Incidental Mutation 'IGL01718:Mars1'
| ID |
105000 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Mars1
|
| Ensembl Gene |
ENSMUSG00000040354 |
| Gene Name |
methionine-tRNA synthetase 1 |
| Synonyms |
MetRS, Mars, methionine tRNA ligase, methionyl-tRNA synthetase |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.967)
|
| Stock # |
IGL01718
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
127132090-127147655 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 127141707 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glycine
at position 266
(R266G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000130666
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037290]
[ENSMUST00000171564]
|
| AlphaFold |
Q68FL6 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000037290
AA Change: R266G
PolyPhen 2
Score 0.955 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000037446
Gene: ENSMUSG00000040354
AA Change: R266G
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:4BL7|A
|
1 |
220 |
1e-118 |
PDB |
|
low complexity region
|
221 |
233 |
N/A |
INTRINSIC |
|
Pfam:tRNA-synt_1g
|
268 |
660 |
6.8e-142 |
PFAM |
|
WHEP-TRS
|
847 |
902 |
7.95e-14 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128369
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145275
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000171564
AA Change: R266G
PolyPhen 2
Score 0.955 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000130666
Gene: ENSMUSG00000040354
AA Change: R266G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
26 |
N/A |
INTRINSIC |
|
Pfam:GST_C
|
94 |
180 |
1e-6 |
PFAM |
|
low complexity region
|
205 |
213 |
N/A |
INTRINSIC |
|
low complexity region
|
221 |
233 |
N/A |
INTRINSIC |
|
Pfam:tRNA-synt_1g
|
268 |
660 |
9.6e-149 |
PFAM |
|
WHEP-TRS
|
855 |
910 |
7.95e-14 |
SMART |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: The encoded protein belongs to the class I family of tRNA synthetases, a class of enzymes that charge tRNAs with their cognate amino acids. The related human gene product is essential for the translation initiation of mRNAs. This gene has an overlapping 3' UTR tail-to-tail arrangement with an adjacent gene on the opposite strand that encodes an inhibitor of the CCAAT/enhancer-binding protein's DNA binding activity. This arrangement, conserved in human and mouse, may be involved in mRNA stability and possible functional and regulatory interaction of these adjacent overlapping genes. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2010]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 28 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aldh1a3 |
A |
G |
7: 66,049,953 (GRCm39) |
F422L |
possibly damaging |
Het |
| Ap2m1 |
T |
C |
16: 20,360,944 (GRCm39) |
|
probably benign |
Het |
| Asic1 |
A |
G |
15: 99,569,883 (GRCm39) |
Y68C |
probably damaging |
Het |
| Ccdc18 |
A |
G |
5: 108,349,214 (GRCm39) |
D1002G |
possibly damaging |
Het |
| Cyp2c29 |
A |
T |
19: 39,318,704 (GRCm39) |
I434F |
possibly damaging |
Het |
| Diaph3 |
T |
A |
14: 86,893,774 (GRCm39) |
R78S |
unknown |
Het |
| Dnase1l2 |
T |
C |
17: 24,660,690 (GRCm39) |
D188G |
possibly damaging |
Het |
| Exosc9 |
T |
C |
3: 36,608,078 (GRCm39) |
|
probably benign |
Het |
| Fgf23 |
G |
A |
6: 127,057,436 (GRCm39) |
V251I |
probably benign |
Het |
| Fndc3c1 |
T |
C |
X: 105,489,534 (GRCm39) |
T296A |
probably benign |
Het |
| Gm5592 |
A |
G |
7: 40,938,617 (GRCm39) |
E633G |
probably damaging |
Het |
| Gpr155 |
T |
C |
2: 73,212,576 (GRCm39) |
M16V |
probably benign |
Het |
| Jakmip3 |
T |
G |
7: 138,591,121 (GRCm39) |
S2A |
possibly damaging |
Het |
| Lrba |
T |
A |
3: 86,258,555 (GRCm39) |
N1347K |
probably damaging |
Het |
| Mplkipl1 |
A |
G |
19: 61,164,199 (GRCm39) |
S79P |
probably damaging |
Het |
| Mrgpra1 |
A |
T |
7: 46,985,675 (GRCm39) |
|
probably null |
Het |
| Or7g20 |
T |
A |
9: 18,946,584 (GRCm39) |
L55* |
probably null |
Het |
| Pdzk1ip1 |
T |
A |
4: 114,950,111 (GRCm39) |
|
probably benign |
Het |
| Ppid |
G |
T |
3: 79,500,986 (GRCm39) |
C52F |
probably damaging |
Het |
| Reln |
A |
G |
5: 22,152,512 (GRCm39) |
I2318T |
possibly damaging |
Het |
| Rhpn2 |
G |
A |
7: 35,070,179 (GRCm39) |
D146N |
probably benign |
Het |
| Tspoap1 |
G |
T |
11: 87,671,081 (GRCm39) |
R1670L |
possibly damaging |
Het |
| Ttc22 |
G |
A |
4: 106,495,773 (GRCm39) |
V376M |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,560,746 (GRCm39) |
L29218F |
probably damaging |
Het |
| Ttn |
A |
T |
2: 76,560,748 (GRCm39) |
L29218I |
probably damaging |
Het |
| Zfp609 |
G |
A |
9: 65,609,682 (GRCm39) |
Q1094* |
probably null |
Het |
| Zfp831 |
C |
T |
2: 174,485,631 (GRCm39) |
T102I |
possibly damaging |
Het |
| Zglp1 |
C |
T |
9: 20,974,675 (GRCm39) |
C171Y |
probably benign |
Het |
|
| Other mutations in Mars1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00230:Mars1
|
APN |
10 |
127,133,875 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL00813:Mars1
|
APN |
10 |
127,135,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01292:Mars1
|
APN |
10 |
127,141,387 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02505:Mars1
|
APN |
10 |
127,140,113 (GRCm39) |
nonsense |
probably null |
|
|
IGL02986:Mars1
|
APN |
10 |
127,133,438 (GRCm39) |
missense |
probably benign |
0.09 |
|
menschen
|
UTSW |
10 |
127,132,549 (GRCm39) |
unclassified |
probably benign |
|
|
PIT4366001:Mars1
|
UTSW |
10 |
127,135,267 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R0149:Mars1
|
UTSW |
10 |
127,135,903 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1445:Mars1
|
UTSW |
10 |
127,133,857 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R1702:Mars1
|
UTSW |
10 |
127,145,948 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R1998:Mars1
|
UTSW |
10 |
127,138,740 (GRCm39) |
missense |
probably benign |
|
|
R1998:Mars1
|
UTSW |
10 |
127,136,347 (GRCm39) |
nonsense |
probably null |
|
|
R2089:Mars1
|
UTSW |
10 |
127,135,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2091:Mars1
|
UTSW |
10 |
127,135,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2091:Mars1
|
UTSW |
10 |
127,135,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4597:Mars1
|
UTSW |
10 |
127,136,322 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4809:Mars1
|
UTSW |
10 |
127,136,084 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4923:Mars1
|
UTSW |
10 |
127,132,549 (GRCm39) |
unclassified |
probably benign |
|
|
R5563:Mars1
|
UTSW |
10 |
127,144,530 (GRCm39) |
missense |
probably benign |
|
|
R5890:Mars1
|
UTSW |
10 |
127,133,914 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5895:Mars1
|
UTSW |
10 |
127,132,418 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5986:Mars1
|
UTSW |
10 |
127,140,171 (GRCm39) |
nonsense |
probably null |
|
|
R6300:Mars1
|
UTSW |
10 |
127,132,429 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7267:Mars1
|
UTSW |
10 |
127,144,455 (GRCm39) |
missense |
probably benign |
|
|
R7544:Mars1
|
UTSW |
10 |
127,147,479 (GRCm39) |
missense |
probably benign |
0.24 |
|
R7573:Mars1
|
UTSW |
10 |
127,138,679 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7740:Mars1
|
UTSW |
10 |
127,136,444 (GRCm39) |
missense |
probably benign |
0.16 |
|
R7884:Mars1
|
UTSW |
10 |
127,136,114 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8286:Mars1
|
UTSW |
10 |
127,141,348 (GRCm39) |
missense |
probably benign |
0.35 |
|
R8397:Mars1
|
UTSW |
10 |
127,136,368 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R9174:Mars1
|
UTSW |
10 |
127,135,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9607:Mars1
|
UTSW |
10 |
127,144,493 (GRCm39) |
nonsense |
probably null |
|
|
R9662:Mars1
|
UTSW |
10 |
127,136,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0027:Mars1
|
UTSW |
10 |
127,144,218 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2014-01-21 |
Incidental Mutation