Incidental Mutation 'R5201:Mpped2'
| ID |
400752 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mpped2
|
| Ensembl Gene |
ENSMUSG00000016386 |
| Gene Name |
metallophosphoesterase domain containing 2 |
| Synonyms |
239Fb, 2700082O15Rik |
| MMRRC Submission |
042776-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R5201 (G1)
|
| Quality Score |
212 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
106523614-106698701 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 106529847 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Serine
at position 32
(N32S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000114253
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000016530]
[ENSMUST00000111063]
[ENSMUST00000125023]
[ENSMUST00000144155]
|
| AlphaFold |
Q9CZJ0 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000016530
AA Change: N32S
PolyPhen 2
Score 0.506 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000016530
Gene: ENSMUSG00000016386
AA Change: N32S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Metallophos
|
58 |
256 |
3e-13 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000111063
AA Change: N32S
PolyPhen 2
Score 0.506 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000106692
Gene: ENSMUSG00000016386
AA Change: N32S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Metallophos
|
58 |
256 |
1.5e-10 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124461
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000125023
AA Change: N32S
PolyPhen 2
Score 0.719 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000123267
Gene: ENSMUSG00000016386
AA Change: N32S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Metallophos
|
58 |
256 |
1.7e-10 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000144155
AA Change: N32S
PolyPhen 2
Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000114253
Gene: ENSMUSG00000016386
AA Change: N32S
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:3RL3|A
|
1 |
67 |
2e-43 |
PDB |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.0%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene likely encodes a metallophosphoesterase. The encoded protein may play a role a brain development. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930407I10Rik |
C |
A |
15: 81,946,745 (GRCm39) |
T214N |
probably benign |
Het |
| Actn4 |
A |
T |
7: 28,615,680 (GRCm39) |
|
probably null |
Het |
| Arap2 |
T |
C |
5: 62,840,832 (GRCm39) |
E678G |
probably damaging |
Het |
| Atl2 |
T |
C |
17: 80,172,580 (GRCm39) |
N130S |
probably benign |
Het |
| Cby2 |
A |
G |
14: 75,821,449 (GRCm39) |
V101A |
probably damaging |
Het |
| Cyp2b10 |
A |
G |
7: 25,616,419 (GRCm39) |
D342G |
probably damaging |
Het |
| Dnah6 |
A |
G |
6: 73,172,715 (GRCm39) |
Y248H |
possibly damaging |
Het |
| Drd5 |
A |
T |
5: 38,477,366 (GRCm39) |
M120L |
probably damaging |
Het |
| Duox1 |
A |
G |
2: 122,158,403 (GRCm39) |
R629G |
probably benign |
Het |
| Dyrk1b |
A |
G |
7: 27,884,521 (GRCm39) |
Y279C |
probably damaging |
Het |
| Efemp1 |
A |
T |
11: 28,864,590 (GRCm39) |
I215L |
probably benign |
Het |
| Enpp6 |
C |
A |
8: 47,518,486 (GRCm39) |
Q205K |
probably damaging |
Het |
| Fam170a |
A |
T |
18: 50,415,193 (GRCm39) |
T280S |
probably benign |
Het |
| Fam222a |
G |
A |
5: 114,749,127 (GRCm39) |
A108T |
possibly damaging |
Het |
| Fgd3 |
G |
T |
13: 49,449,854 (GRCm39) |
P132T |
probably benign |
Het |
| Fzr1 |
A |
T |
10: 81,203,362 (GRCm39) |
L399H |
probably damaging |
Het |
| Galnt15 |
G |
A |
14: 31,771,822 (GRCm39) |
R289Q |
probably damaging |
Het |
| Hira |
T |
C |
16: 18,770,865 (GRCm39) |
V834A |
probably damaging |
Het |
| Ilf3 |
T |
C |
9: 21,300,679 (GRCm39) |
L93P |
probably damaging |
Het |
| Itgae |
G |
A |
11: 73,001,382 (GRCm39) |
R71Q |
probably benign |
Het |
| Itprid1 |
T |
C |
6: 55,944,991 (GRCm39) |
S571P |
probably benign |
Het |
| Kif14 |
T |
A |
1: 136,431,145 (GRCm39) |
S1181T |
probably benign |
Het |
| Lrig3 |
C |
A |
10: 125,849,020 (GRCm39) |
P946Q |
possibly damaging |
Het |
| Macf1 |
A |
T |
4: 123,369,738 (GRCm39) |
C1674* |
probably null |
Het |
| Malt1 |
A |
G |
18: 65,609,126 (GRCm39) |
K710R |
probably benign |
Het |
| Man1a2 |
A |
T |
3: 100,524,328 (GRCm39) |
N373K |
probably benign |
Het |
| Mrtfb |
A |
C |
16: 13,219,456 (GRCm39) |
T701P |
probably benign |
Het |
| Myh10 |
A |
T |
11: 68,674,021 (GRCm39) |
T652S |
probably damaging |
Het |
| Nfia |
A |
G |
4: 97,999,462 (GRCm39) |
Y485C |
probably damaging |
Het |
| Olfml2b |
A |
T |
1: 170,496,433 (GRCm39) |
T355S |
probably benign |
Het |
| Or10q3 |
A |
T |
19: 11,847,995 (GRCm39) |
I195K |
probably benign |
Het |
| Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
| Pcdh1 |
A |
T |
18: 38,331,971 (GRCm39) |
V344D |
probably damaging |
Het |
| Plekhn1 |
C |
A |
4: 156,314,984 (GRCm39) |
V558L |
probably benign |
Het |
| Prr14l |
A |
G |
5: 32,987,591 (GRCm39) |
S635P |
possibly damaging |
Het |
| Prss46 |
T |
A |
9: 110,680,543 (GRCm39) |
C229* |
probably null |
Het |
| Rad50 |
A |
G |
11: 53,589,647 (GRCm39) |
|
probably null |
Het |
| Slc27a3 |
A |
T |
3: 90,296,526 (GRCm39) |
L191Q |
probably benign |
Het |
| Surf4 |
A |
G |
2: 26,823,778 (GRCm39) |
|
probably benign |
Het |
| Taf3 |
A |
G |
2: 9,956,995 (GRCm39) |
S391P |
probably damaging |
Het |
| Tep1 |
A |
C |
14: 51,105,567 (GRCm39) |
L151R |
probably benign |
Het |
| Tmprss11d |
A |
C |
5: 86,457,214 (GRCm39) |
N148K |
possibly damaging |
Het |
| Tpd52l2 |
G |
A |
2: 181,156,879 (GRCm39) |
V172I |
probably benign |
Het |
| Vmn2r77 |
A |
G |
7: 86,460,846 (GRCm39) |
D724G |
probably damaging |
Het |
| Wdr75 |
T |
A |
1: 45,862,519 (GRCm39) |
D779E |
probably benign |
Het |
| Zfp943 |
A |
T |
17: 22,211,794 (GRCm39) |
K293N |
probably damaging |
Het |
|
| Other mutations in Mpped2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01068:Mpped2
|
APN |
2 |
106,695,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01734:Mpped2
|
APN |
2 |
106,614,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03031:Mpped2
|
APN |
2 |
106,613,968 (GRCm39) |
splice site |
probably benign |
|
|
LCD18:Mpped2
|
UTSW |
2 |
106,551,773 (GRCm39) |
intron |
probably benign |
|
|
R1446:Mpped2
|
UTSW |
2 |
106,614,077 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1460:Mpped2
|
UTSW |
2 |
106,575,237 (GRCm39) |
unclassified |
probably benign |
|
|
R1857:Mpped2
|
UTSW |
2 |
106,613,989 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1888:Mpped2
|
UTSW |
2 |
106,529,790 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1888:Mpped2
|
UTSW |
2 |
106,529,790 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1919:Mpped2
|
UTSW |
2 |
106,697,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2073:Mpped2
|
UTSW |
2 |
106,575,147 (GRCm39) |
nonsense |
probably null |
|
|
R2074:Mpped2
|
UTSW |
2 |
106,575,147 (GRCm39) |
nonsense |
probably null |
|
|
R2075:Mpped2
|
UTSW |
2 |
106,575,147 (GRCm39) |
nonsense |
probably null |
|
|
R2295:Mpped2
|
UTSW |
2 |
106,529,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4720:Mpped2
|
UTSW |
2 |
106,614,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4851:Mpped2
|
UTSW |
2 |
106,529,724 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R6500:Mpped2
|
UTSW |
2 |
106,691,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6603:Mpped2
|
UTSW |
2 |
106,697,322 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6994:Mpped2
|
UTSW |
2 |
106,529,878 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7807:Mpped2
|
UTSW |
2 |
106,575,085 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R8827:Mpped2
|
UTSW |
2 |
106,691,928 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8878:Mpped2
|
UTSW |
2 |
106,575,065 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8932:Mpped2
|
UTSW |
2 |
106,697,395 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R9024:Mpped2
|
UTSW |
2 |
106,614,043 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9207:Mpped2
|
UTSW |
2 |
106,697,319 (GRCm39) |
missense |
probably benign |
0.15 |
|
Z1177:Mpped2
|
UTSW |
2 |
106,691,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Mpped2
|
UTSW |
2 |
106,575,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCTTGGATTCAGAGGTTGGC -3'
(R):5'- CTGTCTGTGAAACTGCAGATACC -3'
Sequencing Primer
(F):5'- GTTGGCTGAAACCCATCATG -3'
(R):5'- CCATCTGTTTGGGAAATCACTGAC -3'
|
| Posted On |
2016-07-06 |
Incidental Mutation