Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
C |
A |
1: 12,045,177 (GRCm39) |
A443E |
unknown |
Het |
Acacb |
A |
T |
5: 114,334,770 (GRCm39) |
Y613F |
probably benign |
Het |
Adam23 |
A |
C |
1: 63,596,615 (GRCm39) |
I566L |
probably benign |
Het |
Adar |
G |
T |
3: 89,646,589 (GRCm39) |
R338L |
probably benign |
Het |
Akap14 |
C |
T |
X: 36,420,779 (GRCm39) |
A476T |
probably damaging |
Het |
Amotl1 |
T |
A |
9: 14,486,697 (GRCm39) |
Q399L |
probably benign |
Het |
Ankrd16 |
T |
G |
2: 11,783,407 (GRCm39) |
L3R |
probably benign |
Het |
Arfgap1 |
G |
C |
2: 180,615,881 (GRCm39) |
G187R |
probably damaging |
Het |
Arhgap19 |
A |
T |
19: 41,767,592 (GRCm39) |
V399D |
probably benign |
Het |
Arl4d |
A |
G |
11: 101,557,578 (GRCm39) |
T35A |
probably damaging |
Het |
Atr |
T |
A |
9: 95,747,150 (GRCm39) |
I144N |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,964,127 (GRCm39) |
M1574T |
probably benign |
Het |
Cacna1h |
T |
A |
17: 25,599,781 (GRCm39) |
D1684V |
probably damaging |
Het |
Celsr1 |
C |
A |
15: 85,916,960 (GRCm39) |
V338F |
probably damaging |
Het |
Cep164 |
T |
C |
9: 45,734,938 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
A |
G |
9: 105,658,301 (GRCm39) |
F637S |
probably damaging |
Het |
Crebrf |
T |
A |
17: 26,961,937 (GRCm39) |
Y345N |
probably benign |
Het |
Cstdc3 |
A |
T |
16: 36,128,449 (GRCm39) |
I15F |
probably damaging |
Het |
Cul1 |
A |
G |
6: 47,502,458 (GRCm39) |
|
probably null |
Het |
Cyb5r4 |
C |
T |
9: 86,923,332 (GRCm39) |
S185L |
probably benign |
Het |
Cyp3a57 |
T |
C |
5: 145,318,059 (GRCm39) |
Y347H |
probably damaging |
Het |
Dgkq |
G |
T |
5: 108,801,597 (GRCm39) |
T487K |
probably benign |
Het |
Dmkn |
T |
C |
7: 30,463,990 (GRCm39) |
V143A |
probably benign |
Het |
Dmp1 |
A |
T |
5: 104,355,496 (GRCm39) |
E32V |
possibly damaging |
Het |
Dsc3 |
T |
C |
18: 20,098,773 (GRCm39) |
D802G |
probably damaging |
Het |
Dse |
T |
C |
10: 34,029,225 (GRCm39) |
T622A |
probably benign |
Het |
Duxf4 |
A |
G |
10: 58,071,602 (GRCm39) |
V204A |
probably benign |
Het |
Dyrk1b |
A |
T |
7: 27,882,071 (GRCm39) |
|
probably null |
Het |
Ehd2 |
T |
C |
7: 15,686,113 (GRCm39) |
T320A |
probably benign |
Het |
Eif3a |
A |
C |
19: 60,770,635 (GRCm39) |
L71V |
probably damaging |
Het |
Eif4e1b |
A |
G |
13: 54,935,091 (GRCm39) |
|
probably null |
Het |
Fam131b |
A |
G |
6: 42,295,914 (GRCm39) |
F161L |
probably damaging |
Het |
Fam171b |
A |
T |
2: 83,683,725 (GRCm39) |
M81L |
probably benign |
Het |
Gal3st4 |
T |
C |
5: 138,269,050 (GRCm39) |
|
probably null |
Het |
Gdf11 |
A |
T |
10: 128,722,315 (GRCm39) |
V180E |
probably damaging |
Het |
Grin3a |
T |
A |
4: 49,792,437 (GRCm39) |
Y432F |
probably benign |
Het |
Hif1a |
C |
A |
12: 73,990,929 (GRCm39) |
H708N |
probably benign |
Het |
Hmcn2 |
G |
T |
2: 31,305,295 (GRCm39) |
|
probably null |
Het |
Hs3st6 |
T |
A |
17: 24,976,973 (GRCm39) |
M151K |
possibly damaging |
Het |
Hyal2 |
T |
A |
9: 107,449,537 (GRCm39) |
L431Q |
probably benign |
Het |
Hyal6 |
A |
T |
6: 24,740,857 (GRCm39) |
T337S |
probably benign |
Het |
Igsf5 |
A |
T |
16: 96,187,829 (GRCm39) |
|
probably null |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Krtap19-3 |
G |
A |
16: 88,674,878 (GRCm39) |
|
probably benign |
Het |
Lgalsl |
T |
C |
11: 20,779,420 (GRCm39) |
D75G |
probably benign |
Het |
Lrrc56 |
A |
G |
7: 140,787,421 (GRCm39) |
M353V |
probably benign |
Het |
Ltbp2 |
T |
A |
12: 84,877,555 (GRCm39) |
K337* |
probably null |
Het |
Mdn1 |
C |
T |
4: 32,730,881 (GRCm39) |
H2917Y |
probably benign |
Het |
Medag |
A |
G |
5: 149,353,259 (GRCm39) |
I151M |
probably damaging |
Het |
Meiob |
T |
C |
17: 25,042,544 (GRCm39) |
V124A |
probably damaging |
Het |
Mmp3 |
A |
G |
9: 7,451,799 (GRCm39) |
H379R |
probably benign |
Het |
Mpg |
A |
G |
11: 32,181,957 (GRCm39) |
|
probably null |
Het |
Ncoa6 |
G |
T |
2: 155,263,559 (GRCm39) |
Q292K |
probably benign |
Het |
Ndufaf6 |
G |
T |
4: 11,053,474 (GRCm39) |
H277Q |
probably benign |
Het |
Nlrp4c |
A |
G |
7: 6,087,655 (GRCm39) |
I763V |
probably benign |
Het |
Nlrp5 |
A |
T |
7: 23,117,586 (GRCm39) |
I437F |
probably damaging |
Het |
Noc2l |
G |
A |
4: 156,329,727 (GRCm39) |
R435Q |
probably damaging |
Het |
Nova2 |
T |
C |
7: 18,692,326 (GRCm39) |
I485T |
probably damaging |
Het |
Nrxn2 |
G |
A |
19: 6,538,825 (GRCm39) |
V794I |
probably benign |
Het |
Nup210l |
A |
G |
3: 90,061,806 (GRCm39) |
T662A |
probably damaging |
Het |
Or2ad1 |
A |
T |
13: 21,326,564 (GRCm39) |
I221N |
probably damaging |
Het |
Or2b28 |
A |
G |
13: 21,531,346 (GRCm39) |
M83V |
possibly damaging |
Het |
Or2p2 |
A |
T |
13: 21,256,641 (GRCm39) |
F277I |
probably damaging |
Het |
Or51aa2 |
G |
A |
7: 103,187,859 (GRCm39) |
T194I |
probably damaging |
Het |
Or51e2 |
A |
C |
7: 102,391,571 (GRCm39) |
I213S |
probably damaging |
Het |
Or51l14 |
G |
A |
7: 103,101,332 (GRCm39) |
V263I |
probably benign |
Het |
Or9g8 |
T |
C |
2: 85,607,582 (GRCm39) |
L218P |
probably damaging |
Het |
Pelp1 |
G |
A |
11: 70,285,568 (GRCm39) |
P767S |
probably damaging |
Het |
Pfdn1 |
C |
A |
18: 36,584,153 (GRCm39) |
M60I |
probably benign |
Het |
Plaat1 |
G |
A |
16: 29,036,470 (GRCm39) |
G36D |
probably damaging |
Het |
Plcxd3 |
T |
A |
15: 4,546,093 (GRCm39) |
|
probably benign |
Het |
Plekhg1 |
C |
A |
10: 3,895,917 (GRCm39) |
D436E |
possibly damaging |
Het |
Ppfibp1 |
G |
A |
6: 146,892,090 (GRCm39) |
V117I |
probably benign |
Het |
Prss44 |
A |
G |
9: 110,643,177 (GRCm39) |
K24R |
probably benign |
Het |
Ptger1 |
G |
T |
8: 84,395,107 (GRCm39) |
G195W |
probably benign |
Het |
Ptgs1 |
A |
C |
2: 36,132,782 (GRCm39) |
D260A |
probably benign |
Het |
Ptprd |
T |
A |
4: 75,865,384 (GRCm39) |
T1198S |
probably damaging |
Het |
Qsox2 |
A |
G |
2: 26,104,074 (GRCm39) |
S319P |
probably damaging |
Het |
Rab35 |
A |
G |
5: 115,778,147 (GRCm39) |
I38V |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 71,861,408 (GRCm39) |
I33V |
possibly damaging |
Het |
Rbbp8nl |
C |
T |
2: 179,924,006 (GRCm39) |
|
probably benign |
Het |
Riok1 |
A |
T |
13: 38,242,694 (GRCm39) |
K473* |
probably null |
Het |
Rtca |
C |
T |
3: 116,287,764 (GRCm39) |
G288S |
probably benign |
Het |
Sag |
A |
T |
1: 87,742,570 (GRCm39) |
D114V |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sec61g |
A |
G |
11: 16,456,371 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
A |
T |
4: 124,623,288 (GRCm39) |
I440F |
probably damaging |
Het |
Sgta |
T |
C |
10: 80,884,695 (GRCm39) |
K205E |
possibly damaging |
Het |
Slc36a4 |
A |
G |
9: 15,632,006 (GRCm39) |
T61A |
probably damaging |
Het |
Slc5a4a |
T |
C |
10: 76,002,569 (GRCm39) |
S242P |
probably benign |
Het |
Srgap3 |
A |
T |
6: 112,748,479 (GRCm39) |
L391Q |
probably damaging |
Het |
Stard13 |
T |
C |
5: 151,018,903 (GRCm39) |
Y60C |
probably damaging |
Het |
Styxl2 |
T |
C |
1: 165,928,415 (GRCm39) |
Y399C |
possibly damaging |
Het |
Syt12 |
G |
T |
19: 4,497,825 (GRCm39) |
H386N |
probably damaging |
Het |
Thyn1 |
T |
A |
9: 26,915,070 (GRCm39) |
M74K |
probably benign |
Het |
Tmem130 |
C |
A |
5: 144,689,093 (GRCm39) |
|
probably null |
Het |
Trim71 |
A |
G |
9: 114,392,016 (GRCm39) |
V57A |
possibly damaging |
Het |
Twf1 |
T |
C |
15: 94,483,428 (GRCm39) |
|
probably benign |
Het |
Tyro3 |
T |
A |
2: 119,632,176 (GRCm39) |
I81N |
possibly damaging |
Het |
Unc13a |
A |
T |
8: 72,105,043 (GRCm39) |
C740S |
probably damaging |
Het |
Vmn1r15 |
A |
T |
6: 57,235,616 (GRCm39) |
K161N |
probably benign |
Het |
Vmn1r16 |
A |
T |
6: 57,299,884 (GRCm39) |
I246N |
probably damaging |
Het |
Vmn1r42 |
A |
G |
6: 89,821,597 (GRCm39) |
I324T |
probably benign |
Het |
Vmn2r35 |
T |
C |
7: 7,819,805 (GRCm39) |
Y155C |
possibly damaging |
Het |
Wif1 |
T |
A |
10: 120,919,788 (GRCm39) |
|
probably null |
Het |
Wscd2 |
G |
A |
5: 113,689,231 (GRCm39) |
R79Q |
possibly damaging |
Het |
Zan |
G |
T |
5: 137,404,139 (GRCm39) |
|
probably benign |
Het |
Zfp9 |
G |
T |
6: 118,442,021 (GRCm39) |
H214N |
probably benign |
Het |
Zfp985 |
A |
T |
4: 147,667,315 (GRCm39) |
Y61F |
probably benign |
Het |
Zscan30 |
A |
G |
18: 24,104,524 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Clock |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00598:Clock
|
APN |
5 |
76,377,311 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00725:Clock
|
APN |
5 |
76,402,260 (GRCm39) |
nonsense |
probably null |
|
IGL01304:Clock
|
APN |
5 |
76,414,202 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01369:Clock
|
APN |
5 |
76,384,933 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01542:Clock
|
APN |
5 |
76,379,322 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02541:Clock
|
APN |
5 |
76,410,519 (GRCm39) |
splice site |
probably null |
|
IGL02602:Clock
|
APN |
5 |
76,402,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02602:Clock
|
APN |
5 |
76,402,273 (GRCm39) |
missense |
probably null |
1.00 |
IGL03186:Clock
|
APN |
5 |
76,390,929 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03309:Clock
|
APN |
5 |
76,379,241 (GRCm39) |
critical splice donor site |
probably null |
|
R6760_Clock_188
|
UTSW |
5 |
76,374,823 (GRCm39) |
missense |
unknown |
|
uhr
|
UTSW |
5 |
76,377,401 (GRCm39) |
nonsense |
probably null |
|
R0304:Clock
|
UTSW |
5 |
76,374,832 (GRCm39) |
missense |
unknown |
|
R0593:Clock
|
UTSW |
5 |
76,413,683 (GRCm39) |
missense |
probably benign |
0.25 |
R0654:Clock
|
UTSW |
5 |
76,374,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0684:Clock
|
UTSW |
5 |
76,393,365 (GRCm39) |
missense |
probably damaging |
0.96 |
R0707:Clock
|
UTSW |
5 |
76,374,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0751:Clock
|
UTSW |
5 |
76,377,208 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0865:Clock
|
UTSW |
5 |
76,414,271 (GRCm39) |
splice site |
probably benign |
|
R0920:Clock
|
UTSW |
5 |
76,378,167 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1396:Clock
|
UTSW |
5 |
76,414,649 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Clock
|
UTSW |
5 |
76,410,578 (GRCm39) |
nonsense |
probably null |
|
R1487:Clock
|
UTSW |
5 |
76,414,201 (GRCm39) |
splice site |
probably null |
|
R1574:Clock
|
UTSW |
5 |
76,390,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Clock
|
UTSW |
5 |
76,390,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Clock
|
UTSW |
5 |
76,396,309 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1905:Clock
|
UTSW |
5 |
76,414,735 (GRCm39) |
splice site |
probably benign |
|
R1937:Clock
|
UTSW |
5 |
76,377,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R2411:Clock
|
UTSW |
5 |
76,379,360 (GRCm39) |
missense |
probably benign |
0.08 |
R2887:Clock
|
UTSW |
5 |
76,393,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R3410:Clock
|
UTSW |
5 |
76,377,401 (GRCm39) |
nonsense |
probably null |
|
R4514:Clock
|
UTSW |
5 |
76,378,046 (GRCm39) |
missense |
probably benign |
0.00 |
R4598:Clock
|
UTSW |
5 |
76,383,657 (GRCm39) |
missense |
probably benign |
0.00 |
R4599:Clock
|
UTSW |
5 |
76,383,657 (GRCm39) |
missense |
probably benign |
0.00 |
R4795:Clock
|
UTSW |
5 |
76,413,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Clock
|
UTSW |
5 |
76,413,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Clock
|
UTSW |
5 |
76,402,258 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5204:Clock
|
UTSW |
5 |
76,391,017 (GRCm39) |
splice site |
probably null |
|
R5271:Clock
|
UTSW |
5 |
76,389,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5547:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5630:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5631:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5632:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5787:Clock
|
UTSW |
5 |
76,384,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Clock
|
UTSW |
5 |
76,385,000 (GRCm39) |
missense |
probably benign |
0.45 |
R6578:Clock
|
UTSW |
5 |
76,364,556 (GRCm39) |
missense |
unknown |
|
R6622:Clock
|
UTSW |
5 |
76,389,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6760:Clock
|
UTSW |
5 |
76,374,823 (GRCm39) |
missense |
unknown |
|
R6793:Clock
|
UTSW |
5 |
76,384,967 (GRCm39) |
frame shift |
probably null |
|
R7406:Clock
|
UTSW |
5 |
76,414,692 (GRCm39) |
start codon destroyed |
probably null |
0.26 |
R7414:Clock
|
UTSW |
5 |
76,410,611 (GRCm39) |
missense |
probably benign |
0.00 |
R7560:Clock
|
UTSW |
5 |
76,390,738 (GRCm39) |
splice site |
probably null |
|
R7593:Clock
|
UTSW |
5 |
76,384,145 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7640:Clock
|
UTSW |
5 |
76,396,225 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7708:Clock
|
UTSW |
5 |
76,414,256 (GRCm39) |
missense |
probably benign |
0.00 |
R7713:Clock
|
UTSW |
5 |
76,393,267 (GRCm39) |
critical splice donor site |
probably null |
|
R7807:Clock
|
UTSW |
5 |
76,390,982 (GRCm39) |
missense |
probably benign |
0.01 |
R8171:Clock
|
UTSW |
5 |
76,414,261 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8190:Clock
|
UTSW |
5 |
76,375,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R8225:Clock
|
UTSW |
5 |
76,389,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R8309:Clock
|
UTSW |
5 |
76,402,269 (GRCm39) |
missense |
probably benign |
0.07 |
R8557:Clock
|
UTSW |
5 |
76,377,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Clock
|
UTSW |
5 |
76,410,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8869:Clock
|
UTSW |
5 |
76,374,889 (GRCm39) |
small deletion |
probably benign |
|
R8870:Clock
|
UTSW |
5 |
76,383,632 (GRCm39) |
missense |
probably benign |
0.17 |
R8980:Clock
|
UTSW |
5 |
76,402,286 (GRCm39) |
missense |
probably benign |
0.01 |
R8982:Clock
|
UTSW |
5 |
76,364,559 (GRCm39) |
missense |
unknown |
|
R9177:Clock
|
UTSW |
5 |
76,377,256 (GRCm39) |
missense |
probably benign |
0.00 |
R9208:Clock
|
UTSW |
5 |
76,384,871 (GRCm39) |
missense |
probably benign |
0.00 |
R9213:Clock
|
UTSW |
5 |
76,393,376 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9307:Clock
|
UTSW |
5 |
76,364,671 (GRCm39) |
missense |
unknown |
|
R9446:Clock
|
UTSW |
5 |
76,396,288 (GRCm39) |
missense |
probably benign |
0.00 |
R9516:Clock
|
UTSW |
5 |
76,377,227 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9572:Clock
|
UTSW |
5 |
76,377,338 (GRCm39) |
missense |
probably benign |
0.00 |
R9630:Clock
|
UTSW |
5 |
76,393,281 (GRCm39) |
missense |
probably benign |
0.03 |
|