Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bche |
A |
G |
3: 73,609,216 (GRCm39) |
L70P |
probably damaging |
Het |
Cacna1h |
C |
A |
17: 25,602,752 (GRCm39) |
|
probably benign |
Het |
Ccdc60 |
A |
T |
5: 116,284,274 (GRCm39) |
|
probably benign |
Het |
Cep152 |
T |
C |
2: 125,460,371 (GRCm39) |
N194D |
probably benign |
Het |
Chodl |
T |
A |
16: 78,738,321 (GRCm39) |
D96E |
probably damaging |
Het |
Clca3b |
C |
A |
3: 144,552,671 (GRCm39) |
G122* |
probably null |
Het |
Crybg1 |
T |
C |
10: 43,865,245 (GRCm39) |
I1411V |
probably damaging |
Het |
Dock9 |
A |
C |
14: 121,876,940 (GRCm39) |
V477G |
probably damaging |
Het |
Fam149a |
T |
A |
8: 45,794,265 (GRCm39) |
E632D |
probably damaging |
Het |
Gabra4 |
A |
G |
5: 71,781,358 (GRCm39) |
V351A |
probably damaging |
Het |
Gen1 |
T |
A |
12: 11,298,265 (GRCm39) |
I319L |
probably benign |
Het |
Gne |
C |
A |
4: 44,055,211 (GRCm39) |
D255Y |
probably damaging |
Het |
Gpr146 |
A |
G |
5: 139,378,705 (GRCm39) |
H169R |
probably benign |
Het |
Htatip2 |
A |
G |
7: 49,409,522 (GRCm39) |
E92G |
probably benign |
Het |
Ipcef1 |
A |
G |
10: 6,869,732 (GRCm39) |
S223P |
probably damaging |
Het |
Kcnmb2 |
T |
A |
3: 32,252,276 (GRCm39) |
*37R |
probably null |
Het |
Lin54 |
A |
T |
5: 100,602,337 (GRCm39) |
V400E |
probably damaging |
Het |
Lyg1 |
A |
G |
1: 37,989,849 (GRCm39) |
|
probably benign |
Het |
Nampt |
T |
A |
12: 32,892,685 (GRCm39) |
V324D |
possibly damaging |
Het |
Nat8b-ps |
T |
G |
6: 85,909,950 (GRCm39) |
|
probably benign |
Het |
Neb |
G |
A |
2: 52,059,100 (GRCm39) |
H213Y |
probably damaging |
Het |
Nfkb1 |
T |
C |
3: 135,324,591 (GRCm39) |
E179G |
possibly damaging |
Het |
Nlrc5 |
T |
A |
8: 95,248,536 (GRCm39) |
|
probably benign |
Het |
Or12d2 |
T |
A |
17: 37,624,664 (GRCm39) |
I204F |
probably benign |
Het |
Or8k38 |
A |
T |
2: 86,488,775 (GRCm39) |
L9Q |
possibly damaging |
Het |
Pcdh15 |
G |
A |
10: 74,191,706 (GRCm39) |
V601M |
probably damaging |
Het |
Pigc |
G |
A |
1: 161,798,345 (GRCm39) |
R109Q |
possibly damaging |
Het |
Plxna2 |
A |
G |
1: 194,483,435 (GRCm39) |
N1582S |
probably damaging |
Het |
Pros1 |
C |
T |
16: 62,728,132 (GRCm39) |
Q279* |
probably null |
Het |
Psmb5 |
A |
G |
14: 54,854,014 (GRCm39) |
S155P |
probably damaging |
Het |
Rock2 |
T |
A |
12: 17,003,341 (GRCm39) |
D393E |
probably benign |
Het |
Slc25a21 |
T |
C |
12: 56,785,410 (GRCm39) |
T156A |
probably benign |
Het |
Slc44a1 |
T |
A |
4: 53,536,374 (GRCm39) |
Y183* |
probably null |
Het |
Sytl2 |
C |
T |
7: 90,041,642 (GRCm39) |
P580L |
probably damaging |
Het |
Tktl2 |
G |
T |
8: 66,964,936 (GRCm39) |
V165F |
probably damaging |
Het |
Trim55 |
A |
G |
3: 19,728,629 (GRCm39) |
E480G |
probably benign |
Het |
Vmn2r92 |
T |
A |
17: 18,386,972 (GRCm39) |
S104T |
possibly damaging |
Het |
Vps51 |
C |
T |
19: 6,120,078 (GRCm39) |
R490H |
probably damaging |
Het |
Wdr43 |
G |
A |
17: 71,948,282 (GRCm39) |
V391I |
probably benign |
Het |
Zranb1 |
T |
G |
7: 132,551,635 (GRCm39) |
Y121* |
probably null |
Het |
|
Other mutations in Ltbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Ltbp1
|
APN |
17 |
75,532,333 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00156:Ltbp1
|
APN |
17 |
75,692,155 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00161:Ltbp1
|
APN |
17 |
75,617,147 (GRCm39) |
splice site |
probably benign |
|
IGL00771:Ltbp1
|
APN |
17 |
75,669,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00822:Ltbp1
|
APN |
17 |
75,458,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01760:Ltbp1
|
APN |
17 |
75,534,145 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01796:Ltbp1
|
APN |
17 |
75,534,240 (GRCm39) |
splice site |
probably benign |
|
IGL01826:Ltbp1
|
APN |
17 |
75,599,835 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02372:Ltbp1
|
APN |
17 |
75,559,401 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02792:Ltbp1
|
APN |
17 |
75,589,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02862:Ltbp1
|
APN |
17 |
75,697,466 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03345:Ltbp1
|
APN |
17 |
75,373,154 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03404:Ltbp1
|
APN |
17 |
75,532,301 (GRCm39) |
missense |
probably damaging |
0.97 |
Hiphop
|
UTSW |
17 |
75,666,452 (GRCm39) |
missense |
probably damaging |
0.99 |
Pygea
|
UTSW |
17 |
75,634,223 (GRCm39) |
nonsense |
probably null |
|
Twist
|
UTSW |
17 |
75,617,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R0010:Ltbp1
|
UTSW |
17 |
75,670,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Ltbp1
|
UTSW |
17 |
75,670,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Ltbp1
|
UTSW |
17 |
75,671,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Ltbp1
|
UTSW |
17 |
75,671,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Ltbp1
|
UTSW |
17 |
75,583,504 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0033:Ltbp1
|
UTSW |
17 |
75,583,504 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0034:Ltbp1
|
UTSW |
17 |
75,354,563 (GRCm39) |
intron |
probably benign |
|
R0068:Ltbp1
|
UTSW |
17 |
75,666,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Ltbp1
|
UTSW |
17 |
75,666,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R0467:Ltbp1
|
UTSW |
17 |
75,589,424 (GRCm39) |
critical splice donor site |
probably null |
|
R0554:Ltbp1
|
UTSW |
17 |
75,532,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R0584:Ltbp1
|
UTSW |
17 |
75,670,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0863:Ltbp1
|
UTSW |
17 |
75,559,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R0991:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1084:Ltbp1
|
UTSW |
17 |
75,666,420 (GRCm39) |
nonsense |
probably null |
|
R1114:Ltbp1
|
UTSW |
17 |
75,667,770 (GRCm39) |
missense |
probably benign |
|
R1177:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1179:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1195:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1195:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1195:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1245:Ltbp1
|
UTSW |
17 |
75,634,189 (GRCm39) |
splice site |
probably benign |
|
R1246:Ltbp1
|
UTSW |
17 |
75,692,156 (GRCm39) |
nonsense |
probably null |
|
R1258:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1259:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1260:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1262:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1265:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1267:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1269:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1272:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1411:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1579:Ltbp1
|
UTSW |
17 |
75,559,362 (GRCm39) |
missense |
probably benign |
0.00 |
R1694:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1705:Ltbp1
|
UTSW |
17 |
75,692,196 (GRCm39) |
splice site |
probably null |
|
R1716:Ltbp1
|
UTSW |
17 |
75,622,019 (GRCm39) |
missense |
probably benign |
0.08 |
R1815:Ltbp1
|
UTSW |
17 |
75,559,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1932:Ltbp1
|
UTSW |
17 |
75,620,029 (GRCm39) |
missense |
probably benign |
0.01 |
R1951:Ltbp1
|
UTSW |
17 |
75,458,372 (GRCm39) |
missense |
probably benign |
0.00 |
R2044:Ltbp1
|
UTSW |
17 |
75,583,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2120:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2121:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2122:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2171:Ltbp1
|
UTSW |
17 |
75,598,312 (GRCm39) |
missense |
probably damaging |
0.99 |
R2237:Ltbp1
|
UTSW |
17 |
75,617,158 (GRCm39) |
missense |
probably benign |
0.31 |
R2655:Ltbp1
|
UTSW |
17 |
75,312,978 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2941:Ltbp1
|
UTSW |
17 |
75,486,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Ltbp1
|
UTSW |
17 |
75,666,273 (GRCm39) |
splice site |
probably null |
|
R3177:Ltbp1
|
UTSW |
17 |
75,583,475 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3277:Ltbp1
|
UTSW |
17 |
75,666,273 (GRCm39) |
splice site |
probably null |
|
R3277:Ltbp1
|
UTSW |
17 |
75,583,475 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3797:Ltbp1
|
UTSW |
17 |
75,669,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R3861:Ltbp1
|
UTSW |
17 |
75,666,333 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3897:Ltbp1
|
UTSW |
17 |
75,581,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R4002:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
probably benign |
0.09 |
R4057:Ltbp1
|
UTSW |
17 |
75,617,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:Ltbp1
|
UTSW |
17 |
75,598,362 (GRCm39) |
nonsense |
probably null |
|
R4375:Ltbp1
|
UTSW |
17 |
75,619,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4458:Ltbp1
|
UTSW |
17 |
75,583,502 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4519:Ltbp1
|
UTSW |
17 |
75,671,492 (GRCm39) |
missense |
probably benign |
0.14 |
R4529:Ltbp1
|
UTSW |
17 |
75,458,355 (GRCm39) |
missense |
probably benign |
0.21 |
R4614:Ltbp1
|
UTSW |
17 |
75,596,989 (GRCm39) |
intron |
probably benign |
|
R4724:Ltbp1
|
UTSW |
17 |
75,620,003 (GRCm39) |
missense |
probably damaging |
0.99 |
R4756:Ltbp1
|
UTSW |
17 |
75,532,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Ltbp1
|
UTSW |
17 |
75,312,899 (GRCm39) |
missense |
probably benign |
|
R4910:Ltbp1
|
UTSW |
17 |
75,634,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Ltbp1
|
UTSW |
17 |
75,628,090 (GRCm39) |
critical splice donor site |
probably null |
|
R5011:Ltbp1
|
UTSW |
17 |
75,373,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R5047:Ltbp1
|
UTSW |
17 |
75,599,881 (GRCm39) |
splice site |
probably benign |
|
R5259:Ltbp1
|
UTSW |
17 |
75,670,357 (GRCm39) |
missense |
probably benign |
0.03 |
R5438:Ltbp1
|
UTSW |
17 |
75,598,321 (GRCm39) |
missense |
probably damaging |
0.98 |
R5583:Ltbp1
|
UTSW |
17 |
75,598,325 (GRCm39) |
missense |
probably benign |
0.00 |
R5757:Ltbp1
|
UTSW |
17 |
75,580,944 (GRCm39) |
splice site |
probably null |
|
R5950:Ltbp1
|
UTSW |
17 |
75,580,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Ltbp1
|
UTSW |
17 |
75,597,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Ltbp1
|
UTSW |
17 |
75,312,984 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6383:Ltbp1
|
UTSW |
17 |
75,666,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R6400:Ltbp1
|
UTSW |
17 |
75,458,397 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6861:Ltbp1
|
UTSW |
17 |
75,534,187 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6880:Ltbp1
|
UTSW |
17 |
75,628,044 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7168:Ltbp1
|
UTSW |
17 |
75,598,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R7198:Ltbp1
|
UTSW |
17 |
75,533,962 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7260:Ltbp1
|
UTSW |
17 |
75,373,139 (GRCm39) |
missense |
probably benign |
0.01 |
R7262:Ltbp1
|
UTSW |
17 |
75,671,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7340:Ltbp1
|
UTSW |
17 |
75,634,223 (GRCm39) |
nonsense |
probably null |
|
R7443:Ltbp1
|
UTSW |
17 |
75,671,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Ltbp1
|
UTSW |
17 |
75,659,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7676:Ltbp1
|
UTSW |
17 |
75,598,292 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7717:Ltbp1
|
UTSW |
17 |
75,597,073 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7720:Ltbp1
|
UTSW |
17 |
75,692,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Ltbp1
|
UTSW |
17 |
75,559,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R7944:Ltbp1
|
UTSW |
17 |
75,697,546 (GRCm39) |
makesense |
probably null |
|
R7945:Ltbp1
|
UTSW |
17 |
75,697,546 (GRCm39) |
makesense |
probably null |
|
R7976:Ltbp1
|
UTSW |
17 |
75,670,358 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8256:Ltbp1
|
UTSW |
17 |
75,622,236 (GRCm39) |
intron |
probably benign |
|
R8295:Ltbp1
|
UTSW |
17 |
75,486,184 (GRCm39) |
missense |
probably benign |
0.10 |
R8423:Ltbp1
|
UTSW |
17 |
75,599,852 (GRCm39) |
missense |
probably benign |
|
R8462:Ltbp1
|
UTSW |
17 |
75,620,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8677:Ltbp1
|
UTSW |
17 |
75,655,753 (GRCm39) |
missense |
probably benign |
0.00 |
R8742:Ltbp1
|
UTSW |
17 |
75,617,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R8766:Ltbp1
|
UTSW |
17 |
75,603,250 (GRCm39) |
nonsense |
probably null |
|
R8873:Ltbp1
|
UTSW |
17 |
75,486,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Ltbp1
|
UTSW |
17 |
75,486,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Ltbp1
|
UTSW |
17 |
75,622,103 (GRCm39) |
missense |
probably damaging |
0.96 |
R9100:Ltbp1
|
UTSW |
17 |
75,622,102 (GRCm39) |
missense |
probably benign |
0.10 |
R9141:Ltbp1
|
UTSW |
17 |
75,598,309 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9204:Ltbp1
|
UTSW |
17 |
75,670,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R9292:Ltbp1
|
UTSW |
17 |
75,583,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R9381:Ltbp1
|
UTSW |
17 |
75,696,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9423:Ltbp1
|
UTSW |
17 |
75,597,112 (GRCm39) |
missense |
probably benign |
|
R9426:Ltbp1
|
UTSW |
17 |
75,598,309 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9448:Ltbp1
|
UTSW |
17 |
75,666,455 (GRCm39) |
nonsense |
probably null |
|
R9519:Ltbp1
|
UTSW |
17 |
75,692,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Ltbp1
|
UTSW |
17 |
75,697,498 (GRCm39) |
missense |
probably benign |
0.29 |
R9625:Ltbp1
|
UTSW |
17 |
75,486,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9671:Ltbp1
|
UTSW |
17 |
75,603,217 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0001:Ltbp1
|
UTSW |
17 |
75,534,173 (GRCm39) |
missense |
probably benign |
0.26 |
|