Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
G |
T |
11: 109,958,933 (GRCm39) |
H730Q |
probably damaging |
Het |
Adam20 |
A |
G |
8: 41,249,408 (GRCm39) |
D506G |
probably damaging |
Het |
Brinp1 |
A |
G |
4: 68,823,190 (GRCm39) |
M1T |
probably null |
Het |
Ccnc |
T |
A |
4: 21,748,158 (GRCm39) |
N273K |
possibly damaging |
Het |
Cfdp1 |
C |
A |
8: 112,567,033 (GRCm39) |
V159L |
possibly damaging |
Het |
Cyb5r1 |
T |
A |
1: 134,334,638 (GRCm39) |
|
probably benign |
Het |
Dsp |
C |
T |
13: 38,351,615 (GRCm39) |
Q145* |
probably null |
Het |
Exosc9 |
G |
A |
3: 36,607,968 (GRCm39) |
V59I |
probably damaging |
Het |
Fermt2 |
C |
G |
14: 45,699,318 (GRCm39) |
R592T |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,211,875 (GRCm39) |
S2381P |
probably damaging |
Het |
Fscn2 |
G |
A |
11: 120,258,082 (GRCm39) |
E335K |
possibly damaging |
Het |
Hapln1 |
T |
C |
13: 89,755,997 (GRCm39) |
I267T |
probably benign |
Het |
Hdac9 |
T |
A |
12: 34,483,209 (GRCm39) |
I93L |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,899,706 (GRCm39) |
D535G |
probably damaging |
Het |
Ighv1-4 |
A |
T |
12: 114,451,165 (GRCm39) |
F9I |
possibly damaging |
Het |
Il3ra |
T |
A |
14: 14,350,773 (GRCm38) |
H262Q |
possibly damaging |
Het |
Kti12 |
A |
C |
4: 108,705,443 (GRCm39) |
E119A |
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,444 (GRCm39) |
E119D |
probably benign |
Het |
Mtg1 |
A |
T |
7: 139,727,178 (GRCm39) |
D227V |
probably damaging |
Het |
Nrcam |
T |
G |
12: 44,620,546 (GRCm39) |
|
probably null |
Het |
Or13g1 |
T |
C |
7: 85,955,686 (GRCm39) |
T212A |
probably damaging |
Het |
Or4f57 |
A |
C |
2: 111,791,310 (GRCm39) |
V36G |
probably damaging |
Het |
Or8b1 |
T |
A |
9: 38,399,905 (GRCm39) |
Y193* |
probably null |
Het |
Pcdha1 |
T |
A |
18: 37,065,254 (GRCm39) |
D639E |
possibly damaging |
Het |
Pcdhga8 |
T |
A |
18: 37,860,669 (GRCm39) |
V575E |
possibly damaging |
Het |
Pcif1 |
G |
T |
2: 164,730,392 (GRCm39) |
R375L |
probably benign |
Het |
Pcna |
A |
T |
2: 132,094,929 (GRCm39) |
S10T |
probably benign |
Het |
Pdzd8 |
A |
G |
19: 59,333,518 (GRCm39) |
S168P |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Polq |
T |
A |
16: 36,885,650 (GRCm39) |
D1842E |
probably benign |
Het |
Rag2 |
A |
T |
2: 101,460,040 (GRCm39) |
N117Y |
probably damaging |
Het |
Scnn1g |
T |
C |
7: 121,342,916 (GRCm39) |
Y290H |
probably damaging |
Het |
Sri |
T |
C |
5: 8,113,409 (GRCm39) |
|
probably null |
Het |
Tek |
T |
C |
4: 94,708,372 (GRCm39) |
V361A |
possibly damaging |
Het |
Terf1 |
T |
A |
1: 15,889,300 (GRCm39) |
L243Q |
probably damaging |
Het |
Thrap3 |
G |
A |
4: 126,069,213 (GRCm39) |
T646I |
probably damaging |
Het |
Vmn2r29 |
A |
G |
7: 7,234,727 (GRCm39) |
S720P |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 44,886,421 (GRCm39) |
N879D |
possibly damaging |
Het |
Zfp266 |
T |
C |
9: 20,416,423 (GRCm39) |
T56A |
probably benign |
Het |
Zxdc |
T |
A |
6: 90,358,991 (GRCm39) |
I541N |
probably damaging |
Het |
|
Other mutations in Uba1y |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02852:Uba1y
|
APN |
Y |
828,841 (GRCm39) |
nonsense |
probably null |
|
R0532:Uba1y
|
UTSW |
Y |
820,911 (GRCm39) |
missense |
probably benign |
0.28 |
R1532:Uba1y
|
UTSW |
Y |
828,862 (GRCm39) |
missense |
probably benign |
0.44 |
R1590:Uba1y
|
UTSW |
Y |
826,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R4668:Uba1y
|
UTSW |
Y |
826,032 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4801:Uba1y
|
UTSW |
Y |
825,890 (GRCm39) |
splice site |
probably null |
|
R4802:Uba1y
|
UTSW |
Y |
825,890 (GRCm39) |
splice site |
probably null |
|
R5101:Uba1y
|
UTSW |
Y |
821,447 (GRCm39) |
splice site |
probably null |
|
R6151:Uba1y
|
UTSW |
Y |
825,984 (GRCm39) |
missense |
probably benign |
0.01 |
R6577:Uba1y
|
UTSW |
Y |
825,465 (GRCm39) |
missense |
probably benign |
0.39 |
R6901:Uba1y
|
UTSW |
Y |
825,496 (GRCm39) |
missense |
probably benign |
0.03 |
R7186:Uba1y
|
UTSW |
Y |
825,537 (GRCm39) |
missense |
probably benign |
|
R7263:Uba1y
|
UTSW |
Y |
822,200 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7305:Uba1y
|
UTSW |
Y |
821,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Uba1y
|
UTSW |
Y |
821,567 (GRCm39) |
missense |
probably benign |
0.44 |
R7873:Uba1y
|
UTSW |
Y |
825,542 (GRCm39) |
missense |
probably benign |
|
R8159:Uba1y
|
UTSW |
Y |
828,806 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8810:Uba1y
|
UTSW |
Y |
828,818 (GRCm39) |
missense |
possibly damaging |
0.89 |
|