Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
T |
C |
16: 8,399,794 (GRCm39) |
|
probably null |
Het |
Adamts4 |
G |
A |
1: 171,086,334 (GRCm39) |
D709N |
probably benign |
Het |
Arhgef12 |
G |
T |
9: 42,903,318 (GRCm39) |
D745E |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,818,473 (GRCm39) |
K883E |
probably benign |
Het |
Cfdp1 |
T |
C |
8: 112,495,415 (GRCm39) |
I268V |
probably benign |
Het |
Cgnl1 |
G |
T |
9: 71,552,853 (GRCm39) |
S1037* |
probably null |
Het |
Clca3b |
T |
C |
3: 144,552,610 (GRCm39) |
N142S |
probably benign |
Het |
Col6a6 |
A |
T |
9: 105,659,253 (GRCm39) |
I564N |
probably damaging |
Het |
Coq4 |
G |
T |
2: 29,678,482 (GRCm39) |
R36L |
probably benign |
Het |
Dact3 |
G |
A |
7: 16,620,131 (GRCm39) |
S542N |
unknown |
Het |
Dcaf1 |
A |
G |
9: 106,751,466 (GRCm39) |
D1480G |
unknown |
Het |
Dcdc2a |
C |
T |
13: 25,389,443 (GRCm39) |
T457I |
probably damaging |
Het |
Ddi2 |
A |
G |
4: 141,411,196 (GRCm39) |
V572A |
probably damaging |
Het |
Ddx54 |
C |
T |
5: 120,761,672 (GRCm39) |
R483C |
probably benign |
Het |
Dennd5b |
G |
A |
6: 148,969,997 (GRCm39) |
S152F |
probably benign |
Het |
Efcab14 |
C |
T |
4: 115,616,072 (GRCm39) |
H252Y |
probably benign |
Het |
Efhb |
A |
T |
17: 53,770,298 (GRCm39) |
F4I |
probably damaging |
Het |
Esrrg |
A |
G |
1: 187,775,569 (GRCm39) |
D32G |
probably benign |
Het |
Far2 |
C |
A |
6: 148,060,448 (GRCm39) |
A267E |
probably damaging |
Het |
Fhip2b |
A |
C |
14: 70,827,621 (GRCm39) |
V158G |
possibly damaging |
Het |
Flnb |
T |
C |
14: 7,929,846 (GRCm38) |
I1992T |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 52,944,527 (GRCm39) |
S169G |
|
Het |
Gbf1 |
C |
A |
19: 46,244,137 (GRCm39) |
N210K |
probably benign |
Het |
Gbp3 |
T |
G |
3: 142,276,283 (GRCm39) |
S460A |
probably benign |
Het |
Gm12185 |
T |
A |
11: 48,806,168 (GRCm39) |
H341L |
probably benign |
Het |
Gm5592 |
A |
T |
7: 40,939,234 (GRCm39) |
I839F |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,267,310 (GRCm39) |
D467G |
probably damaging |
Het |
Grin3a |
A |
T |
4: 49,714,213 (GRCm39) |
M844K |
probably damaging |
Het |
Gtf2a1l |
A |
G |
17: 89,019,020 (GRCm39) |
D368G |
probably benign |
Het |
Herc2 |
G |
C |
7: 55,813,659 (GRCm39) |
|
probably null |
Het |
Hycc1 |
T |
C |
5: 24,184,572 (GRCm39) |
Q302R |
possibly damaging |
Het |
Ins2 |
T |
A |
7: 142,233,185 (GRCm39) |
H29L |
probably damaging |
Het |
Ipo13 |
T |
A |
4: 117,762,778 (GRCm39) |
Y275F |
probably benign |
Het |
Kcnj15 |
T |
A |
16: 95,096,483 (GRCm39) |
M35K |
probably benign |
Het |
Kif21b |
G |
A |
1: 136,076,421 (GRCm39) |
V321M |
probably damaging |
Het |
Lcmt1 |
T |
A |
7: 123,029,375 (GRCm39) |
Y332* |
probably null |
Het |
Malt1 |
A |
G |
18: 65,581,283 (GRCm39) |
Q237R |
probably benign |
Het |
Micall1 |
G |
A |
15: 79,005,032 (GRCm39) |
C168Y |
unknown |
Het |
Muc5ac |
A |
G |
7: 141,360,985 (GRCm39) |
K1432R |
probably benign |
Het |
Nacad |
A |
G |
11: 6,551,662 (GRCm39) |
S510P |
probably benign |
Het |
Nub1 |
T |
C |
5: 24,897,965 (GRCm39) |
L117P |
possibly damaging |
Het |
Or10al3 |
T |
C |
17: 38,012,434 (GRCm39) |
L291P |
probably damaging |
Het |
Or5af1 |
A |
G |
11: 58,722,852 (GRCm39) |
R291G |
probably damaging |
Het |
Or8g24 |
A |
T |
9: 38,989,271 (GRCm39) |
F257I |
possibly damaging |
Het |
Pkdrej |
T |
C |
15: 85,705,268 (GRCm39) |
K223E |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,657,044 (GRCm39) |
Y4046* |
probably null |
Het |
Prpf8 |
A |
G |
11: 75,394,257 (GRCm39) |
N1767D |
probably benign |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
R3hdm2 |
G |
T |
10: 127,280,182 (GRCm39) |
M18I |
unknown |
Het |
Rab35 |
C |
A |
5: 115,778,224 (GRCm39) |
D63E |
probably damaging |
Het |
Ribc2 |
T |
A |
15: 85,027,568 (GRCm39) |
Y350N |
probably benign |
Het |
Sec63 |
A |
G |
10: 42,704,944 (GRCm39) |
I733V |
probably benign |
Het |
Slc23a3 |
ATT |
ATTT |
1: 75,109,925 (GRCm39) |
|
probably null |
Het |
Slc38a4 |
T |
C |
15: 96,896,332 (GRCm39) |
K512E |
probably damaging |
Het |
Stk35 |
G |
A |
2: 129,642,605 (GRCm39) |
V49I |
probably benign |
Het |
Tango6 |
A |
G |
8: 107,576,911 (GRCm39) |
E1055G |
probably damaging |
Het |
Tas2r140 |
A |
G |
6: 40,469,036 (GRCm39) |
I289V |
probably benign |
Het |
Thoc2l |
T |
C |
5: 104,667,101 (GRCm39) |
V541A |
probably benign |
Het |
Tll2 |
C |
T |
19: 41,119,084 (GRCm39) |
V215M |
probably damaging |
Het |
Tmem30a |
A |
T |
9: 79,687,874 (GRCm39) |
N98K |
probably benign |
Het |
Trav9n-4 |
C |
A |
14: 53,532,290 (GRCm39) |
A48E |
probably benign |
Het |
Vinac1 |
A |
T |
2: 128,880,499 (GRCm39) |
S476T |
|
Het |
Vmn1r192 |
A |
G |
13: 22,372,010 (GRCm39) |
F70S |
probably damaging |
Het |
Wdr89 |
A |
G |
12: 75,680,026 (GRCm39) |
V76A |
probably damaging |
Het |
Zfp229 |
A |
T |
17: 21,965,275 (GRCm39) |
T502S |
probably 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 |
R8924:Galnt10
|
UTSW |
11 |
57,674,681 (GRCm39) |
intron |
probably benign |
|
R9143:Galnt10
|
UTSW |
11 |
57,612,146 (GRCm39) |
missense |
probably benign |
|
R9508:Galnt10
|
UTSW |
11 |
57,673,040 (GRCm39) |
missense |
possibly damaging |
0.94 |
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 |
|
|