Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410002F23Rik |
C |
T |
7: 43,900,334 (GRCm39) |
R80W |
probably damaging |
Het |
Ankdd1b |
G |
T |
13: 96,591,294 (GRCm39) |
N68K |
possibly damaging |
Het |
Arhgef1 |
A |
G |
7: 24,619,115 (GRCm39) |
E452G |
probably damaging |
Het |
Cbx8 |
T |
G |
11: 118,930,964 (GRCm39) |
E45D |
probably damaging |
Het |
Ceacam15 |
T |
C |
7: 16,407,316 (GRCm39) |
Y67C |
probably damaging |
Het |
Ceacam20 |
A |
G |
7: 19,723,926 (GRCm39) |
Y570C |
probably damaging |
Het |
Cnga4 |
A |
G |
7: 105,054,977 (GRCm39) |
Y187C |
probably damaging |
Het |
Cntrob |
T |
C |
11: 69,205,679 (GRCm39) |
N385S |
probably benign |
Het |
Coro7 |
A |
G |
16: 4,486,624 (GRCm39) |
V183A |
possibly damaging |
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Dnah7b |
A |
G |
1: 46,264,956 (GRCm39) |
Y2150C |
probably damaging |
Het |
E2f8 |
A |
G |
7: 48,528,394 (GRCm39) |
S25P |
probably damaging |
Het |
Eif1ad7 |
A |
G |
12: 88,238,476 (GRCm39) |
Y95H |
probably damaging |
Het |
Eif3d |
T |
C |
15: 77,843,837 (GRCm39) |
E503G |
probably damaging |
Het |
Elp6 |
T |
A |
9: 110,144,965 (GRCm39) |
V157D |
probably damaging |
Het |
Entpd3 |
T |
C |
9: 120,387,546 (GRCm39) |
Y248H |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,844,561 (GRCm39) |
E561G |
unknown |
Het |
Fbxl13 |
C |
T |
5: 21,728,151 (GRCm39) |
G519S |
probably damaging |
Het |
Fgfr4 |
T |
G |
13: 55,309,228 (GRCm39) |
S422A |
probably damaging |
Het |
Flg2 |
G |
A |
3: 93,121,901 (GRCm39) |
C1357Y |
unknown |
Het |
Fpr3 |
T |
A |
17: 18,191,612 (GRCm39) |
N294K |
probably damaging |
Het |
Gas6 |
T |
C |
8: 13,525,048 (GRCm39) |
Q312R |
possibly damaging |
Het |
Glg1 |
C |
T |
8: 111,926,770 (GRCm39) |
E182K |
probably benign |
Het |
Gucy1b1 |
T |
C |
3: 81,947,087 (GRCm39) |
D374G |
probably damaging |
Het |
Ifrd2 |
C |
T |
9: 107,468,285 (GRCm39) |
T251I |
possibly damaging |
Het |
Igkv4-91 |
C |
T |
6: 68,745,632 (GRCm39) |
G89R |
possibly damaging |
Het |
Kcnk1 |
C |
A |
8: 126,756,322 (GRCm39) |
Y281* |
probably null |
Het |
Kcp |
G |
T |
6: 29,485,100 (GRCm39) |
F1217L |
probably null |
Het |
Lama3 |
G |
A |
18: 12,563,019 (GRCm39) |
G514D |
probably damaging |
Het |
Madd |
A |
G |
2: 91,008,800 (GRCm39) |
L34P |
probably damaging |
Het |
Mak |
T |
A |
13: 41,183,595 (GRCm39) |
T562S |
probably benign |
Het |
Nfatc4 |
A |
G |
14: 56,070,259 (GRCm39) |
E879G |
probably damaging |
Het |
Or5w14 |
A |
T |
2: 87,541,992 (GRCm39) |
V86E |
probably benign |
Het |
Pcdhb19 |
C |
T |
18: 37,631,848 (GRCm39) |
R548C |
probably damaging |
Het |
Peli2 |
A |
G |
14: 48,488,150 (GRCm39) |
I165V |
probably damaging |
Het |
Plekhd1 |
A |
T |
12: 80,753,977 (GRCm39) |
M148L |
probably benign |
Het |
Rars2 |
G |
A |
4: 34,637,014 (GRCm39) |
G172R |
probably damaging |
Het |
Reck |
T |
C |
4: 43,928,310 (GRCm39) |
V537A |
probably damaging |
Het |
Sirpb1a |
C |
T |
3: 15,476,320 (GRCm39) |
C226Y |
probably damaging |
Het |
Speg |
A |
C |
1: 75,394,645 (GRCm39) |
I1785L |
probably benign |
Het |
Spry4 |
T |
C |
18: 38,723,070 (GRCm39) |
N231S |
probably damaging |
Het |
Tchh |
C |
T |
3: 93,355,125 (GRCm39) |
Q1522* |
probably null |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Trav7d-3 |
G |
T |
14: 52,981,820 (GRCm39) |
|
probably benign |
Het |
Vmn2r49 |
A |
C |
7: 9,720,849 (GRCm39) |
V214G |
probably benign |
Het |
Vmn2r80 |
T |
C |
10: 78,984,743 (GRCm39) |
Y32H |
probably benign |
Het |
Vwf |
A |
C |
6: 125,577,662 (GRCm39) |
D501A |
|
Het |
Zfp428 |
A |
G |
7: 24,214,866 (GRCm39) |
T161A |
possibly damaging |
Het |
Zpld2 |
G |
A |
4: 133,929,312 (GRCm39) |
P331L |
probably benign |
Het |
|
Other mutations in Rnf135 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01371:Rnf135
|
APN |
11 |
80,080,081 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02637:Rnf135
|
APN |
11 |
80,089,704 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03179:Rnf135
|
APN |
11 |
80,084,837 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0027:Rnf135
|
UTSW |
11 |
80,084,768 (GRCm39) |
missense |
probably benign |
0.10 |
R0282:Rnf135
|
UTSW |
11 |
80,084,784 (GRCm39) |
missense |
probably damaging |
0.99 |
R0496:Rnf135
|
UTSW |
11 |
80,074,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R1680:Rnf135
|
UTSW |
11 |
80,087,707 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2173:Rnf135
|
UTSW |
11 |
80,080,066 (GRCm39) |
missense |
probably benign |
0.36 |
R3721:Rnf135
|
UTSW |
11 |
80,087,743 (GRCm39) |
missense |
probably benign |
0.05 |
R3722:Rnf135
|
UTSW |
11 |
80,087,743 (GRCm39) |
missense |
probably benign |
0.05 |
R4089:Rnf135
|
UTSW |
11 |
80,089,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Rnf135
|
UTSW |
11 |
80,087,775 (GRCm39) |
critical splice donor site |
probably null |
|
R4901:Rnf135
|
UTSW |
11 |
80,089,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R5640:Rnf135
|
UTSW |
11 |
80,084,733 (GRCm39) |
missense |
probably benign |
0.12 |
R5826:Rnf135
|
UTSW |
11 |
80,089,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6225:Rnf135
|
UTSW |
11 |
80,080,053 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7096:Rnf135
|
UTSW |
11 |
80,080,051 (GRCm39) |
missense |
probably benign |
0.19 |
R7532:Rnf135
|
UTSW |
11 |
80,089,732 (GRCm39) |
missense |
probably benign |
0.03 |
R8255:Rnf135
|
UTSW |
11 |
80,084,713 (GRCm39) |
missense |
probably benign |
0.01 |
R8806:Rnf135
|
UTSW |
11 |
80,089,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R8889:Rnf135
|
UTSW |
11 |
80,074,957 (GRCm39) |
missense |
probably benign |
0.01 |
R8892:Rnf135
|
UTSW |
11 |
80,074,957 (GRCm39) |
missense |
probably benign |
0.01 |
|