Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asb16 |
T |
A |
11: 102,159,885 (GRCm39) |
D79E |
probably benign |
Het |
Atp4a |
G |
A |
7: 30,419,650 (GRCm39) |
R671Q |
probably benign |
Het |
B230307C23Rik |
T |
A |
16: 97,810,199 (GRCm39) |
N62K |
probably benign |
Het |
B3galnt2 |
G |
A |
13: 14,150,220 (GRCm39) |
|
probably null |
Het |
Bnip2 |
T |
A |
9: 69,906,432 (GRCm39) |
Y118N |
probably damaging |
Het |
Bptf |
C |
A |
11: 106,965,024 (GRCm39) |
R1275L |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,349,916 (GRCm39) |
|
probably null |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Cdh4 |
T |
C |
2: 179,422,160 (GRCm39) |
S95P |
probably benign |
Het |
Ceacam5 |
G |
A |
7: 17,494,748 (GRCm39) |
E919K |
possibly damaging |
Het |
Eftud2 |
T |
C |
11: 102,735,027 (GRCm39) |
E624G |
probably damaging |
Het |
Hsp90ab1 |
A |
G |
17: 45,880,214 (GRCm39) |
Y110H |
probably damaging |
Het |
Map3k1 |
A |
G |
13: 111,890,425 (GRCm39) |
V1258A |
probably damaging |
Het |
Naa11 |
A |
T |
5: 97,539,648 (GRCm39) |
V170E |
probably benign |
Het |
Nmd3 |
C |
T |
3: 69,654,095 (GRCm39) |
R413C |
probably damaging |
Het |
Or4k51 |
G |
T |
2: 111,584,914 (GRCm39) |
V107F |
probably benign |
Het |
Or56b2 |
A |
G |
7: 104,337,599 (GRCm39) |
I126V |
probably benign |
Het |
Pgm3 |
G |
T |
9: 86,441,563 (GRCm39) |
P345T |
probably benign |
Het |
Ptpn14 |
C |
A |
1: 189,583,596 (GRCm39) |
D814E |
probably damaging |
Het |
Rab36 |
G |
A |
10: 74,880,328 (GRCm39) |
V63I |
probably damaging |
Het |
Rap1gap2 |
C |
A |
11: 74,298,148 (GRCm39) |
A491S |
possibly damaging |
Het |
Ros1 |
A |
T |
10: 52,021,912 (GRCm39) |
V624E |
probably damaging |
Het |
Sgo2b |
T |
C |
8: 64,384,361 (GRCm39) |
K212E |
probably benign |
Het |
Shisa2 |
T |
A |
14: 59,867,228 (GRCm39) |
L160Q |
probably damaging |
Het |
Strn4 |
A |
G |
7: 16,556,506 (GRCm39) |
Y123C |
probably damaging |
Het |
Sycp2 |
T |
C |
2: 178,016,177 (GRCm39) |
T762A |
probably benign |
Het |
Tiam2 |
A |
G |
17: 3,471,959 (GRCm39) |
K534E |
possibly damaging |
Het |
Trdn |
A |
T |
10: 33,344,185 (GRCm39) |
D633V |
probably benign |
Het |
Ttn |
T |
C |
2: 76,747,333 (GRCm39) |
Y4572C |
possibly damaging |
Het |
Unc79 |
T |
A |
12: 103,054,920 (GRCm39) |
N921K |
probably damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,644,397 (GRCm39) |
V671A |
probably damaging |
Het |
Wdr86 |
T |
A |
5: 24,923,339 (GRCm39) |
T118S |
probably damaging |
Het |
Zfp446 |
T |
A |
7: 12,716,580 (GRCm39) |
I517N |
probably damaging |
Het |
Zfp830 |
G |
A |
11: 82,656,188 (GRCm39) |
E331K |
possibly damaging |
Het |
|
Other mutations in Hr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01805:Hr
|
APN |
14 |
70,802,737 (GRCm39) |
splice site |
probably benign |
|
IGL02020:Hr
|
APN |
14 |
70,793,877 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02372:Hr
|
APN |
14 |
70,795,790 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02380:Hr
|
APN |
14 |
70,795,201 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02554:Hr
|
APN |
14 |
70,797,306 (GRCm39) |
splice site |
probably benign |
|
IGL02949:Hr
|
APN |
14 |
70,797,225 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03406:Hr
|
APN |
14 |
70,800,860 (GRCm39) |
critical splice donor site |
probably null |
|
angie
|
UTSW |
14 |
70,805,273 (GRCm39) |
missense |
probably damaging |
0.97 |
blofeld
|
UTSW |
14 |
70,805,525 (GRCm39) |
missense |
probably damaging |
1.00 |
general
|
UTSW |
14 |
70,801,124 (GRCm39) |
critical splice donor site |
probably null |
|
kaburo
|
UTSW |
14 |
0 () |
unclassified |
|
|
mister_clean
|
UTSW |
14 |
70,797,504 (GRCm39) |
critical splice donor site |
probably benign |
|
mushroom
|
UTSW |
14 |
70,805,525 (GRCm39) |
missense |
probably damaging |
1.00 |
prune
|
UTSW |
14 |
70,808,869 (GRCm39) |
missense |
probably damaging |
1.00 |
ren
|
UTSW |
14 |
70,805,525 (GRCm39) |
missense |
probably damaging |
1.00 |
subclinical
|
UTSW |
14 |
70,799,276 (GRCm39) |
missense |
possibly damaging |
0.89 |
vessel
|
UTSW |
14 |
70,799,305 (GRCm39) |
nonsense |
probably null |
|
yuanxiao
|
UTSW |
14 |
70,808,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R0018:Hr
|
UTSW |
14 |
70,795,717 (GRCm39) |
missense |
probably benign |
|
R0038:Hr
|
UTSW |
14 |
70,805,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Hr
|
UTSW |
14 |
70,793,916 (GRCm39) |
missense |
probably benign |
0.01 |
R0511:Hr
|
UTSW |
14 |
70,799,352 (GRCm39) |
nonsense |
probably null |
|
R0609:Hr
|
UTSW |
14 |
70,797,097 (GRCm39) |
missense |
probably benign |
|
R1828:Hr
|
UTSW |
14 |
70,809,477 (GRCm39) |
critical splice donor site |
probably null |
|
R2030:Hr
|
UTSW |
14 |
70,808,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R2266:Hr
|
UTSW |
14 |
70,795,547 (GRCm39) |
missense |
probably benign |
|
R2267:Hr
|
UTSW |
14 |
70,795,547 (GRCm39) |
missense |
probably benign |
|
R2268:Hr
|
UTSW |
14 |
70,795,547 (GRCm39) |
missense |
probably benign |
|
R2377:Hr
|
UTSW |
14 |
70,795,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R3687:Hr
|
UTSW |
14 |
70,795,236 (GRCm39) |
missense |
probably damaging |
0.98 |
R3754:Hr
|
UTSW |
14 |
70,805,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R3803:Hr
|
UTSW |
14 |
70,795,333 (GRCm39) |
missense |
probably benign |
0.01 |
R3846:Hr
|
UTSW |
14 |
70,808,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R3977:Hr
|
UTSW |
14 |
70,801,024 (GRCm39) |
missense |
probably benign |
0.01 |
R3978:Hr
|
UTSW |
14 |
70,801,024 (GRCm39) |
missense |
probably benign |
0.01 |
R3979:Hr
|
UTSW |
14 |
70,801,024 (GRCm39) |
missense |
probably benign |
0.01 |
R4528:Hr
|
UTSW |
14 |
70,803,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Hr
|
UTSW |
14 |
70,801,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R4834:Hr
|
UTSW |
14 |
70,797,362 (GRCm39) |
missense |
probably damaging |
0.98 |
R4847:Hr
|
UTSW |
14 |
70,793,916 (GRCm39) |
missense |
probably benign |
0.04 |
R4863:Hr
|
UTSW |
14 |
70,809,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R5292:Hr
|
UTSW |
14 |
70,809,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Hr
|
UTSW |
14 |
70,794,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R5717:Hr
|
UTSW |
14 |
70,803,616 (GRCm39) |
missense |
probably benign |
0.34 |
R5902:Hr
|
UTSW |
14 |
70,795,231 (GRCm39) |
missense |
probably benign |
0.02 |
R6000:Hr
|
UTSW |
14 |
70,805,273 (GRCm39) |
missense |
probably damaging |
0.97 |
R6439:Hr
|
UTSW |
14 |
70,799,276 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6823:Hr
|
UTSW |
14 |
70,802,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R7030:Hr
|
UTSW |
14 |
70,801,124 (GRCm39) |
critical splice donor site |
probably null |
|
R7213:Hr
|
UTSW |
14 |
70,795,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R7452:Hr
|
UTSW |
14 |
70,808,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R7468:Hr
|
UTSW |
14 |
70,795,652 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7572:Hr
|
UTSW |
14 |
70,799,293 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7956:Hr
|
UTSW |
14 |
70,797,327 (GRCm39) |
missense |
probably benign |
|
R7996:Hr
|
UTSW |
14 |
70,801,043 (GRCm39) |
nonsense |
probably null |
|
R7997:Hr
|
UTSW |
14 |
70,801,043 (GRCm39) |
nonsense |
probably null |
|
R8076:Hr
|
UTSW |
14 |
70,795,381 (GRCm39) |
missense |
probably benign |
0.00 |
R8101:Hr
|
UTSW |
14 |
70,805,282 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8553:Hr
|
UTSW |
14 |
70,804,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Hr
|
UTSW |
14 |
70,795,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8850:Hr
|
UTSW |
14 |
70,799,305 (GRCm39) |
nonsense |
probably null |
|
R8949:Hr
|
UTSW |
14 |
70,795,328 (GRCm39) |
missense |
probably benign |
0.01 |
R9139:Hr
|
UTSW |
14 |
70,795,079 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9236:Hr
|
UTSW |
14 |
70,809,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Hr
|
UTSW |
14 |
70,808,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R9327:Hr
|
UTSW |
14 |
70,805,228 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9337:Hr
|
UTSW |
14 |
70,797,324 (GRCm39) |
missense |
probably benign |
0.00 |
R9487:Hr
|
UTSW |
14 |
70,794,205 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9487:Hr
|
UTSW |
14 |
70,793,877 (GRCm39) |
missense |
probably benign |
0.01 |
R9700:Hr
|
UTSW |
14 |
70,804,616 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Hr
|
UTSW |
14 |
70,804,391 (GRCm39) |
splice site |
probably null |
|
X0026:Hr
|
UTSW |
14 |
70,805,281 (GRCm39) |
missense |
probably damaging |
0.99 |
|