Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankef1 |
T |
A |
2: 136,395,594 (GRCm39) |
D641E |
probably benign |
Het |
Anln |
A |
G |
9: 22,272,116 (GRCm39) |
|
probably null |
Het |
Areg |
A |
T |
5: 91,292,217 (GRCm39) |
E172D |
probably damaging |
Het |
Ccdc51 |
A |
T |
9: 108,918,482 (GRCm39) |
T24S |
probably benign |
Het |
Cckar |
A |
T |
5: 53,860,424 (GRCm39) |
I135N |
probably damaging |
Het |
Cdca7 |
CGAGGAAGAGGAGGAGGAAGAGGAGGAGGAAGAGGA |
CGAGGAAGAGGAGGAGGAAGAGGA |
2: 72,313,821 (GRCm39) |
|
probably benign |
Het |
Cep295 |
T |
C |
9: 15,235,551 (GRCm39) |
H2056R |
possibly damaging |
Het |
Chrnb2 |
T |
C |
3: 89,664,562 (GRCm39) |
K451E |
probably damaging |
Het |
Ctnna2 |
C |
T |
6: 76,919,249 (GRCm39) |
R663Q |
probably benign |
Het |
Cyp4f37 |
A |
T |
17: 32,853,253 (GRCm39) |
I406F |
probably benign |
Het |
Eml4 |
T |
A |
17: 83,734,640 (GRCm39) |
|
probably benign |
Het |
Fkrp |
G |
T |
7: 16,544,569 (GRCm39) |
T431K |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,806,180 (GRCm39) |
Y833F |
possibly damaging |
Het |
Galnt2 |
T |
C |
8: 125,058,837 (GRCm39) |
|
probably null |
Het |
Gm8180 |
T |
A |
14: 44,019,806 (GRCm39) |
|
probably null |
Het |
Hcn1 |
T |
C |
13: 118,108,171 (GRCm39) |
S552P |
unknown |
Het |
Ifit1 |
A |
C |
19: 34,625,887 (GRCm39) |
E341A |
possibly damaging |
Het |
Iyd |
A |
G |
10: 3,490,250 (GRCm39) |
|
probably benign |
Het |
Krt72 |
A |
T |
15: 101,694,836 (GRCm39) |
S20T |
probably damaging |
Het |
Lemd2 |
G |
T |
17: 27,423,069 (GRCm39) |
D108E |
probably benign |
Het |
Lipn |
A |
T |
19: 34,054,376 (GRCm39) |
I205F |
possibly damaging |
Het |
Nat1 |
G |
T |
8: 67,943,723 (GRCm39) |
R36L |
probably benign |
Het |
Nebl |
A |
T |
2: 17,415,907 (GRCm39) |
M334K |
possibly damaging |
Het |
Nectin4 |
A |
T |
1: 171,214,351 (GRCm39) |
N502I |
probably damaging |
Het |
Nrp1 |
G |
A |
8: 129,214,389 (GRCm39) |
V626I |
probably benign |
Het |
Oprm1 |
G |
A |
10: 6,773,914 (GRCm39) |
|
probably benign |
Het |
Or52w1 |
A |
G |
7: 105,017,680 (GRCm39) |
Y49C |
probably damaging |
Het |
Or8a1b |
C |
T |
9: 37,623,204 (GRCm39) |
V124M |
probably damaging |
Het |
Pde2a |
A |
G |
7: 101,156,927 (GRCm39) |
Y637C |
probably damaging |
Het |
Pde4d |
T |
C |
13: 110,071,924 (GRCm39) |
V306A |
probably damaging |
Het |
Pdzd9 |
G |
A |
7: 120,269,498 (GRCm39) |
|
probably benign |
Het |
Pitpnm3 |
T |
A |
11: 71,947,017 (GRCm39) |
D810V |
probably damaging |
Het |
Pkd1l3 |
A |
T |
8: 110,392,304 (GRCm39) |
H1966L |
probably benign |
Het |
Pmfbp1 |
C |
T |
8: 110,247,661 (GRCm39) |
T319I |
possibly damaging |
Het |
Pramel28 |
T |
C |
4: 143,692,314 (GRCm39) |
Q229R |
probably benign |
Het |
Prb1c |
G |
C |
6: 132,338,856 (GRCm39) |
Q121E |
unknown |
Het |
Psg18 |
T |
A |
7: 18,087,450 (GRCm39) |
R69S |
possibly damaging |
Het |
Ptprg |
A |
T |
14: 12,213,638 (GRCm38) |
Q1002L |
possibly damaging |
Het |
Ptprj |
T |
C |
2: 90,290,984 (GRCm39) |
Y585C |
probably damaging |
Het |
Rad51c |
T |
C |
11: 87,293,542 (GRCm39) |
T105A |
probably benign |
Het |
Rbm12 |
A |
T |
2: 155,937,481 (GRCm39) |
D930E |
unknown |
Het |
Rlf |
A |
C |
4: 121,007,784 (GRCm39) |
S509A |
possibly damaging |
Het |
Slc39a3 |
C |
A |
10: 80,869,499 (GRCm39) |
G53C |
probably damaging |
Het |
Smchd1 |
G |
A |
17: 71,670,017 (GRCm39) |
Q1685* |
probably null |
Het |
Sprr2d |
A |
C |
3: 92,247,715 (GRCm39) |
E52A |
unknown |
Het |
Stat1 |
A |
G |
1: 52,182,086 (GRCm39) |
N355S |
probably damaging |
Het |
Tmem30b |
T |
C |
12: 73,592,923 (GRCm39) |
E64G |
probably benign |
Het |
Ttll11 |
A |
T |
2: 35,869,392 (GRCm39) |
V82D |
probably benign |
Het |
Ttn |
T |
A |
2: 76,570,977 (GRCm39) |
T26639S |
probably damaging |
Het |
Usp53 |
A |
T |
3: 122,727,725 (GRCm39) |
N952K |
probably benign |
Het |
Vmn1r199 |
T |
A |
13: 22,567,724 (GRCm39) |
H339Q |
possibly damaging |
Het |
Vps13b |
G |
A |
15: 35,422,537 (GRCm39) |
D166N |
probably damaging |
Het |
|
Other mutations in Zfp954 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00588:Zfp954
|
APN |
7 |
7,118,366 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01696:Zfp954
|
APN |
7 |
7,118,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Zfp954
|
UTSW |
7 |
7,118,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R1723:Zfp954
|
UTSW |
7 |
7,118,837 (GRCm39) |
missense |
probably benign |
0.04 |
R2112:Zfp954
|
UTSW |
7 |
7,118,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Zfp954
|
UTSW |
7 |
7,118,321 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2410:Zfp954
|
UTSW |
7 |
7,120,808 (GRCm39) |
missense |
probably benign |
0.03 |
R5118:Zfp954
|
UTSW |
7 |
7,118,714 (GRCm39) |
missense |
probably benign |
0.05 |
R5191:Zfp954
|
UTSW |
7 |
7,119,022 (GRCm39) |
missense |
probably damaging |
0.96 |
R5832:Zfp954
|
UTSW |
7 |
7,118,389 (GRCm39) |
missense |
probably damaging |
0.97 |
R5851:Zfp954
|
UTSW |
7 |
7,118,624 (GRCm39) |
nonsense |
probably null |
|
R7633:Zfp954
|
UTSW |
7 |
7,118,823 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7646:Zfp954
|
UTSW |
7 |
7,118,720 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7710:Zfp954
|
UTSW |
7 |
7,120,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Zfp954
|
UTSW |
7 |
7,118,470 (GRCm39) |
missense |
probably benign |
0.02 |
R9192:Zfp954
|
UTSW |
7 |
7,118,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|