Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
T |
C |
8: 72,455,423 (GRCm38) |
S466P |
possibly damaging |
Het |
1700061G19Rik |
A |
G |
17: 56,888,655 (GRCm38) |
N684S |
probably benign |
Het |
4930435E12Rik |
A |
G |
16: 38,828,145 (GRCm38) |
S201P |
probably damaging |
Het |
Ablim1 |
T |
C |
19: 57,079,866 (GRCm38) |
T267A |
probably damaging |
Het |
Acap2 |
A |
T |
16: 31,103,499 (GRCm38) |
L724Q |
possibly damaging |
Het |
Adcy4 |
T |
C |
14: 55,781,927 (GRCm38) |
T89A |
possibly damaging |
Het |
Agrp |
T |
C |
8: 105,567,368 (GRCm38) |
E41G |
probably benign |
Het |
Akap9 |
G |
A |
5: 4,034,916 (GRCm38) |
|
probably benign |
Het |
Akr1d1 |
G |
A |
6: 37,564,491 (GRCm38) |
V308M |
probably damaging |
Het |
Ap1m2 |
C |
T |
9: 21,309,674 (GRCm38) |
R54Q |
probably benign |
Het |
Arhgap45 |
T |
A |
10: 80,027,066 (GRCm38) |
V692E |
probably damaging |
Het |
Arsi |
G |
A |
18: 60,916,651 (GRCm38) |
G202E |
probably benign |
Het |
BC048679 |
T |
C |
7: 81,495,720 (GRCm38) |
N27D |
probably benign |
Het |
Ccdc78 |
A |
G |
17: 25,788,700 (GRCm38) |
N237S |
probably benign |
Het |
Cd46 |
G |
A |
1: 195,062,396 (GRCm38) |
L345F |
possibly damaging |
Het |
Cngb3 |
A |
T |
4: 19,425,569 (GRCm38) |
N459I |
possibly damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,881,167 (GRCm38) |
E731G |
probably damaging |
Het |
Cul1 |
G |
T |
6: 47,517,146 (GRCm38) |
K464N |
probably benign |
Het |
Cul1 |
T |
A |
6: 47,517,191 (GRCm38) |
S479R |
probably damaging |
Het |
Dcaf5 |
A |
T |
12: 80,340,232 (GRCm38) |
D373E |
probably benign |
Het |
Ddx58 |
G |
T |
4: 40,210,000 (GRCm38) |
S644R |
probably damaging |
Het |
Dhcr7 |
A |
G |
7: 143,840,500 (GRCm38) |
Q126R |
probably benign |
Het |
Dnd1 |
C |
T |
18: 36,765,963 (GRCm38) |
|
probably benign |
Het |
Dok2 |
T |
C |
14: 70,777,516 (GRCm38) |
F228L |
probably damaging |
Het |
Dpep3 |
T |
G |
8: 105,976,189 (GRCm38) |
I314L |
probably benign |
Het |
Eps8 |
A |
G |
6: 137,514,295 (GRCm38) |
F362L |
probably damaging |
Het |
Espn |
G |
T |
4: 152,138,846 (GRCm38) |
R250S |
probably damaging |
Het |
Faf1 |
A |
C |
4: 109,742,896 (GRCm38) |
N163H |
probably damaging |
Het |
Fam198b |
C |
A |
3: 79,936,674 (GRCm38) |
S36* |
probably null |
Het |
Fam71e2 |
C |
T |
7: 4,757,469 (GRCm38) |
|
probably null |
Het |
Fcho1 |
C |
T |
8: 71,710,481 (GRCm38) |
V635I |
probably benign |
Het |
Gm7579 |
G |
A |
7: 142,211,908 (GRCm38) |
C17Y |
unknown |
Het |
Gm996 |
T |
C |
2: 25,578,753 (GRCm38) |
Y382C |
probably damaging |
Het |
Gpx8 |
G |
T |
13: 113,045,508 (GRCm38) |
Y130* |
probably null |
Het |
Grm6 |
C |
T |
11: 50,864,612 (GRCm38) |
T857M |
probably benign |
Het |
Gvin1 |
A |
T |
7: 106,163,436 (GRCm38) |
Y609N |
possibly damaging |
Het |
Hectd4 |
T |
A |
5: 121,305,818 (GRCm38) |
M30K |
probably benign |
Het |
Ilkap |
A |
G |
1: 91,387,383 (GRCm38) |
|
probably benign |
Het |
Iqub |
T |
C |
6: 24,450,842 (GRCm38) |
D586G |
probably damaging |
Het |
Klhl22 |
G |
A |
16: 17,777,016 (GRCm38) |
|
silent |
Het |
Klhl25 |
T |
C |
7: 75,867,050 (GRCm38) |
I568T |
probably benign |
Het |
Krr1 |
C |
T |
10: 111,985,691 (GRCm38) |
|
probably benign |
Het |
Larp6 |
A |
G |
9: 60,737,810 (GRCm38) |
E411G |
probably damaging |
Het |
Lepr |
A |
C |
4: 101,789,337 (GRCm38) |
I822L |
probably benign |
Het |
Lrig3 |
C |
A |
10: 126,011,052 (GRCm38) |
D896E |
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,553,824 (GRCm38) |
G3114D |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,486,750 (GRCm38) |
Y1263N |
probably damaging |
Het |
Mapk10 |
T |
C |
5: 102,990,619 (GRCm38) |
D180G |
probably damaging |
Het |
Matr3 |
T |
A |
18: 35,581,640 (GRCm38) |
V113E |
probably damaging |
Het |
Mbd4 |
A |
T |
6: 115,848,926 (GRCm38) |
F368Y |
possibly damaging |
Het |
Mcpt8 |
G |
A |
14: 56,082,280 (GRCm38) |
R238W |
probably benign |
Het |
Mcrip2 |
G |
T |
17: 25,864,647 (GRCm38) |
T86N |
possibly damaging |
Het |
Mink1 |
A |
G |
11: 70,611,592 (GRCm38) |
N1043S |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,635,194 (GRCm38) |
T1128I |
probably benign |
Het |
Nrg2 |
T |
A |
18: 36,196,547 (GRCm38) |
Y205F |
probably damaging |
Het |
Nsmce4a |
A |
T |
7: 130,533,591 (GRCm38) |
|
probably benign |
Het |
Nubp2 |
A |
G |
17: 24,884,456 (GRCm38) |
M149T |
probably benign |
Het |
Olfr1062 |
T |
C |
2: 86,422,957 (GRCm38) |
T240A |
probably damaging |
Het |
Olfr462 |
T |
A |
11: 87,889,225 (GRCm38) |
M224L |
probably damaging |
Het |
Olfr974 |
G |
T |
9: 39,942,504 (GRCm38) |
M81I |
probably benign |
Het |
Pax3 |
A |
G |
1: 78,192,456 (GRCm38) |
I191T |
possibly damaging |
Het |
Pdcd5 |
T |
C |
7: 35,643,710 (GRCm38) |
N137D |
possibly damaging |
Het |
Pik3c2a |
G |
A |
7: 116,340,156 (GRCm38) |
A1649V |
probably damaging |
Het |
Pik3r6 |
T |
A |
11: 68,544,053 (GRCm38) |
|
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,537,378 (GRCm38) |
S2183P |
possibly damaging |
Het |
Plekho1 |
T |
A |
3: 95,988,993 (GRCm38) |
Q388L |
possibly damaging |
Het |
Ppfibp1 |
A |
G |
6: 146,990,514 (GRCm38) |
T91A |
probably benign |
Het |
Ptger4 |
G |
T |
15: 5,242,606 (GRCm38) |
N177K |
probably benign |
Het |
Reln |
A |
G |
5: 21,901,751 (GRCm38) |
F3207S |
probably benign |
Het |
Ripk4 |
C |
T |
16: 97,751,536 (GRCm38) |
R194H |
probably damaging |
Het |
Rnf112 |
A |
T |
11: 61,452,744 (GRCm38) |
C112S |
possibly damaging |
Het |
Rprd1b |
T |
G |
2: 158,074,935 (GRCm38) |
Y278* |
probably null |
Het |
Sel1l |
A |
G |
12: 91,831,602 (GRCm38) |
L140P |
probably damaging |
Het |
Shroom3 |
G |
T |
5: 92,943,086 (GRCm38) |
V1151F |
probably damaging |
Het |
Slc38a3 |
A |
G |
9: 107,655,064 (GRCm38) |
V423A |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,751,883 (GRCm38) |
T131A |
probably damaging |
Het |
Slmap |
A |
T |
14: 26,460,209 (GRCm38) |
V323E |
probably benign |
Het |
Smim6 |
T |
C |
11: 115,913,504 (GRCm38) |
V39A |
probably benign |
Het |
Snapc3 |
C |
T |
4: 83,464,897 (GRCm38) |
|
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,337,005 (GRCm38) |
T382A |
probably benign |
Het |
Sparc |
G |
A |
11: 55,399,211 (GRCm38) |
T218I |
possibly damaging |
Het |
Steap1 |
A |
T |
5: 5,736,589 (GRCm38) |
F283I |
probably damaging |
Het |
Stil |
A |
G |
4: 115,038,474 (GRCm38) |
T586A |
probably benign |
Het |
Tango2 |
A |
G |
16: 18,310,901 (GRCm38) |
|
silent |
Het |
Tbce |
T |
A |
13: 14,019,795 (GRCm38) |
D93V |
probably damaging |
Het |
Tcf12 |
C |
T |
9: 71,858,840 (GRCm38) |
G504S |
probably null |
Het |
Tle4 |
A |
T |
19: 14,464,345 (GRCm38) |
I435K |
probably benign |
Het |
Tmem245 |
A |
G |
4: 56,899,164 (GRCm38) |
F254S |
probably damaging |
Het |
Tmem251 |
A |
T |
12: 102,744,055 (GRCm38) |
|
probably benign |
Het |
Tubgcp3 |
T |
C |
8: 12,649,722 (GRCm38) |
K377R |
probably benign |
Het |
Ulk4 |
G |
A |
9: 121,250,902 (GRCm38) |
T497M |
possibly damaging |
Het |
Ush2a |
A |
T |
1: 188,553,275 (GRCm38) |
T2003S |
probably benign |
Het |
Usp53 |
A |
G |
3: 122,961,363 (GRCm38) |
S32P |
possibly damaging |
Het |
Vmn1r78 |
T |
A |
7: 12,152,756 (GRCm38) |
L98Q |
probably damaging |
Het |
Vmn2r84 |
T |
A |
10: 130,385,843 (GRCm38) |
D836V |
probably damaging |
Het |
Vps13d |
A |
G |
4: 145,087,161 (GRCm38) |
F165L |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,863,785 (GRCm38) |
E103G |
possibly damaging |
Het |
Zfp384 |
G |
A |
6: 125,030,930 (GRCm38) |
|
silent |
Het |
Zfp870 |
A |
T |
17: 32,883,340 (GRCm38) |
C339* |
probably null |
Het |
|
Other mutations in Arid5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Arid5b
|
APN |
10 |
68,128,975 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01731:Arid5b
|
APN |
10 |
68,097,609 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02069:Arid5b
|
APN |
10 |
68,097,399 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02161:Arid5b
|
APN |
10 |
68,096,668 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02555:Arid5b
|
APN |
10 |
68,101,904 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02873:Arid5b
|
APN |
10 |
68,101,950 (GRCm38) |
missense |
probably benign |
0.06 |
IGL03119:Arid5b
|
APN |
10 |
68,243,227 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03271:Arid5b
|
APN |
10 |
68,097,457 (GRCm38) |
missense |
possibly damaging |
0.73 |
gobi
|
UTSW |
10 |
68,118,345 (GRCm38) |
missense |
possibly damaging |
0.92 |
3-1:Arid5b
|
UTSW |
10 |
68,098,589 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4677001:Arid5b
|
UTSW |
10 |
68,098,011 (GRCm38) |
missense |
probably damaging |
0.99 |
R0108:Arid5b
|
UTSW |
10 |
68,278,729 (GRCm38) |
utr 5 prime |
probably benign |
|
R0525:Arid5b
|
UTSW |
10 |
68,097,846 (GRCm38) |
missense |
possibly damaging |
0.90 |
R0533:Arid5b
|
UTSW |
10 |
68,186,033 (GRCm38) |
missense |
probably damaging |
1.00 |
R0646:Arid5b
|
UTSW |
10 |
68,096,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R1066:Arid5b
|
UTSW |
10 |
68,098,356 (GRCm38) |
missense |
probably benign |
0.04 |
R1487:Arid5b
|
UTSW |
10 |
68,097,214 (GRCm38) |
nonsense |
probably null |
|
R1638:Arid5b
|
UTSW |
10 |
68,277,947 (GRCm38) |
missense |
possibly damaging |
0.48 |
R1789:Arid5b
|
UTSW |
10 |
68,186,067 (GRCm38) |
missense |
probably damaging |
0.99 |
R2031:Arid5b
|
UTSW |
10 |
68,278,688 (GRCm38) |
critical splice donor site |
probably null |
|
R2337:Arid5b
|
UTSW |
10 |
68,097,777 (GRCm38) |
missense |
possibly damaging |
0.63 |
R2996:Arid5b
|
UTSW |
10 |
68,098,462 (GRCm38) |
missense |
probably benign |
0.01 |
R2997:Arid5b
|
UTSW |
10 |
68,098,462 (GRCm38) |
missense |
probably benign |
0.01 |
R3547:Arid5b
|
UTSW |
10 |
68,098,462 (GRCm38) |
missense |
probably benign |
0.01 |
R4411:Arid5b
|
UTSW |
10 |
68,096,689 (GRCm38) |
missense |
probably damaging |
1.00 |
R4860:Arid5b
|
UTSW |
10 |
68,243,095 (GRCm38) |
missense |
probably damaging |
0.97 |
R5219:Arid5b
|
UTSW |
10 |
68,278,110 (GRCm38) |
missense |
probably benign |
0.08 |
R5341:Arid5b
|
UTSW |
10 |
68,278,127 (GRCm38) |
missense |
possibly damaging |
0.87 |
R5434:Arid5b
|
UTSW |
10 |
68,096,889 (GRCm38) |
missense |
possibly damaging |
0.67 |
R5757:Arid5b
|
UTSW |
10 |
68,102,079 (GRCm38) |
missense |
probably damaging |
1.00 |
R6114:Arid5b
|
UTSW |
10 |
68,097,744 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6313:Arid5b
|
UTSW |
10 |
68,097,582 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6338:Arid5b
|
UTSW |
10 |
68,098,561 (GRCm38) |
nonsense |
probably null |
|
R6525:Arid5b
|
UTSW |
10 |
68,097,666 (GRCm38) |
missense |
possibly damaging |
0.47 |
R6915:Arid5b
|
UTSW |
10 |
68,186,212 (GRCm38) |
nonsense |
probably null |
|
R7013:Arid5b
|
UTSW |
10 |
68,097,819 (GRCm38) |
missense |
probably damaging |
1.00 |
R7099:Arid5b
|
UTSW |
10 |
68,098,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R7260:Arid5b
|
UTSW |
10 |
68,097,807 (GRCm38) |
missense |
probably damaging |
1.00 |
R7324:Arid5b
|
UTSW |
10 |
68,128,922 (GRCm38) |
missense |
probably benign |
0.44 |
R7334:Arid5b
|
UTSW |
10 |
68,243,177 (GRCm38) |
missense |
possibly damaging |
0.61 |
R7432:Arid5b
|
UTSW |
10 |
68,118,266 (GRCm38) |
missense |
probably damaging |
1.00 |
R7453:Arid5b
|
UTSW |
10 |
68,243,164 (GRCm38) |
missense |
probably benign |
0.01 |
R7649:Arid5b
|
UTSW |
10 |
68,118,345 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7659:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7661:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7662:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7663:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7665:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7666:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7759:Arid5b
|
UTSW |
10 |
68,097,802 (GRCm38) |
missense |
probably damaging |
1.00 |
R7779:Arid5b
|
UTSW |
10 |
68,096,776 (GRCm38) |
missense |
probably damaging |
1.00 |
R7788:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7789:Arid5b
|
UTSW |
10 |
68,098,587 (GRCm38) |
missense |
probably benign |
|
R7875:Arid5b
|
UTSW |
10 |
68,128,941 (GRCm38) |
missense |
probably benign |
0.02 |
R8079:Arid5b
|
UTSW |
10 |
68,098,356 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8096:Arid5b
|
UTSW |
10 |
68,186,152 (GRCm38) |
missense |
probably benign |
0.00 |
R8228:Arid5b
|
UTSW |
10 |
68,278,706 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8377:Arid5b
|
UTSW |
10 |
68,097,387 (GRCm38) |
missense |
probably damaging |
0.96 |
R8757:Arid5b
|
UTSW |
10 |
68,097,810 (GRCm38) |
missense |
probably damaging |
1.00 |
R8910:Arid5b
|
UTSW |
10 |
68,098,278 (GRCm38) |
missense |
|
|
R8954:Arid5b
|
UTSW |
10 |
68,101,980 (GRCm38) |
missense |
possibly damaging |
0.88 |
R9234:Arid5b
|
UTSW |
10 |
68,128,798 (GRCm38) |
missense |
possibly damaging |
0.82 |
R9272:Arid5b
|
UTSW |
10 |
68,102,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R9430:Arid5b
|
UTSW |
10 |
68,186,257 (GRCm38) |
critical splice acceptor site |
probably null |
|
X0066:Arid5b
|
UTSW |
10 |
68,118,302 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Arid5b
|
UTSW |
10 |
68,097,228 (GRCm38) |
missense |
probably damaging |
0.99 |
|