Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
A |
5: 8,878,870 (GRCm39) |
N751K |
possibly damaging |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Baz1a |
A |
T |
12: 54,941,816 (GRCm39) |
Y1466* |
probably null |
Het |
Ccng1 |
G |
A |
11: 40,642,096 (GRCm39) |
H229Y |
probably benign |
Het |
Cenpn |
C |
A |
8: 117,663,976 (GRCm39) |
T256N |
probably benign |
Het |
Ciart |
A |
G |
3: 95,788,629 (GRCm39) |
V70A |
possibly damaging |
Het |
Clcc1 |
A |
G |
3: 108,568,774 (GRCm39) |
N36S |
probably damaging |
Het |
Dmrt1 |
T |
A |
19: 25,523,245 (GRCm39) |
S199T |
possibly damaging |
Het |
Dmrt3 |
T |
C |
19: 25,588,272 (GRCm39) |
V37A |
possibly damaging |
Het |
Dock1 |
T |
A |
7: 134,346,786 (GRCm39) |
D239E |
possibly damaging |
Het |
Dyrk3 |
A |
G |
1: 131,063,995 (GRCm39) |
|
probably null |
Het |
Esyt1 |
T |
C |
10: 128,347,354 (GRCm39) |
E1057G |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,818,793 (GRCm39) |
E4842G |
possibly damaging |
Het |
Gadd45b |
G |
A |
10: 80,766,984 (GRCm39) |
V90I |
probably benign |
Het |
Gfi1 |
T |
A |
5: 107,871,667 (GRCm39) |
H79L |
probably damaging |
Het |
Golm2 |
T |
C |
2: 121,737,242 (GRCm39) |
V261A |
probably benign |
Het |
Idh2 |
T |
C |
7: 79,748,001 (GRCm39) |
H233R |
probably benign |
Het |
Itsn2 |
G |
A |
12: 4,714,553 (GRCm39) |
A950T |
probably benign |
Het |
Kcna5 |
A |
G |
6: 126,510,517 (GRCm39) |
L537P |
probably benign |
Het |
Krtap5-4 |
C |
T |
7: 141,857,671 (GRCm39) |
Q114* |
probably null |
Het |
Loxl3 |
T |
C |
6: 83,027,790 (GRCm39) |
F734S |
possibly damaging |
Het |
Lpcat1 |
C |
T |
13: 73,659,498 (GRCm39) |
T420I |
probably damaging |
Het |
Lrch3 |
A |
T |
16: 32,826,083 (GRCm39) |
D720V |
possibly damaging |
Het |
Lrrk1 |
T |
C |
7: 65,915,222 (GRCm39) |
D1622G |
possibly damaging |
Het |
Meioc |
G |
C |
11: 102,567,569 (GRCm39) |
A788P |
probably damaging |
Het |
Mmp1a |
A |
T |
9: 7,467,236 (GRCm39) |
T271S |
possibly damaging |
Het |
Nrp2 |
C |
T |
1: 62,784,567 (GRCm39) |
R239C |
probably damaging |
Het |
Ntrk3 |
T |
A |
7: 78,103,076 (GRCm39) |
D408V |
probably benign |
Het |
Odf1 |
A |
G |
15: 38,226,840 (GRCm39) |
I247V |
unknown |
Het |
Or14j5 |
A |
T |
17: 38,161,693 (GRCm39) |
D70V |
probably damaging |
Het |
Or8k39 |
A |
G |
2: 86,563,848 (GRCm39) |
L36P |
probably damaging |
Het |
Pcsk1 |
T |
C |
13: 75,274,958 (GRCm39) |
S516P |
probably benign |
Het |
Phactr3 |
A |
C |
2: 177,974,737 (GRCm39) |
R523S |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,294,293 (GRCm39) |
D1411G |
probably damaging |
Het |
Ppcs |
A |
T |
4: 119,276,262 (GRCm39) |
S281T |
probably benign |
Het |
Prkcg |
A |
G |
7: 3,362,708 (GRCm39) |
D294G |
probably benign |
Het |
Pspc1 |
G |
A |
14: 57,009,304 (GRCm39) |
Q177* |
probably null |
Het |
Rbm33 |
G |
A |
5: 28,599,606 (GRCm39) |
G185R |
|
Het |
Rps6ka5 |
T |
C |
12: 100,544,048 (GRCm39) |
E350G |
probably damaging |
Het |
Satb2 |
A |
G |
1: 56,910,917 (GRCm39) |
S243P |
probably benign |
Het |
Serinc5 |
T |
C |
13: 92,797,699 (GRCm39) |
|
probably null |
Het |
Sgce |
T |
C |
6: 4,691,636 (GRCm39) |
D313G |
probably damaging |
Het |
Sntg1 |
C |
T |
1: 8,433,794 (GRCm39) |
V486I |
probably damaging |
Het |
Stxbp5 |
A |
G |
10: 9,692,046 (GRCm39) |
V366A |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,061,687 (GRCm39) |
S2610P |
possibly damaging |
Het |
Tlr3 |
G |
A |
8: 45,853,819 (GRCm39) |
T167M |
not run |
Het |
Tmem200a |
A |
G |
10: 25,869,904 (GRCm39) |
S122P |
probably damaging |
Het |
Tmprss15 |
C |
T |
16: 78,887,751 (GRCm39) |
V19M |
probably damaging |
Het |
Tnks2 |
T |
A |
19: 36,829,901 (GRCm39) |
M194K |
probably benign |
Het |
Trav14d-3-dv8 |
A |
C |
14: 53,316,224 (GRCm39) |
Q28P |
probably damaging |
Het |
Trpm5 |
T |
C |
7: 142,634,106 (GRCm39) |
E700G |
probably benign |
Het |
Ubqln3 |
T |
A |
7: 103,791,797 (GRCm39) |
I98L |
probably benign |
Het |
Uso1 |
A |
T |
5: 92,314,439 (GRCm39) |
E115D |
probably benign |
Het |
Vmn1r28 |
T |
C |
6: 58,242,178 (GRCm39) |
V7A |
probably benign |
Het |
|
Other mutations in Psg28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00673:Psg28
|
APN |
7 |
18,161,816 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01118:Psg28
|
APN |
7 |
18,162,017 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01606:Psg28
|
APN |
7 |
18,164,296 (GRCm39) |
missense |
probably benign |
0.01 |
R0276:Psg28
|
UTSW |
7 |
18,164,321 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Psg28
|
UTSW |
7 |
18,160,098 (GRCm39) |
missense |
probably benign |
0.02 |
R0713:Psg28
|
UTSW |
7 |
18,156,999 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1454:Psg28
|
UTSW |
7 |
18,161,889 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1725:Psg28
|
UTSW |
7 |
18,161,936 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2176:Psg28
|
UTSW |
7 |
18,161,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Psg28
|
UTSW |
7 |
18,160,348 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4520:Psg28
|
UTSW |
7 |
18,156,826 (GRCm39) |
missense |
probably benign |
0.00 |
R5010:Psg28
|
UTSW |
7 |
18,161,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Psg28
|
UTSW |
7 |
18,164,373 (GRCm39) |
missense |
probably benign |
0.15 |
R5772:Psg28
|
UTSW |
7 |
18,164,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Psg28
|
UTSW |
7 |
18,160,107 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6039:Psg28
|
UTSW |
7 |
18,160,107 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6046:Psg28
|
UTSW |
7 |
18,160,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R6275:Psg28
|
UTSW |
7 |
18,164,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:Psg28
|
UTSW |
7 |
18,164,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R6928:Psg28
|
UTSW |
7 |
18,157,003 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7197:Psg28
|
UTSW |
7 |
18,164,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R7237:Psg28
|
UTSW |
7 |
18,161,769 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7859:Psg28
|
UTSW |
7 |
18,160,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7863:Psg28
|
UTSW |
7 |
18,162,042 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7993:Psg28
|
UTSW |
7 |
18,160,401 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8115:Psg28
|
UTSW |
7 |
18,164,311 (GRCm39) |
missense |
probably benign |
0.15 |
R8247:Psg28
|
UTSW |
7 |
18,156,864 (GRCm39) |
missense |
probably benign |
0.01 |
R8984:Psg28
|
UTSW |
7 |
18,156,981 (GRCm39) |
missense |
probably damaging |
0.97 |
R9160:Psg28
|
UTSW |
7 |
18,164,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R9266:Psg28
|
UTSW |
7 |
18,161,752 (GRCm39) |
missense |
probably benign |
0.01 |
R9336:Psg28
|
UTSW |
7 |
18,156,905 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9758:Psg28
|
UTSW |
7 |
18,164,602 (GRCm39) |
missense |
probably benign |
0.18 |
R9758:Psg28
|
UTSW |
7 |
18,156,887 (GRCm39) |
nonsense |
probably null |
|
R9782:Psg28
|
UTSW |
7 |
18,164,331 (GRCm39) |
missense |
probably benign |
0.00 |
RF016:Psg28
|
UTSW |
7 |
18,156,847 (GRCm39) |
missense |
probably damaging |
0.97 |
X0020:Psg28
|
UTSW |
7 |
18,161,864 (GRCm39) |
missense |
possibly damaging |
0.95 |
|