Incidental Mutation 'IGL01014:Meis3'
| ID |
53667 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Meis3
|
| Ensembl Gene |
ENSMUSG00000041420 |
| Gene Name |
Meis homeobox 3 |
| Synonyms |
Mrg2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.105)
|
| Stock # |
IGL01014
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
15909015-15920429 bp(+) (GRCm39) |
| Type of Mutation |
critical splice acceptor site |
| DNA Base Change (assembly) |
C to T
at 15912872 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000002495]
[ENSMUST00000176342]
[ENSMUST00000176446]
[ENSMUST00000176506]
[ENSMUST00000177156]
[ENSMUST00000177540]
|
| AlphaFold |
P97368 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000002495
|
| SMART Domains |
Protein: ENSMUSP00000002495
Gene: ENSMUSG00000041420
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
88 |
101 |
N/A |
INTRINSIC |
|
low complexity region
|
230 |
244 |
N/A |
INTRINSIC |
|
HOX
|
265 |
330 |
9.15e-12 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000175946
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000176083
|
| SMART Domains |
Protein: ENSMUSP00000135196
Gene: ENSMUSG00000041420
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Meis_PKNOX_N
|
99 |
183 |
6.5e-47 |
PFAM |
|
low complexity region
|
230 |
244 |
N/A |
INTRINSIC |
|
HOX
|
265 |
330 |
9.15e-12 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000176342
|
| SMART Domains |
Protein: ENSMUSP00000135302
Gene: ENSMUSG00000041420
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
88 |
101 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000176446
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000176506
|
| SMART Domains |
Protein: ENSMUSP00000134918
Gene: ENSMUSG00000041420
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
88 |
101 |
N/A |
INTRINSIC |
|
low complexity region
|
213 |
227 |
N/A |
INTRINSIC |
|
HOX
|
248 |
313 |
9.15e-12 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000177156
|
| SMART Domains |
Protein: ENSMUSP00000135103
Gene: ENSMUSG00000041420
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
88 |
101 |
N/A |
INTRINSIC |
|
low complexity region
|
230 |
244 |
N/A |
INTRINSIC |
|
Pfam:Homeobox_KN
|
283 |
313 |
2e-12 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183527
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000177540
|
| SMART Domains |
Protein: ENSMUSP00000135388
Gene: ENSMUSG00000041420
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
88 |
101 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: The protein encoding this gene belongs to the three amino acid loop extension family of homeodomain transcription factors, which play essential roles in many embryonic processes. These proteins are characterized by an atypical homeodomain containing a three amino acid loop extension between helices 1 and 2. Expression of this gene begins during the compaction stage of embryogenesis and continues into the blastocyst stage. This gene is also expressed in pancreatic islet cells and beta-cells and regulates beta-cell survival. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgra1 |
G |
A |
7: 139,455,576 (GRCm39) |
M401I |
probably benign |
Het |
| Adgra1 |
C |
T |
7: 139,455,577 (GRCm39) |
H402Y |
probably damaging |
Het |
| Akap13 |
T |
C |
7: 75,400,381 (GRCm39) |
|
probably benign |
Het |
| Akap9 |
A |
G |
5: 4,018,683 (GRCm39) |
E1088G |
probably benign |
Het |
| Aox1 |
T |
C |
1: 58,361,960 (GRCm39) |
F722S |
possibly damaging |
Het |
| Arhgef39 |
G |
A |
4: 43,499,502 (GRCm39) |
R36C |
probably damaging |
Het |
| Art2a |
C |
A |
7: 101,204,115 (GRCm39) |
C141F |
probably damaging |
Het |
| Brwd1 |
A |
G |
16: 95,817,373 (GRCm39) |
F1380L |
probably benign |
Het |
| Cadps2 |
A |
T |
6: 23,496,873 (GRCm39) |
N102K |
possibly damaging |
Het |
| Ccdc30 |
C |
A |
4: 119,250,776 (GRCm39) |
R22L |
possibly damaging |
Het |
| Ccdc74a |
A |
T |
16: 17,467,661 (GRCm39) |
T200S |
possibly damaging |
Het |
| Cd200 |
G |
A |
16: 45,215,063 (GRCm39) |
T196I |
probably benign |
Het |
| Cd244a |
A |
G |
1: 171,401,856 (GRCm39) |
Y194C |
probably damaging |
Het |
| Cdh23 |
T |
C |
10: 60,143,301 (GRCm39) |
T3009A |
probably damaging |
Het |
| Clec12b |
T |
A |
6: 129,362,393 (GRCm39) |
N21Y |
probably damaging |
Het |
| Cntln |
A |
G |
4: 84,968,145 (GRCm39) |
E788G |
probably benign |
Het |
| Col11a1 |
C |
T |
3: 113,917,458 (GRCm39) |
|
probably benign |
Het |
| Cttnbp2 |
T |
A |
6: 18,423,894 (GRCm39) |
N810I |
probably damaging |
Het |
| Dhx15 |
A |
T |
5: 52,309,266 (GRCm39) |
V719D |
probably damaging |
Het |
| Dnah6 |
A |
G |
6: 73,051,764 (GRCm39) |
|
probably benign |
Het |
| Dnajc13 |
A |
G |
9: 104,080,417 (GRCm39) |
I888T |
probably damaging |
Het |
| Fasn |
T |
C |
11: 120,708,055 (GRCm39) |
K666E |
probably damaging |
Het |
| Gnas |
C |
T |
2: 174,139,767 (GRCm39) |
|
probably benign |
Het |
| Lmntd2 |
T |
C |
7: 140,793,952 (GRCm39) |
Q7R |
probably damaging |
Het |
| Lmo7 |
G |
A |
14: 102,157,993 (GRCm39) |
|
probably benign |
Het |
| Lrrc55 |
A |
G |
2: 85,026,559 (GRCm39) |
I155T |
possibly damaging |
Het |
| Mib2 |
C |
T |
4: 155,742,187 (GRCm39) |
V334M |
probably damaging |
Het |
| Myo3a |
A |
G |
2: 22,337,284 (GRCm39) |
I386V |
probably benign |
Het |
| Neb |
C |
A |
2: 52,177,170 (GRCm39) |
M1390I |
probably benign |
Het |
| Nmd3 |
G |
A |
3: 69,633,719 (GRCm39) |
V69I |
probably benign |
Het |
| Nsmce3 |
G |
T |
7: 64,522,382 (GRCm39) |
D95E |
possibly damaging |
Het |
| Or4c12 |
T |
C |
2: 89,773,604 (GRCm39) |
Y285C |
probably damaging |
Het |
| Or4f58 |
A |
G |
2: 111,851,477 (GRCm39) |
S241P |
probably damaging |
Het |
| Or5w16 |
T |
C |
2: 87,577,469 (GRCm39) |
F310L |
probably benign |
Het |
| Pde4d |
T |
C |
13: 110,086,036 (GRCm39) |
V538A |
probably damaging |
Het |
| Pgap6 |
T |
A |
17: 26,335,983 (GRCm39) |
|
probably benign |
Het |
| Plxnb1 |
A |
T |
9: 108,935,102 (GRCm39) |
H982L |
probably benign |
Het |
| Pold2 |
G |
T |
11: 5,822,293 (GRCm39) |
Q459K |
probably benign |
Het |
| Ptpn14 |
G |
A |
1: 189,554,830 (GRCm39) |
R130Q |
probably damaging |
Het |
| Rnf10 |
A |
T |
5: 115,395,042 (GRCm39) |
L182Q |
probably damaging |
Het |
| Syne2 |
G |
A |
12: 75,952,051 (GRCm39) |
D440N |
probably damaging |
Het |
| Tlcd1 |
G |
A |
11: 78,070,283 (GRCm39) |
|
probably null |
Het |
| Tpte |
A |
T |
8: 22,810,898 (GRCm39) |
Y185F |
probably benign |
Het |
|
| Other mutations in Meis3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02508:Meis3
|
APN |
7 |
15,912,722 (GRCm39) |
splice site |
probably null |
|
|
IGL03125:Meis3
|
APN |
7 |
15,912,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03383:Meis3
|
APN |
7 |
15,917,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0032:Meis3
|
UTSW |
7 |
15,916,210 (GRCm39) |
unclassified |
probably benign |
|
|
R1147:Meis3
|
UTSW |
7 |
15,917,701 (GRCm39) |
unclassified |
probably benign |
|
|
R1471:Meis3
|
UTSW |
7 |
15,911,496 (GRCm39) |
nonsense |
probably null |
|
|
R3054:Meis3
|
UTSW |
7 |
15,916,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3927:Meis3
|
UTSW |
7 |
15,911,419 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5314:Meis3
|
UTSW |
7 |
15,917,989 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6713:Meis3
|
UTSW |
7 |
15,916,255 (GRCm39) |
nonsense |
probably null |
|
|
R6847:Meis3
|
UTSW |
7 |
15,917,789 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7218:Meis3
|
UTSW |
7 |
15,918,626 (GRCm39) |
missense |
probably benign |
|
|
R7517:Meis3
|
UTSW |
7 |
15,911,743 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7540:Meis3
|
UTSW |
7 |
15,911,418 (GRCm39) |
nonsense |
probably null |
|
|
R7699:Meis3
|
UTSW |
7 |
15,911,481 (GRCm39) |
missense |
probably benign |
|
|
R7700:Meis3
|
UTSW |
7 |
15,911,481 (GRCm39) |
missense |
probably benign |
|
|
R7790:Meis3
|
UTSW |
7 |
15,916,322 (GRCm39) |
missense |
probably benign |
0.37 |
|
R8902:Meis3
|
UTSW |
7 |
15,911,887 (GRCm39) |
missense |
probably benign |
0.17 |
|
R8909:Meis3
|
UTSW |
7 |
15,919,385 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9095:Meis3
|
UTSW |
7 |
15,917,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-06-28 |
Incidental Mutation