Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap5 |
C |
T |
12: 52,565,518 (GRCm39) |
Q830* |
probably null |
Het |
Atic |
A |
T |
1: 71,617,009 (GRCm39) |
E523V |
possibly damaging |
Het |
Cass4 |
T |
A |
2: 172,268,900 (GRCm39) |
F329L |
probably damaging |
Het |
Cdk17 |
A |
T |
10: 93,062,640 (GRCm39) |
|
probably benign |
Het |
Cep120 |
C |
T |
18: 53,819,033 (GRCm39) |
R886H |
probably benign |
Het |
Cep170 |
A |
C |
1: 176,610,061 (GRCm39) |
|
probably null |
Het |
Dsg3 |
A |
G |
18: 20,654,541 (GRCm39) |
K82E |
probably benign |
Het |
Dtd1 |
C |
T |
2: 144,588,896 (GRCm39) |
R185W |
probably damaging |
Het |
Glt6d1 |
C |
A |
2: 25,684,739 (GRCm39) |
|
probably null |
Het |
Hectd1 |
T |
G |
12: 51,800,608 (GRCm39) |
E2070A |
possibly damaging |
Het |
Ifit1bl2 |
T |
A |
19: 34,596,846 (GRCm39) |
K257* |
probably null |
Het |
Ighv8-5 |
T |
A |
12: 115,031,207 (GRCm39) |
T111S |
possibly damaging |
Het |
Lmtk2 |
G |
T |
5: 144,103,205 (GRCm39) |
L321F |
probably damaging |
Het |
Mcoln2 |
C |
T |
3: 145,889,316 (GRCm39) |
T374M |
probably damaging |
Het |
Mfn1 |
T |
C |
3: 32,592,416 (GRCm39) |
|
probably benign |
Het |
Miox |
C |
T |
15: 89,220,477 (GRCm39) |
L189F |
possibly damaging |
Het |
Mroh8 |
T |
C |
2: 157,071,849 (GRCm39) |
H552R |
possibly damaging |
Het |
Myh2 |
T |
A |
11: 67,069,103 (GRCm39) |
L304Q |
probably damaging |
Het |
Prune1 |
T |
A |
3: 95,169,678 (GRCm39) |
T175S |
probably damaging |
Het |
Rdh10 |
C |
T |
1: 16,199,508 (GRCm39) |
T238I |
probably damaging |
Het |
Rlf |
T |
A |
4: 121,004,039 (GRCm39) |
H1647L |
possibly damaging |
Het |
Scn9a |
A |
T |
2: 66,392,788 (GRCm39) |
M268K |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,313,926 (GRCm39) |
V1893A |
probably benign |
Het |
Snd1 |
T |
A |
6: 28,745,209 (GRCm39) |
L518Q |
probably damaging |
Het |
Stat1 |
T |
A |
1: 52,179,819 (GRCm39) |
V343D |
probably damaging |
Het |
Topors |
A |
G |
4: 40,262,772 (GRCm39) |
S171P |
probably damaging |
Het |
Tubd1 |
C |
T |
11: 86,440,221 (GRCm39) |
Q82* |
probably null |
Het |
Unc13c |
A |
G |
9: 73,576,847 (GRCm39) |
|
probably benign |
Het |
Wdr43 |
G |
T |
17: 71,960,487 (GRCm39) |
G590* |
probably null |
Het |
|
Other mutations in Rreb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Rreb1
|
APN |
13 |
38,100,472 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00336:Rreb1
|
APN |
13 |
38,113,622 (GRCm39) |
nonsense |
probably null |
|
IGL00473:Rreb1
|
APN |
13 |
38,114,767 (GRCm39) |
nonsense |
probably null |
|
IGL01338:Rreb1
|
APN |
13 |
38,115,010 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01836:Rreb1
|
APN |
13 |
38,115,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Rreb1
|
APN |
13 |
38,115,482 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02661:Rreb1
|
APN |
13 |
38,114,778 (GRCm39) |
nonsense |
probably null |
|
IGL02739:Rreb1
|
APN |
13 |
38,077,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Rreb1
|
APN |
13 |
38,116,169 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03332:Rreb1
|
APN |
13 |
38,114,892 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03403:Rreb1
|
APN |
13 |
38,113,550 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0039:Rreb1
|
UTSW |
13 |
38,083,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R0101:Rreb1
|
UTSW |
13 |
38,115,518 (GRCm39) |
missense |
probably benign |
0.04 |
R0265:Rreb1
|
UTSW |
13 |
38,100,131 (GRCm39) |
nonsense |
probably null |
|
R0635:Rreb1
|
UTSW |
13 |
38,125,540 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0939:Rreb1
|
UTSW |
13 |
38,116,207 (GRCm39) |
missense |
probably benign |
0.09 |
R1099:Rreb1
|
UTSW |
13 |
38,132,867 (GRCm39) |
missense |
probably benign |
0.16 |
R1438:Rreb1
|
UTSW |
13 |
38,114,581 (GRCm39) |
missense |
probably benign |
0.16 |
R1457:Rreb1
|
UTSW |
13 |
38,130,904 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1510:Rreb1
|
UTSW |
13 |
38,115,860 (GRCm39) |
missense |
probably benign |
0.04 |
R1672:Rreb1
|
UTSW |
13 |
38,114,513 (GRCm39) |
missense |
probably benign |
0.09 |
R1772:Rreb1
|
UTSW |
13 |
38,114,899 (GRCm39) |
missense |
probably benign |
0.09 |
R2171:Rreb1
|
UTSW |
13 |
38,114,822 (GRCm39) |
missense |
probably benign |
0.00 |
R2371:Rreb1
|
UTSW |
13 |
38,100,513 (GRCm39) |
missense |
probably benign |
0.09 |
R2566:Rreb1
|
UTSW |
13 |
38,113,768 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2571:Rreb1
|
UTSW |
13 |
38,083,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:Rreb1
|
UTSW |
13 |
38,116,429 (GRCm39) |
missense |
probably benign |
0.02 |
R2874:Rreb1
|
UTSW |
13 |
38,100,484 (GRCm39) |
missense |
probably benign |
0.09 |
R2911:Rreb1
|
UTSW |
13 |
38,132,896 (GRCm39) |
missense |
probably benign |
0.00 |
R3722:Rreb1
|
UTSW |
13 |
38,131,074 (GRCm39) |
missense |
probably benign |
0.01 |
R3767:Rreb1
|
UTSW |
13 |
38,113,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3770:Rreb1
|
UTSW |
13 |
38,113,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3885:Rreb1
|
UTSW |
13 |
38,077,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Rreb1
|
UTSW |
13 |
38,082,482 (GRCm39) |
splice site |
probably null |
|
R3887:Rreb1
|
UTSW |
13 |
38,077,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Rreb1
|
UTSW |
13 |
38,077,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3889:Rreb1
|
UTSW |
13 |
38,077,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Rreb1
|
UTSW |
13 |
38,114,293 (GRCm39) |
missense |
probably benign |
0.42 |
R4134:Rreb1
|
UTSW |
13 |
38,131,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4135:Rreb1
|
UTSW |
13 |
38,131,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4174:Rreb1
|
UTSW |
13 |
38,114,126 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4250:Rreb1
|
UTSW |
13 |
38,077,869 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4287:Rreb1
|
UTSW |
13 |
38,115,907 (GRCm39) |
missense |
probably benign |
0.03 |
R4396:Rreb1
|
UTSW |
13 |
38,114,419 (GRCm39) |
nonsense |
probably null |
|
R4658:Rreb1
|
UTSW |
13 |
38,132,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Rreb1
|
UTSW |
13 |
38,100,502 (GRCm39) |
missense |
probably benign |
0.09 |
R4856:Rreb1
|
UTSW |
13 |
38,115,034 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4886:Rreb1
|
UTSW |
13 |
38,115,034 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5092:Rreb1
|
UTSW |
13 |
38,112,254 (GRCm39) |
missense |
probably benign |
0.09 |
R5122:Rreb1
|
UTSW |
13 |
38,114,744 (GRCm39) |
missense |
probably benign |
0.02 |
R5405:Rreb1
|
UTSW |
13 |
38,133,087 (GRCm39) |
missense |
probably damaging |
0.99 |
R5408:Rreb1
|
UTSW |
13 |
38,115,320 (GRCm39) |
missense |
probably benign |
0.01 |
R5446:Rreb1
|
UTSW |
13 |
38,082,473 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5641:Rreb1
|
UTSW |
13 |
38,131,397 (GRCm39) |
missense |
probably benign |
0.00 |
R5859:Rreb1
|
UTSW |
13 |
38,131,385 (GRCm39) |
missense |
probably benign |
0.06 |
R5859:Rreb1
|
UTSW |
13 |
38,131,384 (GRCm39) |
missense |
probably benign |
0.24 |
R6429:Rreb1
|
UTSW |
13 |
38,116,105 (GRCm39) |
missense |
probably benign |
0.03 |
R6678:Rreb1
|
UTSW |
13 |
38,083,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R7130:Rreb1
|
UTSW |
13 |
38,083,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Rreb1
|
UTSW |
13 |
38,125,608 (GRCm39) |
missense |
probably benign |
0.02 |
R7188:Rreb1
|
UTSW |
13 |
38,100,544 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7387:Rreb1
|
UTSW |
13 |
38,131,040 (GRCm39) |
missense |
unknown |
|
R7453:Rreb1
|
UTSW |
13 |
38,125,545 (GRCm39) |
missense |
probably damaging |
0.98 |
R7492:Rreb1
|
UTSW |
13 |
38,115,724 (GRCm39) |
missense |
probably benign |
0.00 |
R7585:Rreb1
|
UTSW |
13 |
38,077,874 (GRCm39) |
missense |
probably benign |
0.07 |
R7621:Rreb1
|
UTSW |
13 |
38,133,042 (GRCm39) |
missense |
|
|
R7645:Rreb1
|
UTSW |
13 |
38,115,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7653:Rreb1
|
UTSW |
13 |
38,114,362 (GRCm39) |
missense |
probably benign |
0.19 |
R7670:Rreb1
|
UTSW |
13 |
38,115,548 (GRCm39) |
missense |
probably benign |
0.00 |
R7701:Rreb1
|
UTSW |
13 |
38,114,092 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7708:Rreb1
|
UTSW |
13 |
38,113,546 (GRCm39) |
missense |
probably benign |
0.18 |
R7874:Rreb1
|
UTSW |
13 |
38,131,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Rreb1
|
UTSW |
13 |
38,125,677 (GRCm39) |
missense |
probably benign |
0.16 |
R8129:Rreb1
|
UTSW |
13 |
38,113,775 (GRCm39) |
missense |
probably benign |
0.00 |
R8239:Rreb1
|
UTSW |
13 |
38,077,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Rreb1
|
UTSW |
13 |
38,131,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8824:Rreb1
|
UTSW |
13 |
38,114,492 (GRCm39) |
missense |
probably damaging |
0.99 |
R8910:Rreb1
|
UTSW |
13 |
38,132,741 (GRCm39) |
missense |
|
|
R8992:Rreb1
|
UTSW |
13 |
38,114,352 (GRCm39) |
missense |
probably benign |
0.30 |
R9064:Rreb1
|
UTSW |
13 |
38,115,326 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9087:Rreb1
|
UTSW |
13 |
38,115,644 (GRCm39) |
missense |
probably benign |
0.33 |
R9130:Rreb1
|
UTSW |
13 |
38,114,282 (GRCm39) |
missense |
probably benign |
0.29 |
R9582:Rreb1
|
UTSW |
13 |
38,114,734 (GRCm39) |
missense |
probably benign |
0.29 |
R9602:Rreb1
|
UTSW |
13 |
38,114,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R9774:Rreb1
|
UTSW |
13 |
38,114,185 (GRCm39) |
missense |
probably benign |
0.18 |
X0024:Rreb1
|
UTSW |
13 |
38,115,556 (GRCm39) |
missense |
probably benign |
0.09 |
X0026:Rreb1
|
UTSW |
13 |
38,115,968 (GRCm39) |
missense |
probably benign |
0.17 |
Z1088:Rreb1
|
UTSW |
13 |
38,132,913 (GRCm39) |
missense |
probably benign |
|
|