Incidental Mutation 'IGL02168:Ankra2'
ID |
282803 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Ankra2
|
Ensembl Gene |
ENSMUSG00000021661 |
Gene Name |
ankyrin repeat family A member 2 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.275)
|
Stock # |
IGL02168
|
Quality Score |
|
Status
|
|
Chromosome |
13 |
Chromosomal Location |
98399584-98411262 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
G to A
at 98409882 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153417
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022164]
[ENSMUST00000091356]
[ENSMUST00000123924]
[ENSMUST00000150352]
[ENSMUST00000150916]
[ENSMUST00000226100]
|
AlphaFold |
Q99PE2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000022164
|
SMART Domains |
Protein: ENSMUSP00000022164 Gene: ENSMUSG00000021661
Domain | Start | End | E-Value | Type |
ANK
|
180 |
209 |
1.45e-6 |
SMART |
ANK
|
213 |
242 |
1.05e-3 |
SMART |
ANK
|
246 |
275 |
1.76e-5 |
SMART |
Blast:ANK
|
279 |
308 |
1e-7 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000091356
|
SMART Domains |
Protein: ENSMUSP00000088915 Gene: ENSMUSG00000021661
Domain | Start | End | E-Value | Type |
ANK
|
20 |
49 |
1.45e-6 |
SMART |
ANK
|
53 |
82 |
1.05e-3 |
SMART |
ANK
|
86 |
115 |
1.76e-5 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123924
|
SMART Domains |
Protein: ENSMUSP00000122701 Gene: ENSMUSG00000021661
Domain | Start | End | E-Value | Type |
ANK
|
180 |
209 |
1.45e-6 |
SMART |
ANK
|
213 |
242 |
1.05e-3 |
SMART |
ANK
|
246 |
275 |
1.76e-5 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150352
|
SMART Domains |
Protein: ENSMUSP00000117508 Gene: ENSMUSG00000021661
Domain | Start | End | E-Value | Type |
ANK
|
180 |
209 |
1.45e-6 |
SMART |
ANK
|
213 |
242 |
1.05e-3 |
SMART |
ANK
|
246 |
275 |
1.76e-5 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150916
|
SMART Domains |
Protein: ENSMUSP00000116590 Gene: ENSMUSG00000021661
Domain | Start | End | E-Value | Type |
ANK
|
20 |
49 |
1.45e-6 |
SMART |
ANK
|
53 |
82 |
1.05e-3 |
SMART |
ANK
|
86 |
115 |
1.76e-5 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155629
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000226100
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
All alleles(3) : Targeted(2) Gene trapped(1)
|
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010007H06Rik |
T |
C |
9: 51,191,801 (GRCm39) |
|
probably benign |
Het |
6030468B19Rik |
T |
A |
11: 117,689,244 (GRCm39) |
|
probably benign |
Het |
Astn1 |
C |
A |
1: 158,436,911 (GRCm39) |
A823E |
possibly damaging |
Het |
Cfap43 |
T |
C |
19: 47,740,362 (GRCm39) |
|
probably benign |
Het |
Clec4b2 |
T |
A |
6: 123,181,156 (GRCm39) |
N180K |
probably damaging |
Het |
Col7a1 |
A |
G |
9: 108,813,143 (GRCm39) |
|
probably benign |
Het |
Dhrs7c |
T |
C |
11: 67,706,693 (GRCm39) |
F284L |
probably benign |
Het |
Dock1 |
T |
C |
7: 134,678,860 (GRCm39) |
|
probably benign |
Het |
Entpd5 |
A |
T |
12: 84,433,752 (GRCm39) |
|
probably null |
Het |
Heatr5b |
A |
T |
17: 79,139,020 (GRCm39) |
|
probably benign |
Het |
Kdm3a |
A |
G |
6: 71,577,101 (GRCm39) |
V738A |
probably damaging |
Het |
Klf10 |
A |
T |
15: 38,297,085 (GRCm39) |
F318L |
probably damaging |
Het |
Mcc |
A |
C |
18: 44,582,366 (GRCm39) |
I770S |
probably damaging |
Het |
Muc19 |
C |
T |
15: 91,778,292 (GRCm39) |
|
noncoding transcript |
Het |
Or9a4 |
A |
T |
6: 40,548,317 (GRCm39) |
|
probably benign |
Het |
Pcdh17 |
A |
G |
14: 84,770,635 (GRCm39) |
T1038A |
probably benign |
Het |
Pole2 |
A |
G |
12: 69,248,660 (GRCm39) |
|
probably benign |
Het |
Polr2c |
A |
G |
8: 95,584,394 (GRCm39) |
R36G |
probably damaging |
Het |
Ptgs2 |
A |
G |
1: 149,979,430 (GRCm39) |
|
probably null |
Het |
Scart1 |
A |
T |
7: 139,803,399 (GRCm39) |
H321L |
probably benign |
Het |
Taf5 |
A |
G |
19: 47,070,917 (GRCm39) |
D747G |
probably damaging |
Het |
Tll1 |
T |
G |
8: 64,507,001 (GRCm39) |
K580T |
possibly damaging |
Het |
Tmc3 |
A |
T |
7: 83,269,203 (GRCm39) |
N768I |
possibly damaging |
Het |
Top1 |
G |
T |
2: 160,546,893 (GRCm39) |
|
probably null |
Het |
Ubtf |
T |
C |
11: 102,204,994 (GRCm39) |
K97E |
probably damaging |
Het |
Vcl |
T |
C |
14: 21,057,355 (GRCm39) |
V509A |
probably benign |
Het |
Vmn2r110 |
A |
T |
17: 20,804,062 (GRCm39) |
|
probably benign |
Het |
Zfp106 |
A |
G |
2: 120,364,712 (GRCm39) |
V565A |
possibly damaging |
Het |
Zfp458 |
A |
T |
13: 67,406,098 (GRCm39) |
C111S |
probably damaging |
Het |
|
Other mutations in Ankra2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02807:Ankra2
|
APN |
13 |
98,408,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03030:Ankra2
|
APN |
13 |
98,409,881 (GRCm39) |
splice site |
probably benign |
|
R0068:Ankra2
|
UTSW |
13 |
98,409,891 (GRCm39) |
nonsense |
probably null |
|
R0068:Ankra2
|
UTSW |
13 |
98,409,891 (GRCm39) |
nonsense |
probably null |
|
R0302:Ankra2
|
UTSW |
13 |
98,408,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Ankra2
|
UTSW |
13 |
98,402,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Ankra2
|
UTSW |
13 |
98,408,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Ankra2
|
UTSW |
13 |
98,407,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Ankra2
|
UTSW |
13 |
98,402,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R2230:Ankra2
|
UTSW |
13 |
98,407,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R2232:Ankra2
|
UTSW |
13 |
98,407,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R3898:Ankra2
|
UTSW |
13 |
98,410,317 (GRCm39) |
missense |
probably benign |
0.13 |
R4605:Ankra2
|
UTSW |
13 |
98,402,742 (GRCm39) |
intron |
probably benign |
|
R4855:Ankra2
|
UTSW |
13 |
98,409,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5806:Ankra2
|
UTSW |
13 |
98,405,005 (GRCm39) |
critical splice donor site |
probably null |
|
R5901:Ankra2
|
UTSW |
13 |
98,407,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R6478:Ankra2
|
UTSW |
13 |
98,404,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R7469:Ankra2
|
UTSW |
13 |
98,402,882 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Ankra2
|
UTSW |
13 |
98,408,785 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Posted On |
2015-04-16 |