Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
G |
A |
15: 101,100,975 (GRCm39) |
R379Q |
probably null |
Het |
Adam23 |
C |
T |
1: 63,574,335 (GRCm39) |
Q276* |
probably null |
Het |
Apob |
A |
T |
12: 8,057,499 (GRCm39) |
S1961C |
probably damaging |
Het |
Atxn7l1 |
C |
T |
12: 33,408,839 (GRCm39) |
P334S |
probably damaging |
Het |
Ccnb1 |
T |
C |
13: 100,917,827 (GRCm39) |
M258V |
possibly damaging |
Het |
Cd34 |
A |
C |
1: 194,630,260 (GRCm39) |
T65P |
possibly damaging |
Het |
Cog6 |
A |
G |
3: 52,907,900 (GRCm39) |
|
probably null |
Het |
Cp |
T |
C |
3: 20,041,734 (GRCm39) |
M953T |
probably damaging |
Het |
Cwc27 |
C |
T |
13: 104,768,130 (GRCm39) |
R455Q |
unknown |
Het |
Dhx57 |
A |
T |
17: 80,588,663 (GRCm39) |
D63E |
probably damaging |
Het |
Elapor1 |
A |
T |
3: 108,378,726 (GRCm39) |
Y409* |
probably null |
Het |
Flt4 |
T |
A |
11: 49,536,786 (GRCm39) |
M1252K |
possibly damaging |
Het |
Itih4 |
C |
T |
14: 30,621,351 (GRCm39) |
Q788* |
probably null |
Het |
Kif18b |
A |
G |
11: 102,803,214 (GRCm39) |
S499P |
probably benign |
Het |
Map1a |
G |
C |
2: 121,130,768 (GRCm39) |
R528P |
probably damaging |
Het |
Map3k5 |
T |
C |
10: 20,003,443 (GRCm39) |
F1152L |
probably damaging |
Het |
Marveld2 |
T |
C |
13: 100,748,599 (GRCm39) |
D160G |
probably benign |
Het |
Mtcl2 |
A |
T |
2: 156,882,013 (GRCm39) |
C680S |
probably benign |
Het |
Mug1 |
A |
T |
6: 121,847,469 (GRCm39) |
M616L |
probably benign |
Het |
Ndst4 |
A |
T |
3: 125,231,823 (GRCm39) |
I131F |
probably benign |
Het |
Neto1 |
G |
T |
18: 86,479,399 (GRCm39) |
A196S |
probably benign |
Het |
Notum |
A |
G |
11: 120,545,237 (GRCm39) |
F441L |
probably benign |
Het |
Nsmce4a |
A |
G |
7: 130,140,769 (GRCm39) |
I239T |
probably benign |
Het |
Or51g1 |
A |
T |
7: 102,633,647 (GRCm39) |
N241K |
possibly damaging |
Het |
Or52z14 |
T |
A |
7: 103,252,943 (GRCm39) |
D27E |
probably benign |
Het |
Or5d35 |
A |
T |
2: 87,855,707 (GRCm39) |
I214F |
probably damaging |
Het |
Or6s1 |
T |
A |
14: 51,307,870 (GRCm39) |
K327* |
probably null |
Het |
Or6x1 |
A |
T |
9: 40,098,980 (GRCm39) |
T190S |
possibly damaging |
Het |
Or8k40 |
A |
G |
2: 86,584,398 (GRCm39) |
M228T |
probably damaging |
Het |
Pde4dip |
A |
T |
3: 97,700,841 (GRCm39) |
V221D |
probably damaging |
Het |
Pkp1 |
T |
C |
1: 135,808,545 (GRCm39) |
Y474C |
probably damaging |
Het |
Ptk6 |
A |
C |
2: 180,838,173 (GRCm39) |
H363Q |
probably benign |
Het |
Rb1cc1 |
T |
C |
1: 6,342,948 (GRCm39) |
W187R |
probably damaging |
Het |
Rbfox3 |
A |
T |
11: 118,394,564 (GRCm39) |
F132L |
probably damaging |
Het |
Rcl1 |
A |
T |
19: 29,099,268 (GRCm39) |
I188F |
possibly damaging |
Het |
Scfd1 |
T |
A |
12: 51,462,299 (GRCm39) |
S385T |
possibly damaging |
Het |
Sema6d |
A |
G |
2: 124,501,508 (GRCm39) |
E483G |
possibly damaging |
Het |
Semp2l2b |
T |
C |
10: 21,943,015 (GRCm39) |
I322V |
possibly damaging |
Het |
Sipa1l1 |
T |
C |
12: 82,388,890 (GRCm39) |
V372A |
probably benign |
Het |
Slc17a6 |
G |
A |
7: 51,317,654 (GRCm39) |
G429D |
probably damaging |
Het |
Slc22a5 |
A |
G |
11: 53,774,532 (GRCm39) |
V151A |
possibly damaging |
Het |
Spidr |
T |
C |
16: 15,936,787 (GRCm39) |
D106G |
probably damaging |
Het |
Tekt3 |
A |
T |
11: 62,974,778 (GRCm39) |
T366S |
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,710,398 (GRCm39) |
M281T |
probably benign |
Het |
Ttn |
A |
G |
2: 76,782,485 (GRCm39) |
V917A |
probably damaging |
Het |
Tubgcp4 |
A |
T |
2: 121,014,110 (GRCm39) |
D221V |
possibly damaging |
Het |
Ubr4 |
C |
T |
4: 139,176,232 (GRCm39) |
R3153W |
probably damaging |
Het |
Vmn1r89 |
A |
C |
7: 12,954,187 (GRCm39) |
T308P |
possibly damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,708,326 (GRCm39) |
I27T |
probably benign |
Het |
Vps13c |
T |
G |
9: 67,895,335 (GRCm39) |
|
probably null |
Het |
Zfp142 |
A |
G |
1: 74,606,191 (GRCm39) |
V1793A |
probably damaging |
Het |
Zfp472 |
T |
A |
17: 33,197,109 (GRCm39) |
C395S |
possibly damaging |
Het |
|
Other mutations in Gfral |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01391:Gfral
|
APN |
9 |
76,072,107 (GRCm39) |
nonsense |
probably null |
|
IGL02383:Gfral
|
APN |
9 |
76,104,374 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02987:Gfral
|
APN |
9 |
76,104,583 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03002:Gfral
|
APN |
9 |
76,104,520 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03055:Gfral
|
UTSW |
9 |
76,115,831 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4585001:Gfral
|
UTSW |
9 |
76,104,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Gfral
|
UTSW |
9 |
76,104,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R0547:Gfral
|
UTSW |
9 |
76,115,924 (GRCm39) |
missense |
probably benign |
0.16 |
R1146:Gfral
|
UTSW |
9 |
76,074,341 (GRCm39) |
missense |
probably benign |
0.00 |
R1146:Gfral
|
UTSW |
9 |
76,074,341 (GRCm39) |
missense |
probably benign |
0.00 |
R1275:Gfral
|
UTSW |
9 |
76,104,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Gfral
|
UTSW |
9 |
76,100,485 (GRCm39) |
missense |
probably benign |
0.01 |
R3709:Gfral
|
UTSW |
9 |
76,100,725 (GRCm39) |
nonsense |
probably null |
|
R4712:Gfral
|
UTSW |
9 |
76,100,727 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5567:Gfral
|
UTSW |
9 |
76,115,900 (GRCm39) |
missense |
probably benign |
0.00 |
R5568:Gfral
|
UTSW |
9 |
76,072,087 (GRCm39) |
makesense |
probably null |
|
R5719:Gfral
|
UTSW |
9 |
76,104,328 (GRCm39) |
missense |
probably benign |
0.02 |
R5789:Gfral
|
UTSW |
9 |
76,104,328 (GRCm39) |
missense |
probably benign |
0.02 |
R5791:Gfral
|
UTSW |
9 |
76,104,328 (GRCm39) |
missense |
probably benign |
0.02 |
R7110:Gfral
|
UTSW |
9 |
76,072,112 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7549:Gfral
|
UTSW |
9 |
76,106,257 (GRCm39) |
missense |
probably benign |
0.14 |
R7782:Gfral
|
UTSW |
9 |
76,100,572 (GRCm39) |
missense |
probably benign |
0.43 |
R7851:Gfral
|
UTSW |
9 |
76,112,737 (GRCm39) |
missense |
probably benign |
0.03 |
R9160:Gfral
|
UTSW |
9 |
76,104,372 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9568:Gfral
|
UTSW |
9 |
76,104,383 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gfral
|
UTSW |
9 |
76,112,671 (GRCm39) |
missense |
probably benign |
0.26 |
|