Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adipoq |
T |
A |
16: 22,975,938 (GRCm39) |
V134E |
possibly damaging |
Het |
Agmat |
A |
G |
4: 141,483,273 (GRCm39) |
T236A |
probably benign |
Het |
Anxa9 |
T |
C |
3: 95,208,425 (GRCm39) |
N197S |
probably benign |
Het |
Arhgap23 |
A |
T |
11: 97,366,932 (GRCm39) |
D1071V |
probably damaging |
Het |
Axdnd1 |
G |
A |
1: 156,208,428 (GRCm39) |
T470M |
probably damaging |
Het |
C3 |
C |
T |
17: 57,512,303 (GRCm39) |
D1542N |
possibly damaging |
Het |
Cdh3 |
A |
T |
8: 107,263,606 (GRCm39) |
|
probably null |
Het |
Cep85l |
A |
T |
10: 53,167,906 (GRCm39) |
I624K |
probably benign |
Het |
Cplx4 |
T |
C |
18: 66,102,998 (GRCm39) |
T41A |
probably benign |
Het |
Dchs1 |
A |
T |
7: 105,406,292 (GRCm39) |
D2313E |
possibly damaging |
Het |
Dock7 |
T |
C |
4: 98,859,066 (GRCm39) |
T1409A |
probably benign |
Het |
Exo1 |
C |
T |
1: 175,714,312 (GRCm39) |
P73L |
probably damaging |
Het |
Fgfrl1 |
C |
A |
5: 108,853,242 (GRCm39) |
H197Q |
possibly damaging |
Het |
Fsbp |
G |
A |
4: 11,583,706 (GRCm39) |
G135D |
probably damaging |
Het |
Herc3 |
G |
A |
6: 58,839,973 (GRCm39) |
R362H |
probably benign |
Het |
Herc3 |
T |
C |
6: 58,853,587 (GRCm39) |
F583L |
probably benign |
Het |
Ifna7 |
T |
C |
4: 88,734,964 (GRCm39) |
V167A |
probably damaging |
Het |
Ighv1-54 |
A |
G |
12: 115,157,596 (GRCm39) |
V17A |
possibly damaging |
Het |
Kcnh5 |
A |
G |
12: 75,134,350 (GRCm39) |
Y400H |
possibly damaging |
Het |
Kcnk16 |
T |
A |
14: 20,319,230 (GRCm39) |
M1L |
possibly damaging |
Het |
Kctd19 |
T |
C |
8: 106,123,112 (GRCm39) |
T101A |
probably benign |
Het |
Klf3 |
A |
G |
5: 64,984,560 (GRCm39) |
|
probably null |
Het |
Krtap12-1 |
G |
T |
10: 77,556,729 (GRCm39) |
V91L |
probably benign |
Het |
Lonp1 |
T |
C |
17: 56,928,952 (GRCm39) |
E270G |
possibly damaging |
Het |
Mgl2 |
T |
C |
11: 70,026,659 (GRCm39) |
L128P |
probably damaging |
Het |
Mrc1 |
A |
G |
2: 14,323,981 (GRCm39) |
Y1106C |
probably damaging |
Het |
Mybpc1 |
G |
T |
10: 88,406,521 (GRCm39) |
|
probably null |
Het |
Mypn |
C |
A |
10: 62,961,486 (GRCm39) |
L1035F |
possibly damaging |
Het |
Neurl1a |
T |
C |
19: 47,228,328 (GRCm39) |
L58P |
probably damaging |
Het |
Nlrp4e |
G |
T |
7: 23,039,988 (GRCm39) |
L770F |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,115,857 (GRCm39) |
*895W |
probably null |
Het |
Nphs2 |
T |
C |
1: 156,140,608 (GRCm39) |
I115T |
probably damaging |
Het |
Or1ad6 |
A |
G |
11: 50,860,385 (GRCm39) |
D180G |
probably damaging |
Het |
Or8g22 |
T |
A |
9: 38,958,707 (GRCm39) |
H47L |
unknown |
Het |
Patj |
A |
T |
4: 98,569,456 (GRCm39) |
K1128* |
probably null |
Het |
Pla2g5 |
C |
G |
4: 138,528,746 (GRCm39) |
C70S |
probably damaging |
Het |
Pole4 |
G |
A |
6: 82,599,095 (GRCm39) |
R119C |
possibly damaging |
Het |
Ppm1h |
G |
T |
10: 122,740,027 (GRCm39) |
L367F |
probably damaging |
Het |
Ppp1r13b |
G |
T |
12: 111,812,851 (GRCm39) |
R123S |
probably damaging |
Het |
Ptpru |
C |
T |
4: 131,535,735 (GRCm39) |
C414Y |
probably damaging |
Het |
Pum2 |
T |
A |
12: 8,769,076 (GRCm39) |
Y323* |
probably null |
Het |
Rhot2 |
T |
C |
17: 26,059,521 (GRCm39) |
D407G |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Scn11a |
T |
A |
9: 119,613,115 (GRCm39) |
D825V |
probably damaging |
Het |
Selenoi |
A |
G |
5: 30,461,187 (GRCm39) |
Y141C |
probably damaging |
Het |
Smcr8 |
A |
G |
11: 60,670,330 (GRCm39) |
T493A |
probably benign |
Het |
Tjp2 |
A |
T |
19: 24,078,190 (GRCm39) |
I901N |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Ttc23l |
T |
A |
15: 10,530,781 (GRCm39) |
Y277F |
possibly damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Wdr1 |
C |
T |
5: 38,697,882 (GRCm39) |
G228R |
probably damaging |
Het |
Xab2 |
T |
C |
8: 3,669,053 (GRCm39) |
N31S |
probably damaging |
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 |
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 |
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 |
|
|