Incidental Mutation 'R8906:Iars1'
ID |
680135 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Iars1
|
Ensembl Gene |
ENSMUSG00000037851 |
Gene Name |
isoleucyl-tRNA synthetase 1 |
Synonyms |
Iars, 2510016L12Rik, E430001P04Rik |
MMRRC Submission |
068699-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R8906 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
49835606-49887743 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 49882177 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Serine
at position 1074
(C1074S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000132082
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047363]
[ENSMUST00000164260]
[ENSMUST00000165316]
|
AlphaFold |
Q8BU30 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000047363
AA Change: C1074S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000048096 Gene: ENSMUSG00000037851 AA Change: C1074S
Domain | Start | End | E-Value | Type |
Pfam:tRNA-synt_1
|
17 |
639 |
9.2e-242 |
PFAM |
Pfam:tRNA-synt_1g
|
46 |
197 |
3.7e-6 |
PFAM |
Pfam:Anticodon_1
|
693 |
852 |
1.1e-23 |
PFAM |
low complexity region
|
1159 |
1167 |
N/A |
INTRINSIC |
low complexity region
|
1169 |
1180 |
N/A |
INTRINSIC |
low complexity region
|
1220 |
1229 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000164260
AA Change: C1074S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000126806 Gene: ENSMUSG00000037851 AA Change: C1074S
Domain | Start | End | E-Value | Type |
Pfam:tRNA-synt_1
|
17 |
639 |
5.5e-238 |
PFAM |
Pfam:tRNA-synt_1g
|
46 |
205 |
5.2e-8 |
PFAM |
Pfam:tRNA-synt_1g
|
521 |
659 |
2.1e-5 |
PFAM |
Pfam:Anticodon_1
|
693 |
852 |
7.1e-24 |
PFAM |
low complexity region
|
1159 |
1167 |
N/A |
INTRINSIC |
low complexity region
|
1169 |
1180 |
N/A |
INTRINSIC |
low complexity region
|
1220 |
1229 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165316
AA Change: C1074S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000132082 Gene: ENSMUSG00000037851 AA Change: C1074S
Domain | Start | End | E-Value | Type |
Pfam:tRNA-synt_1
|
17 |
639 |
5.5e-238 |
PFAM |
Pfam:tRNA-synt_1g
|
46 |
205 |
5.2e-8 |
PFAM |
Pfam:tRNA-synt_1g
|
521 |
659 |
2.1e-5 |
PFAM |
Pfam:Anticodon_1
|
693 |
852 |
7.1e-24 |
PFAM |
low complexity region
|
1159 |
1167 |
N/A |
INTRINSIC |
low complexity region
|
1169 |
1180 |
N/A |
INTRINSIC |
low complexity region
|
1220 |
1229 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.4%
|
Validation Efficiency |
100% (88/88) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAS, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Isoleucine-tRNA synthetase belongs to the class-I aminoacyl-tRNA synthetase family and has been identified as a target of autoantibodies in the autoimmune disease polymyositis/dermatomyositis. Alternatively spliced transcript variants have been found. [provided by RefSeq, Nov 2012]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
A |
C |
19: 3,766,686 (GRCm39) |
N91T |
possibly damaging |
Het |
2510009E07Rik |
CCGGAAGGGGAGGAGCAGTGACCCAGTTTCGGA |
CCGGA |
16: 21,472,148 (GRCm39) |
|
probably null |
Het |
4932414N04Rik |
A |
G |
2: 68,562,498 (GRCm39) |
D375G |
possibly damaging |
Het |
Adad2 |
C |
A |
8: 120,339,725 (GRCm39) |
P69Q |
probably benign |
Het |
Adamts3 |
G |
A |
5: 89,825,575 (GRCm39) |
T1088I |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,726,720 (GRCm39) |
V858A |
probably benign |
Het |
Ankrd13a |
A |
G |
5: 114,939,798 (GRCm39) |
N475S |
probably benign |
Het |
Barhl2 |
G |
A |
5: 106,603,352 (GRCm39) |
T269I |
probably benign |
Het |
Boc |
G |
A |
16: 44,323,931 (GRCm39) |
R157W |
|
Het |
Bsn |
G |
T |
9: 107,984,752 (GRCm39) |
P3101T |
unknown |
Het |
Catsperb |
C |
A |
12: 101,486,904 (GRCm39) |
A477E |
possibly damaging |
Het |
Ccser1 |
T |
A |
6: 61,787,842 (GRCm39) |
I220K |
probably benign |
Het |
Cd200r3 |
A |
T |
16: 44,778,102 (GRCm39) |
I242F |
possibly damaging |
Het |
Cdc34b |
A |
C |
11: 94,632,911 (GRCm39) |
D37A |
probably damaging |
Het |
Chek2 |
A |
G |
5: 111,013,458 (GRCm39) |
|
probably benign |
Het |
Cngb1 |
A |
T |
8: 95,989,736 (GRCm39) |
V792D |
probably damaging |
Het |
Cops7a |
T |
C |
6: 124,939,371 (GRCm39) |
K93E |
possibly damaging |
Het |
Crispld1 |
T |
C |
1: 17,820,995 (GRCm39) |
I345T |
possibly damaging |
Het |
Dgkd |
A |
G |
1: 87,869,157 (GRCm39) |
D1170G |
probably damaging |
Het |
Dhx35 |
A |
G |
2: 158,648,918 (GRCm39) |
T115A |
possibly damaging |
Het |
Dnai1 |
G |
A |
4: 41,625,125 (GRCm39) |
R363H |
probably benign |
Het |
Dnmbp |
T |
A |
19: 43,878,681 (GRCm39) |
Q130L |
probably benign |
Het |
Egfr |
A |
G |
11: 16,861,635 (GRCm39) |
Y1138C |
probably damaging |
Het |
Elf3 |
A |
T |
1: 135,182,678 (GRCm39) |
L329Q |
probably damaging |
Het |
Enkur |
A |
G |
2: 21,201,568 (GRCm39) |
M39T |
probably benign |
Het |
Epha7 |
T |
C |
4: 28,821,615 (GRCm39) |
I260T |
probably damaging |
Het |
Fbxo28 |
A |
T |
1: 182,144,634 (GRCm39) |
I310K |
probably damaging |
Het |
Fga |
C |
A |
3: 82,939,111 (GRCm39) |
N495K |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,601,247 (GRCm39) |
D344G |
probably damaging |
Het |
Gm572 |
A |
G |
4: 148,751,290 (GRCm39) |
Q221R |
probably benign |
Het |
Gpa33 |
G |
A |
1: 165,974,216 (GRCm39) |
A18T |
probably benign |
Het |
Gpatch11 |
C |
T |
17: 79,145,289 (GRCm39) |
T6I |
probably benign |
Het |
Gpr84 |
T |
A |
15: 103,217,625 (GRCm39) |
S151C |
probably damaging |
Het |
H2-M11 |
T |
A |
17: 36,859,851 (GRCm39) |
Y281* |
probably null |
Het |
Hadh |
T |
C |
3: 131,038,891 (GRCm39) |
N155S |
probably benign |
Het |
Hoxd13 |
A |
G |
2: 74,500,266 (GRCm39) |
Y269C |
|
Het |
Ibtk |
G |
T |
9: 85,625,457 (GRCm39) |
H98N |
possibly damaging |
Het |
Igsf10 |
C |
T |
3: 59,233,739 (GRCm39) |
G1665R |
probably benign |
Het |
Inpp5d |
A |
G |
1: 87,625,337 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
C |
1: 135,321,951 (GRCm39) |
V593G |
probably damaging |
Het |
Irx3 |
T |
C |
8: 92,526,915 (GRCm39) |
D263G |
possibly damaging |
Het |
Kif13a |
A |
G |
13: 46,927,154 (GRCm39) |
V1179A |
probably benign |
Het |
Lrrc4c |
T |
C |
2: 97,460,393 (GRCm39) |
Y340H |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,045,219 (GRCm39) |
D155G |
probably damaging |
Het |
Mical2 |
T |
A |
7: 111,980,671 (GRCm39) |
I105N |
probably damaging |
Het |
Mob2 |
A |
T |
7: 141,563,261 (GRCm39) |
L66Q |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,096,739 (GRCm39) |
S337G |
probably benign |
Het |
Neb |
T |
C |
2: 52,096,259 (GRCm39) |
D1002G |
probably benign |
Het |
Nebl |
A |
T |
2: 17,382,928 (GRCm39) |
N116K |
probably benign |
Het |
Nkx2-6 |
T |
C |
14: 69,412,623 (GRCm39) |
S264P |
probably benign |
Het |
Nlgn3 |
T |
C |
X: 100,352,390 (GRCm39) |
V179A |
probably damaging |
Het |
Nlrp4e |
A |
G |
7: 23,020,556 (GRCm39) |
T348A |
possibly damaging |
Het |
Nomo1 |
A |
T |
7: 45,722,004 (GRCm39) |
I982F |
probably benign |
Het |
Or10j5 |
A |
G |
1: 172,784,186 (GRCm39) |
|
probably benign |
Het |
Or11g24 |
T |
G |
14: 50,662,291 (GRCm39) |
F105C |
probably damaging |
Het |
Or1j19 |
A |
T |
2: 36,676,621 (GRCm39) |
Y28F |
probably benign |
Het |
Or8g22 |
A |
G |
9: 38,958,077 (GRCm39) |
F213L |
possibly damaging |
Het |
Palld |
A |
G |
8: 62,003,198 (GRCm39) |
|
probably null |
Het |
Pcdh7 |
A |
G |
5: 57,879,154 (GRCm39) |
Y903C |
probably damaging |
Het |
Pknox2 |
G |
A |
9: 36,804,167 (GRCm39) |
T460M |
possibly damaging |
Het |
Ppm1h |
C |
T |
10: 122,714,451 (GRCm39) |
T330I |
probably damaging |
Het |
Ppp2r2b |
C |
T |
18: 42,821,399 (GRCm39) |
R253H |
probably damaging |
Het |
Pramel58 |
G |
T |
5: 94,831,413 (GRCm39) |
R140L |
possibly damaging |
Het |
Prr18 |
G |
A |
17: 8,560,476 (GRCm39) |
A211T |
probably benign |
Het |
Ptgs2 |
A |
G |
1: 149,979,859 (GRCm39) |
I321M |
|
Het |
Rara |
G |
T |
11: 98,860,989 (GRCm39) |
R159L |
probably damaging |
Het |
Rasa4 |
T |
A |
5: 136,133,446 (GRCm39) |
I635N |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,989,888 (GRCm39) |
H423L |
possibly damaging |
Het |
Scn4b |
A |
G |
9: 45,059,169 (GRCm39) |
I147V |
possibly damaging |
Het |
Scrn3 |
G |
A |
2: 73,161,352 (GRCm39) |
V313I |
probably benign |
Het |
Scrn3 |
C |
A |
2: 73,161,355 (GRCm39) |
P314T |
possibly damaging |
Het |
Sh2b1 |
A |
G |
7: 126,070,292 (GRCm39) |
|
probably null |
Het |
Slc26a10 |
T |
C |
10: 127,016,459 (GRCm39) |
Q3R |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,149,139 (GRCm39) |
I524T |
probably damaging |
Het |
Smcp |
T |
A |
3: 92,491,530 (GRCm39) |
N106Y |
unknown |
Het |
Spata31h1 |
T |
C |
10: 82,122,379 (GRCm39) |
T3544A |
probably benign |
Het |
St8sia5 |
G |
A |
18: 77,336,172 (GRCm39) |
V202M |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,028,526 (GRCm39) |
D512E |
probably damaging |
Het |
Tas1r2 |
A |
G |
4: 139,397,046 (GRCm39) |
E795G |
probably damaging |
Het |
Tdrd1 |
T |
A |
19: 56,831,145 (GRCm39) |
V320D |
probably damaging |
Het |
Tmem71 |
T |
A |
15: 66,404,606 (GRCm39) |
I261L |
probably benign |
Het |
Tns2 |
T |
C |
15: 102,020,039 (GRCm39) |
L643P |
probably damaging |
Het |
Upf1 |
G |
A |
8: 70,786,815 (GRCm39) |
Q890* |
probably null |
Het |
Usp43 |
A |
T |
11: 67,782,307 (GRCm39) |
H370Q |
possibly damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,507,356 (GRCm39) |
I158N |
possibly damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,286,532 (GRCm39) |
N343K |
probably benign |
Het |
Vwa8 |
T |
C |
14: 79,329,815 (GRCm39) |
S1216P |
probably benign |
Het |
Yars1 |
A |
C |
4: 129,090,747 (GRCm39) |
D97A |
probably damaging |
Het |
Zer1 |
G |
A |
2: 30,001,035 (GRCm39) |
H129Y |
probably benign |
Het |
Zfat |
C |
T |
15: 67,956,404 (GRCm39) |
D1143N |
possibly damaging |
Het |
|
Other mutations in Iars1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00697:Iars1
|
APN |
13 |
49,863,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00764:Iars1
|
APN |
13 |
49,865,303 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01153:Iars1
|
APN |
13 |
49,865,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01481:Iars1
|
APN |
13 |
49,882,174 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01596:Iars1
|
APN |
13 |
49,856,652 (GRCm39) |
missense |
probably benign |
|
IGL01682:Iars1
|
APN |
13 |
49,863,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01885:Iars1
|
APN |
13 |
49,844,975 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01907:Iars1
|
APN |
13 |
49,863,131 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Iars1
|
APN |
13 |
49,841,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02121:Iars1
|
APN |
13 |
49,878,172 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02365:Iars1
|
APN |
13 |
49,844,975 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02704:Iars1
|
APN |
13 |
49,874,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02838:Iars1
|
APN |
13 |
49,843,965 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02975:Iars1
|
APN |
13 |
49,858,325 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Iars1
|
APN |
13 |
49,863,185 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03034:Iars1
|
APN |
13 |
49,843,965 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03060:Iars1
|
APN |
13 |
49,843,923 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03156:Iars1
|
APN |
13 |
49,856,655 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03206:Iars1
|
APN |
13 |
49,846,546 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03343:Iars1
|
APN |
13 |
49,878,223 (GRCm39) |
missense |
probably benign |
0.12 |
gannett_peak
|
UTSW |
13 |
49,861,897 (GRCm39) |
missense |
probably damaging |
1.00 |
missouri
|
UTSW |
13 |
49,841,752 (GRCm39) |
missense |
possibly damaging |
0.82 |
spacex
|
UTSW |
13 |
49,876,478 (GRCm39) |
missense |
possibly damaging |
0.85 |
wind_river
|
UTSW |
13 |
49,855,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Iars1
|
UTSW |
13 |
49,846,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Iars1
|
UTSW |
13 |
49,846,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Iars1
|
UTSW |
13 |
49,875,688 (GRCm39) |
missense |
probably benign |
0.00 |
R0200:Iars1
|
UTSW |
13 |
49,879,678 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0356:Iars1
|
UTSW |
13 |
49,856,709 (GRCm39) |
missense |
probably benign |
0.03 |
R0383:Iars1
|
UTSW |
13 |
49,885,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R0657:Iars1
|
UTSW |
13 |
49,855,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R1005:Iars1
|
UTSW |
13 |
49,840,921 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1427:Iars1
|
UTSW |
13 |
49,857,745 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1449:Iars1
|
UTSW |
13 |
49,887,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R1647:Iars1
|
UTSW |
13 |
49,876,478 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1648:Iars1
|
UTSW |
13 |
49,876,478 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1664:Iars1
|
UTSW |
13 |
49,865,251 (GRCm39) |
missense |
probably damaging |
0.98 |
R1763:Iars1
|
UTSW |
13 |
49,876,553 (GRCm39) |
critical splice donor site |
probably null |
|
R2192:Iars1
|
UTSW |
13 |
49,841,605 (GRCm39) |
splice site |
probably null |
|
R2203:Iars1
|
UTSW |
13 |
49,876,151 (GRCm39) |
missense |
probably benign |
0.00 |
R2357:Iars1
|
UTSW |
13 |
49,841,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R3724:Iars1
|
UTSW |
13 |
49,840,860 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4785:Iars1
|
UTSW |
13 |
49,878,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R4934:Iars1
|
UTSW |
13 |
49,871,460 (GRCm39) |
missense |
probably benign |
0.17 |
R4999:Iars1
|
UTSW |
13 |
49,863,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Iars1
|
UTSW |
13 |
49,841,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R5268:Iars1
|
UTSW |
13 |
49,843,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R5394:Iars1
|
UTSW |
13 |
49,875,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Iars1
|
UTSW |
13 |
49,863,049 (GRCm39) |
splice site |
probably null |
|
R5960:Iars1
|
UTSW |
13 |
49,878,113 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5972:Iars1
|
UTSW |
13 |
49,863,108 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5978:Iars1
|
UTSW |
13 |
49,876,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R6031:Iars1
|
UTSW |
13 |
49,859,307 (GRCm39) |
missense |
probably damaging |
0.98 |
R6031:Iars1
|
UTSW |
13 |
49,859,307 (GRCm39) |
missense |
probably damaging |
0.98 |
R6092:Iars1
|
UTSW |
13 |
49,861,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R6167:Iars1
|
UTSW |
13 |
49,876,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R6313:Iars1
|
UTSW |
13 |
49,861,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R6358:Iars1
|
UTSW |
13 |
49,880,619 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6385:Iars1
|
UTSW |
13 |
49,855,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R6403:Iars1
|
UTSW |
13 |
49,840,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6575:Iars1
|
UTSW |
13 |
49,878,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R6675:Iars1
|
UTSW |
13 |
49,873,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R6957:Iars1
|
UTSW |
13 |
49,875,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Iars1
|
UTSW |
13 |
49,841,791 (GRCm39) |
critical splice donor site |
probably null |
|
R7254:Iars1
|
UTSW |
13 |
49,876,554 (GRCm39) |
critical splice donor site |
probably null |
|
R7354:Iars1
|
UTSW |
13 |
49,857,796 (GRCm39) |
missense |
probably benign |
|
R7397:Iars1
|
UTSW |
13 |
49,882,153 (GRCm39) |
missense |
probably benign |
0.00 |
R7696:Iars1
|
UTSW |
13 |
49,860,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Iars1
|
UTSW |
13 |
49,876,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R7828:Iars1
|
UTSW |
13 |
49,878,748 (GRCm39) |
missense |
probably benign |
|
R8679:Iars1
|
UTSW |
13 |
49,856,675 (GRCm39) |
unclassified |
probably benign |
|
R8768:Iars1
|
UTSW |
13 |
49,878,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R8797:Iars1
|
UTSW |
13 |
49,841,738 (GRCm39) |
missense |
probably benign |
0.12 |
R8990:Iars1
|
UTSW |
13 |
49,841,752 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9134:Iars1
|
UTSW |
13 |
49,855,323 (GRCm39) |
missense |
probably benign |
0.00 |
R9137:Iars1
|
UTSW |
13 |
49,855,350 (GRCm39) |
missense |
probably benign |
|
R9394:Iars1
|
UTSW |
13 |
49,883,536 (GRCm39) |
missense |
probably benign |
|
R9668:Iars1
|
UTSW |
13 |
49,840,885 (GRCm39) |
missense |
probably damaging |
0.98 |
R9741:Iars1
|
UTSW |
13 |
49,844,978 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Iars1
|
UTSW |
13 |
49,874,564 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- TGCAGTATATGAGAGAGCTGGC -3'
(R):5'- GTAAAGGACTCACTCGGGTGAC -3'
Sequencing Primer
(F):5'- CGAGGAGGTTGAGTTTGTACC -3'
(R):5'- CTCACTCGGGTGACAAGAG -3'
|
Posted On |
2021-08-31 |