Incidental Mutation 'R8255:Wdr31'
| ID |
640596 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Wdr31
|
| Ensembl Gene |
ENSMUSG00000028391 |
| Gene Name |
WD repeat domain 31 |
| Synonyms |
5430402I10Rik |
| MMRRC Submission |
067681-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.078)
|
| Stock # |
R8255 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
62366890-62389133 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 62381634 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Threonine
at position 66
(S66T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030087
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030087]
[ENSMUST00000107452]
[ENSMUST00000120095]
[ENSMUST00000132263]
[ENSMUST00000135811]
[ENSMUST00000155522]
|
| AlphaFold |
Q9JHB4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030087
AA Change: S66T
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000030087
Gene: ENSMUSG00000028391
AA Change: S66T
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
51 |
89 |
8.88e0 |
SMART |
|
WD40
|
92 |
131 |
6.38e-7 |
SMART |
|
WD40
|
135 |
174 |
2.82e-8 |
SMART |
|
WD40
|
177 |
216 |
5.31e-4 |
SMART |
|
Blast:WD40
|
219 |
263 |
2e-10 |
BLAST |
|
WD40
|
267 |
310 |
1.03e-1 |
SMART |
|
Blast:WD40
|
313 |
352 |
2e-15 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000107452
AA Change: S65T
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000103076
Gene: ENSMUSG00000028391
AA Change: S65T
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
50 |
88 |
8.88e0 |
SMART |
|
WD40
|
91 |
130 |
6.38e-7 |
SMART |
|
WD40
|
134 |
173 |
2.82e-8 |
SMART |
|
WD40
|
176 |
215 |
5.31e-4 |
SMART |
|
Blast:WD40
|
218 |
262 |
2e-10 |
BLAST |
|
WD40
|
266 |
309 |
1.03e-1 |
SMART |
|
Blast:WD40
|
312 |
351 |
2e-15 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000120095
AA Change: S66T
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000112719
Gene: ENSMUSG00000028391
AA Change: S66T
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
51 |
89 |
8.88e0 |
SMART |
|
WD40
|
92 |
131 |
6.38e-7 |
SMART |
|
WD40
|
135 |
174 |
2.82e-8 |
SMART |
|
WD40
|
177 |
216 |
5.31e-4 |
SMART |
|
Blast:WD40
|
219 |
263 |
2e-10 |
BLAST |
|
WD40
|
267 |
310 |
1.03e-1 |
SMART |
|
Blast:WD40
|
313 |
352 |
2e-15 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000132263
|
| SMART Domains |
Protein: ENSMUSP00000120684
Gene: ENSMUSG00000028391
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
16 |
55 |
5.31e-4 |
SMART |
|
Blast:WD40
|
58 |
100 |
3e-9 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135811
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000155522
AA Change: S66T
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000123624
Gene: ENSMUSG00000028391
AA Change: S66T
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:WD40
|
51 |
83 |
3e-16 |
BLAST |
|
| Meta Mutation Damage Score |
0.0734 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
| Validation Efficiency |
100% (46/46) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
A |
T |
13: 77,415,850 (GRCm39) |
T648S |
possibly damaging |
Het |
| Abca12 |
T |
A |
1: 71,359,058 (GRCm39) |
I583F |
probably benign |
Het |
| Abca4 |
A |
T |
3: 121,948,926 (GRCm39) |
M1732L |
probably benign |
Het |
| Ank2 |
A |
G |
3: 126,740,398 (GRCm39) |
S1742P |
unknown |
Het |
| Birc6 |
G |
A |
17: 74,969,775 (GRCm39) |
A4273T |
probably damaging |
Het |
| Chd5 |
A |
G |
4: 152,463,880 (GRCm39) |
T1450A |
probably damaging |
Het |
| Dhx32 |
T |
C |
7: 133,339,120 (GRCm39) |
N305S |
probably benign |
Het |
| Dnah7c |
T |
C |
1: 46,698,589 (GRCm39) |
S2174P |
probably damaging |
Het |
| Fat2 |
T |
A |
11: 55,161,101 (GRCm39) |
I3210F |
probably benign |
Het |
| Gm12888 |
A |
G |
4: 121,181,994 (GRCm39) |
S33P |
probably damaging |
Het |
| Gpaa1 |
T |
C |
15: 76,217,438 (GRCm39) |
L292P |
probably damaging |
Het |
| Gzmg |
T |
A |
14: 56,395,753 (GRCm39) |
R69W |
probably damaging |
Het |
| Hat1 |
A |
G |
2: 71,239,347 (GRCm39) |
D40G |
probably damaging |
Het |
| Hcrtr2 |
T |
A |
9: 76,140,203 (GRCm39) |
I362F |
probably damaging |
Het |
| Hmmr |
T |
C |
11: 40,598,262 (GRCm39) |
E650G |
probably damaging |
Het |
| Ifi35 |
A |
T |
11: 101,348,608 (GRCm39) |
M180L |
probably benign |
Het |
| Ifi44 |
A |
T |
3: 151,451,619 (GRCm39) |
H162Q |
probably benign |
Het |
| Il1rl2 |
T |
C |
1: 40,404,471 (GRCm39) |
F531L |
probably damaging |
Het |
| Ipcef1 |
T |
G |
10: 6,870,007 (GRCm39) |
K182T |
probably benign |
Het |
| Med27 |
C |
A |
2: 29,414,376 (GRCm39) |
|
probably null |
Het |
| Med31 |
G |
A |
11: 72,106,294 (GRCm39) |
|
probably benign |
Het |
| Moxd1 |
A |
G |
10: 24,099,700 (GRCm39) |
T67A |
probably benign |
Het |
| Myh3 |
A |
G |
11: 66,985,848 (GRCm39) |
E1266G |
probably damaging |
Het |
| Nkx2-4 |
C |
A |
2: 146,925,924 (GRCm39) |
E313* |
probably null |
Het |
| Nol6 |
G |
T |
4: 41,120,168 (GRCm39) |
R487S |
probably benign |
Het |
| Or2v1 |
C |
A |
11: 49,025,307 (GRCm39) |
A96D |
probably benign |
Het |
| Or2z8 |
T |
A |
8: 72,811,607 (GRCm39) |
F28I |
possibly damaging |
Het |
| Or4k15c |
C |
T |
14: 50,321,329 (GRCm39) |
V270I |
noncoding transcript |
Het |
| Or5p51 |
A |
G |
7: 107,444,368 (GRCm39) |
S191P |
probably damaging |
Het |
| Rnf135 |
A |
G |
11: 80,084,713 (GRCm39) |
D162G |
probably benign |
Het |
| Sdr42e1 |
G |
T |
8: 118,390,502 (GRCm39) |
N46K |
probably benign |
Het |
| Skor2 |
T |
C |
18: 76,946,664 (GRCm39) |
S129P |
unknown |
Het |
| Slc7a11 |
A |
T |
3: 50,382,177 (GRCm39) |
I190N |
probably damaging |
Het |
| Smc5 |
A |
T |
19: 23,186,290 (GRCm39) |
F1056I |
|
Het |
| Son |
A |
T |
16: 91,461,824 (GRCm39) |
Q2243L |
unknown |
Het |
| Sult1a1 |
T |
A |
7: 126,274,280 (GRCm39) |
I101F |
possibly damaging |
Het |
| Sult3a2 |
T |
C |
10: 33,655,747 (GRCm39) |
I77M |
probably benign |
Het |
| Tas1r1 |
A |
T |
4: 152,116,774 (GRCm39) |
S287T |
probably benign |
Het |
| Thbs3 |
A |
C |
3: 89,132,565 (GRCm39) |
T836P |
probably benign |
Het |
| Tlcd3b |
G |
A |
7: 126,423,275 (GRCm39) |
V6M |
probably benign |
Het |
| Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
| Tnfrsf8 |
A |
T |
4: 145,041,653 (GRCm39) |
M1K |
probably null |
Het |
| Vmn1r121 |
T |
G |
7: 20,831,679 (GRCm39) |
N254H |
probably benign |
Het |
| Vmn1r179 |
C |
T |
7: 23,628,436 (GRCm39) |
A209V |
probably benign |
Het |
| Zbtb18 |
T |
C |
1: 177,275,003 (GRCm39) |
V121A |
probably damaging |
Het |
| Zfp30 |
T |
A |
7: 29,488,826 (GRCm39) |
M82K |
probably benign |
Het |
| Zzef1 |
A |
G |
11: 72,765,955 (GRCm39) |
Q1494R |
probably benign |
Het |
|
| Other mutations in Wdr31 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00970:Wdr31
|
APN |
4 |
62,375,757 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01315:Wdr31
|
APN |
4 |
62,374,074 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02345:Wdr31
|
APN |
4 |
62,377,083 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL03192:Wdr31
|
APN |
4 |
62,372,149 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0045:Wdr31
|
UTSW |
4 |
62,382,270 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R0257:Wdr31
|
UTSW |
4 |
62,378,755 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0486:Wdr31
|
UTSW |
4 |
62,372,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1983:Wdr31
|
UTSW |
4 |
62,378,840 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2081:Wdr31
|
UTSW |
4 |
62,374,180 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3620:Wdr31
|
UTSW |
4 |
62,375,701 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4256:Wdr31
|
UTSW |
4 |
62,375,675 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4303:Wdr31
|
UTSW |
4 |
62,378,626 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4562:Wdr31
|
UTSW |
4 |
62,372,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5747:Wdr31
|
UTSW |
4 |
62,381,637 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5986:Wdr31
|
UTSW |
4 |
62,374,113 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6170:Wdr31
|
UTSW |
4 |
62,381,661 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6887:Wdr31
|
UTSW |
4 |
62,375,802 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7126:Wdr31
|
UTSW |
4 |
62,381,666 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7469:Wdr31
|
UTSW |
4 |
62,375,768 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7653:Wdr31
|
UTSW |
4 |
62,381,666 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7727:Wdr31
|
UTSW |
4 |
62,378,873 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8704:Wdr31
|
UTSW |
4 |
62,380,442 (GRCm39) |
missense |
probably benign |
|
|
R9798:Wdr31
|
UTSW |
4 |
62,381,651 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AAGCATGTAGGTGGCCTGAC -3'
(R):5'- CCCTTGCCTGAATTGATATCAC -3'
Sequencing Primer
(F):5'- GAGGTCCTCATGGAATCCTCATG -3'
(R):5'- GCCTGAATTGATATCACTGCCAC -3'
|
| Posted On |
2020-07-28 |
Incidental Mutation