Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
C |
T |
5: 4,114,086 (GRCm39) |
L3122F |
probably damaging |
Het |
Atp6v1b1 |
A |
T |
6: 83,730,632 (GRCm39) |
|
probably null |
Het |
Ccdc178 |
A |
T |
18: 22,153,946 (GRCm39) |
V621E |
probably damaging |
Het |
Cfap126 |
T |
C |
1: 170,941,671 (GRCm39) |
|
probably null |
Het |
Cog2 |
T |
C |
8: 125,252,488 (GRCm39) |
I64T |
probably damaging |
Het |
Dhx9 |
A |
C |
1: 153,349,210 (GRCm39) |
|
probably null |
Het |
Efcab7 |
A |
G |
4: 99,761,931 (GRCm39) |
D407G |
possibly damaging |
Het |
Eif2b5 |
G |
T |
16: 20,324,033 (GRCm39) |
G459C |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,793,765 (GRCm39) |
E1168G |
probably damaging |
Het |
Flnc |
AGCTGTCAAGTATGCTG |
AGCTG |
6: 29,450,901 (GRCm39) |
|
probably benign |
Het |
Fry |
A |
G |
5: 150,419,777 (GRCm39) |
T980A |
probably benign |
Het |
Gabbr2 |
A |
G |
4: 46,787,574 (GRCm39) |
V363A |
possibly damaging |
Het |
Ggt6 |
T |
A |
11: 72,328,346 (GRCm39) |
L244* |
probably null |
Het |
Gprc6a |
T |
A |
10: 51,491,233 (GRCm39) |
I768F |
probably damaging |
Het |
Grk1 |
G |
A |
8: 13,466,237 (GRCm39) |
M560I |
probably benign |
Het |
Hapln4 |
G |
A |
8: 70,537,740 (GRCm39) |
E145K |
probably damaging |
Het |
Hoxd9 |
C |
T |
2: 74,528,733 (GRCm39) |
P112S |
probably benign |
Het |
Ly6g6f |
T |
A |
17: 35,304,550 (GRCm39) |
M1L |
probably benign |
Het |
Mast1 |
T |
C |
8: 85,644,383 (GRCm39) |
T849A |
probably benign |
Het |
Mob4 |
A |
T |
1: 55,175,872 (GRCm39) |
M39L |
possibly damaging |
Het |
Mrgpre |
A |
T |
7: 143,335,260 (GRCm39) |
L81Q |
probably damaging |
Het |
Mst1 |
T |
C |
9: 107,957,774 (GRCm39) |
|
probably null |
Het |
Muc5b |
A |
T |
7: 141,411,559 (GRCm39) |
R1502* |
probably null |
Het |
Or4b13 |
T |
A |
2: 90,082,868 (GRCm39) |
I155L |
probably benign |
Het |
Or5ap2 |
T |
A |
2: 85,680,567 (GRCm39) |
I257N |
probably damaging |
Het |
Or9e1 |
T |
C |
11: 58,732,113 (GRCm39) |
Y58H |
probably damaging |
Het |
Pdc |
A |
G |
1: 150,208,769 (GRCm39) |
D84G |
probably damaging |
Het |
Peak1 |
T |
C |
9: 56,114,523 (GRCm39) |
N443D |
probably benign |
Het |
Pkd1l3 |
T |
A |
8: 110,341,401 (GRCm39) |
W85R |
unknown |
Het |
Pramel31 |
G |
T |
4: 144,089,227 (GRCm39) |
V182L |
probably benign |
Het |
Rfc1 |
G |
A |
5: 65,459,347 (GRCm39) |
Q190* |
probably null |
Het |
Rfc1 |
A |
G |
5: 65,470,304 (GRCm39) |
S68P |
probably damaging |
Het |
Rnf145 |
T |
C |
11: 44,452,317 (GRCm39) |
V432A |
probably benign |
Het |
Ror2 |
A |
G |
13: 53,273,018 (GRCm39) |
S204P |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,162,631 (GRCm39) |
E205G |
probably damaging |
Het |
Slc2a8 |
A |
C |
2: 32,866,189 (GRCm39) |
M277R |
probably damaging |
Het |
Slc4a1 |
T |
C |
11: 102,245,249 (GRCm39) |
Y566C |
probably damaging |
Het |
Slc6a12 |
A |
G |
6: 121,331,262 (GRCm39) |
N185S |
probably benign |
Het |
Srcap |
GCTCCTCCTCCTCCTCCT |
GCTCCTCCTCCTCCT |
7: 127,157,482 (GRCm39) |
|
probably benign |
Het |
Stk33 |
T |
A |
7: 108,926,823 (GRCm39) |
T279S |
possibly damaging |
Het |
Taok3 |
A |
G |
5: 117,379,015 (GRCm39) |
|
probably benign |
Het |
Tlr11 |
A |
G |
14: 50,599,561 (GRCm39) |
T516A |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,641,093 (GRCm39) |
L1088Q |
possibly damaging |
Het |
Tmem132d |
T |
A |
5: 127,861,485 (GRCm39) |
M879L |
probably benign |
Het |
Tnk2 |
A |
G |
16: 32,489,687 (GRCm39) |
E322G |
probably damaging |
Het |
Ttc28 |
T |
C |
5: 111,433,302 (GRCm39) |
V2081A |
probably benign |
Het |
Ttn |
C |
T |
2: 76,624,753 (GRCm39) |
|
probably null |
Het |
Zswim2 |
T |
C |
2: 83,745,753 (GRCm39) |
R562G |
probably benign |
Het |
|
Other mutations in Zfp105 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1416:Zfp105
|
UTSW |
9 |
122,759,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R1717:Zfp105
|
UTSW |
9 |
122,759,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Zfp105
|
UTSW |
9 |
122,758,743 (GRCm39) |
nonsense |
probably null |
|
R4522:Zfp105
|
UTSW |
9 |
122,759,121 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4953:Zfp105
|
UTSW |
9 |
122,758,880 (GRCm39) |
missense |
probably benign |
0.10 |
R5523:Zfp105
|
UTSW |
9 |
122,755,454 (GRCm39) |
missense |
probably benign |
0.00 |
R6943:Zfp105
|
UTSW |
9 |
122,754,303 (GRCm39) |
missense |
probably benign |
|
R7102:Zfp105
|
UTSW |
9 |
122,758,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R7827:Zfp105
|
UTSW |
9 |
122,759,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R8065:Zfp105
|
UTSW |
9 |
122,754,194 (GRCm39) |
missense |
probably benign |
|
R8823:Zfp105
|
UTSW |
9 |
122,759,568 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9037:Zfp105
|
UTSW |
9 |
122,758,836 (GRCm39) |
missense |
possibly damaging |
0.90 |
|