Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amigo1 |
A |
G |
3: 108,095,751 (GRCm39) |
M417V |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,823,306 (GRCm39) |
Q1701K |
probably benign |
Het |
Cfhr2 |
G |
T |
1: 139,741,219 (GRCm39) |
T252K |
possibly damaging |
Het |
Cntnap4 |
T |
A |
8: 113,602,211 (GRCm39) |
V1205E |
possibly damaging |
Het |
Ctsb |
T |
C |
14: 63,370,881 (GRCm39) |
I31T |
probably benign |
Het |
Cyp4f13 |
G |
C |
17: 33,143,833 (GRCm39) |
P497R |
probably damaging |
Het |
Dna2 |
A |
G |
10: 62,809,094 (GRCm39) |
D1062G |
probably benign |
Het |
Dnah7a |
A |
C |
1: 53,657,139 (GRCm39) |
M879R |
probably benign |
Het |
Gcc1 |
C |
A |
6: 28,418,029 (GRCm39) |
S768I |
probably benign |
Het |
Gm29106 |
T |
C |
1: 118,128,218 (GRCm39) |
Y637H |
probably damaging |
Het |
Gm4787 |
T |
C |
12: 81,425,840 (GRCm39) |
D106G |
probably damaging |
Het |
Gm527 |
T |
A |
12: 64,967,782 (GRCm39) |
V68D |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,955,605 (GRCm39) |
Y226* |
probably null |
Het |
Hkdc1 |
T |
C |
10: 62,221,662 (GRCm39) |
R799G |
probably benign |
Het |
Ier2 |
T |
C |
8: 85,389,353 (GRCm39) |
I10V |
probably damaging |
Het |
Ifi209 |
A |
G |
1: 173,470,069 (GRCm39) |
N219S |
probably benign |
Het |
Iqcn |
T |
C |
8: 71,162,625 (GRCm39) |
I606T |
probably benign |
Het |
Krt88 |
A |
G |
15: 101,351,406 (GRCm39) |
S138G |
probably benign |
Het |
Lrrc3 |
T |
C |
10: 77,736,824 (GRCm39) |
D204G |
probably damaging |
Het |
Mllt6 |
T |
C |
11: 97,567,688 (GRCm39) |
I705T |
possibly damaging |
Het |
Mpl |
G |
A |
4: 118,306,207 (GRCm39) |
P278S |
probably benign |
Het |
Nkx3-2 |
T |
C |
5: 41,920,989 (GRCm39) |
E100G |
probably benign |
Het |
Or13p8 |
A |
T |
4: 118,583,822 (GRCm39) |
Y126F |
possibly damaging |
Het |
Or56b1b |
A |
T |
7: 108,164,833 (GRCm39) |
C56* |
probably null |
Het |
Or8b12b |
G |
A |
9: 37,684,560 (GRCm39) |
V202M |
probably damaging |
Het |
Pcdh15 |
G |
A |
10: 74,317,974 (GRCm39) |
V992I |
probably damaging |
Het |
Pcdhgc5 |
A |
G |
18: 37,953,487 (GRCm39) |
N254D |
probably damaging |
Het |
Pdgfd |
A |
G |
9: 6,288,655 (GRCm39) |
E103G |
probably damaging |
Het |
Ppp2r1b |
C |
T |
9: 50,778,194 (GRCm39) |
R304* |
probably null |
Het |
Pramel30 |
A |
G |
4: 144,058,233 (GRCm39) |
D280G |
probably benign |
Het |
Prdm2 |
G |
A |
4: 142,907,467 (GRCm39) |
A35V |
probably damaging |
Het |
Psd |
T |
C |
19: 46,312,788 (GRCm39) |
N194S |
probably damaging |
Het |
Rasgef1c |
A |
T |
11: 49,862,248 (GRCm39) |
E379V |
probably damaging |
Het |
Rnf43 |
A |
T |
11: 87,618,267 (GRCm39) |
I186F |
probably damaging |
Het |
Ros1 |
C |
T |
10: 52,055,047 (GRCm39) |
C85Y |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,378,989 (GRCm39) |
L935I |
probably damaging |
Het |
Slc2a5 |
A |
G |
4: 150,210,590 (GRCm39) |
Q46R |
probably benign |
Het |
Ss18l1 |
A |
T |
2: 179,699,968 (GRCm39) |
Q276L |
probably damaging |
Het |
Tas2r129 |
A |
T |
6: 132,928,815 (GRCm39) |
M251L |
probably benign |
Het |
Thoc1 |
A |
G |
18: 9,989,693 (GRCm39) |
E458G |
probably benign |
Het |
Wdr35 |
T |
A |
12: 9,058,626 (GRCm39) |
N594K |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,744,148 (GRCm39) |
C835S |
probably damaging |
Het |
|
Other mutations in 3110009E18Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00690:3110009E18Rik
|
APN |
1 |
120,078,336 (GRCm39) |
unclassified |
probably benign |
|
IGL00696:3110009E18Rik
|
APN |
1 |
120,099,156 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01482:3110009E18Rik
|
APN |
1 |
120,099,201 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01996:3110009E18Rik
|
APN |
1 |
120,078,430 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0033:3110009E18Rik
|
UTSW |
1 |
120,115,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:3110009E18Rik
|
UTSW |
1 |
120,093,906 (GRCm39) |
splice site |
probably benign |
|
R1025:3110009E18Rik
|
UTSW |
1 |
120,099,192 (GRCm39) |
missense |
probably damaging |
0.97 |
R1535:3110009E18Rik
|
UTSW |
1 |
120,099,203 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4676:3110009E18Rik
|
UTSW |
1 |
120,078,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:3110009E18Rik
|
UTSW |
1 |
120,096,850 (GRCm39) |
intron |
probably benign |
|
R4955:3110009E18Rik
|
UTSW |
1 |
120,096,849 (GRCm39) |
intron |
probably benign |
|
R4955:3110009E18Rik
|
UTSW |
1 |
120,096,840 (GRCm39) |
intron |
probably benign |
|
R4956:3110009E18Rik
|
UTSW |
1 |
120,096,850 (GRCm39) |
intron |
probably benign |
|
R4956:3110009E18Rik
|
UTSW |
1 |
120,096,849 (GRCm39) |
intron |
probably benign |
|
R4956:3110009E18Rik
|
UTSW |
1 |
120,096,840 (GRCm39) |
intron |
probably benign |
|
R4957:3110009E18Rik
|
UTSW |
1 |
120,096,850 (GRCm39) |
intron |
probably benign |
|
R4957:3110009E18Rik
|
UTSW |
1 |
120,096,849 (GRCm39) |
intron |
probably benign |
|
R4957:3110009E18Rik
|
UTSW |
1 |
120,096,840 (GRCm39) |
intron |
probably benign |
|
R5866:3110009E18Rik
|
UTSW |
1 |
120,096,814 (GRCm39) |
intron |
probably benign |
|
R6151:3110009E18Rik
|
UTSW |
1 |
120,099,216 (GRCm39) |
splice site |
probably null |
|
R6229:3110009E18Rik
|
UTSW |
1 |
120,099,213 (GRCm39) |
critical splice donor site |
probably null |
|
R8187:3110009E18Rik
|
UTSW |
1 |
120,115,913 (GRCm39) |
makesense |
probably null |
|
R9049:3110009E18Rik
|
UTSW |
1 |
120,115,900 (GRCm39) |
missense |
probably null |
|
R9075:3110009E18Rik
|
UTSW |
1 |
120,097,014 (GRCm39) |
missense |
|
|
R9211:3110009E18Rik
|
UTSW |
1 |
120,099,161 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9492:3110009E18Rik
|
UTSW |
1 |
120,078,472 (GRCm39) |
missense |
probably damaging |
0.99 |
R9564:3110009E18Rik
|
UTSW |
1 |
120,097,006 (GRCm39) |
missense |
|
|
|