Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
A |
T |
16: 97,866,959 (GRCm39) |
Y334* |
probably null |
Het |
Abcc2 |
A |
C |
19: 43,786,515 (GRCm39) |
I116L |
probably benign |
Het |
Adamts17 |
T |
A |
7: 66,559,148 (GRCm39) |
Y313N |
possibly damaging |
Het |
Adamts17 |
A |
G |
7: 66,654,101 (GRCm39) |
T444A |
probably benign |
Het |
Adamtsl1 |
A |
G |
4: 86,075,091 (GRCm39) |
I153V |
probably damaging |
Het |
Ambra1 |
C |
T |
2: 91,747,761 (GRCm39) |
Q1046* |
probably null |
Het |
Ap1g2 |
A |
T |
14: 55,336,722 (GRCm39) |
V750D |
possibly damaging |
Het |
Bcl7a |
T |
C |
5: 123,507,519 (GRCm39) |
|
probably null |
Het |
C4bp |
A |
T |
1: 130,585,009 (GRCm39) |
L9Q |
probably damaging |
Het |
Cadps2 |
A |
C |
6: 23,583,458 (GRCm39) |
V344G |
probably damaging |
Het |
Car7 |
A |
G |
8: 105,270,213 (GRCm39) |
D15G |
possibly damaging |
Het |
Cep126 |
G |
C |
9: 8,112,101 (GRCm39) |
H157Q |
probably null |
Het |
Cntrob |
G |
A |
11: 69,200,317 (GRCm39) |
R526* |
probably null |
Het |
Cul1 |
A |
G |
6: 47,493,443 (GRCm39) |
T445A |
probably benign |
Het |
Dclre1c |
T |
C |
2: 3,454,206 (GRCm39) |
V363A |
possibly damaging |
Het |
Dock10 |
T |
A |
1: 80,481,365 (GRCm39) |
|
probably benign |
Het |
Donson |
A |
G |
16: 91,478,107 (GRCm39) |
Y465H |
probably benign |
Het |
Eif3e |
G |
A |
15: 43,135,685 (GRCm39) |
A118V |
probably benign |
Het |
Fam47e |
A |
T |
5: 92,713,911 (GRCm39) |
Q180L |
probably damaging |
Het |
Fat1 |
T |
G |
8: 45,496,982 (GRCm39) |
C4156G |
probably damaging |
Het |
Fermt2 |
A |
T |
14: 45,702,599 (GRCm39) |
I441K |
probably damaging |
Het |
Frmd4b |
C |
T |
6: 97,282,158 (GRCm39) |
R510Q |
probably damaging |
Het |
Fscn1 |
C |
T |
5: 142,946,415 (GRCm39) |
A71V |
probably damaging |
Het |
Gfap |
G |
A |
11: 102,787,783 (GRCm39) |
A54V |
possibly damaging |
Het |
Gjc3 |
C |
T |
5: 137,955,759 (GRCm39) |
M175I |
probably benign |
Het |
Gm10645 |
C |
T |
8: 83,892,581 (GRCm39) |
|
probably benign |
Het |
Haus5 |
G |
A |
7: 30,357,040 (GRCm39) |
P464S |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,872,221 (GRCm39) |
I2584F |
probably damaging |
Het |
Mak |
T |
A |
13: 41,186,067 (GRCm39) |
I534L |
probably benign |
Het |
Map3k9 |
T |
C |
12: 81,819,777 (GRCm39) |
D159G |
probably benign |
Het |
Mcat |
A |
G |
15: 83,432,132 (GRCm39) |
|
probably benign |
Het |
Meltf |
A |
G |
16: 31,698,980 (GRCm39) |
D30G |
probably benign |
Het |
Ntng2 |
T |
A |
2: 29,087,041 (GRCm39) |
Y452F |
probably benign |
Het |
Or10ag60 |
T |
C |
2: 87,437,957 (GRCm39) |
L75P |
probably damaging |
Het |
Or4a72 |
T |
A |
2: 89,405,333 (GRCm39) |
I246F |
probably benign |
Het |
Or5b118 |
T |
A |
19: 13,448,725 (GRCm39) |
Y130* |
probably null |
Het |
Or5p53 |
A |
T |
7: 107,532,966 (GRCm39) |
I80L |
probably benign |
Het |
Paip1 |
C |
T |
13: 119,587,306 (GRCm39) |
T390I |
possibly damaging |
Het |
Pianp |
T |
A |
6: 124,976,353 (GRCm39) |
V54D |
possibly damaging |
Het |
Ptprn |
T |
C |
1: 75,237,293 (GRCm39) |
D103G |
possibly damaging |
Het |
Rhcg |
A |
G |
7: 79,250,279 (GRCm39) |
V268A |
probably benign |
Het |
Rhoj |
T |
A |
12: 75,422,163 (GRCm39) |
Y74N |
probably damaging |
Het |
Rigi |
A |
G |
4: 40,225,697 (GRCm39) |
S235P |
probably benign |
Het |
Snx13 |
A |
C |
12: 35,169,788 (GRCm39) |
T578P |
possibly damaging |
Het |
Star |
T |
A |
8: 26,301,851 (GRCm39) |
H227Q |
probably benign |
Het |
Stau2 |
A |
C |
1: 16,460,229 (GRCm39) |
M204R |
probably damaging |
Het |
Steap4 |
A |
G |
5: 8,025,568 (GRCm39) |
Y43C |
probably damaging |
Het |
Syt8 |
A |
G |
7: 141,993,158 (GRCm39) |
E21G |
probably benign |
Het |
Tacr3 |
T |
C |
3: 134,535,500 (GRCm39) |
V156A |
probably damaging |
Het |
Tmem106b |
C |
T |
6: 13,082,422 (GRCm39) |
T199M |
probably benign |
Het |
Tmem131 |
T |
C |
1: 36,835,373 (GRCm39) |
T1583A |
probably damaging |
Het |
Tom1 |
G |
A |
8: 75,778,593 (GRCm39) |
V87I |
probably null |
Het |
Treml4 |
G |
T |
17: 48,579,847 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,544,457 (GRCm39) |
K32843R |
probably damaging |
Het |
Wdr95 |
T |
G |
5: 149,505,315 (GRCm39) |
C223W |
probably damaging |
Het |
Wipi1 |
C |
T |
11: 109,494,590 (GRCm39) |
R81Q |
probably benign |
Het |
Zc3h7a |
G |
A |
16: 10,967,088 (GRCm39) |
T568I |
probably benign |
Het |
Zfp287 |
A |
T |
11: 62,615,643 (GRCm39) |
I228N |
probably damaging |
Het |
Zfp606 |
T |
A |
7: 12,223,519 (GRCm39) |
V10E |
probably damaging |
Het |
|
Other mutations in Chst11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Chst11
|
APN |
10 |
83,027,467 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00659:Chst11
|
APN |
10 |
83,027,639 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02676:Chst11
|
APN |
10 |
83,027,563 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02999:Chst11
|
APN |
10 |
83,027,538 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03368:Chst11
|
APN |
10 |
82,927,980 (GRCm39) |
missense |
probably benign |
0.39 |
lavoisier
|
UTSW |
10 |
83,027,020 (GRCm39) |
missense |
possibly damaging |
0.81 |
Mendeleev
|
UTSW |
10 |
83,027,302 (GRCm39) |
missense |
probably damaging |
1.00 |
BB002:Chst11
|
UTSW |
10 |
83,026,788 (GRCm39) |
missense |
probably damaging |
0.98 |
BB012:Chst11
|
UTSW |
10 |
83,026,788 (GRCm39) |
missense |
probably damaging |
0.98 |
R1929:Chst11
|
UTSW |
10 |
83,027,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R2271:Chst11
|
UTSW |
10 |
83,027,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R4844:Chst11
|
UTSW |
10 |
83,026,923 (GRCm39) |
nonsense |
probably null |
|
R5040:Chst11
|
UTSW |
10 |
83,026,780 (GRCm39) |
missense |
probably benign |
0.02 |
R5396:Chst11
|
UTSW |
10 |
83,027,083 (GRCm39) |
missense |
probably damaging |
0.98 |
R6512:Chst11
|
UTSW |
10 |
83,027,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7803:Chst11
|
UTSW |
10 |
83,027,020 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7925:Chst11
|
UTSW |
10 |
83,026,788 (GRCm39) |
missense |
probably damaging |
0.98 |
R9194:Chst11
|
UTSW |
10 |
83,027,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R9406:Chst11
|
UTSW |
10 |
83,026,881 (GRCm39) |
missense |
possibly damaging |
0.70 |
X0033:Chst11
|
UTSW |
10 |
83,026,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|