Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apcdd1 |
G |
T |
18: 63,070,120 (GRCm39) |
R129L |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 98,101,943 (GRCm39) |
V844I |
probably damaging |
Het |
Arhgef5 |
T |
C |
6: 43,265,665 (GRCm39) |
V1569A |
probably damaging |
Het |
Atr |
T |
A |
9: 95,748,747 (GRCm39) |
S431T |
probably benign |
Het |
Cdh11 |
T |
C |
8: 103,360,953 (GRCm39) |
D795G |
possibly damaging |
Het |
Crygf |
T |
C |
1: 65,967,130 (GRCm39) |
S85P |
probably benign |
Het |
Dip2c |
T |
A |
13: 9,709,314 (GRCm39) |
Y1385N |
probably damaging |
Het |
Dnah14 |
G |
A |
1: 181,454,509 (GRCm39) |
V840I |
possibly damaging |
Het |
Dsg1a |
T |
C |
18: 20,461,795 (GRCm39) |
F299L |
possibly damaging |
Het |
Fgfr4 |
A |
T |
13: 55,314,013 (GRCm39) |
S576C |
probably damaging |
Het |
Frmd8 |
T |
C |
19: 5,919,546 (GRCm39) |
D167G |
probably damaging |
Het |
Gm5105 |
G |
A |
3: 137,755,319 (GRCm39) |
T89I |
unknown |
Het |
Grhl1 |
C |
T |
12: 24,625,996 (GRCm39) |
S35L |
possibly damaging |
Het |
Gsn |
A |
G |
2: 35,183,518 (GRCm39) |
E242G |
probably benign |
Het |
Hcrtr1 |
A |
G |
4: 130,029,661 (GRCm39) |
I140T |
probably damaging |
Het |
Ifnlr1 |
T |
C |
4: 135,431,135 (GRCm39) |
Y208H |
possibly damaging |
Het |
Ighv1-58 |
T |
C |
12: 115,275,985 (GRCm39) |
Y51C |
probably damaging |
Het |
Iqcj |
T |
A |
3: 67,948,580 (GRCm39) |
Y21* |
probably null |
Het |
Kcnc4 |
T |
C |
3: 107,366,178 (GRCm39) |
Y10C |
probably benign |
Het |
Kcnk7 |
G |
T |
19: 5,756,160 (GRCm39) |
G129W |
probably damaging |
Het |
Kcnq2 |
T |
A |
2: 180,723,517 (GRCm39) |
R620* |
probably null |
Het |
Klk13 |
C |
A |
7: 43,376,126 (GRCm39) |
P267Q |
probably benign |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 68,793,938 (GRCm39) |
R314H |
probably damaging |
Het |
Lamc2 |
T |
A |
1: 153,012,488 (GRCm39) |
M729L |
probably benign |
Het |
Lyst |
T |
G |
13: 13,918,044 (GRCm39) |
|
probably null |
Het |
Med13l |
G |
A |
5: 118,890,051 (GRCm39) |
R1909H |
probably damaging |
Het |
Mstn |
T |
A |
1: 53,103,243 (GRCm39) |
L193Q |
possibly damaging |
Het |
Mylk |
T |
C |
16: 34,820,796 (GRCm39) |
V125A |
possibly damaging |
Het |
Nalcn |
T |
A |
14: 123,647,233 (GRCm39) |
M547L |
probably damaging |
Het |
Nckap5 |
A |
G |
1: 125,952,785 (GRCm39) |
S1256P |
probably damaging |
Het |
Nkain1 |
T |
C |
4: 130,532,118 (GRCm38) |
Y189C |
probably damaging |
Het |
Oosp3 |
T |
A |
19: 11,676,783 (GRCm39) |
D47E |
probably benign |
Het |
Or14j8 |
A |
T |
17: 38,263,393 (GRCm39) |
I174N |
probably damaging |
Het |
Or5h25 |
A |
G |
16: 58,930,970 (GRCm39) |
M1T |
probably null |
Het |
Or5p66 |
T |
G |
7: 107,885,551 (GRCm39) |
I261L |
probably benign |
Het |
Pcdh15 |
G |
T |
10: 74,302,186 (GRCm39) |
G942W |
probably damaging |
Het |
Pcyox1l |
C |
A |
18: 61,840,625 (GRCm39) |
|
probably benign |
Het |
Peg3 |
T |
C |
7: 6,711,838 (GRCm39) |
E1128G |
possibly damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Plscr1 |
T |
A |
9: 92,146,715 (GRCm39) |
V119D |
probably damaging |
Het |
Prss56 |
A |
T |
1: 87,113,670 (GRCm39) |
D258V |
possibly damaging |
Het |
Ptpn23 |
T |
G |
9: 110,214,884 (GRCm39) |
K85Q |
possibly damaging |
Het |
Ranbp3l |
C |
A |
15: 9,037,159 (GRCm39) |
S7Y |
probably benign |
Het |
Rnf31 |
T |
C |
14: 55,829,690 (GRCm39) |
L85P |
probably damaging |
Het |
Rptn |
T |
C |
3: 93,305,207 (GRCm39) |
C847R |
possibly damaging |
Het |
Six4 |
T |
A |
12: 73,155,727 (GRCm39) |
E413D |
probably benign |
Het |
Slc30a2 |
G |
A |
4: 134,074,726 (GRCm39) |
R161Q |
probably damaging |
Het |
Sned1 |
T |
C |
1: 93,212,143 (GRCm39) |
V1115A |
probably damaging |
Het |
Spen |
T |
C |
4: 141,220,755 (GRCm39) |
K401E |
unknown |
Het |
Srbd1 |
T |
A |
17: 86,443,843 (GRCm39) |
R128W |
possibly damaging |
Het |
Strc |
A |
T |
2: 121,199,539 (GRCm39) |
I1300N |
probably damaging |
Het |
Susd1 |
T |
G |
4: 59,390,627 (GRCm39) |
T230P |
probably benign |
Het |
Thumpd2 |
G |
T |
17: 81,363,326 (GRCm39) |
S47* |
probably null |
Het |
Tmprss11a |
C |
T |
5: 86,576,429 (GRCm39) |
V141I |
probably damaging |
Het |
Tmprss15 |
T |
C |
16: 78,821,741 (GRCm39) |
Y438C |
possibly damaging |
Het |
Tnfrsf1a |
T |
C |
6: 125,333,914 (GRCm39) |
S56P |
probably damaging |
Het |
Ttc39d |
T |
C |
17: 80,523,610 (GRCm39) |
W90R |
probably benign |
Het |
Utp25 |
A |
G |
1: 192,797,163 (GRCm39) |
I563T |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Wdr20rt |
A |
T |
12: 65,272,536 (GRCm39) |
|
probably null |
Het |
Zfp646 |
C |
A |
7: 127,481,494 (GRCm39) |
Q1224K |
probably benign |
Het |
|
Other mutations in Or5d37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01522:Or5d37
|
APN |
2 |
87,923,360 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02894:Or5d37
|
APN |
2 |
87,924,107 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02977:Or5d37
|
APN |
2 |
87,923,915 (GRCm39) |
missense |
probably benign |
|
R0234:Or5d37
|
UTSW |
2 |
87,923,366 (GRCm39) |
nonsense |
probably null |
|
R0234:Or5d37
|
UTSW |
2 |
87,923,366 (GRCm39) |
nonsense |
probably null |
|
R0480:Or5d37
|
UTSW |
2 |
87,923,972 (GRCm39) |
missense |
probably benign |
|
R0644:Or5d37
|
UTSW |
2 |
87,923,633 (GRCm39) |
missense |
probably benign |
0.02 |
R1479:Or5d37
|
UTSW |
2 |
87,923,630 (GRCm39) |
missense |
probably benign |
0.05 |
R2047:Or5d37
|
UTSW |
2 |
87,924,237 (GRCm39) |
missense |
probably benign |
0.01 |
R2311:Or5d37
|
UTSW |
2 |
87,924,178 (GRCm39) |
missense |
probably benign |
0.00 |
R2973:Or5d37
|
UTSW |
2 |
87,923,458 (GRCm39) |
missense |
probably benign |
0.00 |
R3683:Or5d37
|
UTSW |
2 |
87,923,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R3685:Or5d37
|
UTSW |
2 |
87,923,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R4258:Or5d37
|
UTSW |
2 |
87,923,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Or5d37
|
UTSW |
2 |
87,923,876 (GRCm39) |
missense |
probably benign |
0.08 |
R4970:Or5d37
|
UTSW |
2 |
87,923,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Or5d37
|
UTSW |
2 |
87,923,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5258:Or5d37
|
UTSW |
2 |
87,923,762 (GRCm39) |
missense |
probably benign |
0.22 |
R5884:Or5d37
|
UTSW |
2 |
87,924,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Or5d37
|
UTSW |
2 |
87,924,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:Or5d37
|
UTSW |
2 |
87,923,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7055:Or5d37
|
UTSW |
2 |
87,924,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7314:Or5d37
|
UTSW |
2 |
87,923,458 (GRCm39) |
missense |
probably benign |
0.00 |
R7350:Or5d37
|
UTSW |
2 |
87,923,542 (GRCm39) |
missense |
probably benign |
0.01 |
R7527:Or5d37
|
UTSW |
2 |
87,923,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R8003:Or5d37
|
UTSW |
2 |
87,923,589 (GRCm39) |
nonsense |
probably null |
|
R8814:Or5d37
|
UTSW |
2 |
87,923,315 (GRCm39) |
missense |
probably benign |
|
R9072:Or5d37
|
UTSW |
2 |
87,924,172 (GRCm39) |
missense |
probably benign |
0.25 |
R9073:Or5d37
|
UTSW |
2 |
87,924,172 (GRCm39) |
missense |
probably benign |
0.25 |
R9189:Or5d37
|
UTSW |
2 |
87,924,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Or5d37
|
UTSW |
2 |
87,923,806 (GRCm39) |
missense |
probably benign |
|
R9284:Or5d37
|
UTSW |
2 |
87,924,278 (GRCm39) |
start codon destroyed |
probably benign |
|
Z1176:Or5d37
|
UTSW |
2 |
87,923,678 (GRCm39) |
missense |
probably damaging |
0.99 |
|