Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810474O19Rik |
A |
T |
6: 149,328,375 |
Q973L |
probably damaging |
Het |
Adamts9 |
T |
C |
6: 92,858,113 |
T679A |
possibly damaging |
Het |
Ahr |
T |
C |
12: 35,508,194 |
T276A |
probably benign |
Het |
Akap9 |
A |
T |
5: 4,064,136 |
Q3138H |
probably damaging |
Het |
Armt1 |
T |
A |
10: 4,432,689 |
F7I |
probably benign |
Het |
B3galt2 |
A |
G |
1: 143,646,140 |
R5G |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,801,233 |
N2750S |
probably benign |
Het |
Cadps2 |
T |
A |
6: 23,583,396 |
E365V |
probably damaging |
Het |
Cd200r3 |
T |
A |
16: 44,957,717 |
|
probably null |
Het |
Cst7 |
T |
A |
2: 150,575,886 |
|
probably benign |
Het |
Defb30 |
A |
T |
14: 63,049,763 |
|
probably benign |
Het |
Dido1 |
C |
T |
2: 180,659,851 |
G2087S |
probably benign |
Het |
Dio2 |
A |
G |
12: 90,738,071 |
Y72H |
probably benign |
Het |
Dnah11 |
C |
T |
12: 117,987,469 |
E3035K |
probably damaging |
Het |
Dnajb13 |
T |
C |
7: 100,503,249 |
K287E |
possibly damaging |
Het |
Dnajc11 |
G |
A |
4: 151,973,628 |
V244I |
possibly damaging |
Het |
Ect2 |
C |
T |
3: 27,139,652 |
A226T |
probably damaging |
Het |
Ercc8 |
G |
A |
13: 108,174,061 |
|
probably null |
Het |
Fam120b |
T |
A |
17: 15,402,927 |
M389K |
probably benign |
Het |
Fam151a |
A |
G |
4: 106,747,931 |
M497V |
probably benign |
Het |
Fam186b |
C |
A |
15: 99,280,128 |
G439V |
probably benign |
Het |
Fank1 |
A |
G |
7: 133,876,765 |
Y185C |
probably damaging |
Het |
Gart |
T |
C |
16: 91,630,602 |
|
probably benign |
Het |
Glb1l |
T |
C |
1: 75,199,720 |
Y572C |
probably damaging |
Het |
Gm11563 |
C |
T |
11: 99,658,437 |
A164T |
unknown |
Het |
Gnb4 |
C |
T |
3: 32,591,207 |
V112I |
probably benign |
Het |
Gsdmc3 |
T |
A |
15: 63,859,693 |
D330V |
probably damaging |
Het |
H2-DMa |
C |
T |
17: 34,137,960 |
T144M |
probably damaging |
Het |
Haus6 |
A |
T |
4: 86,583,514 |
F707I |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,594,016 |
T4971S |
probably benign |
Het |
Ints6 |
A |
T |
14: 62,696,759 |
F766L |
probably benign |
Het |
Kdm5d |
T |
A |
Y: 927,330 |
M650K |
probably damaging |
Het |
Kif21b |
T |
C |
1: 136,159,428 |
F881S |
possibly damaging |
Het |
Klrk1 |
C |
A |
6: 129,614,635 |
Q176H |
possibly damaging |
Het |
Ky |
T |
C |
9: 102,537,621 |
V244A |
probably benign |
Het |
Mia2 |
T |
A |
12: 59,154,419 |
L191M |
possibly damaging |
Het |
Miga2 |
T |
A |
2: 30,381,744 |
|
probably benign |
Het |
Mtss1l |
C |
T |
8: 110,737,948 |
P322S |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,299,141 |
|
probably benign |
Het |
Ncbp3 |
T |
A |
11: 73,049,845 |
|
probably benign |
Het |
Nprl3 |
G |
A |
11: 32,234,876 |
L378F |
probably damaging |
Het |
Ntrk2 |
A |
T |
13: 58,846,821 |
M184L |
probably benign |
Het |
Olfr311 |
T |
G |
11: 58,841,443 |
C110G |
probably damaging |
Het |
Olfr738 |
G |
T |
14: 50,413,697 |
C51F |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 109,083,128 |
E287G |
probably damaging |
Het |
Parva |
T |
C |
7: 112,576,411 |
F250L |
probably damaging |
Het |
Pcdhb11 |
C |
T |
18: 37,421,811 |
Q65* |
probably null |
Het |
Phtf1 |
A |
G |
3: 103,993,765 |
T377A |
probably damaging |
Het |
Pkp4 |
G |
A |
2: 59,322,643 |
V612I |
possibly damaging |
Het |
Plscr2 |
C |
A |
9: 92,287,654 |
S52R |
probably benign |
Het |
Pnisr |
C |
T |
4: 21,874,092 |
|
probably benign |
Het |
Pole2 |
A |
C |
12: 69,209,879 |
S291A |
probably damaging |
Het |
Ppp2r5d |
A |
G |
17: 46,684,018 |
F586L |
probably benign |
Het |
Prrx1 |
G |
A |
1: 163,257,816 |
R182C |
probably damaging |
Het |
Ptprs |
A |
G |
17: 56,429,103 |
I110T |
possibly damaging |
Het |
Rasgrf2 |
G |
A |
13: 91,919,817 |
|
probably benign |
Het |
Riox2 |
T |
C |
16: 59,491,892 |
V464A |
probably benign |
Het |
Robo2 |
A |
G |
16: 73,967,802 |
V646A |
possibly damaging |
Het |
Ros1 |
T |
A |
10: 52,118,348 |
I1279F |
probably damaging |
Het |
Siglec1 |
G |
A |
2: 131,074,268 |
T1254M |
probably benign |
Het |
Snx7 |
T |
C |
3: 117,846,675 |
N62D |
probably damaging |
Het |
Sp100 |
G |
A |
1: 85,659,867 |
|
probably null |
Het |
Stil |
A |
T |
4: 115,007,159 |
I86L |
possibly damaging |
Het |
Tbc1d16 |
T |
A |
11: 119,209,038 |
D170V |
probably benign |
Het |
Tmem2 |
T |
A |
19: 21,817,971 |
S743T |
probably benign |
Het |
Trappc13 |
G |
A |
13: 104,161,081 |
T105M |
probably damaging |
Het |
Trhr |
T |
A |
15: 44,229,500 |
S378T |
probably benign |
Het |
Ttc7b |
T |
C |
12: 100,500,073 |
|
probably null |
Het |
Vegfc |
A |
T |
8: 54,157,139 |
Y110F |
probably benign |
Het |
Vmn1r184 |
C |
A |
7: 26,267,177 |
P116H |
possibly damaging |
Het |
Vmn2r5 |
A |
T |
3: 64,503,814 |
C444* |
probably null |
Het |
Zfp819 |
T |
A |
7: 43,616,444 |
V41E |
probably benign |
Het |
|
Other mutations in Zfp341 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Zfp341
|
APN |
2 |
154,634,231 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01352:Zfp341
|
APN |
2 |
154,628,896 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01748:Zfp341
|
APN |
2 |
154,628,927 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02260:Zfp341
|
APN |
2 |
154,642,049 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL02329:Zfp341
|
APN |
2 |
154,632,304 (GRCm38) |
missense |
possibly damaging |
0.90 |
casanova_grimbacher
|
UTSW |
2 |
154,624,881 (GRCm38) |
missense |
probably damaging |
1.00 |
Specious
|
UTSW |
2 |
154,646,134 (GRCm38) |
missense |
possibly damaging |
0.63 |
R0079:Zfp341
|
UTSW |
2 |
154,624,994 (GRCm38) |
nonsense |
probably null |
|
R0570:Zfp341
|
UTSW |
2 |
154,646,068 (GRCm38) |
missense |
probably benign |
0.02 |
R1018:Zfp341
|
UTSW |
2 |
154,646,052 (GRCm38) |
missense |
probably damaging |
1.00 |
R1611:Zfp341
|
UTSW |
2 |
154,645,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R1733:Zfp341
|
UTSW |
2 |
154,641,378 (GRCm38) |
missense |
probably benign |
0.19 |
R1822:Zfp341
|
UTSW |
2 |
154,646,134 (GRCm38) |
missense |
possibly damaging |
0.63 |
R1956:Zfp341
|
UTSW |
2 |
154,638,212 (GRCm38) |
missense |
probably benign |
0.09 |
R2437:Zfp341
|
UTSW |
2 |
154,628,801 (GRCm38) |
missense |
probably damaging |
0.97 |
R3623:Zfp341
|
UTSW |
2 |
154,624,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R4417:Zfp341
|
UTSW |
2 |
154,628,987 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4806:Zfp341
|
UTSW |
2 |
154,645,866 (GRCm38) |
utr 3 prime |
probably benign |
|
R4807:Zfp341
|
UTSW |
2 |
154,645,866 (GRCm38) |
utr 3 prime |
probably benign |
|
R4863:Zfp341
|
UTSW |
2 |
154,645,866 (GRCm38) |
utr 3 prime |
probably benign |
|
R4955:Zfp341
|
UTSW |
2 |
154,638,030 (GRCm38) |
missense |
probably damaging |
0.98 |
R4962:Zfp341
|
UTSW |
2 |
154,626,814 (GRCm38) |
missense |
possibly damaging |
0.80 |
R5484:Zfp341
|
UTSW |
2 |
154,625,001 (GRCm38) |
missense |
probably benign |
0.00 |
R5864:Zfp341
|
UTSW |
2 |
154,643,554 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5877:Zfp341
|
UTSW |
2 |
154,632,289 (GRCm38) |
missense |
probably damaging |
1.00 |
R5975:Zfp341
|
UTSW |
2 |
154,630,441 (GRCm38) |
missense |
probably damaging |
1.00 |
R5990:Zfp341
|
UTSW |
2 |
154,645,659 (GRCm38) |
missense |
probably damaging |
0.98 |
R6057:Zfp341
|
UTSW |
2 |
154,625,034 (GRCm38) |
missense |
probably benign |
0.01 |
R6882:Zfp341
|
UTSW |
2 |
154,638,023 (GRCm38) |
missense |
probably damaging |
1.00 |
R7686:Zfp341
|
UTSW |
2 |
154,624,861 (GRCm38) |
missense |
probably damaging |
0.96 |
R7701:Zfp341
|
UTSW |
2 |
154,634,080 (GRCm38) |
splice site |
probably null |
|
R7847:Zfp341
|
UTSW |
2 |
154,634,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R8109:Zfp341
|
UTSW |
2 |
154,627,900 (GRCm38) |
missense |
probably benign |
0.04 |
R9313:Zfp341
|
UTSW |
2 |
154,627,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R9484:Zfp341
|
UTSW |
2 |
154,643,843 (GRCm38) |
missense |
probably damaging |
1.00 |
|