Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
G |
A |
7: 12,246,809 (GRCm39) |
R63Q |
probably benign |
Het |
Adamts20 |
A |
T |
15: 94,243,871 (GRCm39) |
C619S |
probably damaging |
Het |
Alx1 |
T |
C |
10: 102,861,165 (GRCm39) |
D121G |
possibly damaging |
Het |
Anks3 |
A |
C |
16: 4,771,748 (GRCm39) |
M215R |
probably benign |
Het |
Anxa4 |
T |
A |
6: 86,718,893 (GRCm39) |
|
probably null |
Het |
Arhgef25 |
A |
G |
10: 127,021,733 (GRCm39) |
V222A |
probably damaging |
Het |
Bglap2 |
A |
G |
3: 88,285,932 (GRCm39) |
|
probably benign |
Het |
Cars2 |
A |
G |
8: 11,564,674 (GRCm39) |
V22A |
probably benign |
Het |
Ccdc198 |
G |
T |
14: 49,473,420 (GRCm39) |
L102I |
probably damaging |
Het |
Cenpe |
T |
A |
3: 134,945,606 (GRCm39) |
I1040N |
probably damaging |
Het |
Cep170 |
C |
T |
1: 176,583,335 (GRCm39) |
D1015N |
probably damaging |
Het |
Chia1 |
T |
A |
3: 106,038,181 (GRCm39) |
I359N |
probably damaging |
Het |
Crot |
A |
T |
5: 9,038,248 (GRCm39) |
V93E |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dnmbp |
T |
C |
19: 43,891,186 (GRCm39) |
I194V |
probably damaging |
Het |
Dock4 |
T |
A |
12: 40,783,267 (GRCm39) |
C734S |
probably benign |
Het |
Eif4e3 |
T |
C |
6: 99,617,662 (GRCm39) |
S70G |
probably benign |
Het |
Entpd3 |
G |
A |
9: 120,387,441 (GRCm39) |
D213N |
probably benign |
Het |
Ern2 |
T |
G |
7: 121,775,759 (GRCm39) |
Y445S |
probably benign |
Het |
Fasn |
A |
G |
11: 120,704,133 (GRCm39) |
S1429P |
probably benign |
Het |
Fat4 |
A |
G |
3: 39,036,532 (GRCm39) |
I3395V |
probably benign |
Het |
Fbln2 |
C |
A |
6: 91,233,399 (GRCm39) |
Q628K |
possibly damaging |
Het |
Fbxo28 |
T |
C |
1: 182,153,845 (GRCm39) |
N164D |
probably benign |
Het |
Fez1 |
T |
C |
9: 36,779,063 (GRCm39) |
S247P |
probably damaging |
Het |
Gars1 |
A |
G |
6: 55,040,153 (GRCm39) |
D360G |
probably benign |
Het |
Gcfc2 |
A |
T |
6: 81,933,873 (GRCm39) |
Q710L |
probably damaging |
Het |
Ggt5 |
A |
G |
10: 75,446,376 (GRCm39) |
|
probably null |
Het |
Glp1r |
A |
G |
17: 31,148,909 (GRCm39) |
|
probably null |
Het |
Hspa14 |
T |
C |
2: 3,492,697 (GRCm39) |
D356G |
possibly damaging |
Het |
Htt |
T |
A |
5: 35,006,288 (GRCm39) |
I1399N |
probably damaging |
Het |
Kmt2e |
G |
A |
5: 23,704,484 (GRCm39) |
|
probably benign |
Het |
Krt36 |
C |
A |
11: 99,996,374 (GRCm39) |
G17C |
probably damaging |
Het |
Lama2 |
T |
C |
10: 27,088,092 (GRCm39) |
E895G |
probably damaging |
Het |
Lamb2 |
G |
A |
9: 108,364,586 (GRCm39) |
R1142H |
probably benign |
Het |
Lhcgr |
C |
T |
17: 89,072,575 (GRCm39) |
|
probably null |
Het |
Lpin2 |
A |
G |
17: 71,532,064 (GRCm39) |
T140A |
probably benign |
Het |
Metap1 |
A |
G |
3: 138,186,443 (GRCm39) |
|
probably benign |
Het |
Mpeg1 |
T |
C |
19: 12,440,486 (GRCm39) |
V648A |
probably benign |
Het |
Mroh2a |
A |
G |
1: 88,186,386 (GRCm39) |
S64G |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,752,369 (GRCm38) |
I749N |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,965,862 (GRCm39) |
F1304L |
probably damaging |
Het |
Nup85 |
A |
G |
11: 115,459,239 (GRCm39) |
E114G |
probably benign |
Het |
Or2a5 |
A |
G |
6: 42,874,254 (GRCm39) |
S290G |
probably damaging |
Het |
Or4c10 |
A |
G |
2: 89,761,010 (GRCm39) |
T286A |
possibly damaging |
Het |
Or6b2b |
A |
T |
1: 92,418,822 (GRCm39) |
Y218* |
probably null |
Het |
Pafah2 |
GCCCC |
GCCCCC |
4: 134,152,852 (GRCm39) |
|
probably null |
Het |
Parp2 |
T |
A |
14: 51,052,843 (GRCm39) |
C145* |
probably null |
Het |
Plpp6 |
T |
C |
19: 28,941,680 (GRCm39) |
S94P |
probably benign |
Het |
Polr1a |
T |
C |
6: 71,953,172 (GRCm39) |
I1580T |
probably damaging |
Het |
Polrmt |
A |
T |
10: 79,574,043 (GRCm39) |
V860E |
probably damaging |
Het |
Ppp1r17 |
A |
G |
6: 55,999,412 (GRCm39) |
E15G |
possibly damaging |
Het |
Prl7b1 |
A |
T |
13: 27,786,831 (GRCm39) |
W133R |
probably damaging |
Het |
Ptk7 |
A |
G |
17: 46,887,416 (GRCm39) |
|
probably null |
Het |
Rad23b |
C |
T |
4: 55,383,637 (GRCm39) |
Q290* |
probably null |
Het |
Rorb |
C |
T |
19: 18,932,445 (GRCm39) |
E369K |
probably damaging |
Het |
Rusc1 |
T |
C |
3: 88,999,452 (GRCm39) |
D110G |
probably damaging |
Het |
Smg7 |
A |
G |
1: 152,724,601 (GRCm39) |
S527P |
probably damaging |
Het |
Ssbp2 |
C |
T |
13: 91,812,268 (GRCm39) |
P105L |
probably damaging |
Het |
Stt3a |
C |
T |
9: 36,674,681 (GRCm39) |
R34H |
probably damaging |
Het |
Sufu |
T |
A |
19: 46,439,386 (GRCm39) |
I202N |
possibly damaging |
Het |
Thsd7b |
G |
A |
1: 129,540,993 (GRCm39) |
R289Q |
probably damaging |
Het |
Tph1 |
A |
T |
7: 46,309,863 (GRCm39) |
S130T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,776,030 (GRCm39) |
S1671P |
probably damaging |
Het |
Usp4 |
A |
G |
9: 108,249,935 (GRCm39) |
I441V |
probably benign |
Het |
Vmn1r8 |
A |
G |
6: 57,013,413 (GRCm39) |
N155D |
probably benign |
Het |
Vmn2r115 |
A |
C |
17: 23,578,357 (GRCm39) |
K610T |
probably damaging |
Het |
Vmn2r62 |
G |
A |
7: 42,438,546 (GRCm39) |
P97S |
probably damaging |
Het |
Zbtb40 |
T |
C |
4: 136,735,150 (GRCm39) |
D297G |
probably benign |
Het |
Zfp174 |
C |
A |
16: 3,672,599 (GRCm39) |
Q383K |
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,724,592 (GRCm39) |
D2198E |
probably benign |
Het |
Zgrf1 |
T |
A |
3: 127,409,112 (GRCm39) |
N1695K |
probably damaging |
Het |
|
Other mutations in Zfp628 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00849:Zfp628
|
APN |
7 |
4,923,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Zfp628
|
UTSW |
7 |
4,923,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Zfp628
|
UTSW |
7 |
4,922,732 (GRCm39) |
missense |
probably benign |
|
R0450:Zfp628
|
UTSW |
7 |
4,922,732 (GRCm39) |
missense |
probably benign |
|
R0469:Zfp628
|
UTSW |
7 |
4,922,732 (GRCm39) |
missense |
probably benign |
|
R0480:Zfp628
|
UTSW |
7 |
4,924,615 (GRCm39) |
missense |
probably benign |
0.00 |
R0518:Zfp628
|
UTSW |
7 |
4,922,939 (GRCm39) |
missense |
probably damaging |
0.97 |
R0521:Zfp628
|
UTSW |
7 |
4,922,939 (GRCm39) |
missense |
probably damaging |
0.97 |
R1081:Zfp628
|
UTSW |
7 |
4,923,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Zfp628
|
UTSW |
7 |
4,923,767 (GRCm39) |
missense |
probably benign |
0.00 |
R1997:Zfp628
|
UTSW |
7 |
4,921,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R2221:Zfp628
|
UTSW |
7 |
4,923,830 (GRCm39) |
missense |
probably benign |
0.00 |
R2364:Zfp628
|
UTSW |
7 |
4,923,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R3077:Zfp628
|
UTSW |
7 |
4,924,199 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3964:Zfp628
|
UTSW |
7 |
4,924,744 (GRCm39) |
missense |
probably benign |
0.00 |
R3966:Zfp628
|
UTSW |
7 |
4,924,744 (GRCm39) |
missense |
probably benign |
0.00 |
R6058:Zfp628
|
UTSW |
7 |
4,923,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Zfp628
|
UTSW |
7 |
4,922,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6516:Zfp628
|
UTSW |
7 |
4,923,201 (GRCm39) |
nonsense |
probably null |
|
R6962:Zfp628
|
UTSW |
7 |
4,922,549 (GRCm39) |
missense |
probably benign |
0.03 |
R7180:Zfp628
|
UTSW |
7 |
4,924,063 (GRCm39) |
missense |
probably benign |
0.18 |
R7347:Zfp628
|
UTSW |
7 |
4,924,817 (GRCm39) |
missense |
probably damaging |
0.99 |
R7348:Zfp628
|
UTSW |
7 |
4,924,817 (GRCm39) |
missense |
probably damaging |
0.99 |
R7349:Zfp628
|
UTSW |
7 |
4,924,817 (GRCm39) |
missense |
probably damaging |
0.99 |
R8016:Zfp628
|
UTSW |
7 |
4,922,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R8074:Zfp628
|
UTSW |
7 |
4,923,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R8161:Zfp628
|
UTSW |
7 |
4,921,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R8328:Zfp628
|
UTSW |
7 |
4,922,813 (GRCm39) |
missense |
probably benign |
|
R9116:Zfp628
|
UTSW |
7 |
4,924,202 (GRCm39) |
missense |
probably benign |
0.06 |
R9158:Zfp628
|
UTSW |
7 |
4,922,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R9251:Zfp628
|
UTSW |
7 |
4,923,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Zfp628
|
UTSW |
7 |
4,922,549 (GRCm39) |
missense |
probably benign |
|
RF018:Zfp628
|
UTSW |
7 |
4,923,948 (GRCm39) |
unclassified |
probably benign |
|
X0022:Zfp628
|
UTSW |
7 |
4,922,408 (GRCm39) |
missense |
probably damaging |
1.00 |
|