Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
C |
17: 48,348,357 (GRCm39) |
I27V |
probably benign |
Het |
A2ml1 |
T |
A |
6: 128,537,632 (GRCm39) |
H693L |
probably benign |
Het |
Acacb |
A |
G |
5: 114,354,744 (GRCm39) |
E1206G |
probably benign |
Het |
Acoxl |
A |
G |
2: 127,726,432 (GRCm39) |
T269A |
probably benign |
Het |
Ak9 |
A |
G |
10: 41,309,235 (GRCm39) |
K1879R |
unknown |
Het |
Amot |
A |
T |
X: 144,244,745 (GRCm39) |
L435H |
|
Het |
Bnc2 |
A |
T |
4: 84,329,731 (GRCm39) |
L95Q |
|
Het |
Bpifa2 |
G |
T |
2: 153,851,741 (GRCm39) |
W59L |
probably benign |
Het |
Cd209a |
T |
A |
8: 3,795,602 (GRCm39) |
Q156H |
probably damaging |
Het |
Cep104 |
T |
A |
4: 154,078,971 (GRCm39) |
|
probably null |
Het |
Cpt1c |
A |
G |
7: 44,608,925 (GRCm39) |
*799R |
probably null |
Het |
Csn2 |
A |
T |
5: 87,842,418 (GRCm39) |
M203K |
possibly damaging |
Het |
Dclre1a |
C |
G |
19: 56,526,801 (GRCm39) |
A872P |
probably damaging |
Het |
Dlg5 |
C |
A |
14: 24,196,309 (GRCm39) |
L1629F |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,011,992 (GRCm39) |
D1383G |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,121,924 (GRCm39) |
V1381A |
probably damaging |
Het |
Dnttip2 |
G |
T |
3: 122,070,355 (GRCm39) |
E523D |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,114,883 (GRCm39) |
V2425D |
probably damaging |
Het |
Eif1ad11 |
A |
G |
12: 87,994,077 (GRCm39) |
S102G |
possibly damaging |
Het |
Eif2a |
G |
A |
3: 58,452,695 (GRCm39) |
R199Q |
probably damaging |
Het |
F10 |
T |
C |
8: 13,089,564 (GRCm39) |
F60L |
probably benign |
Het |
Faf2 |
A |
G |
13: 54,799,951 (GRCm39) |
I253V |
probably benign |
Het |
Flt1 |
T |
A |
5: 147,552,047 (GRCm39) |
S715C |
probably damaging |
Het |
Garin4 |
A |
G |
1: 190,895,258 (GRCm39) |
S462P |
probably benign |
Het |
Gm5150 |
G |
T |
3: 16,045,060 (GRCm39) |
T55K |
probably damaging |
Het |
Gria1 |
T |
C |
11: 57,076,759 (GRCm39) |
F121L |
possibly damaging |
Het |
Gucy2d |
A |
G |
7: 98,103,271 (GRCm39) |
Q505R |
probably benign |
Het |
Gzma |
A |
T |
13: 113,237,455 (GRCm39) |
S11T |
probably benign |
Het |
Hoxa6 |
G |
A |
6: 52,185,535 (GRCm39) |
Q24* |
probably null |
Het |
Kcnj14 |
T |
A |
7: 45,469,068 (GRCm39) |
I146L |
possibly damaging |
Het |
Kiss1r |
G |
A |
10: 79,756,605 (GRCm39) |
R149H |
probably damaging |
Het |
Lama2 |
A |
G |
10: 26,929,022 (GRCm39) |
|
probably null |
Het |
Lama5 |
C |
A |
2: 179,821,286 (GRCm39) |
R3092L |
probably damaging |
Het |
Lca5l |
T |
A |
16: 95,977,218 (GRCm39) |
N196I |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,022,394 (GRCm39) |
L462S |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,912,289 (GRCm39) |
V1166E |
probably benign |
Het |
Nr2c1 |
T |
A |
10: 94,017,465 (GRCm39) |
F401Y |
probably benign |
Het |
Or10ak12 |
T |
A |
4: 118,666,195 (GRCm39) |
R289* |
probably null |
Het |
Or14c43 |
A |
T |
7: 86,114,825 (GRCm39) |
M69L |
probably benign |
Het |
Or4e5 |
A |
G |
14: 52,727,830 (GRCm39) |
I197T |
possibly damaging |
Het |
Or5an9 |
A |
T |
19: 12,187,286 (GRCm39) |
M119L |
probably damaging |
Het |
Otop3 |
A |
C |
11: 115,235,424 (GRCm39) |
Y352S |
possibly damaging |
Het |
Plekha6 |
T |
G |
1: 133,200,375 (GRCm39) |
L318R |
probably damaging |
Het |
Pm20d1 |
G |
T |
1: 131,743,825 (GRCm39) |
V497F |
possibly damaging |
Het |
Pnma2 |
G |
A |
14: 67,154,572 (GRCm39) |
R332H |
probably damaging |
Het |
Ppip5k1 |
C |
A |
2: 121,162,045 (GRCm39) |
G1013C |
probably damaging |
Het |
Prdm13 |
C |
G |
4: 21,679,659 (GRCm39) |
R277P |
unknown |
Het |
Prdm2 |
A |
G |
4: 142,858,674 (GRCm39) |
S1539P |
possibly damaging |
Het |
Ptger2 |
A |
G |
14: 45,227,235 (GRCm39) |
T272A |
probably damaging |
Het |
Qser1 |
T |
C |
2: 104,618,815 (GRCm39) |
T576A |
probably benign |
Het |
Rest |
GGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGAGCCTGCCCCTCCCACGGGGC |
GGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGAGCCTGCCCCTCCCACGGGGC |
5: 77,429,651 (GRCm39) |
|
probably benign |
Het |
Sacm1l |
G |
T |
9: 123,398,021 (GRCm39) |
V238L |
probably damaging |
Het |
Sanbr |
T |
C |
11: 23,565,244 (GRCm39) |
I248V |
probably benign |
Het |
Sec16a |
C |
T |
2: 26,313,645 (GRCm39) |
G454D |
|
Het |
Sil1 |
A |
G |
18: 35,450,899 (GRCm39) |
S259P |
possibly damaging |
Het |
Sirpb1b |
A |
G |
3: 15,639,964 (GRCm39) |
L16P |
probably damaging |
Het |
Slc22a20 |
A |
T |
19: 6,032,879 (GRCm39) |
V262D |
probably damaging |
Het |
Slc4a9 |
G |
T |
18: 36,666,676 (GRCm39) |
R580L |
probably benign |
Het |
Ssr3 |
A |
G |
3: 65,290,521 (GRCm39) |
V128A |
probably damaging |
Het |
Stpg2 |
G |
T |
3: 139,014,993 (GRCm39) |
S386I |
possibly damaging |
Het |
Taar8c |
C |
A |
10: 23,977,500 (GRCm39) |
C104F |
probably damaging |
Het |
Tex2 |
T |
C |
11: 106,458,095 (GRCm39) |
E445G |
unknown |
Het |
Tmem253 |
A |
C |
14: 52,256,099 (GRCm39) |
D126A |
probably benign |
Het |
Tox4 |
A |
G |
14: 52,523,247 (GRCm39) |
Q69R |
possibly damaging |
Het |
Tpi1 |
T |
A |
6: 124,788,501 (GRCm39) |
S254C |
probably benign |
Het |
Trmt12 |
T |
G |
15: 58,745,594 (GRCm39) |
S331A |
probably benign |
Het |
Ttn |
A |
G |
2: 76,543,350 (GRCm39) |
V33212A |
probably damaging |
Het |
Tubb4a |
C |
T |
17: 57,387,734 (GRCm39) |
E431K |
unknown |
Het |
Ugt1a10 |
A |
T |
1: 87,983,509 (GRCm39) |
E102D |
probably benign |
Het |
Unc80 |
A |
T |
1: 66,589,000 (GRCm39) |
E1055V |
probably null |
Het |
Vav1 |
C |
A |
17: 57,618,895 (GRCm39) |
S708R |
probably damaging |
Het |
Vmn1r20 |
A |
G |
6: 57,409,246 (GRCm39) |
M191V |
probably damaging |
Het |
Vmn1r37 |
A |
T |
6: 66,709,054 (GRCm39) |
T227S |
probably damaging |
Het |
Vmn1r72 |
C |
A |
7: 11,412,951 (GRCm39) |
|
probably benign |
Het |
Vps33b |
G |
A |
7: 79,924,434 (GRCm39) |
|
probably null |
Het |
Vrtn |
T |
A |
12: 84,697,251 (GRCm39) |
L667Q |
probably benign |
Het |
Xirp1 |
G |
A |
9: 119,847,302 (GRCm39) |
T527M |
probably benign |
Het |
Ylpm1 |
T |
A |
12: 85,077,342 (GRCm39) |
Y1356N |
probably damaging |
Het |
Zmym2 |
A |
T |
14: 57,185,464 (GRCm39) |
Y1032F |
probably damaging |
Het |
|
Other mutations in Zfp980 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00828:Zfp980
|
APN |
4 |
145,428,561 (GRCm39) |
missense |
probably benign |
0.00 |
R0164:Zfp980
|
UTSW |
4 |
145,428,567 (GRCm39) |
missense |
probably benign |
|
R0164:Zfp980
|
UTSW |
4 |
145,428,567 (GRCm39) |
missense |
probably benign |
|
R1186:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R1761:Zfp980
|
UTSW |
4 |
145,428,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R3726:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R4049:Zfp980
|
UTSW |
4 |
145,429,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R4467:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R4610:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R4622:Zfp980
|
UTSW |
4 |
145,428,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R5008:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R5027:Zfp980
|
UTSW |
4 |
145,428,653 (GRCm39) |
missense |
probably benign |
|
R5497:Zfp980
|
UTSW |
4 |
145,428,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Zfp980
|
UTSW |
4 |
145,428,479 (GRCm39) |
nonsense |
probably null |
|
R6125:Zfp980
|
UTSW |
4 |
145,429,208 (GRCm39) |
makesense |
probably null |
|
R7353:Zfp980
|
UTSW |
4 |
145,428,714 (GRCm39) |
missense |
probably benign |
0.06 |
R7675:Zfp980
|
UTSW |
4 |
145,428,164 (GRCm39) |
nonsense |
probably null |
|
R7939:Zfp980
|
UTSW |
4 |
145,428,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Zfp980
|
UTSW |
4 |
145,427,596 (GRCm39) |
missense |
probably benign |
0.00 |
R9122:Zfp980
|
UTSW |
4 |
145,428,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9361:Zfp980
|
UTSW |
4 |
145,427,999 (GRCm39) |
missense |
probably benign |
0.08 |
R9469:Zfp980
|
UTSW |
4 |
145,427,687 (GRCm39) |
missense |
probably benign |
0.14 |
|