Other mutations in this stock |
Total: 139 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931403M11Rik |
C |
A |
14: 24,671,419 (GRCm39) |
|
noncoding transcript |
Het |
Abca7 |
A |
G |
10: 79,838,562 (GRCm39) |
K612R |
probably damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,223,822 (GRCm39) |
V275A |
possibly damaging |
Het |
Afg3l1 |
G |
A |
8: 124,215,065 (GRCm39) |
|
probably null |
Het |
Ajm1 |
G |
A |
2: 25,469,759 (GRCm39) |
R51C |
possibly damaging |
Het |
Alcam |
T |
A |
16: 52,089,176 (GRCm39) |
H508L |
probably benign |
Het |
Ankrd45 |
G |
A |
1: 160,982,942 (GRCm39) |
R151H |
probably damaging |
Het |
Aqr |
G |
A |
2: 113,980,990 (GRCm39) |
L264F |
probably damaging |
Het |
Arfgef2 |
G |
A |
2: 166,677,533 (GRCm39) |
A53T |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,236,880 (GRCm39) |
T1085A |
probably benign |
Het |
Atp10a |
T |
C |
7: 58,435,055 (GRCm39) |
V314A |
probably damaging |
Het |
Bdp1 |
T |
C |
13: 100,187,627 (GRCm39) |
D1580G |
probably benign |
Het |
Btbd17 |
T |
A |
11: 114,684,917 (GRCm39) |
T41S |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,728,400 (GRCm39) |
N378S |
probably damaging |
Het |
Camsap1 |
G |
T |
2: 25,825,562 (GRCm39) |
Q1375K |
probably benign |
Het |
Catsper2 |
G |
T |
2: 121,227,604 (GRCm39) |
|
probably null |
Het |
Cblif |
A |
G |
19: 11,729,583 (GRCm39) |
T181A |
probably benign |
Het |
Ccar1 |
A |
G |
10: 62,588,997 (GRCm39) |
S829P |
unknown |
Het |
Ccdc180 |
T |
C |
4: 45,909,308 (GRCm39) |
L492P |
probably damaging |
Het |
Ccser2 |
A |
T |
14: 36,662,343 (GRCm39) |
N280K |
probably damaging |
Het |
Cd37 |
T |
C |
7: 44,883,359 (GRCm39) |
D271G |
probably damaging |
Het |
Cdcp1 |
G |
A |
9: 123,011,194 (GRCm39) |
|
probably benign |
Het |
Cemip2 |
T |
C |
19: 21,833,528 (GRCm39) |
V1322A |
probably benign |
Het |
Cep85 |
T |
A |
4: 133,892,062 (GRCm39) |
|
probably benign |
Het |
Cfi |
C |
T |
3: 129,666,726 (GRCm39) |
P483L |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 15,945,674 (GRCm39) |
|
probably benign |
Het |
Cytl1 |
G |
T |
5: 37,892,918 (GRCm39) |
L9F |
unknown |
Het |
Defb26 |
T |
C |
2: 152,350,085 (GRCm39) |
E65G |
possibly damaging |
Het |
Degs1 |
G |
A |
1: 182,104,370 (GRCm39) |
T305I |
probably damaging |
Het |
Dnttip2 |
T |
G |
3: 122,070,241 (GRCm39) |
C485W |
probably damaging |
Het |
Ecel1 |
G |
A |
1: 87,076,449 (GRCm39) |
|
probably benign |
Het |
Edrf1 |
G |
T |
7: 133,260,339 (GRCm39) |
M83I |
probably damaging |
Het |
Elmo2 |
A |
T |
2: 165,137,209 (GRCm39) |
C562S |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,344,922 (GRCm39) |
|
probably null |
Het |
F2r |
A |
C |
13: 95,740,905 (GRCm39) |
V210G |
probably damaging |
Het |
Fam171a1 |
T |
A |
2: 3,224,546 (GRCm39) |
V179E |
probably damaging |
Het |
Fmod |
G |
T |
1: 133,967,977 (GRCm39) |
V6F |
possibly damaging |
Het |
Foxr2 |
A |
G |
X: 151,913,312 (GRCm39) |
Q61R |
probably damaging |
Het |
Gabra4 |
G |
A |
5: 71,729,546 (GRCm39) |
H76Y |
probably benign |
Het |
Gck |
A |
T |
11: 5,859,150 (GRCm39) |
M139K |
possibly damaging |
Het |
Gm10192 |
C |
G |
4: 97,071,345 (GRCm39) |
S20T |
probably null |
Het |
Gm44501 |
T |
C |
17: 40,887,515 (GRCm39) |
L11P |
unknown |
Het |
Gm572 |
T |
C |
4: 148,751,302 (GRCm39) |
|
probably null |
Het |
Gnas |
A |
G |
2: 174,139,882 (GRCm39) |
K17R |
possibly damaging |
Het |
Grm2 |
T |
A |
9: 106,527,865 (GRCm39) |
S340C |
probably damaging |
Het |
Gsc |
T |
A |
12: 104,438,274 (GRCm39) |
H198L |
probably damaging |
Het |
H2-Q3 |
A |
T |
17: 35,578,424 (GRCm39) |
|
noncoding transcript |
Het |
H4c1 |
T |
C |
13: 23,944,935 (GRCm39) |
D69G |
probably damaging |
Het |
Hivep3 |
A |
G |
4: 119,980,131 (GRCm39) |
E1723G |
probably damaging |
Het |
Hk3 |
A |
T |
13: 55,154,405 (GRCm39) |
L757Q |
probably damaging |
Het |
Homer2 |
A |
T |
7: 81,299,311 (GRCm39) |
D51E |
probably benign |
Het |
Ier3ip1 |
T |
A |
18: 77,027,227 (GRCm39) |
|
probably benign |
Het |
Itch |
T |
A |
2: 155,059,897 (GRCm39) |
|
probably null |
Het |
Kalrn |
T |
A |
16: 33,991,700 (GRCm39) |
Q974L |
probably damaging |
Het |
Kirrel3 |
G |
T |
9: 34,924,601 (GRCm39) |
G296W |
probably damaging |
Het |
Klhl17 |
A |
G |
4: 156,315,082 (GRCm39) |
V525A |
probably benign |
Het |
Klhl9 |
T |
C |
4: 88,640,182 (GRCm39) |
K20E |
probably benign |
Het |
Kmt2a |
G |
T |
9: 44,732,977 (GRCm39) |
|
probably benign |
Het |
Krt17 |
C |
A |
11: 100,147,305 (GRCm39) |
V409L |
probably benign |
Het |
Lmx1b |
T |
C |
2: 33,454,802 (GRCm39) |
N322S |
probably benign |
Het |
Lrrc63 |
G |
C |
14: 75,363,406 (GRCm39) |
P242A |
probably benign |
Het |
Ltk |
T |
C |
2: 119,583,708 (GRCm39) |
N256D |
probably damaging |
Het |
Map3k19 |
T |
A |
1: 127,745,470 (GRCm39) |
E1328V |
probably damaging |
Het |
Map4k2 |
C |
T |
19: 6,394,033 (GRCm39) |
A280V |
probably benign |
Het |
Micall1 |
C |
T |
15: 79,016,048 (GRCm39) |
R802* |
probably null |
Het |
Mmp14 |
A |
G |
14: 54,673,662 (GRCm39) |
R109G |
probably damaging |
Het |
Mmp27 |
A |
T |
9: 7,581,369 (GRCm39) |
H544L |
probably benign |
Het |
Mpeg1 |
A |
G |
19: 12,440,434 (GRCm39) |
T631A |
probably damaging |
Het |
Mpnd |
A |
G |
17: 56,318,641 (GRCm39) |
M217V |
probably benign |
Het |
Mrc2 |
T |
C |
11: 105,232,034 (GRCm39) |
V862A |
probably damaging |
Het |
Mug2 |
T |
A |
6: 122,058,154 (GRCm39) |
S1239T |
probably damaging |
Het |
Myb |
T |
A |
10: 21,002,137 (GRCm39) |
M616L |
probably benign |
Het |
Myo18b |
A |
T |
5: 113,022,346 (GRCm39) |
|
probably benign |
Het |
Myo1c |
C |
A |
11: 75,560,053 (GRCm39) |
T703N |
probably damaging |
Het |
Myt1l |
T |
G |
12: 29,936,138 (GRCm39) |
C909G |
unknown |
Het |
Nbea |
T |
C |
3: 55,912,776 (GRCm39) |
S1004G |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,186,319 (GRCm39) |
N918D |
probably benign |
Het |
Nrtn |
T |
C |
17: 57,058,636 (GRCm39) |
T122A |
probably damaging |
Het |
Nsd3 |
A |
T |
8: 26,188,939 (GRCm39) |
S1042C |
probably damaging |
Het |
Ntmt2 |
A |
T |
1: 163,530,633 (GRCm39) |
C269S |
probably benign |
Het |
Nvl |
A |
G |
1: 180,945,191 (GRCm39) |
L461S |
probably damaging |
Het |
Onecut2 |
A |
T |
18: 64,473,998 (GRCm39) |
H183L |
possibly damaging |
Het |
Or13p5 |
A |
C |
4: 118,591,885 (GRCm39) |
H53P |
probably benign |
Het |
Or2h2 |
G |
A |
17: 37,396,343 (GRCm39) |
T238I |
probably damaging |
Het |
Or4d10 |
C |
G |
19: 12,051,679 (GRCm39) |
G106R |
probably damaging |
Het |
Or52e4 |
A |
G |
7: 104,705,689 (GRCm39) |
T79A |
possibly damaging |
Het |
Or5c1 |
T |
G |
2: 37,222,601 (GRCm39) |
F281V |
probably damaging |
Het |
Or6c1b |
A |
C |
10: 129,273,248 (GRCm39) |
D189A |
possibly damaging |
Het |
Or6z5 |
A |
T |
7: 6,477,612 (GRCm39) |
I168F |
probably damaging |
Het |
Pcdhb21 |
G |
T |
18: 37,648,130 (GRCm39) |
V420F |
possibly damaging |
Het |
Pcdhb9 |
G |
A |
18: 37,536,286 (GRCm39) |
G760D |
probably benign |
Het |
Pglyrp2 |
G |
A |
17: 32,637,771 (GRCm39) |
P86S |
probably benign |
Het |
Phyhip |
T |
A |
14: 70,704,765 (GRCm39) |
V328E |
probably damaging |
Het |
Pitpnb |
A |
T |
5: 111,530,862 (GRCm39) |
K218N |
possibly damaging |
Het |
Pitrm1 |
A |
G |
13: 6,628,596 (GRCm39) |
D963G |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,258,792 (GRCm39) |
Y699C |
probably damaging |
Het |
Pmpcb |
T |
A |
5: 21,945,660 (GRCm39) |
|
probably benign |
Het |
Polg |
A |
T |
7: 79,114,353 (GRCm39) |
W203R |
probably damaging |
Het |
Pramel22 |
A |
G |
4: 143,380,971 (GRCm39) |
S351P |
probably benign |
Het |
Prss41 |
A |
T |
17: 24,055,977 (GRCm39) |
M252K |
probably benign |
Het |
Prss46 |
A |
T |
9: 110,673,618 (GRCm39) |
M1L |
possibly damaging |
Het |
Rimklb |
T |
C |
6: 122,441,051 (GRCm39) |
|
probably null |
Het |
Rngtt |
T |
C |
4: 33,500,335 (GRCm39) |
I556T |
unknown |
Het |
Rock1 |
A |
C |
18: 10,122,698 (GRCm39) |
D374E |
probably benign |
Het |
Rspry1 |
C |
A |
8: 95,385,417 (GRCm39) |
H450N |
probably benign |
Het |
Rusc2 |
T |
C |
4: 43,423,942 (GRCm39) |
V1032A |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,449,647 (GRCm39) |
R3898G |
probably damaging |
Het |
Scnn1b |
A |
T |
7: 121,502,110 (GRCm39) |
H256L |
probably benign |
Het |
Sh3gl2 |
T |
A |
4: 85,297,494 (GRCm39) |
H157Q |
probably benign |
Het |
Sipa1l1 |
C |
A |
12: 82,389,107 (GRCm39) |
S444R |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,433,818 (GRCm39) |
I478F |
probably damaging |
Het |
Spata31e2 |
A |
G |
1: 26,722,628 (GRCm39) |
Y851H |
probably benign |
Het |
Sptb |
G |
T |
12: 76,655,811 (GRCm39) |
L1424M |
probably benign |
Het |
Sry |
T |
A |
Y: 2,663,105 (GRCm39) |
H185L |
unknown |
Het |
Stox2 |
T |
G |
8: 47,656,198 (GRCm39) |
T93P |
probably damaging |
Het |
Tatdn2 |
T |
A |
6: 113,681,566 (GRCm39) |
F472Y |
possibly damaging |
Het |
Tefm |
A |
T |
11: 80,031,185 (GRCm39) |
V17D |
possibly damaging |
Het |
Tekt2 |
G |
T |
4: 126,218,460 (GRCm39) |
T70N |
probably benign |
Het |
Ticam1 |
T |
C |
17: 56,578,642 (GRCm39) |
D151G |
probably damaging |
Het |
Tmem63c |
A |
G |
12: 87,136,139 (GRCm39) |
E785G |
probably damaging |
Het |
Tnmd |
A |
T |
X: 132,765,551 (GRCm39) |
N219I |
probably benign |
Het |
Ttc14 |
T |
A |
3: 33,861,024 (GRCm39) |
L407* |
probably null |
Het |
Ttll7 |
T |
C |
3: 146,599,932 (GRCm39) |
M1T |
probably null |
Het |
Ttn |
T |
A |
2: 76,746,835 (GRCm39) |
|
probably null |
Het |
Uchl1 |
T |
C |
5: 66,833,780 (GRCm39) |
M12T |
probably benign |
Het |
Uggt2 |
A |
T |
14: 119,315,062 (GRCm39) |
|
probably null |
Het |
Uggt2 |
T |
C |
14: 119,286,665 (GRCm39) |
T224A |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,218,175 (GRCm39) |
E1254G |
probably damaging |
Het |
Unc5d |
A |
G |
8: 29,156,927 (GRCm39) |
F773L |
probably benign |
Het |
Unc80 |
C |
A |
1: 66,683,606 (GRCm39) |
P2216Q |
probably damaging |
Het |
Usp40 |
T |
A |
1: 87,913,923 (GRCm39) |
|
probably null |
Het |
Vmn1r117 |
A |
T |
7: 20,617,421 (GRCm39) |
M209K |
probably damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,380,985 (GRCm39) |
W303R |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,224,478 (GRCm39) |
R268C |
probably damaging |
Het |
Wnt2 |
T |
C |
6: 18,023,125 (GRCm39) |
K175E |
possibly damaging |
Het |
Zfp125 |
A |
G |
12: 20,950,459 (GRCm39) |
|
noncoding transcript |
Het |
Zfp512b |
A |
C |
2: 181,228,856 (GRCm39) |
V703G |
probably damaging |
Het |
Zglp1 |
A |
T |
9: 20,973,957 (GRCm39) |
I243N |
probably benign |
Het |
Zgpat |
T |
C |
2: 181,020,651 (GRCm39) |
S275P |
probably benign |
Het |
|
Other mutations in Xkr6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Xkr6
|
APN |
14 |
64,056,664 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01419:Xkr6
|
APN |
14 |
64,056,325 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01450:Xkr6
|
APN |
14 |
64,035,664 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02010:Xkr6
|
APN |
14 |
64,056,653 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02352:Xkr6
|
APN |
14 |
64,057,156 (GRCm39) |
missense |
unknown |
|
IGL02359:Xkr6
|
APN |
14 |
64,057,156 (GRCm39) |
missense |
unknown |
|
R0148:Xkr6
|
UTSW |
14 |
64,056,998 (GRCm39) |
missense |
unknown |
|
R0521:Xkr6
|
UTSW |
14 |
64,056,871 (GRCm39) |
missense |
probably benign |
0.28 |
R1555:Xkr6
|
UTSW |
14 |
64,056,374 (GRCm39) |
missense |
unknown |
|
R1619:Xkr6
|
UTSW |
14 |
64,056,766 (GRCm39) |
missense |
probably benign |
0.39 |
R1874:Xkr6
|
UTSW |
14 |
64,035,745 (GRCm39) |
missense |
unknown |
|
R2864:Xkr6
|
UTSW |
14 |
64,057,205 (GRCm39) |
missense |
unknown |
|
R2960:Xkr6
|
UTSW |
14 |
63,844,586 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3014:Xkr6
|
UTSW |
14 |
64,056,793 (GRCm39) |
missense |
unknown |
|
R5019:Xkr6
|
UTSW |
14 |
64,056,515 (GRCm39) |
missense |
unknown |
|
R5193:Xkr6
|
UTSW |
14 |
64,056,356 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5354:Xkr6
|
UTSW |
14 |
64,056,353 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5485:Xkr6
|
UTSW |
14 |
64,056,833 (GRCm39) |
missense |
unknown |
|
R5825:Xkr6
|
UTSW |
14 |
64,056,481 (GRCm39) |
missense |
probably benign |
0.39 |
R5885:Xkr6
|
UTSW |
14 |
63,844,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R6074:Xkr6
|
UTSW |
14 |
63,844,519 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6861:Xkr6
|
UTSW |
14 |
64,057,093 (GRCm39) |
missense |
probably benign |
0.39 |
R7289:Xkr6
|
UTSW |
14 |
64,035,748 (GRCm39) |
missense |
unknown |
|
R7477:Xkr6
|
UTSW |
14 |
63,844,129 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7525:Xkr6
|
UTSW |
14 |
64,056,610 (GRCm39) |
missense |
probably benign |
0.39 |
R7528:Xkr6
|
UTSW |
14 |
64,056,610 (GRCm39) |
missense |
probably benign |
0.39 |
R7529:Xkr6
|
UTSW |
14 |
64,056,610 (GRCm39) |
missense |
probably benign |
0.39 |
R7646:Xkr6
|
UTSW |
14 |
63,844,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R7686:Xkr6
|
UTSW |
14 |
63,844,295 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7697:Xkr6
|
UTSW |
14 |
63,844,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R8331:Xkr6
|
UTSW |
14 |
64,056,392 (GRCm39) |
missense |
unknown |
|
R8702:Xkr6
|
UTSW |
14 |
64,057,103 (GRCm39) |
missense |
unknown |
|
R9169:Xkr6
|
UTSW |
14 |
63,844,067 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1176:Xkr6
|
UTSW |
14 |
63,844,394 (GRCm39) |
missense |
probably benign |
0.08 |
|