Incidental Mutation 'R2942:Aox2'
ID |
255189 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Aox2
|
Ensembl Gene |
ENSMUSG00000079554 |
Gene Name |
aldehyde oxidase 2 |
Synonyms |
Aox3l1 |
Accession Numbers |
|
Is this an essential gene? |
Probably non essential
(E-score: 0.068)
|
Stock # |
R2942 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
58278326-58380259 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 58337381 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Leucine
at position 907
(R907L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000110006
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000114366]
|
AlphaFold |
Q5SGK3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000114366
AA Change: R907L
PolyPhen 2
Score 0.030 (Sensitivity: 0.95; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000110006 Gene: ENSMUSG00000079554 AA Change: R907L
Domain | Start | End | E-Value | Type |
Pfam:Fer2
|
13 |
83 |
3.4e-9 |
PFAM |
Pfam:Fer2_2
|
92 |
166 |
4.2e-30 |
PFAM |
Pfam:FAD_binding_5
|
241 |
421 |
5.1e-46 |
PFAM |
CO_deh_flav_C
|
428 |
532 |
1.4e-23 |
SMART |
Ald_Xan_dh_C
|
604 |
707 |
4.64e-47 |
SMART |
Pfam:Ald_Xan_dh_C2
|
717 |
1251 |
1.3e-178 |
PFAM |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1285 |
1303 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 9 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Fat4 |
A |
G |
3: 38,982,336 |
N3379S |
probably damaging |
Het |
Kcnv1 |
A |
G |
15: 45,109,185 |
F434S |
probably damaging |
Het |
Parg |
A |
G |
14: 32,209,337 |
K305E |
probably damaging |
Het |
Phlpp1 |
G |
A |
1: 106,172,772 |
V257I |
probably benign |
Het |
Pth2r |
G |
A |
1: 65,388,476 |
R436K |
probably benign |
Het |
Srsf9 |
T |
C |
5: 115,332,693 |
Y215H |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 65,318,006 |
V798A |
probably damaging |
Het |
Trmt13 |
A |
T |
3: 116,585,772 |
I242N |
probably damaging |
Het |
Vmn1r31 |
G |
A |
6: 58,472,598 |
T94I |
possibly damaging |
Het |
|
Other mutations in Aox2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01014:Aox2
|
APN |
1 |
58322801 |
missense |
possibly damaging |
0.73 |
IGL01288:Aox2
|
APN |
1 |
58294407 |
missense |
probably damaging |
0.99 |
IGL01383:Aox2
|
APN |
1 |
58294305 |
missense |
probably benign |
0.09 |
IGL01734:Aox2
|
APN |
1 |
58354310 |
missense |
possibly damaging |
0.95 |
IGL01793:Aox2
|
APN |
1 |
58336624 |
missense |
possibly damaging |
0.79 |
IGL01834:Aox2
|
APN |
1 |
58309024 |
missense |
possibly damaging |
0.90 |
IGL01924:Aox2
|
APN |
1 |
58287743 |
missense |
possibly damaging |
0.90 |
IGL02591:Aox2
|
APN |
1 |
58358999 |
nonsense |
probably null |
|
IGL02645:Aox2
|
APN |
1 |
58334724 |
missense |
probably damaging |
1.00 |
IGL02710:Aox2
|
APN |
1 |
58334769 |
critical splice donor site |
probably null |
|
IGL02801:Aox2
|
APN |
1 |
58354177 |
missense |
probably damaging |
1.00 |
IGL02988:Aox2
|
APN |
1 |
58337350 |
missense |
probably benign |
|
IGL03104:Aox2
|
APN |
1 |
58282759 |
missense |
probably benign |
|
IGL03121:Aox2
|
APN |
1 |
58358954 |
missense |
probably damaging |
1.00 |
IGL03191:Aox2
|
APN |
1 |
58359069 |
missense |
probably null |
0.98 |
IGL03236:Aox2
|
APN |
1 |
58309997 |
nonsense |
probably null |
|
IGL03409:Aox2
|
APN |
1 |
58354429 |
missense |
possibly damaging |
0.91 |
PIT4362001:Aox2
|
UTSW |
1 |
58282680 |
missense |
probably damaging |
1.00 |
R0035:Aox2
|
UTSW |
1 |
58354422 |
missense |
probably benign |
0.00 |
R0035:Aox2
|
UTSW |
1 |
58354422 |
missense |
probably benign |
0.00 |
R0267:Aox2
|
UTSW |
1 |
58339446 |
splice site |
probably benign |
|
R0388:Aox2
|
UTSW |
1 |
58354406 |
missense |
probably damaging |
1.00 |
R0409:Aox2
|
UTSW |
1 |
58336624 |
missense |
possibly damaging |
0.90 |
R0547:Aox2
|
UTSW |
1 |
58310042 |
missense |
probably damaging |
0.96 |
R0630:Aox2
|
UTSW |
1 |
58337321 |
splice site |
probably benign |
|
R0726:Aox2
|
UTSW |
1 |
58334782 |
splice site |
probably benign |
|
R0734:Aox2
|
UTSW |
1 |
58305341 |
missense |
probably benign |
0.22 |
R0831:Aox2
|
UTSW |
1 |
58339683 |
missense |
probably benign |
0.28 |
R0961:Aox2
|
UTSW |
1 |
58310071 |
missense |
probably benign |
0.00 |
R1404:Aox2
|
UTSW |
1 |
58346212 |
splice site |
probably benign |
|
R1512:Aox2
|
UTSW |
1 |
58307351 |
missense |
probably benign |
0.00 |
R1573:Aox2
|
UTSW |
1 |
58309027 |
missense |
probably benign |
0.00 |
R1592:Aox2
|
UTSW |
1 |
58300694 |
missense |
probably benign |
0.00 |
R1747:Aox2
|
UTSW |
1 |
58339592 |
missense |
probably benign |
0.01 |
R1768:Aox2
|
UTSW |
1 |
58354195 |
missense |
probably benign |
0.00 |
R1809:Aox2
|
UTSW |
1 |
58294325 |
missense |
probably benign |
|
R1823:Aox2
|
UTSW |
1 |
58312359 |
missense |
probably benign |
0.02 |
R1834:Aox2
|
UTSW |
1 |
58308991 |
missense |
probably benign |
0.08 |
R1835:Aox2
|
UTSW |
1 |
58308991 |
missense |
probably benign |
0.08 |
R1836:Aox2
|
UTSW |
1 |
58308991 |
missense |
probably benign |
0.08 |
R2219:Aox2
|
UTSW |
1 |
58349130 |
splice site |
probably null |
|
R2220:Aox2
|
UTSW |
1 |
58349130 |
splice site |
probably null |
|
R2508:Aox2
|
UTSW |
1 |
58343673 |
missense |
probably benign |
0.38 |
R2967:Aox2
|
UTSW |
1 |
58322834 |
missense |
probably damaging |
0.96 |
R3082:Aox2
|
UTSW |
1 |
58283600 |
splice site |
probably benign |
|
R3161:Aox2
|
UTSW |
1 |
58304438 |
missense |
possibly damaging |
0.91 |
R3408:Aox2
|
UTSW |
1 |
58343668 |
missense |
probably benign |
0.32 |
R3803:Aox2
|
UTSW |
1 |
58289899 |
splice site |
probably null |
|
R3894:Aox2
|
UTSW |
1 |
58334678 |
critical splice acceptor site |
probably null |
|
R4214:Aox2
|
UTSW |
1 |
58307444 |
critical splice donor site |
probably null |
|
R4249:Aox2
|
UTSW |
1 |
58299819 |
missense |
probably benign |
0.01 |
R4666:Aox2
|
UTSW |
1 |
58304597 |
nonsense |
probably null |
|
R4668:Aox2
|
UTSW |
1 |
58334694 |
missense |
possibly damaging |
0.63 |
R4703:Aox2
|
UTSW |
1 |
58358957 |
missense |
possibly damaging |
0.78 |
R4758:Aox2
|
UTSW |
1 |
58332582 |
missense |
probably benign |
0.00 |
R4890:Aox2
|
UTSW |
1 |
58334703 |
missense |
probably benign |
0.11 |
R4900:Aox2
|
UTSW |
1 |
58305385 |
missense |
probably benign |
|
R4924:Aox2
|
UTSW |
1 |
58305344 |
missense |
probably damaging |
1.00 |
R4970:Aox2
|
UTSW |
1 |
58310095 |
splice site |
probably null |
|
R5112:Aox2
|
UTSW |
1 |
58310095 |
splice site |
probably null |
|
R5987:Aox2
|
UTSW |
1 |
58307359 |
missense |
probably benign |
0.00 |
R6239:Aox2
|
UTSW |
1 |
58305391 |
critical splice donor site |
probably null |
|
R6273:Aox2
|
UTSW |
1 |
58339672 |
missense |
probably benign |
0.00 |
R6291:Aox2
|
UTSW |
1 |
58330806 |
missense |
probably damaging |
0.98 |
R6334:Aox2
|
UTSW |
1 |
58307407 |
nonsense |
probably null |
|
R6764:Aox2
|
UTSW |
1 |
58350282 |
missense |
probably damaging |
0.97 |
R6766:Aox2
|
UTSW |
1 |
58349068 |
missense |
possibly damaging |
0.95 |
R6789:Aox2
|
UTSW |
1 |
58304485 |
missense |
probably benign |
0.01 |
R6804:Aox2
|
UTSW |
1 |
58304598 |
missense |
probably benign |
0.04 |
R7007:Aox2
|
UTSW |
1 |
58330892 |
missense |
probably damaging |
1.00 |
R7015:Aox2
|
UTSW |
1 |
58282758 |
missense |
probably benign |
0.00 |
R7055:Aox2
|
UTSW |
1 |
58299768 |
missense |
probably benign |
0.08 |
R7089:Aox2
|
UTSW |
1 |
58336649 |
missense |
probably benign |
0.01 |
R7157:Aox2
|
UTSW |
1 |
58283492 |
missense |
probably benign |
0.00 |
R7303:Aox2
|
UTSW |
1 |
58334765 |
nonsense |
probably null |
|
R7426:Aox2
|
UTSW |
1 |
58289983 |
nonsense |
probably null |
|
R7762:Aox2
|
UTSW |
1 |
58349104 |
missense |
probably damaging |
1.00 |
R7899:Aox2
|
UTSW |
1 |
58281237 |
splice site |
probably null |
|
R7942:Aox2
|
UTSW |
1 |
58337431 |
missense |
probably damaging |
1.00 |
R7975:Aox2
|
UTSW |
1 |
58309028 |
missense |
probably benign |
0.02 |
R8029:Aox2
|
UTSW |
1 |
58343668 |
missense |
probably benign |
0.32 |
R8032:Aox2
|
UTSW |
1 |
58350283 |
missense |
probably benign |
0.01 |
R8147:Aox2
|
UTSW |
1 |
58300662 |
missense |
probably benign |
0.02 |
R8165:Aox2
|
UTSW |
1 |
58308929 |
missense |
probably benign |
0.08 |
R8326:Aox2
|
UTSW |
1 |
58295887 |
missense |
probably benign |
|
R8770:Aox2
|
UTSW |
1 |
58339604 |
missense |
probably benign |
0.10 |
R8973:Aox2
|
UTSW |
1 |
58289954 |
missense |
probably benign |
0.34 |
R9015:Aox2
|
UTSW |
1 |
58343692 |
missense |
probably damaging |
1.00 |
R9097:Aox2
|
UTSW |
1 |
58287728 |
missense |
possibly damaging |
0.82 |
R9101:Aox2
|
UTSW |
1 |
58332637 |
missense |
probably benign |
0.03 |
R9108:Aox2
|
UTSW |
1 |
58282692 |
missense |
probably damaging |
1.00 |
R9180:Aox2
|
UTSW |
1 |
58339618 |
nonsense |
probably null |
|
R9258:Aox2
|
UTSW |
1 |
58312356 |
missense |
probably damaging |
1.00 |
R9293:Aox2
|
UTSW |
1 |
58322794 |
missense |
possibly damaging |
0.86 |
R9519:Aox2
|
UTSW |
1 |
58334767 |
missense |
probably damaging |
0.98 |
R9581:Aox2
|
UTSW |
1 |
58330896 |
critical splice donor site |
probably null |
|
Z1177:Aox2
|
UTSW |
1 |
58354397 |
missense |
possibly damaging |
0.69 |
|
Predicted Primers |
PCR Primer
(F):5'- GCCCCTTCAGAGATAACATGCA -3'
(R):5'- AGCTTGGTTATGAGCCTCATT -3'
Sequencing Primer
(F):5'- TGTAAGTCTCCCGGTAAAACTGC -3'
(R):5'- GCTTGGTTATGAGCCTCATTATAATC -3'
|
Posted On |
2014-12-29 |