Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
T |
C |
7: 66,559,224 (GRCm39) |
V338A |
probably damaging |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Bivm |
G |
T |
1: 44,165,561 (GRCm39) |
A4S |
probably benign |
Het |
Cacng3 |
G |
A |
7: 122,367,822 (GRCm39) |
R234Q |
probably damaging |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cftr |
A |
G |
6: 18,267,967 (GRCm39) |
D642G |
probably damaging |
Het |
Cltc |
A |
G |
11: 86,615,949 (GRCm39) |
V443A |
probably damaging |
Het |
Csmd3 |
C |
T |
15: 47,721,356 (GRCm39) |
R1425H |
probably damaging |
Het |
Cttnbp2 |
G |
C |
6: 18,426,092 (GRCm39) |
A762G |
possibly damaging |
Het |
Dscam |
T |
C |
16: 96,442,064 (GRCm39) |
T1588A |
probably benign |
Het |
Gabra4 |
A |
G |
5: 71,798,206 (GRCm39) |
M207T |
probably damaging |
Het |
Galnt3 |
A |
G |
2: 65,926,243 (GRCm39) |
Y322H |
probably damaging |
Het |
Glud1 |
A |
T |
14: 34,051,244 (GRCm39) |
|
probably null |
Het |
Gm47189 |
A |
G |
14: 41,492,011 (GRCm39) |
Y89H |
probably damaging |
Het |
Klhl1 |
A |
T |
14: 96,374,186 (GRCm39) |
M620K |
possibly damaging |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Mocs2 |
A |
G |
13: 114,957,382 (GRCm39) |
E62G |
probably damaging |
Het |
Myh7 |
C |
G |
14: 55,226,258 (GRCm39) |
D461H |
probably damaging |
Het |
Nek10 |
C |
T |
14: 15,001,017 (GRCm38) |
P1066S |
probably benign |
Het |
Nfxl1 |
T |
C |
5: 72,671,632 (GRCm39) |
K876E |
possibly damaging |
Het |
Nipsnap3a |
T |
A |
4: 52,997,279 (GRCm39) |
F182I |
probably damaging |
Het |
Nlrc3 |
C |
T |
16: 3,783,327 (GRCm39) |
G60S |
possibly damaging |
Het |
Notch2 |
T |
C |
3: 98,014,443 (GRCm39) |
Y666H |
probably damaging |
Het |
Or9m1b |
T |
C |
2: 87,836,355 (GRCm39) |
I247V |
probably benign |
Het |
Pars2 |
T |
A |
4: 106,511,276 (GRCm39) |
Y353N |
probably damaging |
Het |
Pcdhb11 |
A |
G |
18: 37,556,962 (GRCm39) |
E764G |
probably damaging |
Het |
Pcdhb3 |
T |
A |
18: 37,435,982 (GRCm39) |
D649E |
probably benign |
Het |
Pde7b |
T |
G |
10: 20,319,051 (GRCm39) |
R90S |
probably damaging |
Het |
Pik3r5 |
T |
C |
11: 68,384,483 (GRCm39) |
V625A |
probably damaging |
Het |
Prdm9 |
G |
A |
17: 15,779,311 (GRCm39) |
R113W |
probably damaging |
Het |
Psg26 |
A |
G |
7: 18,216,572 (GRCm39) |
V89A |
not run |
Het |
Rad1 |
T |
C |
15: 10,493,404 (GRCm39) |
V277A |
probably benign |
Het |
Rb1 |
A |
T |
14: 73,435,983 (GRCm39) |
L894Q |
probably damaging |
Het |
Rorb |
A |
T |
19: 18,965,460 (GRCm39) |
C10S |
probably damaging |
Het |
Ryk |
C |
T |
9: 102,768,432 (GRCm39) |
Q361* |
probably null |
Het |
Serpina3b |
A |
G |
12: 104,099,223 (GRCm39) |
N246S |
probably benign |
Het |
Srr |
A |
G |
11: 74,799,524 (GRCm39) |
V317A |
possibly damaging |
Het |
Timd2 |
A |
T |
11: 46,561,781 (GRCm39) |
C288S |
probably benign |
Het |
Tomm70a |
C |
T |
16: 56,965,136 (GRCm39) |
A440V |
probably damaging |
Het |
Trio |
C |
G |
15: 27,749,952 (GRCm39) |
V2250L |
probably benign |
Het |
Ubr5 |
G |
A |
15: 37,980,076 (GRCm39) |
A2434V |
probably null |
Het |
Unc13d |
A |
T |
11: 115,967,109 (GRCm39) |
V91D |
probably damaging |
Het |
Vmn1r159 |
T |
A |
7: 22,542,487 (GRCm39) |
I182F |
possibly damaging |
Het |
Vmn1r230 |
T |
A |
17: 21,066,823 (GRCm39) |
V4D |
probably benign |
Het |
Zfp27 |
T |
C |
7: 29,595,815 (GRCm39) |
Y50C |
possibly damaging |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp518b |
T |
C |
5: 38,829,741 (GRCm39) |
I755V |
not run |
Het |
|
Other mutations in Trim62 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01530:Trim62
|
APN |
4 |
128,778,252 (GRCm39) |
missense |
probably benign |
0.05 |
R0201:Trim62
|
UTSW |
4 |
128,796,343 (GRCm39) |
missense |
probably benign |
|
R0744:Trim62
|
UTSW |
4 |
128,778,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Trim62
|
UTSW |
4 |
128,803,281 (GRCm39) |
missense |
probably damaging |
0.98 |
R1834:Trim62
|
UTSW |
4 |
128,803,018 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5223:Trim62
|
UTSW |
4 |
128,803,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R5494:Trim62
|
UTSW |
4 |
128,778,999 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6909:Trim62
|
UTSW |
4 |
128,778,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Trim62
|
UTSW |
4 |
128,802,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7507:Trim62
|
UTSW |
4 |
128,790,664 (GRCm39) |
missense |
probably benign |
0.01 |
R7544:Trim62
|
UTSW |
4 |
128,796,346 (GRCm39) |
missense |
probably benign |
0.04 |
R7612:Trim62
|
UTSW |
4 |
128,790,677 (GRCm39) |
missense |
probably benign |
0.03 |
R7624:Trim62
|
UTSW |
4 |
128,777,471 (GRCm39) |
start gained |
probably benign |
|
R8404:Trim62
|
UTSW |
4 |
128,803,233 (GRCm39) |
missense |
probably benign |
0.01 |
R8502:Trim62
|
UTSW |
4 |
128,803,233 (GRCm39) |
missense |
probably benign |
0.01 |
R8692:Trim62
|
UTSW |
4 |
128,794,465 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9061:Trim62
|
UTSW |
4 |
128,802,963 (GRCm39) |
missense |
probably damaging |
1.00 |
|