Incidental Mutation 'R0392:Cyp2b13'
| ID |
31756 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cyp2b13
|
| Ensembl Gene |
ENSMUSG00000040583 |
| Gene Name |
cytochrome P450, family 2, subfamily b, polypeptide 13 |
| Synonyms |
phenobarbital inducible, type c |
| MMRRC Submission |
038598-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0392 (G1)
|
| Quality Score |
182 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
25760922-25795622 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 25785308 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 226
(Y226H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000005669
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000005669]
|
| AlphaFold |
A6H6J2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000005669
AA Change: Y226H
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000005669
Gene: ENSMUSG00000040583
AA Change: Y226H
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
Pfam:p450
|
31 |
488 |
9.8e-150 |
PFAM |
|
| Meta Mutation Damage Score |
0.1178 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.0%
- 10x: 95.5%
- 20x: 90.6%
|
| Validation Efficiency |
100% (31/31) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930527J03Rik |
ACCC |
ACC |
1: 178,276,503 (GRCm38) |
|
noncoding transcript |
Het |
| Bcan |
T |
A |
3: 87,900,869 (GRCm39) |
K455* |
probably null |
Het |
| Casp12 |
T |
A |
9: 5,348,973 (GRCm39) |
|
probably benign |
Het |
| Ccdc61 |
T |
C |
7: 18,625,027 (GRCm39) |
M504V |
probably benign |
Het |
| Cd53 |
A |
T |
3: 106,670,592 (GRCm39) |
V147E |
probably damaging |
Het |
| Cyp2j7 |
T |
C |
4: 96,087,671 (GRCm39) |
D413G |
probably damaging |
Het |
| Dcbld1 |
T |
C |
10: 52,193,230 (GRCm39) |
I254T |
possibly damaging |
Het |
| Ddx39a |
T |
G |
8: 84,448,366 (GRCm39) |
M206R |
probably damaging |
Het |
| Dgki |
T |
A |
6: 36,977,113 (GRCm39) |
T666S |
probably damaging |
Het |
| Dnaaf8 |
T |
C |
16: 4,795,363 (GRCm39) |
|
noncoding transcript |
Het |
| Dnah7a |
C |
A |
1: 53,543,357 (GRCm39) |
C2271F |
probably damaging |
Het |
| Emilin3 |
A |
G |
2: 160,752,799 (GRCm39) |
|
probably benign |
Het |
| Epha4 |
T |
C |
1: 77,483,610 (GRCm39) |
K133R |
probably benign |
Het |
| Gm11146 |
T |
A |
16: 77,394,054 (GRCm39) |
|
probably benign |
Het |
| Ift88 |
A |
T |
14: 57,733,617 (GRCm39) |
|
probably benign |
Het |
| Ighv10-3 |
A |
G |
12: 114,487,460 (GRCm39) |
|
probably benign |
Het |
| Lamp5 |
T |
C |
2: 135,902,817 (GRCm39) |
S179P |
probably damaging |
Het |
| Map4 |
T |
C |
9: 109,907,113 (GRCm39) |
S788P |
probably damaging |
Het |
| Or5m13 |
T |
A |
2: 85,749,106 (GRCm39) |
I279N |
possibly damaging |
Het |
| Otog |
T |
C |
7: 45,899,499 (GRCm39) |
W267R |
probably benign |
Het |
| Pafah1b2 |
T |
C |
9: 45,880,151 (GRCm39) |
I175M |
probably benign |
Het |
| Pcdhb12 |
A |
G |
18: 37,570,011 (GRCm39) |
K386E |
possibly damaging |
Het |
| Pcnt |
T |
C |
10: 76,220,660 (GRCm39) |
N2056S |
probably benign |
Het |
| Pold2 |
T |
C |
11: 5,826,776 (GRCm39) |
I53V |
possibly damaging |
Het |
| Rsf1 |
T |
A |
7: 97,328,212 (GRCm39) |
D1071E |
probably benign |
Het |
| Rtp3 |
A |
T |
9: 110,818,621 (GRCm39) |
M20K |
probably damaging |
Het |
| S1pr5 |
T |
A |
9: 21,156,277 (GRCm39) |
I50F |
probably damaging |
Het |
| Slc47a1 |
A |
G |
11: 61,262,608 (GRCm39) |
S94P |
probably damaging |
Het |
| Slitrk5 |
G |
A |
14: 111,916,465 (GRCm39) |
V30I |
probably benign |
Het |
| St8sia5 |
G |
A |
18: 77,342,102 (GRCm39) |
V271M |
probably damaging |
Het |
| Sult2b1 |
G |
T |
7: 45,383,062 (GRCm39) |
T240N |
probably damaging |
Het |
|
| Other mutations in Cyp2b13 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00980:Cyp2b13
|
APN |
7 |
25,781,152 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL01134:Cyp2b13
|
APN |
7 |
25,781,125 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02386:Cyp2b13
|
APN |
7 |
25,785,438 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02531:Cyp2b13
|
APN |
7 |
25,761,030 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
IGL02960:Cyp2b13
|
APN |
7 |
25,761,101 (GRCm39) |
missense |
probably benign |
0.33 |
|
R0018:Cyp2b13
|
UTSW |
7 |
25,785,375 (GRCm39) |
missense |
probably benign |
0.30 |
|
R0018:Cyp2b13
|
UTSW |
7 |
25,785,375 (GRCm39) |
missense |
probably benign |
0.30 |
|
R0103:Cyp2b13
|
UTSW |
7 |
25,788,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0121:Cyp2b13
|
UTSW |
7 |
25,786,010 (GRCm39) |
missense |
probably benign |
|
|
R0540:Cyp2b13
|
UTSW |
7 |
25,781,136 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1887:Cyp2b13
|
UTSW |
7 |
25,788,075 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2416:Cyp2b13
|
UTSW |
7 |
25,795,246 (GRCm39) |
makesense |
probably null |
|
|
R2879:Cyp2b13
|
UTSW |
7 |
25,785,456 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4654:Cyp2b13
|
UTSW |
7 |
25,761,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4735:Cyp2b13
|
UTSW |
7 |
25,787,720 (GRCm39) |
missense |
probably benign |
|
|
R4969:Cyp2b13
|
UTSW |
7 |
25,780,413 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5174:Cyp2b13
|
UTSW |
7 |
25,788,118 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R6243:Cyp2b13
|
UTSW |
7 |
25,761,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6616:Cyp2b13
|
UTSW |
7 |
25,785,306 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6647:Cyp2b13
|
UTSW |
7 |
25,785,324 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R6766:Cyp2b13
|
UTSW |
7 |
25,781,236 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6844:Cyp2b13
|
UTSW |
7 |
25,781,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7431:Cyp2b13
|
UTSW |
7 |
25,760,976 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7593:Cyp2b13
|
UTSW |
7 |
25,780,416 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R7719:Cyp2b13
|
UTSW |
7 |
25,795,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7857:Cyp2b13
|
UTSW |
7 |
25,788,153 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8406:Cyp2b13
|
UTSW |
7 |
25,781,223 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9418:Cyp2b13
|
UTSW |
7 |
25,761,110 (GRCm39) |
missense |
probably benign |
0.36 |
|
R9557:Cyp2b13
|
UTSW |
7 |
25,780,123 (GRCm39) |
missense |
probably benign |
0.05 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCAAGTTGTTGGGACAGCTAGACTAGG -3'
(R):5'- GCCTCTCTCATCCATGCAGGATTAACC -3'
Sequencing Primer
(F):5'- tctccattgttcttcctgcc -3'
(R):5'- ATCCATGCAGGATTAACCTTCTC -3'
|
| Posted On |
2013-04-24 |
Incidental Mutation