Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
T |
5: 109,884,643 (GRCm39) |
I405K |
possibly damaging |
Het |
4930562C15Rik |
G |
A |
16: 4,682,227 (GRCm39) |
G180E |
probably damaging |
Het |
Adgrg6 |
A |
T |
10: 14,296,248 (GRCm39) |
W1079R |
probably damaging |
Het |
Arsa |
T |
C |
15: 89,357,478 (GRCm39) |
H495R |
probably benign |
Het |
Bptf |
T |
C |
11: 106,952,590 (GRCm39) |
T2088A |
probably damaging |
Het |
Brsk2 |
T |
C |
7: 141,541,643 (GRCm39) |
L152P |
probably damaging |
Het |
C8a |
T |
C |
4: 104,673,042 (GRCm39) |
|
probably benign |
Het |
Ccdc177 |
G |
A |
12: 80,804,816 (GRCm39) |
A486V |
unknown |
Het |
Cpa2 |
A |
G |
6: 30,544,180 (GRCm39) |
T38A |
probably benign |
Het |
Crim1 |
T |
G |
17: 78,545,236 (GRCm39) |
C133G |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,364,177 (GRCm39) |
|
probably null |
Het |
Ep400 |
G |
A |
5: 110,824,550 (GRCm39) |
Q2392* |
probably null |
Het |
Exoc2 |
C |
T |
13: 31,109,738 (GRCm39) |
S210N |
possibly damaging |
Het |
Gm7003 |
A |
G |
12: 113,766,847 (GRCm39) |
|
probably benign |
Het |
Hydin |
A |
G |
8: 111,245,863 (GRCm39) |
K2192R |
probably damaging |
Het |
Ica1l |
T |
C |
1: 60,053,010 (GRCm39) |
D176G |
probably damaging |
Het |
Ints10 |
G |
A |
8: 69,246,693 (GRCm39) |
E8K |
possibly damaging |
Het |
Itgb8 |
T |
C |
12: 119,131,740 (GRCm39) |
E635G |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,749,990 (GRCm39) |
|
probably benign |
Het |
Kng1 |
A |
G |
16: 22,897,887 (GRCm39) |
H429R |
probably benign |
Het |
Mcm3 |
T |
C |
1: 20,884,661 (GRCm39) |
I281V |
probably benign |
Het |
Msi1 |
T |
C |
5: 115,579,450 (GRCm39) |
S200P |
possibly damaging |
Het |
Nat3 |
T |
C |
8: 68,000,514 (GRCm39) |
L131P |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,104,177 (GRCm39) |
E1752G |
probably damaging |
Het |
Nnt |
C |
T |
13: 119,505,131 (GRCm39) |
A414T |
possibly damaging |
Het |
Nrp2 |
C |
T |
1: 62,786,370 (GRCm39) |
Q292* |
probably null |
Het |
Or51ah3 |
T |
A |
7: 103,209,780 (GRCm39) |
L32Q |
probably damaging |
Het |
Or52k2 |
G |
A |
7: 102,253,615 (GRCm39) |
G18D |
probably damaging |
Het |
Otop1 |
A |
T |
5: 38,457,059 (GRCm39) |
I273F |
probably damaging |
Het |
Phactr3 |
T |
A |
2: 177,920,694 (GRCm39) |
N177K |
probably benign |
Het |
Pik3c2b |
C |
T |
1: 133,027,440 (GRCm39) |
T1313I |
possibly damaging |
Het |
Pikfyve |
C |
A |
1: 65,274,192 (GRCm39) |
D677E |
probably damaging |
Het |
Poc1a |
T |
C |
9: 106,165,209 (GRCm39) |
F157L |
probably damaging |
Het |
Prodh2 |
G |
T |
7: 30,193,948 (GRCm39) |
R185L |
possibly damaging |
Het |
Rcc1 |
T |
C |
4: 132,061,497 (GRCm39) |
I350M |
probably benign |
Het |
Rhd |
G |
A |
4: 134,611,928 (GRCm39) |
A249T |
probably damaging |
Het |
Rtf2 |
A |
G |
2: 172,287,252 (GRCm39) |
Y57C |
probably damaging |
Het |
Shmt1 |
A |
G |
11: 60,685,725 (GRCm39) |
S284P |
possibly damaging |
Het |
Shpk |
T |
C |
11: 73,090,361 (GRCm39) |
V6A |
probably benign |
Het |
Slc4a5 |
T |
C |
6: 83,262,836 (GRCm39) |
V661A |
probably benign |
Het |
Tas1r2 |
C |
A |
4: 139,387,320 (GRCm39) |
Q231K |
probably benign |
Het |
Tcp11l1 |
T |
C |
2: 104,518,856 (GRCm39) |
Y280C |
probably benign |
Het |
Tnip1 |
T |
C |
11: 54,801,625 (GRCm39) |
|
probably benign |
Het |
Topbp1 |
T |
A |
9: 103,192,395 (GRCm39) |
D295E |
probably benign |
Het |
Unc79 |
C |
T |
12: 103,078,397 (GRCm39) |
L1521F |
probably damaging |
Het |
Usp10 |
T |
C |
8: 120,683,406 (GRCm39) |
I759T |
probably benign |
Het |
Vmn1r30 |
A |
T |
6: 58,412,759 (GRCm39) |
C24* |
probably null |
Het |
Vmn2r104 |
T |
A |
17: 20,250,343 (GRCm39) |
I643F |
probably damaging |
Het |
Wwc1 |
T |
A |
11: 35,758,199 (GRCm39) |
T716S |
probably damaging |
Het |
Zfp949 |
C |
T |
9: 88,451,537 (GRCm39) |
T369M |
probably benign |
Het |
Zhx3 |
A |
G |
2: 160,621,938 (GRCm39) |
V743A |
probably benign |
Het |
|
Other mutations in Spesp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02557:Spesp1
|
APN |
9 |
62,180,416 (GRCm39) |
missense |
possibly damaging |
0.85 |
BB001:Spesp1
|
UTSW |
9 |
62,180,733 (GRCm39) |
missense |
probably benign |
|
BB011:Spesp1
|
UTSW |
9 |
62,180,733 (GRCm39) |
missense |
probably benign |
|
R0735:Spesp1
|
UTSW |
9 |
62,179,967 (GRCm39) |
missense |
probably benign |
0.32 |
R1051:Spesp1
|
UTSW |
9 |
62,179,924 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2266:Spesp1
|
UTSW |
9 |
62,180,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R3153:Spesp1
|
UTSW |
9 |
62,189,376 (GRCm39) |
start gained |
probably benign |
|
R3154:Spesp1
|
UTSW |
9 |
62,189,376 (GRCm39) |
start gained |
probably benign |
|
R3737:Spesp1
|
UTSW |
9 |
62,180,318 (GRCm39) |
missense |
probably benign |
|
R4035:Spesp1
|
UTSW |
9 |
62,180,318 (GRCm39) |
missense |
probably benign |
|
R5425:Spesp1
|
UTSW |
9 |
62,189,331 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6278:Spesp1
|
UTSW |
9 |
62,179,921 (GRCm39) |
missense |
probably benign |
0.05 |
R6475:Spesp1
|
UTSW |
9 |
62,179,715 (GRCm39) |
missense |
probably benign |
0.33 |
R6941:Spesp1
|
UTSW |
9 |
62,180,152 (GRCm39) |
missense |
probably damaging |
0.98 |
R7003:Spesp1
|
UTSW |
9 |
62,189,302 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7611:Spesp1
|
UTSW |
9 |
62,179,987 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7924:Spesp1
|
UTSW |
9 |
62,180,733 (GRCm39) |
missense |
probably benign |
|
R8694:Spesp1
|
UTSW |
9 |
62,180,242 (GRCm39) |
missense |
probably benign |
0.00 |
R8993:Spesp1
|
UTSW |
9 |
62,180,552 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9044:Spesp1
|
UTSW |
9 |
62,180,623 (GRCm39) |
missense |
probably benign |
0.06 |
R9639:Spesp1
|
UTSW |
9 |
62,180,238 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9684:Spesp1
|
UTSW |
9 |
62,180,545 (GRCm39) |
missense |
probably damaging |
0.99 |
|