Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot5 |
A |
G |
12: 84,122,655 (GRCm39) |
D413G |
probably benign |
Het |
Actr5 |
G |
T |
2: 158,478,057 (GRCm39) |
V476F |
possibly damaging |
Het |
Adhfe1 |
G |
A |
1: 9,637,125 (GRCm39) |
D426N |
probably benign |
Het |
Adra1a |
T |
C |
14: 66,875,727 (GRCm39) |
L234P |
probably damaging |
Het |
Akap9 |
G |
T |
5: 4,022,791 (GRCm39) |
V1207L |
possibly damaging |
Het |
Anapc2 |
A |
G |
2: 25,164,724 (GRCm39) |
D36G |
probably benign |
Het |
Apol8 |
A |
G |
15: 77,633,566 (GRCm39) |
S337P |
possibly damaging |
Het |
Asxl3 |
A |
T |
18: 22,585,492 (GRCm39) |
D139V |
probably damaging |
Het |
Atp13a4 |
A |
T |
16: 29,227,746 (GRCm39) |
V1037E |
probably damaging |
Het |
Baat |
A |
T |
4: 49,490,231 (GRCm39) |
F284L |
probably benign |
Het |
Bltp3b |
T |
C |
10: 89,618,448 (GRCm39) |
V141A |
probably damaging |
Het |
C1qtnf6 |
A |
T |
15: 78,411,640 (GRCm39) |
F40Y |
probably damaging |
Het |
Caskin2 |
G |
A |
11: 115,693,608 (GRCm39) |
H508Y |
probably damaging |
Het |
Cass4 |
A |
T |
2: 172,269,654 (GRCm39) |
I579F |
probably damaging |
Het |
Cdk15 |
A |
G |
1: 59,328,917 (GRCm39) |
Y277C |
probably damaging |
Het |
Cit |
G |
A |
5: 116,105,956 (GRCm39) |
D947N |
probably damaging |
Het |
Clint1 |
T |
A |
11: 45,778,237 (GRCm39) |
I126K |
probably damaging |
Het |
Col6a4 |
C |
T |
9: 105,903,671 (GRCm39) |
G1640E |
probably damaging |
Het |
Ddx10 |
T |
C |
9: 53,149,371 (GRCm39) |
K119E |
probably damaging |
Het |
Dennd1a |
G |
A |
2: 37,690,209 (GRCm39) |
Q964* |
probably null |
Het |
Dnhd1 |
T |
C |
7: 105,343,035 (GRCm39) |
F1460L |
probably benign |
Het |
Edc3 |
T |
C |
9: 57,655,462 (GRCm39) |
|
probably null |
Het |
Edn1 |
A |
G |
13: 42,458,826 (GRCm39) |
E163G |
probably benign |
Het |
Efl1 |
A |
T |
7: 82,332,929 (GRCm39) |
D317V |
possibly damaging |
Het |
Elapor2 |
T |
G |
5: 9,478,407 (GRCm39) |
C424G |
probably damaging |
Het |
F2 |
A |
T |
2: 91,459,175 (GRCm39) |
Y430* |
probably null |
Het |
Faap100 |
C |
T |
11: 120,265,407 (GRCm39) |
V490M |
probably damaging |
Het |
Fuz |
G |
T |
7: 44,546,415 (GRCm39) |
G104W |
probably damaging |
Het |
Greb1l |
C |
A |
18: 10,553,848 (GRCm39) |
H1616Q |
probably benign |
Het |
Grm1 |
G |
T |
10: 10,622,538 (GRCm39) |
|
probably null |
Het |
Gucy2d |
G |
T |
7: 98,126,437 (GRCm39) |
A1098S |
probably benign |
Het |
H1f0 |
T |
A |
15: 78,913,195 (GRCm39) |
S92T |
possibly damaging |
Het |
Hbb-bt |
T |
A |
7: 103,463,083 (GRCm39) |
|
probably benign |
Het |
Heg1 |
G |
A |
16: 33,527,549 (GRCm39) |
A170T |
probably benign |
Het |
Hspa4l |
A |
T |
3: 40,736,049 (GRCm39) |
K578* |
probably null |
Het |
Ikbke |
A |
G |
1: 131,186,947 (GRCm39) |
S582P |
possibly damaging |
Het |
Itga6 |
T |
A |
2: 71,650,510 (GRCm39) |
F185L |
probably damaging |
Het |
Itgal |
T |
A |
7: 126,906,099 (GRCm39) |
D396E |
probably benign |
Het |
Kif5b |
T |
C |
18: 6,213,427 (GRCm39) |
H687R |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,504,182 (GRCm39) |
N3709D |
probably benign |
Het |
Lipf |
A |
T |
19: 33,943,066 (GRCm39) |
K125* |
probably null |
Het |
Lrif1 |
A |
T |
3: 106,640,452 (GRCm39) |
E512D |
probably damaging |
Het |
Matn2 |
T |
A |
15: 34,345,420 (GRCm39) |
Y142* |
probably null |
Het |
Med13l |
A |
G |
5: 118,880,060 (GRCm39) |
T1051A |
probably damaging |
Het |
Mro |
C |
T |
18: 74,009,806 (GRCm39) |
S159L |
probably benign |
Het |
Myh15 |
T |
A |
16: 48,913,145 (GRCm39) |
D367E |
probably damaging |
Het |
Myo1g |
T |
C |
11: 6,462,490 (GRCm39) |
Q547R |
probably benign |
Het |
Neb |
T |
C |
2: 52,097,733 (GRCm39) |
I902M |
probably benign |
Het |
Nsd1 |
G |
A |
13: 55,394,711 (GRCm39) |
D771N |
probably damaging |
Het |
Or10x4 |
A |
G |
1: 174,219,486 (GRCm39) |
I284V |
probably benign |
Het |
Or14a256 |
T |
C |
7: 86,265,664 (GRCm39) |
N63S |
probably damaging |
Het |
Or2a20 |
T |
C |
6: 43,194,494 (GRCm39) |
S216P |
probably damaging |
Het |
Or4e5 |
A |
C |
14: 52,728,051 (GRCm39) |
Y40* |
probably null |
Het |
Or8b48 |
C |
T |
9: 38,492,585 (GRCm39) |
T4I |
probably benign |
Het |
Penk |
A |
G |
4: 4,134,240 (GRCm39) |
Y136H |
probably damaging |
Het |
Prdm6 |
C |
T |
18: 53,673,272 (GRCm39) |
S144L |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,522,155 (GRCm39) |
I599F |
probably damaging |
Het |
Racgap1 |
A |
T |
15: 99,526,650 (GRCm39) |
C304* |
probably null |
Het |
Rbp3 |
T |
C |
14: 33,678,866 (GRCm39) |
V938A |
probably benign |
Het |
Rpp30 |
A |
G |
19: 36,071,827 (GRCm39) |
K132E |
probably damaging |
Het |
Rxfp2 |
A |
T |
5: 149,966,564 (GRCm39) |
R101* |
probably null |
Het |
Ryr1 |
A |
T |
7: 28,801,295 (GRCm39) |
V823E |
probably damaging |
Het |
S100pbp |
A |
T |
4: 129,075,886 (GRCm39) |
D146E |
probably damaging |
Het |
Sdr9c7 |
T |
A |
10: 127,738,127 (GRCm39) |
V135E |
probably damaging |
Het |
Serpinb12 |
A |
G |
1: 106,874,344 (GRCm39) |
D23G |
probably damaging |
Het |
Serpinf1 |
T |
A |
11: 75,304,807 (GRCm39) |
T185S |
probably null |
Het |
Slc23a1 |
A |
C |
18: 35,758,904 (GRCm39) |
C96G |
possibly damaging |
Het |
Slc5a4a |
C |
T |
10: 76,025,103 (GRCm39) |
|
probably null |
Het |
Spmap1 |
A |
G |
11: 97,662,435 (GRCm39) |
F146L |
probably damaging |
Het |
Suco |
A |
T |
1: 161,661,623 (GRCm39) |
L936Q |
probably damaging |
Het |
Tmem144 |
T |
C |
3: 79,732,606 (GRCm39) |
Y224C |
probably damaging |
Het |
Tpm4 |
T |
A |
8: 72,898,598 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,560,414 (GRCm39) |
E29329G |
probably damaging |
Het |
Txn1 |
T |
C |
4: 57,943,922 (GRCm39) |
I101V |
probably benign |
Het |
Ube2o |
A |
T |
11: 116,435,433 (GRCm39) |
C452S |
probably benign |
Het |
Uxs1 |
A |
T |
1: 43,804,081 (GRCm39) |
I278N |
probably damaging |
Het |
Vps54 |
T |
C |
11: 21,256,519 (GRCm39) |
F663L |
probably damaging |
Het |
Wdfy3 |
CG |
C |
5: 102,074,391 (GRCm39) |
|
probably null |
Het |
Zc3h11a |
A |
G |
1: 133,549,439 (GRCm39) |
S741P |
probably damaging |
Het |
Zdbf2 |
G |
A |
1: 63,342,436 (GRCm39) |
V272I |
possibly damaging |
Het |
Zdhhc24 |
A |
G |
19: 4,928,979 (GRCm39) |
N68S |
probably damaging |
Het |
Znfx1 |
A |
T |
2: 166,885,986 (GRCm39) |
L858* |
probably null |
Het |
|
Other mutations in Mpp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Mpp3
|
APN |
11 |
101,892,929 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01337:Mpp3
|
APN |
11 |
101,891,411 (GRCm39) |
missense |
probably benign |
|
IGL01393:Mpp3
|
APN |
11 |
101,916,304 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01544:Mpp3
|
APN |
11 |
101,909,485 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02152:Mpp3
|
APN |
11 |
101,916,216 (GRCm39) |
nonsense |
probably null |
|
IGL02441:Mpp3
|
APN |
11 |
101,900,501 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02656:Mpp3
|
APN |
11 |
101,899,427 (GRCm39) |
missense |
probably benign |
|
R0013:Mpp3
|
UTSW |
11 |
101,896,251 (GRCm39) |
missense |
probably benign |
0.27 |
R0117:Mpp3
|
UTSW |
11 |
101,891,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R0564:Mpp3
|
UTSW |
11 |
101,896,173 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1372:Mpp3
|
UTSW |
11 |
101,891,401 (GRCm39) |
missense |
probably damaging |
0.96 |
R1531:Mpp3
|
UTSW |
11 |
101,899,475 (GRCm39) |
missense |
probably benign |
|
R1639:Mpp3
|
UTSW |
11 |
101,914,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Mpp3
|
UTSW |
11 |
101,909,378 (GRCm39) |
intron |
probably benign |
|
R2064:Mpp3
|
UTSW |
11 |
101,891,516 (GRCm39) |
missense |
probably benign |
0.01 |
R2363:Mpp3
|
UTSW |
11 |
101,911,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R3775:Mpp3
|
UTSW |
11 |
101,914,193 (GRCm39) |
nonsense |
probably null |
|
R3776:Mpp3
|
UTSW |
11 |
101,914,193 (GRCm39) |
nonsense |
probably null |
|
R4208:Mpp3
|
UTSW |
11 |
101,891,426 (GRCm39) |
missense |
probably benign |
|
R4287:Mpp3
|
UTSW |
11 |
101,914,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R4327:Mpp3
|
UTSW |
11 |
101,914,337 (GRCm39) |
intron |
probably benign |
|
R4329:Mpp3
|
UTSW |
11 |
101,914,337 (GRCm39) |
intron |
probably benign |
|
R4367:Mpp3
|
UTSW |
11 |
101,914,246 (GRCm39) |
missense |
probably benign |
0.01 |
R4856:Mpp3
|
UTSW |
11 |
101,915,962 (GRCm39) |
missense |
probably benign |
|
R4886:Mpp3
|
UTSW |
11 |
101,915,962 (GRCm39) |
missense |
probably benign |
|
R4904:Mpp3
|
UTSW |
11 |
101,891,413 (GRCm39) |
missense |
probably benign |
0.01 |
R4946:Mpp3
|
UTSW |
11 |
101,895,848 (GRCm39) |
missense |
probably benign |
0.01 |
R5405:Mpp3
|
UTSW |
11 |
101,901,047 (GRCm39) |
missense |
probably benign |
|
R5935:Mpp3
|
UTSW |
11 |
101,916,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Mpp3
|
UTSW |
11 |
101,909,365 (GRCm39) |
intron |
probably benign |
|
R6056:Mpp3
|
UTSW |
11 |
101,902,515 (GRCm39) |
splice site |
probably null |
|
R6151:Mpp3
|
UTSW |
11 |
101,899,392 (GRCm39) |
missense |
probably benign |
0.11 |
R6677:Mpp3
|
UTSW |
11 |
101,899,444 (GRCm39) |
missense |
probably benign |
|
R6784:Mpp3
|
UTSW |
11 |
101,892,974 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6855:Mpp3
|
UTSW |
11 |
101,904,151 (GRCm39) |
missense |
probably benign |
0.09 |
R7227:Mpp3
|
UTSW |
11 |
101,895,904 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7635:Mpp3
|
UTSW |
11 |
101,916,209 (GRCm39) |
missense |
probably damaging |
0.97 |
R7974:Mpp3
|
UTSW |
11 |
101,899,180 (GRCm39) |
critical splice donor site |
probably null |
|
R8330:Mpp3
|
UTSW |
11 |
101,899,453 (GRCm39) |
missense |
probably benign |
0.20 |
R8331:Mpp3
|
UTSW |
11 |
101,902,541 (GRCm39) |
splice site |
probably null |
|
R8993:Mpp3
|
UTSW |
11 |
101,891,491 (GRCm39) |
missense |
probably benign |
0.03 |
R9154:Mpp3
|
UTSW |
11 |
101,911,328 (GRCm39) |
missense |
|
|
R9593:Mpp3
|
UTSW |
11 |
101,907,506 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9655:Mpp3
|
UTSW |
11 |
101,899,481 (GRCm39) |
missense |
probably benign |
|
Z1176:Mpp3
|
UTSW |
11 |
101,899,182 (GRCm39) |
missense |
probably damaging |
0.96 |
|