Incidental Mutation 'R7423:Aox3'
| ID |
575795 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Aox3
|
| Ensembl Gene |
ENSMUSG00000064294 |
| Gene Name |
aldehyde oxidase 3 |
| Synonyms |
1200011D03Rik, AOH1 |
| MMRRC Submission |
045501-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7423 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
58152289-58239857 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 58160228 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 137
(E137G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049391
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040999]
[ENSMUST00000162011]
|
| AlphaFold |
G3X982 |
| PDB Structure |
Crystal structure of the mouse liver Aldehyde Oxidase 3 (mAOX3) [X-RAY DIFFRACTION]
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000040999
AA Change: E137G
PolyPhen 2
Score 0.803 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000049391
Gene: ENSMUSG00000064294
AA Change: E137G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Fer2
|
12 |
82 |
1.4e-9 |
PFAM |
|
Pfam:Fer2_2
|
91 |
165 |
1e-29 |
PFAM |
|
Pfam:FAD_binding_5
|
239 |
419 |
1e-44 |
PFAM |
|
CO_deh_flav_C
|
426 |
530 |
9.26e-24 |
SMART |
|
Ald_Xan_dh_C
|
594 |
697 |
2.27e-41 |
SMART |
|
Pfam:Ald_Xan_dh_C2
|
708 |
1241 |
8.7e-183 |
PFAM |
|
low complexity region
|
1275 |
1286 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000162011
AA Change: E137G
PolyPhen 2
Score 0.820 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000140140
Gene: ENSMUSG00000064294
AA Change: E137G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Fer2
|
12 |
82 |
3.6e-8 |
PFAM |
|
Pfam:Fer2_2
|
91 |
166 |
2.5e-29 |
PFAM |
|
transmembrane domain
|
242 |
264 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 98.8%
|
| Validation Efficiency |
96% (91/95) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acsbg2 |
A |
T |
17: 57,175,257 (GRCm39) |
M85K |
probably benign |
Het |
| Actn4 |
C |
T |
7: 28,593,680 (GRCm39) |
A905T |
probably damaging |
Het |
| Aff1 |
T |
A |
5: 103,994,967 (GRCm39) |
V1055D |
probably damaging |
Het |
| Apaf1 |
A |
T |
10: 90,895,468 (GRCm39) |
D443E |
probably damaging |
Het |
| Arl5b |
C |
A |
2: 15,072,983 (GRCm39) |
A28E |
probably damaging |
Het |
| Atg16l1 |
T |
C |
1: 87,714,023 (GRCm39) |
V478A |
probably damaging |
Het |
| Atp6v1f |
G |
C |
6: 29,468,105 (GRCm39) |
E13Q |
probably null |
Het |
| Atpaf1 |
A |
T |
4: 115,647,827 (GRCm39) |
K162M |
probably damaging |
Het |
| C3 |
A |
T |
17: 57,521,767 (GRCm39) |
L1100Q |
probably damaging |
Het |
| Ccr1 |
A |
G |
9: 123,764,422 (GRCm39) |
L36P |
probably damaging |
Het |
| Cct3 |
T |
C |
3: 88,216,503 (GRCm39) |
L153S |
probably benign |
Het |
| Chd4 |
A |
G |
6: 125,105,822 (GRCm39) |
D1813G |
possibly damaging |
Het |
| Chrm3 |
T |
C |
13: 9,928,845 (GRCm39) |
I64V |
probably benign |
Het |
| Cnot2 |
A |
T |
10: 116,328,303 (GRCm39) |
V477E |
probably damaging |
Het |
| Csf2rb2 |
T |
A |
15: 78,176,760 (GRCm39) |
I211F |
possibly damaging |
Het |
| Dnah8 |
T |
C |
17: 30,923,743 (GRCm39) |
L1237P |
possibly damaging |
Het |
| Dnttip2 |
T |
C |
3: 122,069,175 (GRCm39) |
V130A |
probably benign |
Het |
| Dock10 |
G |
A |
1: 80,501,497 (GRCm39) |
A1852V |
possibly damaging |
Het |
| Dock3 |
A |
G |
9: 106,844,370 (GRCm39) |
V910A |
probably damaging |
Het |
| Drgx |
A |
G |
14: 32,350,778 (GRCm39) |
S205G |
probably damaging |
Het |
| Fbrs |
G |
A |
7: 127,088,633 (GRCm39) |
W738* |
probably null |
Het |
| Fmnl3 |
T |
A |
15: 99,227,281 (GRCm39) |
D162V |
probably damaging |
Het |
| Fosl2 |
A |
G |
5: 32,307,807 (GRCm39) |
R133G |
probably damaging |
Het |
| Frmpd1 |
A |
G |
4: 45,256,948 (GRCm39) |
Q172R |
probably damaging |
Het |
| Fsd1l |
A |
T |
4: 53,686,406 (GRCm39) |
D273V |
probably damaging |
Het |
| Fstl4 |
T |
A |
11: 52,959,382 (GRCm39) |
M141K |
possibly damaging |
Het |
| Gcfc2 |
A |
G |
6: 81,923,541 (GRCm39) |
D535G |
probably damaging |
Het |
| Gm19410 |
A |
C |
8: 36,271,761 (GRCm39) |
D1277A |
probably benign |
Het |
| Gnmt |
T |
A |
17: 47,037,066 (GRCm39) |
N211Y |
probably damaging |
Het |
| Hic2 |
A |
G |
16: 17,075,993 (GRCm39) |
D274G |
probably damaging |
Het |
| Hnrnpu |
A |
G |
1: 178,156,849 (GRCm39) |
|
probably benign |
Het |
| Icam5 |
T |
C |
9: 20,948,201 (GRCm39) |
S670P |
probably benign |
Het |
| Ighv5-4 |
A |
T |
12: 113,561,120 (GRCm39) |
L100Q |
probably damaging |
Het |
| Il17rb |
A |
T |
14: 29,719,072 (GRCm39) |
S337T |
probably damaging |
Het |
| Inf2 |
G |
T |
12: 112,576,172 (GRCm39) |
R883L |
unknown |
Het |
| Inhbc |
C |
T |
10: 127,193,275 (GRCm39) |
C247Y |
probably damaging |
Het |
| Ints4 |
A |
G |
7: 97,156,926 (GRCm39) |
K333E |
probably damaging |
Het |
| Iyd |
A |
T |
10: 3,497,088 (GRCm39) |
I148F |
probably damaging |
Het |
| Klk1b26 |
A |
T |
7: 43,664,193 (GRCm39) |
D16V |
probably damaging |
Het |
| Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
| Lama2 |
A |
T |
10: 27,088,222 (GRCm39) |
S852T |
probably benign |
Het |
| Mbtd1 |
A |
G |
11: 93,834,622 (GRCm39) |
E600G |
probably benign |
Het |
| Mfap3 |
T |
G |
11: 57,420,329 (GRCm39) |
N103K |
probably damaging |
Het |
| Mtor |
G |
A |
4: 148,640,801 (GRCm39) |
E2536K |
possibly damaging |
Het |
| Mug2 |
G |
A |
6: 122,056,685 (GRCm39) |
S1210N |
probably benign |
Het |
| Nat8 |
G |
A |
6: 85,807,477 (GRCm39) |
L219F |
probably benign |
Het |
| Nisch |
A |
G |
14: 30,893,658 (GRCm39) |
V1305A |
probably benign |
Het |
| Nup153 |
A |
T |
13: 46,850,120 (GRCm39) |
|
probably null |
Het |
| Or3a1b |
G |
A |
11: 74,012,811 (GRCm39) |
R232H |
probably benign |
Het |
| Otud6b |
A |
T |
4: 14,825,858 (GRCm39) |
|
probably null |
Het |
| Pbld2 |
A |
G |
10: 62,883,783 (GRCm39) |
T83A |
probably damaging |
Het |
| Pcx |
A |
T |
19: 4,671,206 (GRCm39) |
M1144L |
probably benign |
Het |
| Pdpk1 |
C |
A |
17: 24,329,874 (GRCm39) |
R81L |
probably benign |
Het |
| Pik3cd |
A |
T |
4: 149,736,220 (GRCm39) |
|
probably null |
Het |
| Plch2 |
A |
C |
4: 155,068,194 (GRCm39) |
D1477E |
probably damaging |
Het |
| Plek2 |
A |
G |
12: 78,946,884 (GRCm39) |
I51T |
probably damaging |
Het |
| Plekhn1 |
A |
G |
4: 156,315,142 (GRCm39) |
V505A |
probably benign |
Het |
| Pofut2 |
T |
C |
10: 77,098,273 (GRCm39) |
S129P |
possibly damaging |
Het |
| Prdx5 |
C |
A |
19: 6,887,370 (GRCm39) |
|
probably benign |
Het |
| Proca1 |
G |
T |
11: 78,085,643 (GRCm39) |
|
probably benign |
Het |
| Ptprs |
A |
C |
17: 56,721,793 (GRCm39) |
Y1752D |
probably damaging |
Het |
| Pum1 |
G |
A |
4: 130,501,856 (GRCm39) |
V1127M |
probably damaging |
Het |
| Ralbp1 |
T |
C |
17: 66,165,976 (GRCm39) |
R403G |
probably damaging |
Het |
| Reps1 |
A |
T |
10: 17,969,635 (GRCm39) |
H246L |
possibly damaging |
Het |
| Rps6kc1 |
A |
C |
1: 190,531,293 (GRCm39) |
M903R |
probably damaging |
Het |
| Rubcnl |
A |
G |
14: 75,287,083 (GRCm39) |
T584A |
probably benign |
Het |
| Samd9l |
A |
T |
6: 3,374,408 (GRCm39) |
V951E |
probably damaging |
Het |
| Sbf2 |
A |
G |
7: 110,038,055 (GRCm39) |
F463L |
possibly damaging |
Het |
| Sdr16c6 |
G |
A |
4: 4,076,921 (GRCm39) |
|
probably benign |
Het |
| Shoc1 |
A |
T |
4: 59,076,264 (GRCm39) |
S560T |
probably benign |
Het |
| Slc26a8 |
A |
G |
17: 28,867,177 (GRCm39) |
I548T |
probably benign |
Het |
| Slc2a13 |
T |
A |
15: 91,456,883 (GRCm39) |
I140F |
probably damaging |
Het |
| Smtn |
A |
T |
11: 3,481,200 (GRCm39) |
|
probably null |
Het |
| Sobp |
G |
T |
10: 42,898,564 (GRCm39) |
C340* |
probably null |
Het |
| Sox6 |
A |
T |
7: 115,149,258 (GRCm39) |
V413E |
probably benign |
Het |
| Spin1 |
T |
C |
13: 51,277,326 (GRCm39) |
|
probably null |
Het |
| Sra1 |
T |
C |
18: 36,800,536 (GRCm39) |
T224A |
probably benign |
Het |
| Sv2c |
A |
T |
13: 96,185,056 (GRCm39) |
F207Y |
probably benign |
Het |
| Tcp10c |
T |
A |
17: 13,581,503 (GRCm39) |
|
probably null |
Het |
| Tkt |
G |
A |
14: 30,292,992 (GRCm39) |
G490S |
possibly damaging |
Het |
| Tpgs1 |
G |
T |
10: 79,511,655 (GRCm39) |
A266S |
probably damaging |
Het |
| Tprg1 |
T |
G |
16: 25,241,003 (GRCm39) |
S260A |
probably damaging |
Het |
| Trdv2-1 |
T |
A |
14: 54,183,935 (GRCm39) |
W56R |
probably damaging |
Het |
| Trgv6 |
G |
T |
13: 19,374,814 (GRCm39) |
G40W |
possibly damaging |
Het |
| Trpc4 |
T |
A |
3: 54,225,450 (GRCm39) |
V933E |
probably benign |
Het |
| Ulk4 |
A |
T |
9: 120,932,687 (GRCm39) |
M1051K |
possibly damaging |
Het |
| Unc119b |
A |
G |
5: 115,272,743 (GRCm39) |
L76P |
probably damaging |
Het |
| Vmn2r15 |
G |
A |
5: 109,445,394 (GRCm39) |
S10F |
probably benign |
Het |
| Vwce |
A |
G |
19: 10,641,704 (GRCm39) |
E810G |
probably benign |
Het |
| Wdr7 |
T |
A |
18: 63,910,451 (GRCm39) |
|
probably null |
Het |
| Wnk2 |
T |
A |
13: 49,191,608 (GRCm39) |
E1283V |
probably benign |
Het |
| Zfp28 |
T |
C |
7: 6,396,956 (GRCm39) |
C464R |
probably damaging |
Het |
| Zpld1 |
C |
T |
16: 55,054,027 (GRCm39) |
C255Y |
probably damaging |
Het |
|
| Other mutations in Aox3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01599:Aox3
|
APN |
1 |
58,208,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01747:Aox3
|
APN |
1 |
58,198,817 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01883:Aox3
|
APN |
1 |
58,177,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01911:Aox3
|
APN |
1 |
58,191,719 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02017:Aox3
|
APN |
1 |
58,160,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02120:Aox3
|
APN |
1 |
58,166,809 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02466:Aox3
|
APN |
1 |
58,197,431 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL02545:Aox3
|
APN |
1 |
58,222,645 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02572:Aox3
|
APN |
1 |
58,197,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02746:Aox3
|
APN |
1 |
58,222,701 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL02808:Aox3
|
APN |
1 |
58,181,859 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02812:Aox3
|
APN |
1 |
58,205,055 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02982:Aox3
|
APN |
1 |
58,166,846 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03056:Aox3
|
APN |
1 |
58,198,180 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03182:Aox3
|
APN |
1 |
58,205,046 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03234:Aox3
|
APN |
1 |
58,191,845 (GRCm39) |
missense |
probably benign |
|
|
IGL03374:Aox3
|
APN |
1 |
58,211,007 (GRCm39) |
missense |
probably damaging |
1.00 |
|
amber
|
UTSW |
1 |
58,211,050 (GRCm39) |
nonsense |
probably null |
|
|
R0071:Aox3
|
UTSW |
1 |
58,211,050 (GRCm39) |
nonsense |
probably null |
|
|
R0071:Aox3
|
UTSW |
1 |
58,211,050 (GRCm39) |
nonsense |
probably null |
|
|
R0135:Aox3
|
UTSW |
1 |
58,164,247 (GRCm39) |
splice site |
probably benign |
|
|
R0332:Aox3
|
UTSW |
1 |
58,181,910 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0626:Aox3
|
UTSW |
1 |
58,211,458 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1325:Aox3
|
UTSW |
1 |
58,215,726 (GRCm39) |
nonsense |
probably null |
|
|
R1435:Aox3
|
UTSW |
1 |
58,202,605 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1438:Aox3
|
UTSW |
1 |
58,192,337 (GRCm39) |
missense |
probably benign |
|
|
R1567:Aox3
|
UTSW |
1 |
58,233,852 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1575:Aox3
|
UTSW |
1 |
58,191,713 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1759:Aox3
|
UTSW |
1 |
58,209,805 (GRCm39) |
splice site |
probably null |
|
|
R1785:Aox3
|
UTSW |
1 |
58,209,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1786:Aox3
|
UTSW |
1 |
58,209,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1921:Aox3
|
UTSW |
1 |
58,219,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1984:Aox3
|
UTSW |
1 |
58,192,220 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R2012:Aox3
|
UTSW |
1 |
58,177,391 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2080:Aox3
|
UTSW |
1 |
58,225,439 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2121:Aox3
|
UTSW |
1 |
58,191,708 (GRCm39) |
splice site |
probably benign |
|
|
R2126:Aox3
|
UTSW |
1 |
58,197,375 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2130:Aox3
|
UTSW |
1 |
58,209,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2131:Aox3
|
UTSW |
1 |
58,209,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2132:Aox3
|
UTSW |
1 |
58,209,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2133:Aox3
|
UTSW |
1 |
58,209,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2385:Aox3
|
UTSW |
1 |
58,177,448 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2495:Aox3
|
UTSW |
1 |
58,227,567 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4200:Aox3
|
UTSW |
1 |
58,227,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4231:Aox3
|
UTSW |
1 |
58,154,044 (GRCm39) |
missense |
probably benign |
0.12 |
|
R4591:Aox3
|
UTSW |
1 |
58,191,815 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4627:Aox3
|
UTSW |
1 |
58,164,194 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4831:Aox3
|
UTSW |
1 |
58,191,725 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4864:Aox3
|
UTSW |
1 |
58,215,646 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4976:Aox3
|
UTSW |
1 |
58,227,683 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5007:Aox3
|
UTSW |
1 |
58,202,583 (GRCm39) |
missense |
probably benign |
|
|
R5119:Aox3
|
UTSW |
1 |
58,227,683 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5175:Aox3
|
UTSW |
1 |
58,211,487 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5360:Aox3
|
UTSW |
1 |
58,185,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5784:Aox3
|
UTSW |
1 |
58,192,658 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6050:Aox3
|
UTSW |
1 |
58,219,814 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6056:Aox3
|
UTSW |
1 |
58,209,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6162:Aox3
|
UTSW |
1 |
58,198,890 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6181:Aox3
|
UTSW |
1 |
58,198,105 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6374:Aox3
|
UTSW |
1 |
58,211,320 (GRCm39) |
missense |
probably benign |
0.11 |
|
R6662:Aox3
|
UTSW |
1 |
58,157,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6809:Aox3
|
UTSW |
1 |
58,157,840 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6810:Aox3
|
UTSW |
1 |
58,180,590 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6821:Aox3
|
UTSW |
1 |
58,189,547 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7039:Aox3
|
UTSW |
1 |
58,215,714 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7116:Aox3
|
UTSW |
1 |
58,192,689 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7146:Aox3
|
UTSW |
1 |
58,197,688 (GRCm39) |
splice site |
probably null |
|
|
R7163:Aox3
|
UTSW |
1 |
58,158,671 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7243:Aox3
|
UTSW |
1 |
58,177,466 (GRCm39) |
missense |
unknown |
|
|
R7319:Aox3
|
UTSW |
1 |
58,191,761 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7664:Aox3
|
UTSW |
1 |
58,158,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7709:Aox3
|
UTSW |
1 |
58,219,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7745:Aox3
|
UTSW |
1 |
58,215,676 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R7751:Aox3
|
UTSW |
1 |
58,218,494 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7912:Aox3
|
UTSW |
1 |
58,181,855 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7940:Aox3
|
UTSW |
1 |
58,227,596 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8143:Aox3
|
UTSW |
1 |
58,198,074 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8178:Aox3
|
UTSW |
1 |
58,189,481 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R8719:Aox3
|
UTSW |
1 |
58,158,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8861:Aox3
|
UTSW |
1 |
58,189,460 (GRCm39) |
missense |
probably benign |
|
|
R9379:Aox3
|
UTSW |
1 |
58,208,959 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R9459:Aox3
|
UTSW |
1 |
58,189,468 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9472:Aox3
|
UTSW |
1 |
58,215,669 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R9479:Aox3
|
UTSW |
1 |
58,177,568 (GRCm39) |
missense |
probably benign |
0.23 |
|
R9521:Aox3
|
UTSW |
1 |
58,164,222 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9750:Aox3
|
UTSW |
1 |
58,215,648 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGTACACACATATGCACACATG -3'
(R):5'- AGGGAGACTTTTCGACACCG -3'
Sequencing Primer
(F):5'- ACATATGCACACATGTATGAACTC -3'
(R):5'- GGAGACTTTTCGACACCGATTAG -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation