Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110082I17Rik |
T |
C |
5: 139,349,855 (GRCm39) |
K65E |
probably damaging |
Het |
Acp5 |
C |
A |
9: 22,041,233 (GRCm39) |
A65S |
probably benign |
Het |
Adad2 |
G |
A |
8: 120,342,397 (GRCm39) |
R345H |
probably damaging |
Het |
Adamts7 |
G |
T |
9: 90,067,793 (GRCm39) |
G428W |
probably damaging |
Het |
Amy1 |
A |
G |
3: 113,355,498 (GRCm39) |
S326P |
probably damaging |
Het |
Ankrd44 |
C |
T |
1: 54,703,071 (GRCm39) |
D482N |
probably damaging |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ano8 |
G |
C |
8: 71,935,640 (GRCm39) |
P326R |
probably damaging |
Het |
Arhgef26 |
A |
G |
3: 62,367,046 (GRCm39) |
E793G |
probably damaging |
Het |
Cd9 |
A |
T |
6: 125,440,703 (GRCm39) |
V96E |
probably damaging |
Het |
Cdh9 |
A |
G |
15: 16,850,914 (GRCm39) |
N561S |
probably benign |
Het |
Col16a1 |
G |
A |
4: 129,948,272 (GRCm39) |
|
probably null |
Het |
Cpne7 |
G |
A |
8: 123,860,498 (GRCm39) |
G484R |
probably damaging |
Het |
Dcun1d4 |
A |
T |
5: 73,701,463 (GRCm39) |
K194* |
probably null |
Het |
Dock3 |
A |
G |
9: 106,818,515 (GRCm39) |
V1193A |
probably damaging |
Het |
Dst |
A |
G |
1: 34,007,904 (GRCm39) |
R113G |
possibly damaging |
Het |
Epha5 |
A |
T |
5: 84,381,502 (GRCm39) |
S450T |
probably damaging |
Het |
Gm5581 |
A |
T |
6: 131,144,190 (GRCm39) |
|
noncoding transcript |
Het |
Grhl3 |
A |
G |
4: 135,279,918 (GRCm39) |
Y379H |
probably damaging |
Het |
Herpud1 |
T |
C |
8: 95,117,454 (GRCm39) |
S13P |
probably benign |
Het |
Jam2 |
C |
T |
16: 84,606,435 (GRCm39) |
Q150* |
probably null |
Het |
Jph2 |
C |
G |
2: 163,217,668 (GRCm39) |
R336P |
probably damaging |
Het |
Kansl3 |
T |
A |
1: 36,387,764 (GRCm39) |
|
probably null |
Het |
Kctd1 |
G |
A |
18: 15,195,580 (GRCm39) |
P348S |
probably damaging |
Het |
Klhl30 |
T |
A |
1: 91,285,106 (GRCm39) |
S321T |
possibly damaging |
Het |
Klhl5 |
T |
C |
5: 65,310,033 (GRCm39) |
|
probably benign |
Het |
Letm2 |
T |
C |
8: 26,084,108 (GRCm39) |
H41R |
possibly damaging |
Het |
Ltn1 |
A |
T |
16: 87,194,679 (GRCm39) |
C1407S |
probably benign |
Het |
Map1b |
T |
C |
13: 99,572,161 (GRCm39) |
T187A |
probably damaging |
Het |
Marveld2 |
T |
C |
13: 100,748,431 (GRCm39) |
N216S |
probably benign |
Het |
Matn1 |
A |
G |
4: 130,680,234 (GRCm39) |
Y437C |
probably damaging |
Het |
Ofcc1 |
A |
G |
13: 40,417,035 (GRCm39) |
|
probably null |
Het |
Or2m12 |
C |
A |
16: 19,104,726 (GRCm39) |
G256W |
probably damaging |
Het |
Or4k51 |
A |
T |
2: 111,584,750 (GRCm39) |
D52V |
probably damaging |
Het |
Or8g34 |
A |
G |
9: 39,373,183 (GRCm39) |
Y152C |
probably damaging |
Het |
Otof |
C |
A |
5: 30,540,837 (GRCm39) |
|
probably benign |
Het |
Pcdh15 |
G |
T |
10: 74,215,249 (GRCm39) |
|
probably null |
Het |
Pgk2 |
G |
A |
17: 40,518,412 (GRCm39) |
P339S |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,186,032 (GRCm39) |
|
probably null |
Het |
Prex2 |
A |
G |
1: 11,168,705 (GRCm39) |
T234A |
possibly damaging |
Het |
Rasgrf1 |
C |
T |
9: 89,826,922 (GRCm39) |
T177M |
probably benign |
Het |
Rgs1 |
A |
T |
1: 144,124,309 (GRCm39) |
|
probably null |
Het |
Snx25 |
T |
C |
8: 46,521,229 (GRCm39) |
N239S |
probably damaging |
Het |
Spata31d1a |
T |
A |
13: 59,849,716 (GRCm39) |
H804L |
possibly damaging |
Het |
Spon2 |
A |
T |
5: 33,371,896 (GRCm39) |
Y303* |
probably null |
Het |
Spopfm2 |
A |
T |
3: 94,082,841 (GRCm39) |
C323* |
probably null |
Het |
Thrb |
G |
A |
14: 18,011,076 (GRCm38) |
D151N |
probably benign |
Het |
Tns1 |
A |
G |
1: 73,975,074 (GRCm39) |
V1170A |
probably benign |
Het |
Trbv19 |
A |
T |
6: 41,155,706 (GRCm39) |
I26F |
probably damaging |
Het |
Tstd2 |
T |
C |
4: 46,120,467 (GRCm39) |
N311S |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,715,746 (GRCm39) |
|
probably benign |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Vmn1r185 |
G |
A |
7: 26,310,716 (GRCm39) |
A263V |
probably benign |
Het |
Zfp316 |
T |
C |
5: 143,239,169 (GRCm39) |
H950R |
probably damaging |
Het |
Zfp51 |
A |
G |
17: 21,676,615 (GRCm39) |
K29E |
probably benign |
Het |
Zfp644 |
T |
C |
5: 106,766,081 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Oas1h |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01676:Oas1h
|
APN |
5 |
121,009,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01890:Oas1h
|
APN |
5 |
121,000,852 (GRCm39) |
splice site |
probably null |
|
IGL02745:Oas1h
|
APN |
5 |
120,999,542 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02888:Oas1h
|
APN |
5 |
120,999,610 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02970:Oas1h
|
APN |
5 |
120,999,698 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0125:Oas1h
|
UTSW |
5 |
121,000,626 (GRCm39) |
nonsense |
probably null |
|
R1261:Oas1h
|
UTSW |
5 |
121,009,930 (GRCm39) |
missense |
probably benign |
0.01 |
R1506:Oas1h
|
UTSW |
5 |
121,009,951 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1565:Oas1h
|
UTSW |
5 |
121,000,663 (GRCm39) |
missense |
probably damaging |
0.97 |
R1696:Oas1h
|
UTSW |
5 |
121,000,885 (GRCm39) |
critical splice donor site |
probably null |
|
R1750:Oas1h
|
UTSW |
5 |
121,009,840 (GRCm39) |
splice site |
probably null |
|
R3116:Oas1h
|
UTSW |
5 |
120,999,679 (GRCm39) |
nonsense |
probably null |
|
R4814:Oas1h
|
UTSW |
5 |
121,000,728 (GRCm39) |
missense |
probably damaging |
0.99 |
R4906:Oas1h
|
UTSW |
5 |
121,005,172 (GRCm39) |
nonsense |
probably null |
|
R4944:Oas1h
|
UTSW |
5 |
121,000,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Oas1h
|
UTSW |
5 |
121,009,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Oas1h
|
UTSW |
5 |
121,009,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R5903:Oas1h
|
UTSW |
5 |
121,009,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Oas1h
|
UTSW |
5 |
121,005,229 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7062:Oas1h
|
UTSW |
5 |
120,999,528 (GRCm39) |
unclassified |
probably benign |
|
R7966:Oas1h
|
UTSW |
5 |
121,009,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R7975:Oas1h
|
UTSW |
5 |
121,009,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Oas1h
|
UTSW |
5 |
121,005,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777-TAIL:Oas1h
|
UTSW |
5 |
121,005,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R8951:Oas1h
|
UTSW |
5 |
121,000,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Oas1h
|
UTSW |
5 |
121,005,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Oas1h
|
UTSW |
5 |
121,005,088 (GRCm39) |
missense |
probably damaging |
0.99 |
|