Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
G |
11: 109,838,003 (GRCm39) |
V1145A |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,589,011 (GRCm39) |
M562T |
probably benign |
Het |
Atn1 |
A |
T |
6: 124,722,211 (GRCm39) |
S881T |
probably benign |
Het |
B3galt1 |
C |
T |
2: 67,949,059 (GRCm39) |
T258I |
probably benign |
Het |
Bahcc1 |
C |
T |
11: 120,167,591 (GRCm39) |
L1331F |
probably benign |
Het |
Capn12 |
G |
A |
7: 28,582,628 (GRCm39) |
V168M |
probably damaging |
Het |
Card14 |
T |
C |
11: 119,216,930 (GRCm39) |
V338A |
possibly damaging |
Het |
Cd27 |
T |
C |
6: 125,213,432 (GRCm39) |
|
probably benign |
Het |
Cd37 |
A |
G |
7: 44,888,109 (GRCm39) |
L37P |
probably damaging |
Het |
Cd96 |
A |
G |
16: 45,919,385 (GRCm39) |
L212P |
probably damaging |
Het |
Celsr1 |
T |
C |
15: 85,916,671 (GRCm39) |
E434G |
possibly damaging |
Het |
Cep152 |
A |
G |
2: 125,444,778 (GRCm39) |
M456T |
possibly damaging |
Het |
Ces3b |
G |
A |
8: 105,811,619 (GRCm39) |
R45H |
probably benign |
Het |
Cfap54 |
T |
G |
10: 92,837,685 (GRCm39) |
T1072P |
probably damaging |
Het |
Chodl |
A |
T |
16: 78,738,659 (GRCm39) |
M172L |
possibly damaging |
Het |
Cilp2 |
A |
G |
8: 70,339,108 (GRCm39) |
S47P |
probably damaging |
Het |
Clasrp |
T |
C |
7: 19,318,232 (GRCm39) |
I596V |
unknown |
Het |
Clcn2 |
C |
T |
16: 20,530,930 (GRCm39) |
V267I |
probably damaging |
Het |
Cntln |
T |
A |
4: 84,806,936 (GRCm39) |
D139E |
probably damaging |
Het |
Cyp2j12 |
A |
C |
4: 95,994,685 (GRCm39) |
N379K |
probably damaging |
Het |
Defb21 |
T |
C |
2: 152,416,704 (GRCm39) |
V60A |
possibly damaging |
Het |
Dnajc16 |
G |
T |
4: 141,494,018 (GRCm39) |
S543* |
probably null |
Het |
Efcab12 |
G |
T |
6: 115,800,664 (GRCm39) |
H120N |
probably benign |
Het |
Efcab3 |
AACTCTA |
AA |
11: 104,806,253 (GRCm39) |
|
probably null |
Het |
Efl1 |
G |
A |
7: 82,412,161 (GRCm39) |
G850D |
probably benign |
Het |
Efna1 |
T |
C |
3: 89,183,635 (GRCm39) |
M64V |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,870,003 (GRCm39) |
W897R |
probably damaging |
Het |
Eif2ak4 |
T |
A |
2: 118,258,513 (GRCm39) |
F621Y |
probably damaging |
Het |
Erbin |
C |
A |
13: 103,975,966 (GRCm39) |
E643* |
probably null |
Het |
Esr1 |
G |
A |
10: 4,807,176 (GRCm39) |
W364* |
probably null |
Het |
Fam171a2 |
T |
C |
11: 102,330,861 (GRCm39) |
E206G |
possibly damaging |
Het |
Fam90a1a |
T |
C |
8: 22,451,429 (GRCm39) |
F97L |
probably benign |
Het |
Fap |
A |
T |
2: 62,378,165 (GRCm39) |
F181I |
probably benign |
Het |
Fem1b |
T |
C |
9: 62,704,916 (GRCm39) |
N115D |
probably damaging |
Het |
Gal3st2b |
G |
T |
1: 93,868,653 (GRCm39) |
A295S |
probably benign |
Het |
Gcfc2 |
T |
C |
6: 81,909,879 (GRCm39) |
V224A |
probably damaging |
Het |
Gh |
T |
C |
11: 106,191,634 (GRCm39) |
E136G |
probably damaging |
Het |
Gjd3 |
C |
T |
11: 98,873,325 (GRCm39) |
C173Y |
probably damaging |
Het |
Gm12695 |
T |
A |
4: 96,651,046 (GRCm39) |
M136L |
probably benign |
Het |
Gnas |
A |
G |
2: 174,141,277 (GRCm39) |
E482G |
unknown |
Het |
Gpa33 |
T |
C |
1: 165,980,351 (GRCm39) |
L138P |
probably damaging |
Het |
Hlf |
T |
C |
11: 90,236,714 (GRCm39) |
D181G |
probably damaging |
Het |
Irgm1 |
A |
G |
11: 48,756,698 (GRCm39) |
L387S |
probably benign |
Het |
Kctd1 |
T |
C |
18: 15,102,745 (GRCm39) |
E812G |
possibly damaging |
Het |
Klra2 |
T |
C |
6: 131,205,214 (GRCm39) |
E209G |
probably benign |
Het |
Klra3 |
C |
T |
6: 130,312,732 (GRCm39) |
V11M |
probably benign |
Het |
Klrh1 |
G |
T |
6: 129,745,084 (GRCm39) |
H171N |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,503,885 (GRCm39) |
S3808G |
probably benign |
Het |
Krtap24-1 |
A |
C |
16: 88,408,888 (GRCm39) |
S79R |
probably benign |
Het |
Limch1 |
T |
A |
5: 67,190,475 (GRCm39) |
H759Q |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,490,433 (GRCm39) |
Y333H |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,974,091 (GRCm39) |
Y377C |
probably damaging |
Het |
Ms4a14 |
A |
T |
19: 11,281,113 (GRCm39) |
Y482N |
possibly damaging |
Het |
Myo9b |
A |
G |
8: 71,801,675 (GRCm39) |
S1277G |
probably benign |
Het |
Nab1 |
T |
C |
1: 52,529,667 (GRCm39) |
T77A |
possibly damaging |
Het |
Obsl1 |
T |
C |
1: 75,482,841 (GRCm39) |
S10G |
probably benign |
Het |
Odc1 |
A |
G |
12: 17,598,329 (GRCm39) |
T157A |
possibly damaging |
Het |
Or2a5 |
T |
G |
6: 42,873,964 (GRCm39) |
L193R |
probably damaging |
Het |
Or8b52 |
T |
C |
9: 38,576,780 (GRCm39) |
D120G |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Plpp1 |
T |
A |
13: 112,943,057 (GRCm39) |
|
probably benign |
Het |
Prdm13 |
G |
A |
4: 21,679,125 (GRCm39) |
A455V |
possibly damaging |
Het |
Ptpn13 |
A |
T |
5: 103,739,101 (GRCm39) |
Y2289F |
probably damaging |
Het |
Ptpn18 |
G |
T |
1: 34,498,966 (GRCm39) |
R21L |
probably benign |
Het |
Ptprd |
A |
G |
4: 75,916,736 (GRCm39) |
|
probably null |
Het |
Rcn3 |
G |
T |
7: 44,733,095 (GRCm39) |
D258E |
probably damaging |
Het |
Ro60 |
C |
T |
1: 143,641,170 (GRCm39) |
|
probably null |
Het |
Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Sacs |
T |
A |
14: 61,429,895 (GRCm39) |
H651Q |
probably benign |
Het |
Sacs |
T |
C |
14: 61,448,702 (GRCm39) |
S3583P |
probably damaging |
Het |
Scel |
A |
G |
14: 103,829,807 (GRCm39) |
N463S |
possibly damaging |
Het |
Serpinb2 |
A |
T |
1: 107,443,284 (GRCm39) |
I28F |
possibly damaging |
Het |
Sin3b |
A |
G |
8: 73,473,131 (GRCm39) |
K484E |
probably benign |
Het |
Snrnp48 |
T |
A |
13: 38,400,397 (GRCm39) |
V168D |
probably damaging |
Het |
Snx18 |
T |
G |
13: 113,754,931 (GRCm39) |
M1L |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,131,295 (GRCm39) |
N572D |
probably benign |
Het |
Srcap |
T |
A |
7: 127,158,204 (GRCm39) |
N2693K |
unknown |
Het |
Stim1 |
A |
G |
7: 102,078,014 (GRCm39) |
D172G |
|
Het |
Stip1 |
A |
T |
19: 7,002,687 (GRCm39) |
L414H |
probably damaging |
Het |
Sun1 |
A |
G |
5: 139,209,390 (GRCm39) |
H40R |
probably damaging |
Het |
Sva |
T |
A |
6: 42,019,182 (GRCm39) |
D117E |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,943,444 (GRCm39) |
D321G |
probably damaging |
Het |
Trim45 |
A |
G |
3: 100,835,394 (GRCm39) |
D459G |
probably damaging |
Het |
Ttc6 |
G |
A |
12: 57,697,790 (GRCm39) |
W43* |
probably null |
Het |
Ugt2b35 |
A |
G |
5: 87,152,780 (GRCm39) |
T317A |
possibly damaging |
Het |
Usp32 |
C |
T |
11: 84,916,370 (GRCm39) |
R858Q |
probably damaging |
Het |
Vmn2r53 |
G |
T |
7: 12,334,752 (GRCm39) |
Q303K |
probably benign |
Het |
Yeats2 |
T |
C |
16: 19,969,312 (GRCm39) |
|
probably null |
Het |
Zfp804a |
A |
G |
2: 82,088,747 (GRCm39) |
N859D |
probably benign |
Het |
Zscan10 |
A |
T |
17: 23,824,580 (GRCm39) |
Q12L |
possibly damaging |
Het |
|
Other mutations in Galnt10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01367:Galnt10
|
APN |
11 |
57,616,409 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02085:Galnt10
|
APN |
11 |
57,673,104 (GRCm39) |
missense |
probably benign |
|
IGL02154:Galnt10
|
APN |
11 |
57,675,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02418:Galnt10
|
APN |
11 |
57,671,994 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02810:Galnt10
|
APN |
11 |
57,616,412 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03070:Galnt10
|
APN |
11 |
57,616,408 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03191:Galnt10
|
APN |
11 |
57,662,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0257:Galnt10
|
UTSW |
11 |
57,671,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Galnt10
|
UTSW |
11 |
57,672,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Galnt10
|
UTSW |
11 |
57,660,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Galnt10
|
UTSW |
11 |
57,671,871 (GRCm39) |
splice site |
probably benign |
|
R1436:Galnt10
|
UTSW |
11 |
57,662,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Galnt10
|
UTSW |
11 |
57,656,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R3424:Galnt10
|
UTSW |
11 |
57,536,539 (GRCm39) |
missense |
probably benign |
|
R4445:Galnt10
|
UTSW |
11 |
57,674,517 (GRCm39) |
missense |
probably damaging |
0.98 |
R5183:Galnt10
|
UTSW |
11 |
57,660,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5369:Galnt10
|
UTSW |
11 |
57,656,573 (GRCm39) |
critical splice donor site |
probably null |
|
R5838:Galnt10
|
UTSW |
11 |
57,671,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R6045:Galnt10
|
UTSW |
11 |
57,674,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6148:Galnt10
|
UTSW |
11 |
57,675,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R6442:Galnt10
|
UTSW |
11 |
57,656,448 (GRCm39) |
missense |
probably benign |
0.03 |
R6851:Galnt10
|
UTSW |
11 |
57,656,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Galnt10
|
UTSW |
11 |
57,672,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7013:Galnt10
|
UTSW |
11 |
57,656,410 (GRCm39) |
missense |
probably benign |
0.22 |
R7696:Galnt10
|
UTSW |
11 |
57,660,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R7950:Galnt10
|
UTSW |
11 |
57,674,549 (GRCm39) |
missense |
probably damaging |
0.99 |
R8208:Galnt10
|
UTSW |
11 |
57,536,398 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8264:Galnt10
|
UTSW |
11 |
57,673,032 (GRCm39) |
missense |
probably benign |
0.01 |
R8743:Galnt10
|
UTSW |
11 |
57,675,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R9143:Galnt10
|
UTSW |
11 |
57,612,146 (GRCm39) |
missense |
probably benign |
|
R9508:Galnt10
|
UTSW |
11 |
57,673,040 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9760:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
R9777:Galnt10
|
UTSW |
11 |
57,672,065 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1088:Galnt10
|
UTSW |
11 |
57,612,157 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Galnt10
|
UTSW |
11 |
57,627,826 (GRCm39) |
missense |
probably benign |
0.43 |
Z1186:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
Z1187:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
Z1188:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
Z1189:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
Z1190:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
Z1191:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
Z1192:Galnt10
|
UTSW |
11 |
57,656,514 (GRCm39) |
missense |
probably benign |
|
|