Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020N15Rik |
A |
G |
X: 68,989,391 (GRCm39) |
S96G |
unknown |
Het |
4930447C04Rik |
T |
C |
12: 72,956,830 (GRCm39) |
D120G |
probably damaging |
Het |
Actmap |
A |
T |
7: 26,902,072 (GRCm39) |
H233L |
probably damaging |
Het |
Adgrg5 |
T |
A |
8: 95,660,785 (GRCm39) |
|
probably null |
Het |
Afg3l2 |
G |
T |
18: 67,548,627 (GRCm39) |
H534Q |
possibly damaging |
Het |
Ankar |
G |
A |
1: 72,695,380 (GRCm39) |
|
probably benign |
Het |
Arid2 |
T |
A |
15: 96,299,930 (GRCm39) |
F1814L |
possibly damaging |
Het |
Asb15 |
C |
T |
6: 24,566,163 (GRCm39) |
A372V |
probably damaging |
Het |
Atg16l1 |
A |
T |
1: 87,709,421 (GRCm39) |
D403V |
possibly damaging |
Het |
Bnc2 |
T |
C |
4: 84,211,433 (GRCm39) |
D407G |
probably benign |
Het |
Ccdc121 |
T |
C |
5: 31,643,312 (GRCm39) |
|
probably benign |
Het |
Cdan1 |
A |
G |
2: 120,556,526 (GRCm39) |
V633A |
probably benign |
Het |
Cfap46 |
T |
C |
7: 139,185,571 (GRCm39) |
Y2482C |
unknown |
Het |
Chd8 |
T |
C |
14: 52,439,761 (GRCm39) |
E964G |
probably benign |
Het |
Cyp2s1 |
A |
G |
7: 25,508,683 (GRCm39) |
V253A |
probably damaging |
Het |
Depdc1b |
A |
G |
13: 108,460,443 (GRCm39) |
N18D |
probably damaging |
Het |
Fis1 |
T |
A |
5: 136,991,048 (GRCm39) |
V4E |
probably damaging |
Het |
Gba2 |
T |
A |
4: 43,570,424 (GRCm39) |
|
probably null |
Het |
Gm2381 |
C |
T |
7: 42,469,504 (GRCm39) |
G207R |
probably damaging |
Het |
Gpr89 |
T |
A |
3: 96,804,640 (GRCm39) |
|
probably benign |
Het |
Gtf2i |
A |
G |
5: 134,290,691 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
G |
7: 55,762,958 (GRCm39) |
S896A |
probably damaging |
Het |
Huwe1 |
T |
C |
X: 150,659,309 (GRCm39) |
S921P |
probably damaging |
Het |
Iqgap1 |
T |
A |
7: 80,386,143 (GRCm39) |
K936I |
probably damaging |
Het |
Kcna4 |
T |
A |
2: 107,125,927 (GRCm39) |
Y220* |
probably null |
Het |
Krt18 |
A |
G |
15: 101,937,920 (GRCm39) |
D139G |
possibly damaging |
Het |
Krt87 |
T |
C |
15: 101,384,921 (GRCm39) |
N392D |
probably damaging |
Het |
L3mbtl4 |
G |
A |
17: 69,081,286 (GRCm39) |
C558Y |
probably damaging |
Het |
Lamc2 |
T |
A |
1: 153,019,622 (GRCm39) |
I440F |
possibly damaging |
Het |
Lrrc28 |
T |
C |
7: 67,267,833 (GRCm39) |
N98S |
probably damaging |
Het |
Lrrk1 |
G |
A |
7: 65,942,084 (GRCm39) |
A718V |
probably damaging |
Het |
Mrgprx2 |
T |
C |
7: 48,132,666 (GRCm39) |
I51V |
probably damaging |
Het |
Myt1 |
A |
T |
2: 181,424,408 (GRCm39) |
R25* |
probably null |
Het |
Npdc1 |
C |
T |
2: 25,298,021 (GRCm39) |
T199I |
probably benign |
Het |
Nup98 |
T |
A |
7: 101,801,660 (GRCm39) |
Y755F |
probably damaging |
Het |
Or51q1c |
A |
G |
7: 103,652,446 (GRCm39) |
|
probably null |
Het |
Or5p69 |
T |
A |
7: 107,966,996 (GRCm39) |
C100S |
probably damaging |
Het |
Or5p76 |
G |
T |
7: 108,122,289 (GRCm39) |
N289K |
probably damaging |
Het |
Or8g22 |
T |
A |
9: 38,957,996 (GRCm39) |
M240L |
probably benign |
Het |
Osgin1 |
A |
T |
8: 120,172,211 (GRCm39) |
Y335F |
probably damaging |
Het |
Pde10a |
A |
T |
17: 9,161,797 (GRCm39) |
I493F |
probably damaging |
Het |
Pdgfrb |
A |
G |
18: 61,212,780 (GRCm39) |
I895V |
probably benign |
Het |
Peg10 |
T |
TCCCCANNANNNN |
6: 4,756,475 (GRCm39) |
|
probably benign |
Het |
Pidd1 |
A |
T |
7: 141,020,726 (GRCm39) |
L457* |
probably null |
Het |
Pik3c2a |
A |
G |
7: 115,945,482 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
C |
G |
8: 110,350,281 (GRCm39) |
D375E |
possibly damaging |
Het |
Plcg1 |
C |
T |
2: 160,595,283 (GRCm39) |
|
probably benign |
Het |
Prr13 |
A |
C |
15: 102,370,650 (GRCm39) |
*138C |
probably null |
Het |
Prrc2b |
T |
C |
2: 32,119,267 (GRCm39) |
|
probably benign |
Het |
Psph |
T |
C |
5: 129,868,633 (GRCm39) |
|
probably benign |
Het |
Ripor1 |
A |
G |
8: 106,344,746 (GRCm39) |
|
probably benign |
Het |
Scg3 |
A |
G |
9: 75,576,617 (GRCm39) |
S253P |
probably damaging |
Het |
Sema6a |
G |
A |
18: 47,423,112 (GRCm39) |
|
probably null |
Het |
Sgk1 |
A |
G |
10: 21,758,556 (GRCm39) |
N7D |
probably damaging |
Het |
Skor2 |
T |
C |
18: 76,964,255 (GRCm39) |
F940L |
probably benign |
Het |
Slbp |
T |
C |
5: 33,802,833 (GRCm39) |
|
probably benign |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Susd5 |
A |
T |
9: 113,911,603 (GRCm39) |
H171L |
possibly damaging |
Het |
Sybu |
T |
C |
15: 44,536,664 (GRCm39) |
E354G |
probably benign |
Het |
Synpo |
T |
C |
18: 60,735,412 (GRCm39) |
N845D |
possibly damaging |
Het |
Tdrd6 |
A |
T |
17: 43,939,050 (GRCm39) |
I666N |
probably damaging |
Het |
Tm9sf4 |
T |
C |
2: 153,029,285 (GRCm39) |
I111T |
probably benign |
Het |
Tnc |
T |
C |
4: 63,926,971 (GRCm39) |
T852A |
probably benign |
Het |
Tnfrsf10b |
T |
A |
14: 70,013,625 (GRCm39) |
I185K |
probably damaging |
Het |
Tnks1bp1 |
A |
G |
2: 84,892,974 (GRCm39) |
E305G |
possibly damaging |
Het |
Tnrc6b |
T |
C |
15: 80,668,959 (GRCm39) |
V22A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,598,956 (GRCm39) |
F19319Y |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 38,031,051 (GRCm39) |
|
probably benign |
Het |
Ugt2b5 |
T |
A |
5: 87,287,627 (GRCm39) |
Q191L |
probably benign |
Het |
Urod |
T |
C |
4: 116,848,473 (GRCm39) |
T300A |
probably benign |
Het |
Znfx1 |
G |
A |
2: 166,889,574 (GRCm39) |
Q723* |
probably null |
Het |
|
Other mutations in Vmn1r213 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0018:Vmn1r213
|
UTSW |
13 |
23,196,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Vmn1r213
|
UTSW |
13 |
23,195,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Vmn1r213
|
UTSW |
13 |
23,195,588 (GRCm39) |
intron |
probably benign |
|
R0389:Vmn1r213
|
UTSW |
13 |
23,195,932 (GRCm39) |
missense |
probably benign |
0.00 |
R0652:Vmn1r213
|
UTSW |
13 |
23,195,564 (GRCm39) |
intron |
probably benign |
|
R1902:Vmn1r213
|
UTSW |
13 |
23,196,476 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1996:Vmn1r213
|
UTSW |
13 |
23,196,473 (GRCm39) |
missense |
probably benign |
0.02 |
R1997:Vmn1r213
|
UTSW |
13 |
23,196,473 (GRCm39) |
missense |
probably benign |
0.02 |
R4214:Vmn1r213
|
UTSW |
13 |
23,196,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4409:Vmn1r213
|
UTSW |
13 |
23,195,593 (GRCm39) |
intron |
probably benign |
|
R4650:Vmn1r213
|
UTSW |
13 |
23,196,422 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4685:Vmn1r213
|
UTSW |
13 |
23,195,800 (GRCm39) |
missense |
probably benign |
0.05 |
R4698:Vmn1r213
|
UTSW |
13 |
23,195,507 (GRCm39) |
intron |
probably benign |
|
R4799:Vmn1r213
|
UTSW |
13 |
23,196,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Vmn1r213
|
UTSW |
13 |
23,195,775 (GRCm39) |
nonsense |
probably null |
|
R5853:Vmn1r213
|
UTSW |
13 |
23,195,684 (GRCm39) |
missense |
probably benign |
0.32 |
R7389:Vmn1r213
|
UTSW |
13 |
23,196,556 (GRCm39) |
missense |
probably benign |
0.18 |
R7414:Vmn1r213
|
UTSW |
13 |
23,195,446 (GRCm39) |
missense |
unknown |
|
R8054:Vmn1r213
|
UTSW |
13 |
23,195,910 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9069:Vmn1r213
|
UTSW |
13 |
23,196,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Vmn1r213
|
UTSW |
13 |
23,196,343 (GRCm39) |
nonsense |
probably null |
|
R9428:Vmn1r213
|
UTSW |
13 |
23,195,944 (GRCm39) |
missense |
|
|
R9469:Vmn1r213
|
UTSW |
13 |
23,196,101 (GRCm39) |
missense |
probably benign |
0.22 |
R9633:Vmn1r213
|
UTSW |
13 |
23,195,519 (GRCm39) |
missense |
unknown |
|
|