Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
C |
9: 44,192,705 (GRCm39) |
K177E |
probably damaging |
Het |
Acvr1 |
T |
C |
2: 58,349,029 (GRCm39) |
T378A |
probably damaging |
Het |
Agtpbp1 |
A |
G |
13: 59,630,394 (GRCm39) |
V779A |
probably benign |
Het |
Alms1 |
C |
T |
6: 85,618,311 (GRCm39) |
Q2786* |
probably null |
Het |
Arhgef28 |
A |
C |
13: 98,097,968 (GRCm39) |
L882R |
probably damaging |
Het |
Cbx2 |
A |
G |
11: 118,919,775 (GRCm39) |
T447A |
probably benign |
Het |
Ch25h |
A |
G |
19: 34,451,863 (GRCm39) |
W222R |
probably damaging |
Het |
Chsy3 |
T |
G |
18: 59,309,469 (GRCm39) |
S241A |
probably damaging |
Het |
Cyfip1 |
T |
C |
7: 55,541,749 (GRCm39) |
S345P |
possibly damaging |
Het |
Cyp4a30b |
C |
A |
4: 115,316,063 (GRCm39) |
D291E |
probably damaging |
Het |
Dcstamp |
A |
G |
15: 39,622,936 (GRCm39) |
Y419C |
probably damaging |
Het |
Eif3d |
G |
A |
15: 77,846,047 (GRCm39) |
R359C |
probably damaging |
Het |
Elavl4 |
C |
A |
4: 110,063,800 (GRCm39) |
G267V |
probably benign |
Het |
Gars1 |
T |
C |
6: 55,042,592 (GRCm39) |
S442P |
probably damaging |
Het |
Gas6 |
C |
T |
8: 13,516,764 (GRCm39) |
R578Q |
probably null |
Het |
H4c4 |
C |
A |
13: 23,765,779 (GRCm39) |
N65K |
possibly damaging |
Het |
Ifitm6 |
T |
C |
7: 140,595,985 (GRCm39) |
I103V |
probably benign |
Het |
Igsf5 |
T |
A |
16: 96,187,731 (GRCm39) |
I241N |
possibly damaging |
Het |
Iqce |
A |
G |
5: 140,657,560 (GRCm39) |
|
probably null |
Het |
Khdc4 |
A |
C |
3: 88,600,403 (GRCm39) |
H164P |
probably damaging |
Het |
Kif20b |
C |
A |
19: 34,928,949 (GRCm39) |
Q1192K |
probably damaging |
Het |
Lap3 |
A |
G |
5: 45,662,093 (GRCm39) |
N298D |
probably benign |
Het |
Lca5 |
A |
T |
9: 83,283,796 (GRCm39) |
S246T |
probably damaging |
Het |
Mrps5 |
G |
A |
2: 127,444,355 (GRCm39) |
G330S |
probably damaging |
Het |
Myh15 |
C |
T |
16: 48,889,900 (GRCm39) |
R164C |
probably benign |
Het |
Myo19 |
C |
G |
11: 84,801,274 (GRCm39) |
P940R |
probably damaging |
Het |
Or10j7 |
T |
C |
1: 173,011,585 (GRCm39) |
R139G |
probably benign |
Het |
Or5b12b |
T |
C |
19: 12,861,751 (GRCm39) |
F169L |
probably benign |
Het |
Pcdh10 |
A |
G |
3: 45,338,603 (GRCm39) |
D920G |
probably damaging |
Het |
Pgm5 |
A |
T |
19: 24,801,815 (GRCm39) |
|
probably null |
Het |
Phactr4 |
T |
C |
4: 132,105,766 (GRCm39) |
E137G |
probably damaging |
Het |
Pkn1 |
C |
T |
8: 84,411,351 (GRCm39) |
V239M |
probably damaging |
Het |
Plcz1 |
T |
A |
6: 139,985,481 (GRCm39) |
D20V |
probably damaging |
Het |
Prkca |
A |
T |
11: 107,872,473 (GRCm39) |
I429N |
probably damaging |
Het |
Ptk2 |
A |
T |
15: 73,176,294 (GRCm39) |
Y251N |
probably damaging |
Het |
R3hdm2 |
T |
C |
10: 127,280,271 (GRCm39) |
F31S |
probably damaging |
Het |
Rab11fip1 |
T |
A |
8: 27,642,003 (GRCm39) |
E932V |
probably damaging |
Het |
Rilp |
A |
G |
11: 75,402,251 (GRCm39) |
Y250C |
probably damaging |
Het |
Slc14a2 |
T |
A |
18: 78,202,381 (GRCm39) |
D583V |
possibly damaging |
Het |
Slc30a4 |
A |
G |
2: 122,528,903 (GRCm39) |
I324T |
probably damaging |
Het |
Slc6a5 |
G |
A |
7: 49,577,321 (GRCm39) |
V326I |
probably benign |
Het |
Slco1c1 |
C |
T |
6: 141,513,222 (GRCm39) |
T617I |
probably damaging |
Het |
Sntg1 |
A |
G |
1: 8,484,495 (GRCm39) |
S442P |
possibly damaging |
Het |
Sys1 |
G |
T |
2: 164,306,429 (GRCm39) |
A128S |
possibly damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tmed5 |
A |
G |
5: 108,272,462 (GRCm39) |
I212T |
probably benign |
Het |
Tnks |
T |
C |
8: 35,432,819 (GRCm39) |
M1V |
probably null |
Het |
Trpa1 |
T |
C |
1: 14,968,492 (GRCm39) |
H452R |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,955,937 (GRCm39) |
V1133A |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,555,395 (GRCm39) |
I30537F |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,530,024 (GRCm39) |
V3271A |
possibly damaging |
Het |
Utp20 |
C |
G |
10: 88,587,329 (GRCm39) |
G2489R |
probably damaging |
Het |
Vmn1r70 |
A |
T |
7: 10,368,402 (GRCm39) |
S278C |
probably benign |
Het |
Wdpcp |
G |
A |
11: 21,661,732 (GRCm39) |
A335T |
probably benign |
Het |
Zc3h18 |
G |
T |
8: 123,113,659 (GRCm39) |
R217L |
probably damaging |
Het |
Zfp384 |
ACAGCAGCAGCAGCAGCAGCAGC |
ACAGCAGCAGCAGCAGCAGC |
6: 125,013,472 (GRCm39) |
|
probably benign |
Het |
Zfp955b |
C |
T |
17: 33,521,161 (GRCm39) |
T210I |
possibly damaging |
Het |
|
Other mutations in Sclt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01069:Sclt1
|
APN |
3 |
41,696,426 (GRCm39) |
unclassified |
probably benign |
|
IGL01106:Sclt1
|
APN |
3 |
41,629,754 (GRCm39) |
splice site |
probably benign |
|
IGL01368:Sclt1
|
APN |
3 |
41,665,610 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02001:Sclt1
|
APN |
3 |
41,636,156 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02897:Sclt1
|
APN |
3 |
41,629,822 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03066:Sclt1
|
APN |
3 |
41,672,278 (GRCm39) |
missense |
probably benign |
0.00 |
R0038:Sclt1
|
UTSW |
3 |
41,583,943 (GRCm39) |
splice site |
probably benign |
|
R0038:Sclt1
|
UTSW |
3 |
41,583,943 (GRCm39) |
splice site |
probably benign |
|
R0172:Sclt1
|
UTSW |
3 |
41,672,222 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0359:Sclt1
|
UTSW |
3 |
41,616,005 (GRCm39) |
critical splice donor site |
probably null |
|
R1281:Sclt1
|
UTSW |
3 |
41,602,055 (GRCm39) |
missense |
probably benign |
0.01 |
R1831:Sclt1
|
UTSW |
3 |
41,681,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R1832:Sclt1
|
UTSW |
3 |
41,681,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R1833:Sclt1
|
UTSW |
3 |
41,681,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R2027:Sclt1
|
UTSW |
3 |
41,685,323 (GRCm39) |
missense |
probably benign |
0.00 |
R4578:Sclt1
|
UTSW |
3 |
41,625,900 (GRCm39) |
nonsense |
probably null |
|
R5502:Sclt1
|
UTSW |
3 |
41,611,710 (GRCm39) |
missense |
probably benign |
0.28 |
R5601:Sclt1
|
UTSW |
3 |
41,685,354 (GRCm39) |
missense |
probably benign |
|
R5710:Sclt1
|
UTSW |
3 |
41,618,398 (GRCm39) |
nonsense |
probably null |
|
R6041:Sclt1
|
UTSW |
3 |
41,581,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R6274:Sclt1
|
UTSW |
3 |
41,583,951 (GRCm39) |
critical splice donor site |
probably null |
|
R6765:Sclt1
|
UTSW |
3 |
41,685,337 (GRCm39) |
missense |
unknown |
|
R7171:Sclt1
|
UTSW |
3 |
41,672,195 (GRCm39) |
missense |
probably benign |
0.00 |
R7489:Sclt1
|
UTSW |
3 |
41,584,032 (GRCm39) |
missense |
probably damaging |
0.99 |
R7988:Sclt1
|
UTSW |
3 |
41,617,889 (GRCm39) |
makesense |
probably null |
|
R8040:Sclt1
|
UTSW |
3 |
41,611,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8158:Sclt1
|
UTSW |
3 |
41,625,917 (GRCm39) |
missense |
probably benign |
0.36 |
R8383:Sclt1
|
UTSW |
3 |
41,696,450 (GRCm39) |
missense |
probably benign |
0.13 |
R8956:Sclt1
|
UTSW |
3 |
41,636,209 (GRCm39) |
missense |
probably benign |
0.01 |
R8971:Sclt1
|
UTSW |
3 |
41,681,541 (GRCm39) |
missense |
probably benign |
0.01 |
R9227:Sclt1
|
UTSW |
3 |
41,665,631 (GRCm39) |
missense |
probably benign |
0.01 |
R9230:Sclt1
|
UTSW |
3 |
41,665,631 (GRCm39) |
missense |
probably benign |
0.01 |
R9463:Sclt1
|
UTSW |
3 |
41,601,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Sclt1
|
UTSW |
3 |
41,629,837 (GRCm39) |
nonsense |
probably null |
|
|