Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl1 |
A |
G |
8: 46,945,930 (GRCm39) |
Y21C |
probably damaging |
Het |
Adamts7 |
A |
T |
9: 90,060,218 (GRCm39) |
I290F |
probably damaging |
Het |
Adcy5 |
G |
A |
16: 35,124,052 (GRCm39) |
V1244I |
probably damaging |
Het |
Adnp |
A |
T |
2: 168,025,945 (GRCm39) |
I450N |
probably damaging |
Het |
AL732309.1 |
A |
T |
2: 25,136,211 (GRCm39) |
M1K |
probably null |
Het |
Alox15 |
C |
T |
11: 70,236,370 (GRCm39) |
G510D |
possibly damaging |
Het |
Arhgef16 |
C |
A |
4: 154,363,502 (GRCm39) |
E685* |
probably null |
Het |
Atp13a2 |
A |
G |
4: 140,730,038 (GRCm39) |
E643G |
probably damaging |
Het |
AW554918 |
C |
A |
18: 25,423,061 (GRCm39) |
Q171K |
probably damaging |
Het |
Bdkrb2 |
A |
G |
12: 105,558,352 (GRCm39) |
T198A |
probably benign |
Het |
C7 |
T |
C |
15: 5,023,645 (GRCm39) |
E721G |
probably damaging |
Het |
Cc2d2b |
T |
C |
19: 40,797,848 (GRCm39) |
Y823H |
unknown |
Het |
Cd74 |
T |
C |
18: 60,944,366 (GRCm39) |
V192A |
probably benign |
Het |
Cdc42bpg |
G |
A |
19: 6,361,067 (GRCm39) |
A231T |
probably damaging |
Het |
Cers6 |
G |
A |
2: 68,777,706 (GRCm39) |
|
probably benign |
Het |
Copg2 |
T |
C |
6: 30,788,637 (GRCm39) |
I555M |
probably benign |
Het |
Cracd |
T |
G |
5: 76,988,757 (GRCm39) |
V36G |
unknown |
Het |
Crnkl1 |
A |
G |
2: 145,770,216 (GRCm39) |
V209A |
possibly damaging |
Het |
Dock7 |
T |
C |
4: 98,971,272 (GRCm39) |
T98A |
|
Het |
Enpp5 |
T |
C |
17: 44,396,414 (GRCm39) |
I442T |
probably benign |
Het |
Fbxw19 |
T |
C |
9: 109,310,641 (GRCm39) |
Y427C |
probably damaging |
Het |
Fktn |
T |
C |
4: 53,744,653 (GRCm39) |
V311A |
probably benign |
Het |
Fyb1 |
T |
G |
15: 6,674,358 (GRCm39) |
S665A |
possibly damaging |
Het |
Igkv6-20 |
T |
C |
6: 70,313,417 (GRCm39) |
Y16C |
probably benign |
Het |
Ints10 |
A |
G |
8: 69,261,129 (GRCm39) |
R370G |
possibly damaging |
Het |
Iqub |
A |
T |
6: 24,446,198 (GRCm39) |
I742N |
possibly damaging |
Het |
Kcnn3 |
T |
C |
3: 89,574,407 (GRCm39) |
Y640H |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,341,303 (GRCm39) |
V959A |
probably benign |
Het |
Marcksl1 |
A |
G |
4: 129,408,816 (GRCm39) |
S132G |
probably benign |
Het |
Mfsd4b3-ps |
T |
A |
10: 39,824,010 (GRCm39) |
K83N |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,760,862 (GRCm39) |
E384G |
possibly damaging |
Het |
Morn5 |
G |
T |
2: 35,939,553 (GRCm39) |
G5W |
probably damaging |
Het |
Mrpl46 |
A |
G |
7: 78,432,671 (GRCm39) |
S36P |
probably benign |
Het |
Naalad2 |
T |
C |
9: 18,274,534 (GRCm39) |
N336S |
probably benign |
Het |
Nepro |
A |
G |
16: 44,544,790 (GRCm39) |
N22S |
probably benign |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Or10x4 |
C |
T |
1: 174,219,109 (GRCm39) |
T158I |
probably benign |
Het |
Or1e1f |
A |
T |
11: 73,856,135 (GRCm39) |
I234F |
probably benign |
Het |
Or2d36 |
T |
C |
7: 106,747,387 (GRCm39) |
I288T |
probably damaging |
Het |
Or8c16 |
T |
A |
9: 38,130,498 (GRCm39) |
Y123* |
probably null |
Het |
Or9r7 |
A |
G |
10: 129,962,335 (GRCm39) |
V197A |
possibly damaging |
Het |
Pcnx1 |
A |
T |
12: 82,020,047 (GRCm39) |
N724Y |
|
Het |
Pde8b |
G |
A |
13: 95,164,204 (GRCm39) |
R669C |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,397,290 (GRCm39) |
|
probably null |
Het |
Pls1 |
A |
G |
9: 95,655,696 (GRCm39) |
V352A |
probably damaging |
Het |
Prb1b |
T |
C |
6: 132,288,972 (GRCm39) |
N284S |
unknown |
Het |
Prtg |
A |
T |
9: 72,758,977 (GRCm39) |
I444F |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,219,776 (GRCm39) |
H1998L |
probably damaging |
Het |
Qrich2 |
A |
T |
11: 116,356,450 (GRCm39) |
V133D |
probably benign |
Het |
Rab35 |
C |
A |
5: 115,778,246 (GRCm39) |
R71S |
probably damaging |
Het |
Scgb2b12 |
A |
G |
7: 32,026,054 (GRCm39) |
L46P |
probably damaging |
Het |
Sdha |
A |
T |
13: 74,475,483 (GRCm39) |
|
probably benign |
Het |
Sdr39u1 |
C |
A |
14: 56,135,209 (GRCm39) |
V245F |
probably benign |
Het |
Sgo2a |
T |
A |
1: 58,058,772 (GRCm39) |
V1117E |
possibly damaging |
Het |
Slc12a2 |
T |
C |
18: 58,074,867 (GRCm39) |
S1154P |
probably damaging |
Het |
Slc6a1 |
A |
T |
6: 114,287,554 (GRCm39) |
Q441L |
possibly damaging |
Het |
Smtnl2 |
A |
T |
11: 72,293,835 (GRCm39) |
|
probably null |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tmem38b |
A |
T |
4: 53,848,924 (GRCm39) |
I110F |
probably damaging |
Het |
Ubqln1 |
A |
G |
13: 58,325,721 (GRCm39) |
I573T |
probably damaging |
Het |
Usp9y |
T |
C |
Y: 1,356,235 (GRCm39) |
I1155M |
possibly damaging |
Het |
Vipr1 |
A |
G |
9: 121,490,118 (GRCm39) |
I164V |
probably benign |
Het |
Vps13b |
T |
G |
15: 35,623,925 (GRCm39) |
S1281A |
possibly damaging |
Het |
Vps13d |
A |
G |
4: 144,882,374 (GRCm39) |
L1073P |
|
Het |
Wipi1 |
C |
T |
11: 109,473,952 (GRCm39) |
|
probably null |
Het |
Zdhhc8 |
G |
A |
16: 18,042,686 (GRCm39) |
P505S |
probably damaging |
Het |
Zfp292 |
C |
T |
4: 34,839,899 (GRCm39) |
V84I |
probably benign |
Het |
Zfp712 |
T |
C |
13: 67,188,791 (GRCm39) |
T579A |
probably benign |
Het |
Zfp788 |
G |
A |
7: 41,299,638 (GRCm39) |
R758Q |
probably benign |
Het |
|
Other mutations in Mtif2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00942:Mtif2
|
APN |
11 |
29,488,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Mtif2
|
APN |
11 |
29,494,973 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01323:Mtif2
|
APN |
11 |
29,491,447 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01360:Mtif2
|
APN |
11 |
29,480,110 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01744:Mtif2
|
APN |
11 |
29,494,417 (GRCm39) |
unclassified |
probably benign |
|
IGL01757:Mtif2
|
APN |
11 |
29,491,337 (GRCm39) |
unclassified |
probably benign |
|
IGL02247:Mtif2
|
APN |
11 |
29,490,642 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02642:Mtif2
|
APN |
11 |
29,494,395 (GRCm39) |
missense |
probably benign |
|
IGL03093:Mtif2
|
APN |
11 |
29,480,702 (GRCm39) |
splice site |
probably benign |
|
R0418:Mtif2
|
UTSW |
11 |
29,483,401 (GRCm39) |
splice site |
probably benign |
|
R0554:Mtif2
|
UTSW |
11 |
29,483,398 (GRCm39) |
critical splice donor site |
probably null |
|
R0577:Mtif2
|
UTSW |
11 |
29,490,862 (GRCm39) |
critical splice donor site |
probably null |
|
R1159:Mtif2
|
UTSW |
11 |
29,490,729 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1168:Mtif2
|
UTSW |
11 |
29,486,914 (GRCm39) |
missense |
probably benign |
0.11 |
R1344:Mtif2
|
UTSW |
11 |
29,495,002 (GRCm39) |
missense |
probably benign |
|
R1418:Mtif2
|
UTSW |
11 |
29,495,002 (GRCm39) |
missense |
probably benign |
|
R1482:Mtif2
|
UTSW |
11 |
29,486,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Mtif2
|
UTSW |
11 |
29,490,721 (GRCm39) |
missense |
probably benign |
0.00 |
R1850:Mtif2
|
UTSW |
11 |
29,490,683 (GRCm39) |
missense |
probably benign |
0.03 |
R3692:Mtif2
|
UTSW |
11 |
29,490,718 (GRCm39) |
missense |
probably benign |
0.03 |
R4471:Mtif2
|
UTSW |
11 |
29,490,053 (GRCm39) |
splice site |
probably benign |
|
R4730:Mtif2
|
UTSW |
11 |
29,490,834 (GRCm39) |
missense |
probably benign |
0.00 |
R5248:Mtif2
|
UTSW |
11 |
29,486,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R5343:Mtif2
|
UTSW |
11 |
29,486,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5989:Mtif2
|
UTSW |
11 |
29,480,098 (GRCm39) |
missense |
probably damaging |
0.96 |
R6511:Mtif2
|
UTSW |
11 |
29,486,949 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7209:Mtif2
|
UTSW |
11 |
29,479,996 (GRCm39) |
missense |
probably benign |
0.00 |
R7318:Mtif2
|
UTSW |
11 |
29,490,115 (GRCm39) |
missense |
probably benign |
0.25 |
R9120:Mtif2
|
UTSW |
11 |
29,483,951 (GRCm39) |
missense |
probably benign |
0.00 |
R9224:Mtif2
|
UTSW |
11 |
29,494,364 (GRCm39) |
missense |
probably benign |
0.09 |
R9266:Mtif2
|
UTSW |
11 |
29,480,065 (GRCm39) |
missense |
probably benign |
0.00 |
R9745:Mtif2
|
UTSW |
11 |
29,476,587 (GRCm39) |
start gained |
probably benign |
|
X0064:Mtif2
|
UTSW |
11 |
29,488,760 (GRCm39) |
missense |
probably benign |
0.07 |
|