Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
C |
6: 146,853,909 (GRCm39) |
I249M |
possibly damaging |
Het |
1700102P08Rik |
T |
A |
9: 108,270,809 (GRCm39) |
D124E |
possibly damaging |
Het |
4930544D05Rik |
A |
G |
11: 70,507,249 (GRCm39) |
E98G |
probably damaging |
Het |
Abca8a |
A |
T |
11: 109,980,768 (GRCm39) |
M90K |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,849,769 (GRCm39) |
|
probably null |
Het |
Adora3 |
A |
C |
3: 105,812,152 (GRCm39) |
N13H |
possibly damaging |
Het |
Aen |
A |
T |
7: 78,557,073 (GRCm39) |
D307V |
probably damaging |
Het |
Akr1c18 |
T |
A |
13: 4,193,287 (GRCm39) |
N126I |
probably benign |
Het |
Ankmy2 |
T |
A |
12: 36,220,467 (GRCm39) |
M51K |
possibly damaging |
Het |
Antkmt |
C |
A |
17: 26,010,319 (GRCm39) |
|
probably null |
Het |
Apc |
A |
G |
18: 34,405,521 (GRCm39) |
E159G |
probably damaging |
Het |
Arhgef28 |
G |
T |
13: 98,282,081 (GRCm39) |
S4R |
probably damaging |
Het |
Atg2b |
G |
A |
12: 105,620,351 (GRCm39) |
T784M |
probably benign |
Het |
Atp11a |
A |
G |
8: 12,862,324 (GRCm39) |
N59D |
probably damaging |
Het |
Cacna1h |
T |
C |
17: 25,595,861 (GRCm39) |
Y1875C |
probably benign |
Het |
Capza1 |
A |
T |
3: 104,747,096 (GRCm39) |
|
probably null |
Het |
Ccdc81 |
T |
C |
7: 89,515,819 (GRCm39) |
E620G |
possibly damaging |
Het |
Cdcp2 |
T |
C |
4: 106,959,899 (GRCm39) |
F105L |
probably damaging |
Het |
Cdhr18 |
A |
C |
14: 13,828,607 (GRCm38) |
Y718D |
probably damaging |
Het |
Cep152 |
A |
T |
2: 125,462,225 (GRCm39) |
M58K |
probably benign |
Het |
Comtd1 |
A |
G |
14: 21,897,809 (GRCm39) |
L108P |
probably damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,788,075 (GRCm39) |
Y401C |
probably damaging |
Het |
Dap3 |
A |
G |
3: 88,838,281 (GRCm39) |
L86P |
probably damaging |
Het |
Dmxl1 |
G |
A |
18: 49,992,202 (GRCm39) |
R316H |
probably benign |
Het |
Eea1 |
T |
A |
10: 95,854,073 (GRCm39) |
|
probably null |
Het |
Eeig1 |
T |
A |
2: 32,450,140 (GRCm39) |
N129K |
possibly damaging |
Het |
Ezhip |
GTCATCATCATCATC |
GTCATCATCATCATCATC |
X: 5,994,645 (GRCm39) |
|
probably benign |
Het |
Fam171a1 |
T |
C |
2: 3,221,380 (GRCm39) |
V157A |
probably damaging |
Het |
Fat3 |
T |
A |
9: 15,878,357 (GRCm39) |
I3375F |
probably damaging |
Het |
Fmod |
A |
G |
1: 133,968,551 (GRCm39) |
E197G |
possibly damaging |
Het |
Fsd1l |
T |
C |
4: 53,696,984 (GRCm39) |
|
probably null |
Het |
Gbp2b |
A |
G |
3: 142,314,063 (GRCm39) |
T448A |
probably benign |
Het |
Gpatch1 |
A |
T |
7: 35,002,813 (GRCm39) |
N232K |
probably damaging |
Het |
H2-Q4 |
A |
G |
17: 35,599,113 (GRCm39) |
R128G |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,924,623 (GRCm39) |
I435V |
probably benign |
Het |
Hmgxb3 |
A |
G |
18: 61,270,473 (GRCm39) |
|
probably null |
Het |
Il23r |
A |
T |
6: 67,450,785 (GRCm39) |
D231E |
possibly damaging |
Het |
Irag1 |
A |
G |
7: 110,523,740 (GRCm39) |
|
probably null |
Het |
Kcnt2 |
T |
A |
1: 140,511,985 (GRCm39) |
S1023T |
probably damaging |
Het |
Klc2 |
A |
G |
19: 5,158,640 (GRCm39) |
V618A |
probably benign |
Het |
Lzts1 |
T |
C |
8: 69,591,485 (GRCm39) |
D221G |
probably damaging |
Het |
Mdn1 |
G |
C |
4: 32,742,540 (GRCm39) |
R3926P |
probably damaging |
Het |
Med24 |
A |
G |
11: 98,609,642 (GRCm39) |
|
probably benign |
Het |
Mga |
T |
A |
2: 119,754,098 (GRCm39) |
L869Q |
probably damaging |
Het |
Mob3a |
G |
A |
10: 80,527,068 (GRCm39) |
Q86* |
probably null |
Het |
Ncoa7 |
T |
C |
10: 30,524,448 (GRCm39) |
N823S |
possibly damaging |
Het |
Nlrp5 |
T |
A |
7: 23,116,909 (GRCm39) |
V211D |
probably damaging |
Het |
Nr1h4 |
A |
T |
10: 89,290,729 (GRCm39) |
M433K |
possibly damaging |
Het |
Ofcc1 |
T |
C |
13: 40,360,100 (GRCm39) |
S310G |
possibly damaging |
Het |
Or4k49 |
G |
T |
2: 111,495,099 (GRCm39) |
S176I |
probably damaging |
Het |
Or5p57 |
T |
C |
7: 107,665,985 (GRCm39) |
N7D |
probably benign |
Het |
Or8k22 |
A |
G |
2: 86,163,617 (GRCm39) |
F28L |
possibly damaging |
Het |
Pdlim7 |
C |
T |
13: 55,653,981 (GRCm39) |
G212D |
probably benign |
Het |
Pdzd4 |
G |
A |
X: 72,839,052 (GRCm39) |
R419C |
probably damaging |
Het |
Pik3cd |
T |
A |
4: 149,737,091 (GRCm39) |
I902F |
probably damaging |
Het |
Pip5kl1 |
A |
G |
2: 32,468,517 (GRCm39) |
T198A |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,647,499 (GRCm39) |
V3641A |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,265,839 (GRCm39) |
V475A |
probably benign |
Het |
Rpl37 |
C |
T |
15: 5,148,072 (GRCm39) |
T83M |
possibly damaging |
Het |
Scml4 |
A |
G |
10: 42,788,223 (GRCm39) |
Y51C |
probably damaging |
Het |
Serinc5 |
A |
T |
13: 92,838,214 (GRCm39) |
D340V |
possibly damaging |
Het |
Stambpl1 |
A |
G |
19: 34,213,808 (GRCm39) |
I346V |
probably benign |
Het |
Syna |
G |
A |
5: 134,588,106 (GRCm39) |
S281L |
probably benign |
Het |
Tcstv2a |
G |
T |
13: 120,725,604 (GRCm39) |
K89N |
probably damaging |
Het |
Tet2 |
T |
C |
3: 133,193,094 (GRCm39) |
T447A |
possibly damaging |
Het |
Tmc7 |
A |
T |
7: 118,160,310 (GRCm39) |
F176I |
possibly damaging |
Het |
Trip4 |
T |
A |
9: 65,782,163 (GRCm39) |
I190F |
probably null |
Het |
Ttc6 |
T |
A |
12: 57,720,044 (GRCm39) |
S872T |
probably benign |
Het |
Ttc7b |
C |
T |
12: 100,381,389 (GRCm39) |
|
probably null |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,182,871 (GRCm39) |
L419P |
probably damaging |
Het |
Ush2a |
C |
A |
1: 188,132,177 (GRCm39) |
Q800K |
probably benign |
Het |
Vmn2r115 |
T |
C |
17: 23,565,007 (GRCm39) |
I298T |
possibly damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,491,288 (GRCm39) |
T320A |
possibly damaging |
Het |
Zfp804b |
T |
C |
5: 6,820,376 (GRCm39) |
R860G |
probably damaging |
Het |
|
Other mutations in Tgfbr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00966:Tgfbr3
|
APN |
5 |
107,290,367 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01135:Tgfbr3
|
APN |
5 |
107,362,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01375:Tgfbr3
|
APN |
5 |
107,284,837 (GRCm39) |
missense |
probably benign |
|
IGL01457:Tgfbr3
|
APN |
5 |
107,297,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01599:Tgfbr3
|
APN |
5 |
107,266,317 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01646:Tgfbr3
|
APN |
5 |
107,269,279 (GRCm39) |
splice site |
probably benign |
|
IGL01945:Tgfbr3
|
APN |
5 |
107,269,224 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03039:Tgfbr3
|
APN |
5 |
107,325,665 (GRCm39) |
splice site |
probably benign |
|
IGL03202:Tgfbr3
|
APN |
5 |
107,257,630 (GRCm39) |
splice site |
probably benign |
|
IGL03378:Tgfbr3
|
APN |
5 |
107,257,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Tgfbr3
|
UTSW |
5 |
107,280,682 (GRCm39) |
missense |
probably benign |
0.00 |
R0452:Tgfbr3
|
UTSW |
5 |
107,288,289 (GRCm39) |
missense |
probably benign |
0.00 |
R0665:Tgfbr3
|
UTSW |
5 |
107,325,716 (GRCm39) |
missense |
probably benign |
0.11 |
R0667:Tgfbr3
|
UTSW |
5 |
107,325,716 (GRCm39) |
missense |
probably benign |
0.11 |
R0751:Tgfbr3
|
UTSW |
5 |
107,287,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Tgfbr3
|
UTSW |
5 |
107,362,809 (GRCm39) |
missense |
probably benign |
0.01 |
R1777:Tgfbr3
|
UTSW |
5 |
107,284,796 (GRCm39) |
missense |
probably benign |
0.31 |
R3019:Tgfbr3
|
UTSW |
5 |
107,285,412 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3552:Tgfbr3
|
UTSW |
5 |
107,287,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R3617:Tgfbr3
|
UTSW |
5 |
107,288,485 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3901:Tgfbr3
|
UTSW |
5 |
107,362,753 (GRCm39) |
splice site |
probably benign |
|
R4830:Tgfbr3
|
UTSW |
5 |
107,257,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4939:Tgfbr3
|
UTSW |
5 |
107,278,335 (GRCm39) |
missense |
probably benign |
|
R5020:Tgfbr3
|
UTSW |
5 |
107,362,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Tgfbr3
|
UTSW |
5 |
107,284,795 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5619:Tgfbr3
|
UTSW |
5 |
107,288,380 (GRCm39) |
missense |
probably benign |
0.23 |
R5752:Tgfbr3
|
UTSW |
5 |
107,287,673 (GRCm39) |
missense |
probably benign |
0.01 |
R5768:Tgfbr3
|
UTSW |
5 |
107,297,761 (GRCm39) |
missense |
probably benign |
|
R5799:Tgfbr3
|
UTSW |
5 |
107,257,474 (GRCm39) |
utr 3 prime |
probably benign |
|
R5818:Tgfbr3
|
UTSW |
5 |
107,280,869 (GRCm39) |
missense |
probably benign |
|
R5846:Tgfbr3
|
UTSW |
5 |
107,288,521 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5859:Tgfbr3
|
UTSW |
5 |
107,288,381 (GRCm39) |
missense |
probably benign |
0.00 |
R6049:Tgfbr3
|
UTSW |
5 |
107,266,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R6378:Tgfbr3
|
UTSW |
5 |
107,325,679 (GRCm39) |
missense |
probably benign |
0.00 |
R6696:Tgfbr3
|
UTSW |
5 |
107,284,796 (GRCm39) |
missense |
probably benign |
0.02 |
R6823:Tgfbr3
|
UTSW |
5 |
107,297,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R6994:Tgfbr3
|
UTSW |
5 |
107,280,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Tgfbr3
|
UTSW |
5 |
107,362,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Tgfbr3
|
UTSW |
5 |
107,288,368 (GRCm39) |
missense |
probably benign |
0.00 |
R7978:Tgfbr3
|
UTSW |
5 |
107,287,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8201:Tgfbr3
|
UTSW |
5 |
107,278,431 (GRCm39) |
missense |
probably benign |
0.01 |
R8296:Tgfbr3
|
UTSW |
5 |
107,287,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R8758:Tgfbr3
|
UTSW |
5 |
107,297,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Tgfbr3
|
UTSW |
5 |
107,290,361 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9360:Tgfbr3
|
UTSW |
5 |
107,257,550 (GRCm39) |
missense |
unknown |
|
R9784:Tgfbr3
|
UTSW |
5 |
107,297,799 (GRCm39) |
missense |
probably benign |
0.00 |
X0022:Tgfbr3
|
UTSW |
5 |
107,284,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|