39) |
I557N |
probably damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,428,455 (GRCm39) |
I497V |
possibly damaging |
Het |
Ticam2 |
A |
C |
18: 46,693,998 (GRCm39) |
S30A |
probably benign |
Het |
Timp3 |
T |
C |
10: 86,181,638 (GRCm39) |
S170P |
possibly damaging |
Het |
Top1mt |
C |
T |
15: 75,547,973 (GRCm39) |
E38K |
probably benign |
Het |
Tpp1 |
G |
A |
7: 105,398,171 (GRCm39) |
L331F |
probably damaging |
Het |
Ttc23 |
A |
G |
7: 67,319,476 (GRCm39) |
E112G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,715,296 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,726,934 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,850,969 (GRCm39) |
C1796S |
probably damaging |
Het |
Ugt2b34 |
C |
T |
5: 87,040,675 (GRCm39) |
V416I |
probably benign |
Het |
Uqcrb |
A |
G |
13: 67,048,827 (GRCm39) |
|
probably benign |
Het |
Vps26b |
A |
G |
9: 26,921,760 (GRCm39) |
L255P |
probably benign |
Het |
Wdr59 |
A |
G |
8: 112,223,512 (GRCm39) |
V154A |
probably damaging |
Het |
|
Other mutations in Trpm7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00232:Trpm7
|
APN |
2 |
126,670,951 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01084:Trpm7
|
APN |
2 |
126,687,992 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01634:Trpm7
|
APN |
2 |
126,668,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01678:Trpm7
|
APN |
2 |
126,658,719 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02005:Trpm7
|
APN |
2 |
126,655,104 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02064:Trpm7
|
APN |
2 |
126,639,863 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02156:Trpm7
|
APN |
2 |
126,641,163 (GRCm39) |
unclassified |
probably benign |
|
IGL02172:Trpm7
|
APN |
2 |
126,637,248 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02334:Trpm7
|
APN |
2 |
126,649,282 (GRCm39) |
missense |
probably benign |
|
IGL02375:Trpm7
|
APN |
2 |
126,667,664 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02388:Trpm7
|
APN |
2 |
126,661,811 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02552:Trpm7
|
APN |
2 |
126,682,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02684:Trpm7
|
APN |
2 |
126,688,079 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02901:Trpm7
|
APN |
2 |
126,649,207 (GRCm39) |
critical splice donor site |
probably null |
|
Accused
|
UTSW |
2 |
126,668,657 (GRCm39) |
missense |
probably damaging |
0.99 |
Condemned
|
UTSW |
2 |
126,677,428 (GRCm39) |
missense |
probably damaging |
1.00 |
denounced
|
UTSW |
2 |
126,654,941 (GRCm39) |
missense |
probably benign |
0.00 |
deposed
|
UTSW |
2 |
126,639,418 (GRCm39) |
missense |
probably benign |
0.01 |
Summac
|
UTSW |
2 |
126,661,883 (GRCm39) |
missense |
probably damaging |
1.00 |
Vacated
|
UTSW |
2 |
126,691,842 (GRCm39) |
missense |
probably damaging |
1.00 |
P0037:Trpm7
|
UTSW |
2 |
126,658,677 (GRCm39) |
splice site |
probably benign |
|
R0038:Trpm7
|
UTSW |
2 |
126,637,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R0139:Trpm7
|
UTSW |
2 |
126,654,691 (GRCm39) |
missense |
probably benign |
|
R0165:Trpm7
|
UTSW |
2 |
126,639,433 (GRCm39) |
missense |
probably damaging |
0.97 |
R0511:Trpm7
|
UTSW |
2 |
126,668,638 (GRCm39) |
nonsense |
probably null |
|
R0543:Trpm7
|
UTSW |
2 |
126,690,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Trpm7
|
UTSW |
2 |
126,687,992 (GRCm39) |
critical splice donor site |
probably null |
|
R0844:Trpm7
|
UTSW |
2 |
126,677,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R0865:Trpm7
|
UTSW |
2 |
126,641,159 (GRCm39) |
splice site |
probably null |
|
R0919:Trpm7
|
UTSW |
2 |
126,673,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Trpm7
|
UTSW |
2 |
126,646,969 (GRCm39) |
missense |
probably benign |
|
R1109:Trpm7
|
UTSW |
2 |
126,639,713 (GRCm39) |
missense |
probably benign |
0.01 |
R1118:Trpm7
|
UTSW |
2 |
126,664,406 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1278:Trpm7
|
UTSW |
2 |
126,667,374 (GRCm39) |
nonsense |
probably null |
|
R1527:Trpm7
|
UTSW |
2 |
126,672,082 (GRCm39) |
missense |
probably benign |
0.18 |
R1542:Trpm7
|
UTSW |
2 |
126,664,519 (GRCm39) |
nonsense |
probably null |
|
R1882:Trpm7
|
UTSW |
2 |
126,654,697 (GRCm39) |
missense |
probably benign |
0.00 |
R1951:Trpm7
|
UTSW |
2 |
126,673,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Trpm7
|
UTSW |
2 |
126,665,917 (GRCm39) |
nonsense |
probably null |
|
R2012:Trpm7
|
UTSW |
2 |
126,665,917 (GRCm39) |
nonsense |
probably null |
|
R2026:Trpm7
|
UTSW |
2 |
126,654,658 (GRCm39) |
missense |
probably benign |
0.39 |
R2067:Trpm7
|
UTSW |
2 |
126,639,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R2926:Trpm7
|
UTSW |
2 |
126,700,329 (GRCm39) |
splice site |
probably benign |
|
R3082:Trpm7
|
UTSW |
2 |
126,686,342 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3552:Trpm7
|
UTSW |
2 |
126,668,630 (GRCm39) |
splice site |
probably benign |
|
R3607:Trpm7
|
UTSW |
2 |
126,638,348 (GRCm39) |
intron |
probably benign |
|
R3739:Trpm7
|
UTSW |
2 |
126,693,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R3943:Trpm7
|
UTSW |
2 |
126,673,138 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4161:Trpm7
|
UTSW |
2 |
126,658,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Trpm7
|
UTSW |
2 |
126,671,083 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4392:Trpm7
|
UTSW |
2 |
126,690,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R4392:Trpm7
|
UTSW |
2 |
126,637,429 (GRCm39) |
splice site |
probably null |
|
R4404:Trpm7
|
UTSW |
2 |
126,675,635 (GRCm39) |
missense |
probably damaging |
0.97 |
R4574:Trpm7
|
UTSW |
2 |
126,639,131 (GRCm39) |
missense |
probably benign |
0.01 |
R4714:Trpm7
|
UTSW |
2 |
126,682,703 (GRCm39) |
nonsense |
probably null |
|
R4807:Trpm7
|
UTSW |
2 |
126,673,149 (GRCm39) |
missense |
probably benign |
0.00 |
R4815:Trpm7
|
UTSW |
2 |
126,700,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R4846:Trpm7
|
UTSW |
2 |
126,655,105 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4972:Trpm7
|
UTSW |
2 |
126,665,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Trpm7
|
UTSW |
2 |
126,638,256 (GRCm39) |
critical splice donor site |
probably null |
|
R5263:Trpm7
|
UTSW |
2 |
126,663,137 (GRCm39) |
missense |
probably benign |
0.34 |
R5361:Trpm7
|
UTSW |
2 |
126,671,161 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5377:Trpm7
|
UTSW |
2 |
126,684,775 (GRCm39) |
critical splice donor site |
probably null |
|
R5574:Trpm7
|
UTSW |
2 |
126,654,950 (GRCm39) |
missense |
probably benign |
|
R5782:Trpm7
|
UTSW |
2 |
126,639,634 (GRCm39) |
missense |
probably benign |
0.04 |
R5840:Trpm7
|
UTSW |
2 |
126,664,531 (GRCm39) |
nonsense |
probably null |
|
R6044:Trpm7
|
UTSW |
2 |
126,656,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Trpm7
|
UTSW |
2 |
126,679,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6196:Trpm7
|
UTSW |
2 |
126,667,559 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6457:Trpm7
|
UTSW |
2 |
126,649,214 (GRCm39) |
missense |
probably benign |
|
R6530:Trpm7
|
UTSW |
2 |
126,654,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6764:Trpm7
|
UTSW |
2 |
126,686,340 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6868:Trpm7
|
UTSW |
2 |
126,679,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Trpm7
|
UTSW |
2 |
126,668,685 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7402:Trpm7
|
UTSW |
2 |
126,641,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Trpm7
|
UTSW |
2 |
126,668,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R7486:Trpm7
|
UTSW |
2 |
126,673,115 (GRCm39) |
critical splice donor site |
probably null |
|
R7509:Trpm7
|
UTSW |
2 |
126,691,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7586:Trpm7
|
UTSW |
2 |
126,652,085 (GRCm39) |
missense |
probably benign |
|
R7774:Trpm7
|
UTSW |
2 |
126,655,158 (GRCm39) |
missense |
probably benign |
0.09 |
R7793:Trpm7
|
UTSW |
2 |
126,665,995 (GRCm39) |
nonsense |
probably null |
|
R7812:Trpm7
|
UTSW |
2 |
126,641,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Trpm7
|
UTSW |
2 |
126,639,418 (GRCm39) |
missense |
probably benign |
0.01 |
R7951:Trpm7
|
UTSW |
2 |
126,655,188 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7965:Trpm7
|
UTSW |
2 |
126,667,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R7992:Trpm7
|
UTSW |
2 |
126,667,454 (GRCm39) |
missense |
probably benign |
|
R8034:Trpm7
|
UTSW |
2 |
126,688,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R8199:Trpm7
|
UTSW |
2 |
126,691,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Trpm7
|
UTSW |
2 |
126,639,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R8405:Trpm7
|
UTSW |
2 |
126,658,755 (GRCm39) |
missense |
probably benign |
0.26 |
R8674:Trpm7
|
UTSW |
2 |
126,641,086 (GRCm39) |
unclassified |
probably benign |
|
R8742:Trpm7
|
UTSW |
2 |
126,667,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8754:Trpm7
|
UTSW |
2 |
126,664,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R8842:Trpm7
|
UTSW |
2 |
126,663,131 (GRCm39) |
missense |
probably benign |
0.05 |
R8850:Trpm7
|
UTSW |
2 |
126,652,100 (GRCm39) |
missense |
probably benign |
0.00 |
R8881:Trpm7
|
UTSW |
2 |
126,661,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R8898:Trpm7
|
UTSW |
2 |
126,664,661 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9339:Trpm7
|
UTSW |
2 |
126,665,906 (GRCm39) |
missense |
probably benign |
0.04 |
R9428:Trpm7
|
UTSW |
2 |
126,671,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R9446:Trpm7
|
UTSW |
2 |
126,672,185 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9568:Trpm7
|
UTSW |
2 |
126,664,510 (GRCm39) |
missense |
probably benign |
0.02 |
R9647:Trpm7
|
UTSW |
2 |
126,667,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R9678:Trpm7
|
UTSW |
2 |
126,686,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R9746:Trpm7
|
UTSW |
2 |
126,664,578 (GRCm39) |
missense |
possibly damaging |
0.47 |
X0026:Trpm7
|
UTSW |
2 |
126,671,210 (GRCm39) |
missense |
probably benign |
|
Z1088:Trpm7
|
UTSW |
2 |
126,639,201 (GRCm39) |
missense |
probably damaging |
1.00 |
|