Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830005F24Rik |
T |
G |
13: 48,667,727 (GRCm39) |
W10G |
unknown |
Het |
Abca13 |
A |
T |
11: 9,328,269 (GRCm39) |
K3447N |
possibly damaging |
Het |
Agtr1a |
T |
G |
13: 30,565,745 (GRCm39) |
V270G |
probably benign |
Het |
Apob |
A |
T |
12: 8,059,033 (GRCm39) |
H2505L |
probably benign |
Het |
Babam1 |
T |
A |
8: 71,850,629 (GRCm39) |
V86D |
possibly damaging |
Het |
Cacna1s |
C |
A |
1: 136,015,075 (GRCm39) |
N654K |
probably damaging |
Het |
Ccdc146 |
A |
T |
5: 21,506,469 (GRCm39) |
|
probably benign |
Het |
Ccdc8 |
T |
C |
7: 16,729,326 (GRCm39) |
S272P |
probably damaging |
Het |
Cnksr1 |
T |
C |
4: 133,956,730 (GRCm39) |
E510G |
probably damaging |
Het |
Cnot6l |
A |
T |
5: 96,239,535 (GRCm39) |
D255E |
probably benign |
Het |
Ddx1 |
A |
C |
12: 13,274,280 (GRCm39) |
|
probably benign |
Het |
Dyrk1a |
A |
G |
16: 94,492,650 (GRCm39) |
T628A |
probably benign |
Het |
Elavl1 |
A |
T |
8: 4,351,786 (GRCm39) |
I110N |
probably damaging |
Het |
Emilin2 |
C |
G |
17: 71,562,141 (GRCm39) |
D954H |
probably damaging |
Het |
Erich3 |
C |
T |
3: 154,410,586 (GRCm39) |
T147I |
|
Het |
Galnt1 |
A |
T |
18: 24,404,686 (GRCm39) |
H341L |
probably damaging |
Het |
Gm14325 |
A |
T |
2: 177,473,592 (GRCm39) |
C497S |
probably damaging |
Het |
Gm4922 |
A |
T |
10: 18,659,536 (GRCm39) |
N395K |
probably benign |
Het |
Hsd17b2 |
G |
A |
8: 118,469,155 (GRCm39) |
C189Y |
probably damaging |
Het |
Kcnn1 |
A |
T |
8: 71,305,449 (GRCm39) |
S254T |
possibly damaging |
Het |
Lce1l |
G |
C |
3: 92,757,766 (GRCm39) |
P31A |
unknown |
Het |
Lrpprc |
A |
G |
17: 85,080,524 (GRCm39) |
Y199H |
probably damaging |
Het |
Lrrtm3 |
A |
T |
10: 63,925,487 (GRCm39) |
|
probably null |
Het |
Mon2 |
G |
T |
10: 122,838,688 (GRCm39) |
A1598E |
probably damaging |
Het |
Myh3 |
A |
T |
11: 66,986,833 (GRCm39) |
|
probably null |
Het |
Naa11 |
A |
T |
5: 97,539,737 (GRCm39) |
D140E |
probably damaging |
Het |
Nadk2 |
G |
A |
15: 9,103,420 (GRCm39) |
R350Q |
probably benign |
Het |
Npc1 |
T |
C |
18: 12,326,455 (GRCm39) |
I1162V |
probably damaging |
Het |
Or4e1 |
A |
G |
14: 52,701,280 (GRCm39) |
M62T |
probably damaging |
Het |
Or5v1 |
T |
C |
17: 37,810,148 (GRCm39) |
I202T |
probably benign |
Het |
Otogl |
A |
T |
10: 107,613,461 (GRCm39) |
N2001K |
possibly damaging |
Het |
Peg10 |
ACATCAGGATCC |
ACATCAGGATCCCCATCAGGATCC |
6: 4,756,454 (GRCm39) |
|
probably benign |
Het |
Pi4ka |
A |
G |
16: 17,171,912 (GRCm39) |
|
probably null |
Het |
Ppp2r5c |
A |
T |
12: 110,512,259 (GRCm39) |
T185S |
possibly damaging |
Het |
Psd2 |
A |
T |
18: 36,112,766 (GRCm39) |
S154C |
probably damaging |
Het |
Rnasel |
G |
A |
1: 153,630,734 (GRCm39) |
V417M |
possibly damaging |
Het |
Slc35g2 |
A |
G |
9: 100,434,841 (GRCm39) |
S277P |
probably damaging |
Het |
Slc36a2 |
A |
T |
11: 55,070,158 (GRCm39) |
W140R |
possibly damaging |
Het |
Slc6a12 |
A |
G |
6: 121,340,250 (GRCm39) |
K512E |
probably damaging |
Het |
Sox7 |
C |
T |
14: 64,181,275 (GRCm39) |
S24L |
probably benign |
Het |
Specc1 |
A |
G |
11: 62,023,171 (GRCm39) |
K659E |
probably damaging |
Het |
Stx18 |
T |
A |
5: 38,285,383 (GRCm39) |
|
probably null |
Het |
Svs5 |
C |
A |
2: 164,080,091 (GRCm39) |
G25W |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,297,829 (GRCm39) |
M1156T |
probably benign |
Het |
Tars2 |
T |
A |
3: 95,658,271 (GRCm39) |
I185F |
probably benign |
Het |
Thsd7a |
T |
C |
6: 12,396,612 (GRCm39) |
I839V |
|
Het |
Vmn1r115 |
T |
C |
7: 20,578,819 (GRCm39) |
N31S |
probably damaging |
Het |
Vmn1r57 |
A |
G |
7: 5,224,024 (GRCm39) |
D183G |
probably damaging |
Het |
Wdr7 |
C |
T |
18: 63,868,756 (GRCm39) |
T275I |
probably damaging |
Het |
Ybx2 |
A |
G |
11: 69,831,194 (GRCm39) |
E263G |
probably damaging |
Het |
Zfp329 |
A |
T |
7: 12,544,116 (GRCm39) |
C469* |
probably null |
Het |
Zfp868 |
A |
T |
8: 70,066,446 (GRCm39) |
L40H |
probably damaging |
Het |
|
Other mutations in Zbtb6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01951:Zbtb6
|
APN |
2 |
37,319,343 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02981:Zbtb6
|
APN |
2 |
37,319,176 (GRCm39) |
nonsense |
probably null |
|
IGL03390:Zbtb6
|
APN |
2 |
37,319,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Zbtb6
|
UTSW |
2 |
37,319,600 (GRCm39) |
nonsense |
probably null |
|
R0164:Zbtb6
|
UTSW |
2 |
37,319,600 (GRCm39) |
nonsense |
probably null |
|
R0470:Zbtb6
|
UTSW |
2 |
37,319,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R1472:Zbtb6
|
UTSW |
2 |
37,319,356 (GRCm39) |
missense |
probably benign |
|
R1606:Zbtb6
|
UTSW |
2 |
37,319,130 (GRCm39) |
missense |
probably benign |
0.00 |
R1824:Zbtb6
|
UTSW |
2 |
37,319,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R4594:Zbtb6
|
UTSW |
2 |
37,319,054 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4838:Zbtb6
|
UTSW |
2 |
37,318,728 (GRCm39) |
nonsense |
probably null |
|
R5000:Zbtb6
|
UTSW |
2 |
37,319,251 (GRCm39) |
missense |
probably benign |
|
R5816:Zbtb6
|
UTSW |
2 |
37,319,227 (GRCm39) |
missense |
probably benign |
0.01 |
R6005:Zbtb6
|
UTSW |
2 |
37,318,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R6152:Zbtb6
|
UTSW |
2 |
37,319,255 (GRCm39) |
missense |
probably benign |
0.18 |
R6390:Zbtb6
|
UTSW |
2 |
37,318,690 (GRCm39) |
missense |
probably benign |
0.01 |
R7657:Zbtb6
|
UTSW |
2 |
37,319,087 (GRCm39) |
missense |
probably benign |
|
R7866:Zbtb6
|
UTSW |
2 |
37,319,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R8969:Zbtb6
|
UTSW |
2 |
37,318,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|