Incidental Mutation 'IGL01635:Prorsd1'
ID 92945
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prorsd1
Ensembl Gene ENSMUSG00000032673
Gene Name prolyl-tRNA synthetase domain containing 1
Synonyms Prdxdd1, Ncrna00117, 2010316F05Rik
Accession Numbers
Essential gene? Not available question?
Stock # IGL01635
Quality Score
Status
Chromosome 11
Chromosomal Location 29461757-29465033 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 29463467 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 98 (K98N)
Ref Sequence ENSEMBL: ENSMUSP00000048099 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039900] [ENSMUST00000040182] [ENSMUST00000133103]
AlphaFold Q9D820
Predicted Effect probably benign
Transcript: ENSMUST00000039900
AA Change: K98N

PolyPhen 2 Score 0.034 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000048099
Gene: ENSMUSG00000032673
AA Change: K98N

DomainStartEndE-ValueType
Pfam:tRNA_edit 26 155 9.6e-30 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000040182
SMART Domains Protein: ENSMUSP00000048978
Gene: ENSMUSG00000032740

DomainStartEndE-ValueType
Pfam:HOOK 14 590 8.1e-36 PFAM
low complexity region 614 625 N/A INTRINSIC
Blast:BRLZ 665 719 6e-22 BLAST
low complexity region 826 839 N/A INTRINSIC
low complexity region 883 895 N/A INTRINSIC
low complexity region 955 985 N/A INTRINSIC
low complexity region 1093 1104 N/A INTRINSIC
coiled coil region 1268 1385 N/A INTRINSIC
low complexity region 1437 1444 N/A INTRINSIC
low complexity region 1566 1576 N/A INTRINSIC
internal_repeat_1 1609 1702 2.38e-6 PROSPERO
internal_repeat_1 1708 1808 2.38e-6 PROSPERO
low complexity region 1811 1824 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000133103
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138402
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abat A G 16: 8,431,910 (GRCm39) I396V probably benign Het
Bag2 T A 1: 33,786,013 (GRCm39) N103I possibly damaging Het
Cfap95 T C 19: 23,536,379 (GRCm39) Y176C probably damaging Het
Chd1 T C 17: 17,598,858 (GRCm39) S107P probably damaging Het
Chd3 A T 11: 69,252,076 (GRCm39) probably benign Het
Cytip T C 2: 58,038,243 (GRCm39) E106G probably damaging Het
Dcp1b T A 6: 119,183,498 (GRCm39) I195N probably damaging Het
Ddhd1 C A 14: 45,867,037 (GRCm39) V322F probably null Het
Esrrg A T 1: 187,930,797 (GRCm39) D296V probably damaging Het
F5 A G 1: 164,035,427 (GRCm39) K1867R probably benign Het
Gm10717 C A 9: 3,025,511 (GRCm39) A32D probably damaging Het
Gm10717 C A 9: 3,025,506 (GRCm39) F30L possibly damaging Het
Gstt1 G T 10: 75,629,951 (GRCm39) T54K probably damaging Het
Ighmbp2 C T 19: 3,317,265 (GRCm39) V536I possibly damaging Het
Mphosph8 A T 14: 56,910,003 (GRCm39) R119W probably damaging Het
Negr1 A G 3: 156,267,929 (GRCm39) D33G probably benign Het
Or2l13b A G 16: 19,348,845 (GRCm39) V275A probably benign Het
Or7d10 A T 9: 19,831,780 (GRCm39) I92L probably damaging Het
Plbd2 T C 5: 120,637,114 (GRCm39) D116G probably damaging Het
Pold1 A T 7: 44,185,401 (GRCm39) V733E probably damaging Het
Rasal2 G T 1: 156,991,394 (GRCm39) L611I probably damaging Het
Rffl G A 11: 82,703,378 (GRCm39) R147C probably benign Het
Rpl27rt A T 18: 34,870,795 (GRCm39) M110L probably benign Het
Sdad1 A G 5: 92,445,019 (GRCm39) M315T probably damaging Het
Shprh T A 10: 11,045,763 (GRCm39) Y861* probably null Het
Six4 G A 12: 73,155,971 (GRCm39) A324V probably benign Het
Stab2 T C 10: 86,816,992 (GRCm39) D135G probably benign Het
Tada3 T C 6: 113,352,973 (GRCm39) H12R probably benign Het
Zap70 A G 1: 36,810,238 (GRCm39) D116G probably damaging Het
Other mutations in Prorsd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2192:Prorsd1 UTSW 11 29,463,592 (GRCm39) missense probably benign 0.01
R6991:Prorsd1 UTSW 11 29,464,486 (GRCm39) unclassified probably benign
R8459:Prorsd1 UTSW 11 29,463,286 (GRCm39) missense probably damaging 1.00
R9244:Prorsd1 UTSW 11 29,463,271 (GRCm39) missense probably benign
Posted On 2013-12-09