Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
A |
C |
19: 3,766,686 (GRCm39) |
N91T |
possibly damaging |
Het |
2510009E07Rik |
CCGGAAGGGGAGGAGCAGTGACCCAGTTTCGGA |
CCGGA |
16: 21,472,148 (GRCm39) |
|
probably null |
Het |
4932414N04Rik |
A |
G |
2: 68,562,498 (GRCm39) |
D375G |
possibly damaging |
Het |
Adad2 |
C |
A |
8: 120,339,725 (GRCm39) |
P69Q |
probably benign |
Het |
Adamts3 |
G |
A |
5: 89,825,575 (GRCm39) |
T1088I |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,726,720 (GRCm39) |
V858A |
probably benign |
Het |
Ankrd13a |
A |
G |
5: 114,939,798 (GRCm39) |
N475S |
probably benign |
Het |
Barhl2 |
G |
A |
5: 106,603,352 (GRCm39) |
T269I |
probably benign |
Het |
Boc |
G |
A |
16: 44,323,931 (GRCm39) |
R157W |
|
Het |
Bsn |
G |
T |
9: 107,984,752 (GRCm39) |
P3101T |
unknown |
Het |
Catsperb |
C |
A |
12: 101,486,904 (GRCm39) |
A477E |
possibly damaging |
Het |
Ccser1 |
T |
A |
6: 61,787,842 (GRCm39) |
I220K |
probably benign |
Het |
Cd200r3 |
A |
T |
16: 44,778,102 (GRCm39) |
I242F |
possibly damaging |
Het |
Cdc34b |
A |
C |
11: 94,632,911 (GRCm39) |
D37A |
probably damaging |
Het |
Chek2 |
A |
G |
5: 111,013,458 (GRCm39) |
|
probably benign |
Het |
Cngb1 |
A |
T |
8: 95,989,736 (GRCm39) |
V792D |
probably damaging |
Het |
Cops7a |
T |
C |
6: 124,939,371 (GRCm39) |
K93E |
possibly damaging |
Het |
Crispld1 |
T |
C |
1: 17,820,995 (GRCm39) |
I345T |
possibly damaging |
Het |
Dgkd |
A |
G |
1: 87,869,157 (GRCm39) |
D1170G |
probably damaging |
Het |
Dhx35 |
A |
G |
2: 158,648,918 (GRCm39) |
T115A |
possibly damaging |
Het |
Dnai1 |
G |
A |
4: 41,625,125 (GRCm39) |
R363H |
probably benign |
Het |
Dnmbp |
T |
A |
19: 43,878,681 (GRCm39) |
Q130L |
probably benign |
Het |
Egfr |
A |
G |
11: 16,861,635 (GRCm39) |
Y1138C |
probably damaging |
Het |
Enkur |
A |
G |
2: 21,201,568 (GRCm39) |
M39T |
probably benign |
Het |
Epha7 |
T |
C |
4: 28,821,615 (GRCm39) |
I260T |
probably damaging |
Het |
Fbxo28 |
A |
T |
1: 182,144,634 (GRCm39) |
I310K |
probably damaging |
Het |
Fga |
C |
A |
3: 82,939,111 (GRCm39) |
N495K |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,601,247 (GRCm39) |
D344G |
probably damaging |
Het |
Gm572 |
A |
G |
4: 148,751,290 (GRCm39) |
Q221R |
probably benign |
Het |
Gpa33 |
G |
A |
1: 165,974,216 (GRCm39) |
A18T |
probably benign |
Het |
Gpatch11 |
C |
T |
17: 79,145,289 (GRCm39) |
T6I |
probably benign |
Het |
Gpr84 |
T |
A |
15: 103,217,625 (GRCm39) |
S151C |
probably damaging |
Het |
H2-M11 |
T |
A |
17: 36,859,851 (GRCm39) |
Y281* |
probably null |
Het |
Hadh |
T |
C |
3: 131,038,891 (GRCm39) |
N155S |
probably benign |
Het |
Hoxd13 |
A |
G |
2: 74,500,266 (GRCm39) |
Y269C |
|
Het |
Iars1 |
T |
A |
13: 49,882,177 (GRCm39) |
C1074S |
probably benign |
Het |
Ibtk |
G |
T |
9: 85,625,457 (GRCm39) |
H98N |
possibly damaging |
Het |
Igsf10 |
C |
T |
3: 59,233,739 (GRCm39) |
G1665R |
probably benign |
Het |
Inpp5d |
A |
G |
1: 87,625,337 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
C |
1: 135,321,951 (GRCm39) |
V593G |
probably damaging |
Het |
Irx3 |
T |
C |
8: 92,526,915 (GRCm39) |
D263G |
possibly damaging |
Het |
Kif13a |
A |
G |
13: 46,927,154 (GRCm39) |
V1179A |
probably benign |
Het |
Lrrc4c |
T |
C |
2: 97,460,393 (GRCm39) |
Y340H |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,045,219 (GRCm39) |
D155G |
probably damaging |
Het |
Mical2 |
T |
A |
7: 111,980,671 (GRCm39) |
I105N |
probably damaging |
Het |
Mob2 |
A |
T |
7: 141,563,261 (GRCm39) |
L66Q |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,096,739 (GRCm39) |
S337G |
probably benign |
Het |
Neb |
T |
C |
2: 52,096,259 (GRCm39) |
D1002G |
probably benign |
Het |
Nebl |
A |
T |
2: 17,382,928 (GRCm39) |
N116K |
probably benign |
Het |
Nkx2-6 |
T |
C |
14: 69,412,623 (GRCm39) |
S264P |
probably benign |
Het |
Nlgn3 |
T |
C |
X: 100,352,390 (GRCm39) |
V179A |
probably damaging |
Het |
Nlrp4e |
A |
G |
7: 23,020,556 (GRCm39) |
T348A |
possibly damaging |
Het |
Nomo1 |
A |
T |
7: 45,722,004 (GRCm39) |
I982F |
probably benign |
Het |
Or10j5 |
A |
G |
1: 172,784,186 (GRCm39) |
|
probably benign |
Het |
Or11g24 |
T |
G |
14: 50,662,291 (GRCm39) |
F105C |
probably damaging |
Het |
Or1j19 |
A |
T |
2: 36,676,621 (GRCm39) |
Y28F |
probably benign |
Het |
Or8g22 |
A |
G |
9: 38,958,077 (GRCm39) |
F213L |
possibly damaging |
Het |
Palld |
A |
G |
8: 62,003,198 (GRCm39) |
|
probably null |
Het |
Pcdh7 |
A |
G |
5: 57,879,154 (GRCm39) |
Y903C |
probably damaging |
Het |
Pknox2 |
G |
A |
9: 36,804,167 (GRCm39) |
T460M |
possibly damaging |
Het |
Ppm1h |
C |
T |
10: 122,714,451 (GRCm39) |
T330I |
probably damaging |
Het |
Ppp2r2b |
C |
T |
18: 42,821,399 (GRCm39) |
R253H |
probably damaging |
Het |
Pramel58 |
G |
T |
5: 94,831,413 (GRCm39) |
R140L |
possibly damaging |
Het |
Prr18 |
G |
A |
17: 8,560,476 (GRCm39) |
A211T |
probably benign |
Het |
Ptgs2 |
A |
G |
1: 149,979,859 (GRCm39) |
I321M |
|
Het |
Rara |
G |
T |
11: 98,860,989 (GRCm39) |
R159L |
probably damaging |
Het |
Rasa4 |
T |
A |
5: 136,133,446 (GRCm39) |
I635N |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,989,888 (GRCm39) |
H423L |
possibly damaging |
Het |
Scn4b |
A |
G |
9: 45,059,169 (GRCm39) |
I147V |
possibly damaging |
Het |
Scrn3 |
G |
A |
2: 73,161,352 (GRCm39) |
V313I |
probably benign |
Het |
Scrn3 |
C |
A |
2: 73,161,355 (GRCm39) |
P314T |
possibly damaging |
Het |
Sh2b1 |
A |
G |
7: 126,070,292 (GRCm39) |
|
probably null |
Het |
Slc26a10 |
T |
C |
10: 127,016,459 (GRCm39) |
Q3R |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,149,139 (GRCm39) |
I524T |
probably damaging |
Het |
Smcp |
T |
A |
3: 92,491,530 (GRCm39) |
N106Y |
unknown |
Het |
Spata31h1 |
T |
C |
10: 82,122,379 (GRCm39) |
T3544A |
probably benign |
Het |
St8sia5 |
G |
A |
18: 77,336,172 (GRCm39) |
V202M |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,028,526 (GRCm39) |
D512E |
probably damaging |
Het |
Tas1r2 |
A |
G |
4: 139,397,046 (GRCm39) |
E795G |
probably damaging |
Het |
Tdrd1 |
T |
A |
19: 56,831,145 (GRCm39) |
V320D |
probably damaging |
Het |
Tmem71 |
T |
A |
15: 66,404,606 (GRCm39) |
I261L |
probably benign |
Het |
Tns2 |
T |
C |
15: 102,020,039 (GRCm39) |
L643P |
probably damaging |
Het |
Upf1 |
G |
A |
8: 70,786,815 (GRCm39) |
Q890* |
probably null |
Het |
Usp43 |
A |
T |
11: 67,782,307 (GRCm39) |
H370Q |
possibly damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,507,356 (GRCm39) |
I158N |
possibly damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,286,532 (GRCm39) |
N343K |
probably benign |
Het |
Vwa8 |
T |
C |
14: 79,329,815 (GRCm39) |
S1216P |
probably benign |
Het |
Yars1 |
A |
C |
4: 129,090,747 (GRCm39) |
D97A |
probably damaging |
Het |
Zer1 |
G |
A |
2: 30,001,035 (GRCm39) |
H129Y |
probably benign |
Het |
Zfat |
C |
T |
15: 67,956,404 (GRCm39) |
D1143N |
possibly damaging |
Het |
|
Other mutations in Elf3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02141:Elf3
|
APN |
1 |
135,185,445 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02470:Elf3
|
APN |
1 |
135,182,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03018:Elf3
|
APN |
1 |
135,183,803 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03252:Elf3
|
APN |
1 |
135,182,691 (GRCm39) |
missense |
probably damaging |
1.00 |
P0026:Elf3
|
UTSW |
1 |
135,183,711 (GRCm39) |
critical splice donor site |
probably null |
|
R0087:Elf3
|
UTSW |
1 |
135,184,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:Elf3
|
UTSW |
1 |
135,184,531 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1897:Elf3
|
UTSW |
1 |
135,184,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R2081:Elf3
|
UTSW |
1 |
135,184,814 (GRCm39) |
missense |
probably benign |
0.12 |
R4049:Elf3
|
UTSW |
1 |
135,182,015 (GRCm39) |
missense |
probably benign |
0.21 |
R4467:Elf3
|
UTSW |
1 |
135,184,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4630:Elf3
|
UTSW |
1 |
135,184,478 (GRCm39) |
intron |
probably benign |
|
R4715:Elf3
|
UTSW |
1 |
135,185,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R4923:Elf3
|
UTSW |
1 |
135,184,473 (GRCm39) |
intron |
probably benign |
|
R5226:Elf3
|
UTSW |
1 |
135,184,977 (GRCm39) |
missense |
probably benign |
0.07 |
R5422:Elf3
|
UTSW |
1 |
135,182,778 (GRCm39) |
missense |
probably damaging |
0.98 |
R5706:Elf3
|
UTSW |
1 |
135,184,220 (GRCm39) |
missense |
probably benign |
0.01 |
R7115:Elf3
|
UTSW |
1 |
135,184,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Elf3
|
UTSW |
1 |
135,184,244 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7855:Elf3
|
UTSW |
1 |
135,182,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R7940:Elf3
|
UTSW |
1 |
135,184,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R8315:Elf3
|
UTSW |
1 |
135,184,314 (GRCm39) |
missense |
probably benign |
0.00 |
R8723:Elf3
|
UTSW |
1 |
135,185,385 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8724:Elf3
|
UTSW |
1 |
135,182,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R8960:Elf3
|
UTSW |
1 |
135,182,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|