Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
T |
C |
16: 8,399,794 (GRCm39) |
|
probably null |
Het |
Adamts4 |
G |
A |
1: 171,086,334 (GRCm39) |
D709N |
probably benign |
Het |
Arhgef12 |
G |
T |
9: 42,903,318 (GRCm39) |
D745E |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,818,473 (GRCm39) |
K883E |
probably benign |
Het |
Cfdp1 |
T |
C |
8: 112,495,415 (GRCm39) |
I268V |
probably benign |
Het |
Cgnl1 |
G |
T |
9: 71,552,853 (GRCm39) |
S1037* |
probably null |
Het |
Clca3b |
T |
C |
3: 144,552,610 (GRCm39) |
N142S |
probably benign |
Het |
Col6a6 |
A |
T |
9: 105,659,253 (GRCm39) |
I564N |
probably damaging |
Het |
Coq4 |
G |
T |
2: 29,678,482 (GRCm39) |
R36L |
probably benign |
Het |
Dact3 |
G |
A |
7: 16,620,131 (GRCm39) |
S542N |
unknown |
Het |
Dcaf1 |
A |
G |
9: 106,751,466 (GRCm39) |
D1480G |
unknown |
Het |
Dcdc2a |
C |
T |
13: 25,389,443 (GRCm39) |
T457I |
probably damaging |
Het |
Ddi2 |
A |
G |
4: 141,411,196 (GRCm39) |
V572A |
probably damaging |
Het |
Ddx54 |
C |
T |
5: 120,761,672 (GRCm39) |
R483C |
probably benign |
Het |
Dennd5b |
G |
A |
6: 148,969,997 (GRCm39) |
S152F |
probably benign |
Het |
Efcab14 |
C |
T |
4: 115,616,072 (GRCm39) |
H252Y |
probably benign |
Het |
Efhb |
A |
T |
17: 53,770,298 (GRCm39) |
F4I |
probably damaging |
Het |
Esrrg |
A |
G |
1: 187,775,569 (GRCm39) |
D32G |
probably benign |
Het |
Far2 |
C |
A |
6: 148,060,448 (GRCm39) |
A267E |
probably damaging |
Het |
Fhip2b |
A |
C |
14: 70,827,621 (GRCm39) |
V158G |
possibly damaging |
Het |
Flnb |
T |
C |
14: 7,929,846 (GRCm38) |
I1992T |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 52,944,527 (GRCm39) |
S169G |
|
Het |
Galnt10 |
G |
A |
11: 57,656,514 (GRCm39) |
V233I |
probably benign |
Het |
Gbf1 |
C |
A |
19: 46,244,137 (GRCm39) |
N210K |
probably benign |
Het |
Gbp3 |
T |
G |
3: 142,276,283 (GRCm39) |
S460A |
probably benign |
Het |
Gm12185 |
T |
A |
11: 48,806,168 (GRCm39) |
H341L |
probably benign |
Het |
Gm5592 |
A |
T |
7: 40,939,234 (GRCm39) |
I839F |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,267,310 (GRCm39) |
D467G |
probably damaging |
Het |
Grin3a |
A |
T |
4: 49,714,213 (GRCm39) |
M844K |
probably damaging |
Het |
Gtf2a1l |
A |
G |
17: 89,019,020 (GRCm39) |
D368G |
probably benign |
Het |
Herc2 |
G |
C |
7: 55,813,659 (GRCm39) |
|
probably null |
Het |
Hycc1 |
T |
C |
5: 24,184,572 (GRCm39) |
Q302R |
possibly damaging |
Het |
Ins2 |
T |
A |
7: 142,233,185 (GRCm39) |
H29L |
probably damaging |
Het |
Ipo13 |
T |
A |
4: 117,762,778 (GRCm39) |
Y275F |
probably benign |
Het |
Kcnj15 |
T |
A |
16: 95,096,483 (GRCm39) |
M35K |
probably benign |
Het |
Kif21b |
G |
A |
1: 136,076,421 (GRCm39) |
V321M |
probably damaging |
Het |
Malt1 |
A |
G |
18: 65,581,283 (GRCm39) |
Q237R |
probably benign |
Het |
Micall1 |
G |
A |
15: 79,005,032 (GRCm39) |
C168Y |
unknown |
Het |
Muc5ac |
A |
G |
7: 141,360,985 (GRCm39) |
K1432R |
probably benign |
Het |
Nacad |
A |
G |
11: 6,551,662 (GRCm39) |
S510P |
probably benign |
Het |
Nub1 |
T |
C |
5: 24,897,965 (GRCm39) |
L117P |
possibly damaging |
Het |
Or10al3 |
T |
C |
17: 38,012,434 (GRCm39) |
L291P |
probably damaging |
Het |
Or5af1 |
A |
G |
11: 58,722,852 (GRCm39) |
R291G |
probably damaging |
Het |
Or8g24 |
A |
T |
9: 38,989,271 (GRCm39) |
F257I |
possibly damaging |
Het |
Pkdrej |
T |
C |
15: 85,705,268 (GRCm39) |
K223E |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,657,044 (GRCm39) |
Y4046* |
probably null |
Het |
Prpf8 |
A |
G |
11: 75,394,257 (GRCm39) |
N1767D |
probably benign |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
R3hdm2 |
G |
T |
10: 127,280,182 (GRCm39) |
M18I |
unknown |
Het |
Rab35 |
C |
A |
5: 115,778,224 (GRCm39) |
D63E |
probably damaging |
Het |
Ribc2 |
T |
A |
15: 85,027,568 (GRCm39) |
Y350N |
probably benign |
Het |
Sec63 |
A |
G |
10: 42,704,944 (GRCm39) |
I733V |
probably benign |
Het |
Slc23a3 |
ATT |
ATTT |
1: 75,109,925 (GRCm39) |
|
probably null |
Het |
Slc38a4 |
T |
C |
15: 96,896,332 (GRCm39) |
K512E |
probably damaging |
Het |
Stk35 |
G |
A |
2: 129,642,605 (GRCm39) |
V49I |
probably benign |
Het |
Tango6 |
A |
G |
8: 107,576,911 (GRCm39) |
E1055G |
probably damaging |
Het |
Tas2r140 |
A |
G |
6: 40,469,036 (GRCm39) |
I289V |
probably benign |
Het |
Thoc2l |
T |
C |
5: 104,667,101 (GRCm39) |
V541A |
probably benign |
Het |
Tll2 |
C |
T |
19: 41,119,084 (GRCm39) |
V215M |
probably damaging |
Het |
Tmem30a |
A |
T |
9: 79,687,874 (GRCm39) |
N98K |
probably benign |
Het |
Trav9n-4 |
C |
A |
14: 53,532,290 (GRCm39) |
A48E |
probably benign |
Het |
Vinac1 |
A |
T |
2: 128,880,499 (GRCm39) |
S476T |
|
Het |
Vmn1r192 |
A |
G |
13: 22,372,010 (GRCm39) |
F70S |
probably damaging |
Het |
Wdr89 |
A |
G |
12: 75,680,026 (GRCm39) |
V76A |
probably damaging |
Het |
Zfp229 |
A |
T |
17: 21,965,275 (GRCm39) |
T502S |
probably damaging |
Het |
|
Other mutations in Lcmt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01472:Lcmt1
|
APN |
7 |
123,027,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01536:Lcmt1
|
APN |
7 |
123,021,966 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01564:Lcmt1
|
APN |
7 |
123,003,663 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02598:Lcmt1
|
APN |
7 |
123,020,871 (GRCm39) |
splice site |
probably benign |
|
rancho
|
UTSW |
7 |
123,000,718 (GRCm39) |
missense |
probably benign |
0.03 |
relasso
|
UTSW |
7 |
123,000,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R0665:Lcmt1
|
UTSW |
7 |
123,002,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R0668:Lcmt1
|
UTSW |
7 |
123,002,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R0943:Lcmt1
|
UTSW |
7 |
123,000,662 (GRCm39) |
splice site |
probably null |
|
R1574:Lcmt1
|
UTSW |
7 |
123,002,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Lcmt1
|
UTSW |
7 |
123,002,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R2896:Lcmt1
|
UTSW |
7 |
123,020,809 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3017:Lcmt1
|
UTSW |
7 |
123,029,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Lcmt1
|
UTSW |
7 |
122,999,702 (GRCm39) |
missense |
probably benign |
0.07 |
R3714:Lcmt1
|
UTSW |
7 |
123,003,683 (GRCm39) |
missense |
probably damaging |
0.98 |
R4092:Lcmt1
|
UTSW |
7 |
123,017,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Lcmt1
|
UTSW |
7 |
123,010,035 (GRCm39) |
nonsense |
probably null |
|
R5062:Lcmt1
|
UTSW |
7 |
123,010,053 (GRCm39) |
splice site |
probably null |
|
R5096:Lcmt1
|
UTSW |
7 |
123,000,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Lcmt1
|
UTSW |
7 |
123,027,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Lcmt1
|
UTSW |
7 |
123,000,686 (GRCm39) |
missense |
probably benign |
0.03 |
R5931:Lcmt1
|
UTSW |
7 |
123,020,839 (GRCm39) |
missense |
probably benign |
|
R6331:Lcmt1
|
UTSW |
7 |
122,977,405 (GRCm39) |
intron |
probably benign |
|
R7752:Lcmt1
|
UTSW |
7 |
122,969,030 (GRCm39) |
missense |
unknown |
|
R7784:Lcmt1
|
UTSW |
7 |
123,000,718 (GRCm39) |
missense |
probably benign |
0.03 |
R8447:Lcmt1
|
UTSW |
7 |
123,020,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R8499:Lcmt1
|
UTSW |
7 |
123,029,371 (GRCm39) |
missense |
probably benign |
0.02 |
R8743:Lcmt1
|
UTSW |
7 |
122,999,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Lcmt1
|
UTSW |
7 |
123,000,669 (GRCm39) |
missense |
probably damaging |
1.00 |
RF013:Lcmt1
|
UTSW |
7 |
122,969,059 (GRCm39) |
frame shift |
probably null |
|
RF025:Lcmt1
|
UTSW |
7 |
122,969,057 (GRCm39) |
frame shift |
probably null |
|
RF046:Lcmt1
|
UTSW |
7 |
122,969,057 (GRCm39) |
frame shift |
probably null |
|
|