Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,132,880 (GRCm39) |
K1270E |
possibly damaging |
Het |
Adgrb2 |
T |
C |
4: 129,903,877 (GRCm39) |
S668P |
probably damaging |
Het |
Ahdc1 |
T |
G |
4: 132,791,588 (GRCm39) |
L943R |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,739,125 (GRCm39) |
K2253R |
unknown |
Het |
Arhgap23 |
T |
C |
11: 97,354,387 (GRCm39) |
S767P |
probably damaging |
Het |
Arhgef12 |
A |
G |
9: 42,901,285 (GRCm39) |
I839T |
possibly damaging |
Het |
Begain |
CGCCGC |
CGCCGCGGCCGC |
12: 108,999,350 (GRCm39) |
|
probably benign |
Het |
Btbd19 |
A |
T |
4: 116,979,472 (GRCm39) |
C116S |
probably damaging |
Het |
Cbr1 |
C |
T |
16: 93,407,067 (GRCm39) |
A261V |
probably benign |
Het |
Ccdc137 |
A |
G |
11: 120,349,022 (GRCm39) |
R18G |
probably benign |
Het |
Cdsn |
AG |
AGACAGGAAGTAGTAGCTCTCAG |
17: 35,865,876 (GRCm39) |
|
probably benign |
Het |
Celsr3 |
C |
T |
9: 108,726,256 (GRCm39) |
R3162C |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,791,224 (GRCm39) |
V1300E |
probably benign |
Het |
Cluh |
G |
GCCAGAT |
11: 74,560,364 (GRCm39) |
|
probably benign |
Het |
Cmya5 |
G |
T |
13: 93,205,799 (GRCm39) |
Q3357K |
possibly damaging |
Het |
Col6a2 |
T |
G |
10: 76,442,043 (GRCm39) |
|
probably null |
Het |
Cyp2j9 |
T |
A |
4: 96,465,889 (GRCm39) |
T315S |
probably damaging |
Het |
Cyp3a13 |
CATTATT |
CATT |
5: 137,892,525 (GRCm39) |
|
probably null |
Het |
Dnah6 |
T |
A |
6: 73,095,040 (GRCm39) |
Y2181F |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,412,421 (GRCm39) |
D4010G |
possibly damaging |
Het |
E4f1 |
CCG |
CCGACG |
17: 24,674,169 (GRCm39) |
|
probably benign |
Het |
Ep300 |
A |
T |
15: 81,470,772 (GRCm39) |
|
probably benign |
Het |
Fam234a |
A |
G |
17: 26,437,725 (GRCm39) |
V90A |
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,623 (GRCm39) |
|
probably benign |
Het |
Gal3st1 |
A |
G |
11: 3,948,153 (GRCm39) |
Y120C |
possibly damaging |
Het |
Garin5a |
GGA |
GGAAGGGTGGATCCTGGATACCTGGGTCTGAGGGAAGA |
7: 44,149,959 (GRCm39) |
|
probably null |
Het |
Gm5475 |
GTGGAAGGAAAGGT |
G |
15: 100,325,030 (GRCm39) |
|
probably null |
Het |
Gm6665 |
T |
TC |
18: 31,953,430 (GRCm39) |
|
probably null |
Het |
Hdlbp |
T |
C |
1: 93,368,456 (GRCm39) |
T8A |
probably benign |
Het |
Hnrnpa2b1 |
T |
A |
6: 51,443,674 (GRCm39) |
K92N |
probably damaging |
Het |
Hsdl2 |
GGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
GGAGCAGCCACAGCTGCAGGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
4: 59,610,640 (GRCm39) |
|
probably benign |
Het |
Klhl10 |
C |
G |
11: 100,332,896 (GRCm39) |
Q14E |
probably benign |
Het |
Klra2 |
GAAAGAAATCCA |
GAAAGAAATCCAAAGAAATCCA |
6: 131,198,801 (GRCm39) |
|
probably null |
Het |
Kmt2b |
CC |
CCTCCTGC |
7: 30,285,807 (GRCm39) |
|
probably benign |
Het |
Krt1c |
A |
G |
15: 101,726,403 (GRCm39) |
I45T |
unknown |
Het |
Ksr2 |
T |
C |
5: 117,693,283 (GRCm39) |
S244P |
probably benign |
Het |
Lama5 |
A |
T |
2: 179,837,971 (GRCm39) |
M915K |
probably benign |
Het |
Lrp1b |
A |
C |
2: 41,660,858 (GRCm39) |
H197Q |
|
Het |
Lrrc1 |
T |
C |
9: 77,359,913 (GRCm39) |
E293G |
probably damaging |
Het |
Med12l |
AACA |
AACAACA |
3: 59,183,379 (GRCm39) |
|
probably benign |
Het |
Mgam |
T |
A |
6: 40,662,243 (GRCm39) |
Y1179N |
probably damaging |
Het |
Mgat4c |
A |
G |
10: 102,224,928 (GRCm39) |
I381V |
probably benign |
Het |
Mrgprx1 |
A |
AGAC |
7: 47,671,259 (GRCm39) |
|
probably benign |
Het |
Myc |
A |
T |
15: 61,857,672 (GRCm39) |
|
probably benign |
Het |
Nipbl |
A |
G |
15: 8,388,418 (GRCm39) |
S401P |
probably damaging |
Het |
Nlrp9c |
A |
T |
7: 26,084,649 (GRCm39) |
I310N |
probably benign |
Het |
Nwd2 |
C |
A |
5: 63,963,066 (GRCm39) |
Y883* |
probably null |
Het |
Oas1e |
T |
A |
5: 120,932,383 (GRCm39) |
T87S |
possibly damaging |
Het |
Or10n7-ps1 |
GA |
GATACA |
9: 39,598,049 (GRCm39) |
|
probably null |
Het |
Or51a5 |
A |
T |
7: 102,771,098 (GRCm39) |
C294S |
probably benign |
Het |
Or8b38 |
G |
A |
9: 37,972,620 (GRCm39) |
M1I |
probably null |
Het |
Pappa |
T |
G |
4: 65,123,282 (GRCm39) |
S872R |
possibly damaging |
Het |
Parp4 |
T |
C |
14: 56,884,806 (GRCm39) |
L1295P |
unknown |
Het |
Pcdh15 |
A |
T |
10: 74,021,242 (GRCm39) |
Y152F |
probably damaging |
Het |
Pdk1 |
A |
T |
2: 71,714,240 (GRCm39) |
I217L |
possibly damaging |
Het |
Phldb1 |
A |
C |
9: 44,609,243 (GRCm39) |
C450W |
probably damaging |
Het |
Pnma8a |
C |
CCATGATGCACCTGCTTCAACATCA |
7: 16,695,376 (GRCm39) |
|
probably benign |
Het |
Prl2c5 |
G |
A |
13: 13,360,497 (GRCm39) |
G55S |
probably benign |
Het |
Psme2b |
A |
T |
11: 48,836,397 (GRCm39) |
H183Q |
probably damaging |
Het |
Ptms |
CCTCCTC |
CCTCCTCCTC |
6: 124,891,412 (GRCm39) |
|
probably benign |
Het |
Rln3 |
T |
C |
8: 84,769,931 (GRCm39) |
T73A |
probably benign |
Het |
Rprd1a |
T |
A |
18: 24,663,062 (GRCm39) |
Q21L |
probably damaging |
Het |
Septin3 |
A |
T |
15: 82,168,662 (GRCm39) |
D155V |
probably damaging |
Het |
Sh3rf3 |
T |
A |
10: 58,649,590 (GRCm39) |
V65E |
probably damaging |
Het |
Shank3 |
A |
G |
15: 89,384,593 (GRCm39) |
N155S |
probably benign |
Het |
Shox2 |
G |
T |
3: 66,881,146 (GRCm39) |
P278Q |
probably damaging |
Het |
Slc1a1 |
T |
C |
19: 28,856,555 (GRCm39) |
|
probably null |
Het |
Slc39a10 |
A |
T |
1: 46,849,175 (GRCm39) |
F814I |
probably damaging |
Het |
Slc5a1 |
T |
C |
5: 33,290,773 (GRCm39) |
I119T |
probably damaging |
Het |
Slc6a13 |
T |
C |
6: 121,301,310 (GRCm39) |
|
probably null |
Het |
Spmap2l |
CAGCGATCCTCCCCAGTCCCGCAAGGC |
CAGCGATCCTCCCCAGTCCCGCAAGGCGAGCGATCCTCCCCAGTCCCGCAAGGC |
5: 77,164,247 (GRCm39) |
|
probably benign |
Het |
Spta1 |
A |
G |
1: 174,041,010 (GRCm39) |
D1270G |
probably benign |
Het |
Spta1 |
T |
A |
1: 174,045,469 (GRCm39) |
F1542L |
probably damaging |
Het |
Tacc3 |
T |
A |
5: 33,818,568 (GRCm39) |
M1K |
probably null |
Het |
Tax1bp1 |
T |
C |
6: 52,698,339 (GRCm39) |
V17A |
probably damaging |
Het |
Tmem156 |
T |
A |
5: 65,248,890 (GRCm39) |
E3D |
probably benign |
Het |
Tmem209 |
T |
A |
6: 30,487,417 (GRCm39) |
M530L |
probably benign |
Het |
Trpc2 |
A |
G |
7: 101,745,433 (GRCm39) |
D883G |
unknown |
Het |
Tsen34 |
GGAGCCAAAAT |
G |
7: 3,698,795 (GRCm39) |
|
probably null |
Het |
Uhrf2 |
T |
C |
19: 30,063,791 (GRCm39) |
Y585H |
probably damaging |
Het |
Vmn1r26 |
T |
A |
6: 57,985,705 (GRCm39) |
K161N |
probably benign |
Het |
Vmn1r29 |
A |
G |
6: 58,284,528 (GRCm39) |
S83G |
probably benign |
Het |
Vps13b |
G |
T |
15: 35,925,552 (GRCm39) |
W3829L |
probably null |
Het |
Vwce |
G |
A |
19: 10,630,449 (GRCm39) |
G503R |
probably damaging |
Het |
Zc3h11a |
T |
C |
1: 133,554,735 (GRCm39) |
E415G |
possibly damaging |
Het |
Zc3h14 |
T |
A |
12: 98,746,541 (GRCm39) |
|
probably null |
Het |
Zfp119b |
A |
T |
17: 56,246,499 (GRCm39) |
M229K |
probably benign |
Het |
Zfp384 |
CCAAGCTCAAGC |
CCAAGC |
6: 125,013,418 (GRCm39) |
|
probably benign |
Het |
Zfp384 |
GGCCCAGGC |
GGCCCAGGCCCACGCCCAGGC |
6: 125,013,451 (GRCm39) |
|
probably benign |
Het |
Zyx |
T |
A |
6: 42,334,330 (GRCm39) |
L518Q |
probably damaging |
Het |
|
Other mutations in Or52d3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01588:Or52d3
|
APN |
7 |
104,229,150 (GRCm39) |
missense |
probably damaging |
1.00 |
I2288:Or52d3
|
UTSW |
7 |
104,229,593 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Or52d3
|
UTSW |
7 |
104,229,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R0325:Or52d3
|
UTSW |
7 |
104,229,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Or52d3
|
UTSW |
7 |
104,229,268 (GRCm39) |
nonsense |
probably null |
|
R1599:Or52d3
|
UTSW |
7 |
104,228,855 (GRCm39) |
start codon destroyed |
probably null |
|
R1956:Or52d3
|
UTSW |
7 |
104,229,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Or52d3
|
UTSW |
7 |
104,228,848 (GRCm39) |
start gained |
probably benign |
|
R2418:Or52d3
|
UTSW |
7 |
104,229,141 (GRCm39) |
missense |
probably benign |
0.00 |
R2483:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4049:Or52d3
|
UTSW |
7 |
104,229,575 (GRCm39) |
missense |
probably benign |
|
R4755:Or52d3
|
UTSW |
7 |
104,229,268 (GRCm39) |
nonsense |
probably null |
|
R4757:Or52d3
|
UTSW |
7 |
104,229,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4828:Or52d3
|
UTSW |
7 |
104,229,180 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4842:Or52d3
|
UTSW |
7 |
104,229,422 (GRCm39) |
missense |
probably benign |
0.45 |
R5496:Or52d3
|
UTSW |
7 |
104,229,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Or52d3
|
UTSW |
7 |
104,229,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Or52d3
|
UTSW |
7 |
104,229,645 (GRCm39) |
nonsense |
probably null |
|
R7590:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7968:Or52d3
|
UTSW |
7 |
104,229,595 (GRCm39) |
nonsense |
probably null |
|
R8491:Or52d3
|
UTSW |
7 |
104,229,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R9306:Or52d3
|
UTSW |
7 |
104,229,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Or52d3
|
UTSW |
7 |
104,228,855 (GRCm39) |
start codon destroyed |
probably null |
|
R9557:Or52d3
|
UTSW |
7 |
104,229,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9682:Or52d3
|
UTSW |
7 |
104,229,434 (GRCm39) |
missense |
probably damaging |
1.00 |
|