Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
C |
6: 128,522,000 (GRCm39) |
E1274G |
possibly damaging |
Het |
Abi3bp |
A |
G |
16: 56,472,563 (GRCm39) |
E424G |
probably damaging |
Het |
Ankrd10 |
A |
G |
8: 11,662,644 (GRCm39) |
I363T |
probably benign |
Het |
Ankrd12 |
A |
T |
17: 66,334,361 (GRCm39) |
N204K |
probably damaging |
Het |
Brca2 |
C |
A |
5: 150,463,098 (GRCm39) |
S954* |
probably null |
Het |
Col11a1 |
A |
C |
3: 114,001,872 (GRCm39) |
D432A |
possibly damaging |
Het |
Dagla |
G |
T |
19: 10,240,461 (GRCm39) |
D256E |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,713,720 (GRCm39) |
F230L |
probably benign |
Het |
Elp5 |
T |
C |
11: 69,861,388 (GRCm39) |
Q197R |
probably null |
Het |
Emilin2 |
A |
T |
17: 71,581,258 (GRCm39) |
D489E |
probably benign |
Het |
Entrep3 |
T |
C |
3: 89,091,754 (GRCm39) |
V87A |
probably damaging |
Het |
Ermp1 |
A |
G |
19: 29,623,365 (GRCm39) |
|
probably null |
Het |
Fam149a |
A |
G |
8: 45,794,321 (GRCm39) |
Y614H |
probably benign |
Het |
Fnbp1 |
T |
C |
2: 30,926,131 (GRCm39) |
|
probably null |
Het |
Gabrb3 |
T |
C |
7: 57,241,061 (GRCm39) |
F13S |
probably benign |
Het |
Hydin |
G |
A |
8: 111,320,452 (GRCm39) |
A4499T |
probably benign |
Het |
Islr2 |
A |
T |
9: 58,107,183 (GRCm39) |
C26S |
probably damaging |
Het |
Jup |
T |
A |
11: 100,263,287 (GRCm39) |
D696V |
probably benign |
Het |
Kcnq5 |
A |
C |
1: 21,605,392 (GRCm39) |
V171G |
probably damaging |
Het |
Kntc1 |
T |
G |
5: 123,914,680 (GRCm39) |
S667A |
possibly damaging |
Het |
Loxhd1 |
A |
G |
18: 77,418,755 (GRCm39) |
T293A |
possibly damaging |
Het |
Lrp1b |
C |
A |
2: 41,298,405 (GRCm39) |
C138F |
probably damaging |
Het |
Lrrc37 |
T |
A |
11: 103,427,426 (GRCm39) |
H1388L |
unknown |
Het |
Mctp2 |
A |
G |
7: 71,909,085 (GRCm39) |
I76T |
probably benign |
Het |
Or2z8 |
A |
G |
8: 72,812,028 (GRCm39) |
Y168C |
probably damaging |
Het |
Or5k16 |
T |
C |
16: 58,736,947 (GRCm39) |
D19G |
probably benign |
Het |
Pbx1 |
A |
G |
1: 168,018,841 (GRCm39) |
|
probably null |
Het |
Pelp1 |
A |
T |
11: 70,287,693 (GRCm39) |
W410R |
probably damaging |
Het |
Phaf1 |
T |
C |
8: 105,967,763 (GRCm39) |
L218P |
probably benign |
Het |
Pkd1 |
T |
C |
17: 24,806,971 (GRCm39) |
L3482P |
probably benign |
Het |
Plekhn1 |
C |
T |
4: 156,306,258 (GRCm39) |
G604E |
probably benign |
Het |
Ptpn22 |
A |
G |
3: 103,793,561 (GRCm39) |
T571A |
probably benign |
Het |
Qrsl1 |
A |
T |
10: 43,760,828 (GRCm39) |
S252T |
probably damaging |
Het |
Rab3gap2 |
T |
A |
1: 184,978,863 (GRCm39) |
M280K |
probably damaging |
Het |
Serpinh1 |
T |
C |
7: 98,996,206 (GRCm39) |
M293V |
probably benign |
Het |
Six4 |
G |
A |
12: 73,155,605 (GRCm39) |
T454I |
probably damaging |
Het |
Slc26a8 |
T |
A |
17: 28,866,973 (GRCm39) |
E585D |
probably benign |
Het |
Slc34a2 |
T |
G |
5: 53,224,910 (GRCm39) |
C350W |
probably damaging |
Het |
Slit2 |
T |
A |
5: 48,394,586 (GRCm39) |
|
probably null |
Het |
Trip11 |
G |
A |
12: 101,861,957 (GRCm39) |
Q203* |
probably null |
Het |
Usp38 |
A |
C |
8: 81,719,928 (GRCm39) |
S434A |
probably benign |
Het |
Zbtb16 |
A |
G |
9: 48,571,101 (GRCm39) |
F555S |
probably damaging |
Het |
Zfp141 |
A |
T |
7: 42,125,705 (GRCm39) |
S256T |
probably benign |
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 |
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 |
R6841:Trpm7
|
UTSW |
2 |
126,654,941 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|