Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam4 |
T |
C |
12: 81,466,516 (GRCm39) |
K702E |
probably benign |
Het |
Agbl1 |
T |
C |
7: 75,985,069 (GRCm39) |
I162T |
|
Het |
Agpat2 |
A |
T |
2: 26,487,230 (GRCm39) |
I101N |
possibly damaging |
Het |
Amot |
A |
T |
X: 144,244,745 (GRCm39) |
L435H |
|
Het |
Arhgap32 |
G |
A |
9: 32,162,039 (GRCm39) |
R330H |
possibly damaging |
Het |
Asb4 |
T |
A |
6: 5,390,775 (GRCm39) |
I56N |
probably benign |
Het |
Atp2a2 |
C |
T |
5: 122,604,087 (GRCm39) |
V449M |
possibly damaging |
Het |
Bend4 |
A |
G |
5: 67,575,080 (GRCm39) |
L267P |
probably damaging |
Het |
Catspere2 |
T |
A |
1: 177,967,949 (GRCm39) |
N745K |
probably benign |
Het |
Celf2 |
A |
G |
2: 6,554,646 (GRCm39) |
F484L |
possibly damaging |
Het |
Chd3 |
T |
C |
11: 69,241,648 (GRCm39) |
D1495G |
possibly damaging |
Het |
Chrna3 |
A |
T |
9: 54,933,671 (GRCm39) |
V8D |
unknown |
Het |
Cog3 |
T |
C |
14: 75,966,802 (GRCm39) |
Y466C |
probably damaging |
Het |
Col5a1 |
A |
G |
2: 27,841,363 (GRCm39) |
E328G |
unknown |
Het |
Col7a1 |
A |
G |
9: 108,785,707 (GRCm39) |
Y392C |
unknown |
Het |
Crtc3 |
A |
T |
7: 80,248,697 (GRCm39) |
N255K |
probably damaging |
Het |
Dnaaf1 |
T |
C |
8: 120,302,195 (GRCm39) |
I32T |
probably benign |
Het |
Dner |
A |
T |
1: 84,512,647 (GRCm39) |
C307S |
probably damaging |
Het |
Dzip3 |
T |
C |
16: 48,772,401 (GRCm39) |
K423E |
possibly damaging |
Het |
Eif2b4 |
A |
G |
5: 31,345,393 (GRCm39) |
S414P |
probably damaging |
Het |
Elp4 |
T |
C |
2: 105,624,891 (GRCm39) |
E334G |
probably damaging |
Het |
Emilin2 |
T |
A |
17: 71,587,689 (GRCm39) |
N141I |
probably benign |
Het |
Fstl1 |
T |
A |
16: 37,647,140 (GRCm39) |
V170E |
probably damaging |
Het |
Fxn |
A |
G |
19: 24,244,687 (GRCm39) |
I151T |
probably damaging |
Het |
Gtf3c4 |
A |
T |
2: 28,730,214 (GRCm39) |
V9E |
possibly damaging |
Het |
Ino80d |
A |
G |
1: 63,132,607 (GRCm39) |
S19P |
probably damaging |
Het |
Kank3 |
T |
G |
17: 34,037,242 (GRCm39) |
L370R |
probably damaging |
Het |
Large1 |
T |
A |
8: 73,542,645 (GRCm39) |
Y693F |
probably benign |
Het |
Lig4 |
C |
A |
8: 10,022,202 (GRCm39) |
W526L |
probably damaging |
Het |
Mib1 |
C |
T |
18: 10,726,437 (GRCm39) |
P45S |
probably benign |
Het |
Ndufaf6 |
T |
C |
4: 11,070,301 (GRCm39) |
K107E |
probably benign |
Het |
Nf1 |
T |
C |
11: 79,436,291 (GRCm39) |
L1977P |
probably damaging |
Het |
Nme4 |
G |
T |
17: 26,314,389 (GRCm39) |
A13E |
probably benign |
Het |
Or52s6 |
G |
A |
7: 103,091,850 (GRCm39) |
P160L |
probably damaging |
Het |
Or52z15 |
T |
A |
7: 103,332,404 (GRCm39) |
F160I |
probably benign |
Het |
Pappa |
G |
A |
4: 65,258,962 (GRCm39) |
R1570Q |
probably damaging |
Het |
Parp6 |
G |
A |
9: 59,531,213 (GRCm39) |
A32T |
|
Het |
Pclo |
A |
G |
5: 14,731,068 (GRCm39) |
Q64R |
|
Het |
Pde8a |
C |
T |
7: 80,982,619 (GRCm39) |
T746I |
probably damaging |
Het |
Perm1 |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
4: 156,302,525 (GRCm39) |
|
probably benign |
Het |
Pramel21 |
T |
C |
4: 143,341,600 (GRCm39) |
S10P |
possibly damaging |
Het |
Prdm13 |
C |
G |
4: 21,679,659 (GRCm39) |
R277P |
unknown |
Het |
Prf1 |
A |
C |
10: 61,136,216 (GRCm39) |
D164A |
probably damaging |
Het |
Rarres1 |
A |
G |
3: 67,386,924 (GRCm39) |
V226A |
probably damaging |
Het |
Rest |
GGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGAGCCTGCCCCTCCCACGGGGC |
GGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGAGCCTGCCCCTCCCACGGGGC |
5: 77,429,651 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
A |
G |
9: 107,948,375 (GRCm39) |
L106P |
probably damaging |
Het |
Scnn1b |
A |
T |
7: 121,511,326 (GRCm39) |
T338S |
probably benign |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,103,384 (GRCm39) |
|
probably benign |
Het |
Slc9a5 |
T |
C |
8: 106,080,139 (GRCm39) |
V94A |
probably damaging |
Het |
Slco4a1 |
A |
G |
2: 180,106,478 (GRCm39) |
D220G |
probably benign |
Het |
Spata31e2 |
T |
A |
1: 26,723,485 (GRCm39) |
Q565L |
possibly damaging |
Het |
Sult1c2 |
T |
C |
17: 54,269,200 (GRCm39) |
D272G |
possibly damaging |
Het |
Tgm1 |
T |
C |
14: 55,946,355 (GRCm39) |
N427S |
probably damaging |
Het |
Themis |
C |
A |
10: 28,658,233 (GRCm39) |
T420N |
probably benign |
Het |
Tnni3 |
A |
T |
7: 4,521,376 (GRCm39) |
F209L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,745,912 (GRCm39) |
S5046C |
probably damaging |
Het |
Tubb2a |
T |
A |
13: 34,260,628 (GRCm39) |
I24L |
probably benign |
Het |
Uevld |
C |
A |
7: 46,587,746 (GRCm39) |
G318V |
probably damaging |
Het |
Unkl |
T |
C |
17: 25,448,350 (GRCm39) |
S308P |
probably benign |
Het |
Vmn1r159 |
C |
A |
7: 22,542,765 (GRCm39) |
C89F |
probably damaging |
Het |
Wee2 |
T |
G |
6: 40,437,977 (GRCm39) |
S302A |
probably benign |
Het |
Ydjc |
T |
C |
16: 16,965,666 (GRCm39) |
C144R |
probably benign |
Het |
Zc3h12c |
A |
G |
9: 52,027,419 (GRCm39) |
S667P |
probably benign |
Het |
Zfp280b |
T |
A |
10: 75,874,651 (GRCm39) |
Y177N |
probably benign |
Het |
|
Other mutations in Zfp354b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02029:Zfp354b
|
APN |
11 |
50,814,664 (GRCm39) |
missense |
probably benign |
|
R1299:Zfp354b
|
UTSW |
11 |
50,814,297 (GRCm39) |
missense |
probably benign |
0.04 |
R1353:Zfp354b
|
UTSW |
11 |
50,814,240 (GRCm39) |
missense |
probably damaging |
0.96 |
R1860:Zfp354b
|
UTSW |
11 |
50,814,369 (GRCm39) |
missense |
probably benign |
|
R2072:Zfp354b
|
UTSW |
11 |
50,813,279 (GRCm39) |
nonsense |
probably null |
|
R5221:Zfp354b
|
UTSW |
11 |
50,813,917 (GRCm39) |
missense |
probably benign |
0.00 |
R5231:Zfp354b
|
UTSW |
11 |
50,813,917 (GRCm39) |
missense |
probably benign |
0.00 |
R5258:Zfp354b
|
UTSW |
11 |
50,813,917 (GRCm39) |
missense |
probably benign |
0.00 |
R5775:Zfp354b
|
UTSW |
11 |
50,813,647 (GRCm39) |
missense |
probably benign |
0.00 |
R5847:Zfp354b
|
UTSW |
11 |
50,814,043 (GRCm39) |
missense |
probably damaging |
0.96 |
R5929:Zfp354b
|
UTSW |
11 |
50,813,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R6443:Zfp354b
|
UTSW |
11 |
50,813,581 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6748:Zfp354b
|
UTSW |
11 |
50,813,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Zfp354b
|
UTSW |
11 |
50,813,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7706:Zfp354b
|
UTSW |
11 |
50,819,390 (GRCm39) |
critical splice donor site |
probably null |
|
R7819:Zfp354b
|
UTSW |
11 |
50,814,632 (GRCm39) |
nonsense |
probably null |
|
R7830:Zfp354b
|
UTSW |
11 |
50,814,136 (GRCm39) |
missense |
probably benign |
0.28 |
R8508:Zfp354b
|
UTSW |
11 |
50,814,297 (GRCm39) |
missense |
probably benign |
0.04 |
R9157:Zfp354b
|
UTSW |
11 |
50,813,887 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9303:Zfp354b
|
UTSW |
11 |
50,820,256 (GRCm39) |
missense |
probably damaging |
0.97 |
R9462:Zfp354b
|
UTSW |
11 |
50,814,523 (GRCm39) |
missense |
probably benign |
|
|