Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh1a2 |
T |
C |
9: 71,169,049 (GRCm39) |
I177T |
probably damaging |
Het |
Aopep |
T |
A |
13: 63,388,139 (GRCm39) |
F39L |
probably damaging |
Het |
Arl4c |
A |
G |
1: 88,629,350 (GRCm39) |
S13P |
possibly damaging |
Het |
Bst1 |
G |
T |
5: 43,976,306 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
G |
A |
14: 55,741,302 (GRCm39) |
R1029Q |
probably benign |
Het |
Cflar |
A |
G |
1: 58,780,202 (GRCm39) |
T269A |
probably benign |
Het |
Clcnka |
T |
A |
4: 141,121,798 (GRCm39) |
Y236F |
probably damaging |
Het |
Clmp |
T |
A |
9: 40,682,405 (GRCm39) |
I63N |
probably damaging |
Het |
Cln6 |
T |
C |
9: 62,751,908 (GRCm39) |
L44P |
probably damaging |
Het |
Col5a3 |
C |
T |
9: 20,718,915 (GRCm39) |
A280T |
unknown |
Het |
Dact2 |
A |
G |
17: 14,417,567 (GRCm39) |
L211P |
probably damaging |
Het |
Dclk2 |
G |
T |
3: 86,813,272 (GRCm39) |
Q225K |
probably damaging |
Het |
Ddx60 |
T |
C |
8: 62,453,616 (GRCm39) |
F1245S |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,835,259 (GRCm39) |
K3540E |
unknown |
Het |
Eif3i |
T |
C |
4: 129,487,145 (GRCm39) |
N240S |
probably benign |
Het |
Enpp1 |
T |
C |
10: 24,536,152 (GRCm39) |
Y416C |
probably damaging |
Het |
Epb42 |
T |
A |
2: 120,854,889 (GRCm39) |
R565S |
probably benign |
Het |
Eral1 |
G |
A |
11: 77,966,609 (GRCm39) |
P217L |
probably benign |
Het |
Fgd3 |
G |
A |
13: 49,427,224 (GRCm39) |
P503S |
probably benign |
Het |
Frem3 |
T |
C |
8: 81,340,062 (GRCm39) |
L785P |
probably benign |
Het |
Gadl1 |
A |
G |
9: 115,835,769 (GRCm39) |
|
probably null |
Het |
Gm10787 |
C |
T |
10: 76,857,676 (GRCm39) |
|
noncoding transcript |
Het |
Gm6563 |
A |
G |
19: 23,653,246 (GRCm39) |
K12R |
probably benign |
Het |
Grm5 |
T |
C |
7: 87,675,758 (GRCm39) |
L424P |
probably damaging |
Het |
H2ac11 |
A |
G |
13: 22,227,006 (GRCm39) |
V31A |
probably benign |
Het |
Il17re |
T |
C |
6: 113,447,069 (GRCm39) |
S607P |
possibly damaging |
Het |
Ints7 |
A |
G |
1: 191,353,524 (GRCm39) |
|
probably benign |
Het |
Itih1 |
A |
G |
14: 30,651,780 (GRCm39) |
M854T |
possibly damaging |
Het |
Kif1b |
A |
G |
4: 149,348,086 (GRCm39) |
L315P |
probably damaging |
Het |
Ms4a6b |
T |
C |
19: 11,497,734 (GRCm39) |
V11A |
possibly damaging |
Het |
Mxd1 |
C |
A |
6: 86,627,966 (GRCm39) |
D191Y |
probably damaging |
Het |
Nol8 |
T |
A |
13: 49,807,160 (GRCm39) |
|
probably null |
Het |
Ntn4 |
T |
A |
10: 93,543,128 (GRCm39) |
|
probably null |
Het |
Nxph1 |
A |
T |
6: 9,247,103 (GRCm39) |
T25S |
probably benign |
Het |
Or1n1 |
A |
G |
2: 36,749,853 (GRCm39) |
V169A |
probably benign |
Het |
Or2bd2 |
A |
C |
7: 6,443,354 (GRCm39) |
T152P |
possibly damaging |
Het |
Or3a1 |
A |
T |
11: 74,225,961 (GRCm39) |
I32K |
probably benign |
Het |
Or51f1d |
A |
G |
7: 102,700,526 (GRCm39) |
N7S |
probably benign |
Het |
Or5ac20 |
C |
T |
16: 59,104,342 (GRCm39) |
V173I |
probably benign |
Het |
Or6c219 |
A |
G |
10: 129,781,695 (GRCm39) |
F79L |
possibly damaging |
Het |
Oxsm |
T |
A |
14: 16,242,308 (GRCm38) |
M154L |
possibly damaging |
Het |
Papolg |
A |
C |
11: 23,841,815 (GRCm39) |
I36S |
probably benign |
Het |
Pde3b |
T |
A |
7: 114,107,502 (GRCm39) |
H544Q |
probably benign |
Het |
Pdzd2 |
A |
T |
15: 12,592,656 (GRCm39) |
|
probably null |
Het |
Prkce |
C |
A |
17: 86,800,775 (GRCm39) |
P397Q |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,276,765 (GRCm39) |
S492G |
possibly damaging |
Het |
Rnf216 |
A |
G |
5: 143,054,659 (GRCm39) |
Y630H |
probably damaging |
Het |
Ruvbl1 |
C |
T |
6: 88,459,973 (GRCm39) |
T211I |
possibly damaging |
Het |
Scyl2 |
A |
T |
10: 89,481,348 (GRCm39) |
D666E |
probably benign |
Het |
Sertad2 |
A |
G |
11: 20,598,436 (GRCm39) |
T211A |
probably benign |
Het |
Sipa1l1 |
A |
T |
12: 82,487,643 (GRCm39) |
Q1639L |
probably benign |
Het |
Snx5 |
T |
C |
2: 144,101,073 (GRCm39) |
D98G |
probably damaging |
Het |
Sorcs2 |
G |
T |
5: 36,185,332 (GRCm39) |
|
probably null |
Het |
Spmip2 |
T |
C |
3: 79,313,192 (GRCm39) |
S89P |
probably damaging |
Het |
Tanc2 |
G |
A |
11: 105,758,543 (GRCm39) |
R768Q |
probably damaging |
Het |
Tmem132d |
A |
G |
5: 128,346,181 (GRCm39) |
S114P |
probably benign |
Het |
Tns2 |
G |
A |
15: 102,019,846 (GRCm39) |
G579R |
probably damaging |
Het |
Usp37 |
A |
T |
1: 74,517,295 (GRCm39) |
|
probably null |
Het |
Vmn1r79 |
T |
C |
7: 11,910,448 (GRCm39) |
I110T |
probably damaging |
Het |
Vps37a |
C |
T |
8: 40,981,363 (GRCm39) |
L69F |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,338,587 (GRCm39) |
I276N |
possibly damaging |
Het |
Zfp946 |
G |
A |
17: 22,673,821 (GRCm39) |
E192K |
probably benign |
Het |
|
Other mutations in Fbxl16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01307:Fbxl16
|
APN |
17 |
26,038,338 (GRCm39) |
splice site |
probably benign |
|
BB002:Fbxl16
|
UTSW |
17 |
26,035,880 (GRCm39) |
missense |
probably benign |
0.00 |
BB012:Fbxl16
|
UTSW |
17 |
26,035,880 (GRCm39) |
missense |
probably benign |
0.00 |
R1848:Fbxl16
|
UTSW |
17 |
26,035,420 (GRCm39) |
missense |
probably benign |
|
R5413:Fbxl16
|
UTSW |
17 |
26,035,817 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6018:Fbxl16
|
UTSW |
17 |
26,036,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Fbxl16
|
UTSW |
17 |
26,037,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R7068:Fbxl16
|
UTSW |
17 |
26,038,485 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7089:Fbxl16
|
UTSW |
17 |
26,035,703 (GRCm39) |
missense |
probably benign |
0.00 |
R7925:Fbxl16
|
UTSW |
17 |
26,035,880 (GRCm39) |
missense |
probably benign |
0.00 |
R8065:Fbxl16
|
UTSW |
17 |
26,036,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R8067:Fbxl16
|
UTSW |
17 |
26,036,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R9694:Fbxl16
|
UTSW |
17 |
26,036,813 (GRCm39) |
nonsense |
probably null |
|
X0025:Fbxl16
|
UTSW |
17 |
26,037,489 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fbxl16
|
UTSW |
17 |
26,035,985 (GRCm39) |
missense |
possibly damaging |
0.80 |
|