Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Adamts20 |
G |
A |
15: 94,227,928 (GRCm39) |
R1040* |
probably null |
Het |
Akt1 |
A |
G |
12: 112,628,634 (GRCm39) |
L52P |
probably damaging |
Het |
Alk |
T |
A |
17: 72,176,742 (GRCm39) |
T1521S |
probably benign |
Het |
Armt1 |
A |
G |
10: 4,403,488 (GRCm39) |
N191S |
probably damaging |
Het |
Ascl1 |
T |
G |
10: 87,328,562 (GRCm39) |
N130T |
probably damaging |
Het |
Bahcc1 |
T |
G |
11: 120,178,211 (GRCm39) |
S2257A |
probably damaging |
Het |
Cd86 |
T |
C |
16: 36,449,377 (GRCm39) |
M7V |
possibly damaging |
Het |
Cep57 |
A |
T |
9: 13,722,057 (GRCm39) |
S304R |
possibly damaging |
Het |
Cep57l1 |
A |
T |
10: 41,616,918 (GRCm39) |
I123N |
possibly damaging |
Het |
Cers6 |
A |
G |
2: 68,692,008 (GRCm39) |
N10S |
probably benign |
Het |
Chrng |
A |
G |
1: 87,139,074 (GRCm39) |
D475G |
probably damaging |
Het |
Crabp1 |
T |
A |
9: 54,680,129 (GRCm39) |
V128E |
probably damaging |
Het |
Csnk2a1-ps3 |
T |
C |
1: 156,352,425 (GRCm39) |
Y209H |
probably damaging |
Het |
Dcdc2a |
T |
C |
13: 25,240,354 (GRCm39) |
V34A |
possibly damaging |
Het |
Eeig1 |
G |
A |
2: 32,450,102 (GRCm39) |
V117I |
probably benign |
Het |
Fbn1 |
A |
G |
2: 125,308,532 (GRCm39) |
C177R |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,857,844 (GRCm39) |
D2046G |
probably benign |
Het |
Glul |
T |
C |
1: 153,783,087 (GRCm39) |
I220T |
probably benign |
Het |
Gpc6 |
C |
T |
14: 118,202,182 (GRCm39) |
T464M |
probably damaging |
Het |
Gpm6a |
T |
C |
8: 55,511,833 (GRCm39) |
S236P |
probably damaging |
Het |
H2-K2 |
G |
T |
17: 34,218,304 (GRCm39) |
T204K |
probably benign |
Het |
H2-K2 |
T |
C |
17: 34,218,305 (GRCm39) |
T204A |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,963,135 (GRCm39) |
H792R |
possibly damaging |
Het |
Herc4 |
T |
A |
10: 63,110,821 (GRCm39) |
I244K |
possibly damaging |
Het |
Hsd11b2 |
G |
T |
8: 106,249,966 (GRCm39) |
R359L |
possibly damaging |
Het |
Igsf9 |
G |
A |
1: 172,312,456 (GRCm39) |
E56K |
probably damaging |
Het |
Il9 |
T |
C |
13: 56,628,495 (GRCm39) |
T65A |
possibly damaging |
Het |
Kcnip1 |
T |
C |
11: 33,592,478 (GRCm39) |
T102A |
probably damaging |
Het |
L3mbtl2 |
T |
C |
15: 81,551,555 (GRCm39) |
S74P |
probably benign |
Het |
Lamc2 |
C |
T |
1: 153,012,575 (GRCm39) |
D700N |
probably benign |
Het |
Ldb2 |
T |
C |
5: 44,633,905 (GRCm39) |
T322A |
possibly damaging |
Het |
Lix1 |
A |
T |
17: 17,664,012 (GRCm39) |
I117F |
probably damaging |
Het |
Map2 |
T |
A |
1: 66,454,573 (GRCm39) |
D1154E |
probably benign |
Het |
Mark4 |
T |
C |
7: 19,160,310 (GRCm39) |
E650G |
probably benign |
Het |
Mink1 |
A |
G |
11: 70,502,546 (GRCm39) |
T1086A |
possibly damaging |
Het |
Nxf1 |
G |
A |
19: 8,745,186 (GRCm39) |
V479M |
probably damaging |
Het |
Or10v1 |
T |
A |
19: 11,873,388 (GRCm39) |
M1K |
probably null |
Het |
Or11g2 |
T |
C |
14: 50,856,158 (GRCm39) |
F160L |
probably benign |
Het |
Or2n1e |
A |
G |
17: 38,586,150 (GRCm39) |
T163A |
probably damaging |
Het |
Or5h23 |
T |
C |
16: 58,906,273 (GRCm39) |
D191G |
probably damaging |
Het |
Or5h23 |
A |
G |
16: 58,906,792 (GRCm39) |
V18A |
probably benign |
Het |
Or6c5 |
T |
C |
10: 129,074,329 (GRCm39) |
S104P |
probably damaging |
Het |
Otx2 |
T |
C |
14: 48,896,215 (GRCm39) |
D281G |
probably damaging |
Het |
Pcdhga3 |
A |
T |
18: 37,808,141 (GRCm39) |
D198V |
probably damaging |
Het |
Ppp1r13l |
T |
C |
7: 19,104,500 (GRCm39) |
V273A |
probably benign |
Het |
Ppp6r2 |
T |
C |
15: 89,137,455 (GRCm39) |
|
probably null |
Het |
Pramel51 |
T |
A |
12: 88,143,995 (GRCm39) |
I273F |
possibly damaging |
Het |
Prg4 |
C |
T |
1: 150,327,197 (GRCm39) |
G873D |
probably damaging |
Het |
Ptprq |
T |
C |
10: 107,471,135 (GRCm39) |
N1422S |
probably benign |
Het |
Rbm27 |
A |
T |
18: 42,460,570 (GRCm39) |
K839M |
probably damaging |
Het |
Rere |
A |
T |
4: 150,553,255 (GRCm39) |
N149I |
probably damaging |
Het |
Ret |
A |
G |
6: 118,156,280 (GRCm39) |
L340S |
probably benign |
Het |
Sel1l2 |
T |
A |
2: 140,082,889 (GRCm39) |
D583V |
possibly damaging |
Het |
Shroom1 |
A |
T |
11: 53,354,308 (GRCm39) |
D76V |
possibly damaging |
Het |
Slc5a3 |
C |
A |
16: 91,875,963 (GRCm39) |
S673R |
probably benign |
Het |
Spink1 |
A |
T |
18: 43,861,247 (GRCm39) |
I74N |
probably damaging |
Het |
Tbc1d1 |
T |
A |
5: 64,435,352 (GRCm39) |
S497T |
probably damaging |
Het |
Trim3 |
C |
T |
7: 105,260,278 (GRCm39) |
R741Q |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,747,022 (GRCm39) |
C4676R |
probably benign |
Het |
Ubqlnl |
G |
A |
7: 103,797,959 (GRCm39) |
P513S |
probably benign |
Het |
Unc13d |
C |
T |
11: 115,964,394 (GRCm39) |
|
probably null |
Het |
Vmn1r125 |
TGG |
TG |
7: 21,006,144 (GRCm39) |
|
probably null |
Het |
Vmn2r7 |
A |
T |
3: 64,632,436 (GRCm39) |
C9S |
probably benign |
Het |
Xdh |
T |
A |
17: 74,213,264 (GRCm39) |
M829L |
probably damaging |
Het |
Zcrb1 |
A |
G |
15: 93,285,463 (GRCm39) |
F173L |
probably benign |
Het |
Zfp41 |
T |
C |
15: 75,490,372 (GRCm39) |
V108A |
probably damaging |
Het |
Zfp438 |
T |
C |
18: 5,213,209 (GRCm39) |
E583G |
probably damaging |
Het |
Zfp628 |
T |
C |
7: 4,923,917 (GRCm39) |
L713P |
probably damaging |
Het |
Zfp664 |
T |
A |
5: 124,963,042 (GRCm39) |
C145* |
probably null |
Het |
Zfp683 |
T |
C |
4: 133,786,042 (GRCm39) |
C390R |
probably damaging |
Het |
Zfp941 |
G |
A |
7: 140,392,010 (GRCm39) |
P450S |
probably damaging |
Het |
|
Other mutations in Marco |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Marco
|
APN |
1 |
120,413,432 (GRCm39) |
missense |
probably benign |
|
IGL01343:Marco
|
APN |
1 |
120,422,469 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02117:Marco
|
APN |
1 |
120,418,683 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02338:Marco
|
APN |
1 |
120,422,508 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03293:Marco
|
APN |
1 |
120,422,524 (GRCm39) |
missense |
probably benign |
0.08 |
P0027:Marco
|
UTSW |
1 |
120,402,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Marco
|
UTSW |
1 |
120,419,767 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Marco
|
UTSW |
1 |
120,404,474 (GRCm39) |
splice site |
probably benign |
|
R1958:Marco
|
UTSW |
1 |
120,412,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R2444:Marco
|
UTSW |
1 |
120,422,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Marco
|
UTSW |
1 |
120,422,514 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4740:Marco
|
UTSW |
1 |
120,422,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Marco
|
UTSW |
1 |
120,421,954 (GRCm39) |
missense |
probably benign |
0.02 |
R5393:Marco
|
UTSW |
1 |
120,413,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R5536:Marco
|
UTSW |
1 |
120,432,464 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6022:Marco
|
UTSW |
1 |
120,416,294 (GRCm39) |
missense |
probably benign |
0.00 |
R6028:Marco
|
UTSW |
1 |
120,418,671 (GRCm39) |
missense |
probably damaging |
0.97 |
R7565:Marco
|
UTSW |
1 |
120,402,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Marco
|
UTSW |
1 |
120,421,771 (GRCm39) |
critical splice donor site |
probably null |
|
R8002:Marco
|
UTSW |
1 |
120,422,509 (GRCm39) |
missense |
probably benign |
0.18 |
R9157:Marco
|
UTSW |
1 |
120,421,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Marco
|
UTSW |
1 |
120,421,814 (GRCm39) |
missense |
probably damaging |
1.00 |
T0722:Marco
|
UTSW |
1 |
120,402,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|