Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
A |
G |
17: 36,270,144 (GRCm39) |
F638S |
possibly damaging |
Het |
Actl6b |
T |
A |
5: 137,562,762 (GRCm39) |
N159K |
probably damaging |
Het |
Adam6a |
T |
G |
12: 113,508,655 (GRCm39) |
S343A |
probably benign |
Het |
Ankrd17 |
G |
A |
5: 90,380,173 (GRCm39) |
T2505I |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,433,382 (GRCm39) |
T728A |
probably benign |
Het |
Asap2 |
G |
T |
12: 21,315,964 (GRCm39) |
E919* |
probably null |
Het |
Atp10b |
A |
T |
11: 43,136,291 (GRCm39) |
I1140F |
probably damaging |
Het |
Cep126 |
A |
T |
9: 8,103,383 (GRCm39) |
V209E |
probably damaging |
Het |
Cfap65 |
C |
T |
1: 74,965,792 (GRCm39) |
R406Q |
probably benign |
Het |
Cldn1 |
T |
C |
16: 26,190,376 (GRCm39) |
M1V |
probably null |
Het |
Cryl1 |
C |
T |
14: 57,512,956 (GRCm39) |
D304N |
probably benign |
Het |
D3Ertd751e |
T |
C |
3: 41,708,212 (GRCm39) |
|
probably null |
Het |
D630044L22Rik |
A |
T |
17: 26,181,090 (GRCm39) |
M156L |
probably benign |
Het |
Ddx21 |
T |
C |
10: 62,427,634 (GRCm39) |
D423G |
possibly damaging |
Het |
Dock2 |
T |
A |
11: 34,260,363 (GRCm39) |
M993L |
probably benign |
Het |
Dusp29 |
A |
T |
14: 21,727,129 (GRCm39) |
I173N |
probably damaging |
Het |
Eif4g1 |
C |
T |
16: 20,500,252 (GRCm39) |
A675V |
probably damaging |
Het |
Eml1 |
C |
T |
12: 108,472,810 (GRCm39) |
S206L |
probably benign |
Het |
Farp2 |
A |
C |
1: 93,531,181 (GRCm39) |
I560L |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,223,969 (GRCm39) |
D593E |
probably benign |
Het |
Fetub |
A |
G |
16: 22,748,007 (GRCm39) |
D61G |
possibly damaging |
Het |
Fpgs |
T |
C |
2: 32,576,641 (GRCm39) |
K329E |
probably benign |
Het |
Fpgt |
T |
C |
3: 154,797,120 (GRCm39) |
Y45C |
probably damaging |
Het |
Gas2l1 |
A |
T |
11: 5,011,106 (GRCm39) |
C574* |
probably null |
Het |
Gm9747 |
G |
T |
1: 82,211,837 (GRCm39) |
C12F |
unknown |
Het |
H2-T23 |
T |
C |
17: 36,342,709 (GRCm39) |
Y143C |
probably damaging |
Het |
Hhip |
A |
T |
8: 80,719,142 (GRCm39) |
S462T |
probably benign |
Het |
Hnf1a |
C |
T |
5: 115,091,446 (GRCm39) |
G416R |
probably damaging |
Het |
Hoxa5 |
C |
T |
6: 52,181,023 (GRCm39) |
C103Y |
probably damaging |
Het |
Kansl3 |
G |
T |
1: 36,390,848 (GRCm39) |
D395E |
possibly damaging |
Het |
Marchf10 |
A |
G |
11: 105,299,502 (GRCm39) |
S116P |
probably benign |
Het |
Med12l |
C |
T |
3: 59,001,180 (GRCm39) |
Q748* |
probably null |
Het |
Mtbp |
T |
G |
15: 55,421,961 (GRCm39) |
D61E |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,411,391 (GRCm39) |
I1446L |
unknown |
Het |
Myh15 |
T |
C |
16: 48,901,705 (GRCm39) |
V266A |
possibly damaging |
Het |
Nap1l1 |
G |
A |
10: 111,330,655 (GRCm39) |
|
probably null |
Het |
Napsa |
A |
G |
7: 44,235,159 (GRCm39) |
T315A |
probably benign |
Het |
Nlrc5 |
A |
T |
8: 95,206,350 (GRCm39) |
I734F |
probably damaging |
Het |
Nnt |
A |
G |
13: 119,531,198 (GRCm39) |
V183A |
probably damaging |
Het |
Nploc4 |
A |
T |
11: 120,276,614 (GRCm39) |
D477E |
probably benign |
Het |
Nrip3 |
A |
G |
7: 109,364,695 (GRCm39) |
S144P |
probably damaging |
Het |
Ntng1 |
A |
T |
3: 109,842,445 (GRCm39) |
F109L |
probably benign |
Het |
Or5p61 |
A |
G |
7: 107,758,883 (GRCm39) |
Y66H |
probably damaging |
Het |
Or5v1 |
T |
A |
17: 37,809,776 (GRCm39) |
V78D |
probably damaging |
Het |
Or6aa1 |
G |
A |
7: 86,044,752 (GRCm39) |
|
probably benign |
Het |
Or8b36 |
A |
G |
9: 37,937,795 (GRCm39) |
E231G |
probably benign |
Het |
Pacsin1 |
G |
A |
17: 27,921,707 (GRCm39) |
D30N |
probably damaging |
Het |
Pbld2 |
A |
T |
10: 62,860,368 (GRCm39) |
|
probably benign |
Het |
Pcnx4 |
C |
T |
12: 72,613,750 (GRCm39) |
T565I |
probably damaging |
Het |
Pdzk1 |
A |
T |
3: 96,763,246 (GRCm39) |
T225S |
probably benign |
Het |
Phyhip |
T |
G |
14: 70,704,639 (GRCm39) |
I286S |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,813,086 (GRCm39) |
Y3903N |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,942,698 (GRCm39) |
L222Q |
probably damaging |
Het |
Plcd4 |
T |
A |
1: 74,593,662 (GRCm39) |
H262Q |
probably benign |
Het |
Plekhh1 |
C |
T |
12: 79,109,390 (GRCm39) |
A474V |
probably benign |
Het |
Plppr3 |
T |
C |
10: 79,701,537 (GRCm39) |
E435G |
probably damaging |
Het |
Poln |
T |
A |
5: 34,276,340 (GRCm39) |
N305I |
possibly damaging |
Het |
Pou3f2 |
T |
C |
4: 22,486,874 (GRCm39) |
T420A |
probably benign |
Het |
Ppdpf |
T |
C |
2: 180,829,523 (GRCm39) |
Y17H |
probably damaging |
Het |
Prrx2 |
C |
A |
2: 30,768,485 (GRCm39) |
T104K |
probably damaging |
Het |
Ptprj |
A |
T |
2: 90,294,822 (GRCm39) |
L462H |
probably benign |
Het |
Radil |
T |
C |
5: 142,471,304 (GRCm39) |
T991A |
probably damaging |
Het |
Rbsn |
T |
C |
6: 92,178,608 (GRCm39) |
E147G |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,300,742 (GRCm39) |
V35M |
probably benign |
Het |
Rps6ka1 |
T |
C |
4: 133,599,373 (GRCm39) |
Q18R |
probably benign |
Het |
Setbp1 |
T |
A |
18: 78,902,734 (GRCm39) |
D311V |
possibly damaging |
Het |
Setd2 |
C |
T |
9: 110,377,865 (GRCm39) |
S560L |
possibly damaging |
Het |
Slc12a5 |
A |
T |
2: 164,816,878 (GRCm39) |
I134F |
probably damaging |
Het |
Speer1h |
C |
T |
5: 11,647,706 (GRCm39) |
T148I |
possibly damaging |
Het |
Svil |
A |
G |
18: 5,116,080 (GRCm39) |
D2035G |
probably damaging |
Het |
Syngap1 |
T |
C |
17: 27,178,985 (GRCm39) |
Y665H |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,043,519 (GRCm39) |
Y547H |
possibly damaging |
Het |
Tgm2 |
A |
G |
2: 157,980,812 (GRCm39) |
V83A |
probably benign |
Het |
Tmem233 |
T |
C |
5: 116,189,429 (GRCm39) |
I117V |
probably benign |
Het |
Tsen34 |
A |
G |
7: 3,703,640 (GRCm39) |
T293A |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,709,023 (GRCm39) |
V8752A |
unknown |
Het |
Ubac1 |
A |
G |
2: 25,904,974 (GRCm39) |
V88A |
probably benign |
Het |
Uchl4 |
T |
C |
9: 64,142,621 (GRCm39) |
V34A |
probably damaging |
Het |
Ugt2a2 |
C |
T |
5: 87,608,435 (GRCm39) |
R468H |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,749 (GRCm39) |
T255S |
probably benign |
Het |
Wdr6 |
T |
A |
9: 108,450,564 (GRCm39) |
N988I |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,903,389 (GRCm39) |
I2359N |
unknown |
Het |
Ybey |
A |
G |
10: 76,304,025 (GRCm39) |
V59A |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,349,375 (GRCm39) |
C271S |
possibly damaging |
Het |
Zfp397 |
A |
G |
18: 24,090,122 (GRCm39) |
N142S |
probably benign |
Het |
Zfy1 |
A |
T |
Y: 725,788 (GRCm39) |
V659E |
probably damaging |
Het |
|
Other mutations in Mroh7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01722:Mroh7
|
APN |
4 |
106,560,358 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01729:Mroh7
|
APN |
4 |
106,561,402 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01834:Mroh7
|
APN |
4 |
106,538,071 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02003:Mroh7
|
APN |
4 |
106,559,726 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02135:Mroh7
|
APN |
4 |
106,559,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02335:Mroh7
|
APN |
4 |
106,564,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02532:Mroh7
|
APN |
4 |
106,577,788 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02896:Mroh7
|
APN |
4 |
106,557,013 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03066:Mroh7
|
APN |
4 |
106,549,595 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03298:Mroh7
|
APN |
4 |
106,571,288 (GRCm39) |
nonsense |
probably null |
|
holy
|
UTSW |
4 |
106,567,152 (GRCm39) |
splice site |
probably null |
|
moley
|
UTSW |
4 |
106,551,509 (GRCm39) |
splice site |
probably null |
|
P0016:Mroh7
|
UTSW |
4 |
106,565,054 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0019:Mroh7
|
UTSW |
4 |
106,578,623 (GRCm39) |
missense |
probably benign |
0.07 |
R0094:Mroh7
|
UTSW |
4 |
106,560,381 (GRCm39) |
missense |
probably damaging |
0.98 |
R0105:Mroh7
|
UTSW |
4 |
106,568,467 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0105:Mroh7
|
UTSW |
4 |
106,568,467 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0515:Mroh7
|
UTSW |
4 |
106,548,861 (GRCm39) |
missense |
probably benign |
0.01 |
R0828:Mroh7
|
UTSW |
4 |
106,557,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R0831:Mroh7
|
UTSW |
4 |
106,537,990 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1107:Mroh7
|
UTSW |
4 |
106,564,791 (GRCm39) |
splice site |
probably null |
|
R1301:Mroh7
|
UTSW |
4 |
106,577,692 (GRCm39) |
missense |
probably damaging |
0.99 |
R1456:Mroh7
|
UTSW |
4 |
106,552,338 (GRCm39) |
splice site |
probably benign |
|
R1491:Mroh7
|
UTSW |
4 |
106,560,255 (GRCm39) |
missense |
probably benign |
0.11 |
R1540:Mroh7
|
UTSW |
4 |
106,560,273 (GRCm39) |
missense |
probably benign |
0.11 |
R1560:Mroh7
|
UTSW |
4 |
106,568,451 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1645:Mroh7
|
UTSW |
4 |
106,577,865 (GRCm39) |
missense |
probably benign |
0.19 |
R1804:Mroh7
|
UTSW |
4 |
106,551,589 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2162:Mroh7
|
UTSW |
4 |
106,557,378 (GRCm39) |
missense |
probably damaging |
0.96 |
R2265:Mroh7
|
UTSW |
4 |
106,578,124 (GRCm39) |
missense |
probably benign |
0.01 |
R2866:Mroh7
|
UTSW |
4 |
106,548,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Mroh7
|
UTSW |
4 |
106,561,407 (GRCm39) |
missense |
probably benign |
0.25 |
R3718:Mroh7
|
UTSW |
4 |
106,561,407 (GRCm39) |
missense |
probably benign |
0.25 |
R4530:Mroh7
|
UTSW |
4 |
106,577,634 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4661:Mroh7
|
UTSW |
4 |
106,548,710 (GRCm39) |
critical splice donor site |
probably null |
|
R4706:Mroh7
|
UTSW |
4 |
106,548,821 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4910:Mroh7
|
UTSW |
4 |
106,567,152 (GRCm39) |
splice site |
probably null |
|
R4965:Mroh7
|
UTSW |
4 |
106,548,184 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4969:Mroh7
|
UTSW |
4 |
106,538,070 (GRCm39) |
missense |
probably benign |
|
R4971:Mroh7
|
UTSW |
4 |
106,548,749 (GRCm39) |
missense |
probably benign |
0.04 |
R5083:Mroh7
|
UTSW |
4 |
106,547,515 (GRCm39) |
missense |
probably benign |
0.03 |
R5207:Mroh7
|
UTSW |
4 |
106,578,583 (GRCm39) |
missense |
probably damaging |
0.97 |
R5364:Mroh7
|
UTSW |
4 |
106,548,840 (GRCm39) |
missense |
probably benign |
0.10 |
R5392:Mroh7
|
UTSW |
4 |
106,568,448 (GRCm39) |
critical splice donor site |
probably null |
|
R5630:Mroh7
|
UTSW |
4 |
106,577,764 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5691:Mroh7
|
UTSW |
4 |
106,559,815 (GRCm39) |
missense |
probably damaging |
0.96 |
R5703:Mroh7
|
UTSW |
4 |
106,565,757 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5707:Mroh7
|
UTSW |
4 |
106,539,082 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5919:Mroh7
|
UTSW |
4 |
106,551,509 (GRCm39) |
splice site |
probably null |
|
R5979:Mroh7
|
UTSW |
4 |
106,578,123 (GRCm39) |
missense |
probably benign |
0.00 |
R6479:Mroh7
|
UTSW |
4 |
106,560,385 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6520:Mroh7
|
UTSW |
4 |
106,578,460 (GRCm39) |
missense |
probably benign |
0.00 |
R6657:Mroh7
|
UTSW |
4 |
106,559,697 (GRCm39) |
nonsense |
probably null |
|
R6732:Mroh7
|
UTSW |
4 |
106,537,910 (GRCm39) |
frame shift |
probably null |
|
R6817:Mroh7
|
UTSW |
4 |
106,571,312 (GRCm39) |
missense |
probably benign |
0.00 |
R6980:Mroh7
|
UTSW |
4 |
106,557,434 (GRCm39) |
missense |
probably benign |
0.05 |
R7062:Mroh7
|
UTSW |
4 |
106,541,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Mroh7
|
UTSW |
4 |
106,568,517 (GRCm39) |
missense |
probably benign |
0.07 |
R7169:Mroh7
|
UTSW |
4 |
106,548,836 (GRCm39) |
missense |
probably damaging |
0.99 |
R7419:Mroh7
|
UTSW |
4 |
106,541,115 (GRCm39) |
missense |
probably benign |
|
R7516:Mroh7
|
UTSW |
4 |
106,548,316 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Mroh7
|
UTSW |
4 |
106,566,899 (GRCm39) |
missense |
probably benign |
0.22 |
R7540:Mroh7
|
UTSW |
4 |
106,577,595 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7849:Mroh7
|
UTSW |
4 |
106,578,287 (GRCm39) |
missense |
probably benign |
|
R7920:Mroh7
|
UTSW |
4 |
106,564,773 (GRCm39) |
missense |
probably benign |
|
R7998:Mroh7
|
UTSW |
4 |
106,568,478 (GRCm39) |
missense |
probably benign |
0.02 |
R8026:Mroh7
|
UTSW |
4 |
106,578,634 (GRCm39) |
missense |
probably benign |
0.01 |
R8122:Mroh7
|
UTSW |
4 |
106,559,726 (GRCm39) |
missense |
probably damaging |
0.96 |
R8249:Mroh7
|
UTSW |
4 |
106,578,409 (GRCm39) |
missense |
probably benign |
0.00 |
R9188:Mroh7
|
UTSW |
4 |
106,566,789 (GRCm39) |
missense |
probably benign |
0.01 |
|