Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,240,350 (GRCm39) |
S738P |
probably benign |
Het |
Abi3bp |
C |
A |
16: 56,408,348 (GRCm39) |
P261Q |
probably damaging |
Het |
Adam19 |
A |
G |
11: 46,018,105 (GRCm39) |
N389S |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,637,196 (GRCm39) |
V3415D |
possibly damaging |
Het |
Ankrd33 |
A |
T |
15: 101,017,432 (GRCm39) |
I282F |
probably damaging |
Het |
Arhgap39 |
C |
T |
15: 76,619,383 (GRCm39) |
V734M |
probably damaging |
Het |
Arsg |
T |
C |
11: 109,454,100 (GRCm39) |
|
probably null |
Het |
Atp8b4 |
C |
T |
2: 126,245,301 (GRCm39) |
G283R |
probably benign |
Het |
B3galnt2 |
T |
G |
13: 14,166,119 (GRCm39) |
L338* |
probably null |
Het |
Cdc14a |
A |
T |
3: 116,216,296 (GRCm39) |
Y1* |
probably null |
Het |
Ceacam16 |
T |
C |
7: 19,592,803 (GRCm39) |
E35G |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,220,323 (GRCm39) |
D1244V |
possibly damaging |
Het |
Chordc1 |
T |
C |
9: 18,223,274 (GRCm39) |
Y245H |
probably damaging |
Het |
Col6a6 |
C |
A |
9: 105,579,469 (GRCm39) |
V1919F |
probably damaging |
Het |
Cped1 |
T |
C |
6: 22,237,727 (GRCm39) |
C948R |
probably damaging |
Het |
Cyfip2 |
T |
C |
11: 46,089,846 (GRCm39) |
D1189G |
probably damaging |
Het |
Cyp27b1 |
T |
C |
10: 126,884,952 (GRCm39) |
Y72H |
possibly damaging |
Het |
Dagla |
A |
G |
19: 10,248,378 (GRCm39) |
M94T |
probably benign |
Het |
Dip2a |
A |
G |
10: 76,153,797 (GRCm39) |
S178P |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,967,858 (GRCm39) |
V1220A |
probably benign |
Het |
Dpysl2 |
T |
C |
14: 67,105,840 (GRCm39) |
|
probably benign |
Het |
E2f6 |
T |
C |
12: 16,868,884 (GRCm39) |
V69A |
probably benign |
Het |
Fat3 |
T |
C |
9: 15,826,636 (GRCm39) |
T4439A |
probably benign |
Het |
Fn1 |
T |
C |
1: 71,663,418 (GRCm39) |
I1023M |
probably damaging |
Het |
Gabrr2 |
G |
A |
4: 33,077,481 (GRCm39) |
V83M |
probably damaging |
Het |
Gfral |
T |
C |
9: 76,100,485 (GRCm39) |
N318D |
probably benign |
Het |
Gm5611 |
A |
T |
9: 16,942,073 (GRCm39) |
|
noncoding transcript |
Het |
Gpat3 |
A |
T |
5: 101,041,046 (GRCm39) |
M369L |
probably benign |
Het |
Grik5 |
T |
C |
7: 24,745,726 (GRCm39) |
D449G |
possibly damaging |
Het |
Gucy2g |
T |
A |
19: 55,211,362 (GRCm39) |
T623S |
possibly damaging |
Het |
H2-T22 |
T |
C |
17: 36,352,434 (GRCm39) |
T164A |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,404,881 (GRCm39) |
C4484S |
possibly damaging |
Het |
Hira |
T |
C |
16: 18,766,164 (GRCm39) |
S659P |
probably damaging |
Het |
Hoxa7 |
T |
C |
6: 52,194,307 (GRCm39) |
T27A |
possibly damaging |
Het |
Hoxd1 |
T |
C |
2: 74,593,866 (GRCm39) |
S141P |
probably damaging |
Het |
Kank1 |
C |
A |
19: 25,388,396 (GRCm39) |
Q690K |
probably benign |
Het |
Kera |
A |
G |
10: 97,445,009 (GRCm39) |
K123E |
probably benign |
Het |
Kifbp |
T |
C |
10: 62,395,106 (GRCm39) |
Y512C |
probably damaging |
Het |
Lepr |
A |
C |
4: 101,592,874 (GRCm39) |
Y163S |
probably damaging |
Het |
Leprotl1 |
T |
C |
8: 34,607,922 (GRCm39) |
I29V |
probably benign |
Het |
Lrriq1 |
T |
G |
10: 102,997,620 (GRCm39) |
T1332P |
probably benign |
Het |
Mrps15 |
A |
G |
4: 125,949,200 (GRCm39) |
K223E |
probably damaging |
Het |
Mrps7 |
T |
A |
11: 115,497,811 (GRCm39) |
N225K |
probably benign |
Het |
Nav3 |
T |
A |
10: 109,659,184 (GRCm39) |
D811V |
probably damaging |
Het |
Ndst3 |
T |
A |
3: 123,342,587 (GRCm39) |
R741S |
probably damaging |
Het |
Nos3 |
T |
C |
5: 24,575,131 (GRCm39) |
Y356H |
probably damaging |
Het |
Nxpe3 |
A |
G |
16: 55,686,444 (GRCm39) |
V188A |
probably damaging |
Het |
Or13n4 |
T |
C |
7: 106,423,317 (GRCm39) |
R139G |
probably benign |
Het |
Or5p50 |
T |
A |
7: 107,422,578 (GRCm39) |
I33F |
probably benign |
Het |
Or8j3b |
T |
C |
2: 86,205,487 (GRCm39) |
K90E |
possibly damaging |
Het |
Pdia4 |
A |
T |
6: 47,773,695 (GRCm39) |
C551* |
probably null |
Het |
Pex13 |
A |
G |
11: 23,605,513 (GRCm39) |
F239S |
probably damaging |
Het |
Pigq |
A |
G |
17: 26,153,980 (GRCm39) |
M273T |
probably benign |
Het |
Plppr2 |
C |
T |
9: 21,859,047 (GRCm39) |
P388L |
probably damaging |
Het |
Polr3b |
C |
T |
10: 84,528,786 (GRCm39) |
Q737* |
probably null |
Het |
Ppfibp1 |
T |
C |
6: 146,923,757 (GRCm39) |
|
probably null |
Het |
Ppfibp2 |
C |
A |
7: 107,236,504 (GRCm39) |
D17E |
probably damaging |
Het |
Pramel34 |
A |
T |
5: 93,785,545 (GRCm39) |
I245K |
probably benign |
Het |
Prr35 |
T |
C |
17: 26,165,691 (GRCm39) |
D532G |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,691,325 (GRCm39) |
D1064G |
probably benign |
Het |
Qtrt2 |
A |
T |
16: 43,692,018 (GRCm39) |
S168T |
probably damaging |
Het |
Rbp3 |
T |
C |
14: 33,676,601 (GRCm39) |
V183A |
probably benign |
Het |
Shprh |
T |
C |
10: 11,062,655 (GRCm39) |
|
probably null |
Het |
Slc39a10 |
T |
C |
1: 46,875,230 (GRCm39) |
H24R |
probably damaging |
Het |
Slc7a13 |
A |
T |
4: 19,819,046 (GRCm39) |
H82L |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,782,569 (GRCm39) |
I502V |
probably benign |
Het |
Syne2 |
C |
T |
12: 76,156,636 (GRCm39) |
R6811C |
probably damaging |
Het |
Syt12 |
A |
G |
19: 4,506,911 (GRCm39) |
V78A |
probably benign |
Het |
Tbck |
T |
A |
3: 132,543,772 (GRCm39) |
D874E |
probably benign |
Het |
Tesc |
A |
T |
5: 118,184,394 (GRCm39) |
I25L |
probably damaging |
Het |
Thoc5 |
T |
G |
11: 4,864,608 (GRCm39) |
D351E |
probably benign |
Het |
Tor1aip1 |
A |
T |
1: 155,883,308 (GRCm39) |
M180K |
probably damaging |
Het |
Trps1 |
T |
C |
15: 50,524,532 (GRCm39) |
S842G |
probably damaging |
Het |
Unc79 |
A |
T |
12: 103,100,737 (GRCm39) |
T1858S |
probably damaging |
Het |
Vmn1r193 |
T |
C |
13: 22,403,561 (GRCm39) |
T144A |
probably benign |
Het |
Vwa8 |
T |
C |
14: 79,318,576 (GRCm39) |
F1046S |
probably benign |
Het |
Wdr26 |
A |
T |
1: 181,019,340 (GRCm39) |
W346R |
probably damaging |
Het |
Zfp740 |
T |
A |
15: 102,116,336 (GRCm39) |
V22E |
probably damaging |
Het |
Zw10 |
C |
A |
9: 48,981,041 (GRCm39) |
S480R |
probably damaging |
Het |
|
Other mutations in Colgalt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01312:Colgalt1
|
APN |
8 |
72,075,420 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01888:Colgalt1
|
APN |
8 |
72,070,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03191:Colgalt1
|
APN |
8 |
72,075,731 (GRCm39) |
splice site |
probably null |
|
P0041:Colgalt1
|
UTSW |
8 |
72,075,434 (GRCm39) |
missense |
probably benign |
0.05 |
R0094:Colgalt1
|
UTSW |
8 |
72,075,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Colgalt1
|
UTSW |
8 |
72,075,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R1342:Colgalt1
|
UTSW |
8 |
72,070,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Colgalt1
|
UTSW |
8 |
72,073,401 (GRCm39) |
missense |
probably benign |
0.01 |
R1754:Colgalt1
|
UTSW |
8 |
72,075,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Colgalt1
|
UTSW |
8 |
72,063,995 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2050:Colgalt1
|
UTSW |
8 |
72,070,330 (GRCm39) |
critical splice donor site |
probably null |
|
R2393:Colgalt1
|
UTSW |
8 |
72,076,385 (GRCm39) |
missense |
probably benign |
0.00 |
R2406:Colgalt1
|
UTSW |
8 |
72,070,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R3897:Colgalt1
|
UTSW |
8 |
72,072,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4210:Colgalt1
|
UTSW |
8 |
72,075,350 (GRCm39) |
missense |
probably benign |
0.34 |
R4909:Colgalt1
|
UTSW |
8 |
72,073,277 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5428:Colgalt1
|
UTSW |
8 |
72,075,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Colgalt1
|
UTSW |
8 |
72,075,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Colgalt1
|
UTSW |
8 |
72,074,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R6994:Colgalt1
|
UTSW |
8 |
72,076,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Colgalt1
|
UTSW |
8 |
72,076,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Colgalt1
|
UTSW |
8 |
72,076,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R7691:Colgalt1
|
UTSW |
8 |
72,073,398 (GRCm39) |
missense |
probably benign |
0.00 |
R7877:Colgalt1
|
UTSW |
8 |
72,074,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R8899:Colgalt1
|
UTSW |
8 |
72,076,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R9719:Colgalt1
|
UTSW |
8 |
72,073,456 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Colgalt1
|
UTSW |
8 |
72,076,240 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Colgalt1
|
UTSW |
8 |
72,075,852 (GRCm39) |
missense |
probably damaging |
1.00 |
|