Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
A |
17: 24,510,529 (GRCm39) |
Q983L |
probably benign |
Het |
Agtr1a |
A |
T |
13: 30,564,962 (GRCm39) |
D9V |
probably benign |
Het |
Ahcyl |
T |
C |
16: 45,974,201 (GRCm39) |
E392G |
probably damaging |
Het |
Ano2 |
A |
G |
6: 125,687,696 (GRCm39) |
D67G |
probably benign |
Het |
Arhgef5 |
G |
A |
6: 43,256,507 (GRCm39) |
R1205H |
probably damaging |
Het |
Ascc3 |
T |
A |
10: 50,590,448 (GRCm39) |
Y1055* |
probably null |
Het |
Atad5 |
C |
T |
11: 80,023,862 (GRCm39) |
A1658V |
probably benign |
Het |
Atp6ap1l |
T |
C |
13: 91,031,926 (GRCm39) |
D252G |
probably damaging |
Het |
Bdkrb2 |
T |
C |
12: 105,558,800 (GRCm39) |
V347A |
possibly damaging |
Het |
Ccdc187 |
A |
T |
2: 26,146,007 (GRCm39) |
L1194Q |
probably damaging |
Het |
Chd9 |
A |
C |
8: 91,710,115 (GRCm39) |
D770A |
unknown |
Het |
Chd9 |
A |
G |
8: 91,760,846 (GRCm39) |
D2197G |
unknown |
Het |
Clip2 |
C |
A |
5: 134,531,484 (GRCm39) |
E774* |
probably null |
Het |
Clspn |
A |
G |
4: 126,459,993 (GRCm39) |
T407A |
probably benign |
Het |
Col24a1 |
T |
A |
3: 144,998,926 (GRCm39) |
|
probably null |
Het |
Cradd |
T |
A |
10: 95,158,637 (GRCm39) |
T37S |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,456,501 (GRCm39) |
D849G |
|
Het |
Ctbp2 |
A |
G |
7: 132,600,610 (GRCm39) |
F70S |
probably damaging |
Het |
D3Ertd751e |
A |
T |
3: 41,701,000 (GRCm39) |
E6D |
probably damaging |
Het |
Dst |
T |
A |
1: 34,230,754 (GRCm39) |
F2782L |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,159,479 (GRCm39) |
|
probably null |
Het |
Eif2s1 |
G |
T |
12: 78,927,969 (GRCm39) |
G215V |
probably damaging |
Het |
Epg5 |
A |
T |
18: 78,002,252 (GRCm39) |
D557V |
possibly damaging |
Het |
Eya4 |
C |
T |
10: 22,999,749 (GRCm39) |
|
probably null |
Het |
Fpr1 |
C |
A |
17: 18,097,242 (GRCm39) |
R249L |
probably damaging |
Het |
Fry |
A |
G |
5: 150,339,788 (GRCm39) |
T1520A |
probably benign |
Het |
Gapvd1 |
C |
T |
2: 34,580,473 (GRCm39) |
|
probably null |
Het |
Gemin4 |
A |
C |
11: 76,104,278 (GRCm39) |
L161* |
probably null |
Het |
Gid8 |
A |
T |
2: 180,359,779 (GRCm39) |
K221I |
probably benign |
Het |
Gm21028 |
A |
C |
7: 42,227,913 (GRCm39) |
C34G |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,774,882 (GRCm39) |
S172P |
probably damaging |
Het |
Herc2 |
A |
G |
7: 55,832,423 (GRCm39) |
I3040V |
possibly damaging |
Het |
Hmcn2 |
T |
A |
2: 31,306,824 (GRCm39) |
V3190E |
probably damaging |
Het |
Hrnr |
G |
T |
3: 93,230,448 (GRCm39) |
G229* |
probably null |
Het |
Igfn1 |
A |
T |
1: 135,891,738 (GRCm39) |
V2259D |
probably damaging |
Het |
Ism2 |
A |
G |
12: 87,326,814 (GRCm39) |
F375S |
probably damaging |
Het |
Kcnk4 |
T |
A |
19: 6,903,478 (GRCm39) |
D357V |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,901,040 (GRCm39) |
R914G |
possibly damaging |
Het |
Mars2 |
T |
C |
1: 55,276,729 (GRCm39) |
S111P |
probably damaging |
Het |
Mogat2 |
G |
A |
7: 98,881,673 (GRCm39) |
P88S |
possibly damaging |
Het |
Msh2 |
T |
A |
17: 88,024,957 (GRCm39) |
S612T |
possibly damaging |
Het |
Nvl |
A |
G |
1: 180,962,601 (GRCm39) |
L123P |
probably damaging |
Het |
Or1j20 |
T |
C |
2: 36,759,890 (GRCm39) |
V104A |
probably benign |
Het |
Or2d3c |
A |
T |
7: 106,526,111 (GRCm39) |
L185Q |
probably damaging |
Het |
Or51v15-ps1 |
A |
G |
7: 103,278,390 (GRCm39) |
L259P |
unknown |
Het |
Or5m11b |
T |
A |
2: 85,805,780 (GRCm39) |
S64R |
possibly damaging |
Het |
Or6c202 |
T |
A |
10: 128,995,939 (GRCm39) |
I305F |
probably benign |
Het |
Or7e174 |
A |
T |
9: 20,012,169 (GRCm39) |
Y38F |
probably damaging |
Het |
P2rx7 |
A |
T |
5: 122,804,205 (GRCm39) |
|
probably null |
Het |
Pard3 |
A |
T |
8: 128,319,573 (GRCm39) |
I1149L |
probably damaging |
Het |
Pcdha8 |
T |
A |
18: 37,125,830 (GRCm39) |
I104N |
probably damaging |
Het |
Pecr |
G |
A |
1: 72,306,624 (GRCm39) |
T219I |
probably benign |
Het |
Pgap2 |
A |
T |
7: 101,859,774 (GRCm39) |
|
probably benign |
Het |
Phf7 |
T |
C |
14: 30,963,745 (GRCm39) |
R76G |
probably benign |
Het |
Pigu |
T |
C |
2: 155,141,090 (GRCm39) |
T268A |
probably damaging |
Het |
Piwil4 |
T |
C |
9: 14,641,289 (GRCm39) |
T231A |
possibly damaging |
Het |
Pkd1l1 |
T |
G |
11: 8,895,202 (GRCm39) |
E636A |
|
Het |
Plscr3 |
T |
C |
11: 69,738,316 (GRCm39) |
S55P |
unknown |
Het |
Pnlip |
T |
A |
19: 58,664,976 (GRCm39) |
I268N |
probably damaging |
Het |
Podxl |
A |
T |
6: 31,501,929 (GRCm39) |
H343Q |
probably benign |
Het |
Prkcd |
T |
C |
14: 30,327,793 (GRCm39) |
T213A |
probably benign |
Het |
Prss22 |
T |
A |
17: 24,215,419 (GRCm39) |
Q119L |
probably benign |
Het |
Psme3ip1 |
T |
C |
8: 95,302,327 (GRCm39) |
N235D |
possibly damaging |
Het |
Ptprcap |
A |
G |
19: 4,206,238 (GRCm39) |
E107G |
possibly damaging |
Het |
Ptprg |
A |
G |
14: 12,154,198 (GRCm38) |
T640A |
possibly damaging |
Het |
Ptprh |
A |
T |
7: 4,554,006 (GRCm39) |
|
probably null |
Het |
Rasa4 |
A |
G |
5: 136,124,448 (GRCm39) |
T166A |
probably benign |
Het |
Sbf2 |
T |
C |
7: 109,998,555 (GRCm39) |
E626G |
possibly damaging |
Het |
Scn2a |
T |
A |
2: 65,512,850 (GRCm39) |
Y203* |
probably null |
Het |
Serpinb1a |
G |
C |
13: 33,026,981 (GRCm39) |
H320Q |
probably damaging |
Het |
Shisa7 |
G |
A |
7: 4,832,920 (GRCm39) |
T464I |
probably benign |
Het |
Slc47a2 |
G |
A |
11: 61,199,699 (GRCm39) |
A399V |
possibly damaging |
Het |
Snrnp200 |
A |
G |
2: 127,063,746 (GRCm39) |
T642A |
probably benign |
Het |
Spag16 |
A |
G |
1: 69,883,526 (GRCm39) |
H85R |
probably benign |
Het |
Spata31h1 |
A |
G |
10: 82,127,847 (GRCm39) |
L1721S |
possibly damaging |
Het |
Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
Stag3 |
C |
A |
5: 138,299,770 (GRCm39) |
L894M |
probably damaging |
Het |
Sun2 |
A |
T |
15: 79,618,313 (GRCm39) |
F284Y |
probably benign |
Het |
Tpx2 |
T |
A |
2: 152,718,550 (GRCm39) |
N184K |
probably benign |
Het |
Trpa1 |
A |
T |
1: 14,968,334 (GRCm39) |
N477K |
probably damaging |
Het |
Ttbk2 |
C |
T |
2: 120,620,791 (GRCm39) |
R157H |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,537,649 (GRCm39) |
E34760K |
probably benign |
Het |
Tysnd1 |
T |
C |
10: 61,532,427 (GRCm39) |
S360P |
probably damaging |
Het |
Uqcc5 |
A |
G |
14: 30,846,560 (GRCm39) |
V53A |
probably damaging |
Het |
Usp34 |
T |
A |
11: 23,311,683 (GRCm39) |
L511I |
probably damaging |
Het |
Vmn2r71 |
A |
T |
7: 85,273,468 (GRCm39) |
T761S |
possibly damaging |
Het |
Zdhhc18 |
G |
T |
4: 133,360,482 (GRCm39) |
C73* |
probably null |
Het |
Zfp975 |
A |
T |
7: 42,312,215 (GRCm39) |
C133S |
probably damaging |
Het |
Zfy1 |
T |
C |
Y: 735,141 (GRCm39) |
E214G |
unknown |
Het |
Zmym5 |
T |
A |
14: 57,031,597 (GRCm39) |
K504* |
probably null |
Het |
|
Other mutations in Ankrd13c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02313:Ankrd13c
|
APN |
3 |
157,653,571 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02943:Ankrd13c
|
APN |
3 |
157,653,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Ankrd13c
|
UTSW |
3 |
157,697,351 (GRCm39) |
missense |
probably benign |
0.26 |
R0588:Ankrd13c
|
UTSW |
3 |
157,711,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Ankrd13c
|
UTSW |
3 |
157,700,315 (GRCm39) |
missense |
probably null |
0.98 |
R1459:Ankrd13c
|
UTSW |
3 |
157,677,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1530:Ankrd13c
|
UTSW |
3 |
157,697,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Ankrd13c
|
UTSW |
3 |
157,706,757 (GRCm39) |
missense |
probably benign |
0.01 |
R4632:Ankrd13c
|
UTSW |
3 |
157,667,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R4946:Ankrd13c
|
UTSW |
3 |
157,711,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R5154:Ankrd13c
|
UTSW |
3 |
157,694,297 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5672:Ankrd13c
|
UTSW |
3 |
157,666,664 (GRCm39) |
critical splice donor site |
probably null |
|
R5935:Ankrd13c
|
UTSW |
3 |
157,653,220 (GRCm39) |
synonymous |
silent |
|
R6562:Ankrd13c
|
UTSW |
3 |
157,705,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Ankrd13c
|
UTSW |
3 |
157,694,284 (GRCm39) |
missense |
probably benign |
0.33 |
R8543:Ankrd13c
|
UTSW |
3 |
157,709,712 (GRCm39) |
splice site |
probably null |
|
R9166:Ankrd13c
|
UTSW |
3 |
157,705,357 (GRCm39) |
missense |
probably benign |
0.00 |
R9272:Ankrd13c
|
UTSW |
3 |
157,700,358 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9476:Ankrd13c
|
UTSW |
3 |
157,697,396 (GRCm39) |
missense |
probably benign |
0.01 |
R9628:Ankrd13c
|
UTSW |
3 |
157,653,313 (GRCm39) |
missense |
probably benign |
0.00 |
R9629:Ankrd13c
|
UTSW |
3 |
157,653,313 (GRCm39) |
missense |
probably benign |
0.00 |
|