Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
C |
T |
2: 25,337,228 (GRCm39) |
A2361V |
probably damaging |
Het |
Alpi |
A |
G |
1: 87,027,923 (GRCm39) |
I219T |
probably damaging |
Het |
Anapc10 |
T |
A |
8: 80,501,772 (GRCm39) |
M180K |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,713,708 (GRCm39) |
I431V |
probably damaging |
Het |
Atp1a3 |
T |
A |
7: 24,678,808 (GRCm39) |
I945F |
probably damaging |
Het |
Atp2a3 |
T |
C |
11: 72,882,570 (GRCm39) |
S1019P |
probably damaging |
Het |
Cbs |
T |
A |
17: 31,841,448 (GRCm39) |
I258F |
probably damaging |
Het |
Cic |
T |
C |
7: 24,985,386 (GRCm39) |
S277P |
probably damaging |
Het |
Cidea |
T |
A |
18: 67,493,230 (GRCm39) |
V83E |
probably damaging |
Het |
Cilp |
G |
A |
9: 65,186,997 (GRCm39) |
G1031S |
probably damaging |
Het |
Clca3a2 |
A |
G |
3: 144,516,477 (GRCm39) |
I373T |
possibly damaging |
Het |
Cpvl |
T |
A |
6: 53,903,886 (GRCm39) |
D293V |
probably damaging |
Het |
Cryz |
A |
G |
3: 154,317,147 (GRCm39) |
N122S |
probably benign |
Het |
Dmap1 |
T |
C |
4: 117,533,319 (GRCm39) |
E245G |
probably damaging |
Het |
Epha2 |
C |
T |
4: 141,045,916 (GRCm39) |
|
probably benign |
Het |
Fam222b |
C |
T |
11: 78,045,347 (GRCm39) |
L303F |
probably damaging |
Het |
Fastkd1 |
T |
C |
2: 69,542,492 (GRCm39) |
D105G |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,943,009 (GRCm39) |
L634Q |
probably damaging |
Het |
Fbxo10 |
A |
T |
4: 45,042,036 (GRCm39) |
I731N |
possibly damaging |
Het |
Fig4 |
A |
G |
10: 41,141,423 (GRCm39) |
F279L |
probably damaging |
Het |
Guk1 |
A |
G |
11: 59,077,675 (GRCm39) |
S22P |
probably damaging |
Het |
Kmt2d |
A |
G |
15: 98,762,934 (GRCm39) |
|
probably benign |
Het |
Macf1 |
A |
T |
4: 123,403,639 (GRCm39) |
S727T |
probably benign |
Het |
Mki67 |
T |
A |
7: 135,315,701 (GRCm39) |
K54* |
probably null |
Het |
Ms4a8a |
T |
C |
19: 11,053,696 (GRCm39) |
T137A |
possibly damaging |
Het |
Myo5c |
T |
C |
9: 75,174,313 (GRCm39) |
Y557H |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,689,115 (GRCm39) |
K387N |
probably damaging |
Het |
Oga |
T |
G |
19: 45,765,349 (GRCm39) |
T153P |
possibly damaging |
Het |
Or5bb10 |
G |
T |
19: 12,206,241 (GRCm39) |
A223E |
probably damaging |
Het |
Pde4c |
T |
A |
8: 71,199,508 (GRCm39) |
Y223N |
probably damaging |
Het |
Psd |
T |
G |
19: 46,303,237 (GRCm39) |
E715A |
probably damaging |
Het |
Rpl7 |
A |
T |
1: 16,172,807 (GRCm39) |
S171T |
probably benign |
Het |
Rrm1 |
A |
G |
7: 102,116,112 (GRCm39) |
*66W |
probably null |
Het |
Scgb1b3 |
T |
A |
7: 31,075,388 (GRCm39) |
H79Q |
probably damaging |
Het |
Serpinb9 |
A |
T |
13: 33,199,469 (GRCm39) |
M255L |
probably benign |
Het |
Slc35a4 |
T |
C |
18: 36,816,058 (GRCm39) |
V296A |
probably benign |
Het |
Smgc |
G |
A |
15: 91,722,596 (GRCm39) |
A9T |
possibly damaging |
Het |
Snx11 |
C |
A |
11: 96,661,522 (GRCm39) |
W161L |
probably benign |
Het |
Spag17 |
A |
G |
3: 99,929,068 (GRCm39) |
K533E |
possibly damaging |
Het |
Spata31g1 |
A |
G |
4: 42,971,512 (GRCm39) |
I282V |
probably benign |
Het |
Speer4b |
A |
G |
5: 27,702,011 (GRCm39) |
S250P |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,041,061 (GRCm39) |
H1287L |
probably benign |
Het |
Surf2 |
T |
C |
2: 26,809,767 (GRCm39) |
F239S |
probably damaging |
Het |
Tada1 |
G |
A |
1: 166,214,319 (GRCm39) |
R106H |
possibly damaging |
Het |
Tbc1d22a |
C |
A |
15: 86,235,852 (GRCm39) |
|
probably null |
Het |
Tbcd |
A |
G |
11: 121,387,886 (GRCm39) |
Q339R |
probably benign |
Het |
Tdrd7 |
A |
G |
4: 45,994,445 (GRCm39) |
H281R |
probably benign |
Het |
Tomm5 |
A |
G |
4: 45,107,915 (GRCm39) |
|
probably null |
Het |
Ttc7 |
T |
C |
17: 87,669,373 (GRCm39) |
|
probably null |
Het |
Ulk1 |
A |
T |
5: 110,937,382 (GRCm39) |
F638Y |
probably damaging |
Het |
Vps35l |
T |
A |
7: 118,409,195 (GRCm39) |
I612N |
probably damaging |
Het |
Wdr93 |
C |
A |
7: 79,418,109 (GRCm39) |
D277E |
probably damaging |
Het |
Znrf3 |
T |
C |
11: 5,231,477 (GRCm39) |
R583G |
probably damaging |
Het |
Zscan29 |
T |
A |
2: 120,991,641 (GRCm39) |
I716F |
probably damaging |
Het |
|
Other mutations in Anxa8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01300:Anxa8
|
APN |
14 |
33,821,700 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01335:Anxa8
|
APN |
14 |
33,811,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02131:Anxa8
|
APN |
14 |
33,812,588 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02675:Anxa8
|
APN |
14 |
33,815,371 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02887:Anxa8
|
APN |
14 |
33,818,481 (GRCm39) |
splice site |
probably null |
|
R0095:Anxa8
|
UTSW |
14 |
33,808,028 (GRCm39) |
missense |
probably benign |
0.19 |
R0095:Anxa8
|
UTSW |
14 |
33,808,028 (GRCm39) |
missense |
probably benign |
0.19 |
R0138:Anxa8
|
UTSW |
14 |
33,819,897 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0138:Anxa8
|
UTSW |
14 |
33,819,896 (GRCm39) |
missense |
probably benign |
0.01 |
R0452:Anxa8
|
UTSW |
14 |
33,816,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Anxa8
|
UTSW |
14 |
33,811,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Anxa8
|
UTSW |
14 |
33,818,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Anxa8
|
UTSW |
14 |
33,813,873 (GRCm39) |
critical splice donor site |
probably null |
|
R3921:Anxa8
|
UTSW |
14 |
33,816,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Anxa8
|
UTSW |
14 |
33,814,579 (GRCm39) |
critical splice donor site |
probably null |
|
R5372:Anxa8
|
UTSW |
14 |
33,815,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Anxa8
|
UTSW |
14 |
33,819,850 (GRCm39) |
missense |
probably damaging |
0.98 |
R6823:Anxa8
|
UTSW |
14 |
33,816,722 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6837:Anxa8
|
UTSW |
14 |
33,814,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Anxa8
|
UTSW |
14 |
33,816,769 (GRCm39) |
missense |
probably benign |
0.00 |
R8405:Anxa8
|
UTSW |
14 |
33,819,881 (GRCm39) |
missense |
probably damaging |
0.96 |
R9301:Anxa8
|
UTSW |
14 |
33,819,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Anxa8
|
UTSW |
14 |
33,814,509 (GRCm39) |
missense |
possibly damaging |
0.78 |
|