Incidental Mutation 'R0499:Aox4'
| ID |
46982 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Aox4
|
| Ensembl Gene |
ENSMUSG00000038242 |
| Gene Name |
aldehyde oxidase 4 |
| Synonyms |
AOH2, 2310003G12Rik |
| MMRRC Submission |
038695-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0499 (G1)
|
| Quality Score |
121 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
58249556-58307756 bp(+) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 58302556 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000048929
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040442]
|
| AlphaFold |
Q3TYQ9 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000040442
|
| SMART Domains |
Protein: ENSMUSP00000048929
Gene: ENSMUSG00000038242
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Fer2
|
12 |
82 |
1.6e-10 |
PFAM |
|
Pfam:Fer2_2
|
91 |
165 |
4.6e-30 |
PFAM |
|
Pfam:FAD_binding_5
|
240 |
421 |
2.7e-47 |
PFAM |
|
CO_deh_flav_C
|
428 |
532 |
1.19e-26 |
SMART |
|
Ald_Xan_dh_C
|
596 |
699 |
8.22e-39 |
SMART |
|
Pfam:Ald_Xan_dh_C2
|
709 |
1243 |
1.1e-178 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161126
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161833
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.2%
|
| Validation Efficiency |
99% (97/98) |
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a null allele exhibit a slight decrease in prenatal survival and epidermal thickening that is exacerbated by UV treatment. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acad9 |
T |
C |
3: 36,139,564 (GRCm39) |
V388A |
probably damaging |
Het |
| Acp3 |
T |
C |
9: 104,197,201 (GRCm39) |
E146G |
probably damaging |
Het |
| Adap2 |
A |
T |
11: 80,066,905 (GRCm39) |
R276S |
probably damaging |
Het |
| Agbl3 |
A |
T |
6: 34,816,270 (GRCm39) |
M727L |
probably benign |
Het |
| Ahnak |
T |
A |
19: 8,977,628 (GRCm39) |
|
probably benign |
Het |
| Ankmy1 |
G |
T |
1: 92,813,948 (GRCm39) |
D410E |
probably damaging |
Het |
| Ankra2 |
T |
C |
13: 98,402,962 (GRCm39) |
S70P |
probably damaging |
Het |
| Arl13b |
G |
A |
16: 62,622,096 (GRCm39) |
T399I |
probably benign |
Het |
| Atad2 |
A |
T |
15: 57,966,636 (GRCm39) |
D652E |
possibly damaging |
Het |
| Atad2 |
T |
G |
15: 57,984,345 (GRCm39) |
M328L |
probably benign |
Het |
| Ccnb1 |
T |
C |
13: 100,916,642 (GRCm39) |
|
probably null |
Het |
| Ccr2 |
G |
C |
9: 123,905,976 (GRCm39) |
K85N |
possibly damaging |
Het |
| Ccr2 |
A |
T |
9: 123,906,163 (GRCm39) |
T148S |
possibly damaging |
Het |
| Cdc20b |
T |
C |
13: 113,192,484 (GRCm39) |
V59A |
probably benign |
Het |
| Cdin1 |
C |
T |
2: 115,473,172 (GRCm39) |
R101W |
probably damaging |
Het |
| Cdkl3 |
T |
C |
11: 51,923,243 (GRCm39) |
S507P |
possibly damaging |
Het |
| Celf6 |
C |
A |
9: 59,510,161 (GRCm39) |
T86K |
probably benign |
Het |
| Ces1g |
A |
G |
8: 94,060,317 (GRCm39) |
F101L |
probably benign |
Het |
| Cimap1d |
T |
C |
10: 79,476,099 (GRCm39) |
D155G |
probably damaging |
Het |
| Cntnap3 |
C |
T |
13: 65,006,492 (GRCm39) |
D107N |
probably benign |
Het |
| Col15a1 |
A |
T |
4: 47,262,950 (GRCm39) |
D534V |
probably damaging |
Het |
| Col27a1 |
A |
G |
4: 63,218,978 (GRCm39) |
|
probably benign |
Het |
| Csmd3 |
T |
C |
15: 47,710,527 (GRCm39) |
T1687A |
probably benign |
Het |
| Cstf3 |
A |
G |
2: 104,479,950 (GRCm39) |
I272M |
possibly damaging |
Het |
| Cyp2d40 |
T |
C |
15: 82,645,418 (GRCm39) |
T150A |
probably benign |
Het |
| Dnah8 |
T |
A |
17: 30,934,483 (GRCm39) |
F1489L |
possibly damaging |
Het |
| Dop1b |
A |
T |
16: 93,567,325 (GRCm39) |
T1251S |
probably benign |
Het |
| Dtx2 |
G |
A |
5: 136,057,957 (GRCm39) |
G421R |
probably damaging |
Het |
| Epb41l3 |
T |
A |
17: 69,554,654 (GRCm39) |
D251E |
probably benign |
Het |
| Erg |
A |
C |
16: 95,161,842 (GRCm39) |
Y305* |
probably null |
Het |
| Exosc4 |
G |
A |
15: 76,213,766 (GRCm39) |
A197T |
probably benign |
Het |
| Fam227b |
T |
A |
2: 125,942,829 (GRCm39) |
I323L |
probably benign |
Het |
| Far1 |
G |
T |
7: 113,153,503 (GRCm39) |
|
probably benign |
Het |
| Fmod |
A |
G |
1: 133,968,934 (GRCm39) |
I325V |
possibly damaging |
Het |
| Fshr |
C |
G |
17: 89,316,713 (GRCm39) |
S169T |
probably benign |
Het |
| Gm4076 |
G |
T |
13: 85,275,345 (GRCm39) |
|
noncoding transcript |
Het |
| Gm5134 |
A |
T |
10: 75,828,359 (GRCm39) |
Y313F |
probably benign |
Het |
| H2-Q6 |
T |
A |
17: 35,644,179 (GRCm39) |
F54I |
probably damaging |
Het |
| Hcrtr2 |
C |
A |
9: 76,161,954 (GRCm39) |
L145F |
probably damaging |
Het |
| Hepacam2 |
A |
G |
6: 3,476,121 (GRCm39) |
L268P |
probably damaging |
Het |
| Herc2 |
C |
A |
7: 55,834,117 (GRCm39) |
C3107* |
probably null |
Het |
| Herc4 |
T |
C |
10: 63,099,811 (GRCm39) |
V78A |
probably damaging |
Het |
| Hyal5 |
T |
C |
6: 24,877,920 (GRCm39) |
W339R |
probably damaging |
Het |
| Igfbp6 |
T |
A |
15: 102,056,419 (GRCm39) |
|
probably null |
Het |
| Il18rap |
A |
T |
1: 40,564,218 (GRCm39) |
H112L |
probably benign |
Het |
| Il1r2 |
T |
A |
1: 40,162,309 (GRCm39) |
Y317* |
probably null |
Het |
| Ints8 |
C |
A |
4: 11,246,097 (GRCm39) |
V190L |
probably benign |
Het |
| Ipo11 |
T |
C |
13: 107,061,595 (GRCm39) |
T22A |
probably benign |
Het |
| Itgb4 |
C |
A |
11: 115,870,521 (GRCm39) |
R117S |
probably benign |
Het |
| Lcorl |
C |
G |
5: 45,891,711 (GRCm39) |
G214A |
probably benign |
Het |
| Lgals3bp |
T |
A |
11: 118,289,019 (GRCm39) |
|
probably null |
Het |
| Lyst |
T |
A |
13: 13,791,298 (GRCm39) |
L54I |
probably damaging |
Het |
| Mcm9 |
T |
C |
10: 53,414,250 (GRCm39) |
T1015A |
probably benign |
Het |
| Mef2d |
T |
A |
3: 88,063,825 (GRCm39) |
I84N |
probably damaging |
Het |
| Mmrn2 |
A |
G |
14: 34,119,913 (GRCm39) |
N261S |
probably damaging |
Het |
| Mpdz |
T |
C |
4: 81,210,768 (GRCm39) |
T1693A |
probably benign |
Het |
| Mss51 |
T |
A |
14: 20,534,756 (GRCm39) |
Q338L |
possibly damaging |
Het |
| Mstn |
T |
A |
1: 53,103,143 (GRCm39) |
Y160N |
probably damaging |
Het |
| Muc6 |
T |
C |
7: 141,226,735 (GRCm39) |
T1431A |
probably benign |
Het |
| Nek9 |
A |
T |
12: 85,348,657 (GRCm39) |
M959K |
probably benign |
Het |
| Or2ak6 |
G |
A |
11: 58,593,069 (GRCm39) |
V181I |
probably benign |
Het |
| Or4f58 |
A |
T |
2: 111,851,777 (GRCm39) |
C141S |
probably damaging |
Het |
| Or8b47 |
A |
T |
9: 38,435,801 (GRCm39) |
M258L |
probably benign |
Het |
| Otog |
G |
T |
7: 45,923,256 (GRCm39) |
G1044W |
probably damaging |
Het |
| Pcdh9 |
G |
A |
14: 94,123,671 (GRCm39) |
T833M |
probably damaging |
Het |
| Pdcd10 |
T |
C |
3: 75,434,958 (GRCm39) |
K111R |
probably damaging |
Het |
| Pde5a |
A |
G |
3: 122,542,107 (GRCm39) |
N199S |
probably damaging |
Het |
| Plekhg1 |
T |
C |
10: 3,887,971 (GRCm39) |
V355A |
probably damaging |
Het |
| Podn |
G |
T |
4: 107,878,791 (GRCm39) |
L359I |
probably damaging |
Het |
| Psd |
T |
C |
19: 46,310,600 (GRCm39) |
E483G |
probably damaging |
Het |
| Ptch2 |
T |
A |
4: 116,968,340 (GRCm39) |
L905* |
probably null |
Het |
| Rxfp2 |
T |
A |
5: 149,989,880 (GRCm39) |
N420K |
probably damaging |
Het |
| Scpppq1 |
C |
A |
5: 104,222,747 (GRCm39) |
G24* |
probably null |
Het |
| Sde2 |
T |
A |
1: 180,689,992 (GRCm39) |
D237E |
probably benign |
Het |
| Serpina1d |
A |
T |
12: 103,732,016 (GRCm39) |
L281Q |
probably damaging |
Het |
| Serpina9 |
T |
C |
12: 103,967,729 (GRCm39) |
N222S |
probably benign |
Het |
| Sh3bgrl2 |
A |
G |
9: 83,459,612 (GRCm39) |
K57E |
probably damaging |
Het |
| Shc3 |
C |
T |
13: 51,634,264 (GRCm39) |
|
probably benign |
Het |
| Sik3 |
T |
C |
9: 46,120,038 (GRCm39) |
M659T |
possibly damaging |
Het |
| Slc23a2 |
A |
G |
2: 131,913,937 (GRCm39) |
L280P |
probably damaging |
Het |
| Smchd1 |
G |
T |
17: 71,694,083 (GRCm39) |
Q1221K |
probably benign |
Het |
| Spmip2 |
T |
A |
3: 79,313,093 (GRCm39) |
W56R |
probably damaging |
Het |
| Spocd1 |
A |
G |
4: 129,849,263 (GRCm39) |
N694S |
possibly damaging |
Het |
| Styxl2 |
C |
A |
1: 165,926,670 (GRCm39) |
V981L |
probably benign |
Het |
| Tecta |
T |
C |
9: 42,263,359 (GRCm39) |
D1409G |
probably damaging |
Het |
| Tmem131 |
A |
T |
1: 36,880,754 (GRCm39) |
V172D |
probably damaging |
Het |
| Trpm3 |
T |
C |
19: 22,964,237 (GRCm39) |
M1244T |
possibly damaging |
Het |
| Ugcg |
G |
C |
4: 59,217,036 (GRCm39) |
V187L |
possibly damaging |
Het |
| Usp17le |
T |
C |
7: 104,417,708 (GRCm39) |
N478S |
probably benign |
Het |
| Usp36 |
A |
G |
11: 118,164,397 (GRCm39) |
V205A |
probably damaging |
Het |
| Vmn1r25 |
T |
A |
6: 57,955,494 (GRCm39) |
Q265L |
probably damaging |
Het |
| Vwf |
A |
T |
6: 125,615,077 (GRCm39) |
H1176L |
probably benign |
Het |
| Zfyve28 |
C |
T |
5: 34,389,550 (GRCm39) |
D217N |
possibly damaging |
Het |
| Zranb3 |
A |
C |
1: 127,882,817 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Aox4 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00959:Aox4
|
APN |
1 |
58,278,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01011:Aox4
|
APN |
1 |
58,279,934 (GRCm39) |
nonsense |
probably null |
|
|
IGL01634:Aox4
|
APN |
1 |
58,261,089 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL01689:Aox4
|
APN |
1 |
58,284,320 (GRCm39) |
splice site |
probably benign |
|
|
IGL01874:Aox4
|
APN |
1 |
58,291,243 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02104:Aox4
|
APN |
1 |
58,275,816 (GRCm39) |
splice site |
probably benign |
|
|
IGL02744:Aox4
|
APN |
1 |
58,294,711 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02751:Aox4
|
APN |
1 |
58,298,211 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03225:Aox4
|
APN |
1 |
58,286,386 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL03247:Aox4
|
APN |
1 |
58,303,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03369:Aox4
|
APN |
1 |
58,301,746 (GRCm39) |
missense |
probably benign |
0.01 |
|
BB008:Aox4
|
UTSW |
1 |
58,294,645 (GRCm39) |
missense |
probably benign |
0.07 |
|
BB018:Aox4
|
UTSW |
1 |
58,294,645 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0138:Aox4
|
UTSW |
1 |
58,268,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0243:Aox4
|
UTSW |
1 |
58,252,235 (GRCm39) |
missense |
probably benign |
|
|
R0368:Aox4
|
UTSW |
1 |
58,252,238 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0513:Aox4
|
UTSW |
1 |
58,286,459 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0513:Aox4
|
UTSW |
1 |
58,256,678 (GRCm39) |
missense |
probably benign |
|
|
R0546:Aox4
|
UTSW |
1 |
58,289,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0591:Aox4
|
UTSW |
1 |
58,278,261 (GRCm39) |
splice site |
probably benign |
|
|
R0825:Aox4
|
UTSW |
1 |
58,288,068 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R1912:Aox4
|
UTSW |
1 |
58,303,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1934:Aox4
|
UTSW |
1 |
58,285,095 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2180:Aox4
|
UTSW |
1 |
58,252,226 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2293:Aox4
|
UTSW |
1 |
58,261,096 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3017:Aox4
|
UTSW |
1 |
58,274,363 (GRCm39) |
missense |
probably benign |
|
|
R3744:Aox4
|
UTSW |
1 |
58,285,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3745:Aox4
|
UTSW |
1 |
58,285,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3830:Aox4
|
UTSW |
1 |
58,294,670 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3856:Aox4
|
UTSW |
1 |
58,293,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4214:Aox4
|
UTSW |
1 |
58,261,051 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4484:Aox4
|
UTSW |
1 |
58,301,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4706:Aox4
|
UTSW |
1 |
58,305,946 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4710:Aox4
|
UTSW |
1 |
58,294,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4729:Aox4
|
UTSW |
1 |
58,298,236 (GRCm39) |
nonsense |
probably null |
|
|
R4769:Aox4
|
UTSW |
1 |
58,298,307 (GRCm39) |
missense |
probably null |
1.00 |
|
R4809:Aox4
|
UTSW |
1 |
58,305,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4989:Aox4
|
UTSW |
1 |
58,275,835 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5082:Aox4
|
UTSW |
1 |
58,270,642 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R5102:Aox4
|
UTSW |
1 |
58,279,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5114:Aox4
|
UTSW |
1 |
58,285,445 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5133:Aox4
|
UTSW |
1 |
58,275,835 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5134:Aox4
|
UTSW |
1 |
58,275,835 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5185:Aox4
|
UTSW |
1 |
58,293,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5217:Aox4
|
UTSW |
1 |
58,285,400 (GRCm39) |
nonsense |
probably null |
|
|
R5426:Aox4
|
UTSW |
1 |
58,259,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5443:Aox4
|
UTSW |
1 |
58,273,151 (GRCm39) |
splice site |
probably null |
|
|
R5708:Aox4
|
UTSW |
1 |
58,285,032 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R6052:Aox4
|
UTSW |
1 |
58,293,477 (GRCm39) |
nonsense |
probably null |
|
|
R6167:Aox4
|
UTSW |
1 |
58,303,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6179:Aox4
|
UTSW |
1 |
58,270,662 (GRCm39) |
missense |
probably benign |
|
|
R6196:Aox4
|
UTSW |
1 |
58,256,685 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6513:Aox4
|
UTSW |
1 |
58,252,212 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6781:Aox4
|
UTSW |
1 |
58,284,268 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6885:Aox4
|
UTSW |
1 |
58,303,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7082:Aox4
|
UTSW |
1 |
58,263,352 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7127:Aox4
|
UTSW |
1 |
58,268,033 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7153:Aox4
|
UTSW |
1 |
58,289,378 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7371:Aox4
|
UTSW |
1 |
58,303,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7690:Aox4
|
UTSW |
1 |
58,303,076 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7745:Aox4
|
UTSW |
1 |
58,279,866 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7752:Aox4
|
UTSW |
1 |
58,293,107 (GRCm39) |
missense |
not run |
|
|
R7767:Aox4
|
UTSW |
1 |
58,274,366 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7782:Aox4
|
UTSW |
1 |
58,270,251 (GRCm39) |
splice site |
probably null |
|
|
R7931:Aox4
|
UTSW |
1 |
58,294,645 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7978:Aox4
|
UTSW |
1 |
58,274,366 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7982:Aox4
|
UTSW |
1 |
58,296,400 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R8316:Aox4
|
UTSW |
1 |
58,293,470 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R8361:Aox4
|
UTSW |
1 |
58,279,998 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8829:Aox4
|
UTSW |
1 |
58,294,649 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8832:Aox4
|
UTSW |
1 |
58,294,649 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8896:Aox4
|
UTSW |
1 |
58,291,233 (GRCm39) |
missense |
probably benign |
|
|
R9103:Aox4
|
UTSW |
1 |
58,296,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9241:Aox4
|
UTSW |
1 |
58,291,345 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9282:Aox4
|
UTSW |
1 |
58,285,028 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R9487:Aox4
|
UTSW |
1 |
58,288,097 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9493:Aox4
|
UTSW |
1 |
58,286,434 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9557:Aox4
|
UTSW |
1 |
58,285,095 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9616:Aox4
|
UTSW |
1 |
58,268,020 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R9644:Aox4
|
UTSW |
1 |
58,267,278 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9683:Aox4
|
UTSW |
1 |
58,278,462 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9727:Aox4
|
UTSW |
1 |
58,286,473 (GRCm39) |
missense |
probably benign |
0.43 |
|
R9767:Aox4
|
UTSW |
1 |
58,274,357 (GRCm39) |
missense |
probably benign |
0.05 |
|
X0021:Aox4
|
UTSW |
1 |
58,286,454 (GRCm39) |
nonsense |
probably null |
|
|
X0028:Aox4
|
UTSW |
1 |
58,293,342 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1176:Aox4
|
UTSW |
1 |
58,285,510 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTTGGTGCAAGCAAGAAGAAAGCCC -3'
(R):5'- AAGGTCTCAGGTGAACCTCAGCAG -3'
Sequencing Primer
(F):5'- GCCCAGCATGGAAGGAAC -3'
(R):5'- ACTGAGAGGATCCTCTGACCA -3'
|
| Posted On |
2013-06-12 |
Incidental Mutation