Incidental Mutation 'R5903:Cyp2j8'
| ID |
456433 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cyp2j8
|
| Ensembl Gene |
ENSMUSG00000082932 |
| Gene Name |
cytochrome P450, family 2, subfamily j, polypeptide 8 |
| Synonyms |
Cyp2j8-ps, OTTMUSG00000007938 |
| MMRRC Submission |
044101-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.066)
|
| Stock # |
R5903 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
96444596-96507386 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 96507277 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Isoleucine
at position 37
(N37I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134591
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000124729]
|
| AlphaFold |
G3UZ38 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000124729
AA Change: N37I
PolyPhen 2
Score 0.464 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000134591
Gene: ENSMUSG00000082932
AA Change: N37I
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
13 |
35 |
N/A |
INTRINSIC |
|
Pfam:p450
|
44 |
500 |
1.2e-134 |
PFAM |
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.6%
- 20x: 92.8%
|
| Validation Efficiency |
98% (58/59) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 50 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9130230L23Rik |
A |
G |
5: 65,988,318 |
V150A |
unknown |
Het |
| Abraxas1 |
T |
C |
5: 100,817,958 |
|
probably null |
Het |
| Actl7a |
G |
T |
4: 56,743,827 |
R118L |
probably damaging |
Het |
| Atg2b |
T |
C |
12: 105,639,359 |
D1449G |
possibly damaging |
Het |
| Atg7 |
G |
A |
6: 114,706,293 |
W439* |
probably null |
Het |
| Atp6v0a2 |
T |
A |
5: 124,712,279 |
I370N |
probably damaging |
Het |
| B4galt1 |
T |
C |
4: 40,807,760 |
D347G |
probably damaging |
Het |
| Baz2b |
C |
T |
2: 59,959,889 |
C660Y |
probably damaging |
Het |
| Ccdc88c |
T |
C |
12: 100,930,542 |
Y1390C |
probably damaging |
Het |
| Cdcp1 |
G |
A |
9: 123,173,772 |
Q745* |
probably null |
Het |
| Cep97 |
G |
A |
16: 55,919,526 |
S185L |
probably damaging |
Het |
| Clec4d |
A |
G |
6: 123,267,061 |
H43R |
probably damaging |
Het |
| Cntn3 |
T |
A |
6: 102,242,133 |
M509L |
probably benign |
Het |
| Cntrob |
A |
C |
11: 69,309,375 |
S564R |
possibly damaging |
Het |
| Edc4 |
A |
G |
8: 105,890,587 |
T1029A |
probably benign |
Het |
| Fam160b2 |
A |
T |
14: 70,591,681 |
V64E |
probably damaging |
Het |
| Fmnl1 |
G |
T |
11: 103,171,444 |
|
probably null |
Het |
| Fzd6 |
T |
A |
15: 39,007,388 |
M1K |
probably null |
Het |
| Gle1 |
C |
A |
2: 29,940,281 |
T283N |
probably benign |
Het |
| Hsd17b14 |
T |
C |
7: 45,565,962 |
V161A |
probably damaging |
Het |
| Hsf2 |
T |
C |
10: 57,504,723 |
S218P |
probably benign |
Het |
| Ipo7 |
T |
A |
7: 110,050,813 |
C736S |
probably damaging |
Het |
| Itpkb |
G |
T |
1: 180,413,975 |
V737L |
probably damaging |
Het |
| Itpr1 |
T |
C |
6: 108,489,797 |
|
probably benign |
Het |
| Kcnh8 |
G |
T |
17: 52,803,336 |
V192L |
possibly damaging |
Het |
| Kctd10 |
G |
A |
5: 114,380,462 |
|
probably benign |
Het |
| Kdm3a |
C |
A |
6: 71,632,250 |
|
probably benign |
Het |
| Kif5a |
T |
A |
10: 127,230,578 |
M990L |
probably benign |
Het |
| Klf12 |
A |
G |
14: 100,022,688 |
S202P |
probably damaging |
Het |
| Krt81 |
T |
G |
15: 101,460,202 |
Q390P |
probably damaging |
Het |
| Lrig3 |
T |
C |
10: 126,008,478 |
S604P |
probably damaging |
Het |
| Ms4a1 |
A |
T |
19: 11,258,248 |
V48D |
probably damaging |
Het |
| Mta1 |
C |
T |
12: 113,136,619 |
P688L |
probably damaging |
Het |
| Oas1h |
T |
C |
5: 120,870,977 |
V250A |
probably damaging |
Het |
| Olfr618 |
G |
T |
7: 103,597,921 |
G202* |
probably null |
Het |
| Olfr95 |
A |
T |
17: 37,211,021 |
Y277* |
probably null |
Het |
| P2rx3 |
T |
C |
2: 85,000,727 |
E265G |
possibly damaging |
Het |
| Pdzd8 |
A |
G |
19: 59,345,286 |
I101T |
possibly damaging |
Het |
| Psme4 |
A |
T |
11: 30,841,589 |
N1148I |
probably benign |
Het |
| Rnf213 |
T |
C |
11: 119,421,369 |
L874P |
probably damaging |
Het |
| Sart3 |
T |
C |
5: 113,751,239 |
Y508C |
probably damaging |
Het |
| Sez6l2 |
T |
C |
7: 126,970,133 |
|
probably benign |
Het |
| Slc9b1 |
C |
T |
3: 135,392,894 |
|
probably benign |
Het |
| Stmn3 |
T |
C |
2: 181,308,780 |
K78E |
possibly damaging |
Het |
| Thsd4 |
T |
A |
9: 60,394,106 |
N302I |
possibly damaging |
Het |
| Trdv5 |
A |
T |
14: 54,148,785 |
H74Q |
probably benign |
Het |
| Tubb4b |
C |
T |
2: 25,223,981 |
R77H |
probably benign |
Het |
| Ugt1a6a |
C |
T |
1: 88,215,123 |
P113L |
probably damaging |
Het |
| Unc5a |
T |
A |
13: 54,999,690 |
C438S |
possibly damaging |
Het |
| Zan |
C |
A |
5: 137,442,134 |
C1946F |
unknown |
Het |
|
| Other mutations in Cyp2j8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00088:Cyp2j8
|
APN |
4 |
96,503,842 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL00418:Cyp2j8
|
APN |
4 |
96,444,616 (GRCm38) |
missense |
possibly damaging |
0.85 |
|
IGL01577:Cyp2j8
|
APN |
4 |
96,479,071 (GRCm38) |
missense |
probably damaging |
0.96 |
|
IGL01629:Cyp2j8
|
APN |
4 |
96,499,603 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01928:Cyp2j8
|
APN |
4 |
96,470,476 (GRCm38) |
splice site |
probably benign |
|
|
IGL01978:Cyp2j8
|
APN |
4 |
96,504,009 (GRCm38) |
splice site |
probably null |
|
|
IGL02053:Cyp2j8
|
APN |
4 |
96,470,654 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02500:Cyp2j8
|
APN |
4 |
96,470,650 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02947:Cyp2j8
|
APN |
4 |
96,470,578 (GRCm38) |
missense |
probably damaging |
1.00 |
|
cyprus
|
UTSW |
4 |
96,499,603 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0558:Cyp2j8
|
UTSW |
4 |
96,444,634 (GRCm38) |
missense |
probably benign |
0.01 |
|
R0718:Cyp2j8
|
UTSW |
4 |
96,501,196 (GRCm38) |
missense |
probably benign |
|
|
R1553:Cyp2j8
|
UTSW |
4 |
96,475,557 (GRCm38) |
missense |
probably benign |
|
|
R1557:Cyp2j8
|
UTSW |
4 |
96,470,476 (GRCm38) |
splice site |
probably benign |
|
|
R1632:Cyp2j8
|
UTSW |
4 |
96,447,324 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1708:Cyp2j8
|
UTSW |
4 |
96,499,595 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2119:Cyp2j8
|
UTSW |
4 |
96,507,201 (GRCm38) |
missense |
probably benign |
|
|
R2220:Cyp2j8
|
UTSW |
4 |
96,444,625 (GRCm38) |
missense |
probably benign |
0.03 |
|
R3123:Cyp2j8
|
UTSW |
4 |
96,501,213 (GRCm38) |
splice site |
probably benign |
|
|
R3735:Cyp2j8
|
UTSW |
4 |
96,444,599 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3736:Cyp2j8
|
UTSW |
4 |
96,444,599 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4326:Cyp2j8
|
UTSW |
4 |
96,507,329 (GRCm38) |
missense |
probably benign |
0.10 |
|
R4327:Cyp2j8
|
UTSW |
4 |
96,507,329 (GRCm38) |
missense |
probably benign |
0.10 |
|
R4762:Cyp2j8
|
UTSW |
4 |
96,470,649 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4901:Cyp2j8
|
UTSW |
4 |
96,479,086 (GRCm38) |
missense |
probably benign |
0.16 |
|
R4960:Cyp2j8
|
UTSW |
4 |
96,507,377 (GRCm38) |
missense |
probably benign |
|
|
R5260:Cyp2j8
|
UTSW |
4 |
96,501,064 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R5562:Cyp2j8
|
UTSW |
4 |
96,470,653 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5596:Cyp2j8
|
UTSW |
4 |
96,507,341 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5741:Cyp2j8
|
UTSW |
4 |
96,444,643 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5825:Cyp2j8
|
UTSW |
4 |
96,507,214 (GRCm38) |
missense |
probably benign |
0.01 |
|
R6122:Cyp2j8
|
UTSW |
4 |
96,444,640 (GRCm38) |
missense |
probably benign |
|
|
R6232:Cyp2j8
|
UTSW |
4 |
96,507,190 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R6748:Cyp2j8
|
UTSW |
4 |
96,475,545 (GRCm38) |
missense |
probably benign |
0.01 |
|
R6931:Cyp2j8
|
UTSW |
4 |
96,444,781 (GRCm38) |
splice site |
probably null |
|
|
R7000:Cyp2j8
|
UTSW |
4 |
96,447,351 (GRCm38) |
missense |
probably benign |
0.06 |
|
R7183:Cyp2j8
|
UTSW |
4 |
96,479,181 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R7186:Cyp2j8
|
UTSW |
4 |
96,475,550 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7348:Cyp2j8
|
UTSW |
4 |
96,444,640 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7575:Cyp2j8
|
UTSW |
4 |
96,470,548 (GRCm38) |
missense |
possibly damaging |
0.63 |
|
R7648:Cyp2j8
|
UTSW |
4 |
96,499,603 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7975:Cyp2j8
|
UTSW |
4 |
96,470,539 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R7993:Cyp2j8
|
UTSW |
4 |
96,447,219 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8878:Cyp2j8
|
UTSW |
4 |
96,470,570 (GRCm38) |
missense |
possibly damaging |
0.56 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTACTGGATAGGTTAGCAGGCAG -3'
(R):5'- GATAGGCAGGCTTGGGTAAC -3'
Sequencing Primer
(F):5'- AGCATCAGCCTCCAGCCTG -3'
(R):5'- CAAGGAACAAGGTAGAACTTAGCAC -3'
|
| Posted On |
2017-02-15 |
Incidental Mutation