Incidental Mutation 'IGL03170:Cyp4f37'
ID |
411817 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Cyp4f37
|
Ensembl Gene |
ENSMUSG00000062464 |
Gene Name |
cytochrome P450, family 4, subfamily f, polypeptide 37 |
Synonyms |
Gm9705 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.222)
|
Stock # |
IGL03170
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
32840283-32855158 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
C to T
at 32844093 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000076827
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077639]
|
AlphaFold |
Q3V1F1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000077639
|
SMART Domains |
Protein: ENSMUSP00000076827 Gene: ENSMUSG00000062464
Domain | Start | End | E-Value | Type |
Pfam:p450
|
52 |
515 |
1.1e-136 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cand2 |
A |
G |
6: 115,774,861 (GRCm39) |
D1023G |
probably damaging |
Het |
Ccn1 |
C |
A |
3: 145,355,514 (GRCm39) |
A12S |
probably benign |
Het |
Cyp2c54 |
A |
G |
19: 40,060,809 (GRCm39) |
|
probably null |
Het |
Entpd2 |
T |
C |
2: 25,289,493 (GRCm39) |
F325S |
probably damaging |
Het |
Flnb |
T |
C |
14: 7,818,261 (GRCm38) |
I37T |
possibly damaging |
Het |
Gtpbp10 |
A |
G |
5: 5,605,355 (GRCm39) |
V116A |
probably benign |
Het |
H2-T9 |
C |
T |
17: 36,439,605 (GRCm39) |
G125E |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 40,587,456 (GRCm39) |
N164I |
unknown |
Het |
Nle1 |
T |
A |
11: 82,795,096 (GRCm39) |
T312S |
probably benign |
Het |
Or10ab5 |
T |
C |
7: 108,245,307 (GRCm39) |
I159V |
probably benign |
Het |
Pim1 |
T |
A |
17: 29,710,152 (GRCm39) |
L12Q |
possibly damaging |
Het |
Plb1 |
G |
T |
5: 32,442,246 (GRCm39) |
C246F |
probably damaging |
Het |
Ppp4r4 |
T |
C |
12: 103,557,033 (GRCm39) |
|
probably benign |
Het |
Prl6a1 |
T |
A |
13: 27,499,406 (GRCm39) |
V63D |
possibly damaging |
Het |
Ptprz1 |
G |
A |
6: 22,959,766 (GRCm39) |
A88T |
probably benign |
Het |
Ranbp3l |
A |
T |
15: 9,029,611 (GRCm39) |
E31V |
probably damaging |
Het |
Relch |
C |
T |
1: 105,663,680 (GRCm39) |
T943I |
probably damaging |
Het |
Rgs9 |
G |
A |
11: 109,150,681 (GRCm39) |
T209I |
probably benign |
Het |
Smg8 |
A |
G |
11: 86,977,434 (GRCm39) |
V49A |
probably damaging |
Het |
Smim6 |
A |
T |
11: 115,804,314 (GRCm39) |
T34S |
possibly damaging |
Het |
Snw1 |
T |
G |
12: 87,519,022 (GRCm39) |
T4P |
probably benign |
Het |
Sod2 |
C |
A |
17: 13,227,257 (GRCm39) |
H70Q |
probably benign |
Het |
Tro |
A |
G |
X: 149,438,556 (GRCm39) |
S34P |
probably benign |
Het |
Tshr |
T |
A |
12: 91,504,643 (GRCm39) |
M527K |
probably damaging |
Het |
Uggt1 |
A |
C |
1: 36,202,342 (GRCm39) |
V1085G |
probably damaging |
Het |
Vmn1r21 |
A |
G |
6: 57,820,847 (GRCm39) |
V199A |
probably damaging |
Het |
Xkr9 |
T |
C |
1: 13,771,036 (GRCm39) |
I184T |
possibly damaging |
Het |
Zfp369 |
T |
C |
13: 65,442,224 (GRCm39) |
S273P |
probably damaging |
Het |
Zpld2 |
C |
T |
4: 133,920,345 (GRCm39) |
V607I |
possibly damaging |
Het |
|
Other mutations in Cyp4f37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Cyp4f37
|
APN |
17 |
32,848,027 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01994:Cyp4f37
|
APN |
17 |
32,844,150 (GRCm39) |
nonsense |
probably null |
|
IGL02073:Cyp4f37
|
APN |
17 |
32,846,825 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02145:Cyp4f37
|
APN |
17 |
32,849,009 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02814:Cyp4f37
|
APN |
17 |
32,853,645 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02873:Cyp4f37
|
APN |
17 |
32,844,142 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02937:Cyp4f37
|
APN |
17 |
32,844,163 (GRCm39) |
missense |
probably benign |
0.00 |
R0625:Cyp4f37
|
UTSW |
17 |
32,853,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Cyp4f37
|
UTSW |
17 |
32,848,864 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1871:Cyp4f37
|
UTSW |
17 |
32,853,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Cyp4f37
|
UTSW |
17 |
32,853,244 (GRCm39) |
missense |
probably benign |
0.23 |
R2847:Cyp4f37
|
UTSW |
17 |
32,848,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R2848:Cyp4f37
|
UTSW |
17 |
32,848,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Cyp4f37
|
UTSW |
17 |
32,850,646 (GRCm39) |
missense |
probably benign |
0.00 |
R4463:Cyp4f37
|
UTSW |
17 |
32,846,710 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4517:Cyp4f37
|
UTSW |
17 |
32,850,566 (GRCm39) |
missense |
probably benign |
0.00 |
R4573:Cyp4f37
|
UTSW |
17 |
32,848,061 (GRCm39) |
missense |
probably benign |
0.23 |
R4670:Cyp4f37
|
UTSW |
17 |
32,844,126 (GRCm39) |
missense |
probably benign |
|
R5752:Cyp4f37
|
UTSW |
17 |
32,850,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Cyp4f37
|
UTSW |
17 |
32,848,957 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6248:Cyp4f37
|
UTSW |
17 |
32,848,864 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7412:Cyp4f37
|
UTSW |
17 |
32,848,818 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7969:Cyp4f37
|
UTSW |
17 |
32,844,181 (GRCm39) |
missense |
probably benign |
0.00 |
R8066:Cyp4f37
|
UTSW |
17 |
32,854,047 (GRCm39) |
missense |
probably benign |
0.21 |
R8187:Cyp4f37
|
UTSW |
17 |
32,854,171 (GRCm39) |
missense |
probably benign |
|
R8303:Cyp4f37
|
UTSW |
17 |
32,853,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8309:Cyp4f37
|
UTSW |
17 |
32,853,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Cyp4f37
|
UTSW |
17 |
32,853,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8869:Cyp4f37
|
UTSW |
17 |
32,844,096 (GRCm39) |
missense |
probably benign |
0.01 |
R9054:Cyp4f37
|
UTSW |
17 |
32,853,253 (GRCm39) |
missense |
probably benign |
0.25 |
R9565:Cyp4f37
|
UTSW |
17 |
32,844,205 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9674:Cyp4f37
|
UTSW |
17 |
32,846,841 (GRCm39) |
critical splice donor site |
probably null |
|
X0057:Cyp4f37
|
UTSW |
17 |
32,844,198 (GRCm39) |
missense |
probably benign |
0.01 |
|
Posted On |
2016-08-02 |