Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
A |
T |
11: 23,467,237 (GRCm39) |
V132E |
probably benign |
Het |
4930563M21Rik |
C |
T |
9: 55,895,250 (GRCm39) |
V315M |
probably damaging |
Het |
Aadacl4fm1 |
T |
C |
4: 144,255,126 (GRCm39) |
I182T |
probably benign |
Het |
Alb |
G |
C |
5: 90,615,214 (GRCm39) |
R242P |
probably damaging |
Het |
Amotl1 |
A |
T |
9: 14,461,798 (GRCm39) |
V805D |
probably damaging |
Het |
Arhgef3 |
T |
C |
14: 27,107,881 (GRCm39) |
L179P |
probably damaging |
Het |
Atp8b3 |
G |
A |
10: 80,366,858 (GRCm39) |
L247F |
possibly damaging |
Het |
Ccdc191 |
T |
C |
16: 43,735,968 (GRCm39) |
|
probably null |
Het |
Celsr3 |
A |
G |
9: 108,705,530 (GRCm39) |
H671R |
probably benign |
Het |
Cemip |
C |
A |
7: 83,652,616 (GRCm39) |
|
probably benign |
Het |
Cfap97 |
G |
T |
8: 46,623,482 (GRCm39) |
V291F |
possibly damaging |
Het |
Clca3a2 |
A |
G |
3: 144,777,288 (GRCm39) |
V861A |
possibly damaging |
Het |
Cln8 |
A |
T |
8: 14,944,950 (GRCm39) |
D88V |
probably damaging |
Het |
Col18a1 |
C |
A |
10: 76,916,685 (GRCm39) |
G330V |
unknown |
Het |
Dis3 |
C |
T |
14: 99,327,471 (GRCm39) |
R344Q |
probably benign |
Het |
Esyt2 |
T |
A |
12: 116,305,848 (GRCm39) |
S359R |
possibly damaging |
Het |
Fbxo41 |
A |
T |
6: 85,450,211 (GRCm39) |
L844Q |
probably damaging |
Het |
Fn1 |
G |
A |
1: 71,651,761 (GRCm39) |
T1372M |
probably damaging |
Het |
Gbp5 |
G |
A |
3: 142,213,500 (GRCm39) |
R472H |
probably benign |
Het |
Gm4559 |
C |
T |
7: 141,827,553 (GRCm39) |
R183K |
unknown |
Het |
Gm9507 |
T |
A |
10: 77,647,604 (GRCm39) |
E25V |
unknown |
Het |
Golgb1 |
A |
G |
16: 36,738,995 (GRCm39) |
I2486V |
probably damaging |
Het |
Ifitm10 |
A |
T |
7: 141,924,704 (GRCm39) |
V45D |
probably damaging |
Het |
Ift80 |
A |
G |
3: 68,823,478 (GRCm39) |
Y595H |
probably benign |
Het |
Itga8 |
C |
T |
2: 12,247,244 (GRCm39) |
V326I |
probably benign |
Het |
Kif14 |
A |
T |
1: 136,399,186 (GRCm39) |
H449L |
possibly damaging |
Het |
Klrh1 |
A |
G |
6: 129,743,658 (GRCm39) |
Y209H |
probably benign |
Het |
Ldlrad1 |
G |
A |
4: 107,066,688 (GRCm39) |
A8T |
probably benign |
Het |
Lrrc8b |
C |
A |
5: 105,627,883 (GRCm39) |
S76R |
possibly damaging |
Het |
Lrrn1 |
T |
C |
6: 107,545,783 (GRCm39) |
L527P |
probably damaging |
Het |
Luc7l |
T |
C |
17: 26,474,047 (GRCm39) |
V35A |
probably damaging |
Het |
Luzp1 |
T |
G |
4: 136,270,402 (GRCm39) |
V875G |
probably damaging |
Het |
Mcf2l |
G |
T |
8: 13,048,494 (GRCm39) |
|
probably null |
Het |
Mcoln2 |
T |
C |
3: 145,896,169 (GRCm39) |
M497T |
probably damaging |
Het |
Mrgprb4 |
A |
T |
7: 47,848,203 (GRCm39) |
S242T |
probably benign |
Het |
Muc21 |
TCAGTGGTGGTCAGGATGGGGGTAGAGCCTGAGCCACTCCTGGATGCAGTGGTGGTCAGG |
TCAGTGGTGGTCAGG |
17: 35,930,628 (GRCm39) |
|
probably benign |
Het |
Nipbl |
T |
A |
15: 8,340,734 (GRCm39) |
R1995S |
possibly damaging |
Het |
Nup35 |
A |
G |
2: 80,469,280 (GRCm39) |
|
probably null |
Het |
Or13a17 |
C |
T |
7: 140,271,046 (GRCm39) |
S76F |
probably benign |
Het |
Or2o1 |
A |
G |
11: 49,051,312 (GRCm39) |
D157G |
probably damaging |
Het |
Prdm12 |
A |
G |
2: 31,532,316 (GRCm39) |
K109E |
probably damaging |
Het |
Ptch1 |
A |
T |
13: 63,688,626 (GRCm39) |
L444Q |
probably damaging |
Het |
Qtrt1 |
C |
T |
9: 21,331,392 (GRCm39) |
R374* |
probably null |
Het |
Rnase11 |
T |
C |
14: 51,287,398 (GRCm39) |
D52G |
probably damaging |
Het |
Rps6 |
A |
G |
4: 86,774,158 (GRCm39) |
S148P |
probably benign |
Het |
Rrm2b |
T |
C |
15: 37,947,044 (GRCm39) |
K86E |
possibly damaging |
Het |
Sh2d1b2 |
A |
G |
1: 170,075,742 (GRCm39) |
K59E |
possibly damaging |
Het |
Six6 |
T |
A |
12: 72,987,100 (GRCm39) |
W91R |
probably damaging |
Het |
Slc23a2 |
C |
A |
2: 131,931,092 (GRCm39) |
A136S |
possibly damaging |
Het |
Slc9a5 |
G |
A |
8: 106,086,012 (GRCm39) |
R593H |
probably damaging |
Het |
Smbd1 |
T |
C |
16: 32,630,804 (GRCm39) |
M1V |
probably null |
Het |
Ssbp4 |
T |
C |
8: 71,051,647 (GRCm39) |
Y239C |
probably damaging |
Het |
Stox1 |
T |
C |
10: 62,501,345 (GRCm39) |
E405G |
probably damaging |
Het |
Tle7 |
C |
T |
8: 110,836,735 (GRCm39) |
T207M |
probably damaging |
Het |
Tmem192 |
A |
G |
8: 65,418,196 (GRCm39) |
I194V |
probably benign |
Het |
Tns3 |
A |
T |
11: 8,395,667 (GRCm39) |
C1246S |
probably damaging |
Het |
Ugt1a6a |
A |
T |
1: 88,066,575 (GRCm39) |
Q127L |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,275,025 (GRCm39) |
I1833V |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 84,656,093 (GRCm39) |
Y308N |
probably benign |
Het |
Vti1a |
T |
G |
19: 55,564,917 (GRCm39) |
L191R |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,570,153 (GRCm39) |
N310K |
probably benign |
Het |
|
Other mutations in Or6k2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Or6k2
|
APN |
1 |
173,986,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02479:Or6k2
|
APN |
1 |
173,986,520 (GRCm39) |
nonsense |
probably null |
|
IGL03190:Or6k2
|
APN |
1 |
173,987,110 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03270:Or6k2
|
APN |
1 |
173,987,119 (GRCm39) |
missense |
probably benign |
0.04 |
R0645:Or6k2
|
UTSW |
1 |
173,986,920 (GRCm39) |
missense |
probably benign |
0.00 |
R0834:Or6k2
|
UTSW |
1 |
173,986,930 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1432:Or6k2
|
UTSW |
1 |
173,986,483 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1508:Or6k2
|
UTSW |
1 |
173,986,930 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2351:Or6k2
|
UTSW |
1 |
173,986,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R3440:Or6k2
|
UTSW |
1 |
173,986,746 (GRCm39) |
missense |
probably benign |
0.14 |
R3441:Or6k2
|
UTSW |
1 |
173,986,746 (GRCm39) |
missense |
probably benign |
0.14 |
R4571:Or6k2
|
UTSW |
1 |
173,986,494 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5072:Or6k2
|
UTSW |
1 |
173,986,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R6060:Or6k2
|
UTSW |
1 |
173,986,907 (GRCm39) |
nonsense |
probably null |
|
R6166:Or6k2
|
UTSW |
1 |
173,986,659 (GRCm39) |
missense |
probably benign |
0.43 |
R6228:Or6k2
|
UTSW |
1 |
173,979,712 (GRCm39) |
missense |
probably benign |
0.00 |
R6272:Or6k2
|
UTSW |
1 |
173,986,741 (GRCm39) |
missense |
probably benign |
0.02 |
R6298:Or6k2
|
UTSW |
1 |
173,979,748 (GRCm39) |
missense |
probably benign |
0.02 |
R6400:Or6k2
|
UTSW |
1 |
173,986,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7581:Or6k2
|
UTSW |
1 |
173,986,337 (GRCm39) |
splice site |
probably null |
|
R7677:Or6k2
|
UTSW |
1 |
173,986,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Or6k2
|
UTSW |
1 |
173,987,254 (GRCm39) |
missense |
probably benign |
0.12 |
R7829:Or6k2
|
UTSW |
1 |
173,986,425 (GRCm39) |
missense |
probably benign |
0.00 |
R8519:Or6k2
|
UTSW |
1 |
173,986,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R9106:Or6k2
|
UTSW |
1 |
173,986,369 (GRCm39) |
missense |
probably benign |
0.00 |
R9205:Or6k2
|
UTSW |
1 |
173,986,456 (GRCm39) |
missense |
probably benign |
0.33 |
R9507:Or6k2
|
UTSW |
1 |
173,986,552 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9797:Or6k2
|
UTSW |
1 |
173,986,417 (GRCm39) |
missense |
probably benign |
|
Z1187:Or6k2
|
UTSW |
1 |
173,986,907 (GRCm39) |
nonsense |
probably null |
|
Z1192:Or6k2
|
UTSW |
1 |
173,986,907 (GRCm39) |
nonsense |
probably null |
|
|