Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
TGTTGATCCATA |
T |
2: 69,154,216 (GRCm39) |
|
probably null |
Het |
Abcb11 |
GTTGATCCATACA |
G |
2: 69,154,217 (GRCm39) |
|
probably benign |
Het |
Abcc10 |
T |
C |
17: 46,634,999 (GRCm39) |
T335A |
probably benign |
Het |
Actr3b |
T |
C |
5: 26,036,657 (GRCm39) |
Y245H |
probably benign |
Het |
Afm |
G |
A |
5: 90,695,727 (GRCm39) |
M411I |
probably benign |
Het |
Ahr |
T |
C |
12: 35,554,169 (GRCm39) |
N650S |
possibly damaging |
Het |
Ap5m1 |
A |
G |
14: 49,311,232 (GRCm39) |
R101G |
probably benign |
Het |
Armcx5 |
AGACAAAGCTAAAGAGGTCTGTGTCAAATCCAGGGCTGGGGACAAAGCTAAAGAGGTCTGTGTCAAATCCAGGGCTGGGGACAAAGCTA |
AGACAAAGCTAAAGAGGTCTGTGTCAAATCCAGGGCTGGGGACAAAGCTA |
X: 134,646,453 (GRCm39) |
|
probably benign |
Het |
Atp13a4 |
T |
C |
16: 29,215,284 (GRCm39) |
Q1151R |
|
Het |
Bcl9 |
A |
G |
3: 97,112,567 (GRCm39) |
V1296A |
possibly damaging |
Het |
Bsn |
A |
C |
9: 107,989,065 (GRCm39) |
M2229R |
probably damaging |
Het |
Cfap74 |
T |
C |
4: 155,514,351 (GRCm39) |
V529A |
|
Het |
Clip1 |
C |
T |
5: 123,760,861 (GRCm39) |
V767M |
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,766,382 (GRCm39) |
I1846T |
possibly damaging |
Het |
Crisp1 |
A |
T |
17: 40,618,656 (GRCm39) |
D68E |
probably benign |
Het |
Csmd1 |
A |
T |
8: 17,584,935 (GRCm39) |
L19Q |
possibly damaging |
Het |
Cul7 |
T |
C |
17: 46,968,931 (GRCm39) |
I892T |
probably benign |
Het |
Efcab3 |
A |
T |
11: 104,889,061 (GRCm39) |
Y4159F |
probably benign |
Het |
Elavl3 |
G |
A |
9: 21,929,846 (GRCm39) |
R353C |
probably damaging |
Het |
Fam184a |
C |
A |
10: 53,509,802 (GRCm39) |
E126* |
probably null |
Het |
Fbxo3 |
A |
G |
2: 103,883,757 (GRCm39) |
D327G |
possibly damaging |
Het |
Galr1 |
T |
C |
18: 82,424,256 (GRCm39) |
N7S |
probably benign |
Het |
Glyatl3 |
T |
C |
17: 41,215,802 (GRCm39) |
T235A |
probably damaging |
Het |
Gm5145 |
A |
C |
17: 20,790,967 (GRCm39) |
Q115P |
probably benign |
Het |
Grm5 |
T |
C |
7: 87,780,069 (GRCm39) |
S1202P |
probably benign |
Het |
Itsn1 |
G |
A |
16: 91,615,446 (GRCm39) |
R397H |
unknown |
Het |
Jmjd1c |
A |
G |
10: 67,075,644 (GRCm39) |
N1837S |
probably damaging |
Het |
Jph3 |
A |
T |
8: 122,516,136 (GRCm39) |
|
probably null |
Het |
Kcna6 |
A |
G |
6: 126,715,761 (GRCm39) |
L376P |
probably damaging |
Het |
Kcne3 |
C |
G |
7: 99,833,520 (GRCm39) |
R46G |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 180,722,934 (GRCm39) |
D842G |
probably damaging |
Het |
Klhl12 |
A |
T |
1: 134,386,219 (GRCm39) |
I4F |
probably benign |
Het |
Kpna1 |
T |
A |
16: 35,854,235 (GRCm39) |
I525N |
probably benign |
Het |
Krtap31-1 |
T |
C |
11: 99,798,949 (GRCm39) |
C51R |
possibly damaging |
Het |
Ms4a12 |
C |
T |
19: 11,207,723 (GRCm39) |
G61D |
possibly damaging |
Het |
Nol4 |
T |
C |
18: 22,956,400 (GRCm39) |
N115D |
|
Het |
Pcdh15 |
A |
G |
10: 74,289,827 (GRCm39) |
Y882C |
probably damaging |
Het |
Pde8b |
T |
A |
13: 95,244,202 (GRCm39) |
H79L |
probably benign |
Het |
Pdia2 |
T |
C |
17: 26,417,207 (GRCm39) |
E79G |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,590,167 (GRCm39) |
F90L |
probably damaging |
Het |
Pik3cd |
T |
A |
4: 149,741,726 (GRCm39) |
T407S |
probably benign |
Het |
Pkd1l2 |
G |
T |
8: 117,724,827 (GRCm39) |
F2361L |
possibly damaging |
Het |
Pla2g12b |
A |
T |
10: 59,246,816 (GRCm39) |
R77* |
probably null |
Het |
Ppfia2 |
A |
G |
10: 106,655,399 (GRCm39) |
Y322C |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,341,108 (GRCm39) |
Q382R |
possibly damaging |
Het |
Ptprq |
A |
G |
10: 107,546,484 (GRCm39) |
V270A |
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Robo2 |
T |
C |
16: 73,695,838 (GRCm39) |
E1431G |
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,764,027 (GRCm39) |
I253T |
possibly damaging |
Het |
Sox9 |
A |
C |
11: 112,675,635 (GRCm39) |
I275L |
probably benign |
Het |
Tlr4 |
A |
G |
4: 66,758,058 (GRCm39) |
I284V |
probably benign |
Het |
Unc13b |
A |
G |
4: 43,171,860 (GRCm39) |
D896G |
unknown |
Het |
Usp48 |
A |
T |
4: 137,371,739 (GRCm39) |
H955L |
probably damaging |
Het |
Vps54 |
T |
C |
11: 21,213,307 (GRCm39) |
I30T |
probably benign |
Het |
Zfp106 |
G |
A |
2: 120,366,096 (GRCm39) |
R59* |
probably null |
Het |
Zmym4 |
A |
T |
4: 126,783,332 (GRCm39) |
D1169E |
possibly damaging |
Het |
Zscan2 |
T |
A |
7: 80,525,448 (GRCm39) |
Y390N |
probably damaging |
Het |
|
Other mutations in Nudt16l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1547:Nudt16l2
|
UTSW |
9 |
105,021,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R4258:Nudt16l2
|
UTSW |
9 |
105,020,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R4675:Nudt16l2
|
UTSW |
9 |
105,021,647 (GRCm39) |
missense |
probably benign |
0.19 |
R4754:Nudt16l2
|
UTSW |
9 |
105,021,592 (GRCm39) |
missense |
probably benign |
0.01 |
R4890:Nudt16l2
|
UTSW |
9 |
105,021,786 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6680:Nudt16l2
|
UTSW |
9 |
105,020,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R6703:Nudt16l2
|
UTSW |
9 |
105,021,758 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7170:Nudt16l2
|
UTSW |
9 |
105,020,600 (GRCm39) |
splice site |
probably null |
|
R7397:Nudt16l2
|
UTSW |
9 |
105,021,621 (GRCm39) |
missense |
probably damaging |
0.97 |
R8828:Nudt16l2
|
UTSW |
9 |
105,021,648 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Nudt16l2
|
UTSW |
9 |
105,021,659 (GRCm39) |
missense |
possibly damaging |
0.80 |
|