Incidental Mutation 'IGL03124:Cyp4f15'
| ID |
410118 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Cyp4f15
|
| Ensembl Gene |
ENSMUSG00000073424 |
| Gene Name |
cytochrome P450, family 4, subfamily f, polypeptide 15 |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.651)
|
| Stock # |
IGL03124
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
17 |
| Chromosomal Location |
32904605-32922329 bp(+) (GRCm39) |
| Type of Mutation |
critical splice donor site (1 bp from exon) |
| DNA Base Change (assembly) |
G to A
at 32904786 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000129264
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000008801]
[ENSMUST00000168171]
|
| AlphaFold |
Q99N18 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000008801
|
| SMART Domains |
Protein: ENSMUSP00000008801
Gene: ENSMUSG00000073424
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
16 |
37 |
N/A |
INTRINSIC |
|
Pfam:p450
|
57 |
520 |
8.4e-137 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000163907
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000167789
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000168171
|
| SMART Domains |
Protein: ENSMUSP00000129264
Gene: ENSMUSG00000073424
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
16 |
37 |
N/A |
INTRINSIC |
|
Pfam:p450
|
57 |
527 |
3.2e-133 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene, CYP4F8, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and functions as a 19-hydroxylase of prostaglandins in seminal vesicles. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F3, is approximately 18 kb away. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700018B08Rik |
C |
A |
8: 122,268,449 (GRCm39) |
|
probably benign |
Het |
| 4931414P19Rik |
A |
G |
14: 54,832,596 (GRCm39) |
V193A |
probably benign |
Het |
| Acap3 |
T |
C |
4: 155,989,490 (GRCm39) |
S645P |
probably benign |
Het |
| Alms1 |
A |
G |
6: 85,655,401 (GRCm39) |
I3316V |
probably benign |
Het |
| Apc |
T |
G |
18: 34,433,038 (GRCm39) |
H424Q |
probably damaging |
Het |
| Camsap2 |
A |
T |
1: 136,202,537 (GRCm39) |
|
probably null |
Het |
| Car13 |
C |
T |
3: 14,722,000 (GRCm39) |
P182L |
possibly damaging |
Het |
| Ccdc87 |
T |
G |
19: 4,891,082 (GRCm39) |
S525A |
probably damaging |
Het |
| Ces1f |
T |
C |
8: 94,002,012 (GRCm39) |
N39D |
probably benign |
Het |
| Cyp2j13 |
C |
A |
4: 95,950,159 (GRCm39) |
A281S |
possibly damaging |
Het |
| Fat4 |
C |
A |
3: 39,035,701 (GRCm39) |
R3118S |
possibly damaging |
Het |
| Glg1 |
C |
T |
8: 111,926,803 (GRCm39) |
V171M |
probably damaging |
Het |
| Hivep1 |
G |
T |
13: 42,312,380 (GRCm39) |
G1540V |
possibly damaging |
Het |
| Ighm |
T |
C |
12: 113,385,258 (GRCm39) |
D234G |
unknown |
Het |
| Igsf10 |
T |
C |
3: 59,227,086 (GRCm39) |
T2196A |
probably benign |
Het |
| Kctd19 |
T |
A |
8: 106,113,702 (GRCm39) |
Q657L |
possibly damaging |
Het |
| Klhl40 |
T |
A |
9: 121,609,751 (GRCm39) |
I512N |
probably damaging |
Het |
| Lima1 |
A |
T |
15: 99,694,615 (GRCm39) |
|
probably benign |
Het |
| Map2k4 |
A |
C |
11: 65,581,617 (GRCm39) |
I365S |
probably damaging |
Het |
| Mast4 |
T |
A |
13: 102,874,753 (GRCm39) |
K1346N |
probably damaging |
Het |
| Met |
T |
A |
6: 17,492,077 (GRCm39) |
F280I |
probably benign |
Het |
| Ncapg |
A |
G |
5: 45,828,551 (GRCm39) |
T101A |
probably benign |
Het |
| Nup214 |
T |
C |
2: 31,886,452 (GRCm39) |
F605L |
probably benign |
Het |
| Odr4 |
A |
G |
1: 150,262,176 (GRCm39) |
V88A |
probably benign |
Het |
| Or51k1 |
G |
T |
7: 103,661,001 (GRCm39) |
Q303K |
probably benign |
Het |
| Or5ae2 |
T |
A |
7: 84,505,931 (GRCm39) |
M118K |
probably damaging |
Het |
| Or7e177 |
T |
A |
9: 20,212,459 (GRCm39) |
M322K |
probably benign |
Het |
| Pck2 |
C |
T |
14: 55,782,790 (GRCm39) |
T373I |
probably damaging |
Het |
| Pcna |
C |
T |
2: 132,093,673 (GRCm39) |
E109K |
probably benign |
Het |
| Pecr |
A |
C |
1: 72,316,499 (GRCm39) |
S69A |
probably benign |
Het |
| Pgap6 |
G |
A |
17: 26,335,808 (GRCm39) |
R65Q |
probably damaging |
Het |
| Pitpnb |
A |
G |
5: 111,478,696 (GRCm39) |
E6G |
possibly damaging |
Het |
| Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
| Plbd2 |
A |
T |
5: 120,631,142 (GRCm39) |
F212I |
possibly damaging |
Het |
| Rfk |
T |
A |
19: 17,375,959 (GRCm39) |
H84Q |
possibly damaging |
Het |
| Scp2 |
T |
A |
4: 107,921,103 (GRCm39) |
I36F |
probably damaging |
Het |
| Slc9a4 |
A |
G |
1: 40,619,895 (GRCm39) |
T74A |
probably damaging |
Het |
| Spmip6 |
T |
C |
4: 41,507,287 (GRCm39) |
N170D |
possibly damaging |
Het |
| St6galnac1 |
G |
A |
11: 116,666,125 (GRCm39) |
A35V |
probably benign |
Het |
| Tasor2 |
A |
T |
13: 3,624,704 (GRCm39) |
Y1749N |
probably benign |
Het |
| Trav17 |
T |
C |
14: 54,044,106 (GRCm39) |
V4A |
probably benign |
Het |
| Vmn1r57 |
A |
T |
7: 5,224,021 (GRCm39) |
H182L |
possibly damaging |
Het |
| Vwa8 |
A |
T |
14: 79,296,255 (GRCm39) |
|
probably benign |
Het |
| Zgpat |
A |
G |
2: 181,007,973 (GRCm39) |
Y170C |
probably benign |
Het |
|
| Other mutations in Cyp4f15 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01812:Cyp4f15
|
APN |
17 |
32,905,131 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01813:Cyp4f15
|
APN |
17 |
32,905,131 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02394:Cyp4f15
|
APN |
17 |
32,911,609 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
IGL02547:Cyp4f15
|
APN |
17 |
32,919,229 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02743:Cyp4f15
|
APN |
17 |
32,918,926 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
IGL03120:Cyp4f15
|
APN |
17 |
32,909,738 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL03342:Cyp4f15
|
APN |
17 |
32,916,910 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4472001:Cyp4f15
|
UTSW |
17 |
32,921,798 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2016:Cyp4f15
|
UTSW |
17 |
32,921,133 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2892:Cyp4f15
|
UTSW |
17 |
32,905,182 (GRCm39) |
missense |
probably benign |
|
|
R3812:Cyp4f15
|
UTSW |
17 |
32,905,151 (GRCm39) |
missense |
probably benign |
|
|
R4803:Cyp4f15
|
UTSW |
17 |
32,911,554 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5180:Cyp4f15
|
UTSW |
17 |
32,909,714 (GRCm39) |
missense |
probably benign |
0.21 |
|
R5199:Cyp4f15
|
UTSW |
17 |
32,921,346 (GRCm39) |
missense |
probably benign |
|
|
R5787:Cyp4f15
|
UTSW |
17 |
32,921,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6695:Cyp4f15
|
UTSW |
17 |
32,911,586 (GRCm39) |
nonsense |
probably null |
|
|
R8311:Cyp4f15
|
UTSW |
17 |
32,916,914 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8342:Cyp4f15
|
UTSW |
17 |
32,909,733 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8369:Cyp4f15
|
UTSW |
17 |
32,916,939 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8488:Cyp4f15
|
UTSW |
17 |
32,920,948 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8503:Cyp4f15
|
UTSW |
17 |
32,914,338 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8778:Cyp4f15
|
UTSW |
17 |
32,921,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9052:Cyp4f15
|
UTSW |
17 |
32,911,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9179:Cyp4f15
|
UTSW |
17 |
32,919,185 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9183:Cyp4f15
|
UTSW |
17 |
32,919,205 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9311:Cyp4f15
|
UTSW |
17 |
32,905,139 (GRCm39) |
missense |
probably benign |
|
|
Z1088:Cyp4f15
|
UTSW |
17 |
32,911,664 (GRCm39) |
splice site |
probably null |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation