Incidental Mutation 'IGL01490:Mex3b'
| ID |
88836 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Mex3b
|
| Ensembl Gene |
ENSMUSG00000057706 |
| Gene Name |
mex3 RNA binding family member B |
| Synonyms |
Rkhd3, 4931439A04Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.541)
|
| Stock # |
IGL01490
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
82516541-82520723 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 82519035 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Glutamine
at position 450
(P450Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000082168
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000082237]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000082237
AA Change: P450Q
PolyPhen 2
Score 0.713 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000082168
Gene: ENSMUSG00000057706
AA Change: P450Q
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
32 |
N/A |
INTRINSIC |
|
low complexity region
|
35 |
61 |
N/A |
INTRINSIC |
|
KH
|
71 |
139 |
2.54e-9 |
SMART |
|
KH
|
166 |
233 |
1.6e-15 |
SMART |
|
low complexity region
|
262 |
270 |
N/A |
INTRINSIC |
|
low complexity region
|
295 |
306 |
N/A |
INTRINSIC |
|
low complexity region
|
309 |
320 |
N/A |
INTRINSIC |
|
low complexity region
|
337 |
346 |
N/A |
INTRINSIC |
|
low complexity region
|
367 |
380 |
N/A |
INTRINSIC |
|
low complexity region
|
389 |
424 |
N/A |
INTRINSIC |
|
low complexity region
|
472 |
486 |
N/A |
INTRINSIC |
|
low complexity region
|
494 |
515 |
N/A |
INTRINSIC |
|
RING
|
525 |
564 |
3.24e-4 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000209046
|
| 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 an RNA-binding phosphoprotein that is part of the MEX3 (muscle excess 3) family of translational regulators. The encoded protein contains N-terminal nuclear export and nuclear localization signals and is exported from the cytoplasm to the nucleus. The protein binds to RNA via two KH domains and also colocalizes with MEX3A, Dcp1A decapping factor and Argonaute proteins within P (processing) bodies. [provided by RefSeq, Oct 2012]
PHENOTYPE: Homozygous inactivation of this gene leads to partial neonatal lethality, decreased body weight and subfertility. Males show seminiferous tubule obstruction, oligozoospermia, abnormalities in Sertoli cell barrier morphology and function, and impaired Sertoli cell and macrophage phagocytosis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 34 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca2 |
A |
G |
2: 25,336,023 (GRCm39) |
Y2131C |
probably damaging |
Het |
| Ano6 |
T |
A |
15: 95,846,291 (GRCm39) |
S510T |
probably benign |
Het |
| Asb16 |
A |
T |
11: 102,167,575 (GRCm39) |
N314Y |
probably damaging |
Het |
| Atp6v0b |
G |
A |
4: 117,742,303 (GRCm39) |
Q150* |
probably null |
Het |
| Chct1 |
A |
G |
11: 85,069,138 (GRCm39) |
D52G |
probably damaging |
Het |
| Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
| Cmklr2 |
T |
C |
1: 63,222,455 (GRCm39) |
Y260C |
probably damaging |
Het |
| Crim1 |
A |
G |
17: 78,642,725 (GRCm39) |
D481G |
possibly damaging |
Het |
| Dnajb2 |
T |
C |
1: 75,213,534 (GRCm39) |
S3P |
probably damaging |
Het |
| Dnajb9 |
A |
T |
12: 44,253,869 (GRCm39) |
S179R |
possibly damaging |
Het |
| Dock2 |
A |
T |
11: 34,596,608 (GRCm39) |
I416N |
probably damaging |
Het |
| Dock7 |
G |
T |
4: 98,833,355 (GRCm39) |
|
probably benign |
Het |
| Eif6 |
T |
C |
2: 155,668,102 (GRCm39) |
I46V |
probably benign |
Het |
| Fcgr1 |
T |
C |
3: 96,191,686 (GRCm39) |
D374G |
probably benign |
Het |
| Gatad2b |
A |
G |
3: 90,259,385 (GRCm39) |
I374V |
possibly damaging |
Het |
| Gfpt2 |
T |
C |
11: 49,717,954 (GRCm39) |
|
probably benign |
Het |
| H2-M10.2 |
G |
T |
17: 36,596,377 (GRCm39) |
T156K |
probably damaging |
Het |
| Il20rb |
T |
A |
9: 100,355,207 (GRCm39) |
I79F |
probably damaging |
Het |
| Kcnip3 |
C |
T |
2: 127,352,799 (GRCm39) |
R44H |
probably benign |
Het |
| Lama1 |
A |
T |
17: 68,057,579 (GRCm39) |
D551V |
possibly damaging |
Het |
| Mmp20 |
T |
C |
9: 7,628,330 (GRCm39) |
L26P |
probably benign |
Het |
| Msh3 |
G |
A |
13: 92,436,813 (GRCm39) |
T499M |
probably damaging |
Het |
| Myo18b |
T |
C |
5: 112,957,566 (GRCm39) |
S1466G |
possibly damaging |
Het |
| Myom3 |
A |
G |
4: 135,538,089 (GRCm39) |
R1324G |
possibly damaging |
Het |
| Nxph3 |
A |
G |
11: 95,401,919 (GRCm39) |
I165T |
possibly damaging |
Het |
| Prex2 |
G |
A |
1: 11,254,769 (GRCm39) |
|
probably null |
Het |
| Ptpn6 |
T |
A |
6: 124,705,307 (GRCm39) |
E208V |
probably damaging |
Het |
| Qpct |
T |
C |
17: 79,397,169 (GRCm39) |
V354A |
probably benign |
Het |
| Rfx4 |
A |
G |
10: 84,676,715 (GRCm39) |
I108V |
possibly damaging |
Het |
| Tmem67 |
A |
G |
4: 12,057,422 (GRCm39) |
|
probably benign |
Het |
| Trappc12 |
A |
T |
12: 28,796,914 (GRCm39) |
I206N |
probably damaging |
Het |
| Vmn1r173 |
A |
T |
7: 23,402,132 (GRCm39) |
K122N |
probably benign |
Het |
| Wdr35 |
G |
T |
12: 9,027,381 (GRCm39) |
G54V |
probably damaging |
Het |
| Zfyve26 |
A |
T |
12: 79,291,147 (GRCm39) |
C2153S |
probably damaging |
Het |
|
| Other mutations in Mex3b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00565:Mex3b
|
APN |
7 |
82,518,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01112:Mex3b
|
APN |
7 |
82,518,911 (GRCm39) |
missense |
probably benign |
0.41 |
|
IGL01809:Mex3b
|
APN |
7 |
82,518,920 (GRCm39) |
missense |
probably benign |
|
|
IGL02328:Mex3b
|
APN |
7 |
82,518,920 (GRCm39) |
missense |
probably benign |
|
|
R0218:Mex3b
|
UTSW |
7 |
82,518,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0653:Mex3b
|
UTSW |
7 |
82,518,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2360:Mex3b
|
UTSW |
7 |
82,517,070 (GRCm39) |
missense |
probably benign |
0.16 |
|
R4184:Mex3b
|
UTSW |
7 |
82,519,238 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4397:Mex3b
|
UTSW |
7 |
82,519,031 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4771:Mex3b
|
UTSW |
7 |
82,518,273 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4945:Mex3b
|
UTSW |
7 |
82,519,382 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5189:Mex3b
|
UTSW |
7 |
82,518,459 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6962:Mex3b
|
UTSW |
7 |
82,518,473 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7021:Mex3b
|
UTSW |
7 |
82,519,080 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R7381:Mex3b
|
UTSW |
7 |
82,518,073 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7483:Mex3b
|
UTSW |
7 |
82,517,114 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8398:Mex3b
|
UTSW |
7 |
82,518,842 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9288:Mex3b
|
UTSW |
7 |
82,518,159 (GRCm39) |
missense |
probably benign |
0.02 |
|
RF009:Mex3b
|
UTSW |
7 |
82,516,968 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2013-11-18 |
Incidental Mutation