Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
G |
A |
9: 44,186,063 (GRCm39) |
Q603* |
probably null |
Het |
Adar |
A |
G |
3: 89,647,516 (GRCm39) |
Y165C |
probably damaging |
Het |
Afp |
A |
G |
5: 90,651,500 (GRCm39) |
T372A |
probably benign |
Het |
Asah1 |
T |
A |
8: 41,800,061 (GRCm39) |
L184F |
probably damaging |
Het |
Bltp1 |
A |
G |
3: 37,067,132 (GRCm39) |
E3548G |
probably damaging |
Het |
Bpifb2 |
A |
T |
2: 153,731,046 (GRCm39) |
I206F |
possibly damaging |
Het |
Btn1a1 |
C |
A |
13: 23,648,741 (GRCm39) |
D31Y |
possibly damaging |
Het |
C4b |
T |
A |
17: 34,952,892 (GRCm39) |
D1110V |
probably damaging |
Het |
Ccdc162 |
T |
A |
10: 41,429,178 (GRCm39) |
D1901V |
probably damaging |
Het |
Cd101 |
A |
G |
3: 100,910,817 (GRCm39) |
V947A |
probably benign |
Het |
Cd55b |
A |
T |
1: 130,338,375 (GRCm39) |
S238T |
possibly damaging |
Het |
Cdc25c |
T |
C |
18: 34,866,329 (GRCm39) |
I437V |
possibly damaging |
Het |
Cfap97 |
T |
C |
8: 46,623,605 (GRCm39) |
S332P |
probably damaging |
Het |
Chpf |
A |
G |
1: 75,452,398 (GRCm39) |
L352P |
probably damaging |
Het |
Cntln |
T |
A |
4: 85,018,961 (GRCm39) |
M1217K |
possibly damaging |
Het |
Cntrl |
A |
G |
2: 35,052,053 (GRCm39) |
E1629G |
possibly damaging |
Het |
Csnk1g2 |
T |
C |
10: 80,474,396 (GRCm39) |
Y206H |
probably damaging |
Het |
Cyp2c55 |
T |
A |
19: 38,995,547 (GRCm39) |
W20R |
probably null |
Het |
Dhx35 |
A |
T |
2: 158,657,393 (GRCm39) |
H130L |
possibly damaging |
Het |
Dnm1 |
A |
G |
2: 32,202,741 (GRCm39) |
V54A |
probably damaging |
Het |
Eea1 |
T |
A |
10: 95,864,381 (GRCm39) |
S967T |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,820,772 (GRCm39) |
|
probably benign |
Het |
Elf3 |
A |
T |
1: 135,182,813 (GRCm39) |
I304N |
probably damaging |
Het |
Eps8l1 |
G |
T |
7: 4,481,214 (GRCm39) |
R672L |
probably damaging |
Het |
Fam163a |
A |
T |
1: 155,954,862 (GRCm39) |
C96* |
probably null |
Het |
Fancd2 |
T |
C |
6: 113,540,129 (GRCm39) |
|
probably null |
Het |
Fbxo3 |
C |
T |
2: 103,858,274 (GRCm39) |
L23F |
possibly damaging |
Het |
Fbxw14 |
A |
G |
9: 109,114,367 (GRCm39) |
V121A |
possibly damaging |
Het |
Fgd6 |
T |
A |
10: 93,880,868 (GRCm39) |
V574D |
probably benign |
Het |
Gask1b |
T |
C |
3: 79,794,293 (GRCm39) |
S254P |
probably benign |
Het |
Gbp11 |
A |
G |
5: 105,479,251 (GRCm39) |
F124S |
probably damaging |
Het |
Grin1 |
A |
T |
2: 25,195,428 (GRCm39) |
|
probably benign |
Het |
Grm2 |
T |
G |
9: 106,531,345 (GRCm39) |
E48A |
probably benign |
Het |
H2-M10.5 |
T |
A |
17: 37,084,770 (GRCm39) |
Y165N |
probably benign |
Het |
Ifih1 |
T |
A |
2: 62,442,235 (GRCm39) |
K376N |
possibly damaging |
Het |
Insrr |
C |
A |
3: 87,720,386 (GRCm39) |
T1008K |
probably damaging |
Het |
Itih1 |
A |
G |
14: 30,655,414 (GRCm39) |
S594P |
probably damaging |
Het |
Kidins220 |
T |
C |
12: 25,106,914 (GRCm39) |
S1365P |
probably benign |
Het |
Malrd1 |
A |
T |
2: 15,570,241 (GRCm39) |
K158* |
probably null |
Het |
Man2c1 |
G |
A |
9: 57,045,279 (GRCm39) |
G504R |
probably damaging |
Het |
Mbd1 |
T |
C |
18: 74,406,890 (GRCm39) |
|
probably null |
Het |
Micall2 |
G |
A |
5: 139,702,025 (GRCm39) |
A323V |
probably benign |
Het |
Mroh9 |
A |
C |
1: 162,883,196 (GRCm39) |
F428V |
probably benign |
Het |
Myo7b |
T |
A |
18: 32,127,299 (GRCm39) |
|
probably benign |
Het |
Niban1 |
A |
T |
1: 151,591,463 (GRCm39) |
H535L |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,922,438 (GRCm39) |
V6567E |
probably damaging |
Het |
Or1e28-ps1 |
A |
C |
11: 73,615,230 (GRCm39) |
S207A |
unknown |
Het |
Or1e33 |
A |
T |
11: 73,738,167 (GRCm39) |
C261* |
probably null |
Het |
Or2g25 |
T |
A |
17: 37,970,760 (GRCm39) |
T155S |
probably benign |
Het |
Or2y1d |
A |
T |
11: 49,321,543 (GRCm39) |
Q80L |
probably benign |
Het |
Or5h25 |
T |
A |
16: 58,930,555 (GRCm39) |
R139S |
probably benign |
Het |
Or8b53 |
A |
T |
9: 38,667,385 (GRCm39) |
I134F |
possibly damaging |
Het |
Pde4dip |
T |
C |
3: 97,700,464 (GRCm39) |
D238G |
probably damaging |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Pgbd5 |
T |
A |
8: 125,111,175 (GRCm39) |
Y172F |
probably benign |
Het |
Pkd1 |
A |
G |
17: 24,795,176 (GRCm39) |
T2288A |
probably damaging |
Het |
Ppp6r2 |
T |
A |
15: 89,137,239 (GRCm39) |
M1K |
probably null |
Het |
Rc3h1 |
A |
G |
1: 160,774,164 (GRCm39) |
T344A |
probably damaging |
Het |
Rgs5 |
T |
C |
1: 169,504,461 (GRCm39) |
V37A |
possibly damaging |
Het |
Rgs9 |
A |
G |
11: 109,139,815 (GRCm39) |
S17P |
possibly damaging |
Het |
Rusc1 |
T |
A |
3: 88,991,865 (GRCm39) |
D407V |
probably damaging |
Het |
Rwdd1 |
T |
A |
10: 33,895,383 (GRCm39) |
I18F |
possibly damaging |
Het |
Satb2 |
C |
T |
1: 56,910,470 (GRCm39) |
|
probably null |
Het |
Sds |
A |
G |
5: 120,621,659 (GRCm39) |
E267G |
probably damaging |
Het |
Sema4b |
T |
A |
7: 79,875,076 (GRCm39) |
V822E |
probably damaging |
Het |
Sfxn5 |
A |
T |
6: 85,266,176 (GRCm39) |
M107K |
probably damaging |
Het |
Slc5a8 |
C |
T |
10: 88,722,035 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,387,048 (GRCm39) |
D6G |
probably damaging |
Het |
Syt14 |
A |
C |
1: 192,666,515 (GRCm39) |
|
probably benign |
Het |
Vmn2r124 |
T |
G |
17: 18,283,291 (GRCm39) |
Y328* |
probably null |
Het |
Vmn2r86 |
T |
A |
10: 130,289,672 (GRCm39) |
E74D |
probably benign |
Het |
Vmo1 |
A |
C |
11: 70,404,476 (GRCm39) |
L175W |
probably damaging |
Het |
Vps13a |
G |
T |
19: 16,683,247 (GRCm39) |
L982I |
possibly damaging |
Het |
Wdr19 |
T |
C |
5: 65,398,211 (GRCm39) |
V812A |
probably benign |
Het |
Wdr27 |
T |
C |
17: 15,103,908 (GRCm39) |
I733V |
probably benign |
Het |
Wdr54 |
A |
T |
6: 83,132,739 (GRCm39) |
H38Q |
probably damaging |
Het |
Wdr76 |
G |
A |
2: 121,341,104 (GRCm39) |
V50I |
probably damaging |
Het |
Zfp930 |
T |
A |
8: 69,680,541 (GRCm39) |
N59K |
probably damaging |
Het |
Zfyve9 |
T |
C |
4: 108,501,558 (GRCm39) |
N1218S |
possibly damaging |
Het |
|
Other mutations in Hoxa13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
H8786:Hoxa13
|
UTSW |
6 |
52,260,636 (GRCm38) |
frame shift |
probably null |
|
PIT4131001:Hoxa13
|
UTSW |
6 |
52,260,648 (GRCm38) |
utr 5 prime |
probably benign |
|
PIT4131001:Hoxa13
|
UTSW |
6 |
52,260,647 (GRCm38) |
utr 5 prime |
probably benign |
|
PIT4142001:Hoxa13
|
UTSW |
6 |
52,260,648 (GRCm38) |
utr 5 prime |
probably benign |
|
PIT4142001:Hoxa13
|
UTSW |
6 |
52,260,647 (GRCm38) |
utr 5 prime |
probably benign |
|
R0458:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R0496:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R0502:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R0512:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R0784:Hoxa13
|
UTSW |
6 |
52,236,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R1062:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R1157:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R1192:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R1310:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R1341:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R1343:Hoxa13
|
UTSW |
6 |
52,237,618 (GRCm39) |
frame shift |
probably null |
|
R1398:Hoxa13
|
UTSW |
6 |
52,260,648 (GRCm38) |
utr 5 prime |
probably benign |
|
R1398:Hoxa13
|
UTSW |
6 |
52,260,647 (GRCm38) |
utr 5 prime |
probably benign |
|
R1400:Hoxa13
|
UTSW |
6 |
52,260,648 (GRCm38) |
utr 5 prime |
probably benign |
|
R1400:Hoxa13
|
UTSW |
6 |
52,260,647 (GRCm38) |
utr 5 prime |
probably benign |
|
R1450:Hoxa13
|
UTSW |
6 |
52,260,648 (GRCm38) |
utr 5 prime |
probably benign |
|
R1450:Hoxa13
|
UTSW |
6 |
52,260,647 (GRCm38) |
utr 5 prime |
probably benign |
|
R1632:Hoxa13
|
UTSW |
6 |
52,236,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R2382:Hoxa13
|
UTSW |
6 |
52,236,125 (GRCm39) |
missense |
probably damaging |
0.98 |
R3149:Hoxa13
|
UTSW |
6 |
52,237,284 (GRCm39) |
intron |
probably benign |
|
R4012:Hoxa13
|
UTSW |
6 |
52,236,107 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4426:Hoxa13
|
UTSW |
6 |
52,237,714 (GRCm39) |
utr 5 prime |
probably benign |
|
R5535:Hoxa13
|
UTSW |
6 |
52,237,520 (GRCm39) |
frame shift |
probably null |
|
R6175:Hoxa13
|
UTSW |
6 |
52,236,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R7365:Hoxa13
|
UTSW |
6 |
52,236,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R7770:Hoxa13
|
UTSW |
6 |
52,237,247 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R7926:Hoxa13
|
UTSW |
6 |
52,237,619 (GRCm39) |
frame shift |
probably null |
|
R7931:Hoxa13
|
UTSW |
6 |
52,237,620 (GRCm39) |
frame shift |
probably null |
|
R8982:Hoxa13
|
UTSW |
6 |
52,235,916 (GRCm39) |
nonsense |
probably null |
|
R9060:Hoxa13
|
UTSW |
6 |
52,236,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R9698:Hoxa13
|
UTSW |
6 |
52,236,024 (GRCm39) |
missense |
probably benign |
0.00 |
X0018:Hoxa13
|
UTSW |
6 |
52,237,099 (GRCm39) |
missense |
probably benign |
0.13 |
|