Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833439L19Rik |
A |
G |
13: 54,701,057 (GRCm39) |
S174P |
probably damaging |
Het |
4931414P19Rik |
T |
C |
14: 54,823,168 (GRCm39) |
E343G |
probably damaging |
Het |
Abca14 |
T |
C |
7: 119,851,497 (GRCm39) |
V825A |
probably damaging |
Het |
Abca8b |
G |
T |
11: 109,827,210 (GRCm39) |
T1466K |
possibly damaging |
Het |
Adcy8 |
A |
G |
15: 64,678,553 (GRCm39) |
S467P |
probably damaging |
Het |
Agbl4 |
T |
C |
4: 110,976,237 (GRCm39) |
V198A |
possibly damaging |
Het |
Agpat4 |
A |
G |
17: 12,417,699 (GRCm39) |
K80R |
probably benign |
Het |
Akap8 |
T |
C |
17: 32,535,208 (GRCm39) |
T269A |
probably benign |
Het |
Ankhd1 |
A |
T |
18: 36,758,080 (GRCm39) |
I925F |
possibly damaging |
Het |
Aste1 |
A |
G |
9: 105,282,203 (GRCm39) |
Y57C |
probably damaging |
Het |
Axdnd1 |
A |
G |
1: 156,247,980 (GRCm39) |
S7P |
possibly damaging |
Het |
BC051019 |
T |
A |
7: 109,319,789 (GRCm39) |
R91S |
probably null |
Het |
Cavin2 |
C |
A |
1: 51,340,398 (GRCm39) |
N358K |
probably benign |
Het |
Cd2 |
T |
C |
3: 101,190,355 (GRCm39) |
N196S |
probably benign |
Het |
Clca3a1 |
C |
T |
3: 144,436,483 (GRCm39) |
V867I |
probably benign |
Het |
Col6a4 |
T |
A |
9: 105,952,262 (GRCm39) |
K545N |
probably damaging |
Het |
Cps1 |
T |
A |
1: 67,268,679 (GRCm39) |
|
probably null |
Het |
Cyp2c65 |
A |
T |
19: 39,076,009 (GRCm39) |
|
probably null |
Het |
Dcaf6 |
T |
C |
1: 165,157,572 (GRCm39) |
D856G |
possibly damaging |
Het |
Epcam |
T |
C |
17: 87,949,580 (GRCm39) |
I181T |
probably damaging |
Het |
Esrp2 |
A |
G |
8: 106,859,061 (GRCm39) |
S562P |
probably damaging |
Het |
Fcgbpl1 |
A |
C |
7: 27,856,383 (GRCm39) |
I2057L |
probably benign |
Het |
Ffar4 |
A |
G |
19: 38,085,627 (GRCm39) |
D18G |
probably benign |
Het |
Gen1 |
C |
T |
12: 11,296,347 (GRCm39) |
V337I |
probably damaging |
Het |
Gimap8 |
C |
T |
6: 48,633,581 (GRCm39) |
P467S |
possibly damaging |
Het |
Gnl3 |
T |
A |
14: 30,738,803 (GRCm39) |
H82L |
possibly damaging |
Het |
Grid2 |
T |
C |
6: 64,053,862 (GRCm39) |
S354P |
probably benign |
Het |
Ighmbp2 |
T |
A |
19: 3,315,084 (GRCm39) |
T779S |
possibly damaging |
Het |
Ints15 |
C |
T |
5: 143,293,443 (GRCm39) |
E345K |
possibly damaging |
Het |
Kif19a |
C |
A |
11: 114,673,923 (GRCm39) |
T348N |
probably damaging |
Het |
Lrrc15 |
T |
A |
16: 30,092,172 (GRCm39) |
N389I |
probably damaging |
Het |
Mrps26 |
A |
G |
2: 130,405,886 (GRCm39) |
Y63C |
probably damaging |
Het |
Myd88 |
C |
A |
9: 119,166,889 (GRCm39) |
V223F |
possibly damaging |
Het |
Nox4 |
T |
A |
7: 87,025,450 (GRCm39) |
W526R |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,185,838 (GRCm39) |
N300K |
probably damaging |
Het |
Nsmf |
T |
C |
2: 24,950,464 (GRCm39) |
|
probably benign |
Het |
Patl2 |
A |
C |
2: 121,954,283 (GRCm39) |
H429Q |
probably benign |
Het |
Pcdhb12 |
A |
T |
18: 37,568,907 (GRCm39) |
K18* |
probably null |
Het |
Peg10 |
T |
A |
6: 4,754,511 (GRCm39) |
D97E |
probably benign |
Het |
Runx1t1 |
C |
T |
4: 13,846,830 (GRCm39) |
Q205* |
probably null |
Het |
Selenon |
T |
C |
4: 134,275,284 (GRCm39) |
K138R |
probably damaging |
Het |
Slc13a3 |
T |
C |
2: 165,262,000 (GRCm39) |
E369G |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,248,190 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
A |
T |
7: 27,068,816 (GRCm39) |
M499K |
probably damaging |
Het |
Sra1 |
A |
T |
18: 36,803,012 (GRCm39) |
|
probably benign |
Het |
Stra6 |
T |
C |
9: 58,048,429 (GRCm39) |
L174P |
probably damaging |
Het |
Syngr1 |
T |
C |
15: 80,000,086 (GRCm39) |
Y66H |
probably damaging |
Het |
Synpo |
G |
T |
18: 60,735,831 (GRCm39) |
S466* |
probably null |
Het |
Tenm3 |
T |
A |
8: 48,795,343 (GRCm39) |
M595L |
probably benign |
Het |
Tnks |
T |
C |
8: 35,308,963 (GRCm39) |
T1099A |
probably benign |
Het |
Tram1l1 |
G |
T |
3: 124,115,400 (GRCm39) |
V187F |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,965,639 (GRCm39) |
E529G |
probably benign |
Het |
Virma |
T |
C |
4: 11,519,392 (GRCm39) |
Y880H |
probably benign |
Het |
Vmn1r214 |
C |
T |
13: 23,219,571 (GRCm39) |
T355I |
possibly damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,598,205 (GRCm39) |
K784R |
possibly damaging |
Het |
Wrap53 |
C |
T |
11: 69,453,273 (GRCm39) |
W389* |
probably null |
Het |
Zfp748 |
A |
G |
13: 67,689,638 (GRCm39) |
S541P |
probably damaging |
Het |
|
Other mutations in Usp17la |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Usp17la
|
APN |
7 |
104,510,522 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01482:Usp17la
|
APN |
7 |
104,508,600 (GRCm39) |
start codon destroyed |
probably benign |
0.28 |
IGL02236:Usp17la
|
APN |
7 |
104,510,353 (GRCm39) |
nonsense |
probably null |
|
IGL03239:Usp17la
|
APN |
7 |
104,509,827 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0512:Usp17la
|
UTSW |
7 |
104,510,246 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1632:Usp17la
|
UTSW |
7 |
104,510,118 (GRCm39) |
missense |
probably benign |
0.02 |
R1828:Usp17la
|
UTSW |
7 |
104,510,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Usp17la
|
UTSW |
7 |
104,509,953 (GRCm39) |
missense |
probably benign |
0.11 |
R1976:Usp17la
|
UTSW |
7 |
104,509,527 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2058:Usp17la
|
UTSW |
7 |
104,510,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Usp17la
|
UTSW |
7 |
104,510,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R2078:Usp17la
|
UTSW |
7 |
104,508,600 (GRCm39) |
start codon destroyed |
probably benign |
0.28 |
R2197:Usp17la
|
UTSW |
7 |
104,509,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R3610:Usp17la
|
UTSW |
7 |
104,510,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Usp17la
|
UTSW |
7 |
104,510,937 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4480:Usp17la
|
UTSW |
7 |
104,509,897 (GRCm39) |
missense |
probably benign |
0.15 |
R4633:Usp17la
|
UTSW |
7 |
104,509,428 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4701:Usp17la
|
UTSW |
7 |
104,509,856 (GRCm39) |
nonsense |
probably null |
|
R4907:Usp17la
|
UTSW |
7 |
104,510,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Usp17la
|
UTSW |
7 |
104,510,330 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5313:Usp17la
|
UTSW |
7 |
104,510,457 (GRCm39) |
missense |
probably benign |
0.00 |
R6269:Usp17la
|
UTSW |
7 |
104,509,557 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7054:Usp17la
|
UTSW |
7 |
104,510,514 (GRCm39) |
missense |
probably benign |
0.38 |
R7395:Usp17la
|
UTSW |
7 |
104,510,792 (GRCm39) |
missense |
probably benign |
0.30 |
R7570:Usp17la
|
UTSW |
7 |
104,509,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R7633:Usp17la
|
UTSW |
7 |
104,510,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7641:Usp17la
|
UTSW |
7 |
104,510,654 (GRCm39) |
nonsense |
probably null |
|
R7674:Usp17la
|
UTSW |
7 |
104,510,654 (GRCm39) |
nonsense |
probably null |
|
R8098:Usp17la
|
UTSW |
7 |
104,510,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Usp17la
|
UTSW |
7 |
104,510,307 (GRCm39) |
missense |
probably benign |
0.07 |
R9416:Usp17la
|
UTSW |
7 |
104,508,531 (GRCm39) |
start gained |
probably benign |
|
R9739:Usp17la
|
UTSW |
7 |
104,510,736 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9786:Usp17la
|
UTSW |
7 |
104,510,864 (GRCm39) |
missense |
probably benign |
0.32 |
X0062:Usp17la
|
UTSW |
7 |
104,510,685 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Usp17la
|
UTSW |
7 |
104,510,233 (GRCm39) |
nonsense |
probably null |
|
|