Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts5 |
A |
T |
16: 85,696,854 (GRCm39) |
L101Q |
probably damaging |
Het |
Arhgap18 |
A |
T |
10: 26,746,007 (GRCm39) |
I293F |
possibly damaging |
Het |
Atp8b1 |
T |
A |
18: 64,678,346 (GRCm39) |
Q850L |
probably damaging |
Het |
B4galnt3 |
A |
T |
6: 120,202,148 (GRCm39) |
F118Y |
probably benign |
Het |
Bcl6 |
A |
G |
16: 23,790,163 (GRCm39) |
|
probably null |
Het |
Cc2d2b |
T |
A |
19: 40,744,974 (GRCm39) |
L31Q |
probably benign |
Het |
Cd5l |
G |
T |
3: 87,275,162 (GRCm39) |
E234* |
probably null |
Het |
Cemip2 |
C |
T |
19: 21,807,321 (GRCm39) |
L917F |
probably benign |
Het |
Cfap65 |
T |
C |
1: 74,965,784 (GRCm39) |
T409A |
probably benign |
Het |
Chst5 |
A |
T |
8: 112,617,557 (GRCm39) |
I21N |
probably benign |
Het |
Cldn20 |
T |
C |
17: 3,583,030 (GRCm39) |
Y68H |
probably benign |
Het |
Col4a4 |
T |
C |
1: 82,506,514 (GRCm39) |
M269V |
unknown |
Het |
Dgkh |
A |
G |
14: 78,832,585 (GRCm39) |
|
probably null |
Het |
Dpp6 |
A |
G |
5: 27,656,242 (GRCm39) |
T166A |
probably benign |
Het |
Drosha |
A |
G |
15: 12,881,731 (GRCm39) |
D754G |
probably damaging |
Het |
Epb41l4a |
C |
A |
18: 33,987,326 (GRCm39) |
K350N |
probably damaging |
Het |
Fsd1 |
T |
G |
17: 56,295,150 (GRCm39) |
D46E |
probably benign |
Het |
Gabra1 |
T |
C |
11: 42,024,418 (GRCm39) |
D419G |
probably damaging |
Het |
Golga4 |
T |
A |
9: 118,377,770 (GRCm39) |
D458E |
probably damaging |
Het |
Grm6 |
C |
A |
11: 50,742,369 (GRCm39) |
A134E |
probably benign |
Het |
Ikzf1 |
T |
A |
11: 11,698,339 (GRCm39) |
S63R |
probably damaging |
Het |
Ilvbl |
G |
A |
10: 78,412,500 (GRCm39) |
V74I |
probably benign |
Het |
Kcng2 |
C |
T |
18: 80,339,305 (GRCm39) |
V328M |
probably benign |
Het |
Kpna7 |
T |
C |
5: 144,941,855 (GRCm39) |
E145G |
probably benign |
Het |
Krt81 |
A |
G |
15: 101,357,448 (GRCm39) |
V428A |
probably damaging |
Het |
Lalba |
T |
C |
15: 98,380,549 (GRCm39) |
M2V |
probably benign |
Het |
Lrpprc |
T |
C |
17: 85,084,375 (GRCm39) |
S113G |
probably benign |
Het |
Mboat1 |
A |
C |
13: 30,410,289 (GRCm39) |
M249L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,571,538 (GRCm39) |
H327L |
unknown |
Het |
Myh1 |
A |
G |
11: 67,106,748 (GRCm39) |
I1277V |
probably benign |
Het |
Naf1 |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
8: 67,313,200 (GRCm39) |
|
probably benign |
Het |
Naga |
C |
A |
15: 82,214,348 (GRCm39) |
V388L |
probably benign |
Het |
Nfkb1 |
A |
C |
3: 135,291,162 (GRCm39) |
M957R |
possibly damaging |
Het |
Nol12 |
C |
A |
15: 78,824,793 (GRCm39) |
S157* |
probably null |
Het |
Or13c25 |
A |
G |
4: 52,911,368 (GRCm39) |
V142A |
possibly damaging |
Het |
Or5g23 |
A |
G |
2: 85,438,751 (GRCm39) |
F168L |
possibly damaging |
Het |
Or8u3-ps |
A |
T |
2: 85,952,840 (GRCm39) |
D191V |
possibly damaging |
Het |
Pcdhga5 |
T |
C |
18: 37,828,098 (GRCm39) |
V182A |
probably benign |
Het |
Pik3r4 |
A |
G |
9: 105,547,081 (GRCm39) |
E953G |
probably damaging |
Het |
Piwil2 |
C |
T |
14: 70,631,506 (GRCm39) |
R646Q |
probably damaging |
Het |
Plxnc1 |
T |
C |
10: 94,779,971 (GRCm39) |
H157R |
probably damaging |
Het |
Prrg4 |
A |
T |
2: 104,669,723 (GRCm39) |
F131L |
probably benign |
Het |
Prss3b |
C |
A |
6: 41,010,127 (GRCm39) |
R69L |
probably benign |
Het |
Rab28 |
A |
G |
5: 41,865,313 (GRCm39) |
S4P |
probably damaging |
Het |
Ranbp2 |
C |
A |
10: 58,291,260 (GRCm39) |
Q209K |
probably benign |
Het |
Schip1 |
G |
A |
3: 67,972,317 (GRCm39) |
D15N |
probably benign |
Het |
Serpina3f |
T |
G |
12: 104,184,477 (GRCm39) |
M207R |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,422,193 (GRCm39) |
M487K |
possibly damaging |
Het |
Sh3tc2 |
A |
T |
18: 62,122,651 (GRCm39) |
I471F |
probably benign |
Het |
Slamf1 |
G |
A |
1: 171,602,467 (GRCm39) |
V65I |
possibly damaging |
Het |
Slit3 |
T |
C |
11: 35,574,871 (GRCm39) |
C1062R |
probably damaging |
Het |
Snapc4 |
T |
G |
2: 26,263,446 (GRCm39) |
K344N |
probably damaging |
Het |
Sorl1 |
A |
G |
9: 41,895,822 (GRCm39) |
Y1778H |
probably damaging |
Het |
Spon2 |
G |
A |
5: 33,373,019 (GRCm39) |
R228C |
probably damaging |
Het |
Sv2c |
A |
G |
13: 96,113,203 (GRCm39) |
I582T |
possibly damaging |
Het |
Tamm41 |
C |
T |
6: 114,993,139 (GRCm39) |
V205M |
probably damaging |
Het |
Trpm2 |
T |
C |
10: 77,761,623 (GRCm39) |
D1009G |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,831,613 (GRCm39) |
S1493P |
probably damaging |
Het |
Ttc34 |
G |
A |
4: 154,923,731 (GRCm39) |
V147I |
possibly damaging |
Het |
Tut7 |
A |
G |
13: 59,947,496 (GRCm39) |
F942L |
probably benign |
Het |
Uba2 |
C |
T |
7: 33,850,275 (GRCm39) |
A393T |
probably damaging |
Het |
Ubn2 |
T |
A |
6: 38,440,873 (GRCm39) |
N416K |
probably benign |
Het |
Uevld |
T |
C |
7: 46,593,553 (GRCm39) |
N233S |
probably benign |
Het |
Upp2 |
G |
A |
2: 58,664,160 (GRCm39) |
M142I |
possibly damaging |
Het |
Vps52 |
T |
A |
17: 34,181,108 (GRCm39) |
V450D |
probably benign |
Het |
Wdr31 |
A |
T |
4: 62,378,873 (GRCm39) |
F118Y |
probably damaging |
Het |
Zfp110 |
T |
A |
7: 12,582,922 (GRCm39) |
D523E |
possibly damaging |
Het |
Zfp367 |
A |
T |
13: 64,293,457 (GRCm39) |
V143D |
probably damaging |
Het |
Zfp950 |
T |
C |
19: 61,108,379 (GRCm39) |
I235V |
probably benign |
Het |
|
Other mutations in Meltf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01811:Meltf
|
APN |
16 |
31,707,803 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02942:Meltf
|
APN |
16 |
31,709,596 (GRCm39) |
nonsense |
probably null |
|
IGL03340:Meltf
|
APN |
16 |
31,711,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Meltf
|
UTSW |
16 |
31,700,776 (GRCm39) |
missense |
probably damaging |
0.99 |
R1023:Meltf
|
UTSW |
16 |
31,703,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Meltf
|
UTSW |
16 |
31,702,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1767:Meltf
|
UTSW |
16 |
31,702,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Meltf
|
UTSW |
16 |
31,715,395 (GRCm39) |
missense |
probably benign |
0.00 |
R1900:Meltf
|
UTSW |
16 |
31,700,787 (GRCm39) |
critical splice donor site |
probably null |
|
R1993:Meltf
|
UTSW |
16 |
31,711,440 (GRCm39) |
nonsense |
probably null |
|
R3423:Meltf
|
UTSW |
16 |
31,715,343 (GRCm39) |
nonsense |
probably null |
|
R3425:Meltf
|
UTSW |
16 |
31,715,343 (GRCm39) |
nonsense |
probably null |
|
R3804:Meltf
|
UTSW |
16 |
31,703,816 (GRCm39) |
missense |
probably benign |
0.23 |
R4724:Meltf
|
UTSW |
16 |
31,711,323 (GRCm39) |
missense |
probably benign |
0.03 |
R4976:Meltf
|
UTSW |
16 |
31,713,532 (GRCm39) |
missense |
probably benign |
0.01 |
R5007:Meltf
|
UTSW |
16 |
31,706,380 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5058:Meltf
|
UTSW |
16 |
31,706,421 (GRCm39) |
splice site |
probably null |
|
R5534:Meltf
|
UTSW |
16 |
31,709,632 (GRCm39) |
critical splice donor site |
probably null |
|
R5661:Meltf
|
UTSW |
16 |
31,700,744 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6028:Meltf
|
UTSW |
16 |
31,706,294 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6424:Meltf
|
UTSW |
16 |
31,699,080 (GRCm39) |
nonsense |
probably null |
|
R6464:Meltf
|
UTSW |
16 |
31,709,594 (GRCm39) |
missense |
probably benign |
0.19 |
R6479:Meltf
|
UTSW |
16 |
31,700,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Meltf
|
UTSW |
16 |
31,707,717 (GRCm39) |
nonsense |
probably null |
|
R6629:Meltf
|
UTSW |
16 |
31,703,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6964:Meltf
|
UTSW |
16 |
31,698,980 (GRCm39) |
missense |
probably benign |
0.41 |
R7133:Meltf
|
UTSW |
16 |
31,711,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7169:Meltf
|
UTSW |
16 |
31,698,980 (GRCm39) |
missense |
probably benign |
0.41 |
R7198:Meltf
|
UTSW |
16 |
31,702,617 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7212:Meltf
|
UTSW |
16 |
31,709,632 (GRCm39) |
critical splice donor site |
probably null |
|
R7246:Meltf
|
UTSW |
16 |
31,713,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7407:Meltf
|
UTSW |
16 |
31,713,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Meltf
|
UTSW |
16 |
31,703,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Meltf
|
UTSW |
16 |
31,700,756 (GRCm39) |
missense |
probably benign |
0.12 |
R7764:Meltf
|
UTSW |
16 |
31,699,085 (GRCm39) |
missense |
probably benign |
0.01 |
R8220:Meltf
|
UTSW |
16 |
31,706,233 (GRCm39) |
missense |
probably benign |
0.01 |
R8840:Meltf
|
UTSW |
16 |
31,716,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R8896:Meltf
|
UTSW |
16 |
31,709,522 (GRCm39) |
splice site |
probably benign |
|
R9214:Meltf
|
UTSW |
16 |
31,697,763 (GRCm39) |
missense |
probably benign |
|
R9563:Meltf
|
UTSW |
16 |
31,703,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R9638:Meltf
|
UTSW |
16 |
31,706,409 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0062:Meltf
|
UTSW |
16 |
31,699,018 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Meltf
|
UTSW |
16 |
31,699,052 (GRCm39) |
missense |
probably damaging |
1.00 |
|