Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,613,338 (GRCm39) |
S31P |
probably damaging |
Het |
Abca12 |
G |
T |
1: 71,283,999 (GRCm39) |
H2524Q |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,266,586 (GRCm39) |
V135A |
probably benign |
Het |
Actl11 |
T |
G |
9: 107,806,736 (GRCm39) |
L353R |
possibly damaging |
Het |
Adcy6 |
G |
T |
15: 98,496,379 (GRCm39) |
|
probably null |
Het |
B230104I21Rik |
A |
G |
4: 154,425,694 (GRCm39) |
I697T |
probably damaging |
Het |
BC061237 |
G |
A |
14: 44,738,700 (GRCm39) |
R33K |
possibly damaging |
Het |
Brf1 |
C |
A |
12: 112,963,964 (GRCm39) |
V5F |
possibly damaging |
Het |
Chmp2a |
C |
T |
7: 12,767,863 (GRCm39) |
A21T |
possibly damaging |
Het |
Cwh43 |
A |
G |
5: 73,610,417 (GRCm39) |
N607S |
probably benign |
Het |
Ddhd2 |
G |
A |
8: 26,231,688 (GRCm39) |
L445F |
possibly damaging |
Het |
Dicer1 |
C |
A |
12: 104,669,143 (GRCm39) |
D1180Y |
possibly damaging |
Het |
Dnaaf4 |
A |
T |
9: 72,867,909 (GRCm39) |
I57L |
probably damaging |
Het |
Dock5 |
A |
T |
14: 68,083,511 (GRCm39) |
S133T |
possibly damaging |
Het |
Efs |
A |
T |
14: 55,154,620 (GRCm39) |
C540S |
possibly damaging |
Het |
Ehd4 |
C |
T |
2: 119,921,973 (GRCm39) |
G428S |
probably benign |
Het |
Eml1 |
C |
T |
12: 108,504,476 (GRCm39) |
R812* |
probably null |
Het |
Enpp1 |
C |
T |
10: 24,530,786 (GRCm39) |
D557N |
possibly damaging |
Het |
Fn3krp |
A |
G |
11: 121,315,803 (GRCm39) |
T65A |
probably damaging |
Het |
Galnt5 |
A |
G |
2: 57,888,615 (GRCm39) |
R72G |
probably benign |
Het |
Gfod1 |
C |
T |
13: 43,354,336 (GRCm39) |
R213H |
possibly damaging |
Het |
Gm10518 |
A |
G |
1: 179,631,210 (GRCm39) |
|
probably benign |
Het |
Gm5431 |
A |
G |
11: 48,780,082 (GRCm39) |
F558S |
probably damaging |
Het |
Got1 |
C |
T |
19: 43,504,119 (GRCm39) |
|
probably null |
Het |
Gucy2g |
C |
T |
19: 55,226,191 (GRCm39) |
V242I |
probably benign |
Het |
Hdgfl2 |
T |
A |
17: 56,406,874 (GRCm39) |
V606E |
possibly damaging |
Het |
Hoxa3 |
T |
C |
6: 52,146,979 (GRCm39) |
|
probably benign |
Het |
Iqub |
T |
A |
6: 24,491,670 (GRCm39) |
I339L |
probably benign |
Het |
Kdm4c |
C |
T |
4: 74,263,720 (GRCm39) |
T668I |
probably benign |
Het |
Klhl32 |
T |
C |
4: 24,617,474 (GRCm39) |
I592V |
probably benign |
Het |
Mfsd12 |
G |
T |
10: 81,197,921 (GRCm39) |
M296I |
probably benign |
Het |
Mfsd4b4 |
C |
T |
10: 39,768,437 (GRCm39) |
A219T |
probably damaging |
Het |
Mrpl52 |
T |
C |
14: 54,664,414 (GRCm39) |
S9P |
possibly damaging |
Het |
Nbr1 |
A |
G |
11: 101,458,040 (GRCm39) |
Y273C |
possibly damaging |
Het |
Ncf4 |
G |
T |
15: 78,144,846 (GRCm39) |
G217V |
probably damaging |
Het |
Neo1 |
T |
C |
9: 58,897,668 (GRCm39) |
E96G |
probably benign |
Het |
Nid2 |
T |
A |
14: 19,818,344 (GRCm39) |
N279K |
probably damaging |
Het |
Nr5a2 |
A |
G |
1: 136,872,732 (GRCm39) |
Y56H |
probably damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,101,049 (GRCm39) |
T280A |
probably benign |
Het |
Or1o2 |
A |
G |
17: 37,542,434 (GRCm39) |
Y276H |
probably damaging |
Het |
Or2b28 |
T |
A |
13: 21,531,116 (GRCm39) |
I6N |
probably benign |
Het |
Or2w2 |
A |
G |
13: 21,758,426 (GRCm39) |
F67L |
probably benign |
Het |
Or55b10 |
A |
G |
7: 102,143,266 (GRCm39) |
S239P |
possibly damaging |
Het |
Or5b109 |
T |
C |
19: 13,212,393 (GRCm39) |
Y260H |
probably damaging |
Het |
Otog |
G |
A |
7: 45,895,707 (GRCm39) |
C107Y |
probably damaging |
Het |
Ptprn |
A |
G |
1: 75,230,766 (GRCm39) |
V565A |
probably benign |
Het |
Rbm6 |
T |
G |
9: 107,730,102 (GRCm39) |
D182A |
probably damaging |
Het |
Rhbg |
A |
G |
3: 88,151,859 (GRCm39) |
F400L |
probably benign |
Het |
Rpl22l1 |
T |
A |
3: 28,860,738 (GRCm39) |
N33K |
possibly damaging |
Het |
Rtp1 |
T |
A |
16: 23,249,959 (GRCm39) |
I108N |
probably damaging |
Het |
Sirpa |
C |
T |
2: 129,458,296 (GRCm39) |
T304I |
possibly damaging |
Het |
Slc22a29 |
A |
G |
19: 8,184,430 (GRCm39) |
I257T |
probably benign |
Het |
Slc41a1 |
T |
C |
1: 131,768,938 (GRCm39) |
I256T |
probably damaging |
Het |
Smg6 |
A |
G |
11: 75,033,674 (GRCm39) |
K1208R |
probably damaging |
Het |
Sorcs1 |
G |
T |
19: 50,210,633 (GRCm39) |
P744Q |
probably damaging |
Het |
Sptbn5 |
T |
C |
2: 119,900,943 (GRCm39) |
T213A |
probably benign |
Het |
St18 |
A |
G |
1: 6,872,936 (GRCm39) |
T224A |
probably benign |
Het |
Stat3 |
T |
C |
11: 100,785,655 (GRCm39) |
N465S |
probably damaging |
Het |
Stmn2 |
T |
A |
3: 8,610,636 (GRCm39) |
M40K |
probably benign |
Het |
Tespa1 |
A |
G |
10: 130,184,108 (GRCm39) |
D63G |
probably benign |
Het |
Thrb |
T |
A |
14: 18,008,674 (GRCm38) |
C133S |
probably damaging |
Het |
Tmem25 |
C |
T |
9: 44,707,780 (GRCm39) |
V172M |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trhde |
T |
A |
10: 114,636,754 (GRCm39) |
Y151F |
probably damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,280,229 (GRCm39) |
T912A |
probably damaging |
Het |
Unc79 |
C |
A |
12: 103,135,951 (GRCm39) |
A2269E |
probably damaging |
Het |
Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
Zfp758 |
T |
G |
17: 22,594,823 (GRCm39) |
S436R |
probably damaging |
Het |
Zfp791 |
G |
T |
8: 85,837,312 (GRCm39) |
T184K |
probably benign |
Het |
Znrf3 |
A |
G |
11: 5,231,062 (GRCm39) |
V817A |
probably benign |
Het |
|
Other mutations in Sema6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00324:Sema6b
|
APN |
17 |
56,437,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01102:Sema6b
|
APN |
17 |
56,439,761 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01533:Sema6b
|
APN |
17 |
56,436,499 (GRCm39) |
splice site |
probably benign |
|
IGL01611:Sema6b
|
APN |
17 |
56,436,969 (GRCm39) |
splice site |
probably null |
|
IGL01996:Sema6b
|
APN |
17 |
56,438,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02118:Sema6b
|
APN |
17 |
56,439,821 (GRCm39) |
missense |
probably benign |
|
R0010:Sema6b
|
UTSW |
17 |
56,431,105 (GRCm39) |
missense |
probably benign |
0.06 |
R0066:Sema6b
|
UTSW |
17 |
56,435,271 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0066:Sema6b
|
UTSW |
17 |
56,435,271 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0525:Sema6b
|
UTSW |
17 |
56,433,630 (GRCm39) |
missense |
probably damaging |
0.96 |
R0635:Sema6b
|
UTSW |
17 |
56,436,971 (GRCm39) |
critical splice donor site |
probably null |
|
R1129:Sema6b
|
UTSW |
17 |
56,431,347 (GRCm39) |
missense |
probably benign |
|
R2211:Sema6b
|
UTSW |
17 |
56,431,741 (GRCm39) |
missense |
probably benign |
0.00 |
R4081:Sema6b
|
UTSW |
17 |
56,435,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R5013:Sema6b
|
UTSW |
17 |
56,439,497 (GRCm39) |
critical splice donor site |
probably null |
|
R5296:Sema6b
|
UTSW |
17 |
56,434,091 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5314:Sema6b
|
UTSW |
17 |
56,435,413 (GRCm39) |
nonsense |
probably null |
|
R6317:Sema6b
|
UTSW |
17 |
56,431,047 (GRCm39) |
missense |
probably benign |
0.26 |
R6419:Sema6b
|
UTSW |
17 |
56,439,784 (GRCm39) |
nonsense |
probably null |
|
R7255:Sema6b
|
UTSW |
17 |
56,432,336 (GRCm39) |
missense |
probably benign |
0.01 |
R7289:Sema6b
|
UTSW |
17 |
56,432,573 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7805:Sema6b
|
UTSW |
17 |
56,438,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Sema6b
|
UTSW |
17 |
56,435,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Sema6b
|
UTSW |
17 |
56,431,803 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8305:Sema6b
|
UTSW |
17 |
56,434,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R9502:Sema6b
|
UTSW |
17 |
56,439,500 (GRCm39) |
missense |
probably benign |
0.13 |
|