Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Astn1 |
C |
T |
1: 158,338,520 (GRCm39) |
|
probably benign |
Het |
Bms1 |
C |
A |
6: 118,366,290 (GRCm39) |
V1068F |
probably benign |
Het |
Cand1 |
A |
T |
10: 119,047,626 (GRCm39) |
N621K |
probably damaging |
Het |
Cd44 |
C |
T |
2: 102,661,732 (GRCm39) |
E418K |
possibly damaging |
Het |
Clip2 |
A |
T |
5: 134,531,425 (GRCm39) |
N758K |
probably benign |
Het |
Cst11 |
A |
T |
2: 148,613,161 (GRCm39) |
Y55N |
probably damaging |
Het |
Cytip |
A |
T |
2: 58,023,872 (GRCm39) |
L316* |
probably null |
Het |
Ddx52 |
T |
C |
11: 83,843,057 (GRCm39) |
M352T |
probably damaging |
Het |
Fancd2 |
G |
A |
6: 113,512,720 (GRCm39) |
|
probably benign |
Het |
Fat4 |
A |
T |
3: 39,034,068 (GRCm39) |
E2573D |
probably benign |
Het |
Fbxl13 |
T |
G |
5: 21,695,454 (GRCm39) |
D646A |
probably damaging |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Grid2ip |
A |
G |
5: 143,374,664 (GRCm39) |
D928G |
probably benign |
Het |
Hmgxb3 |
A |
G |
18: 61,265,285 (GRCm39) |
L1231P |
probably damaging |
Het |
Ifitm7 |
A |
G |
16: 13,801,541 (GRCm39) |
F73L |
probably damaging |
Het |
Ikbkb |
T |
A |
8: 23,155,919 (GRCm39) |
T583S |
probably benign |
Het |
Kdm6b |
G |
A |
11: 69,296,893 (GRCm39) |
A458V |
possibly damaging |
Het |
Klra2 |
T |
C |
6: 131,207,180 (GRCm39) |
K143R |
probably benign |
Het |
Kmt2d |
A |
G |
15: 98,764,309 (GRCm39) |
S42P |
possibly damaging |
Het |
Krt78 |
T |
A |
15: 101,857,028 (GRCm39) |
M360L |
probably benign |
Het |
Lamb1 |
A |
G |
12: 31,350,250 (GRCm39) |
N677S |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,168,113 (GRCm39) |
T426A |
probably benign |
Het |
Net1 |
T |
C |
13: 3,937,663 (GRCm39) |
Y146C |
probably damaging |
Het |
Nlrp4d |
T |
A |
7: 10,122,625 (GRCm39) |
|
noncoding transcript |
Het |
Notch4 |
A |
T |
17: 34,787,445 (GRCm39) |
N335I |
probably damaging |
Het |
Or14j6 |
A |
T |
17: 38,215,134 (GRCm39) |
E232D |
probably benign |
Het |
Or5ac20 |
A |
T |
16: 59,104,584 (GRCm39) |
I92K |
probably damaging |
Het |
Or8b53 |
A |
T |
9: 38,667,784 (GRCm39) |
T267S |
probably benign |
Het |
Pax3 |
A |
T |
1: 78,171,969 (GRCm39) |
H80Q |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,729,508 (GRCm39) |
|
probably benign |
Het |
Pdgfra |
A |
G |
5: 75,348,567 (GRCm39) |
D869G |
probably damaging |
Het |
Per2 |
T |
C |
1: 91,373,332 (GRCm39) |
Y152C |
probably damaging |
Het |
Pilrb2 |
T |
C |
5: 137,865,125 (GRCm39) |
D223G |
probably benign |
Het |
Rag1 |
T |
A |
2: 101,473,733 (GRCm39) |
I470F |
probably damaging |
Het |
Rap1gap |
T |
C |
4: 137,445,317 (GRCm39) |
S333P |
probably damaging |
Het |
Rundc3b |
A |
G |
5: 8,542,530 (GRCm39) |
Y430H |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,793,472 (GRCm39) |
D1332G |
probably benign |
Het |
Sgo1 |
G |
A |
17: 53,986,567 (GRCm39) |
A208V |
possibly damaging |
Het |
Skint5 |
C |
T |
4: 113,794,778 (GRCm39) |
|
probably null |
Het |
Slc26a4 |
C |
T |
12: 31,578,853 (GRCm39) |
|
probably benign |
Het |
Slc28a3 |
A |
T |
13: 58,706,451 (GRCm39) |
S597T |
probably benign |
Het |
Slc4a5 |
T |
A |
6: 83,248,085 (GRCm39) |
|
probably benign |
Het |
Slc52a3 |
A |
G |
2: 151,847,448 (GRCm39) |
|
probably benign |
Het |
Stac3 |
A |
G |
10: 127,339,768 (GRCm39) |
D158G |
probably benign |
Het |
Tdo2 |
T |
C |
3: 81,871,224 (GRCm39) |
|
probably benign |
Het |
Usp25 |
A |
T |
16: 76,912,335 (GRCm39) |
E1018V |
probably damaging |
Het |
Vmn1r46 |
T |
A |
6: 89,953,886 (GRCm39) |
F245Y |
probably damaging |
Het |
|
Other mutations in Lrrc9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Lrrc9
|
APN |
12 |
72,533,017 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL00843:Lrrc9
|
APN |
12 |
72,510,191 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01923:Lrrc9
|
APN |
12 |
72,557,186 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02027:Lrrc9
|
APN |
12 |
72,517,108 (GRCm39) |
splice site |
probably benign |
|
IGL02398:Lrrc9
|
APN |
12 |
72,513,677 (GRCm39) |
missense |
probably benign |
|
IGL02795:Lrrc9
|
APN |
12 |
72,525,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02931:Lrrc9
|
APN |
12 |
72,500,923 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03257:Lrrc9
|
APN |
12 |
72,496,542 (GRCm39) |
missense |
probably benign |
|
BB006:Lrrc9
|
UTSW |
12 |
72,533,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
BB016:Lrrc9
|
UTSW |
12 |
72,533,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02799:Lrrc9
|
UTSW |
12 |
72,553,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R0172:Lrrc9
|
UTSW |
12 |
72,510,260 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0315:Lrrc9
|
UTSW |
12 |
72,502,802 (GRCm39) |
missense |
probably damaging |
0.96 |
R0492:Lrrc9
|
UTSW |
12 |
72,525,537 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0617:Lrrc9
|
UTSW |
12 |
72,529,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0639:Lrrc9
|
UTSW |
12 |
72,533,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R0987:Lrrc9
|
UTSW |
12 |
72,557,156 (GRCm39) |
missense |
probably benign |
0.00 |
R1325:Lrrc9
|
UTSW |
12 |
72,543,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Lrrc9
|
UTSW |
12 |
72,547,533 (GRCm39) |
missense |
probably benign |
0.05 |
R1465:Lrrc9
|
UTSW |
12 |
72,547,533 (GRCm39) |
missense |
probably benign |
0.05 |
R1479:Lrrc9
|
UTSW |
12 |
72,507,599 (GRCm39) |
nonsense |
probably null |
|
R1564:Lrrc9
|
UTSW |
12 |
72,533,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R1626:Lrrc9
|
UTSW |
12 |
72,542,435 (GRCm39) |
splice site |
probably null |
|
R1632:Lrrc9
|
UTSW |
12 |
72,506,794 (GRCm39) |
splice site |
probably null |
|
R1715:Lrrc9
|
UTSW |
12 |
72,524,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Lrrc9
|
UTSW |
12 |
72,502,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Lrrc9
|
UTSW |
12 |
72,502,772 (GRCm39) |
nonsense |
probably null |
|
R1866:Lrrc9
|
UTSW |
12 |
72,543,912 (GRCm39) |
missense |
probably damaging |
0.97 |
R1878:Lrrc9
|
UTSW |
12 |
72,522,938 (GRCm39) |
critical splice donor site |
probably null |
|
R1990:Lrrc9
|
UTSW |
12 |
72,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R2361:Lrrc9
|
UTSW |
12 |
72,510,244 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3752:Lrrc9
|
UTSW |
12 |
72,507,580 (GRCm39) |
nonsense |
probably null |
|
R3833:Lrrc9
|
UTSW |
12 |
72,529,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R4134:Lrrc9
|
UTSW |
12 |
72,513,740 (GRCm39) |
missense |
probably benign |
0.00 |
R4651:Lrrc9
|
UTSW |
12 |
72,524,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Lrrc9
|
UTSW |
12 |
72,524,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Lrrc9
|
UTSW |
12 |
72,517,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Lrrc9
|
UTSW |
12 |
72,546,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Lrrc9
|
UTSW |
12 |
72,546,466 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5017:Lrrc9
|
UTSW |
12 |
72,553,099 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5163:Lrrc9
|
UTSW |
12 |
72,496,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5279:Lrrc9
|
UTSW |
12 |
72,542,368 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5434:Lrrc9
|
UTSW |
12 |
72,500,862 (GRCm39) |
missense |
probably damaging |
0.98 |
R5783:Lrrc9
|
UTSW |
12 |
72,502,827 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6021:Lrrc9
|
UTSW |
12 |
72,516,005 (GRCm39) |
missense |
probably damaging |
0.97 |
R6214:Lrrc9
|
UTSW |
12 |
72,506,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R6255:Lrrc9
|
UTSW |
12 |
72,533,797 (GRCm39) |
missense |
probably benign |
0.33 |
R6538:Lrrc9
|
UTSW |
12 |
72,547,703 (GRCm39) |
missense |
probably benign |
0.08 |
R6563:Lrrc9
|
UTSW |
12 |
72,533,169 (GRCm39) |
splice site |
probably null |
|
R6672:Lrrc9
|
UTSW |
12 |
72,520,710 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6919:Lrrc9
|
UTSW |
12 |
72,553,167 (GRCm39) |
missense |
probably benign |
0.01 |
R6929:Lrrc9
|
UTSW |
12 |
72,497,546 (GRCm39) |
missense |
probably benign |
0.41 |
R7092:Lrrc9
|
UTSW |
12 |
72,510,238 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7150:Lrrc9
|
UTSW |
12 |
72,513,726 (GRCm39) |
missense |
probably benign |
0.00 |
R7338:Lrrc9
|
UTSW |
12 |
72,510,305 (GRCm39) |
splice site |
probably null |
|
R7398:Lrrc9
|
UTSW |
12 |
72,547,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R7477:Lrrc9
|
UTSW |
12 |
72,550,301 (GRCm39) |
critical splice donor site |
probably null |
|
R7501:Lrrc9
|
UTSW |
12 |
72,496,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R7542:Lrrc9
|
UTSW |
12 |
72,553,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R7816:Lrrc9
|
UTSW |
12 |
72,542,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R7870:Lrrc9
|
UTSW |
12 |
72,532,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R7929:Lrrc9
|
UTSW |
12 |
72,533,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8042:Lrrc9
|
UTSW |
12 |
72,507,680 (GRCm39) |
missense |
probably benign |
0.02 |
R8108:Lrrc9
|
UTSW |
12 |
72,500,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Lrrc9
|
UTSW |
12 |
72,496,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R8244:Lrrc9
|
UTSW |
12 |
72,546,384 (GRCm39) |
missense |
probably benign |
0.22 |
R8333:Lrrc9
|
UTSW |
12 |
72,528,317 (GRCm39) |
missense |
probably benign |
0.38 |
R9288:Lrrc9
|
UTSW |
12 |
72,522,858 (GRCm39) |
missense |
probably benign |
0.01 |
R9324:Lrrc9
|
UTSW |
12 |
72,496,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9342:Lrrc9
|
UTSW |
12 |
72,506,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R9557:Lrrc9
|
UTSW |
12 |
72,532,981 (GRCm39) |
missense |
probably benign |
0.01 |
R9624:Lrrc9
|
UTSW |
12 |
72,497,586 (GRCm39) |
missense |
probably benign |
0.19 |
R9677:Lrrc9
|
UTSW |
12 |
72,497,539 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Lrrc9
|
UTSW |
12 |
72,543,834 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lrrc9
|
UTSW |
12 |
72,524,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|