Incidental Mutation 'IGL01095:Ddx42'
| ID |
52276 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ddx42
|
| Ensembl Gene |
ENSMUSG00000020705 |
| Gene Name |
DEAD box helicase 42 |
| Synonyms |
DEAD (Asp-Glu-Ala-Asp) box polypeptide 42, B430002H05Rik, 1810047H21Rik, SF3b125 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01095
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
106107752-106139965 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 106138325 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 708
(Y708C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000021046
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021046]
[ENSMUST00000021048]
|
| AlphaFold |
Q810A7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000021046
AA Change: Y708C
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000021046
Gene: ENSMUSG00000020705
AA Change: Y708C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
35 |
52 |
N/A |
INTRINSIC |
|
low complexity region
|
68 |
82 |
N/A |
INTRINSIC |
|
low complexity region
|
108 |
114 |
N/A |
INTRINSIC |
|
coiled coil region
|
116 |
143 |
N/A |
INTRINSIC |
|
low complexity region
|
149 |
158 |
N/A |
INTRINSIC |
|
DEXDc
|
272 |
474 |
7.61e-68 |
SMART |
|
HELICc
|
512 |
593 |
1.58e-33 |
SMART |
|
low complexity region
|
644 |
659 |
N/A |
INTRINSIC |
|
low complexity region
|
722 |
737 |
N/A |
INTRINSIC |
|
low complexity region
|
814 |
838 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021048
|
| SMART Domains |
Protein: ENSMUSP00000021048
Gene: ENSMUSG00000020706
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:FtsJ
|
24 |
200 |
2.8e-56 |
PFAM |
|
low complexity region
|
203 |
218 |
N/A |
INTRINSIC |
|
Pfam:DUF3381
|
231 |
398 |
1.3e-48 |
PFAM |
|
low complexity region
|
456 |
475 |
N/A |
INTRINSIC |
|
low complexity region
|
560 |
568 |
N/A |
INTRINSIC |
|
Pfam:Spb1_C
|
597 |
831 |
1.8e-72 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126938
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154635
|
| 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 Asp-Glu-Ala-Asp (DEAD) box protein family. Members of this protein family are putative RNA helicases, and 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. Members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam34l |
T |
A |
8: 44,079,133 (GRCm39) |
I364L |
probably benign |
Het |
| Adgra1 |
A |
G |
7: 139,425,570 (GRCm39) |
T28A |
possibly damaging |
Het |
| Aldh8a1 |
A |
G |
10: 21,265,180 (GRCm39) |
E269G |
probably benign |
Het |
| Alkbh7 |
A |
G |
17: 57,304,470 (GRCm39) |
|
probably null |
Het |
| Ap1g2 |
T |
C |
14: 55,342,571 (GRCm39) |
T129A |
probably benign |
Het |
| Ap1s1 |
A |
G |
5: 137,070,663 (GRCm39) |
I117T |
probably damaging |
Het |
| Brca1 |
G |
A |
11: 101,415,195 (GRCm39) |
P119S |
possibly damaging |
Het |
| Chid1 |
A |
G |
7: 141,110,142 (GRCm39) |
V62A |
probably damaging |
Het |
| Cpa1 |
A |
T |
6: 30,642,968 (GRCm39) |
I299F |
probably benign |
Het |
| Cuzd1 |
A |
G |
7: 130,917,865 (GRCm39) |
V245A |
probably damaging |
Het |
| Ddx39b |
T |
C |
17: 35,465,937 (GRCm39) |
S71P |
probably benign |
Het |
| Dnah3 |
C |
A |
7: 119,550,820 (GRCm39) |
L3166F |
probably benign |
Het |
| Erap1 |
A |
G |
13: 74,816,213 (GRCm39) |
E114G |
probably benign |
Het |
| Fap |
G |
A |
2: 62,354,545 (GRCm39) |
T448I |
possibly damaging |
Het |
| Fhl2 |
A |
T |
1: 43,170,841 (GRCm39) |
Y158N |
probably benign |
Het |
| Fscb |
A |
G |
12: 64,520,155 (GRCm39) |
V437A |
possibly damaging |
Het |
| Il18 |
A |
T |
9: 50,490,629 (GRCm39) |
D88V |
probably damaging |
Het |
| Il5ra |
A |
T |
6: 106,719,605 (GRCm39) |
|
probably benign |
Het |
| Jakmip3 |
A |
T |
7: 138,622,546 (GRCm39) |
Q302L |
probably damaging |
Het |
| Lrp2 |
A |
T |
2: 69,322,776 (GRCm39) |
Y1857* |
probably null |
Het |
| Meis2 |
T |
C |
2: 115,694,905 (GRCm39) |
T406A |
probably benign |
Het |
| Mre11a |
T |
A |
9: 14,721,120 (GRCm39) |
S346R |
probably benign |
Het |
| Myh15 |
A |
T |
16: 48,952,378 (GRCm39) |
K816M |
probably damaging |
Het |
| Mysm1 |
C |
T |
4: 94,856,106 (GRCm39) |
|
probably null |
Het |
| Nyap1 |
C |
A |
5: 137,736,346 (GRCm39) |
R47L |
probably damaging |
Het |
| Oas3 |
A |
G |
5: 120,910,954 (GRCm39) |
Y209H |
probably damaging |
Het |
| Or2v2 |
T |
G |
11: 49,003,680 (GRCm39) |
Y291S |
probably damaging |
Het |
| Or4g16 |
A |
G |
2: 111,136,966 (GRCm39) |
R139G |
probably benign |
Het |
| Or6c209 |
A |
G |
10: 129,483,498 (GRCm39) |
D167G |
probably benign |
Het |
| Or8b42 |
A |
G |
9: 38,341,811 (GRCm39) |
I78V |
probably benign |
Het |
| Or8d6 |
T |
C |
9: 39,853,976 (GRCm39) |
V140A |
probably benign |
Het |
| Pde4b |
T |
C |
4: 102,363,241 (GRCm39) |
|
probably null |
Het |
| Psd3 |
G |
A |
8: 68,361,165 (GRCm39) |
T99M |
probably damaging |
Het |
| R3hcc1 |
T |
C |
14: 69,937,477 (GRCm39) |
E390G |
probably damaging |
Het |
| Rabgap1l |
A |
C |
1: 160,566,539 (GRCm39) |
C58W |
probably benign |
Het |
| Rasd1 |
A |
G |
11: 59,855,117 (GRCm39) |
I121T |
probably damaging |
Het |
| Spta1 |
A |
G |
1: 174,041,051 (GRCm39) |
N1284D |
probably benign |
Het |
| Tpr |
T |
C |
1: 150,285,891 (GRCm39) |
V525A |
possibly damaging |
Het |
|
| Other mutations in Ddx42 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00719:Ddx42
|
APN |
11 |
106,126,575 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL00833:Ddx42
|
APN |
11 |
106,122,004 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
IGL01651:Ddx42
|
APN |
11 |
106,138,855 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01715:Ddx42
|
APN |
11 |
106,115,101 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02097:Ddx42
|
APN |
11 |
106,129,986 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03182:Ddx42
|
APN |
11 |
106,138,353 (GRCm39) |
missense |
probably benign |
|
|
P0045:Ddx42
|
UTSW |
11 |
106,122,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0504:Ddx42
|
UTSW |
11 |
106,138,675 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0646:Ddx42
|
UTSW |
11 |
106,123,659 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2277:Ddx42
|
UTSW |
11 |
106,133,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2279:Ddx42
|
UTSW |
11 |
106,133,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2297:Ddx42
|
UTSW |
11 |
106,133,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2336:Ddx42
|
UTSW |
11 |
106,121,976 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R2519:Ddx42
|
UTSW |
11 |
106,136,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3413:Ddx42
|
UTSW |
11 |
106,138,636 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3498:Ddx42
|
UTSW |
11 |
106,122,019 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R3883:Ddx42
|
UTSW |
11 |
106,138,518 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4421:Ddx42
|
UTSW |
11 |
106,121,964 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4696:Ddx42
|
UTSW |
11 |
106,138,529 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4953:Ddx42
|
UTSW |
11 |
106,133,766 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5398:Ddx42
|
UTSW |
11 |
106,115,724 (GRCm39) |
missense |
probably benign |
|
|
R5669:Ddx42
|
UTSW |
11 |
106,132,645 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6091:Ddx42
|
UTSW |
11 |
106,125,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6139:Ddx42
|
UTSW |
11 |
106,130,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6643:Ddx42
|
UTSW |
11 |
106,119,646 (GRCm39) |
missense |
probably benign |
0.14 |
|
R6991:Ddx42
|
UTSW |
11 |
106,129,970 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7351:Ddx42
|
UTSW |
11 |
106,138,508 (GRCm39) |
missense |
probably benign |
|
|
R7502:Ddx42
|
UTSW |
11 |
106,138,565 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7792:Ddx42
|
UTSW |
11 |
106,127,822 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8145:Ddx42
|
UTSW |
11 |
106,130,887 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8425:Ddx42
|
UTSW |
11 |
106,138,550 (GRCm39) |
missense |
probably benign |
|
|
R9265:Ddx42
|
UTSW |
11 |
106,132,435 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9523:Ddx42
|
UTSW |
11 |
106,132,606 (GRCm39) |
missense |
probably benign |
0.40 |
|
R9681:Ddx42
|
UTSW |
11 |
106,125,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF018:Ddx42
|
UTSW |
11 |
106,123,630 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
| Posted On |
2013-06-21 |
Incidental Mutation