Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Aamdc |
A |
G |
7: 97,224,808 (GRCm39) |
V18A |
probably benign |
Het |
Adam12 |
T |
A |
7: 133,509,373 (GRCm39) |
I796F |
probably benign |
Het |
Adcy7 |
T |
A |
8: 89,037,646 (GRCm39) |
V238E |
possibly damaging |
Het |
Adgrv1 |
G |
A |
13: 81,691,497 (GRCm39) |
H1697Y |
probably damaging |
Het |
Adrb1 |
A |
G |
19: 56,711,825 (GRCm39) |
D341G |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,354,275 (GRCm39) |
Y80H |
probably benign |
Het |
Akap9 |
C |
T |
5: 4,105,709 (GRCm39) |
L2927F |
probably damaging |
Het |
Alox8 |
T |
A |
11: 69,075,950 (GRCm39) |
D667V |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,236,002 (GRCm39) |
E792G |
probably benign |
Het |
Arhgef16 |
A |
G |
4: 154,365,432 (GRCm39) |
V561A |
possibly damaging |
Het |
Bcap29 |
A |
T |
12: 31,676,756 (GRCm39) |
Y105N |
probably damaging |
Het |
Best2 |
T |
A |
8: 85,740,147 (GRCm39) |
T6S |
|
Het |
Bfsp2 |
C |
A |
9: 103,357,251 (GRCm39) |
V59L |
possibly damaging |
Het |
Brd3 |
T |
A |
2: 27,349,815 (GRCm39) |
D246V |
|
Het |
Btnl1 |
T |
A |
17: 34,600,118 (GRCm39) |
V207E |
probably benign |
Het |
Ccdc122 |
T |
A |
14: 77,329,408 (GRCm39) |
Y154N |
|
Het |
Cfap43 |
A |
G |
19: 47,773,814 (GRCm39) |
Y656H |
probably damaging |
Het |
Clca3a2 |
A |
T |
3: 144,508,808 (GRCm39) |
Y670* |
probably null |
Het |
Coprs |
T |
C |
8: 13,935,081 (GRCm39) |
Y158C |
probably damaging |
Het |
Desi2 |
T |
G |
1: 178,084,170 (GRCm39) |
M106R |
unknown |
Het |
Dnaaf3 |
T |
C |
7: 4,531,100 (GRCm39) |
E111G |
probably damaging |
Het |
Epha10 |
T |
A |
4: 124,775,704 (GRCm39) |
F13I |
probably benign |
Het |
Fbn1 |
C |
A |
2: 125,207,551 (GRCm39) |
A981S |
probably benign |
Het |
Gga2 |
T |
A |
7: 121,611,448 (GRCm39) |
T37S |
probably damaging |
Het |
Glra3 |
T |
A |
8: 56,578,299 (GRCm39) |
F452Y |
probably damaging |
Het |
Gm10338 |
T |
A |
14: 19,280,438 (GRCm39) |
N96I |
probably damaging |
Het |
Gpd2 |
A |
T |
2: 57,195,866 (GRCm39) |
E149V |
possibly damaging |
Het |
Gpr137c |
T |
G |
14: 45,516,229 (GRCm39) |
L321* |
probably null |
Het |
Gsdmc2 |
T |
C |
15: 63,702,678 (GRCm39) |
I196M |
probably benign |
Het |
Habp2 |
A |
G |
19: 56,295,253 (GRCm39) |
D48G |
probably benign |
Het |
Hdc |
G |
T |
2: 126,458,149 (GRCm39) |
P58T |
probably damaging |
Het |
Heatr5a |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGTGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
12: 51,934,702 (GRCm39) |
|
probably benign |
Het |
Hnrnpr |
G |
T |
4: 136,063,615 (GRCm39) |
V342F |
probably damaging |
Het |
Hyal6 |
T |
A |
6: 24,734,929 (GRCm39) |
Y287* |
probably null |
Het |
Igsf8 |
T |
C |
1: 172,146,525 (GRCm39) |
Y571H |
|
Het |
Kalrn |
A |
G |
16: 33,854,864 (GRCm39) |
S1999P |
probably damaging |
Het |
Lama2 |
T |
A |
10: 26,877,170 (GRCm39) |
N2672I |
probably benign |
Het |
Lrrc7 |
T |
C |
3: 157,867,105 (GRCm39) |
R879G |
probably damaging |
Het |
Lrwd1 |
T |
G |
5: 136,160,413 (GRCm39) |
H307P |
probably benign |
Het |
Mau2 |
T |
C |
8: 70,480,153 (GRCm39) |
Y318C |
probably damaging |
Het |
Med13 |
T |
C |
11: 86,199,727 (GRCm39) |
Q660R |
probably benign |
Het |
Mepce |
G |
C |
5: 137,783,759 (GRCm39) |
P189R |
probably damaging |
Het |
Mical3 |
T |
A |
6: 121,001,758 (GRCm39) |
N578I |
probably damaging |
Het |
Mug1 |
T |
C |
6: 121,861,635 (GRCm39) |
S1366P |
probably damaging |
Het |
Nol11 |
A |
T |
11: 107,064,278 (GRCm39) |
D511E |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,994,340 (GRCm39) |
H1514L |
probably benign |
Het |
Onecut3 |
C |
A |
10: 80,331,887 (GRCm39) |
S349* |
probably null |
Het |
Or2l13b |
C |
T |
16: 19,349,026 (GRCm39) |
A215T |
probably benign |
Het |
Or4f57 |
A |
G |
2: 111,790,584 (GRCm39) |
V278A |
possibly damaging |
Het |
Or5ap2b-ps1 |
A |
T |
2: 85,693,922 (GRCm39) |
I56F |
probably damaging |
Het |
Or5b110-ps1 |
G |
A |
19: 13,259,558 (GRCm39) |
T288I |
unknown |
Het |
Or7e169 |
A |
G |
9: 19,757,816 (GRCm39) |
L33P |
possibly damaging |
Het |
Or7g34 |
T |
C |
9: 19,478,396 (GRCm39) |
I95V |
possibly damaging |
Het |
Or8g18 |
T |
C |
9: 39,149,625 (GRCm39) |
T32A |
probably benign |
Het |
Patl2 |
C |
T |
2: 121,955,374 (GRCm39) |
G297E |
probably benign |
Het |
Pdlim5 |
G |
A |
3: 142,010,111 (GRCm39) |
T168M |
probably damaging |
Het |
Pdzd2 |
A |
C |
15: 12,374,621 (GRCm39) |
L1838R |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
T |
C |
8: 110,395,849 (GRCm39) |
V2083A |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,637,741 (GRCm39) |
Y348F |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,198,826 (GRCm39) |
S1005T |
probably benign |
Het |
Ppp4r1 |
T |
A |
17: 66,142,073 (GRCm39) |
N709K |
probably null |
Het |
Pramel32 |
T |
A |
4: 88,546,219 (GRCm39) |
L374F |
possibly damaging |
Het |
Pramel40 |
G |
A |
5: 94,464,924 (GRCm39) |
V437I |
probably benign |
Het |
Reln |
T |
C |
5: 22,125,508 (GRCm39) |
D2725G |
possibly damaging |
Het |
Rnf41 |
T |
A |
10: 128,274,299 (GRCm39) |
I317K |
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,979,444 (GRCm39) |
V268A |
possibly damaging |
Het |
Sema5a |
A |
G |
15: 32,679,373 (GRCm39) |
H884R |
probably damaging |
Het |
Serpinh1 |
A |
T |
7: 98,996,484 (GRCm39) |
M236K |
probably damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,255,610 (GRCm39) |
L1064P |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,715,375 (GRCm39) |
H947R |
probably benign |
Het |
Slc12a3 |
T |
A |
8: 95,083,658 (GRCm39) |
M895K |
possibly damaging |
Het |
Slc22a3 |
C |
A |
17: 12,726,057 (GRCm39) |
R52L |
probably damaging |
Het |
Slc38a1 |
A |
G |
15: 96,487,965 (GRCm39) |
L180P |
probably damaging |
Het |
Slc4a3 |
T |
C |
1: 75,533,612 (GRCm39) |
V1078A |
probably damaging |
Het |
Snx30 |
T |
A |
4: 59,879,241 (GRCm39) |
V160E |
probably damaging |
Het |
Spata18 |
A |
T |
5: 73,829,840 (GRCm39) |
I332F |
|
Het |
Stard9 |
C |
G |
2: 120,534,564 (GRCm39) |
P3607R |
probably damaging |
Het |
Svep1 |
T |
A |
4: 58,084,144 (GRCm39) |
Y1876F |
possibly damaging |
Het |
Sytl1 |
A |
G |
4: 132,986,291 (GRCm39) |
|
probably null |
Het |
Tacc2 |
A |
C |
7: 130,366,041 (GRCm39) |
K567Q |
probably damaging |
Het |
Tfr2 |
A |
G |
5: 137,575,769 (GRCm39) |
D295G |
possibly damaging |
Het |
Tmem53 |
C |
A |
4: 117,125,122 (GRCm39) |
H78Q |
probably benign |
Het |
Tnnt2 |
G |
A |
1: 135,768,640 (GRCm39) |
E10K |
unknown |
Het |
Top2a |
T |
A |
11: 98,902,970 (GRCm39) |
I406F |
probably damaging |
Het |
Ttc1 |
C |
A |
11: 43,621,305 (GRCm39) |
R292I |
|
Het |
Ubr1 |
T |
G |
2: 120,703,627 (GRCm39) |
T1568P |
probably damaging |
Het |
Usp25 |
T |
G |
16: 76,852,076 (GRCm39) |
V197G |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,432,188 (GRCm39) |
N432K |
probably benign |
Het |
Vmn2r26 |
T |
A |
6: 124,038,137 (GRCm39) |
Y571N |
probably damaging |
Het |
Zfp7 |
T |
C |
15: 76,775,484 (GRCm39) |
S509P |
probably damaging |
Het |
|
Other mutations in Fam193a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01981:Fam193a
|
APN |
5 |
34,588,537 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02111:Fam193a
|
APN |
5 |
34,568,001 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02139:Fam193a
|
APN |
5 |
34,602,081 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02218:Fam193a
|
APN |
5 |
34,600,932 (GRCm39) |
missense |
possibly damaging |
0.68 |
BB010:Fam193a
|
UTSW |
5 |
34,623,539 (GRCm39) |
missense |
possibly damaging |
0.53 |
BB020:Fam193a
|
UTSW |
5 |
34,623,539 (GRCm39) |
missense |
possibly damaging |
0.53 |
P0017:Fam193a
|
UTSW |
5 |
34,597,807 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4418001:Fam193a
|
UTSW |
5 |
34,597,879 (GRCm39) |
missense |
probably damaging |
0.97 |
R0172:Fam193a
|
UTSW |
5 |
34,622,957 (GRCm39) |
missense |
probably damaging |
0.97 |
R0413:Fam193a
|
UTSW |
5 |
34,623,552 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0512:Fam193a
|
UTSW |
5 |
34,583,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R0735:Fam193a
|
UTSW |
5 |
34,596,722 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0764:Fam193a
|
UTSW |
5 |
34,600,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R0904:Fam193a
|
UTSW |
5 |
34,619,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Fam193a
|
UTSW |
5 |
34,623,636 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1765:Fam193a
|
UTSW |
5 |
34,593,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1766:Fam193a
|
UTSW |
5 |
34,619,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R1845:Fam193a
|
UTSW |
5 |
34,600,716 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2051:Fam193a
|
UTSW |
5 |
34,619,494 (GRCm39) |
missense |
probably benign |
0.19 |
R2483:Fam193a
|
UTSW |
5 |
34,623,102 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3014:Fam193a
|
UTSW |
5 |
34,623,016 (GRCm39) |
missense |
probably benign |
0.33 |
R4523:Fam193a
|
UTSW |
5 |
34,600,715 (GRCm39) |
missense |
probably benign |
0.07 |
R4723:Fam193a
|
UTSW |
5 |
34,578,130 (GRCm39) |
missense |
probably benign |
0.04 |
R4823:Fam193a
|
UTSW |
5 |
34,616,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R4826:Fam193a
|
UTSW |
5 |
34,593,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Fam193a
|
UTSW |
5 |
34,623,549 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5331:Fam193a
|
UTSW |
5 |
34,622,915 (GRCm39) |
splice site |
probably null |
|
R5364:Fam193a
|
UTSW |
5 |
34,623,597 (GRCm39) |
missense |
probably benign |
0.01 |
R5564:Fam193a
|
UTSW |
5 |
34,578,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R5580:Fam193a
|
UTSW |
5 |
34,578,132 (GRCm39) |
missense |
probably benign |
0.33 |
R5784:Fam193a
|
UTSW |
5 |
34,623,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R5933:Fam193a
|
UTSW |
5 |
34,623,024 (GRCm39) |
missense |
probably damaging |
0.98 |
R5949:Fam193a
|
UTSW |
5 |
34,597,816 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6106:Fam193a
|
UTSW |
5 |
34,616,374 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6181:Fam193a
|
UTSW |
5 |
34,600,884 (GRCm39) |
splice site |
probably null |
|
R7095:Fam193a
|
UTSW |
5 |
34,615,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R7109:Fam193a
|
UTSW |
5 |
34,623,165 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7344:Fam193a
|
UTSW |
5 |
34,643,074 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7401:Fam193a
|
UTSW |
5 |
34,622,979 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7453:Fam193a
|
UTSW |
5 |
34,621,460 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7456:Fam193a
|
UTSW |
5 |
34,578,132 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7648:Fam193a
|
UTSW |
5 |
34,588,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R7768:Fam193a
|
UTSW |
5 |
34,623,135 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7783:Fam193a
|
UTSW |
5 |
34,588,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R7818:Fam193a
|
UTSW |
5 |
34,622,997 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7852:Fam193a
|
UTSW |
5 |
34,568,161 (GRCm39) |
missense |
probably benign |
0.01 |
R7853:Fam193a
|
UTSW |
5 |
34,597,473 (GRCm39) |
missense |
probably benign |
0.12 |
R7894:Fam193a
|
UTSW |
5 |
34,597,877 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7933:Fam193a
|
UTSW |
5 |
34,623,539 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7957:Fam193a
|
UTSW |
5 |
34,619,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Fam193a
|
UTSW |
5 |
34,597,917 (GRCm39) |
missense |
probably damaging |
0.96 |
R8281:Fam193a
|
UTSW |
5 |
34,600,780 (GRCm39) |
missense |
unknown |
|
R8554:Fam193a
|
UTSW |
5 |
34,633,115 (GRCm39) |
missense |
probably benign |
0.05 |
R8743:Fam193a
|
UTSW |
5 |
34,577,501 (GRCm39) |
critical splice donor site |
probably null |
|
R8821:Fam193a
|
UTSW |
5 |
34,616,374 (GRCm39) |
missense |
probably benign |
0.01 |
R8831:Fam193a
|
UTSW |
5 |
34,616,374 (GRCm39) |
missense |
probably benign |
0.01 |
R8896:Fam193a
|
UTSW |
5 |
34,583,828 (GRCm39) |
missense |
probably benign |
0.03 |
R8943:Fam193a
|
UTSW |
5 |
34,597,796 (GRCm39) |
missense |
probably benign |
0.01 |
R9026:Fam193a
|
UTSW |
5 |
34,616,536 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9182:Fam193a
|
UTSW |
5 |
34,623,361 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9210:Fam193a
|
UTSW |
5 |
34,597,481 (GRCm39) |
missense |
probably benign |
0.01 |
R9212:Fam193a
|
UTSW |
5 |
34,597,481 (GRCm39) |
missense |
probably benign |
0.01 |
R9291:Fam193a
|
UTSW |
5 |
34,593,835 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Fam193a
|
UTSW |
5 |
34,578,239 (GRCm39) |
missense |
probably benign |
|
|