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 |
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 |
Vmn1r213 |
A |
G |
13: 23,195,564 (GRCm39) |
|
probably benign |
Het |
Znfx1 |
G |
A |
2: 166,889,574 (GRCm39) |
Q723* |
probably null |
Het |
|
Other mutations in Atg16l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Atg16l1
|
APN |
1 |
87,693,119 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00861:Atg16l1
|
APN |
1 |
87,702,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01065:Atg16l1
|
APN |
1 |
87,713,653 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01068:Atg16l1
|
APN |
1 |
87,702,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01140:Atg16l1
|
APN |
1 |
87,702,575 (GRCm39) |
missense |
probably benign |
0.03 |
R0023:Atg16l1
|
UTSW |
1 |
87,717,187 (GRCm39) |
missense |
probably benign |
0.00 |
R0023:Atg16l1
|
UTSW |
1 |
87,717,187 (GRCm39) |
missense |
probably benign |
0.00 |
R0655:Atg16l1
|
UTSW |
1 |
87,694,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:Atg16l1
|
UTSW |
1 |
87,714,080 (GRCm39) |
splice site |
probably benign |
|
R1549:Atg16l1
|
UTSW |
1 |
87,701,910 (GRCm39) |
missense |
probably benign |
|
R2202:Atg16l1
|
UTSW |
1 |
87,694,737 (GRCm39) |
missense |
probably benign |
0.03 |
R2204:Atg16l1
|
UTSW |
1 |
87,694,737 (GRCm39) |
missense |
probably benign |
0.03 |
R3689:Atg16l1
|
UTSW |
1 |
87,713,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R4012:Atg16l1
|
UTSW |
1 |
87,694,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4391:Atg16l1
|
UTSW |
1 |
87,687,842 (GRCm39) |
missense |
probably damaging |
0.97 |
R4839:Atg16l1
|
UTSW |
1 |
87,693,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R4935:Atg16l1
|
UTSW |
1 |
87,694,764 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4980:Atg16l1
|
UTSW |
1 |
87,694,553 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4990:Atg16l1
|
UTSW |
1 |
87,717,091 (GRCm39) |
missense |
probably benign |
0.00 |
R5011:Atg16l1
|
UTSW |
1 |
87,701,902 (GRCm39) |
nonsense |
probably null |
|
R5457:Atg16l1
|
UTSW |
1 |
87,702,813 (GRCm39) |
missense |
probably damaging |
0.96 |
R5897:Atg16l1
|
UTSW |
1 |
87,713,719 (GRCm39) |
critical splice donor site |
probably null |
|
R6289:Atg16l1
|
UTSW |
1 |
87,683,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R6437:Atg16l1
|
UTSW |
1 |
87,718,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R6727:Atg16l1
|
UTSW |
1 |
87,702,576 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6923:Atg16l1
|
UTSW |
1 |
87,702,078 (GRCm39) |
splice site |
probably null |
|
R7423:Atg16l1
|
UTSW |
1 |
87,714,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Atg16l1
|
UTSW |
1 |
87,687,805 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8493:Atg16l1
|
UTSW |
1 |
87,706,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R8742:Atg16l1
|
UTSW |
1 |
87,694,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Atg16l1
|
UTSW |
1 |
87,714,010 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9035:Atg16l1
|
UTSW |
1 |
87,693,167 (GRCm39) |
critical splice donor site |
probably null |
|
R9071:Atg16l1
|
UTSW |
1 |
87,683,907 (GRCm39) |
intron |
probably benign |
|
R9282:Atg16l1
|
UTSW |
1 |
87,707,906 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9706:Atg16l1
|
UTSW |
1 |
87,713,977 (GRCm39) |
missense |
possibly damaging |
0.64 |
|