Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
T |
6: 128,524,268 (GRCm39) |
N1121K |
probably null |
Het |
Actr10 |
A |
G |
12: 71,006,795 (GRCm39) |
N351D |
probably damaging |
Het |
Adcy7 |
G |
A |
8: 89,044,606 (GRCm39) |
A500T |
probably damaging |
Het |
Arap2 |
G |
A |
5: 62,864,028 (GRCm39) |
T532I |
probably damaging |
Het |
Bag3 |
AAAGG |
AAAGGAAGG |
7: 128,147,493 (GRCm39) |
|
probably null |
Het |
Cc2d2a |
T |
C |
5: 43,841,375 (GRCm39) |
|
probably benign |
Het |
Cep85l |
A |
T |
10: 53,224,827 (GRCm39) |
M254K |
probably benign |
Het |
Clic4 |
A |
G |
4: 134,950,850 (GRCm39) |
S114P |
probably damaging |
Het |
Ctsj |
T |
C |
13: 61,150,363 (GRCm39) |
Y213C |
probably damaging |
Het |
Ddx28 |
A |
G |
8: 106,737,206 (GRCm39) |
V284A |
probably damaging |
Het |
Dnase2b |
T |
A |
3: 146,290,443 (GRCm39) |
D176V |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,729,111 (GRCm39) |
N663K |
probably damaging |
Het |
Dst |
T |
A |
1: 34,235,002 (GRCm39) |
S3694T |
possibly damaging |
Het |
Emilin1 |
T |
C |
5: 31,073,036 (GRCm39) |
S158P |
probably benign |
Het |
Eng |
T |
C |
2: 32,563,752 (GRCm39) |
|
probably benign |
Het |
Entrep2 |
T |
A |
7: 64,409,141 (GRCm39) |
M418L |
probably benign |
Het |
Fdxr |
C |
A |
11: 115,161,208 (GRCm39) |
V223L |
probably benign |
Het |
Fhip1b |
T |
C |
7: 105,037,398 (GRCm39) |
N395S |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,423,994 (GRCm39) |
M3148L |
probably benign |
Het |
Hip1 |
A |
T |
5: 135,460,584 (GRCm39) |
D114E |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,706,183 (GRCm39) |
|
probably benign |
Het |
Kcnt2 |
T |
A |
1: 140,437,179 (GRCm39) |
N487K |
probably damaging |
Het |
Krt6a |
A |
G |
15: 101,601,606 (GRCm39) |
F172L |
probably benign |
Het |
Megf8 |
C |
T |
7: 25,040,170 (GRCm39) |
R1034W |
probably damaging |
Het |
Muc6 |
C |
T |
7: 141,236,075 (GRCm39) |
D451N |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,125,225 (GRCm39) |
T1838A |
possibly damaging |
Het |
N4bp2l2 |
A |
T |
5: 150,585,073 (GRCm39) |
D302E |
probably damaging |
Het |
Nbeal2 |
T |
A |
9: 110,459,318 (GRCm39) |
I1930F |
probably benign |
Het |
Nhsl3 |
A |
G |
4: 129,116,432 (GRCm39) |
V732A |
probably benign |
Het |
Npas4 |
A |
T |
19: 5,037,392 (GRCm39) |
Y301N |
probably benign |
Het |
Nt5m |
A |
G |
11: 59,766,741 (GRCm39) |
K211E |
probably benign |
Het |
Pfn4 |
A |
G |
12: 4,824,382 (GRCm39) |
|
probably null |
Het |
Pfpl |
A |
C |
19: 12,407,843 (GRCm39) |
D698A |
probably benign |
Het |
Pias1 |
G |
T |
9: 62,859,137 (GRCm39) |
H124N |
possibly damaging |
Het |
Pja2 |
A |
T |
17: 64,618,162 (GRCm39) |
|
probably benign |
Het |
Polr3e |
T |
C |
7: 120,531,465 (GRCm39) |
Y185H |
probably benign |
Het |
Pomc |
T |
C |
12: 4,010,275 (GRCm39) |
L172S |
probably benign |
Het |
Rapgef4 |
A |
G |
2: 71,875,533 (GRCm39) |
T129A |
probably damaging |
Het |
Reep1 |
T |
C |
6: 71,750,278 (GRCm39) |
S97P |
probably damaging |
Het |
Rttn |
T |
A |
18: 89,029,067 (GRCm39) |
I595N |
possibly damaging |
Het |
Sap30 |
T |
C |
8: 57,938,506 (GRCm39) |
|
probably null |
Het |
Slc1a7 |
T |
C |
4: 107,850,203 (GRCm39) |
Y105H |
probably damaging |
Het |
Slc5a5 |
C |
T |
8: 71,345,102 (GRCm39) |
M68I |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,776,503 (GRCm39) |
Y791F |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,847,094 (GRCm39) |
H912N |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,847,093 (GRCm39) |
S911R |
probably benign |
Het |
Tgm7 |
A |
T |
2: 120,929,062 (GRCm39) |
F278Y |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,283,039 (GRCm39) |
T310A |
probably damaging |
Het |
Tmem256 |
T |
C |
11: 69,730,271 (GRCm39) |
I93T |
probably benign |
Het |
Trpm2 |
G |
A |
10: 77,756,305 (GRCm39) |
Q1172* |
probably null |
Het |
Ttll8 |
A |
G |
15: 88,818,156 (GRCm39) |
V173A |
possibly damaging |
Het |
Ubr5 |
T |
C |
15: 38,002,543 (GRCm39) |
S1497G |
possibly damaging |
Het |
Ubr7 |
G |
A |
12: 102,727,764 (GRCm39) |
|
probably null |
Het |
Vmn1r37 |
T |
A |
6: 66,708,878 (GRCm39) |
M1K |
probably null |
Het |
Vmn2r14 |
A |
G |
5: 109,366,698 (GRCm39) |
|
probably null |
Het |
Vmn2r72 |
T |
C |
7: 85,387,444 (GRCm39) |
I707V |
probably benign |
Het |
Vps8 |
A |
G |
16: 21,395,507 (GRCm39) |
R1266G |
probably damaging |
Het |
Wdr87-ps |
T |
A |
7: 29,235,950 (GRCm39) |
|
noncoding transcript |
Het |
Zfhx4 |
A |
G |
3: 5,307,349 (GRCm39) |
N192D |
probably damaging |
Het |
Zfp638 |
G |
C |
6: 83,906,500 (GRCm39) |
D222H |
probably damaging |
Het |
Zscan29 |
A |
C |
2: 120,999,883 (GRCm39) |
V106G |
probably damaging |
Het |
|
Other mutations in Ankrd35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Ankrd35
|
APN |
3 |
96,590,350 (GRCm39) |
splice site |
probably null |
|
IGL00896:Ankrd35
|
APN |
3 |
96,591,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01565:Ankrd35
|
APN |
3 |
96,592,101 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01837:Ankrd35
|
APN |
3 |
96,587,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02605:Ankrd35
|
APN |
3 |
96,588,388 (GRCm39) |
splice site |
probably null |
|
IGL02819:Ankrd35
|
APN |
3 |
96,597,524 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02994:Ankrd35
|
APN |
3 |
96,590,307 (GRCm39) |
splice site |
probably benign |
|
IGL03083:Ankrd35
|
APN |
3 |
96,592,117 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Ankrd35
|
APN |
3 |
96,591,373 (GRCm39) |
missense |
probably benign |
|
FR4304:Ankrd35
|
UTSW |
3 |
96,591,163 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4342:Ankrd35
|
UTSW |
3 |
96,590,831 (GRCm39) |
frame shift |
probably null |
|
FR4737:Ankrd35
|
UTSW |
3 |
96,591,165 (GRCm39) |
utr 3 prime |
probably benign |
|
R0003:Ankrd35
|
UTSW |
3 |
96,591,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Ankrd35
|
UTSW |
3 |
96,591,379 (GRCm39) |
missense |
probably benign |
0.00 |
R0551:Ankrd35
|
UTSW |
3 |
96,591,276 (GRCm39) |
missense |
probably benign |
0.08 |
R1420:Ankrd35
|
UTSW |
3 |
96,592,054 (GRCm39) |
missense |
probably benign |
0.13 |
R1455:Ankrd35
|
UTSW |
3 |
96,585,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Ankrd35
|
UTSW |
3 |
96,592,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R3605:Ankrd35
|
UTSW |
3 |
96,589,497 (GRCm39) |
nonsense |
probably null |
|
R4166:Ankrd35
|
UTSW |
3 |
96,586,471 (GRCm39) |
splice site |
probably null |
|
R4651:Ankrd35
|
UTSW |
3 |
96,591,343 (GRCm39) |
missense |
probably benign |
0.00 |
R4668:Ankrd35
|
UTSW |
3 |
96,586,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Ankrd35
|
UTSW |
3 |
96,591,438 (GRCm39) |
missense |
probably benign |
|
R4921:Ankrd35
|
UTSW |
3 |
96,592,140 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4953:Ankrd35
|
UTSW |
3 |
96,590,989 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5180:Ankrd35
|
UTSW |
3 |
96,587,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Ankrd35
|
UTSW |
3 |
96,592,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Ankrd35
|
UTSW |
3 |
96,592,215 (GRCm39) |
missense |
probably benign |
0.02 |
R5613:Ankrd35
|
UTSW |
3 |
96,590,334 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6165:Ankrd35
|
UTSW |
3 |
96,590,623 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6413:Ankrd35
|
UTSW |
3 |
96,592,129 (GRCm39) |
missense |
probably damaging |
0.96 |
R6711:Ankrd35
|
UTSW |
3 |
96,590,784 (GRCm39) |
nonsense |
probably null |
|
R6834:Ankrd35
|
UTSW |
3 |
96,590,599 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6841:Ankrd35
|
UTSW |
3 |
96,577,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Ankrd35
|
UTSW |
3 |
96,590,650 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7396:Ankrd35
|
UTSW |
3 |
96,590,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:Ankrd35
|
UTSW |
3 |
96,592,104 (GRCm39) |
missense |
not run |
|
R7815:Ankrd35
|
UTSW |
3 |
96,592,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Ankrd35
|
UTSW |
3 |
96,592,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Ankrd35
|
UTSW |
3 |
96,586,997 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8318:Ankrd35
|
UTSW |
3 |
96,592,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Ankrd35
|
UTSW |
3 |
96,589,529 (GRCm39) |
critical splice donor site |
probably null |
|
R8527:Ankrd35
|
UTSW |
3 |
96,589,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:Ankrd35
|
UTSW |
3 |
96,589,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8742:Ankrd35
|
UTSW |
3 |
96,586,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Ankrd35
|
UTSW |
3 |
96,587,003 (GRCm39) |
nonsense |
probably null |
|
R9029:Ankrd35
|
UTSW |
3 |
96,591,460 (GRCm39) |
missense |
probably benign |
0.43 |
R9229:Ankrd35
|
UTSW |
3 |
96,592,215 (GRCm39) |
missense |
probably benign |
0.02 |
R9488:Ankrd35
|
UTSW |
3 |
96,589,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R9669:Ankrd35
|
UTSW |
3 |
96,587,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Ankrd35
|
UTSW |
3 |
96,591,733 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:Ankrd35
|
UTSW |
3 |
96,591,086 (GRCm39) |
missense |
probably damaging |
0.96 |
|