Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
A |
G |
7: 29,277,153 (GRCm39) |
|
noncoding transcript |
Het |
Aaas |
A |
T |
15: 102,255,111 (GRCm39) |
|
probably null |
Het |
Abcc3 |
G |
A |
11: 94,255,247 (GRCm39) |
R600W |
probably damaging |
Het |
Abhd13 |
A |
T |
8: 10,038,318 (GRCm39) |
Q305L |
probably benign |
Het |
Adcy5 |
A |
T |
16: 34,977,486 (GRCm39) |
I340F |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,871,994 (GRCm39) |
I964N |
probably damaging |
Het |
Anks1b |
T |
A |
10: 89,912,926 (GRCm39) |
H316Q |
probably damaging |
Het |
Ap3d1 |
A |
T |
10: 80,554,964 (GRCm39) |
F454I |
possibly damaging |
Het |
Apol7c |
T |
C |
15: 77,410,599 (GRCm39) |
R116G |
possibly damaging |
Het |
Arhgap5 |
A |
G |
12: 52,566,695 (GRCm39) |
E1222G |
possibly damaging |
Het |
AW551984 |
A |
G |
9: 39,502,559 (GRCm39) |
V673A |
probably benign |
Het |
Baiap2l1 |
A |
G |
5: 144,218,949 (GRCm39) |
S220P |
probably damaging |
Het |
Bcl6 |
A |
G |
16: 23,791,926 (GRCm39) |
F143L |
probably benign |
Het |
Calb1 |
A |
T |
4: 15,900,811 (GRCm39) |
T165S |
probably benign |
Het |
Ccdc66 |
C |
A |
14: 27,228,668 (GRCm39) |
G6C |
probably damaging |
Het |
Ccdc88a |
A |
G |
11: 29,453,484 (GRCm39) |
I344V |
probably benign |
Het |
Cdh19 |
T |
A |
1: 110,857,587 (GRCm39) |
D249V |
probably damaging |
Het |
Ces1c |
T |
A |
8: 93,854,227 (GRCm39) |
T103S |
probably benign |
Het |
Cfap54 |
T |
A |
10: 92,808,473 (GRCm39) |
K1401* |
probably null |
Het |
Copa |
T |
A |
1: 171,932,789 (GRCm39) |
N371K |
probably damaging |
Het |
Cyp2b10 |
A |
T |
7: 25,616,437 (GRCm39) |
Y348F |
probably damaging |
Het |
Dennd5a |
T |
C |
7: 109,504,928 (GRCm39) |
R861G |
possibly damaging |
Het |
Dhx8 |
T |
C |
11: 101,623,862 (GRCm39) |
|
probably benign |
Het |
Dido1 |
C |
T |
2: 180,301,445 (GRCm39) |
W2153* |
probably null |
Het |
Dlgap1 |
T |
A |
17: 71,125,156 (GRCm39) |
V969D |
probably damaging |
Het |
Dvl3 |
A |
G |
16: 20,336,039 (GRCm39) |
D32G |
probably damaging |
Het |
Epdr1 |
T |
C |
13: 19,778,718 (GRCm39) |
D24G |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,307,043 (GRCm39) |
|
probably null |
Het |
Fhad1 |
C |
T |
4: 141,632,442 (GRCm39) |
M1232I |
probably benign |
Het |
Gcnt2 |
A |
C |
13: 41,014,429 (GRCm39) |
E200A |
probably damaging |
Het |
Gm5174 |
A |
G |
10: 86,492,409 (GRCm39) |
|
noncoding transcript |
Het |
Gm6408 |
T |
A |
5: 146,421,267 (GRCm39) |
F299I |
possibly damaging |
Het |
Gpr85 |
G |
T |
6: 13,836,000 (GRCm39) |
Y301* |
probably null |
Het |
Gucy2e |
G |
T |
11: 69,117,082 (GRCm39) |
P780T |
probably damaging |
Het |
Icam5 |
A |
T |
9: 20,946,116 (GRCm39) |
N316I |
probably damaging |
Het |
Ifit1bl1 |
C |
T |
19: 34,571,677 (GRCm39) |
R260Q |
probably damaging |
Het |
Il1r1 |
A |
C |
1: 40,264,411 (GRCm39) |
|
probably benign |
Het |
Kif3c |
A |
T |
12: 3,439,656 (GRCm39) |
I86F |
probably benign |
Het |
Mast2 |
A |
G |
4: 116,292,760 (GRCm39) |
L9P |
probably damaging |
Het |
Mcoln1 |
G |
T |
8: 3,560,389 (GRCm39) |
C316F |
probably damaging |
Het |
Mon1a |
A |
T |
9: 107,775,894 (GRCm39) |
D4V |
probably damaging |
Het |
Ms4a18 |
T |
A |
19: 10,991,038 (GRCm39) |
M19L |
probably benign |
Het |
Nbea |
T |
C |
3: 55,539,392 (GRCm39) |
K2790E |
probably benign |
Het |
Niban1 |
C |
T |
1: 151,593,307 (GRCm39) |
T664I |
probably benign |
Het |
Noc3l |
C |
T |
19: 38,803,139 (GRCm39) |
E167K |
possibly damaging |
Het |
Nol10 |
G |
A |
12: 17,466,829 (GRCm39) |
E570K |
possibly damaging |
Het |
Nr2e3 |
T |
C |
9: 59,856,484 (GRCm39) |
R69G |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,892,294 (GRCm39) |
R1358* |
probably null |
Het |
Or14j4 |
A |
T |
17: 37,921,145 (GRCm39) |
F166I |
probably damaging |
Het |
Or2b7 |
C |
A |
13: 21,739,266 (GRCm39) |
V309F |
probably damaging |
Het |
Or52e8b |
A |
G |
7: 104,673,428 (GRCm39) |
I253T |
probably damaging |
Het |
Or5b117 |
A |
T |
19: 13,431,746 (GRCm39) |
M45K |
probably benign |
Het |
Pak2 |
A |
T |
16: 31,860,337 (GRCm39) |
D175E |
probably benign |
Het |
Pccb |
C |
T |
9: 100,867,856 (GRCm39) |
V357I |
possibly damaging |
Het |
Pcdhb4 |
C |
T |
18: 37,442,034 (GRCm39) |
P448L |
probably damaging |
Het |
Pcdhb9 |
A |
G |
18: 37,534,167 (GRCm39) |
M54V |
probably benign |
Het |
Ppp3cb |
A |
G |
14: 20,570,758 (GRCm39) |
|
probably benign |
Het |
Ppp4r1 |
A |
G |
17: 66,131,563 (GRCm39) |
D452G |
probably benign |
Het |
Pramel18 |
T |
A |
4: 101,767,317 (GRCm39) |
F189I |
probably benign |
Het |
Prmt3 |
T |
A |
7: 49,476,499 (GRCm39) |
D369E |
probably damaging |
Het |
Psmd12 |
T |
A |
11: 107,377,301 (GRCm39) |
V120D |
probably benign |
Het |
Ptprb |
T |
C |
10: 116,189,732 (GRCm39) |
L1797P |
probably damaging |
Het |
Ptprm |
A |
G |
17: 67,227,191 (GRCm39) |
S653P |
probably damaging |
Het |
Pxdn |
T |
A |
12: 30,053,141 (GRCm39) |
V926D |
probably damaging |
Het |
Retreg3 |
T |
G |
11: 100,997,165 (GRCm39) |
Q105P |
probably damaging |
Het |
Sacs |
A |
T |
14: 61,443,890 (GRCm39) |
R1979* |
probably null |
Het |
Scn2a |
T |
A |
2: 65,537,639 (GRCm39) |
L696* |
probably null |
Het |
Sema3c |
A |
T |
5: 17,916,422 (GRCm39) |
N465Y |
probably damaging |
Het |
Slc25a32 |
A |
T |
15: 38,963,308 (GRCm39) |
V171E |
possibly damaging |
Het |
Slc30a7 |
C |
T |
3: 115,783,700 (GRCm39) |
V158I |
probably benign |
Het |
Slc44a5 |
G |
A |
3: 153,975,802 (GRCm39) |
|
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,685,045 (GRCm39) |
D140G |
probably damaging |
Het |
Slc7a11 |
G |
A |
3: 50,397,532 (GRCm39) |
S60L |
possibly damaging |
Het |
Spryd3 |
A |
T |
15: 102,040,372 (GRCm39) |
H59Q |
probably benign |
Het |
Sqstm1 |
T |
C |
11: 50,093,849 (GRCm39) |
D256G |
probably damaging |
Het |
Sst |
A |
T |
16: 23,708,487 (GRCm39) |
S115T |
probably damaging |
Het |
Stimate |
A |
G |
14: 30,592,776 (GRCm39) |
K166E |
probably damaging |
Het |
Surf1 |
T |
C |
2: 26,805,963 (GRCm39) |
|
probably benign |
Het |
Synj1 |
A |
T |
16: 90,806,865 (GRCm39) |
|
probably benign |
Het |
Tet1 |
C |
A |
10: 62,714,073 (GRCm39) |
C574F |
probably damaging |
Het |
Thnsl1 |
T |
A |
2: 21,217,201 (GRCm39) |
Y318* |
probably null |
Het |
Tomm70a |
A |
G |
16: 56,942,493 (GRCm39) |
E90G |
probably damaging |
Het |
Treml4 |
A |
G |
17: 48,571,927 (GRCm39) |
D110G |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Txnl1 |
C |
T |
18: 63,797,396 (GRCm39) |
G283D |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,282,906 (GRCm39) |
D559G |
probably damaging |
Het |
Usp4 |
T |
C |
9: 108,233,661 (GRCm39) |
V94A |
possibly damaging |
Het |
Vmn2r25 |
A |
C |
6: 123,802,255 (GRCm39) |
C549W |
probably damaging |
Het |
Vmn2r59 |
G |
T |
7: 41,695,105 (GRCm39) |
Q436K |
probably benign |
Het |
Wdr70 |
A |
T |
15: 7,913,769 (GRCm39) |
Y627N |
possibly damaging |
Het |
Xpr1 |
T |
C |
1: 155,188,609 (GRCm39) |
I344V |
probably benign |
Het |
Zfp423 |
T |
A |
8: 88,585,968 (GRCm39) |
Q61L |
possibly damaging |
Het |
|
Other mutations in Klhdc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00900:Klhdc2
|
APN |
12 |
69,350,308 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00990:Klhdc2
|
APN |
12 |
69,353,987 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01024:Klhdc2
|
APN |
12 |
69,352,610 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01457:Klhdc2
|
APN |
12 |
69,343,827 (GRCm39) |
missense |
probably benign |
|
IGL01735:Klhdc2
|
APN |
12 |
69,347,053 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01913:Klhdc2
|
APN |
12 |
69,349,132 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02440:Klhdc2
|
APN |
12 |
69,350,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Dixit_dominus
|
UTSW |
12 |
69,355,750 (GRCm39) |
nonsense |
probably null |
|
R0611:Klhdc2
|
UTSW |
12 |
69,347,053 (GRCm39) |
missense |
probably benign |
0.22 |
R0724:Klhdc2
|
UTSW |
12 |
69,343,822 (GRCm39) |
missense |
probably benign |
|
R1350:Klhdc2
|
UTSW |
12 |
69,352,484 (GRCm39) |
critical splice donor site |
probably null |
|
R1796:Klhdc2
|
UTSW |
12 |
69,347,071 (GRCm39) |
critical splice donor site |
probably null |
|
R1907:Klhdc2
|
UTSW |
12 |
69,343,734 (GRCm39) |
start gained |
probably benign |
|
R4418:Klhdc2
|
UTSW |
12 |
69,354,371 (GRCm39) |
unclassified |
probably benign |
|
R5119:Klhdc2
|
UTSW |
12 |
69,343,736 (GRCm39) |
utr 5 prime |
probably benign |
|
R5987:Klhdc2
|
UTSW |
12 |
69,350,387 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6448:Klhdc2
|
UTSW |
12 |
69,350,694 (GRCm39) |
missense |
probably benign |
|
R6848:Klhdc2
|
UTSW |
12 |
69,355,750 (GRCm39) |
nonsense |
probably null |
|
R7824:Klhdc2
|
UTSW |
12 |
69,354,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R7844:Klhdc2
|
UTSW |
12 |
69,349,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R7886:Klhdc2
|
UTSW |
12 |
69,351,406 (GRCm39) |
splice site |
probably null |
|
R8963:Klhdc2
|
UTSW |
12 |
69,347,065 (GRCm39) |
nonsense |
probably null |
|
R9775:Klhdc2
|
UTSW |
12 |
69,350,393 (GRCm39) |
missense |
probably damaging |
0.99 |
R9790:Klhdc2
|
UTSW |
12 |
69,346,995 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Klhdc2
|
UTSW |
12 |
69,346,995 (GRCm39) |
missense |
probably benign |
0.01 |
RF016:Klhdc2
|
UTSW |
12 |
69,350,660 (GRCm39) |
missense |
probably damaging |
0.97 |
|