Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
G |
5: 36,006,889 (GRCm39) |
K435E |
probably damaging |
Het |
Acly |
T |
C |
11: 100,395,785 (GRCm39) |
T412A |
probably damaging |
Het |
Aldh3b2 |
T |
A |
19: 4,029,489 (GRCm39) |
D287E |
probably benign |
Het |
Asphd1 |
G |
A |
7: 126,547,974 (GRCm39) |
P110S |
|
Het |
Atg7 |
T |
C |
6: 114,654,993 (GRCm39) |
L142P |
probably benign |
Het |
Atp13a4 |
T |
C |
16: 29,239,277 (GRCm39) |
I796V |
|
Het |
Bbx |
A |
G |
16: 50,095,022 (GRCm39) |
V98A |
probably damaging |
Het |
Brca2 |
T |
C |
5: 150,480,410 (GRCm39) |
S2727P |
probably damaging |
Het |
Camk1 |
T |
A |
6: 113,318,850 (GRCm39) |
D21V |
possibly damaging |
Het |
Cdc5l |
A |
T |
17: 45,715,709 (GRCm39) |
D634E |
probably benign |
Het |
Cfap418 |
T |
C |
4: 10,893,304 (GRCm39) |
I141T |
possibly damaging |
Het |
Cyfip1 |
A |
T |
7: 55,528,853 (GRCm39) |
D275V |
possibly damaging |
Het |
Cyp4a30b |
A |
G |
4: 115,328,162 (GRCm39) |
E477G |
probably damaging |
Het |
Cyp4f16 |
C |
T |
17: 32,769,246 (GRCm39) |
P379S |
probably damaging |
Het |
Dchs2 |
C |
T |
3: 83,263,766 (GRCm39) |
Q3345* |
probably null |
Het |
Dnaaf1 |
A |
G |
8: 120,315,001 (GRCm39) |
T270A |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,561,356 (GRCm39) |
V334A |
|
Het |
Dnhd1 |
T |
C |
7: 105,353,342 (GRCm39) |
F2832L |
probably benign |
Het |
Dock8 |
A |
G |
19: 25,098,545 (GRCm39) |
N623S |
probably null |
Het |
Eif4enif1 |
T |
C |
11: 3,165,714 (GRCm39) |
I97T |
probably benign |
Het |
Elmo1 |
C |
G |
13: 20,392,310 (GRCm39) |
P29A |
probably benign |
Het |
Erich6 |
G |
C |
3: 58,544,162 (GRCm39) |
P142A |
possibly damaging |
Het |
Fam135b |
T |
C |
15: 71,397,686 (GRCm39) |
R125G |
probably damaging |
Het |
Fcrla |
T |
A |
1: 170,749,808 (GRCm39) |
H83L |
probably damaging |
Het |
Flt3 |
C |
T |
5: 147,303,841 (GRCm39) |
E366K |
possibly damaging |
Het |
Gabbr2 |
C |
T |
4: 46,724,283 (GRCm39) |
|
probably null |
Het |
Gigyf1 |
T |
A |
5: 137,522,926 (GRCm39) |
L809* |
probably null |
Het |
Glg1 |
C |
T |
8: 111,899,133 (GRCm39) |
G711R |
probably damaging |
Het |
Gp1bb |
T |
C |
16: 18,439,527 (GRCm39) |
E189G |
probably benign |
Het |
H2-Q1 |
A |
T |
17: 35,542,532 (GRCm39) |
I326F |
probably benign |
Het |
Hoxb3 |
A |
T |
11: 96,235,420 (GRCm39) |
K116* |
probably null |
Het |
Kcnb1 |
T |
C |
2: 167,030,161 (GRCm39) |
Y128C |
probably damaging |
Het |
Kif5b |
G |
A |
18: 6,225,672 (GRCm39) |
R171C |
probably damaging |
Het |
Lcn4 |
G |
A |
2: 26,561,228 (GRCm39) |
Q18* |
probably null |
Het |
Lrp1b |
G |
A |
2: 40,779,354 (GRCm39) |
Q2677* |
probably null |
Het |
Map4k3 |
T |
A |
17: 80,958,538 (GRCm39) |
T145S |
probably damaging |
Het |
Mas1 |
T |
C |
17: 13,060,898 (GRCm39) |
E175G |
probably benign |
Het |
Metap2 |
T |
C |
10: 93,707,366 (GRCm39) |
T202A |
probably benign |
Het |
Mras |
A |
T |
9: 99,275,054 (GRCm39) |
M131K |
probably benign |
Het |
Mtor |
T |
C |
4: 148,568,169 (GRCm39) |
V1092A |
probably damaging |
Het |
Mug2 |
T |
C |
6: 122,028,751 (GRCm39) |
S582P |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,848,017 (GRCm39) |
N1085S |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,603,103 (GRCm39) |
T1149A |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,366,373 (GRCm39) |
S1239T |
probably benign |
Het |
Or10a3m |
T |
A |
7: 108,312,677 (GRCm39) |
M39K |
probably benign |
Het |
Or10p1 |
G |
A |
10: 129,444,084 (GRCm39) |
H89Y |
probably benign |
Het |
Or1j1 |
A |
G |
2: 36,702,621 (GRCm39) |
L161P |
probably damaging |
Het |
Or51i2 |
T |
A |
7: 103,689,522 (GRCm39) |
V173D |
probably damaging |
Het |
Pcdh18 |
T |
C |
3: 49,711,229 (GRCm39) |
N29D |
probably benign |
Het |
Pdzrn4 |
T |
C |
15: 92,294,949 (GRCm39) |
W52R |
probably benign |
Het |
Plekhb1 |
T |
C |
7: 100,304,588 (GRCm39) |
K39E |
probably damaging |
Het |
Pramel28 |
A |
G |
4: 143,692,348 (GRCm39) |
S218P |
probably benign |
Het |
Psmb4 |
C |
A |
3: 94,792,285 (GRCm39) |
E212D |
probably benign |
Het |
Rcc1l |
A |
G |
5: 134,205,348 (GRCm39) |
L69P |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,729,952 (GRCm39) |
R1082G |
probably benign |
Het |
Rorb |
T |
C |
19: 18,955,115 (GRCm39) |
Y167C |
probably damaging |
Het |
Sanbr |
T |
A |
11: 23,534,590 (GRCm39) |
K589I |
probably damaging |
Het |
Sbsn |
GGAAATATGGCAGACAAGTTTGGTCAGGGGGCCCACCATGCTTTTGGTCAGGGCAG |
GG |
7: 30,452,067 (GRCm39) |
|
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,248,170 (GRCm39) |
F1164L |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,438,046 (GRCm39) |
M1940K |
probably benign |
Het |
Serpinb2 |
A |
G |
1: 107,452,298 (GRCm39) |
N292S |
probably benign |
Het |
Sparcl1 |
C |
A |
5: 104,234,998 (GRCm39) |
V506L |
possibly damaging |
Het |
Stt3a |
A |
G |
9: 36,661,025 (GRCm39) |
V262A |
possibly damaging |
Het |
Syt17 |
C |
A |
7: 118,036,191 (GRCm39) |
M58I |
probably benign |
Het |
Tas2r134 |
A |
C |
2: 51,518,358 (GRCm39) |
N279T |
possibly damaging |
Het |
Tbc1d2 |
T |
C |
4: 46,609,065 (GRCm39) |
E724G |
probably damaging |
Het |
Teddm1b |
T |
A |
1: 153,750,620 (GRCm39) |
L143Q |
|
Het |
Tlk1 |
T |
A |
2: 70,617,281 (GRCm39) |
R66S |
probably damaging |
Het |
Tmem139 |
A |
T |
6: 42,240,176 (GRCm39) |
|
probably null |
Het |
Tom1l2 |
T |
C |
11: 60,151,942 (GRCm39) |
Y155C |
possibly damaging |
Het |
Trmt1l |
C |
A |
1: 151,304,710 (GRCm39) |
S28* |
probably null |
Het |
Ttf2 |
T |
C |
3: 100,859,918 (GRCm39) |
I679V |
probably benign |
Het |
Unc13b |
T |
G |
4: 43,172,513 (GRCm39) |
F1114V |
|
Het |
Vmn2r25 |
T |
A |
6: 123,816,579 (GRCm39) |
D334V |
probably damaging |
Het |
Vps13c |
T |
G |
9: 67,856,715 (GRCm39) |
Y2581D |
probably damaging |
Het |
Xkr5 |
A |
G |
8: 18,984,247 (GRCm39) |
S432P |
probably benign |
Het |
Zc2hc1b |
G |
A |
10: 13,043,677 (GRCm39) |
P73S |
possibly damaging |
Het |
Zfhx2 |
A |
C |
14: 55,303,483 (GRCm39) |
F1500L |
probably benign |
Het |
Zfp3 |
T |
G |
11: 70,662,739 (GRCm39) |
S233A |
possibly damaging |
Het |
Zmat5 |
T |
C |
11: 4,687,453 (GRCm39) |
W169R |
probably damaging |
Het |
|
Other mutations in Nkpd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Nkpd1
|
APN |
7 |
19,252,674 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01140:Nkpd1
|
APN |
7 |
19,257,387 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01450:Nkpd1
|
APN |
7 |
19,257,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Nkpd1
|
UTSW |
7 |
19,253,852 (GRCm39) |
missense |
probably benign |
|
R0626:Nkpd1
|
UTSW |
7 |
19,257,099 (GRCm39) |
missense |
probably benign |
0.02 |
R1171:Nkpd1
|
UTSW |
7 |
19,258,012 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1637:Nkpd1
|
UTSW |
7 |
19,257,904 (GRCm39) |
missense |
probably benign |
0.00 |
R1722:Nkpd1
|
UTSW |
7 |
19,257,846 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1823:Nkpd1
|
UTSW |
7 |
19,257,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Nkpd1
|
UTSW |
7 |
19,258,162 (GRCm39) |
missense |
probably damaging |
0.99 |
R2224:Nkpd1
|
UTSW |
7 |
19,253,745 (GRCm39) |
missense |
probably benign |
0.00 |
R2225:Nkpd1
|
UTSW |
7 |
19,253,745 (GRCm39) |
missense |
probably benign |
0.00 |
R2226:Nkpd1
|
UTSW |
7 |
19,253,745 (GRCm39) |
missense |
probably benign |
0.00 |
R2274:Nkpd1
|
UTSW |
7 |
19,257,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2275:Nkpd1
|
UTSW |
7 |
19,257,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2374:Nkpd1
|
UTSW |
7 |
19,257,900 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3108:Nkpd1
|
UTSW |
7 |
19,256,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R4940:Nkpd1
|
UTSW |
7 |
19,257,498 (GRCm39) |
nonsense |
probably null |
|
R5182:Nkpd1
|
UTSW |
7 |
19,257,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Nkpd1
|
UTSW |
7 |
19,257,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Nkpd1
|
UTSW |
7 |
19,258,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5681:Nkpd1
|
UTSW |
7 |
19,257,498 (GRCm39) |
nonsense |
probably null |
|
R5684:Nkpd1
|
UTSW |
7 |
19,257,498 (GRCm39) |
nonsense |
probably null |
|
R5685:Nkpd1
|
UTSW |
7 |
19,257,498 (GRCm39) |
nonsense |
probably null |
|
R6177:Nkpd1
|
UTSW |
7 |
19,257,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R6200:Nkpd1
|
UTSW |
7 |
19,258,528 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7348:Nkpd1
|
UTSW |
7 |
19,258,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R7356:Nkpd1
|
UTSW |
7 |
19,257,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8239:Nkpd1
|
UTSW |
7 |
19,253,753 (GRCm39) |
missense |
probably benign |
|
R8791:Nkpd1
|
UTSW |
7 |
19,258,095 (GRCm39) |
missense |
probably benign |
0.08 |
R8936:Nkpd1
|
UTSW |
7 |
19,255,875 (GRCm39) |
missense |
probably damaging |
0.98 |
R9200:Nkpd1
|
UTSW |
7 |
19,257,683 (GRCm39) |
missense |
probably benign |
0.35 |
R9213:Nkpd1
|
UTSW |
7 |
19,258,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Nkpd1
|
UTSW |
7 |
19,257,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Nkpd1
|
UTSW |
7 |
19,257,462 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1177:Nkpd1
|
UTSW |
7 |
19,257,877 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nkpd1
|
UTSW |
7 |
19,257,702 (GRCm39) |
missense |
probably damaging |
1.00 |
|