Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
G |
C |
2: 19,522,357 (GRCm39) |
N247K |
probably damaging |
Het |
AA986860 |
T |
C |
1: 130,670,906 (GRCm39) |
L376P |
probably benign |
Het |
Adamts10 |
T |
C |
17: 33,770,166 (GRCm39) |
|
probably null |
Het |
Adamts7 |
T |
C |
9: 90,070,493 (GRCm39) |
|
probably null |
Het |
Adgrl1 |
T |
C |
8: 84,661,093 (GRCm39) |
I862T |
probably damaging |
Het |
Agbl1 |
G |
A |
7: 76,239,248 (GRCm39) |
V583M |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,341 (GRCm39) |
V177D |
probably benign |
Het |
Arfgap2 |
A |
G |
2: 91,100,586 (GRCm39) |
K297R |
probably benign |
Het |
Armh3 |
A |
T |
19: 45,941,119 (GRCm39) |
L300Q |
probably damaging |
Het |
Atg14 |
A |
T |
14: 47,780,352 (GRCm39) |
I474N |
probably damaging |
Het |
Atp2b4 |
C |
A |
1: 133,642,968 (GRCm39) |
V1046F |
probably benign |
Het |
Best1 |
A |
G |
19: 9,969,443 (GRCm39) |
V205A |
probably benign |
Het |
Bicdl1 |
A |
G |
5: 115,862,638 (GRCm39) |
S206P |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,008,119 (GRCm39) |
V1725A |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,042,405 (GRCm39) |
T2797I |
probably damaging |
Het |
Cacna1h |
C |
T |
17: 25,651,850 (GRCm39) |
C98Y |
possibly damaging |
Het |
Calhm3 |
T |
A |
19: 47,140,430 (GRCm39) |
D221V |
probably damaging |
Het |
Ccdc93 |
T |
A |
1: 121,411,071 (GRCm39) |
|
probably null |
Het |
Cd248 |
A |
T |
19: 5,120,074 (GRCm39) |
I641F |
possibly damaging |
Het |
Chrnb3 |
C |
T |
8: 27,884,262 (GRCm39) |
T333M |
probably damaging |
Het |
Cyb5rl |
A |
G |
4: 106,928,203 (GRCm39) |
H113R |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Ddx59 |
T |
A |
1: 136,344,447 (GRCm39) |
D39E |
probably benign |
Het |
Defa5 |
A |
G |
8: 21,787,513 (GRCm39) |
D20G |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,303,677 (GRCm39) |
V1409E |
probably benign |
Het |
Dlc1 |
A |
T |
8: 37,404,763 (GRCm39) |
V342E |
probably benign |
Het |
Dsc2 |
G |
A |
18: 20,166,351 (GRCm39) |
T760I |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,616,022 (GRCm39) |
I3057V |
probably benign |
Het |
Etnk2 |
T |
G |
1: 133,304,791 (GRCm39) |
|
probably null |
Het |
Fbp2 |
G |
T |
13: 63,006,021 (GRCm39) |
L31I |
probably damaging |
Het |
Gbp7 |
A |
T |
3: 142,240,383 (GRCm39) |
I34F |
probably damaging |
Het |
Gcfc2 |
A |
G |
6: 81,920,460 (GRCm39) |
E415G |
probably damaging |
Het |
Glp1r |
T |
C |
17: 31,144,523 (GRCm39) |
L232P |
probably damaging |
Het |
Gm10822 |
A |
G |
2: 73,729,619 (GRCm39) |
|
noncoding transcript |
Het |
Gm42669 |
G |
A |
5: 107,655,776 (GRCm39) |
V1192M |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,689,062 (GRCm39) |
S12P |
possibly damaging |
Het |
Gpt |
A |
G |
15: 76,582,176 (GRCm39) |
E211G |
possibly damaging |
Het |
Grxcr1 |
T |
C |
5: 68,267,755 (GRCm39) |
I168T |
probably damaging |
Het |
Hat1 |
T |
C |
2: 71,264,378 (GRCm39) |
V272A |
probably benign |
Het |
Igkv8-30 |
A |
C |
6: 70,094,070 (GRCm39) |
C114G |
probably damaging |
Het |
Kcne4 |
T |
C |
1: 78,795,624 (GRCm39) |
S91P |
probably benign |
Het |
Kif5b |
G |
A |
18: 6,213,248 (GRCm39) |
Q715* |
probably null |
Het |
Lamb1 |
T |
A |
12: 31,337,428 (GRCm39) |
N386K |
probably damaging |
Het |
Lcmt2 |
T |
C |
2: 120,969,097 (GRCm39) |
N662S |
probably damaging |
Het |
Lnx1 |
G |
T |
5: 74,780,727 (GRCm39) |
H324N |
probably benign |
Het |
Lrrc4 |
T |
G |
6: 28,830,586 (GRCm39) |
D343A |
probably benign |
Het |
Mars1 |
A |
G |
10: 127,135,154 (GRCm39) |
S646P |
probably damaging |
Het |
Mboat7 |
T |
C |
7: 3,687,010 (GRCm39) |
|
probably benign |
Het |
Mlip |
C |
T |
9: 77,072,145 (GRCm39) |
V341I |
possibly damaging |
Het |
Mterf1b |
A |
T |
5: 4,247,057 (GRCm39) |
T233S |
possibly damaging |
Het |
Myo3a |
A |
T |
2: 22,338,488 (GRCm39) |
H442L |
probably damaging |
Het |
Myrf |
A |
T |
19: 10,201,964 (GRCm39) |
V171D |
possibly damaging |
Het |
Nbas |
G |
A |
12: 13,411,046 (GRCm39) |
D897N |
probably benign |
Het |
Nfx1 |
T |
C |
4: 40,977,004 (GRCm39) |
V226A |
probably benign |
Het |
Nlrp4a |
T |
C |
7: 26,149,578 (GRCm39) |
L395P |
probably damaging |
Het |
Nrros |
C |
T |
16: 31,962,975 (GRCm39) |
W311* |
probably null |
Het |
Nsun6 |
A |
G |
2: 15,044,542 (GRCm39) |
|
probably null |
Het |
Ntrk2 |
A |
G |
13: 59,007,115 (GRCm39) |
H239R |
possibly damaging |
Het |
Or10g9 |
T |
C |
9: 39,912,500 (GRCm39) |
T8A |
probably benign |
Het |
Or4k51 |
A |
T |
2: 111,584,731 (GRCm39) |
M46L |
probably benign |
Het |
Or5aq7 |
T |
C |
2: 86,938,606 (GRCm39) |
N42D |
probably damaging |
Het |
Or5p70 |
A |
G |
7: 107,995,068 (GRCm39) |
H247R |
probably damaging |
Het |
Pate4 |
C |
A |
9: 35,519,553 (GRCm39) |
A46S |
possibly damaging |
Het |
Pcdhb18 |
T |
C |
18: 37,623,653 (GRCm39) |
S328P |
probably damaging |
Het |
Pdk4 |
A |
G |
6: 5,494,857 (GRCm39) |
|
probably benign |
Het |
Pigm |
T |
C |
1: 172,205,100 (GRCm39) |
Y279H |
probably damaging |
Het |
Plaat3 |
A |
G |
19: 7,556,474 (GRCm39) |
I92V |
probably damaging |
Het |
Plxdc2 |
A |
G |
2: 16,718,494 (GRCm39) |
I379M |
probably damaging |
Het |
Ppp1r35 |
A |
G |
5: 137,778,156 (GRCm39) |
N217S |
possibly damaging |
Het |
Prex1 |
G |
A |
2: 166,411,285 (GRCm39) |
T1438I |
possibly damaging |
Het |
Ptger4 |
T |
A |
15: 5,272,326 (GRCm39) |
I98F |
possibly damaging |
Het |
Rasl11a |
T |
A |
5: 146,783,927 (GRCm39) |
I124N |
probably damaging |
Het |
Rest |
A |
G |
5: 77,429,126 (GRCm39) |
K515R |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,785,474 (GRCm39) |
L1746P |
probably damaging |
Het |
Ryr2 |
G |
T |
13: 11,960,863 (GRCm39) |
T25K |
probably benign |
Het |
Sacs |
A |
T |
14: 61,429,368 (GRCm39) |
I476L |
possibly damaging |
Het |
Serpina3g |
A |
T |
12: 104,205,417 (GRCm39) |
D52V |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,703,881 (GRCm39) |
N998S |
probably benign |
Het |
Skp2 |
C |
A |
15: 9,113,786 (GRCm39) |
G376C |
probably damaging |
Het |
Slc10a4 |
G |
A |
5: 73,174,482 (GRCm39) |
|
probably benign |
Het |
Slc24a2 |
G |
T |
4: 86,929,883 (GRCm39) |
P538T |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,665,763 (GRCm39) |
T184S |
probably benign |
Het |
Ssbp1 |
A |
G |
6: 40,453,433 (GRCm39) |
Y73C |
probably null |
Het |
St18 |
G |
A |
1: 6,898,195 (GRCm39) |
V666M |
probably benign |
Het |
Suclg1 |
A |
G |
6: 73,241,259 (GRCm39) |
K193R |
probably benign |
Het |
Tcp11l1 |
T |
C |
2: 104,514,484 (GRCm39) |
I428V |
possibly damaging |
Het |
Th |
T |
A |
7: 142,449,280 (GRCm39) |
D275V |
probably damaging |
Het |
Tnrc18 |
A |
C |
5: 142,759,396 (GRCm39) |
S813R |
unknown |
Het |
Tnrc6a |
T |
C |
7: 122,771,343 (GRCm39) |
|
probably null |
Het |
Trap1 |
A |
C |
16: 3,863,903 (GRCm39) |
Y472* |
probably null |
Het |
Trdv1 |
C |
A |
14: 54,119,626 (GRCm39) |
Q96K |
probably benign |
Het |
Trpm8 |
T |
C |
1: 88,271,048 (GRCm39) |
I446T |
probably damaging |
Het |
Tti2 |
T |
C |
8: 31,644,294 (GRCm39) |
L297P |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,565,355 (GRCm39) |
G26545R |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,587,488 (GRCm39) |
D13208G |
probably damaging |
Het |
Tubb3 |
A |
G |
8: 124,148,417 (GRCm39) |
|
probably null |
Het |
Umodl1 |
A |
G |
17: 31,190,893 (GRCm39) |
M247V |
probably benign |
Het |
Wrn |
T |
A |
8: 33,757,853 (GRCm39) |
H812L |
probably benign |
Het |
Zfp174 |
A |
G |
16: 3,672,506 (GRCm39) |
R352G |
possibly damaging |
Het |
Zfp955a |
T |
A |
17: 33,461,731 (GRCm39) |
K134* |
probably null |
Het |
|
Other mutations in 4930402F06Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00786:4930402F06Rik
|
APN |
2 |
35,265,851 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00805:4930402F06Rik
|
APN |
2 |
35,270,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01647:4930402F06Rik
|
APN |
2 |
35,266,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01927:4930402F06Rik
|
APN |
2 |
35,266,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02315:4930402F06Rik
|
APN |
2 |
35,266,185 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02563:4930402F06Rik
|
APN |
2 |
35,270,410 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02655:4930402F06Rik
|
APN |
2 |
35,270,498 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03341:4930402F06Rik
|
APN |
2 |
35,265,906 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0102:4930402F06Rik
|
UTSW |
2 |
35,265,795 (GRCm39) |
nonsense |
probably null |
|
R0102:4930402F06Rik
|
UTSW |
2 |
35,265,795 (GRCm39) |
nonsense |
probably null |
|
R0309:4930402F06Rik
|
UTSW |
2 |
35,266,271 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0556:4930402F06Rik
|
UTSW |
2 |
35,280,482 (GRCm39) |
splice site |
probably benign |
|
R2089:4930402F06Rik
|
UTSW |
2 |
35,266,079 (GRCm39) |
missense |
probably benign |
0.00 |
R2091:4930402F06Rik
|
UTSW |
2 |
35,266,079 (GRCm39) |
missense |
probably benign |
0.00 |
R2158:4930402F06Rik
|
UTSW |
2 |
35,275,680 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4027:4930402F06Rik
|
UTSW |
2 |
35,270,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:4930402F06Rik
|
UTSW |
2 |
35,266,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7755:4930402F06Rik
|
UTSW |
2 |
35,266,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:4930402F06Rik
|
UTSW |
2 |
35,266,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:4930402F06Rik
|
UTSW |
2 |
35,265,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:4930402F06Rik
|
UTSW |
2 |
35,279,599 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8550:4930402F06Rik
|
UTSW |
2 |
35,265,786 (GRCm39) |
nonsense |
probably null |
|
X0024:4930402F06Rik
|
UTSW |
2 |
35,279,617 (GRCm39) |
missense |
possibly damaging |
0.93 |
|