Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamp |
A |
G |
1: 74,320,705 (GRCm39) |
V288A |
possibly damaging |
Het |
Ankhd1 |
T |
A |
18: 36,711,810 (GRCm39) |
S135R |
|
Het |
Axl |
G |
A |
7: 25,460,846 (GRCm39) |
T721I |
probably damaging |
Het |
Blnk |
G |
A |
19: 40,922,962 (GRCm39) |
A388V |
probably benign |
Het |
C8b |
T |
C |
4: 104,641,631 (GRCm39) |
V189A |
probably damaging |
Het |
Ccdc33 |
G |
C |
9: 57,983,842 (GRCm39) |
I452M |
probably benign |
Het |
Cfap57 |
T |
C |
4: 118,412,048 (GRCm39) |
T1199A |
probably benign |
Het |
Chga |
G |
A |
12: 102,528,144 (GRCm39) |
V212M |
probably benign |
Het |
Cspp1 |
T |
A |
1: 10,186,875 (GRCm39) |
M887K |
probably damaging |
Het |
Cyp3a16 |
G |
C |
5: 145,406,434 (GRCm39) |
A6G |
unknown |
Het |
Cyp4f17 |
G |
T |
17: 32,743,868 (GRCm39) |
E349* |
probably null |
Het |
Dnajc13 |
A |
T |
9: 104,085,039 (GRCm39) |
D791E |
probably benign |
Het |
Dpysl5 |
T |
C |
5: 30,935,397 (GRCm39) |
Y167H |
probably benign |
Het |
Dqx1 |
G |
T |
6: 83,036,759 (GRCm39) |
Q254H |
possibly damaging |
Het |
Eef1g |
A |
G |
19: 8,955,383 (GRCm39) |
T411A |
probably benign |
Het |
Fancl |
C |
A |
11: 26,337,231 (GRCm39) |
A6E |
probably benign |
Het |
Gabrr3 |
A |
G |
16: 59,227,830 (GRCm39) |
Q29R |
probably benign |
Het |
Gtf2h2 |
A |
C |
13: 100,617,778 (GRCm39) |
L168R |
probably damaging |
Het |
Hacl1 |
T |
A |
14: 31,338,338 (GRCm39) |
Q413L |
probably benign |
Het |
Hdc |
A |
T |
2: 126,439,837 (GRCm39) |
V372E |
probably damaging |
Het |
Hr |
A |
T |
14: 70,795,079 (GRCm39) |
H208L |
possibly damaging |
Het |
Htr6 |
T |
C |
4: 138,789,501 (GRCm39) |
R255G |
possibly damaging |
Het |
Jup |
C |
T |
11: 100,270,391 (GRCm39) |
C372Y |
probably damaging |
Het |
Kank2 |
A |
G |
9: 21,681,370 (GRCm39) |
V747A |
probably damaging |
Het |
Kif5c |
A |
G |
2: 49,620,291 (GRCm39) |
T508A |
probably benign |
Het |
Klhdc8b |
A |
G |
9: 108,326,927 (GRCm39) |
V145A |
probably damaging |
Het |
Klk1b21 |
T |
A |
7: 43,754,924 (GRCm39) |
V73D |
probably damaging |
Het |
Ksr1 |
T |
A |
11: 78,911,572 (GRCm39) |
M737L |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,328,564 (GRCm39) |
Y4723C |
probably damaging |
Het |
Mcm7 |
T |
C |
5: 138,167,397 (GRCm39) |
Y182C |
probably damaging |
Het |
Mtf2 |
T |
C |
5: 108,252,398 (GRCm39) |
|
probably null |
Het |
Nrxn2 |
A |
T |
19: 6,498,299 (GRCm39) |
T255S |
probably benign |
Het |
Or10v9 |
A |
G |
19: 11,832,666 (GRCm39) |
L217P |
probably damaging |
Het |
Or10x4 |
A |
T |
1: 174,218,649 (GRCm39) |
T5S |
probably damaging |
Het |
Or11g25 |
T |
C |
14: 50,723,707 (GRCm39) |
L264P |
probably damaging |
Het |
Or2z2 |
T |
A |
11: 58,345,999 (GRCm39) |
T259S |
possibly damaging |
Het |
Or52k2 |
T |
A |
7: 102,254,185 (GRCm39) |
I208N |
probably damaging |
Het |
Or9m1 |
A |
T |
2: 87,733,108 (GRCm39) |
M304K |
probably benign |
Het |
Pamr1 |
T |
A |
2: 102,464,766 (GRCm39) |
V305E |
probably benign |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Peg10 |
C |
T |
6: 4,757,128 (GRCm39) |
T568M |
unknown |
Het |
Polr3a |
A |
G |
14: 24,519,416 (GRCm39) |
F664S |
probably damaging |
Het |
Prb1a |
T |
A |
6: 132,185,306 (GRCm39) |
N109I |
unknown |
Het |
Prdm2 |
T |
C |
4: 142,858,752 (GRCm39) |
I1513V |
probably benign |
Het |
Prkd3 |
A |
C |
17: 79,269,969 (GRCm39) |
V564G |
possibly damaging |
Het |
Prss16 |
A |
G |
13: 22,192,513 (GRCm39) |
S151P |
probably damaging |
Het |
Rnf150 |
C |
T |
8: 83,590,588 (GRCm39) |
|
probably benign |
Het |
Rttn |
A |
G |
18: 89,038,261 (GRCm39) |
T786A |
probably benign |
Het |
Scin |
A |
G |
12: 40,113,236 (GRCm39) |
V645A |
possibly damaging |
Het |
Slc25a20 |
T |
A |
9: 108,557,398 (GRCm39) |
M177K |
probably benign |
Het |
Slc2a6 |
G |
A |
2: 26,914,334 (GRCm39) |
S261L |
possibly damaging |
Het |
Slc4a7 |
A |
T |
14: 14,796,115 (GRCm38) |
D1118V |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,358,709 (GRCm39) |
W351R |
probably damaging |
Het |
Sp8 |
G |
A |
12: 118,812,174 (GRCm39) |
G10S |
probably damaging |
Het |
St8sia2 |
A |
G |
7: 73,616,513 (GRCm39) |
I175T |
probably damaging |
Het |
Tas2r122 |
T |
A |
6: 132,688,779 (GRCm39) |
N38I |
probably benign |
Het |
Trim31 |
C |
T |
17: 37,209,382 (GRCm39) |
T46M |
possibly damaging |
Het |
Trim31 |
A |
G |
17: 37,220,145 (GRCm39) |
K354E |
probably benign |
Het |
Trio |
G |
A |
15: 27,749,922 (GRCm39) |
Q2260* |
probably null |
Het |
Trpm1 |
T |
C |
7: 63,848,943 (GRCm39) |
I63T |
probably benign |
Het |
Usp54 |
T |
C |
14: 20,627,162 (GRCm39) |
T499A |
probably benign |
Het |
Vmn1r35 |
T |
C |
6: 66,655,933 (GRCm39) |
I246V |
probably benign |
Het |
Vmn2r6 |
A |
G |
3: 64,464,277 (GRCm39) |
S186P |
probably benign |
Het |
Vmn2r76 |
T |
A |
7: 85,879,170 (GRCm39) |
M377L |
probably benign |
Het |
Zeb2 |
A |
C |
2: 44,878,637 (GRCm39) |
M1243R |
possibly damaging |
Het |
|
Other mutations in Ugt2b37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00401:Ugt2b37
|
APN |
5 |
87,390,340 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00567:Ugt2b37
|
APN |
5 |
87,401,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00787:Ugt2b37
|
APN |
5 |
87,390,288 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01560:Ugt2b37
|
APN |
5 |
87,399,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01617:Ugt2b37
|
APN |
5 |
87,399,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Ugt2b37
|
APN |
5 |
87,390,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Ugt2b37
|
APN |
5 |
87,390,174 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02323:Ugt2b37
|
APN |
5 |
87,398,423 (GRCm39) |
splice site |
probably benign |
|
IGL02326:Ugt2b37
|
APN |
5 |
87,388,861 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02516:Ugt2b37
|
APN |
5 |
87,388,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03285:Ugt2b37
|
APN |
5 |
87,388,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R0076:Ugt2b37
|
UTSW |
5 |
87,402,080 (GRCm39) |
missense |
probably benign |
0.31 |
R0141:Ugt2b37
|
UTSW |
5 |
87,388,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Ugt2b37
|
UTSW |
5 |
87,398,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Ugt2b37
|
UTSW |
5 |
87,398,443 (GRCm39) |
missense |
probably benign |
0.10 |
R0523:Ugt2b37
|
UTSW |
5 |
87,399,691 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1938:Ugt2b37
|
UTSW |
5 |
87,388,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Ugt2b37
|
UTSW |
5 |
87,402,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R2496:Ugt2b37
|
UTSW |
5 |
87,402,569 (GRCm39) |
missense |
probably damaging |
0.97 |
R3704:Ugt2b37
|
UTSW |
5 |
87,390,846 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4430:Ugt2b37
|
UTSW |
5 |
87,401,951 (GRCm39) |
missense |
probably benign |
0.00 |
R4825:Ugt2b37
|
UTSW |
5 |
87,398,498 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5043:Ugt2b37
|
UTSW |
5 |
87,399,719 (GRCm39) |
nonsense |
probably null |
|
R5098:Ugt2b37
|
UTSW |
5 |
87,390,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Ugt2b37
|
UTSW |
5 |
87,399,739 (GRCm39) |
missense |
probably benign |
0.00 |
R5522:Ugt2b37
|
UTSW |
5 |
87,388,759 (GRCm39) |
missense |
probably benign |
0.14 |
R5879:Ugt2b37
|
UTSW |
5 |
87,402,265 (GRCm39) |
missense |
probably benign |
|
R5999:Ugt2b37
|
UTSW |
5 |
87,402,036 (GRCm39) |
missense |
probably benign |
0.25 |
R6374:Ugt2b37
|
UTSW |
5 |
87,390,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R6454:Ugt2b37
|
UTSW |
5 |
87,388,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Ugt2b37
|
UTSW |
5 |
87,388,705 (GRCm39) |
missense |
probably damaging |
0.98 |
R6875:Ugt2b37
|
UTSW |
5 |
87,390,288 (GRCm39) |
missense |
probably benign |
0.00 |
R6916:Ugt2b37
|
UTSW |
5 |
87,402,459 (GRCm39) |
missense |
probably benign |
0.07 |
R7099:Ugt2b37
|
UTSW |
5 |
87,388,848 (GRCm39) |
missense |
probably benign |
0.00 |
R7239:Ugt2b37
|
UTSW |
5 |
87,402,590 (GRCm39) |
missense |
probably benign |
|
R7470:Ugt2b37
|
UTSW |
5 |
87,401,971 (GRCm39) |
missense |
probably benign |
0.24 |
R7810:Ugt2b37
|
UTSW |
5 |
87,402,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R7841:Ugt2b37
|
UTSW |
5 |
87,398,489 (GRCm39) |
missense |
probably benign |
0.05 |
R7860:Ugt2b37
|
UTSW |
5 |
87,402,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Ugt2b37
|
UTSW |
5 |
87,390,299 (GRCm39) |
nonsense |
probably null |
|
R8200:Ugt2b37
|
UTSW |
5 |
87,388,750 (GRCm39) |
nonsense |
probably null |
|
R8211:Ugt2b37
|
UTSW |
5 |
87,390,235 (GRCm39) |
missense |
probably benign |
0.07 |
R8282:Ugt2b37
|
UTSW |
5 |
87,402,440 (GRCm39) |
missense |
probably benign |
0.01 |
R8312:Ugt2b37
|
UTSW |
5 |
87,390,799 (GRCm39) |
missense |
probably benign |
0.15 |
R8520:Ugt2b37
|
UTSW |
5 |
87,388,714 (GRCm39) |
missense |
probably benign |
0.04 |
R8688:Ugt2b37
|
UTSW |
5 |
87,390,240 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8695:Ugt2b37
|
UTSW |
5 |
87,390,243 (GRCm39) |
missense |
probably benign |
0.00 |
R8772:Ugt2b37
|
UTSW |
5 |
87,402,345 (GRCm39) |
missense |
probably benign |
0.00 |
R8839:Ugt2b37
|
UTSW |
5 |
87,402,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Ugt2b37
|
UTSW |
5 |
87,401,996 (GRCm39) |
missense |
probably benign |
0.01 |
R9424:Ugt2b37
|
UTSW |
5 |
87,402,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R9432:Ugt2b37
|
UTSW |
5 |
87,402,046 (GRCm39) |
missense |
probably damaging |
0.97 |
R9498:Ugt2b37
|
UTSW |
5 |
87,402,244 (GRCm39) |
missense |
probably benign |
0.07 |
R9711:Ugt2b37
|
UTSW |
5 |
87,402,532 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9718:Ugt2b37
|
UTSW |
5 |
87,390,802 (GRCm39) |
missense |
probably benign |
0.11 |
R9783:Ugt2b37
|
UTSW |
5 |
87,388,840 (GRCm39) |
missense |
probably damaging |
1.00 |
|