Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630001G21Rik |
T |
C |
1: 85,652,892 (GRCm39) |
N92S |
probably damaging |
Het |
Abca2 |
T |
C |
2: 25,323,329 (GRCm39) |
L99P |
possibly damaging |
Het |
Adam19 |
T |
A |
11: 46,022,548 (GRCm39) |
Y500* |
probably null |
Het |
Amy1 |
A |
T |
3: 113,358,722 (GRCm39) |
|
probably benign |
Het |
Aox3 |
T |
C |
1: 58,197,526 (GRCm39) |
I624T |
probably damaging |
Het |
Atad3a |
C |
T |
4: 155,838,041 (GRCm39) |
D244N |
possibly damaging |
Het |
Atp5mf |
C |
A |
5: 145,124,047 (GRCm39) |
|
probably benign |
Het |
Bbof1 |
G |
A |
12: 84,475,139 (GRCm39) |
D443N |
probably damaging |
Het |
Bod1l |
G |
A |
5: 41,978,573 (GRCm39) |
Q914* |
probably null |
Het |
C330011M18Rik |
A |
G |
8: 84,793,208 (GRCm39) |
|
probably benign |
Het |
Cgref1 |
A |
G |
5: 31,090,911 (GRCm39) |
V301A |
probably benign |
Het |
Coa6 |
T |
C |
8: 127,149,480 (GRCm39) |
Y19H |
probably damaging |
Het |
Cop1 |
T |
A |
1: 159,136,448 (GRCm39) |
|
probably benign |
Het |
Dmrta1 |
T |
C |
4: 89,579,795 (GRCm39) |
S252P |
probably benign |
Het |
Dnaaf5 |
T |
G |
5: 139,170,384 (GRCm39) |
S484A |
probably benign |
Het |
Dspp |
A |
T |
5: 104,324,935 (GRCm39) |
S433C |
probably damaging |
Het |
Efcab5 |
G |
A |
11: 77,028,714 (GRCm39) |
R206* |
probably null |
Het |
Epop |
A |
T |
11: 97,519,027 (GRCm39) |
S361T |
probably benign |
Het |
Fat3 |
T |
A |
9: 15,871,802 (GRCm39) |
T3530S |
probably benign |
Het |
Flvcr1 |
A |
G |
1: 190,757,843 (GRCm39) |
Y108H |
probably damaging |
Het |
Fsip2 |
T |
G |
2: 82,822,347 (GRCm39) |
S6027A |
probably benign |
Het |
Galnt14 |
A |
G |
17: 73,842,262 (GRCm39) |
L209P |
probably damaging |
Het |
Hif3a |
C |
A |
7: 16,784,513 (GRCm39) |
R25L |
probably null |
Het |
Il22ra2 |
A |
T |
10: 19,502,492 (GRCm39) |
T104S |
probably benign |
Het |
Klrk1 |
A |
G |
6: 129,592,316 (GRCm39) |
S138P |
probably damaging |
Het |
Lrp5 |
G |
T |
19: 3,664,283 (GRCm39) |
Q815K |
probably benign |
Het |
Morn4 |
A |
G |
19: 42,064,886 (GRCm39) |
|
probably benign |
Het |
Nlrp14 |
T |
A |
7: 106,781,929 (GRCm39) |
Y375* |
probably null |
Het |
Nsd1 |
T |
A |
13: 55,443,943 (GRCm39) |
M1714K |
probably damaging |
Het |
Or2aj6 |
T |
A |
16: 19,443,848 (GRCm39) |
M1L |
probably benign |
Het |
Or5aq7 |
G |
A |
2: 86,938,710 (GRCm39) |
T7I |
possibly damaging |
Het |
Or6c213 |
T |
A |
10: 129,574,735 (GRCm39) |
D17V |
possibly damaging |
Het |
Pappa2 |
C |
T |
1: 158,678,786 (GRCm39) |
A877T |
probably benign |
Het |
Pcsk2 |
G |
A |
2: 143,532,262 (GRCm39) |
A137T |
probably damaging |
Het |
Piezo1 |
A |
G |
8: 123,212,044 (GRCm39) |
V2054A |
probably benign |
Het |
Rad52 |
A |
G |
6: 119,892,188 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Rusf1 |
A |
T |
7: 127,889,752 (GRCm39) |
|
probably benign |
Het |
Sbno1 |
A |
G |
5: 124,519,740 (GRCm39) |
|
probably benign |
Het |
Scrn1 |
C |
T |
6: 54,489,186 (GRCm39) |
D312N |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,471,109 (GRCm39) |
Q352R |
probably benign |
Het |
Slc25a28 |
A |
G |
19: 43,652,885 (GRCm39) |
Y259H |
probably damaging |
Het |
Sppl2a |
T |
C |
2: 126,768,216 (GRCm39) |
M151V |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Stra8 |
G |
A |
6: 34,916,094 (GRCm39) |
D280N |
probably damaging |
Het |
Thbs2 |
A |
T |
17: 14,897,275 (GRCm39) |
D744E |
possibly damaging |
Het |
Tiparp |
A |
G |
3: 65,439,310 (GRCm39) |
T27A |
probably benign |
Het |
Tmem38a |
T |
C |
8: 73,333,818 (GRCm39) |
F99S |
probably damaging |
Het |
Tmod3 |
T |
C |
9: 75,416,667 (GRCm39) |
T222A |
probably benign |
Het |
Tnn |
A |
G |
1: 159,913,677 (GRCm39) |
I1272T |
probably damaging |
Het |
Tnpo1 |
A |
T |
13: 98,985,667 (GRCm39) |
I829N |
probably damaging |
Het |
Trpm5 |
A |
T |
7: 142,641,613 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,598,215 (GRCm39) |
V19566A |
probably damaging |
Het |
V1ra8 |
A |
G |
6: 90,180,040 (GRCm39) |
D81G |
probably damaging |
Het |
Zdhhc20 |
A |
G |
14: 58,127,564 (GRCm39) |
V25A |
probably benign |
Het |
|
Other mutations in Hsf5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00514:Hsf5
|
APN |
11 |
87,513,922 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01726:Hsf5
|
APN |
11 |
87,526,951 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02480:Hsf5
|
APN |
11 |
87,522,483 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03113:Hsf5
|
APN |
11 |
87,548,190 (GRCm39) |
missense |
probably benign |
0.03 |
R0015:Hsf5
|
UTSW |
11 |
87,548,161 (GRCm39) |
missense |
probably benign |
|
R0015:Hsf5
|
UTSW |
11 |
87,548,161 (GRCm39) |
missense |
probably benign |
|
R1381:Hsf5
|
UTSW |
11 |
87,528,995 (GRCm39) |
missense |
probably benign |
|
R1807:Hsf5
|
UTSW |
11 |
87,548,168 (GRCm39) |
missense |
probably benign |
0.04 |
R1838:Hsf5
|
UTSW |
11 |
87,526,881 (GRCm39) |
missense |
probably benign |
0.45 |
R2187:Hsf5
|
UTSW |
11 |
87,529,010 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3930:Hsf5
|
UTSW |
11 |
87,522,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R3931:Hsf5
|
UTSW |
11 |
87,522,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4420:Hsf5
|
UTSW |
11 |
87,548,130 (GRCm39) |
missense |
probably benign |
0.02 |
R4423:Hsf5
|
UTSW |
11 |
87,522,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R4744:Hsf5
|
UTSW |
11 |
87,513,617 (GRCm39) |
missense |
probably benign |
0.02 |
R4795:Hsf5
|
UTSW |
11 |
87,526,446 (GRCm39) |
missense |
probably benign |
0.18 |
R5862:Hsf5
|
UTSW |
11 |
87,513,817 (GRCm39) |
missense |
probably damaging |
0.96 |
R6232:Hsf5
|
UTSW |
11 |
87,508,120 (GRCm39) |
missense |
probably benign |
0.05 |
R6234:Hsf5
|
UTSW |
11 |
87,508,120 (GRCm39) |
missense |
probably benign |
0.05 |
R6609:Hsf5
|
UTSW |
11 |
87,526,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R7821:Hsf5
|
UTSW |
11 |
87,528,954 (GRCm39) |
missense |
probably benign |
0.04 |
R7989:Hsf5
|
UTSW |
11 |
87,526,450 (GRCm39) |
missense |
probably benign |
0.07 |
R9299:Hsf5
|
UTSW |
11 |
87,526,770 (GRCm39) |
missense |
probably benign |
|
R9419:Hsf5
|
UTSW |
11 |
87,528,935 (GRCm39) |
missense |
probably benign |
0.02 |
R9752:Hsf5
|
UTSW |
11 |
87,513,709 (GRCm39) |
missense |
probably benign |
0.22 |
Z1177:Hsf5
|
UTSW |
11 |
87,528,959 (GRCm39) |
nonsense |
probably null |
|
|