Incidental Mutation 'IGL01764:Ddx56'
| ID |
153639 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ddx56
|
| Ensembl Gene |
ENSMUSG00000004393 |
| Gene Name |
DEAD box helicase 56 |
| Synonyms |
D11Ertd619e, NOH61, DEAD (Asp-Glu-Ala-Asp) box polypeptide 56, 2600001H07Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.968)
|
| Stock # |
IGL01764
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
6208919-6217772 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 6215692 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glycine
at position 219
(V219G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000122368
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000004507]
[ENSMUST00000004508]
[ENSMUST00000151446]
|
| AlphaFold |
Q9D0R4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000004507
AA Change: V237G
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
| SMART Domains |
Protein: ENSMUSP00000004507
Gene: ENSMUSG00000004393
AA Change: V237G
| Domain | Start | End | E-Value | Type |
|---|
|
DEXDc
|
26 |
234 |
4.13e-46 |
SMART |
|
low complexity region
|
246 |
256 |
N/A |
INTRINSIC |
|
HELICc
|
272 |
380 |
2.42e-20 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000004508
|
| SMART Domains |
Protein: ENSMUSP00000004508
Gene: ENSMUSG00000004394
| Domain | Start | End | E-Value | Type |
|---|
|
EMP24_GP25L
|
29 |
222 |
3.21e-79 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139073
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000151446
AA Change: V219G
PolyPhen 2
Score 0.048 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000122368
Gene: ENSMUSG00000004393
AA Change: V219G
| Domain | Start | End | E-Value | Type |
|---|
|
DEXDc
|
26 |
216 |
3.65e-38 |
SMART |
|
low complexity region
|
228 |
236 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155874
|
| 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 encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene shows ATPase activity in the presence of polynucleotides and associates with nucleoplasmic 65S preribosomal particles. This gene may be involved in ribosome synthesis, most likely during assembly of the large 60S ribosomal subunit. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700113H08Rik |
A |
T |
10: 86,909,910 (GRCm39) |
M1L |
probably benign |
Het |
| BC025920 |
T |
A |
10: 81,444,984 (GRCm39) |
Y36N |
probably damaging |
Het |
| Cdk11b |
G |
A |
4: 155,713,260 (GRCm39) |
R112H |
possibly damaging |
Het |
| Ctu2 |
G |
A |
8: 123,206,161 (GRCm39) |
|
probably benign |
Het |
| Dnah14 |
T |
C |
1: 181,572,342 (GRCm39) |
V2891A |
probably benign |
Het |
| Fbn2 |
G |
T |
18: 58,178,423 (GRCm39) |
N1938K |
probably damaging |
Het |
| Fbxw20 |
A |
G |
9: 109,052,427 (GRCm39) |
M302T |
possibly damaging |
Het |
| Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
| Gpat2 |
T |
C |
2: 127,269,456 (GRCm39) |
I36T |
probably benign |
Het |
| Gsta5 |
A |
T |
9: 78,211,789 (GRCm39) |
|
probably null |
Het |
| Hmcn2 |
A |
G |
2: 31,295,642 (GRCm39) |
E2617G |
possibly damaging |
Het |
| Hrob |
T |
C |
11: 102,146,422 (GRCm39) |
C233R |
probably benign |
Het |
| Krba1 |
C |
T |
6: 48,392,770 (GRCm39) |
R895W |
probably benign |
Het |
| Large2 |
G |
T |
2: 92,197,531 (GRCm39) |
|
probably benign |
Het |
| Lrp1b |
C |
T |
2: 40,587,454 (GRCm39) |
V165M |
unknown |
Het |
| Mapk1 |
T |
A |
16: 16,801,597 (GRCm39) |
M36K |
possibly damaging |
Het |
| Nf1 |
A |
G |
11: 79,275,013 (GRCm39) |
T25A |
probably benign |
Het |
| Nrxn3 |
G |
A |
12: 90,171,524 (GRCm39) |
V1316I |
possibly damaging |
Het |
| Pik3r4 |
G |
A |
9: 105,562,321 (GRCm39) |
|
probably benign |
Het |
| Plekhh1 |
G |
T |
12: 79,101,679 (GRCm39) |
A250S |
probably benign |
Het |
| Polr3g |
G |
A |
13: 81,830,238 (GRCm39) |
T145M |
possibly damaging |
Het |
| Prss32 |
A |
G |
17: 24,075,085 (GRCm39) |
D145G |
probably damaging |
Het |
| Rab11fip3 |
T |
C |
17: 26,287,667 (GRCm39) |
K162R |
probably benign |
Het |
| Spag7 |
A |
G |
11: 70,554,933 (GRCm39) |
|
probably benign |
Het |
| Spata2l |
T |
A |
8: 123,960,914 (GRCm39) |
Q125L |
probably benign |
Het |
| Tlr9 |
G |
T |
9: 106,103,004 (GRCm39) |
C765F |
probably damaging |
Het |
| Trip11 |
A |
T |
12: 101,850,890 (GRCm39) |
I773N |
probably damaging |
Het |
| Vcan |
T |
G |
13: 89,873,507 (GRCm39) |
T116P |
probably damaging |
Het |
| Vmn2r22 |
C |
T |
6: 123,627,379 (GRCm39) |
|
probably null |
Het |
| Yme1l1 |
T |
C |
2: 23,052,556 (GRCm39) |
I70T |
probably benign |
Het |
| Zfp938 |
T |
A |
10: 82,063,624 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Ddx56 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01061:Ddx56
|
APN |
11 |
6,214,671 (GRCm39) |
splice site |
probably null |
|
|
IGL02858:Ddx56
|
APN |
11 |
6,217,667 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03075:Ddx56
|
APN |
11 |
6,211,632 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0972:Ddx56
|
UTSW |
11 |
6,217,718 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|
R1652:Ddx56
|
UTSW |
11 |
6,217,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1744:Ddx56
|
UTSW |
11 |
6,216,396 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1793:Ddx56
|
UTSW |
11 |
6,216,934 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1869:Ddx56
|
UTSW |
11 |
6,213,993 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1917:Ddx56
|
UTSW |
11 |
6,213,937 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2415:Ddx56
|
UTSW |
11 |
6,211,727 (GRCm39) |
unclassified |
probably benign |
|
|
R3839:Ddx56
|
UTSW |
11 |
6,217,712 (GRCm39) |
missense |
probably benign |
0.23 |
|
R4445:Ddx56
|
UTSW |
11 |
6,215,770 (GRCm39) |
splice site |
probably null |
|
|
R5041:Ddx56
|
UTSW |
11 |
6,214,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6925:Ddx56
|
UTSW |
11 |
6,213,980 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7412:Ddx56
|
UTSW |
11 |
6,211,720 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8401:Ddx56
|
UTSW |
11 |
6,214,199 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9088:Ddx56
|
UTSW |
11 |
6,209,612 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9382:Ddx56
|
UTSW |
11 |
6,215,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Ddx56
|
UTSW |
11 |
6,217,445 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2014-02-04 |
Incidental Mutation