Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
A |
T |
5: 8,736,212 (GRCm39) |
I202L |
probably benign |
Het |
Acadsb |
A |
T |
7: 131,045,423 (GRCm39) |
T452S |
unknown |
Het |
Ago2 |
A |
T |
15: 72,991,315 (GRCm39) |
L541Q |
probably damaging |
Het |
Ap2a2 |
A |
T |
7: 141,200,812 (GRCm39) |
E553V |
probably damaging |
Het |
Astn2 |
T |
C |
4: 65,910,663 (GRCm39) |
K442E |
unknown |
Het |
Bicd1 |
A |
G |
6: 149,414,633 (GRCm39) |
T449A |
probably benign |
Het |
Btn1a1 |
T |
A |
13: 23,645,919 (GRCm39) |
Q150L |
probably benign |
Het |
C1ra |
G |
A |
6: 124,499,610 (GRCm39) |
G599R |
probably damaging |
Het |
Camta2 |
T |
A |
11: 70,561,886 (GRCm39) |
Q1076L |
probably benign |
Het |
Capza2 |
T |
A |
6: 17,657,214 (GRCm39) |
C157S |
probably damaging |
Het |
Chd3 |
T |
A |
11: 69,251,483 (GRCm39) |
D516V |
probably damaging |
Het |
Cntnap5b |
A |
G |
1: 99,999,832 (GRCm39) |
T197A |
probably benign |
Het |
Comp |
A |
G |
8: 70,829,110 (GRCm39) |
N260S |
probably damaging |
Het |
Dcp1a |
A |
G |
14: 30,244,883 (GRCm39) |
T570A |
possibly damaging |
Het |
Ddx60 |
T |
A |
8: 62,393,142 (GRCm39) |
|
probably null |
Het |
Defb22 |
C |
T |
2: 152,327,712 (GRCm39) |
V158I |
unknown |
Het |
Diaph3 |
T |
C |
14: 87,103,949 (GRCm39) |
S812G |
probably damaging |
Het |
Dohh |
G |
T |
10: 81,221,844 (GRCm39) |
Q79H |
probably benign |
Het |
Dyrk1b |
T |
G |
7: 27,882,080 (GRCm39) |
V147G |
probably benign |
Het |
Fastkd2 |
C |
T |
1: 63,787,183 (GRCm39) |
T539I |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,306,622 (GRCm39) |
D229N |
probably damaging |
Het |
Kcnv1 |
A |
T |
15: 44,972,754 (GRCm39) |
D376E |
probably benign |
Het |
Kif13a |
C |
A |
13: 46,906,057 (GRCm39) |
V1577F |
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 68,793,938 (GRCm39) |
R314H |
probably damaging |
Het |
Mcoln2 |
A |
C |
3: 145,898,179 (GRCm39) |
N100T |
unknown |
Het |
Mdh1b |
C |
T |
1: 63,759,164 (GRCm39) |
V143M |
possibly damaging |
Het |
Mfsd4b4 |
G |
T |
10: 39,768,101 (GRCm39) |
Q377K |
probably benign |
Het |
Mpv17l |
T |
C |
16: 13,762,584 (GRCm39) |
F122S |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,742,949 (GRCm39) |
S1154P |
probably damaging |
Het |
Myo5b |
A |
G |
18: 74,760,261 (GRCm39) |
Y259C |
probably damaging |
Het |
Nek1 |
G |
A |
8: 61,558,646 (GRCm39) |
V931M |
probably benign |
Het |
Nkd2 |
C |
A |
13: 73,969,437 (GRCm39) |
G343V |
probably damaging |
Het |
Obox8 |
T |
A |
7: 14,065,928 (GRCm39) |
T197S |
probably benign |
Het |
Or10j5 |
T |
A |
1: 172,784,744 (GRCm39) |
C127* |
probably null |
Het |
Or13g1 |
G |
A |
7: 85,955,962 (GRCm39) |
R120C |
probably benign |
Het |
Or4b1b |
A |
G |
2: 90,112,616 (GRCm39) |
F101S |
possibly damaging |
Het |
Or5m11b |
T |
G |
2: 85,806,085 (GRCm39) |
M166R |
probably benign |
Het |
Or5m11b |
T |
C |
2: 85,805,766 (GRCm39) |
Y60H |
probably damaging |
Het |
Or5p57 |
A |
G |
7: 107,664,980 (GRCm39) |
S342P |
probably damaging |
Het |
Or5t7 |
T |
A |
2: 86,507,218 (GRCm39) |
H153L |
probably benign |
Het |
Palb2 |
A |
T |
7: 121,724,097 (GRCm39) |
S551T |
probably damaging |
Het |
Pcdha12 |
T |
A |
18: 37,154,953 (GRCm39) |
D557E |
probably damaging |
Het |
Pcdhb21 |
T |
A |
18: 37,648,921 (GRCm39) |
D683E |
probably benign |
Het |
Plekhb1 |
A |
G |
7: 100,305,936 (GRCm39) |
|
probably benign |
Het |
Plekhg5 |
A |
G |
4: 152,187,464 (GRCm39) |
N90D |
probably damaging |
Het |
Pnpla1 |
A |
G |
17: 29,100,579 (GRCm39) |
D482G |
probably benign |
Het |
Rc3h1 |
A |
T |
1: 160,768,329 (GRCm39) |
|
probably benign |
Het |
Rfpl4 |
C |
T |
7: 5,113,539 (GRCm39) |
R214H |
probably benign |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Setd5 |
T |
C |
6: 113,092,031 (GRCm39) |
I284T |
possibly damaging |
Het |
Smurf1 |
C |
T |
5: 144,830,897 (GRCm39) |
E293K |
possibly damaging |
Het |
Tas2r106 |
A |
T |
6: 131,655,023 (GRCm39) |
I276N |
probably damaging |
Het |
Tbc1d2 |
C |
A |
4: 46,649,791 (GRCm39) |
A82S |
possibly damaging |
Het |
Tex19.2 |
A |
G |
11: 121,008,010 (GRCm39) |
I146T |
possibly damaging |
Het |
Tmem107 |
T |
G |
11: 68,962,281 (GRCm39) |
N79K |
probably damaging |
Het |
Tpsab1 |
A |
T |
17: 25,564,305 (GRCm39) |
S50T |
probably benign |
Het |
Ttn |
T |
A |
2: 76,553,594 (GRCm39) |
K31008* |
probably null |
Het |
Ubox5 |
T |
C |
2: 130,441,629 (GRCm39) |
T353A |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,285,711 (GRCm39) |
H2445Q |
probably damaging |
Het |
Uvrag |
T |
C |
7: 98,537,698 (GRCm39) |
D499G |
probably benign |
Het |
Xndc1 |
A |
T |
7: 101,728,343 (GRCm39) |
N247I |
possibly damaging |
Het |
Yipf2 |
A |
T |
9: 21,501,291 (GRCm39) |
W226R |
probably damaging |
Het |
Zfp335 |
T |
A |
2: 164,739,973 (GRCm39) |
Q793L |
probably damaging |
Het |
Zfp385c |
A |
G |
11: 100,548,291 (GRCm39) |
S54P |
probably damaging |
Het |
Zpld2 |
G |
T |
4: 133,930,278 (GRCm39) |
T9K |
unknown |
Het |
|
Other mutations in Ccnk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02331:Ccnk
|
APN |
12 |
108,155,343 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02341:Ccnk
|
APN |
12 |
108,161,989 (GRCm39) |
missense |
unknown |
|
IGL02557:Ccnk
|
APN |
12 |
108,161,985 (GRCm39) |
missense |
unknown |
|
FR4449:Ccnk
|
UTSW |
12 |
108,168,766 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Ccnk
|
UTSW |
12 |
108,168,766 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Ccnk
|
UTSW |
12 |
108,168,766 (GRCm39) |
unclassified |
probably benign |
|
R0481:Ccnk
|
UTSW |
12 |
108,165,568 (GRCm39) |
unclassified |
probably benign |
|
R0725:Ccnk
|
UTSW |
12 |
108,161,834 (GRCm39) |
splice site |
probably benign |
|
R1839:Ccnk
|
UTSW |
12 |
108,161,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Ccnk
|
UTSW |
12 |
108,155,349 (GRCm39) |
missense |
probably null |
1.00 |
R2903:Ccnk
|
UTSW |
12 |
108,168,647 (GRCm39) |
unclassified |
probably benign |
|
R4660:Ccnk
|
UTSW |
12 |
108,168,575 (GRCm39) |
unclassified |
probably benign |
|
R5131:Ccnk
|
UTSW |
12 |
108,168,890 (GRCm39) |
unclassified |
probably benign |
|
R5404:Ccnk
|
UTSW |
12 |
108,161,882 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5843:Ccnk
|
UTSW |
12 |
108,159,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Ccnk
|
UTSW |
12 |
108,153,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R6522:Ccnk
|
UTSW |
12 |
108,153,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R6864:Ccnk
|
UTSW |
12 |
108,168,473 (GRCm39) |
unclassified |
probably benign |
|
R7135:Ccnk
|
UTSW |
12 |
108,152,734 (GRCm39) |
missense |
probably damaging |
0.96 |
R7179:Ccnk
|
UTSW |
12 |
108,153,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Ccnk
|
UTSW |
12 |
108,159,964 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7592:Ccnk
|
UTSW |
12 |
108,152,724 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8191:Ccnk
|
UTSW |
12 |
108,159,933 (GRCm39) |
missense |
probably benign |
0.27 |
R8273:Ccnk
|
UTSW |
12 |
108,152,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Ccnk
|
UTSW |
12 |
108,159,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Ccnk
|
UTSW |
12 |
108,161,946 (GRCm39) |
missense |
unknown |
|
R9558:Ccnk
|
UTSW |
12 |
108,155,397 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9566:Ccnk
|
UTSW |
12 |
108,152,695 (GRCm39) |
missense |
probably benign |
0.04 |
|