Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
C |
11: 84,255,275 (GRCm39) |
|
probably null |
Het |
Afg2a |
T |
G |
3: 37,474,620 (GRCm39) |
M44R |
probably benign |
Het |
Ankef1 |
C |
A |
2: 136,395,618 (GRCm39) |
N649K |
probably benign |
Het |
Arl5b |
T |
A |
2: 15,079,869 (GRCm39) |
S147T |
probably damaging |
Het |
Arnt2 |
A |
T |
7: 83,918,155 (GRCm39) |
|
probably null |
Het |
Ash1l |
A |
G |
3: 88,890,932 (GRCm39) |
E937G |
possibly damaging |
Het |
Asxl1 |
T |
G |
2: 153,241,854 (GRCm39) |
S802R |
possibly damaging |
Het |
Cacna1h |
T |
A |
17: 25,611,250 (GRCm39) |
H516L |
probably damaging |
Het |
Cad |
A |
G |
5: 31,218,829 (GRCm39) |
Y550C |
probably damaging |
Het |
Cdo1 |
A |
G |
18: 46,861,157 (GRCm39) |
I18T |
probably benign |
Het |
Cfap251 |
A |
T |
5: 123,460,517 (GRCm39) |
I1160F |
probably damaging |
Het |
Chd2 |
A |
G |
7: 73,169,223 (GRCm39) |
|
probably null |
Het |
Dbf4 |
A |
G |
5: 8,458,232 (GRCm39) |
|
probably null |
Het |
Dcdc2a |
A |
T |
13: 25,286,361 (GRCm39) |
R132W |
possibly damaging |
Het |
Dnah10 |
T |
C |
5: 124,859,425 (GRCm39) |
S2131P |
probably damaging |
Het |
Eef2k |
A |
G |
7: 120,494,441 (GRCm39) |
Y599C |
probably damaging |
Het |
Eno2 |
C |
T |
6: 124,744,225 (GRCm39) |
|
probably null |
Het |
Fam124b |
T |
A |
1: 80,191,512 (GRCm39) |
|
probably benign |
Het |
Fezf2 |
A |
G |
14: 12,342,701 (GRCm38) |
I388T |
possibly damaging |
Het |
Gbp11 |
T |
C |
5: 105,472,798 (GRCm39) |
N542S |
probably benign |
Het |
Gdpd1 |
T |
A |
11: 86,932,639 (GRCm39) |
I229F |
probably damaging |
Het |
Gria1 |
T |
A |
11: 57,133,591 (GRCm39) |
V490E |
probably damaging |
Het |
Grm8 |
G |
A |
6: 27,762,422 (GRCm39) |
R268C |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,469,880 (GRCm39) |
S2592T |
probably benign |
Het |
Herpud1 |
C |
T |
8: 95,118,828 (GRCm39) |
T194I |
probably benign |
Het |
Hspa1b |
T |
C |
17: 35,177,167 (GRCm39) |
T273A |
probably benign |
Het |
Iftap |
T |
A |
2: 101,416,747 (GRCm39) |
K67N |
probably benign |
Het |
Ighm |
T |
A |
12: 113,384,873 (GRCm39) |
K327* |
probably null |
Het |
Igkv3-4 |
A |
T |
6: 70,649,297 (GRCm39) |
I99F |
probably damaging |
Het |
Iqca1l |
T |
C |
5: 24,758,643 (GRCm39) |
E117G |
probably damaging |
Het |
Isl2 |
C |
A |
9: 55,449,723 (GRCm39) |
S97R |
probably benign |
Het |
Klhl12 |
A |
T |
1: 134,386,219 (GRCm39) |
I4F |
probably benign |
Het |
Lgalsl2 |
G |
A |
7: 5,362,441 (GRCm39) |
R24H |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,271,710 (GRCm39) |
E4074G |
probably benign |
Het |
Mcm3ap |
A |
G |
10: 76,342,441 (GRCm39) |
N1645D |
probably damaging |
Het |
Mettl23 |
T |
C |
11: 116,736,679 (GRCm39) |
|
probably benign |
Het |
Mettl24 |
A |
G |
10: 40,686,478 (GRCm39) |
E285G |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,196,246 (GRCm39) |
L506P |
probably benign |
Het |
Mup18 |
G |
T |
4: 61,590,925 (GRCm39) |
|
probably null |
Het |
Myom1 |
T |
C |
17: 71,352,747 (GRCm39) |
L357P |
probably benign |
Het |
Nkx2-9 |
G |
A |
12: 56,659,031 (GRCm39) |
A61V |
probably benign |
Het |
Or52n5 |
C |
T |
7: 104,588,573 (GRCm39) |
A280V |
probably damaging |
Het |
Pbx1 |
A |
T |
1: 168,012,616 (GRCm39) |
M340K |
probably benign |
Het |
Pcdhb17 |
A |
T |
18: 37,618,233 (GRCm39) |
N8Y |
probably benign |
Het |
Pex13 |
C |
A |
11: 23,600,929 (GRCm39) |
|
probably null |
Het |
Pierce1 |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
2: 28,356,122 (GRCm39) |
|
probably benign |
Het |
Plxnb1 |
A |
G |
9: 108,943,408 (GRCm39) |
R1884G |
probably damaging |
Het |
Polq |
T |
A |
16: 36,865,245 (GRCm39) |
V699E |
probably damaging |
Het |
Ppl |
C |
T |
16: 4,906,725 (GRCm39) |
R1190H |
probably damaging |
Het |
Prr14l |
A |
T |
5: 32,987,310 (GRCm39) |
H728Q |
probably benign |
Het |
Prss12 |
T |
C |
3: 123,300,145 (GRCm39) |
V752A |
possibly damaging |
Het |
Prss56 |
A |
G |
1: 87,111,921 (GRCm39) |
S51G |
probably benign |
Het |
Pwp2 |
G |
A |
10: 78,009,240 (GRCm39) |
R854W |
probably damaging |
Het |
Rhobtb2 |
C |
T |
14: 70,033,746 (GRCm39) |
C493Y |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rusf1 |
C |
A |
7: 127,897,177 (GRCm39) |
A27S |
probably benign |
Het |
Scap |
A |
G |
9: 110,213,811 (GRCm39) |
N1258S |
possibly damaging |
Het |
Sec31a |
C |
T |
5: 100,547,336 (GRCm39) |
G218R |
probably damaging |
Het |
Siglec15 |
A |
T |
18: 78,086,914 (GRCm39) |
M315K |
probably benign |
Het |
Slc17a6 |
G |
A |
7: 51,308,573 (GRCm39) |
|
probably null |
Het |
Smchd1 |
T |
C |
17: 71,684,813 (GRCm39) |
|
probably null |
Het |
Spag4 |
A |
T |
2: 155,911,244 (GRCm39) |
D393V |
probably damaging |
Het |
Sulf1 |
A |
G |
1: 12,875,518 (GRCm39) |
N176S |
probably damaging |
Het |
Tmem9 |
T |
A |
1: 135,955,125 (GRCm39) |
|
probably null |
Het |
Tnpo3 |
T |
C |
6: 29,565,223 (GRCm39) |
I577V |
probably benign |
Het |
Tti1 |
A |
C |
2: 157,835,390 (GRCm39) |
I956S |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,344,725 (GRCm39) |
R181G |
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,012,995 (GRCm39) |
C1654S |
probably damaging |
Het |
Znrf4 |
A |
G |
17: 56,818,681 (GRCm39) |
C209R |
probably damaging |
Het |
Zzef1 |
T |
G |
11: 72,687,373 (GRCm39) |
L84R |
probably damaging |
Het |
|
Other mutations in Zfp74 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0355:Zfp74
|
UTSW |
7 |
29,653,466 (GRCm39) |
start gained |
probably benign |
|
R0387:Zfp74
|
UTSW |
7 |
29,634,179 (GRCm39) |
missense |
probably benign |
0.05 |
R0948:Zfp74
|
UTSW |
7 |
29,635,362 (GRCm39) |
critical splice donor site |
probably null |
|
R1757:Zfp74
|
UTSW |
7 |
29,634,486 (GRCm39) |
missense |
probably benign |
0.01 |
R1813:Zfp74
|
UTSW |
7 |
29,634,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Zfp74
|
UTSW |
7 |
29,635,470 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1896:Zfp74
|
UTSW |
7 |
29,634,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Zfp74
|
UTSW |
7 |
29,635,136 (GRCm39) |
missense |
probably benign |
0.08 |
R2092:Zfp74
|
UTSW |
7 |
29,653,349 (GRCm39) |
start gained |
probably benign |
|
R2111:Zfp74
|
UTSW |
7 |
29,634,443 (GRCm39) |
nonsense |
probably null |
|
R4894:Zfp74
|
UTSW |
7 |
29,635,470 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R5121:Zfp74
|
UTSW |
7 |
29,631,932 (GRCm39) |
splice site |
probably null |
|
R5123:Zfp74
|
UTSW |
7 |
29,634,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5129:Zfp74
|
UTSW |
7 |
29,631,880 (GRCm39) |
missense |
probably benign |
0.00 |
R5213:Zfp74
|
UTSW |
7 |
29,634,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Zfp74
|
UTSW |
7 |
29,635,316 (GRCm39) |
missense |
probably benign |
0.04 |
R5519:Zfp74
|
UTSW |
7 |
29,634,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R5589:Zfp74
|
UTSW |
7 |
29,633,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R6287:Zfp74
|
UTSW |
7 |
29,635,201 (GRCm39) |
missense |
probably benign |
|
R6330:Zfp74
|
UTSW |
7 |
29,637,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6370:Zfp74
|
UTSW |
7 |
29,631,835 (GRCm39) |
missense |
probably damaging |
0.96 |
R6407:Zfp74
|
UTSW |
7 |
29,635,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R6694:Zfp74
|
UTSW |
7 |
29,634,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R6791:Zfp74
|
UTSW |
7 |
29,633,860 (GRCm39) |
missense |
probably benign |
0.02 |
R7144:Zfp74
|
UTSW |
7 |
29,634,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R7662:Zfp74
|
UTSW |
7 |
29,653,278 (GRCm39) |
critical splice donor site |
probably null |
|
R7667:Zfp74
|
UTSW |
7 |
29,634,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R7940:Zfp74
|
UTSW |
7 |
29,631,867 (GRCm39) |
missense |
probably benign |
0.07 |
R8676:Zfp74
|
UTSW |
7 |
29,634,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Zfp74
|
UTSW |
7 |
29,634,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Zfp74
|
UTSW |
7 |
29,634,772 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9748:Zfp74
|
UTSW |
7 |
29,634,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R9764:Zfp74
|
UTSW |
7 |
29,631,845 (GRCm39) |
missense |
probably benign |
0.11 |
|