Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
T |
C |
4: 88,786,423 (GRCm39) |
E65G |
unknown |
Het |
Aadacl2fm2 |
A |
T |
3: 59,637,318 (GRCm39) |
I27F |
probably benign |
Het |
Abcg5 |
A |
T |
17: 84,981,018 (GRCm39) |
N190K |
possibly damaging |
Het |
Abhd6 |
A |
C |
14: 8,039,792 (GRCm38) |
H55P |
probably benign |
Het |
Acox3 |
A |
T |
5: 35,764,492 (GRCm39) |
Q535L |
probably benign |
Het |
Adora1 |
A |
G |
1: 134,131,276 (GRCm39) |
W132R |
probably damaging |
Het |
Armc3 |
A |
G |
2: 19,258,829 (GRCm39) |
I299V |
possibly damaging |
Het |
Atp11a |
A |
G |
8: 12,901,039 (GRCm39) |
D956G |
possibly damaging |
Het |
Bptf |
C |
A |
11: 106,964,887 (GRCm39) |
V1436F |
probably damaging |
Het |
Brd9 |
A |
G |
13: 74,086,652 (GRCm39) |
Y51C |
probably damaging |
Het |
Cdh18 |
T |
C |
15: 23,410,873 (GRCm39) |
W453R |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,737,920 (GRCm39) |
Q2326R |
unknown |
Het |
Col4a2 |
G |
T |
8: 11,475,453 (GRCm39) |
E626* |
probably null |
Het |
Dpp8 |
A |
G |
9: 64,952,949 (GRCm39) |
I208M |
probably damaging |
Het |
Evi5 |
T |
C |
5: 108,022,860 (GRCm39) |
R16G |
probably benign |
Het |
Gabrg1 |
T |
C |
5: 70,931,675 (GRCm39) |
Y356C |
probably damaging |
Het |
Gbp7 |
G |
T |
3: 142,242,147 (GRCm39) |
V94L |
probably benign |
Het |
Gm4884 |
A |
C |
7: 40,690,122 (GRCm39) |
Q6P |
probably benign |
Het |
Gm9767 |
A |
T |
10: 25,954,255 (GRCm39) |
|
probably benign |
Het |
Gopc |
T |
C |
10: 52,215,845 (GRCm39) |
S448G |
possibly damaging |
Het |
Gpr15 |
A |
T |
16: 58,538,873 (GRCm39) |
I72N |
probably damaging |
Het |
Hsd17b11 |
T |
A |
5: 104,166,132 (GRCm39) |
T76S |
probably damaging |
Het |
Inhbe |
A |
G |
10: 127,186,779 (GRCm39) |
S134P |
possibly damaging |
Het |
Inpp4b |
G |
A |
8: 82,467,949 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,322,062 (GRCm39) |
V556A |
probably benign |
Het |
Krt7 |
G |
A |
15: 101,310,515 (GRCm39) |
G54D |
possibly damaging |
Het |
Mecom |
T |
G |
3: 30,063,973 (GRCm39) |
Y39S |
unknown |
Het |
Mrpl49 |
C |
T |
19: 6,105,200 (GRCm39) |
R87H |
probably damaging |
Het |
Nfat5 |
A |
G |
8: 108,085,300 (GRCm39) |
D531G |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,262,006 (GRCm39) |
K718N |
possibly damaging |
Het |
Ogfr |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,850 (GRCm39) |
|
probably benign |
Het |
Or52d1 |
T |
G |
7: 103,755,690 (GRCm39) |
L68W |
probably damaging |
Het |
Pigu |
A |
C |
2: 155,134,640 (GRCm39) |
Y388* |
probably null |
Het |
Pirb |
A |
T |
7: 3,722,410 (GRCm39) |
C144* |
probably null |
Het |
Pkm |
A |
G |
9: 59,578,005 (GRCm39) |
H274R |
probably benign |
Het |
Plch2 |
C |
A |
4: 155,073,922 (GRCm39) |
D927Y |
probably damaging |
Het |
Rock1 |
T |
G |
18: 10,104,173 (GRCm39) |
K596Q |
probably damaging |
Het |
Scaper |
A |
T |
9: 55,722,732 (GRCm39) |
M692K |
probably benign |
Het |
Serpine1 |
C |
A |
5: 137,100,043 (GRCm39) |
G39* |
probably null |
Het |
Serpine2 |
T |
C |
1: 79,794,516 (GRCm39) |
Q139R |
probably benign |
Het |
Sipa1l1 |
C |
A |
12: 82,444,267 (GRCm39) |
R993S |
probably damaging |
Het |
Slc12a9 |
T |
C |
5: 137,330,448 (GRCm39) |
T86A |
probably damaging |
Het |
Slc30a6 |
G |
A |
17: 74,711,088 (GRCm39) |
|
probably null |
Het |
Snrnp48 |
A |
G |
13: 38,393,965 (GRCm39) |
E90G |
probably null |
Het |
Spaca7b |
A |
T |
8: 11,706,174 (GRCm39) |
I120K |
probably benign |
Het |
Spdl1 |
A |
T |
11: 34,704,170 (GRCm39) |
N554K |
possibly damaging |
Het |
Spon1 |
G |
A |
7: 113,629,567 (GRCm39) |
V404I |
probably benign |
Het |
Tada3 |
C |
T |
6: 113,347,921 (GRCm39) |
R300H |
probably benign |
Het |
Tcl1b5 |
G |
A |
12: 105,142,815 (GRCm39) |
|
probably null |
Het |
Tdrd9 |
A |
G |
12: 111,964,386 (GRCm39) |
Y336C |
possibly damaging |
Het |
Timm44 |
A |
G |
8: 4,319,976 (GRCm39) |
L64P |
possibly damaging |
Het |
Tpo |
A |
G |
12: 30,150,404 (GRCm39) |
L492P |
probably damaging |
Het |
Trip11 |
T |
G |
12: 101,844,403 (GRCm39) |
Q1565P |
probably damaging |
Het |
Trpm2 |
A |
G |
10: 77,759,340 (GRCm39) |
I1148T |
probably benign |
Het |
Tshz1 |
T |
C |
18: 84,032,296 (GRCm39) |
E704G |
probably benign |
Het |
Tysnd1 |
C |
T |
10: 61,537,944 (GRCm39) |
R541* |
probably null |
Het |
|
Other mutations in Klhdc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00900:Klhdc2
|
APN |
12 |
69,350,308 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00990:Klhdc2
|
APN |
12 |
69,353,987 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01024:Klhdc2
|
APN |
12 |
69,352,610 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01457:Klhdc2
|
APN |
12 |
69,343,827 (GRCm39) |
missense |
probably benign |
|
IGL01735:Klhdc2
|
APN |
12 |
69,347,053 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01913:Klhdc2
|
APN |
12 |
69,349,132 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02440:Klhdc2
|
APN |
12 |
69,350,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Dixit_dominus
|
UTSW |
12 |
69,355,750 (GRCm39) |
nonsense |
probably null |
|
R0611:Klhdc2
|
UTSW |
12 |
69,347,053 (GRCm39) |
missense |
probably benign |
0.22 |
R0724:Klhdc2
|
UTSW |
12 |
69,343,822 (GRCm39) |
missense |
probably benign |
|
R1350:Klhdc2
|
UTSW |
12 |
69,352,484 (GRCm39) |
critical splice donor site |
probably null |
|
R1796:Klhdc2
|
UTSW |
12 |
69,347,071 (GRCm39) |
critical splice donor site |
probably null |
|
R1907:Klhdc2
|
UTSW |
12 |
69,343,734 (GRCm39) |
start gained |
probably benign |
|
R4418:Klhdc2
|
UTSW |
12 |
69,354,371 (GRCm39) |
unclassified |
probably benign |
|
R5119:Klhdc2
|
UTSW |
12 |
69,343,736 (GRCm39) |
utr 5 prime |
probably benign |
|
R5586:Klhdc2
|
UTSW |
12 |
69,354,467 (GRCm39) |
splice site |
probably null |
|
R5987:Klhdc2
|
UTSW |
12 |
69,350,387 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6448:Klhdc2
|
UTSW |
12 |
69,350,694 (GRCm39) |
missense |
probably benign |
|
R6848:Klhdc2
|
UTSW |
12 |
69,355,750 (GRCm39) |
nonsense |
probably null |
|
R7824:Klhdc2
|
UTSW |
12 |
69,354,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R7886:Klhdc2
|
UTSW |
12 |
69,351,406 (GRCm39) |
splice site |
probably null |
|
R8963:Klhdc2
|
UTSW |
12 |
69,347,065 (GRCm39) |
nonsense |
probably null |
|
R9775:Klhdc2
|
UTSW |
12 |
69,350,393 (GRCm39) |
missense |
probably damaging |
0.99 |
R9790:Klhdc2
|
UTSW |
12 |
69,346,995 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Klhdc2
|
UTSW |
12 |
69,346,995 (GRCm39) |
missense |
probably benign |
0.01 |
RF016:Klhdc2
|
UTSW |
12 |
69,350,660 (GRCm39) |
missense |
probably damaging |
0.97 |
|