Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
A |
T |
12: 31,234,730 (GRCm39) |
|
noncoding transcript |
Het |
Acad11 |
T |
C |
9: 103,993,495 (GRCm39) |
F541L |
probably damaging |
Het |
Acin1 |
G |
T |
14: 54,884,231 (GRCm39) |
R92S |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,662,213 (GRCm39) |
S490P |
probably benign |
Het |
Aqp9 |
C |
A |
9: 71,037,726 (GRCm39) |
V184L |
probably benign |
Het |
Arih1 |
A |
T |
9: 59,393,266 (GRCm39) |
I122N |
possibly damaging |
Het |
Bmi1 |
T |
C |
2: 18,687,983 (GRCm39) |
|
probably benign |
Het |
Bmpr1a |
G |
A |
14: 34,137,834 (GRCm39) |
T391I |
possibly damaging |
Het |
Cacna1s |
A |
G |
1: 136,041,041 (GRCm39) |
K1256E |
probably damaging |
Het |
Cacng3 |
C |
T |
7: 122,367,795 (GRCm39) |
P225L |
probably damaging |
Het |
Cd101 |
A |
T |
3: 100,925,843 (GRCm39) |
|
probably null |
Het |
Cd55 |
A |
G |
1: 130,390,294 (GRCm39) |
|
probably benign |
Het |
Cenpe |
T |
C |
3: 134,928,016 (GRCm39) |
I258T |
probably damaging |
Het |
Cfap251 |
C |
T |
5: 123,428,117 (GRCm39) |
T538M |
probably damaging |
Het |
Cma2 |
A |
G |
14: 56,211,135 (GRCm39) |
|
probably benign |
Het |
Ddost |
T |
A |
4: 138,036,964 (GRCm39) |
S176T |
probably benign |
Het |
Ddx19b |
A |
T |
8: 111,750,596 (GRCm39) |
|
probably null |
Het |
Dmxl2 |
A |
G |
9: 54,286,223 (GRCm39) |
I2681T |
probably damaging |
Het |
Ern1 |
C |
T |
11: 106,289,412 (GRCm39) |
E964K |
probably benign |
Het |
Exoc1l |
G |
T |
5: 76,648,334 (GRCm39) |
V47L |
possibly damaging |
Het |
Galntl5 |
C |
T |
5: 25,425,172 (GRCm39) |
R430C |
probably benign |
Het |
Gga3 |
A |
G |
11: 115,478,259 (GRCm39) |
L511P |
probably damaging |
Het |
Gria2 |
C |
T |
3: 80,618,165 (GRCm39) |
|
probably benign |
Het |
Hmbs |
A |
T |
9: 44,252,949 (GRCm39) |
L28* |
probably null |
Het |
Iffo2 |
A |
G |
4: 139,330,532 (GRCm39) |
E220G |
probably damaging |
Het |
Ifi30 |
A |
G |
8: 71,217,562 (GRCm39) |
|
probably benign |
Het |
Irf2 |
T |
A |
8: 47,299,096 (GRCm39) |
C297S |
probably benign |
Het |
Izumo4 |
T |
C |
10: 80,538,918 (GRCm39) |
Y94H |
probably damaging |
Het |
Klhdc9 |
A |
G |
1: 171,187,353 (GRCm39) |
V215A |
probably benign |
Het |
Kmt2a |
T |
C |
9: 44,731,261 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,580,955 (GRCm39) |
C513S |
probably damaging |
Het |
Lyg1 |
A |
T |
1: 37,988,977 (GRCm39) |
M81K |
possibly damaging |
Het |
Maip1 |
T |
G |
1: 57,454,852 (GRCm39) |
W279G |
probably damaging |
Het |
Myo7a |
T |
C |
7: 97,721,144 (GRCm39) |
T1263A |
probably benign |
Het |
Naa15 |
T |
A |
3: 51,373,060 (GRCm39) |
I701N |
possibly damaging |
Het |
Ncoa3 |
A |
G |
2: 165,910,463 (GRCm39) |
N1292S |
probably benign |
Het |
Necab2 |
T |
A |
8: 120,180,979 (GRCm39) |
|
probably benign |
Het |
Nfatc1 |
T |
A |
18: 80,741,257 (GRCm39) |
I234F |
possibly damaging |
Het |
Olfm1 |
G |
A |
2: 28,098,223 (GRCm39) |
R95K |
possibly damaging |
Het |
Or10ag56 |
A |
G |
2: 87,139,402 (GRCm39) |
T90A |
probably benign |
Het |
Or10ak8 |
A |
T |
4: 118,773,823 (GRCm39) |
N280K |
possibly damaging |
Het |
Otoa |
T |
C |
7: 120,755,750 (GRCm39) |
|
probably null |
Het |
Padi4 |
GCTGCGTACCTCCAC |
GC |
4: 140,475,760 (GRCm39) |
|
probably benign |
Het |
Pard6g |
A |
G |
18: 80,160,337 (GRCm39) |
D150G |
probably damaging |
Het |
Pax5 |
A |
G |
4: 44,609,783 (GRCm39) |
L215S |
probably damaging |
Het |
Pja2 |
A |
T |
17: 64,594,516 (GRCm39) |
|
probably benign |
Het |
Plk4 |
T |
A |
3: 40,765,654 (GRCm39) |
|
probably benign |
Het |
Polr1a |
A |
T |
6: 71,955,405 (GRCm39) |
H1687L |
possibly damaging |
Het |
Ptcd2 |
G |
A |
13: 99,479,899 (GRCm39) |
L41F |
probably damaging |
Het |
Ropn1 |
T |
A |
16: 34,490,334 (GRCm39) |
S62T |
probably benign |
Het |
Setd1a |
T |
C |
7: 127,395,223 (GRCm39) |
|
probably benign |
Het |
Setdb1 |
T |
C |
3: 95,234,997 (GRCm39) |
D902G |
probably damaging |
Het |
Sik3 |
T |
A |
9: 46,120,068 (GRCm39) |
L719Q |
probably damaging |
Het |
Slc36a1 |
G |
T |
11: 55,123,333 (GRCm39) |
V433F |
probably benign |
Het |
Slc6a3 |
T |
C |
13: 73,705,169 (GRCm39) |
V220A |
possibly damaging |
Het |
Slc6a5 |
A |
T |
7: 49,561,539 (GRCm39) |
R24W |
probably damaging |
Het |
Smox |
G |
T |
2: 131,362,564 (GRCm39) |
R281L |
probably benign |
Het |
Sulf2 |
G |
T |
2: 165,935,436 (GRCm39) |
H226N |
probably damaging |
Het |
Syne2 |
C |
T |
12: 76,106,358 (GRCm39) |
|
probably null |
Het |
Tenm3 |
C |
T |
8: 48,740,826 (GRCm39) |
S1210N |
possibly damaging |
Het |
Tns1 |
A |
T |
1: 73,964,920 (GRCm39) |
V1237E |
probably damaging |
Het |
Trf |
C |
T |
9: 103,094,700 (GRCm39) |
V92M |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,539,717 (GRCm39) |
V34423A |
possibly damaging |
Het |
Vmn2r118 |
A |
G |
17: 55,918,021 (GRCm39) |
|
probably benign |
Het |
Vmn2r19 |
A |
G |
6: 123,286,703 (GRCm39) |
Y112C |
probably damaging |
Het |
Zfp326 |
G |
T |
5: 106,026,641 (GRCm39) |
A15S |
possibly damaging |
Het |
|
Other mutations in 0610040J01Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:0610040J01Rik
|
APN |
5 |
64,055,726 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02229:0610040J01Rik
|
APN |
5 |
64,055,696 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02389:0610040J01Rik
|
APN |
5 |
64,053,826 (GRCm39) |
missense |
probably null |
1.00 |
IGL02411:0610040J01Rik
|
APN |
5 |
64,055,459 (GRCm39) |
missense |
probably benign |
0.31 |
R0243:0610040J01Rik
|
UTSW |
5 |
64,055,806 (GRCm39) |
missense |
probably benign |
0.10 |
R1978:0610040J01Rik
|
UTSW |
5 |
64,055,880 (GRCm39) |
nonsense |
probably null |
|
R2072:0610040J01Rik
|
UTSW |
5 |
64,056,080 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2202:0610040J01Rik
|
UTSW |
5 |
64,056,011 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3161:0610040J01Rik
|
UTSW |
5 |
64,053,833 (GRCm39) |
splice site |
probably benign |
|
R3162:0610040J01Rik
|
UTSW |
5 |
64,053,833 (GRCm39) |
splice site |
probably benign |
|
R4428:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4429:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4430:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4431:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4464:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4465:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4467:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4491:0610040J01Rik
|
UTSW |
5 |
64,055,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5161:0610040J01Rik
|
UTSW |
5 |
64,055,344 (GRCm39) |
nonsense |
probably null |
|
R6115:0610040J01Rik
|
UTSW |
5 |
64,055,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:0610040J01Rik
|
UTSW |
5 |
64,055,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7445:0610040J01Rik
|
UTSW |
5 |
64,055,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R7593:0610040J01Rik
|
UTSW |
5 |
64,055,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R8070:0610040J01Rik
|
UTSW |
5 |
64,055,510 (GRCm39) |
missense |
probably benign |
0.01 |
R8140:0610040J01Rik
|
UTSW |
5 |
64,055,954 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8165:0610040J01Rik
|
UTSW |
5 |
64,055,289 (GRCm39) |
splice site |
probably null |
|
R8557:0610040J01Rik
|
UTSW |
5 |
64,055,954 (GRCm39) |
missense |
probably benign |
0.04 |
R9671:0610040J01Rik
|
UTSW |
5 |
64,055,948 (GRCm39) |
nonsense |
probably null |
|
R9782:0610040J01Rik
|
UTSW |
5 |
64,053,796 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|