Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
A |
G |
4: 124,504,445 (GRCm39) |
S36P |
probably damaging |
Het |
Agmo |
A |
G |
12: 37,302,538 (GRCm39) |
D125G |
probably damaging |
Het |
Arhgap26 |
A |
T |
18: 39,490,880 (GRCm39) |
S328C |
probably null |
Het |
Arl6 |
T |
C |
16: 59,439,169 (GRCm39) |
D175G |
probably damaging |
Het |
Asb3 |
G |
A |
11: 31,005,559 (GRCm39) |
A192T |
probably damaging |
Het |
Atp10b |
A |
T |
11: 43,126,573 (GRCm39) |
M1110L |
possibly damaging |
Het |
Cacna1i |
T |
C |
15: 80,220,883 (GRCm39) |
I175T |
probably damaging |
Het |
Car15 |
A |
T |
16: 17,655,227 (GRCm39) |
I71N |
probably benign |
Het |
Casq1 |
T |
A |
1: 172,044,407 (GRCm39) |
Y140F |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,362,269 (GRCm39) |
T17M |
possibly damaging |
Het |
Cfap46 |
CCTTCTTCT |
CCTTCT |
7: 139,218,816 (GRCm39) |
|
probably benign |
Het |
Ciart |
G |
A |
3: 95,788,323 (GRCm39) |
|
probably benign |
Het |
Cul5 |
A |
T |
9: 53,558,094 (GRCm39) |
V170D |
probably benign |
Het |
Cyb5r3 |
T |
C |
15: 83,038,917 (GRCm39) |
D224G |
probably benign |
Het |
Daam1 |
G |
A |
12: 72,035,723 (GRCm39) |
G964R |
probably damaging |
Het |
Daglb |
T |
A |
5: 143,475,689 (GRCm39) |
L383Q |
probably damaging |
Het |
Dazap2 |
T |
G |
15: 100,514,864 (GRCm39) |
H28Q |
possibly damaging |
Het |
Dnttip2 |
A |
T |
3: 122,068,905 (GRCm39) |
D40V |
probably benign |
Het |
Dynlt2b |
T |
A |
16: 32,245,727 (GRCm39) |
D125E |
possibly damaging |
Het |
Epn1 |
G |
T |
7: 5,098,925 (GRCm39) |
D406Y |
probably damaging |
Het |
Epn1 |
G |
T |
7: 5,098,935 (GRCm39) |
R409L |
probably damaging |
Het |
Evc |
T |
C |
5: 37,457,843 (GRCm39) |
T966A |
probably benign |
Het |
Extl3 |
T |
C |
14: 65,314,375 (GRCm39) |
D269G |
probably damaging |
Het |
Gfra3 |
TGCGC |
TGC |
18: 34,828,864 (GRCm39) |
|
probably null |
Het |
Gpr87 |
A |
T |
3: 59,086,528 (GRCm39) |
F326I |
probably damaging |
Het |
Hivep3 |
C |
A |
4: 119,952,137 (GRCm39) |
P151H |
probably damaging |
Het |
Kcnj14 |
T |
A |
7: 45,467,440 (GRCm39) |
E302V |
probably damaging |
Het |
Kdm5d |
T |
C |
Y: 921,693 (GRCm39) |
Y534H |
probably damaging |
Homo |
Map3k5 |
T |
A |
10: 20,014,006 (GRCm39) |
|
probably null |
Het |
Mdn1 |
A |
G |
4: 32,748,590 (GRCm39) |
T4212A |
probably benign |
Het |
Ms4a6d |
A |
T |
19: 11,564,504 (GRCm39) |
S122R |
probably damaging |
Het |
Mtarc1 |
G |
A |
1: 184,527,648 (GRCm39) |
R271W |
probably damaging |
Het |
Nectin3 |
A |
T |
16: 46,215,513 (GRCm39) |
H76Q |
probably damaging |
Het |
Notch1 |
C |
A |
2: 26,364,182 (GRCm39) |
E846D |
possibly damaging |
Het |
Or1e23 |
A |
G |
11: 73,407,534 (GRCm39) |
S164P |
probably benign |
Het |
Or4a67 |
T |
C |
2: 88,598,632 (GRCm39) |
E9G |
probably damaging |
Het |
Or8b36 |
GTTT |
GTTTGCTTTTT |
9: 37,937,842 (GRCm39) |
|
probably null |
Het |
Or8b36 |
TT |
TTGCTGTGT |
9: 37,937,844 (GRCm39) |
|
probably null |
Het |
Or8b36 |
G |
GGGATTGC |
9: 37,937,833 (GRCm39) |
|
probably null |
Het |
Or8b36 |
TGTTT |
TGTTTGCAGTTT |
9: 37,937,841 (GRCm39) |
|
probably null |
Het |
Pfkl |
C |
T |
10: 77,825,399 (GRCm39) |
|
probably null |
Het |
Pigz |
T |
C |
16: 31,764,424 (GRCm39) |
V494A |
possibly damaging |
Het |
Pik3r4 |
T |
C |
9: 105,531,247 (GRCm39) |
V516A |
probably benign |
Het |
Polr2b |
G |
A |
5: 77,496,141 (GRCm39) |
R1104K |
probably benign |
Het |
Rap1a |
A |
T |
3: 105,639,311 (GRCm39) |
L116* |
probably null |
Het |
Rnf114 |
T |
C |
2: 167,356,649 (GRCm39) |
*230R |
probably null |
Het |
Rtl1 |
G |
T |
12: 109,560,083 (GRCm39) |
N585K |
probably benign |
Het |
Serpinb5 |
G |
T |
1: 106,802,795 (GRCm39) |
R110I |
possibly damaging |
Het |
Spink6 |
T |
C |
18: 44,207,498 (GRCm39) |
|
probably null |
Het |
Spopfm1 |
G |
T |
3: 94,173,208 (GRCm39) |
S72I |
probably damaging |
Het |
Stk39 |
A |
T |
2: 68,137,383 (GRCm39) |
|
probably null |
Het |
Tcstv2a |
T |
C |
13: 120,724,907 (GRCm39) |
|
probably benign |
Het |
Tcte1 |
A |
T |
17: 45,846,085 (GRCm39) |
T230S |
probably benign |
Het |
Tecpr1 |
C |
A |
5: 144,135,394 (GRCm39) |
V1020L |
probably damaging |
Het |
Tmc7 |
T |
C |
7: 118,160,261 (GRCm39) |
Y192C |
possibly damaging |
Het |
Trim63 |
A |
T |
4: 134,050,537 (GRCm39) |
T274S |
probably benign |
Het |
Wdr43 |
G |
A |
17: 71,957,048 (GRCm39) |
|
probably null |
Het |
Zfr |
T |
C |
15: 12,160,677 (GRCm39) |
I750T |
probably benign |
Het |
|
Other mutations in Or8g18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00981:Or8g18
|
APN |
9 |
39,148,901 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01691:Or8g18
|
APN |
9 |
39,149,315 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02606:Or8g18
|
APN |
9 |
39,149,490 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02656:Or8g18
|
APN |
9 |
39,149,456 (GRCm39) |
missense |
probably benign |
0.13 |
R0133:Or8g18
|
UTSW |
9 |
39,149,307 (GRCm39) |
missense |
probably benign |
0.00 |
R0548:Or8g18
|
UTSW |
9 |
39,149,667 (GRCm39) |
missense |
probably benign |
0.13 |
R0558:Or8g18
|
UTSW |
9 |
39,149,496 (GRCm39) |
missense |
probably damaging |
0.96 |
R0616:Or8g18
|
UTSW |
9 |
39,148,946 (GRCm39) |
missense |
probably benign |
0.00 |
R0626:Or8g18
|
UTSW |
9 |
39,149,162 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0826:Or8g18
|
UTSW |
9 |
39,149,725 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R0839:Or8g18
|
UTSW |
9 |
39,149,146 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1074:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1224:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1226:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1252:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1256:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1355:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1356:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1416:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1499:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1658:Or8g18
|
UTSW |
9 |
39,149,255 (GRCm39) |
missense |
probably benign |
0.03 |
R1815:Or8g18
|
UTSW |
9 |
39,149,286 (GRCm39) |
missense |
probably benign |
0.01 |
R2198:Or8g18
|
UTSW |
9 |
39,149,048 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4178:Or8g18
|
UTSW |
9 |
39,149,375 (GRCm39) |
nonsense |
probably null |
|
R5112:Or8g18
|
UTSW |
9 |
39,149,717 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R6850:Or8g18
|
UTSW |
9 |
39,149,271 (GRCm39) |
missense |
probably benign |
0.01 |
R7032:Or8g18
|
UTSW |
9 |
39,148,983 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7573:Or8g18
|
UTSW |
9 |
39,148,977 (GRCm39) |
missense |
probably benign |
0.42 |
R7715:Or8g18
|
UTSW |
9 |
39,149,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7722:Or8g18
|
UTSW |
9 |
39,148,885 (GRCm39) |
nonsense |
probably null |
|
R7729:Or8g18
|
UTSW |
9 |
39,149,546 (GRCm39) |
missense |
probably benign |
0.28 |
R8710:Or8g18
|
UTSW |
9 |
39,149,306 (GRCm39) |
missense |
probably benign |
0.00 |
R9513:Or8g18
|
UTSW |
9 |
39,149,625 (GRCm39) |
missense |
probably benign |
0.05 |
R9515:Or8g18
|
UTSW |
9 |
39,149,625 (GRCm39) |
missense |
probably benign |
0.05 |
|