Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
C |
T |
16: 97,867,651 (GRCm39) |
A104T |
probably damaging |
Het |
Abhd18 |
T |
A |
3: 40,884,627 (GRCm39) |
L222Q |
probably damaging |
Het |
Adam30 |
C |
T |
3: 98,070,348 (GRCm39) |
T727M |
possibly damaging |
Het |
Adh6b |
A |
T |
3: 138,058,729 (GRCm39) |
Q137L |
probably damaging |
Het |
Alpl |
C |
T |
4: 137,475,127 (GRCm39) |
V269I |
probably benign |
Het |
Ang2 |
C |
T |
14: 51,432,996 (GRCm39) |
G129S |
probably benign |
Het |
Atp6v0a1 |
A |
T |
11: 100,920,015 (GRCm39) |
H216L |
possibly damaging |
Het |
BC030500 |
C |
T |
8: 59,366,049 (GRCm39) |
T61I |
unknown |
Het |
Brpf1 |
T |
G |
6: 113,293,491 (GRCm39) |
L520R |
probably damaging |
Het |
Btbd10 |
A |
G |
7: 112,927,626 (GRCm39) |
I243T |
possibly damaging |
Het |
Bub1 |
C |
A |
2: 127,646,139 (GRCm39) |
C947F |
probably damaging |
Het |
C4b |
T |
C |
17: 34,953,459 (GRCm39) |
E1008G |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,155,323 (GRCm39) |
T1188A |
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,875,485 (GRCm39) |
T1770A |
unknown |
Het |
Cnn1 |
G |
T |
9: 22,010,557 (GRCm39) |
|
probably benign |
Het |
Cox15 |
A |
T |
19: 43,735,181 (GRCm39) |
C195* |
probably null |
Het |
Cped1 |
A |
T |
6: 22,059,941 (GRCm39) |
R202S |
possibly damaging |
Het |
Dact2 |
A |
T |
17: 14,417,146 (GRCm39) |
C351* |
probably null |
Het |
Dbnl |
A |
G |
11: 5,738,582 (GRCm39) |
N8S |
probably benign |
Het |
Depdc1a |
T |
A |
3: 159,228,356 (GRCm39) |
N369K |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,415,005 (GRCm39) |
L243Q |
probably damaging |
Het |
Dscaml1 |
T |
A |
9: 45,341,759 (GRCm39) |
Y57N |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,927,944 (GRCm39) |
T388A |
probably benign |
Het |
Eif4h |
A |
C |
5: 134,654,393 (GRCm39) |
|
probably null |
Het |
Elf1 |
C |
T |
14: 79,810,667 (GRCm39) |
Q288* |
probably null |
Het |
Fbxl5 |
A |
T |
5: 43,908,362 (GRCm39) |
|
probably benign |
Het |
Fgl2 |
C |
T |
5: 21,580,677 (GRCm39) |
R340* |
probably null |
Het |
Fut4 |
T |
C |
9: 14,662,082 (GRCm39) |
D404G |
probably damaging |
Het |
Glmn |
G |
A |
5: 107,718,152 (GRCm39) |
P255L |
probably benign |
Het |
Gm14322 |
C |
T |
2: 177,411,481 (GRCm39) |
T97I |
probably benign |
Het |
Gm44511 |
C |
A |
6: 128,797,997 (GRCm39) |
C32F |
probably damaging |
Het |
Gm5478 |
A |
G |
15: 101,553,871 (GRCm39) |
F247S |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,739,563 (GRCm39) |
M2675K |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,849,000 (GRCm39) |
D368G |
possibly damaging |
Het |
Hnrnpul2 |
A |
G |
19: 8,798,064 (GRCm39) |
N140S |
probably benign |
Het |
Htr4 |
A |
T |
18: 62,561,209 (GRCm39) |
I157L |
probably damaging |
Het |
Igf2bp3 |
G |
T |
6: 49,086,009 (GRCm39) |
|
probably benign |
Het |
Kcnma1 |
T |
G |
14: 23,436,332 (GRCm39) |
M790L |
probably benign |
Het |
Kcnv1 |
G |
A |
15: 44,977,999 (GRCm39) |
S13L |
unknown |
Het |
Kctd20 |
C |
T |
17: 29,184,025 (GRCm39) |
R312* |
probably null |
Het |
Kdm3b |
T |
A |
18: 34,960,435 (GRCm39) |
I1340N |
probably damaging |
Het |
Kdm6b |
A |
G |
11: 69,292,919 (GRCm39) |
F1286L |
unknown |
Het |
Knl1 |
T |
A |
2: 118,899,524 (GRCm39) |
F408L |
probably benign |
Het |
Lypd5 |
G |
T |
7: 24,053,101 (GRCm39) |
G253W |
probably damaging |
Het |
Mea1 |
A |
G |
17: 46,992,614 (GRCm39) |
T21A |
probably benign |
Het |
Metrnl |
A |
G |
11: 121,606,842 (GRCm39) |
E299G |
possibly damaging |
Het |
Mindy4 |
T |
A |
6: 55,256,055 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Nbn |
G |
A |
4: 15,963,911 (GRCm39) |
S104N |
probably damaging |
Het |
Nxpe2 |
A |
T |
9: 48,238,073 (GRCm39) |
F61I |
probably benign |
Het |
Or6c1b |
T |
C |
10: 129,273,334 (GRCm39) |
Y218H |
probably benign |
Het |
Or6c70 |
T |
A |
10: 129,710,092 (GRCm39) |
D178V |
probably damaging |
Het |
Pcdhb20 |
C |
T |
18: 37,638,437 (GRCm39) |
A321V |
probably damaging |
Het |
Pgr |
C |
A |
9: 8,901,544 (GRCm39) |
P359Q |
probably damaging |
Het |
Pi4k2b |
G |
A |
5: 52,908,031 (GRCm39) |
V157I |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,242,956 (GRCm39) |
S621N |
probably benign |
Het |
Plekhm1 |
A |
C |
11: 103,258,444 (GRCm39) |
F1031L |
probably damaging |
Het |
Pltp |
A |
G |
2: 164,696,301 (GRCm39) |
S124P |
probably damaging |
Het |
Polr3gl |
T |
A |
3: 96,487,154 (GRCm39) |
E177V |
probably benign |
Het |
Pstk |
G |
T |
7: 130,973,024 (GRCm39) |
R41L |
possibly damaging |
Het |
Ptprk |
C |
A |
10: 28,442,541 (GRCm39) |
|
probably benign |
Het |
Rasgrp1 |
T |
C |
2: 117,119,158 (GRCm39) |
E493G |
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,434,726 (GRCm39) |
L422P |
probably benign |
Het |
Rusc2 |
C |
T |
4: 43,401,351 (GRCm39) |
|
probably benign |
Het |
Sbno2 |
A |
G |
10: 79,911,090 (GRCm39) |
F6S |
probably benign |
Het |
Sh2d4a |
A |
G |
8: 68,798,695 (GRCm39) |
Y348C |
probably damaging |
Het |
Sh3rf3 |
A |
G |
10: 58,939,992 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
T |
C |
8: 126,177,125 (GRCm39) |
E1163G |
probably benign |
Het |
Strip1 |
G |
C |
3: 107,521,964 (GRCm39) |
A738G |
probably damaging |
Het |
Tdrkh |
C |
T |
3: 94,333,299 (GRCm39) |
R255C |
probably benign |
Het |
Tex11 |
C |
T |
X: 100,059,191 (GRCm39) |
V190I |
possibly damaging |
Het |
Tln1 |
A |
T |
4: 43,555,911 (GRCm39) |
M101K |
possibly damaging |
Het |
Trav6-2 |
A |
C |
14: 52,905,028 (GRCm39) |
|
probably benign |
Het |
Tspan11 |
A |
T |
6: 127,900,674 (GRCm39) |
I82F |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,779,320 (GRCm39) |
K1233E |
unknown |
Het |
U2af2 |
T |
A |
7: 5,070,432 (GRCm39) |
|
probably benign |
Het |
Usp29 |
A |
T |
7: 6,965,917 (GRCm39) |
S587C |
probably damaging |
Het |
Vmn1r235 |
A |
T |
17: 21,482,056 (GRCm39) |
Q127L |
probably damaging |
Het |
Vmn1r65 |
C |
A |
7: 6,011,503 (GRCm39) |
A244S |
probably damaging |
Het |
Vmn2r18 |
A |
G |
5: 151,508,462 (GRCm39) |
S221P |
probably damaging |
Het |
Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,930,150 (GRCm39) |
K52E |
probably benign |
Het |
|
Other mutations in Colgalt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01472:Colgalt2
|
APN |
1 |
152,382,629 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02900:Colgalt2
|
APN |
1 |
152,384,481 (GRCm39) |
missense |
probably damaging |
0.99 |
R0280:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0282:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0328:Colgalt2
|
UTSW |
1 |
152,348,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R0409:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0412:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0485:Colgalt2
|
UTSW |
1 |
152,360,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R0518:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0519:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0556:Colgalt2
|
UTSW |
1 |
152,347,564 (GRCm39) |
splice site |
probably benign |
|
R0605:Colgalt2
|
UTSW |
1 |
152,371,543 (GRCm39) |
splice site |
probably benign |
|
R0628:Colgalt2
|
UTSW |
1 |
152,384,312 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0972:Colgalt2
|
UTSW |
1 |
152,347,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Colgalt2
|
UTSW |
1 |
152,378,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Colgalt2
|
UTSW |
1 |
152,348,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Colgalt2
|
UTSW |
1 |
152,379,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Colgalt2
|
UTSW |
1 |
152,360,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Colgalt2
|
UTSW |
1 |
152,360,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R1707:Colgalt2
|
UTSW |
1 |
152,276,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R2285:Colgalt2
|
UTSW |
1 |
152,344,301 (GRCm39) |
missense |
probably benign |
0.00 |
R2917:Colgalt2
|
UTSW |
1 |
152,347,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Colgalt2
|
UTSW |
1 |
152,384,362 (GRCm39) |
nonsense |
probably null |
|
R3917:Colgalt2
|
UTSW |
1 |
152,384,362 (GRCm39) |
nonsense |
probably null |
|
R4250:Colgalt2
|
UTSW |
1 |
152,365,638 (GRCm39) |
missense |
probably benign |
0.00 |
R4282:Colgalt2
|
UTSW |
1 |
152,344,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R4421:Colgalt2
|
UTSW |
1 |
152,360,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R4583:Colgalt2
|
UTSW |
1 |
152,382,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R4743:Colgalt2
|
UTSW |
1 |
152,276,094 (GRCm39) |
missense |
probably damaging |
0.97 |
R4751:Colgalt2
|
UTSW |
1 |
152,365,627 (GRCm39) |
missense |
probably benign |
0.34 |
R4832:Colgalt2
|
UTSW |
1 |
152,360,749 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4930:Colgalt2
|
UTSW |
1 |
152,375,710 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5319:Colgalt2
|
UTSW |
1 |
152,360,620 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5504:Colgalt2
|
UTSW |
1 |
152,276,054 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5916:Colgalt2
|
UTSW |
1 |
152,379,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6006:Colgalt2
|
UTSW |
1 |
152,348,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Colgalt2
|
UTSW |
1 |
152,347,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:Colgalt2
|
UTSW |
1 |
152,382,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7464:Colgalt2
|
UTSW |
1 |
152,379,895 (GRCm39) |
missense |
probably damaging |
0.97 |
R8462:Colgalt2
|
UTSW |
1 |
152,378,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Colgalt2
|
UTSW |
1 |
152,360,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R9118:Colgalt2
|
UTSW |
1 |
152,378,906 (GRCm39) |
intron |
probably benign |
|
R9186:Colgalt2
|
UTSW |
1 |
152,384,403 (GRCm39) |
missense |
probably damaging |
0.98 |
R9393:Colgalt2
|
UTSW |
1 |
152,360,598 (GRCm39) |
nonsense |
probably null |
|
R9611:Colgalt2
|
UTSW |
1 |
152,360,745 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Colgalt2
|
UTSW |
1 |
152,347,471 (GRCm39) |
missense |
probably damaging |
1.00 |
|