Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh1a3 |
T |
C |
7: 66,051,789 (GRCm39) |
D388G |
probably benign |
Het |
Ankhd1 |
C |
A |
18: 36,757,714 (GRCm39) |
Q803K |
probably damaging |
Het |
Arrdc3 |
A |
G |
13: 81,041,499 (GRCm39) |
N180S |
probably benign |
Het |
Atp11b |
G |
A |
3: 35,868,301 (GRCm39) |
E458K |
probably benign |
Het |
Bend6 |
G |
A |
1: 33,901,827 (GRCm39) |
A185V |
probably benign |
Het |
Ccdc121 |
C |
T |
5: 31,644,835 (GRCm39) |
T196I |
probably benign |
Het |
Chd5 |
A |
G |
4: 152,450,670 (GRCm39) |
D632G |
probably damaging |
Het |
Clec4a1 |
A |
T |
6: 122,909,175 (GRCm39) |
H181L |
probably benign |
Het |
Cntnap5a |
T |
A |
1: 116,085,224 (GRCm39) |
D387E |
probably benign |
Het |
Colq |
G |
A |
14: 31,257,599 (GRCm39) |
S256F |
possibly damaging |
Het |
Cracd |
A |
G |
5: 76,996,817 (GRCm39) |
T92A |
possibly damaging |
Het |
Ctdp1 |
A |
G |
18: 80,499,187 (GRCm39) |
Y252H |
probably damaging |
Het |
Cyp4f17 |
T |
A |
17: 32,743,854 (GRCm39) |
L344Q |
probably damaging |
Het |
Fam83b |
A |
G |
9: 76,399,604 (GRCm39) |
Y500H |
probably damaging |
Het |
Gapvd1 |
G |
A |
2: 34,594,203 (GRCm39) |
P949L |
probably damaging |
Het |
Gp5 |
A |
G |
16: 30,128,482 (GRCm39) |
I64T |
probably benign |
Het |
Il31ra |
A |
G |
13: 112,670,401 (GRCm39) |
V248A |
probably damaging |
Het |
Kdm4a |
C |
T |
4: 118,017,366 (GRCm39) |
A567T |
probably benign |
Het |
Kpna7 |
T |
C |
5: 144,930,888 (GRCm39) |
|
probably null |
Het |
Lrrc8c |
G |
A |
5: 105,755,257 (GRCm39) |
R344H |
probably damaging |
Het |
Man1a |
G |
A |
10: 53,801,621 (GRCm39) |
L413F |
probably damaging |
Het |
Man1a2 |
A |
T |
3: 100,591,978 (GRCm39) |
D67E |
probably damaging |
Het |
Mkln1 |
G |
A |
6: 31,426,455 (GRCm39) |
S243N |
probably benign |
Het |
Mmp19 |
T |
A |
10: 128,634,356 (GRCm39) |
M299K |
probably benign |
Het |
Msantd2 |
T |
C |
9: 37,434,686 (GRCm39) |
F309L |
possibly damaging |
Het |
Mstn |
A |
G |
1: 53,101,309 (GRCm39) |
|
probably benign |
Het |
Nat8f5 |
A |
C |
6: 85,794,408 (GRCm39) |
I184R |
probably benign |
Het |
Or5d43 |
C |
T |
2: 88,105,056 (GRCm39) |
M112I |
probably benign |
Het |
Or9m1b |
G |
T |
2: 87,837,117 (GRCm39) |
Q2K |
probably benign |
Het |
Pigc |
A |
G |
1: 161,798,134 (GRCm39) |
K39E |
possibly damaging |
Het |
Pms2 |
T |
A |
5: 143,862,582 (GRCm39) |
L563Q |
probably benign |
Het |
Rpap1 |
A |
G |
2: 119,610,594 (GRCm39) |
S162P |
possibly damaging |
Het |
Rpl3l |
A |
G |
17: 24,951,407 (GRCm39) |
K103E |
probably damaging |
Het |
Slc45a1 |
A |
T |
4: 150,722,447 (GRCm39) |
V479E |
probably damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,600,714 (GRCm39) |
I671L |
possibly damaging |
Het |
Vmn2r6 |
C |
A |
3: 64,445,323 (GRCm39) |
V712L |
possibly damaging |
Het |
Zzz3 |
A |
G |
3: 152,133,752 (GRCm39) |
D270G |
possibly damaging |
Het |
|
Other mutations in Themis2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02192:Themis2
|
APN |
4 |
132,510,658 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02743:Themis2
|
APN |
4 |
132,510,795 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02934:Themis2
|
APN |
4 |
132,516,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R0111:Themis2
|
UTSW |
4 |
132,517,236 (GRCm39) |
missense |
probably benign |
0.17 |
R0598:Themis2
|
UTSW |
4 |
132,516,994 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1445:Themis2
|
UTSW |
4 |
132,510,212 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1484:Themis2
|
UTSW |
4 |
132,519,796 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1719:Themis2
|
UTSW |
4 |
132,516,960 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2076:Themis2
|
UTSW |
4 |
132,513,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Themis2
|
UTSW |
4 |
132,512,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R4620:Themis2
|
UTSW |
4 |
132,513,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R4653:Themis2
|
UTSW |
4 |
132,510,287 (GRCm39) |
missense |
probably benign |
0.40 |
R4891:Themis2
|
UTSW |
4 |
132,510,668 (GRCm39) |
missense |
probably benign |
0.14 |
R5331:Themis2
|
UTSW |
4 |
132,510,244 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5660:Themis2
|
UTSW |
4 |
132,523,567 (GRCm39) |
splice site |
probably null |
|
R6014:Themis2
|
UTSW |
4 |
132,513,291 (GRCm39) |
missense |
probably benign |
0.01 |
R6747:Themis2
|
UTSW |
4 |
132,523,573 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6863:Themis2
|
UTSW |
4 |
132,516,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R7380:Themis2
|
UTSW |
4 |
132,513,528 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7890:Themis2
|
UTSW |
4 |
132,516,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R7998:Themis2
|
UTSW |
4 |
132,519,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R8847:Themis2
|
UTSW |
4 |
132,513,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9503:Themis2
|
UTSW |
4 |
132,510,657 (GRCm39) |
critical splice donor site |
probably null |
|
R9642:Themis2
|
UTSW |
4 |
132,513,047 (GRCm39) |
missense |
possibly damaging |
0.96 |
|