Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
A |
3: 121,846,572 (GRCm39) |
V30M |
probably benign |
Het |
Abcg8 |
C |
T |
17: 85,002,417 (GRCm39) |
|
probably benign |
Het |
Ablim1 |
T |
A |
19: 57,204,397 (GRCm39) |
|
probably null |
Het |
Acvr1c |
A |
T |
2: 58,173,517 (GRCm39) |
N248K |
probably damaging |
Het |
Adgrf3 |
A |
T |
5: 30,407,304 (GRCm39) |
N207K |
probably benign |
Het |
Anapc4 |
T |
A |
5: 52,997,010 (GRCm39) |
D94E |
probably damaging |
Het |
Arfgef2 |
A |
G |
2: 166,705,523 (GRCm39) |
N918S |
probably benign |
Het |
Arhgap45 |
A |
G |
10: 79,866,788 (GRCm39) |
N1097S |
probably damaging |
Het |
Atf2 |
G |
A |
2: 73,676,563 (GRCm39) |
P184S |
probably damaging |
Het |
Atg2a |
A |
G |
19: 6,302,566 (GRCm39) |
Y963C |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Atrn |
T |
C |
2: 130,799,955 (GRCm39) |
V444A |
probably damaging |
Het |
Avpr1a |
G |
A |
10: 122,285,695 (GRCm39) |
|
probably null |
Het |
Best3 |
A |
C |
10: 116,860,291 (GRCm39) |
Q517P |
probably benign |
Het |
C3 |
A |
G |
17: 57,525,829 (GRCm39) |
L851P |
probably damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,386,455 (GRCm39) |
F194S |
probably damaging |
Het |
Carns1 |
T |
C |
19: 4,215,473 (GRCm39) |
E903G |
probably damaging |
Het |
Chn1 |
A |
G |
2: 73,455,245 (GRCm39) |
C39R |
probably damaging |
Het |
Ciao1 |
A |
G |
2: 127,088,380 (GRCm39) |
S148P |
possibly damaging |
Het |
Clrn3 |
A |
C |
7: 135,115,753 (GRCm39) |
I199S |
possibly damaging |
Het |
Cngb1 |
C |
A |
8: 96,026,320 (GRCm39) |
G154W |
probably damaging |
Het |
Cnot2 |
G |
C |
10: 116,334,320 (GRCm39) |
P274R |
possibly damaging |
Het |
Cops7a |
G |
A |
6: 124,939,359 (GRCm39) |
R97* |
probably null |
Het |
Coro7 |
T |
C |
16: 4,446,596 (GRCm39) |
E843G |
probably benign |
Het |
Crocc |
T |
C |
4: 140,761,369 (GRCm39) |
R755G |
possibly damaging |
Het |
Crtam |
G |
C |
9: 40,915,846 (GRCm39) |
P13A |
probably benign |
Het |
Ddrgk1 |
G |
T |
2: 130,505,480 (GRCm39) |
|
probably benign |
Het |
Defb26 |
T |
A |
2: 152,350,195 (GRCm39) |
K28N |
possibly damaging |
Het |
Dnah8 |
G |
A |
17: 30,945,870 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,854,479 (GRCm39) |
E47G |
unknown |
Het |
Dnhd1 |
A |
T |
7: 105,323,183 (GRCm39) |
M564L |
probably benign |
Het |
Dusp15 |
A |
G |
2: 152,787,341 (GRCm39) |
|
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,139,159 (GRCm39) |
|
probably null |
Het |
Eapp |
A |
T |
12: 54,720,513 (GRCm39) |
M234K |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Gfi1b |
T |
C |
2: 28,500,125 (GRCm39) |
K302R |
possibly damaging |
Het |
Gpatch1 |
A |
G |
7: 34,994,947 (GRCm39) |
S440P |
probably damaging |
Het |
Gpr6 |
T |
C |
10: 40,947,477 (GRCm39) |
E35G |
probably benign |
Het |
H2-Q1 |
A |
T |
17: 35,542,469 (GRCm39) |
M305L |
probably benign |
Het |
Hoxa10 |
C |
A |
6: 52,211,350 (GRCm39) |
G189C |
possibly damaging |
Het |
Kbtbd4 |
T |
C |
2: 90,737,895 (GRCm39) |
V215A |
probably damaging |
Het |
Klf16 |
G |
A |
10: 80,412,739 (GRCm39) |
A99V |
probably benign |
Het |
Lvrn |
A |
T |
18: 47,011,387 (GRCm39) |
Y448F |
probably benign |
Het |
Med19 |
A |
G |
2: 84,516,002 (GRCm39) |
H177R |
possibly damaging |
Het |
Mif |
G |
T |
10: 75,695,681 (GRCm39) |
H41N |
possibly damaging |
Het |
Mpl |
A |
G |
4: 118,312,936 (GRCm39) |
M132T |
probably benign |
Het |
Mtcl1 |
G |
T |
17: 66,686,409 (GRCm39) |
H480Q |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,908,222 (GRCm39) |
N2017S |
probably benign |
Het |
Neurl4 |
C |
T |
11: 69,797,959 (GRCm39) |
R740C |
probably damaging |
Het |
Nlgn1 |
G |
T |
3: 26,385,939 (GRCm39) |
|
probably benign |
Het |
Or14j7 |
T |
A |
17: 38,234,993 (GRCm39) |
C179S |
probably damaging |
Het |
Or2ak6 |
T |
A |
11: 58,593,172 (GRCm39) |
L215Q |
probably damaging |
Het |
Or4c11 |
A |
C |
2: 88,695,524 (GRCm39) |
M192L |
probably benign |
Het |
Or6c214 |
A |
G |
10: 129,590,584 (GRCm39) |
V245A |
probably damaging |
Het |
Paip1 |
T |
A |
13: 119,593,550 (GRCm39) |
M463K |
probably damaging |
Het |
Parp3 |
T |
A |
9: 106,351,931 (GRCm39) |
Y147F |
probably damaging |
Het |
Pgrmc2 |
C |
A |
3: 41,037,473 (GRCm39) |
|
probably benign |
Het |
Phldb3 |
G |
A |
7: 24,316,832 (GRCm39) |
A278T |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 108,924,715 (GRCm39) |
|
probably null |
Het |
Pom121 |
G |
A |
5: 135,412,740 (GRCm39) |
R481C |
unknown |
Het |
Psg22 |
A |
T |
7: 18,453,635 (GRCm39) |
N149I |
probably damaging |
Het |
Recql5 |
T |
C |
11: 115,788,017 (GRCm39) |
Y434C |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,386,303 (GRCm39) |
S252P |
probably benign |
Het |
Rtl1 |
A |
G |
12: 109,558,354 (GRCm39) |
S1162P |
probably benign |
Het |
Samd9l |
G |
T |
6: 3,376,269 (GRCm39) |
Q331K |
probably benign |
Het |
Sipa1l1 |
T |
C |
12: 82,419,208 (GRCm39) |
Y629H |
probably damaging |
Het |
Slc12a2 |
A |
T |
18: 58,037,425 (GRCm39) |
I512L |
possibly damaging |
Het |
Slc17a8 |
T |
C |
10: 89,413,777 (GRCm39) |
M484V |
probably benign |
Het |
Slc25a24 |
A |
T |
3: 109,043,581 (GRCm39) |
E79D |
probably damaging |
Het |
Snw1 |
T |
A |
12: 87,506,247 (GRCm39) |
I218F |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,221,082 (GRCm39) |
D545G |
probably damaging |
Het |
Sorcs2 |
A |
G |
5: 36,228,731 (GRCm39) |
S104P |
possibly damaging |
Het |
Spry4 |
A |
G |
18: 38,723,142 (GRCm39) |
I207T |
possibly damaging |
Het |
Tex101 |
A |
G |
7: 24,367,650 (GRCm39) |
V234A |
probably benign |
Het |
Thra |
T |
A |
11: 98,653,899 (GRCm39) |
|
probably benign |
Het |
Tmem161b |
T |
A |
13: 84,441,585 (GRCm39) |
L210Q |
probably damaging |
Het |
Tmem50a |
A |
G |
4: 134,630,953 (GRCm39) |
|
probably benign |
Het |
Tmem63b |
A |
G |
17: 45,989,887 (GRCm39) |
|
probably null |
Het |
Tnrc6c |
A |
G |
11: 117,646,849 (GRCm39) |
D1450G |
possibly damaging |
Het |
Trdmt1 |
A |
G |
2: 13,516,420 (GRCm39) |
L386P |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,771,822 (GRCm39) |
S109G |
possibly damaging |
Het |
Trit1 |
T |
C |
4: 122,948,033 (GRCm39) |
I451T |
probably benign |
Het |
Ttn |
T |
A |
2: 76,577,522 (GRCm39) |
D24457V |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,715,834 (GRCm39) |
|
probably benign |
Het |
Tubgcp4 |
A |
T |
2: 121,009,147 (GRCm39) |
|
probably benign |
Het |
Ubiad1 |
A |
G |
4: 148,528,468 (GRCm39) |
L147P |
probably damaging |
Het |
Vps72 |
T |
A |
3: 95,029,851 (GRCm39) |
V290D |
probably benign |
Het |
Zfp408 |
A |
T |
2: 91,480,093 (GRCm39) |
M1K |
probably null |
Het |
Zfy2 |
C |
A |
Y: 2,121,496 (GRCm39) |
M132I |
probably benign |
Het |
|
Other mutations in Ttc34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03000:Ttc34
|
APN |
4 |
154,949,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03034:Ttc34
|
APN |
4 |
154,945,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03139:Ttc34
|
APN |
4 |
154,945,727 (GRCm39) |
missense |
probably benign |
0.04 |
R1205:Ttc34
|
UTSW |
4 |
154,946,671 (GRCm39) |
missense |
probably benign |
0.01 |
R1775:Ttc34
|
UTSW |
4 |
154,946,671 (GRCm39) |
missense |
probably benign |
0.00 |
R1936:Ttc34
|
UTSW |
4 |
154,950,139 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1937:Ttc34
|
UTSW |
4 |
154,950,139 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1939:Ttc34
|
UTSW |
4 |
154,950,139 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1940:Ttc34
|
UTSW |
4 |
154,950,139 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3701:Ttc34
|
UTSW |
4 |
154,949,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R5181:Ttc34
|
UTSW |
4 |
154,946,703 (GRCm39) |
missense |
probably benign |
0.00 |
R5845:Ttc34
|
UTSW |
4 |
154,949,929 (GRCm39) |
missense |
probably benign |
0.08 |
R6603:Ttc34
|
UTSW |
4 |
154,923,762 (GRCm39) |
missense |
probably benign |
0.34 |
R6930:Ttc34
|
UTSW |
4 |
154,923,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R7209:Ttc34
|
UTSW |
4 |
154,923,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R7548:Ttc34
|
UTSW |
4 |
154,940,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:Ttc34
|
UTSW |
4 |
154,945,841 (GRCm39) |
missense |
probably benign |
|
R7727:Ttc34
|
UTSW |
4 |
154,923,731 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7856:Ttc34
|
UTSW |
4 |
154,945,743 (GRCm39) |
missense |
probably benign |
|
R7893:Ttc34
|
UTSW |
4 |
154,945,757 (GRCm39) |
missense |
probably benign |
0.05 |
R7894:Ttc34
|
UTSW |
4 |
154,943,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7982:Ttc34
|
UTSW |
4 |
154,945,875 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9462:Ttc34
|
UTSW |
4 |
154,942,539 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ttc34
|
UTSW |
4 |
154,949,854 (GRCm39) |
missense |
possibly damaging |
0.73 |
|