Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apof |
G |
A |
10: 128,105,568 (GRCm39) |
V241M |
probably benign |
Het |
Arhgef10 |
T |
A |
8: 15,004,505 (GRCm39) |
I91N |
probably damaging |
Het |
Arhgef17 |
G |
A |
7: 100,578,938 (GRCm39) |
T670I |
probably benign |
Het |
Barhl1 |
T |
C |
2: 28,805,468 (GRCm39) |
D75G |
probably benign |
Het |
Capn13 |
T |
C |
17: 73,638,108 (GRCm39) |
T432A |
probably benign |
Het |
Casd1 |
T |
A |
6: 4,640,951 (GRCm39) |
Y691N |
probably damaging |
Het |
Ccdc175 |
C |
A |
12: 72,191,557 (GRCm39) |
V340L |
probably benign |
Het |
Cdc5l |
A |
T |
17: 45,744,348 (GRCm39) |
M5K |
possibly damaging |
Het |
Cgn |
A |
G |
3: 94,686,544 (GRCm39) |
F253L |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,078,712 (GRCm39) |
K2003R |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,621,259 (GRCm39) |
|
probably null |
Het |
Dnah7a |
T |
C |
1: 53,472,163 (GRCm39) |
N3535D |
possibly damaging |
Het |
Exoc3 |
G |
A |
13: 74,341,232 (GRCm39) |
Q191* |
probably null |
Het |
Fstl5 |
T |
A |
3: 76,337,099 (GRCm39) |
Y219* |
probably null |
Het |
Gad2 |
T |
A |
2: 22,571,367 (GRCm39) |
L435Q |
probably benign |
Het |
Gcnt3 |
A |
G |
9: 69,941,983 (GRCm39) |
V195A |
probably damaging |
Het |
Haus6 |
G |
A |
4: 86,501,343 (GRCm39) |
Q843* |
probably null |
Het |
Hivep2 |
T |
A |
10: 14,006,395 (GRCm39) |
F998I |
probably damaging |
Het |
Klb |
A |
G |
5: 65,540,813 (GRCm39) |
N969D |
probably benign |
Het |
Klhl6 |
T |
A |
16: 19,776,001 (GRCm39) |
S186C |
possibly damaging |
Het |
Klk15 |
T |
C |
7: 43,587,805 (GRCm39) |
F78L |
probably benign |
Het |
Ldlr |
A |
G |
9: 21,651,124 (GRCm39) |
E514G |
possibly damaging |
Het |
Map9 |
T |
A |
3: 82,267,285 (GRCm39) |
|
probably benign |
Het |
Miga2 |
A |
T |
2: 30,274,022 (GRCm39) |
I99F |
possibly damaging |
Het |
Morc4 |
T |
C |
X: 138,758,605 (GRCm39) |
E189G |
probably benign |
Het |
Nhlrc3 |
A |
T |
3: 53,365,984 (GRCm39) |
Y170N |
possibly damaging |
Het |
Or3a1b |
G |
A |
11: 74,012,529 (GRCm39) |
R138Q |
probably benign |
Het |
Or4c111 |
A |
G |
2: 88,844,379 (GRCm39) |
F10L |
probably damaging |
Het |
Or51b6b |
A |
T |
7: 103,309,851 (GRCm39) |
V202D |
possibly damaging |
Het |
Or52u1 |
A |
T |
7: 104,237,940 (GRCm39) |
R310W |
probably benign |
Het |
Or5o1 |
T |
A |
X: 48,815,939 (GRCm39) |
N291Y |
probably damaging |
Het |
Or5w15 |
T |
C |
2: 87,568,506 (GRCm39) |
Q54R |
probably benign |
Het |
Or8g32 |
A |
C |
9: 39,305,981 (GRCm39) |
K295T |
probably damaging |
Het |
Pkd1l1 |
G |
A |
11: 8,784,793 (GRCm39) |
T1997I |
probably benign |
Het |
Poln |
A |
G |
5: 34,274,206 (GRCm39) |
S377P |
probably benign |
Het |
Rab22a |
T |
A |
2: 173,503,265 (GRCm39) |
V26E |
probably damaging |
Het |
Rhbdl3 |
T |
C |
11: 80,244,439 (GRCm39) |
V382A |
possibly damaging |
Het |
Slitrk3 |
G |
T |
3: 72,957,723 (GRCm39) |
Q350K |
probably benign |
Het |
Sult1d1 |
A |
T |
5: 87,707,738 (GRCm39) |
Y127* |
probably null |
Het |
Vmn1r73 |
A |
T |
7: 11,490,527 (GRCm39) |
Y115F |
probably benign |
Het |
Zfp128 |
T |
A |
7: 12,624,314 (GRCm39) |
D227E |
probably benign |
Het |
|
Other mutations in Hsf5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00514:Hsf5
|
APN |
11 |
87,513,922 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01726:Hsf5
|
APN |
11 |
87,526,951 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02480:Hsf5
|
APN |
11 |
87,522,483 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02572:Hsf5
|
APN |
11 |
87,522,521 (GRCm39) |
splice site |
probably benign |
|
R0015:Hsf5
|
UTSW |
11 |
87,548,161 (GRCm39) |
missense |
probably benign |
|
R0015:Hsf5
|
UTSW |
11 |
87,548,161 (GRCm39) |
missense |
probably benign |
|
R1381:Hsf5
|
UTSW |
11 |
87,528,995 (GRCm39) |
missense |
probably benign |
|
R1807:Hsf5
|
UTSW |
11 |
87,548,168 (GRCm39) |
missense |
probably benign |
0.04 |
R1838:Hsf5
|
UTSW |
11 |
87,526,881 (GRCm39) |
missense |
probably benign |
0.45 |
R2187:Hsf5
|
UTSW |
11 |
87,529,010 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3930:Hsf5
|
UTSW |
11 |
87,522,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R3931:Hsf5
|
UTSW |
11 |
87,522,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4420:Hsf5
|
UTSW |
11 |
87,548,130 (GRCm39) |
missense |
probably benign |
0.02 |
R4423:Hsf5
|
UTSW |
11 |
87,522,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R4744:Hsf5
|
UTSW |
11 |
87,513,617 (GRCm39) |
missense |
probably benign |
0.02 |
R4795:Hsf5
|
UTSW |
11 |
87,526,446 (GRCm39) |
missense |
probably benign |
0.18 |
R5862:Hsf5
|
UTSW |
11 |
87,513,817 (GRCm39) |
missense |
probably damaging |
0.96 |
R6232:Hsf5
|
UTSW |
11 |
87,508,120 (GRCm39) |
missense |
probably benign |
0.05 |
R6234:Hsf5
|
UTSW |
11 |
87,508,120 (GRCm39) |
missense |
probably benign |
0.05 |
R6609:Hsf5
|
UTSW |
11 |
87,526,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R7821:Hsf5
|
UTSW |
11 |
87,528,954 (GRCm39) |
missense |
probably benign |
0.04 |
R7989:Hsf5
|
UTSW |
11 |
87,526,450 (GRCm39) |
missense |
probably benign |
0.07 |
R9299:Hsf5
|
UTSW |
11 |
87,526,770 (GRCm39) |
missense |
probably benign |
|
R9419:Hsf5
|
UTSW |
11 |
87,528,935 (GRCm39) |
missense |
probably benign |
0.02 |
R9752:Hsf5
|
UTSW |
11 |
87,513,709 (GRCm39) |
missense |
probably benign |
0.22 |
Z1177:Hsf5
|
UTSW |
11 |
87,528,959 (GRCm39) |
nonsense |
probably null |
|
|