Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A130010J15Rik |
T |
A |
1: 192,857,087 (GRCm39) |
D146E |
probably benign |
Het |
Acaca |
C |
T |
11: 84,271,339 (GRCm39) |
Q2058* |
probably null |
Het |
Adam39 |
T |
A |
8: 41,279,744 (GRCm39) |
C712S |
possibly damaging |
Het |
Aipl1 |
T |
C |
11: 71,921,161 (GRCm39) |
E219G |
probably benign |
Het |
Ankrd24 |
A |
G |
10: 81,475,898 (GRCm39) |
R301G |
unknown |
Het |
Arhgef17 |
A |
G |
7: 100,532,009 (GRCm39) |
F272L |
probably damaging |
Het |
B3galt2 |
T |
A |
1: 143,522,604 (GRCm39) |
Y247N |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,002,090 (GRCm39) |
V1345A |
probably damaging |
Het |
Bnip3l |
G |
A |
14: 67,246,214 (GRCm39) |
P7L |
possibly damaging |
Het |
Cat |
T |
C |
2: 103,285,433 (GRCm39) |
E503G |
probably benign |
Het |
Cemip2 |
T |
C |
19: 21,803,453 (GRCm39) |
S829P |
probably damaging |
Het |
Coro1b |
T |
A |
19: 4,199,497 (GRCm39) |
V52E |
probably damaging |
Het |
D6Ertd527e |
G |
C |
6: 87,088,839 (GRCm39) |
S334T |
unknown |
Het |
Dip2c |
T |
A |
13: 9,704,683 (GRCm39) |
M1344K |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,236,774 (GRCm39) |
I367V |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,178,607 (GRCm39) |
T1807A |
probably benign |
Het |
Dusp10 |
T |
A |
1: 183,806,643 (GRCm39) |
F459I |
probably damaging |
Het |
Elac1 |
A |
T |
18: 73,872,089 (GRCm39) |
L302Q |
probably benign |
Het |
Entrep3 |
T |
A |
3: 89,091,199 (GRCm39) |
S57T |
probably benign |
Het |
Fdx2 |
A |
T |
9: 20,979,097 (GRCm39) |
Y165N |
probably damaging |
Het |
Gabra2 |
C |
T |
5: 71,165,353 (GRCm39) |
V206I |
possibly damaging |
Het |
Gabrg1 |
T |
C |
5: 70,939,808 (GRCm39) |
E108G |
probably damaging |
Het |
Gm29394 |
A |
G |
15: 57,932,722 (GRCm39) |
L5P |
probably benign |
Het |
Gnb1l |
C |
T |
16: 18,362,914 (GRCm39) |
P101S |
probably benign |
Het |
Hectd4 |
C |
A |
5: 121,424,844 (GRCm39) |
S749* |
probably null |
Het |
Hmcn2 |
A |
G |
2: 31,244,742 (GRCm39) |
Y733C |
probably damaging |
Het |
Inafm1 |
G |
A |
7: 16,007,059 (GRCm39) |
L53F |
probably damaging |
Het |
Iqgap3 |
G |
A |
3: 88,011,657 (GRCm39) |
R814H |
probably damaging |
Het |
Map3k19 |
A |
G |
1: 127,778,163 (GRCm39) |
C21R |
probably benign |
Het |
Maz |
A |
G |
7: 126,624,924 (GRCm39) |
F199L |
probably damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,187,628 (GRCm39) |
I825T |
probably damaging |
Het |
Mpp3 |
T |
A |
11: 101,907,506 (GRCm39) |
T211S |
possibly damaging |
Het |
Mtrf1 |
T |
C |
14: 79,656,664 (GRCm39) |
Y389H |
probably damaging |
Het |
Myo3b |
G |
A |
2: 70,075,648 (GRCm39) |
G579R |
probably benign |
Het |
Nlrp4e |
T |
C |
7: 23,020,197 (GRCm39) |
V228A |
probably benign |
Het |
Npepps |
T |
A |
11: 97,149,179 (GRCm39) |
|
probably null |
Het |
Ntng1 |
A |
G |
3: 109,842,224 (GRCm39) |
L183P |
probably damaging |
Het |
Pcdha4 |
A |
C |
18: 37,086,740 (GRCm39) |
I308L |
probably benign |
Het |
Pear1 |
G |
T |
3: 87,658,480 (GRCm39) |
Q964K |
probably benign |
Het |
Plekhg2 |
A |
T |
7: 28,059,710 (GRCm39) |
D1182E |
possibly damaging |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,674,998 (GRCm39) |
D658E |
possibly damaging |
Het |
Ptprq |
T |
C |
10: 107,524,254 (GRCm39) |
Y493C |
possibly damaging |
Het |
Rnd1 |
A |
G |
15: 98,570,526 (GRCm39) |
W107R |
probably damaging |
Het |
Scn5a |
G |
A |
9: 119,315,839 (GRCm39) |
T1623M |
probably damaging |
Het |
Sec23b |
T |
C |
2: 144,410,564 (GRCm39) |
I288T |
probably benign |
Het |
Slfn14 |
T |
A |
11: 83,174,733 (GRCm39) |
H86L |
probably benign |
Het |
Smchd1 |
G |
A |
17: 71,701,828 (GRCm39) |
H1055Y |
probably damaging |
Het |
Sox13 |
G |
A |
1: 133,316,214 (GRCm39) |
P243S |
probably damaging |
Het |
St3gal6 |
C |
A |
16: 58,305,136 (GRCm39) |
E109* |
probably null |
Het |
Traf4 |
T |
C |
11: 78,056,253 (GRCm39) |
D5G |
possibly damaging |
Het |
Trank1 |
G |
T |
9: 111,191,365 (GRCm39) |
C458F |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,549,049 (GRCm39) |
F81S |
probably benign |
Het |
Tulp1 |
C |
T |
17: 28,572,802 (GRCm39) |
W451* |
probably null |
Het |
Tyms |
T |
C |
5: 30,269,110 (GRCm39) |
I171V |
|
Het |
Vmn2r115 |
T |
A |
17: 23,578,184 (GRCm39) |
N552K |
probably damaging |
Het |
Zfp710 |
T |
A |
7: 79,730,909 (GRCm39) |
S29T |
possibly damaging |
Het |
|
Other mutations in Or8c16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01099:Or8c16
|
APN |
9 |
38,131,039 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01772:Or8c16
|
APN |
9 |
38,130,905 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02253:Or8c16
|
APN |
9 |
38,131,031 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02279:Or8c16
|
APN |
9 |
38,130,389 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03031:Or8c16
|
APN |
9 |
38,130,361 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03163:Or8c16
|
APN |
9 |
38,130,710 (GRCm39) |
missense |
probably benign |
0.00 |
R0417:Or8c16
|
UTSW |
9 |
38,130,751 (GRCm39) |
missense |
probably benign |
0.01 |
R0458:Or8c16
|
UTSW |
9 |
38,130,344 (GRCm39) |
missense |
probably damaging |
0.97 |
R1498:Or8c16
|
UTSW |
9 |
38,130,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Or8c16
|
UTSW |
9 |
38,130,548 (GRCm39) |
missense |
probably benign |
0.01 |
R2020:Or8c16
|
UTSW |
9 |
38,130,728 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2282:Or8c16
|
UTSW |
9 |
38,130,124 (GRCm39) |
missense |
probably benign |
0.01 |
R3928:Or8c16
|
UTSW |
9 |
38,130,131 (GRCm39) |
start codon destroyed |
probably null |
0.63 |
R4716:Or8c16
|
UTSW |
9 |
38,130,714 (GRCm39) |
missense |
probably damaging |
0.99 |
R4911:Or8c16
|
UTSW |
9 |
38,130,392 (GRCm39) |
missense |
probably damaging |
0.99 |
R5148:Or8c16
|
UTSW |
9 |
38,130,317 (GRCm39) |
missense |
probably benign |
0.01 |
R7677:Or8c16
|
UTSW |
9 |
38,130,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7971:Or8c16
|
UTSW |
9 |
38,130,843 (GRCm39) |
missense |
probably benign |
0.00 |
R8219:Or8c16
|
UTSW |
9 |
38,130,668 (GRCm39) |
missense |
probably damaging |
0.98 |
R8754:Or8c16
|
UTSW |
9 |
38,130,865 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9248:Or8c16
|
UTSW |
9 |
38,130,706 (GRCm39) |
missense |
probably benign |
0.04 |
R9256:Or8c16
|
UTSW |
9 |
38,130,498 (GRCm39) |
nonsense |
probably null |
|
R9352:Or8c16
|
UTSW |
9 |
38,130,683 (GRCm39) |
missense |
probably damaging |
1.00 |
X0050:Or8c16
|
UTSW |
9 |
38,130,446 (GRCm39) |
missense |
probably benign |
0.00 |
|