Incidental Mutation 'IGL01766:Dcaf13'
ID |
153664 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Dcaf13
|
Ensembl Gene |
ENSMUSG00000022300 |
Gene Name |
DDB1 and CUL4 associated factor 13 |
Synonyms |
Wdsof1, LOC223499 |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.955)
|
Stock # |
IGL01766
|
Quality Score |
|
Status
|
|
Chromosome |
15 |
Chromosomal Location |
38976300-39010251 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 38982145 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 37
(V37A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000022909
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022909]
|
AlphaFold |
Q6PAC3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000022909
AA Change: V37A
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
SMART Domains |
Protein: ENSMUSP00000022909 Gene: ENSMUSG00000022300 AA Change: V37A
Domain | Start | End | E-Value | Type |
WD40
|
55 |
95 |
5.77e-5 |
SMART |
WD40
|
98 |
137 |
4.38e-5 |
SMART |
WD40
|
185 |
225 |
5.97e-1 |
SMART |
Blast:WD40
|
228 |
267 |
1e-18 |
BLAST |
WD40
|
271 |
310 |
2.69e-5 |
SMART |
WD40
|
312 |
353 |
2.96e-2 |
SMART |
Pfam:Sof1
|
354 |
440 |
7.2e-38 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
All alleles(9) : Targeted, other(2) Gene trapped(7) |
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
A |
G |
10: 29,100,557 (GRCm39) |
D310G |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,977,482 (GRCm39) |
T7A |
unknown |
Het |
Arhgap21 |
T |
A |
2: 20,854,448 (GRCm39) |
D1648V |
possibly damaging |
Het |
Cd274 |
T |
C |
19: 29,362,810 (GRCm39) |
*291Q |
probably null |
Het |
Ceacam1 |
G |
A |
7: 25,171,420 (GRCm39) |
S348L |
probably damaging |
Het |
Degs1 |
A |
T |
1: 182,106,660 (GRCm39) |
F200I |
probably damaging |
Het |
Dock4 |
G |
T |
12: 40,496,378 (GRCm39) |
E8* |
probably null |
Het |
Dsc2 |
G |
A |
18: 20,179,399 (GRCm39) |
P223L |
possibly damaging |
Het |
Exo1 |
A |
G |
1: 175,719,587 (GRCm39) |
T171A |
possibly damaging |
Het |
Gen1 |
C |
T |
12: 11,306,895 (GRCm39) |
D92N |
probably damaging |
Het |
Gm572 |
A |
T |
4: 148,739,352 (GRCm39) |
H60L |
possibly damaging |
Het |
Gucy2c |
T |
C |
6: 136,692,971 (GRCm39) |
T719A |
probably benign |
Het |
Heatr5a |
T |
C |
12: 51,936,447 (GRCm39) |
S1575G |
probably benign |
Het |
Hspa12a |
T |
C |
19: 58,787,899 (GRCm39) |
E641G |
probably damaging |
Het |
Itgb4 |
G |
A |
11: 115,879,752 (GRCm39) |
V635I |
probably damaging |
Het |
Luzp1 |
T |
C |
4: 136,270,084 (GRCm39) |
I769T |
possibly damaging |
Het |
Map2k5 |
C |
T |
9: 63,284,509 (GRCm39) |
A11T |
probably benign |
Het |
Myo9b |
A |
G |
8: 71,743,161 (GRCm39) |
E74G |
probably damaging |
Het |
Myom1 |
T |
C |
17: 71,384,283 (GRCm39) |
V666A |
probably damaging |
Het |
Or1e29 |
T |
A |
11: 73,667,901 (GRCm39) |
N84I |
probably benign |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or5ak4 |
A |
G |
2: 85,161,945 (GRCm39) |
L99S |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,747,649 (GRCm39) |
F166S |
probably damaging |
Het |
Plekhg1 |
A |
G |
10: 3,823,400 (GRCm39) |
T123A |
probably damaging |
Het |
Polrmt |
T |
C |
10: 79,572,402 (GRCm39) |
E1077G |
possibly damaging |
Het |
Ptprh |
A |
G |
7: 4,583,915 (GRCm39) |
W226R |
probably benign |
Het |
Robo1 |
A |
G |
16: 72,801,553 (GRCm39) |
H1059R |
probably benign |
Het |
Sesn1 |
A |
G |
10: 41,774,365 (GRCm39) |
T306A |
probably benign |
Het |
Sox14 |
T |
A |
9: 99,757,169 (GRCm39) |
H190L |
probably damaging |
Het |
Spag8 |
G |
T |
4: 43,653,209 (GRCm39) |
|
probably benign |
Het |
Tomm40 |
T |
C |
7: 19,437,007 (GRCm39) |
H20R |
possibly damaging |
Het |
Znhit3 |
G |
T |
11: 84,806,959 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Dcaf13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00787:Dcaf13
|
APN |
15 |
39,007,027 (GRCm39) |
nonsense |
probably null |
|
IGL01081:Dcaf13
|
APN |
15 |
38,982,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02174:Dcaf13
|
APN |
15 |
39,001,544 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02262:Dcaf13
|
APN |
15 |
38,982,102 (GRCm39) |
splice site |
probably benign |
|
IGL02740:Dcaf13
|
APN |
15 |
39,008,495 (GRCm39) |
nonsense |
probably null |
|
IGL03092:Dcaf13
|
APN |
15 |
38,991,371 (GRCm39) |
splice site |
probably benign |
|
IGL03374:Dcaf13
|
APN |
15 |
39,008,543 (GRCm39) |
nonsense |
probably null |
|
R0590:Dcaf13
|
UTSW |
15 |
39,008,480 (GRCm39) |
splice site |
probably benign |
|
R0594:Dcaf13
|
UTSW |
15 |
38,986,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0711:Dcaf13
|
UTSW |
15 |
39,001,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R1036:Dcaf13
|
UTSW |
15 |
39,007,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Dcaf13
|
UTSW |
15 |
38,993,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Dcaf13
|
UTSW |
15 |
38,982,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R1933:Dcaf13
|
UTSW |
15 |
39,001,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Dcaf13
|
UTSW |
15 |
39,008,547 (GRCm39) |
missense |
probably benign |
|
R4113:Dcaf13
|
UTSW |
15 |
38,993,615 (GRCm39) |
missense |
probably damaging |
0.98 |
R4595:Dcaf13
|
UTSW |
15 |
38,982,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Dcaf13
|
UTSW |
15 |
39,001,637 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5431:Dcaf13
|
UTSW |
15 |
38,986,619 (GRCm39) |
missense |
probably benign |
0.16 |
R5454:Dcaf13
|
UTSW |
15 |
38,987,759 (GRCm39) |
missense |
probably benign |
|
R5834:Dcaf13
|
UTSW |
15 |
39,007,037 (GRCm39) |
nonsense |
probably null |
|
R5929:Dcaf13
|
UTSW |
15 |
39,007,048 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5944:Dcaf13
|
UTSW |
15 |
39,010,072 (GRCm39) |
missense |
probably benign |
|
R6319:Dcaf13
|
UTSW |
15 |
39,007,067 (GRCm39) |
missense |
probably benign |
0.00 |
R6394:Dcaf13
|
UTSW |
15 |
39,007,132 (GRCm39) |
missense |
probably benign |
0.04 |
R6664:Dcaf13
|
UTSW |
15 |
38,982,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6884:Dcaf13
|
UTSW |
15 |
38,986,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R7419:Dcaf13
|
UTSW |
15 |
38,993,615 (GRCm39) |
missense |
probably damaging |
0.98 |
R8750:Dcaf13
|
UTSW |
15 |
38,982,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R8944:Dcaf13
|
UTSW |
15 |
39,001,612 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9294:Dcaf13
|
UTSW |
15 |
38,993,687 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9300:Dcaf13
|
UTSW |
15 |
39,010,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Dcaf13
|
UTSW |
15 |
38,982,178 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9696:Dcaf13
|
UTSW |
15 |
39,001,496 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9778:Dcaf13
|
UTSW |
15 |
39,008,586 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Dcaf13
|
UTSW |
15 |
39,008,642 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2014-02-04 |