Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
A |
C |
5: 121,638,856 (GRCm39) |
S730A |
probably benign |
Het |
Adamts9 |
G |
A |
6: 92,856,940 (GRCm39) |
R319* |
probably null |
Het |
Anapc1 |
G |
T |
2: 128,469,115 (GRCm39) |
S1575R |
probably damaging |
Het |
Appbp2 |
A |
T |
11: 85,100,764 (GRCm39) |
|
probably null |
Het |
Bcas2 |
C |
T |
3: 103,081,666 (GRCm39) |
P90S |
probably benign |
Het |
Carmil3 |
GGACGA |
GGA |
14: 55,736,933 (GRCm39) |
|
probably benign |
Het |
Cd101 |
T |
C |
3: 100,920,469 (GRCm39) |
N477D |
probably benign |
Het |
Cdk12 |
A |
G |
11: 98,111,814 (GRCm39) |
|
probably benign |
Het |
Clcn4 |
T |
C |
7: 7,290,804 (GRCm39) |
E634G |
probably benign |
Het |
Cltb |
C |
T |
13: 54,746,574 (GRCm39) |
R64H |
probably damaging |
Het |
Cpt1b |
G |
T |
15: 89,308,247 (GRCm39) |
|
probably null |
Het |
Ctf2 |
T |
G |
7: 127,318,556 (GRCm39) |
T148P |
possibly damaging |
Het |
Ddx23 |
G |
A |
15: 98,545,505 (GRCm39) |
T601I |
probably damaging |
Het |
Dlx6 |
G |
T |
6: 6,865,305 (GRCm39) |
|
probably benign |
Het |
Dmrtb1 |
A |
T |
4: 107,534,265 (GRCm39) |
N183K |
possibly damaging |
Het |
Dnah11 |
A |
G |
12: 117,975,990 (GRCm39) |
|
probably null |
Het |
Dnah5 |
C |
T |
15: 28,367,909 (GRCm39) |
P2765S |
probably benign |
Het |
Dnah6 |
T |
A |
6: 73,063,164 (GRCm39) |
N2698I |
probably damaging |
Het |
Gm4841 |
T |
C |
18: 60,402,998 (GRCm39) |
N365S |
probably benign |
Het |
Gsdmc2 |
C |
T |
15: 63,699,872 (GRCm39) |
|
probably null |
Het |
Irx5 |
G |
A |
8: 93,084,890 (GRCm39) |
V27I |
probably damaging |
Het |
Kmt2e |
T |
A |
5: 23,697,405 (GRCm39) |
V101D |
possibly damaging |
Het |
Maip1 |
A |
C |
1: 57,452,404 (GRCm39) |
K219Q |
possibly damaging |
Het |
Mpp7 |
G |
T |
18: 7,353,228 (GRCm39) |
R493S |
probably benign |
Het |
Ms4a14 |
T |
C |
19: 11,281,335 (GRCm39) |
T408A |
probably benign |
Het |
Mthfr |
A |
G |
4: 148,127,998 (GRCm39) |
N117S |
possibly damaging |
Het |
Mtres1 |
T |
A |
10: 43,409,006 (GRCm39) |
S46C |
probably damaging |
Het |
Myo5c |
A |
G |
9: 75,176,893 (GRCm39) |
I613V |
probably benign |
Het |
Neurl1b |
A |
G |
17: 26,650,860 (GRCm39) |
Q44R |
probably benign |
Het |
Nup54 |
T |
A |
5: 92,573,641 (GRCm39) |
N187I |
probably benign |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or5ak22 |
C |
A |
2: 85,230,370 (GRCm39) |
C169F |
probably damaging |
Het |
Pate2 |
C |
A |
9: 35,596,969 (GRCm39) |
|
probably benign |
Het |
Pccb |
T |
C |
9: 100,867,252 (GRCm39) |
S445G |
probably damaging |
Het |
Pex3 |
G |
A |
10: 13,411,315 (GRCm39) |
Q188* |
probably null |
Het |
Pikfyve |
T |
A |
1: 65,231,351 (GRCm39) |
W74R |
probably damaging |
Het |
Plcl2 |
T |
C |
17: 50,914,874 (GRCm39) |
S628P |
probably damaging |
Het |
Pnldc1 |
T |
C |
17: 13,111,669 (GRCm39) |
H346R |
probably benign |
Het |
Pom121l2 |
T |
A |
13: 22,168,572 (GRCm39) |
C948S |
probably benign |
Het |
Pspc1 |
A |
T |
14: 56,999,404 (GRCm39) |
M284K |
possibly damaging |
Het |
Ralgapa2 |
A |
G |
2: 146,277,919 (GRCm39) |
L414S |
probably damaging |
Het |
Rgs13 |
T |
A |
1: 144,016,583 (GRCm39) |
K53N |
probably damaging |
Het |
Rorc |
T |
C |
3: 94,296,291 (GRCm39) |
S163P |
probably benign |
Het |
Rpl3l |
A |
C |
17: 24,952,984 (GRCm39) |
T315P |
possibly damaging |
Het |
Rsph3b |
A |
G |
17: 7,172,438 (GRCm39) |
V487A |
probably benign |
Het |
Rusc2 |
A |
G |
4: 43,416,080 (GRCm39) |
E462G |
probably damaging |
Het |
Sez6l |
T |
C |
5: 112,576,344 (GRCm39) |
T838A |
probably damaging |
Het |
Slc22a14 |
A |
G |
9: 119,008,561 (GRCm39) |
Y236H |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,442,457 (GRCm39) |
R1984H |
probably damaging |
Het |
Steap3 |
G |
T |
1: 120,169,186 (GRCm39) |
D370E |
probably benign |
Het |
Sumf1 |
A |
G |
6: 108,085,393 (GRCm39) |
|
probably benign |
Het |
Telo2 |
T |
C |
17: 25,320,647 (GRCm39) |
E754G |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,972,353 (GRCm39) |
F604L |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,639,131 (GRCm39) |
D1734E |
probably benign |
Het |
Tsfm |
A |
C |
10: 126,864,242 (GRCm39) |
Y158D |
probably damaging |
Het |
Ubtf |
T |
C |
11: 102,197,591 (GRCm39) |
|
probably benign |
Het |
Upk3a |
G |
T |
15: 84,904,752 (GRCm39) |
V167F |
possibly damaging |
Het |
Vmn2r19 |
C |
T |
6: 123,292,939 (GRCm39) |
S327L |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,858,965 (GRCm39) |
I2805N |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 80,673,534 (GRCm39) |
D166G |
possibly damaging |
Het |
|
Other mutations in Fpr-rs6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02836:Fpr-rs6
|
APN |
17 |
20,403,307 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03380:Fpr-rs6
|
APN |
17 |
20,403,245 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0149:Fpr-rs6
|
UTSW |
17 |
20,402,475 (GRCm39) |
missense |
probably benign |
0.29 |
R0190:Fpr-rs6
|
UTSW |
17 |
20,402,741 (GRCm39) |
missense |
probably benign |
0.07 |
R1347:Fpr-rs6
|
UTSW |
17 |
20,403,011 (GRCm39) |
missense |
probably benign |
0.23 |
R1347:Fpr-rs6
|
UTSW |
17 |
20,403,011 (GRCm39) |
missense |
probably benign |
0.23 |
R1934:Fpr-rs6
|
UTSW |
17 |
20,403,152 (GRCm39) |
missense |
probably benign |
0.36 |
R1965:Fpr-rs6
|
UTSW |
17 |
20,402,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R3690:Fpr-rs6
|
UTSW |
17 |
20,403,137 (GRCm39) |
missense |
probably benign |
0.02 |
R3963:Fpr-rs6
|
UTSW |
17 |
20,402,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R4564:Fpr-rs6
|
UTSW |
17 |
20,403,168 (GRCm39) |
nonsense |
probably null |
|
R5015:Fpr-rs6
|
UTSW |
17 |
20,402,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Fpr-rs6
|
UTSW |
17 |
20,402,375 (GRCm39) |
missense |
probably benign |
0.05 |
R6737:Fpr-rs6
|
UTSW |
17 |
20,403,339 (GRCm39) |
missense |
probably benign |
0.08 |
R6786:Fpr-rs6
|
UTSW |
17 |
20,403,100 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6908:Fpr-rs6
|
UTSW |
17 |
20,402,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Fpr-rs6
|
UTSW |
17 |
20,403,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R7462:Fpr-rs6
|
UTSW |
17 |
20,402,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Fpr-rs6
|
UTSW |
17 |
20,402,999 (GRCm39) |
missense |
probably benign |
0.03 |
R7958:Fpr-rs6
|
UTSW |
17 |
20,402,705 (GRCm39) |
missense |
probably damaging |
0.98 |
R8103:Fpr-rs6
|
UTSW |
17 |
20,402,839 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8772:Fpr-rs6
|
UTSW |
17 |
20,402,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|