Incidental Mutation 'R7003:Alox8'
| ID |
544680 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Alox8
|
| Ensembl Gene |
ENSMUSG00000020891 |
| Gene Name |
arachidonate 8-lipoxygenase |
| Synonyms |
8S-LOX, 8S-lipoxygenase, 8-LOX, Alox15b |
| MMRRC Submission |
045108-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.114)
|
| Stock # |
R7003 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
69074758-69088669 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 69082416 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 170
(D170G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000021262
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021262]
[ENSMUST00000094078]
|
| AlphaFold |
O35936 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000021262
AA Change: D170G
PolyPhen 2
Score 0.696 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000021262
Gene: ENSMUSG00000020891
AA Change: D170G
| Domain | Start | End | E-Value | Type |
|---|
|
LH2
|
2 |
122 |
1.07e-36 |
SMART |
|
Pfam:Lipoxygenase
|
163 |
662 |
5.5e-70 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000094078
AA Change: D170G
PolyPhen 2
Score 0.672 (Sensitivity: 0.86; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000091621
Gene: ENSMUSG00000020891
AA Change: D170G
| Domain | Start | End | E-Value | Type |
|---|
|
LH2
|
2 |
122 |
1.07e-36 |
SMART |
|
Pfam:Lipoxygenase
|
205 |
405 |
6.9e-44 |
PFAM |
|
Pfam:Lipoxygenase
|
402 |
640 |
1.9e-60 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene belongs to the lipoxygenase (LOX) gene family whose members encode enzymes that catalyze the addition of molecular oxygen to polyunsaturated fatty acids (PUFAs) to yield fatty acid hydroperoxides. The encoded enzyme preferentially metabolizes arachidonic acid to yield 8-hydroxyeicosatetraenoic acid (8-HETE), while metabolizing linoleic acid less efficiently. The gene may also function as a tumor suppressor. This gene is located in a cluster of related genes that spans approximately 75 kilobases on chromosome 11. [provided by RefSeq, Jan 2013]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 57 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Actbl2 |
T |
A |
13: 111,392,490 (GRCm39) |
I275N |
probably damaging |
Het |
| Actr3b |
A |
C |
5: 26,003,461 (GRCm39) |
Y21S |
probably damaging |
Het |
| Adam6b |
C |
T |
12: 113,453,662 (GRCm39) |
Q160* |
probably null |
Het |
| Adgrv1 |
C |
T |
13: 81,670,223 (GRCm39) |
|
probably null |
Het |
| Akr1c6 |
A |
G |
13: 4,504,514 (GRCm39) |
N300D |
probably benign |
Het |
| Amhr2 |
A |
G |
15: 102,354,768 (GRCm39) |
N40S |
probably benign |
Het |
| Ap2a2 |
A |
G |
7: 141,209,109 (GRCm39) |
N767S |
probably benign |
Het |
| Armc3 |
T |
C |
2: 19,274,839 (GRCm39) |
I358T |
probably damaging |
Het |
| Atg2b |
A |
G |
12: 105,620,508 (GRCm39) |
S732P |
probably benign |
Het |
| Atp12a |
A |
G |
14: 56,610,837 (GRCm39) |
Y327C |
possibly damaging |
Het |
| Bcr |
T |
C |
10: 74,897,393 (GRCm39) |
V179A |
probably benign |
Het |
| Cep104 |
T |
C |
4: 154,078,018 (GRCm39) |
L642P |
probably benign |
Het |
| Clspn |
T |
A |
4: 126,486,513 (GRCm39) |
S1302R |
possibly damaging |
Het |
| Cmip |
T |
C |
8: 118,111,727 (GRCm39) |
F153L |
probably benign |
Het |
| Cplane1 |
T |
G |
15: 8,258,246 (GRCm39) |
L2164R |
probably damaging |
Het |
| D630039A03Rik |
T |
C |
4: 57,910,521 (GRCm39) |
D97G |
probably damaging |
Het |
| Dok7 |
A |
T |
5: 35,236,899 (GRCm39) |
T396S |
probably benign |
Het |
| Dsel |
C |
T |
1: 111,788,025 (GRCm39) |
V837I |
probably benign |
Het |
| Etl4 |
C |
T |
2: 20,810,695 (GRCm39) |
T926I |
probably benign |
Het |
| Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
| Gpr155 |
A |
G |
2: 73,173,961 (GRCm39) |
I816T |
probably damaging |
Het |
| Hpn |
C |
T |
7: 30,810,367 (GRCm39) |
|
probably benign |
Het |
| Inpp5e |
A |
G |
2: 26,287,877 (GRCm39) |
S640P |
probably benign |
Het |
| Irs3 |
C |
T |
5: 137,643,539 (GRCm39) |
V82I |
probably benign |
Het |
| Kif16b |
A |
C |
2: 142,600,749 (GRCm39) |
D461E |
possibly damaging |
Het |
| Krba1 |
A |
G |
6: 48,390,014 (GRCm39) |
T592A |
possibly damaging |
Het |
| Lgsn |
T |
A |
1: 31,243,024 (GRCm39) |
S369T |
possibly damaging |
Het |
| Lrrc4b |
C |
T |
7: 44,094,580 (GRCm39) |
P83S |
probably damaging |
Het |
| Mplkipl1 |
A |
G |
19: 61,164,319 (GRCm39) |
S39P |
possibly damaging |
Het |
| Neil3 |
T |
C |
8: 54,054,001 (GRCm39) |
T343A |
possibly damaging |
Het |
| Nt5e |
A |
G |
9: 88,246,805 (GRCm39) |
Y347C |
probably damaging |
Het |
| Or1j1 |
A |
G |
2: 36,703,047 (GRCm39) |
I19T |
possibly damaging |
Het |
| Or2d3b |
A |
T |
7: 106,514,319 (GRCm39) |
T305S |
probably benign |
Het |
| Or2f2 |
C |
T |
6: 42,767,399 (GRCm39) |
T142I |
probably benign |
Het |
| Or8g26 |
A |
T |
9: 39,096,239 (GRCm39) |
Y255F |
probably benign |
Het |
| P2rx5 |
T |
C |
11: 73,058,800 (GRCm39) |
|
probably null |
Het |
| Phtf2 |
A |
G |
5: 20,999,399 (GRCm39) |
V248A |
probably benign |
Het |
| Plekhd1 |
T |
C |
12: 80,768,734 (GRCm39) |
C406R |
possibly damaging |
Het |
| Plod3 |
T |
A |
5: 137,018,498 (GRCm39) |
N245K |
probably damaging |
Het |
| Polr3c |
G |
T |
3: 96,630,954 (GRCm39) |
H155Q |
possibly damaging |
Het |
| Psap |
T |
A |
10: 60,135,276 (GRCm39) |
C317S |
probably damaging |
Het |
| Rif1 |
A |
G |
2: 51,967,001 (GRCm39) |
I97V |
probably benign |
Het |
| Rnf123 |
T |
A |
9: 107,940,882 (GRCm39) |
|
probably null |
Het |
| Rnf19a |
G |
A |
15: 36,254,650 (GRCm39) |
R303* |
probably null |
Het |
| Sdk1 |
G |
A |
5: 142,082,489 (GRCm39) |
V1036I |
probably benign |
Het |
| Shc3 |
T |
A |
13: 51,620,588 (GRCm39) |
Y146F |
probably benign |
Het |
| Skint6 |
A |
G |
4: 112,963,109 (GRCm39) |
Y441H |
probably benign |
Het |
| Slc7a12 |
T |
C |
3: 14,570,580 (GRCm39) |
I173T |
probably damaging |
Het |
| Spesp1 |
A |
T |
9: 62,189,302 (GRCm39) |
S15T |
possibly damaging |
Het |
| Tarm1 |
A |
T |
7: 3,545,939 (GRCm39) |
|
probably null |
Het |
| Tenm3 |
T |
C |
8: 48,693,479 (GRCm39) |
Y1817C |
probably damaging |
Het |
| Ttc9c |
A |
T |
19: 8,795,904 (GRCm39) |
L45Q |
probably damaging |
Het |
| Ube3a |
C |
T |
7: 58,926,188 (GRCm39) |
T322I |
probably damaging |
Het |
| Vac14 |
T |
A |
8: 111,439,430 (GRCm39) |
V669E |
probably damaging |
Het |
| Vmn1r225 |
A |
G |
17: 20,723,416 (GRCm39) |
M286V |
probably null |
Het |
| Zfp658 |
A |
G |
7: 43,224,172 (GRCm39) |
K816E |
possibly damaging |
Het |
| Zfp846 |
T |
C |
9: 20,499,188 (GRCm39) |
M1T |
probably null |
Het |
|
| Other mutations in Alox8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01411:Alox8
|
APN |
11 |
69,079,516 (GRCm39) |
missense |
probably benign |
|
|
IGL01878:Alox8
|
APN |
11 |
69,087,864 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02342:Alox8
|
APN |
11 |
69,077,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02694:Alox8
|
APN |
11 |
69,077,455 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03246:Alox8
|
APN |
11 |
69,076,841 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03373:Alox8
|
APN |
11 |
69,077,443 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0567:Alox8
|
UTSW |
11 |
69,082,348 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1575:Alox8
|
UTSW |
11 |
69,076,067 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1688:Alox8
|
UTSW |
11 |
69,080,732 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2021:Alox8
|
UTSW |
11 |
69,077,114 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2041:Alox8
|
UTSW |
11 |
69,088,517 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R2175:Alox8
|
UTSW |
11 |
69,078,592 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R2237:Alox8
|
UTSW |
11 |
69,076,597 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3821:Alox8
|
UTSW |
11 |
69,077,308 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4870:Alox8
|
UTSW |
11 |
69,077,394 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6836:Alox8
|
UTSW |
11 |
69,080,715 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R6836:Alox8
|
UTSW |
11 |
69,077,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7158:Alox8
|
UTSW |
11 |
69,076,696 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7316:Alox8
|
UTSW |
11 |
69,077,064 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7513:Alox8
|
UTSW |
11 |
69,078,670 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9515:Alox8
|
UTSW |
11 |
69,075,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9721:Alox8
|
UTSW |
11 |
69,087,911 (GRCm39) |
missense |
probably benign |
0.19 |
|
X0065:Alox8
|
UTSW |
11 |
69,076,079 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Alox8
|
UTSW |
11 |
69,076,047 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1186:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1187:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1189:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1189:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1190:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1191:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1192:Alox8
|
UTSW |
11 |
69,088,322 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Alox8
|
UTSW |
11 |
69,076,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTGACTTCCTTTGACGATGAAC -3'
(R):5'- TCCAACCCAGTGAGCATAGAAGG -3'
Sequencing Primer
(F):5'- CGGCAATGTGGAAGTGTAAGCTG -3'
(R):5'- GTCTCAGGAGAGCCCCTC -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation