Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
C |
T |
11: 9,225,053 (GRCm39) |
H511Y |
possibly damaging |
Het |
Acp5 |
G |
A |
9: 22,038,489 (GRCm39) |
R271* |
probably null |
Het |
Adamts20 |
A |
T |
15: 94,184,294 (GRCm39) |
V1503E |
possibly damaging |
Het |
Adra2b |
A |
T |
2: 127,206,417 (GRCm39) |
E311D |
probably benign |
Het |
Aldh18a1 |
T |
C |
19: 40,546,230 (GRCm39) |
I556V |
possibly damaging |
Het |
Alox12 |
C |
A |
11: 70,144,146 (GRCm39) |
A116S |
probably benign |
Het |
Alox5 |
G |
T |
6: 116,390,102 (GRCm39) |
A552E |
probably damaging |
Het |
Angpt1 |
G |
T |
15: 42,375,780 (GRCm39) |
L159I |
probably damaging |
Het |
Atp2b4 |
CTT |
CTTTTT |
1: 133,629,485 (GRCm39) |
|
probably benign |
Het |
Bub1b |
T |
A |
2: 118,462,305 (GRCm39) |
L726I |
probably damaging |
Het |
Ccdc78 |
A |
T |
17: 26,006,807 (GRCm39) |
T165S |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,824,791 (GRCm39) |
D1323G |
probably damaging |
Het |
Chek1 |
A |
T |
9: 36,625,033 (GRCm39) |
C349* |
probably null |
Het |
Clec1a |
A |
T |
6: 129,428,617 (GRCm39) |
L21Q |
possibly damaging |
Het |
Col1a1 |
T |
C |
11: 94,833,634 (GRCm39) |
V445A |
possibly damaging |
Het |
Efcab7 |
A |
G |
4: 99,757,791 (GRCm39) |
T313A |
probably null |
Het |
Fads1 |
T |
A |
19: 10,170,325 (GRCm39) |
Y288* |
probably null |
Het |
Fgb |
T |
A |
3: 82,953,969 (GRCm39) |
T90S |
probably benign |
Het |
Glg1 |
C |
A |
8: 111,888,114 (GRCm39) |
V1026L |
probably damaging |
Het |
Hadh |
T |
A |
3: 131,027,825 (GRCm39) |
Y313F |
probably damaging |
Het |
Htr4 |
A |
G |
18: 62,570,853 (GRCm39) |
I303V |
possibly damaging |
Het |
Kcnn3 |
A |
G |
3: 89,552,757 (GRCm39) |
D487G |
possibly damaging |
Het |
L1td1 |
G |
A |
4: 98,625,814 (GRCm39) |
V604I |
probably benign |
Het |
Lefty1 |
C |
A |
1: 180,764,118 (GRCm39) |
A86E |
probably damaging |
Het |
Lmx1b |
T |
C |
2: 33,529,522 (GRCm39) |
Y79C |
|
Het |
Lrp2 |
A |
G |
2: 69,382,745 (GRCm39) |
C47R |
probably damaging |
Het |
Mrc2 |
A |
T |
11: 105,238,465 (GRCm39) |
N1204I |
probably benign |
Het |
Ncf1 |
A |
C |
5: 134,254,145 (GRCm39) |
Y209* |
probably null |
Het |
Or14j7 |
T |
A |
17: 38,235,075 (GRCm39) |
M206K |
probably benign |
Het |
Or2ad1 |
A |
T |
13: 21,326,453 (GRCm39) |
M258K |
possibly damaging |
Het |
Or8k33 |
G |
A |
2: 86,384,297 (GRCm39) |
T57M |
probably damaging |
Het |
Oxtr |
T |
G |
6: 112,466,871 (GRCm39) |
|
probably benign |
Het |
Pcdhac1 |
T |
C |
18: 37,224,942 (GRCm39) |
V585A |
probably damaging |
Het |
Pdcd11 |
T |
G |
19: 47,097,019 (GRCm39) |
L755R |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,358,461 (GRCm39) |
V2705A |
probably damaging |
Het |
Plch2 |
C |
A |
4: 155,070,875 (GRCm39) |
G1168V |
probably benign |
Het |
Prpf39 |
T |
C |
12: 65,089,555 (GRCm39) |
Y98H |
possibly damaging |
Het |
R3hdm2 |
T |
G |
10: 127,293,521 (GRCm39) |
S142A |
probably damaging |
Het |
Rassf10 |
T |
A |
7: 112,554,738 (GRCm39) |
D446E |
probably benign |
Het |
Rgs13 |
T |
C |
1: 144,016,482 (GRCm39) |
Y87C |
probably damaging |
Het |
Serpinb9h |
G |
A |
13: 33,588,204 (GRCm39) |
R263H |
probably benign |
Het |
Smpd3 |
G |
A |
8: 106,982,377 (GRCm39) |
R576C |
probably damaging |
Het |
Spata31e1 |
T |
C |
13: 49,938,704 (GRCm39) |
Y1002C |
probably damaging |
Het |
Srsf11 |
A |
T |
3: 157,718,037 (GRCm39) |
D382E |
unknown |
Het |
Stpg1 |
T |
A |
4: 135,261,108 (GRCm39) |
M306K |
probably benign |
Het |
Svil |
C |
T |
18: 5,059,332 (GRCm39) |
Q696* |
probably null |
Het |
Syna |
C |
T |
5: 134,588,723 (GRCm39) |
M75I |
probably benign |
Het |
Synj2 |
T |
C |
17: 6,036,514 (GRCm39) |
F161S |
possibly damaging |
Het |
Tek |
T |
C |
4: 94,738,037 (GRCm39) |
Y696H |
probably damaging |
Het |
Tgfbr1 |
A |
T |
4: 47,405,555 (GRCm39) |
D386V |
possibly damaging |
Het |
Tgm4 |
G |
T |
9: 122,890,910 (GRCm39) |
G503V |
probably damaging |
Het |
Tnni3k |
T |
C |
3: 154,645,691 (GRCm39) |
E461G |
probably damaging |
Het |
Tom1l1 |
A |
T |
11: 90,561,931 (GRCm39) |
H232Q |
probably benign |
Het |
Ubqln5 |
T |
C |
7: 103,778,329 (GRCm39) |
N165S |
probably benign |
Het |
Vmn1r24 |
G |
A |
6: 57,932,958 (GRCm39) |
L187F |
probably benign |
Het |
Vmn2r82 |
C |
T |
10: 79,213,894 (GRCm39) |
T160I |
probably damaging |
Het |
Vmn2r96 |
G |
T |
17: 18,818,250 (GRCm39) |
G801V |
probably damaging |
Het |
Vps39 |
A |
G |
2: 120,172,506 (GRCm39) |
S176P |
probably damaging |
Het |
Vsig10 |
C |
A |
5: 117,472,981 (GRCm39) |
H191Q |
probably benign |
Het |
Wtap |
G |
A |
17: 13,186,488 (GRCm39) |
S353L |
possibly damaging |
Het |
Zmym4 |
T |
G |
4: 126,816,953 (GRCm39) |
R248S |
probably benign |
Het |
Zscan10 |
A |
G |
17: 23,829,011 (GRCm39) |
S518G |
probably benign |
Het |
Zscan29 |
A |
T |
2: 120,996,876 (GRCm39) |
Y282N |
probably damaging |
Het |
|
Other mutations in Lao1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02105:Lao1
|
APN |
4 |
118,825,640 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02252:Lao1
|
APN |
4 |
118,824,613 (GRCm39) |
missense |
probably benign |
0.19 |
R0139:Lao1
|
UTSW |
4 |
118,821,399 (GRCm39) |
missense |
probably benign |
0.06 |
R0541:Lao1
|
UTSW |
4 |
118,820,999 (GRCm39) |
missense |
probably benign |
0.03 |
R0635:Lao1
|
UTSW |
4 |
118,825,493 (GRCm39) |
missense |
probably benign |
0.04 |
R1164:Lao1
|
UTSW |
4 |
118,822,602 (GRCm39) |
missense |
probably benign |
0.00 |
R4465:Lao1
|
UTSW |
4 |
118,822,504 (GRCm39) |
missense |
probably benign |
0.10 |
R4767:Lao1
|
UTSW |
4 |
118,825,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4950:Lao1
|
UTSW |
4 |
118,822,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R5061:Lao1
|
UTSW |
4 |
118,824,673 (GRCm39) |
missense |
probably benign |
0.00 |
R5488:Lao1
|
UTSW |
4 |
118,824,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Lao1
|
UTSW |
4 |
118,822,433 (GRCm39) |
splice site |
probably null |
|
R6176:Lao1
|
UTSW |
4 |
118,819,197 (GRCm39) |
start codon destroyed |
probably null |
0.40 |
R6189:Lao1
|
UTSW |
4 |
118,825,077 (GRCm39) |
missense |
probably benign |
0.00 |
R6857:Lao1
|
UTSW |
4 |
118,821,023 (GRCm39) |
critical splice donor site |
probably null |
|
R6859:Lao1
|
UTSW |
4 |
118,820,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R7074:Lao1
|
UTSW |
4 |
118,825,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R7878:Lao1
|
UTSW |
4 |
118,824,619 (GRCm39) |
missense |
probably benign |
0.00 |
R8021:Lao1
|
UTSW |
4 |
118,825,674 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Lao1
|
UTSW |
4 |
118,825,719 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Lao1
|
UTSW |
4 |
118,825,637 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lao1
|
UTSW |
4 |
118,825,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|