Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd14b |
A |
G |
9: 106,328,817 (GRCm39) |
D146G |
probably benign |
Het |
Atp5if1 |
T |
C |
4: 132,260,685 (GRCm39) |
D34G |
probably benign |
Het |
Bcr |
T |
C |
10: 74,967,404 (GRCm39) |
F546S |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Ccdc141 |
A |
T |
2: 76,844,739 (GRCm39) |
W1443R |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,839,589 (GRCm39) |
D1375G |
probably damaging |
Het |
Chi3l1 |
A |
T |
1: 134,115,662 (GRCm39) |
Q223H |
probably benign |
Het |
Clcn2 |
A |
T |
16: 20,531,080 (GRCm39) |
F260I |
probably damaging |
Het |
Cpq |
A |
T |
15: 33,594,381 (GRCm39) |
D464V |
probably benign |
Het |
Crygb |
T |
C |
1: 65,121,300 (GRCm39) |
D9G |
probably damaging |
Het |
Cyp2b10 |
A |
G |
7: 25,624,815 (GRCm39) |
K438E |
unknown |
Het |
Cyp46a1 |
A |
T |
12: 108,324,366 (GRCm39) |
D381V |
possibly damaging |
Het |
Dhx40 |
A |
C |
11: 86,667,582 (GRCm39) |
|
probably benign |
Het |
Dnase2b |
G |
T |
3: 146,292,717 (GRCm39) |
P152Q |
probably damaging |
Het |
Duox1 |
A |
T |
2: 122,175,186 (GRCm39) |
H1328L |
probably damaging |
Het |
Ephb6 |
C |
T |
6: 41,590,293 (GRCm39) |
A15V |
probably benign |
Het |
Fam168b |
A |
G |
1: 34,858,862 (GRCm39) |
F102L |
probably benign |
Het |
Fam3b |
T |
A |
16: 97,277,594 (GRCm39) |
D128V |
probably damaging |
Het |
Galnt11 |
T |
G |
5: 25,469,983 (GRCm39) |
H527Q |
possibly damaging |
Het |
Gbp2b |
A |
T |
3: 142,316,730 (GRCm39) |
R460S |
probably benign |
Het |
Hdhd2 |
A |
C |
18: 77,058,366 (GRCm39) |
S246R |
possibly damaging |
Het |
Heatr1 |
T |
C |
13: 12,415,995 (GRCm39) |
M189T |
probably damaging |
Het |
Ift70a1 |
A |
T |
2: 75,810,251 (GRCm39) |
C611S |
probably benign |
Het |
Ino80 |
A |
G |
2: 119,210,059 (GRCm39) |
S1411P |
possibly damaging |
Het |
Jakmip1 |
A |
G |
5: 37,274,882 (GRCm39) |
T467A |
probably benign |
Het |
Kcnh2 |
A |
G |
5: 24,536,868 (GRCm39) |
S239P |
probably benign |
Het |
Lct |
T |
A |
1: 128,228,299 (GRCm39) |
T1065S |
probably damaging |
Het |
Lrrc66 |
T |
C |
5: 73,787,227 (GRCm39) |
D41G |
probably benign |
Het |
Mfsd2b |
A |
T |
12: 4,921,490 (GRCm39) |
D26E |
probably benign |
Het |
Myh1 |
A |
T |
11: 67,096,607 (GRCm39) |
M333L |
probably benign |
Het |
Neurl4 |
T |
C |
11: 69,798,958 (GRCm39) |
V855A |
possibly damaging |
Het |
Nfkb2 |
T |
A |
19: 46,295,304 (GRCm39) |
V80D |
probably damaging |
Het |
Nop9 |
T |
C |
14: 55,983,438 (GRCm39) |
S70P |
possibly damaging |
Het |
Or2t46 |
A |
G |
11: 58,471,738 (GRCm39) |
S23G |
probably benign |
Het |
Pcdhb14 |
G |
T |
18: 37,582,231 (GRCm39) |
D446Y |
probably damaging |
Het |
Pclo |
C |
T |
5: 14,719,325 (GRCm39) |
A1154V |
unknown |
Het |
Pdgfa |
G |
T |
5: 138,971,977 (GRCm39) |
Q141K |
probably damaging |
Het |
Plekhh1 |
G |
T |
12: 79,122,307 (GRCm39) |
L1133F |
probably damaging |
Het |
Pole |
A |
T |
5: 110,471,488 (GRCm39) |
N1411Y |
possibly damaging |
Het |
Primpol |
A |
G |
8: 47,034,597 (GRCm39) |
|
probably benign |
Het |
Psmc5 |
T |
G |
11: 106,152,787 (GRCm39) |
V203G |
probably damaging |
Het |
Ptgdr |
C |
T |
14: 45,096,181 (GRCm39) |
C177Y |
probably damaging |
Het |
Ptgir |
A |
T |
7: 16,641,220 (GRCm39) |
I171F |
probably damaging |
Het |
Ptprg |
T |
A |
14: 12,154,170 (GRCm38) |
H630Q |
probably benign |
Het |
Ptrh2 |
A |
G |
11: 86,580,907 (GRCm39) |
T175A |
possibly damaging |
Het |
Ralgapb |
A |
G |
2: 158,296,197 (GRCm39) |
T857A |
probably damaging |
Het |
Rnf24 |
A |
G |
2: 131,155,197 (GRCm39) |
F10S |
possibly damaging |
Het |
Rreb1 |
C |
A |
13: 38,114,352 (GRCm39) |
S570R |
probably benign |
Het |
Rttn |
A |
G |
18: 88,995,832 (GRCm39) |
N205S |
probably benign |
Het |
Rusc1 |
T |
C |
3: 88,999,365 (GRCm39) |
E139G |
probably benign |
Het |
Scn2a |
A |
G |
2: 65,594,242 (GRCm39) |
N1697S |
probably damaging |
Het |
Serpinb3a |
T |
A |
1: 106,974,907 (GRCm39) |
M209L |
probably damaging |
Het |
Shank3 |
A |
G |
15: 89,432,888 (GRCm39) |
D1211G |
possibly damaging |
Het |
Slc22a12 |
C |
A |
19: 6,592,514 (GRCm39) |
R90L |
possibly damaging |
Het |
Slc6a13 |
G |
A |
6: 121,313,901 (GRCm39) |
W548* |
probably null |
Het |
Srfbp1 |
T |
A |
18: 52,609,392 (GRCm39) |
L59* |
probably null |
Het |
Ss18 |
A |
T |
18: 14,803,380 (GRCm39) |
S73T |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,135,508 (GRCm39) |
K189R |
probably benign |
Het |
Szt2 |
G |
T |
4: 118,239,985 (GRCm39) |
|
probably benign |
Het |
Tbx1 |
T |
A |
16: 18,402,937 (GRCm39) |
H183L |
probably damaging |
Het |
Thop1 |
A |
G |
10: 80,915,972 (GRCm39) |
E385G |
possibly damaging |
Het |
Tmem168 |
C |
A |
6: 13,602,849 (GRCm39) |
M172I |
possibly damaging |
Het |
Tmem67 |
A |
G |
4: 12,058,559 (GRCm39) |
Y513H |
probably damaging |
Het |
Top1 |
A |
G |
2: 160,562,921 (GRCm39) |
D709G |
probably damaging |
Het |
Tprg1l |
A |
C |
4: 154,242,890 (GRCm39) |
S247A |
probably damaging |
Het |
Trim46 |
A |
G |
3: 89,143,692 (GRCm39) |
S602P |
probably damaging |
Het |
Ttc7b |
T |
C |
12: 100,466,433 (GRCm39) |
K60E |
probably benign |
Het |
Ttn |
G |
A |
2: 76,714,815 (GRCm39) |
S8053F |
unknown |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Usp24 |
T |
A |
4: 106,234,762 (GRCm39) |
H956Q |
probably benign |
Het |
Vcp |
T |
C |
4: 42,980,828 (GRCm39) |
T761A |
probably benign |
Het |
Xpc |
G |
A |
6: 91,477,956 (GRCm39) |
T309I |
possibly damaging |
Het |
Zfp560 |
C |
T |
9: 20,260,895 (GRCm39) |
M129I |
probably benign |
Het |
Zpld2 |
G |
A |
4: 133,929,978 (GRCm39) |
T109I |
probably damaging |
Het |
|
Other mutations in Abhd6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02475:Abhd6
|
APN |
14 |
8,039,849 (GRCm38) |
missense |
probably damaging |
0.96 |
R1757:Abhd6
|
UTSW |
14 |
8,049,867 (GRCm38) |
missense |
probably damaging |
1.00 |
R2011:Abhd6
|
UTSW |
14 |
8,042,742 (GRCm38) |
missense |
probably benign |
0.07 |
R2425:Abhd6
|
UTSW |
14 |
8,049,857 (GRCm38) |
missense |
probably benign |
0.29 |
R3810:Abhd6
|
UTSW |
14 |
8,045,603 (GRCm38) |
missense |
probably benign |
0.01 |
R4809:Abhd6
|
UTSW |
14 |
8,039,771 (GRCm38) |
start codon destroyed |
probably null |
1.00 |
R5841:Abhd6
|
UTSW |
14 |
8,049,596 (GRCm38) |
missense |
probably benign |
0.02 |
R5878:Abhd6
|
UTSW |
14 |
8,028,286 (GRCm38) |
missense |
probably benign |
0.13 |
R6439:Abhd6
|
UTSW |
14 |
8,055,589 (GRCm38) |
missense |
probably damaging |
1.00 |
R6582:Abhd6
|
UTSW |
14 |
8,042,828 (GRCm38) |
critical splice donor site |
probably null |
|
R6582:Abhd6
|
UTSW |
14 |
8,042,826 (GRCm38) |
missense |
probably damaging |
1.00 |
R6924:Abhd6
|
UTSW |
14 |
8,049,850 (GRCm38) |
missense |
possibly damaging |
0.71 |
R7684:Abhd6
|
UTSW |
14 |
8,039,807 (GRCm38) |
missense |
probably damaging |
1.00 |
R7844:Abhd6
|
UTSW |
14 |
8,039,792 (GRCm38) |
missense |
probably benign |
0.22 |
R8093:Abhd6
|
UTSW |
14 |
8,028,353 (GRCm38) |
missense |
probably damaging |
0.98 |
R9499:Abhd6
|
UTSW |
14 |
8,028,329 (GRCm38) |
missense |
possibly damaging |
0.80 |
R9552:Abhd6
|
UTSW |
14 |
8,028,329 (GRCm38) |
missense |
possibly damaging |
0.80 |
R9601:Abhd6
|
UTSW |
14 |
8,049,808 (GRCm38) |
missense |
possibly damaging |
0.67 |
|