Incidental Mutation 'IGL02201:Prr23a3'
ID 284198
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prr23a3
Ensembl Gene ENSMUSG00000090470
Gene Name proline rich 23A, member 3
Synonyms 2410012M07Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # IGL02201
Quality Score
Status
Chromosome 9
Chromosomal Location 98746820-98748633 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 98747297 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 84 (V84L)
Ref Sequence ENSEMBL: ENSMUSP00000130716 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167951]
AlphaFold Q9CWP9
Predicted Effect possibly damaging
Transcript: ENSMUST00000167951
AA Change: V84L

PolyPhen 2 Score 0.724 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000130716
Gene: ENSMUSG00000090470
AA Change: V84L

DomainStartEndE-ValueType
Pfam:DUF2476 1 251 8.2e-123 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl3 G A 1: 78,676,870 (GRCm39) G484R probably damaging Het
Adgrb3 A G 1: 25,459,631 (GRCm39) probably benign Het
Akr1c14 A G 13: 4,131,022 (GRCm39) D238G probably damaging Het
Ccdc88b T A 19: 6,823,999 (GRCm39) D1418V probably damaging Het
Cnnm4 A T 1: 36,511,831 (GRCm39) K353M probably damaging Het
Col6a6 A G 9: 105,658,194 (GRCm39) F673L probably damaging Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Dyrk1a A G 16: 94,493,008 (GRCm39) E747G probably benign Het
Eml5 T A 12: 98,760,683 (GRCm39) probably benign Het
Ercc6l2 A G 13: 64,000,783 (GRCm39) N516D probably benign Het
Fbxl17 A G 17: 63,806,024 (GRCm39) L330P probably damaging Het
Fgr A T 4: 132,722,235 (GRCm39) Y168F probably damaging Het
Frem2 T G 3: 53,427,061 (GRCm39) K2962N probably benign Het
Hdac4 G T 1: 91,915,382 (GRCm39) probably null Het
Il1r1 A T 1: 40,352,428 (GRCm39) N533Y probably damaging Het
Kcnab2 T C 4: 152,486,375 (GRCm39) probably benign Het
Knl1 C T 2: 118,899,633 (GRCm39) P445S probably benign Het
Lamb2 G A 9: 108,364,741 (GRCm39) C1165Y probably damaging Het
Nisch C T 14: 30,909,051 (GRCm39) probably benign Het
Or1i2 C T 10: 78,448,104 (GRCm39) V124M probably damaging Het
Or2m12 A T 16: 19,105,212 (GRCm39) S94T probably benign Het
Or8b40 A G 9: 38,027,893 (GRCm39) D267G probably benign Het
Or8h7 A G 2: 86,721,420 (GRCm39) L33P probably damaging Het
Pde3b T A 7: 114,133,843 (GRCm39) M953K probably damaging Het
Pdzph1 A G 17: 59,274,506 (GRCm39) probably benign Het
Plce1 T C 19: 38,757,890 (GRCm39) probably benign Het
Psg26 A G 7: 18,214,071 (GRCm39) V197A probably benign Het
Ptpra T A 2: 30,336,389 (GRCm39) C80S possibly damaging Het
Ripk4 A T 16: 97,556,377 (GRCm39) V122E possibly damaging Het
Scd2 A G 19: 44,289,779 (GRCm39) N258S probably damaging Het
Slc38a1 A T 15: 96,476,679 (GRCm39) V394E probably damaging Het
Slc7a15 A G 12: 8,589,023 (GRCm39) S175P possibly damaging Het
Tacc2 T A 7: 130,227,942 (GRCm39) D1542E possibly damaging Het
Trim67 G T 8: 125,520,797 (GRCm39) R53L probably benign Het
Urah A T 7: 140,415,576 (GRCm39) T38S probably damaging Het
Vps13c A G 9: 67,874,418 (GRCm39) S3362G probably damaging Het
Wwc1 T C 11: 35,734,978 (GRCm39) probably benign Het
Zfyve28 T C 5: 34,400,549 (GRCm39) T50A probably damaging Het
Other mutations in Prr23a3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4564:Prr23a3 UTSW 9 98,747,190 (GRCm39) missense probably damaging 1.00
R4752:Prr23a3 UTSW 9 98,747,700 (GRCm39) missense probably damaging 0.99
R4979:Prr23a3 UTSW 9 98,747,431 (GRCm39) missense possibly damaging 0.83
R5035:Prr23a3 UTSW 9 98,747,183 (GRCm39) missense possibly damaging 0.91
R6171:Prr23a3 UTSW 9 98,747,731 (GRCm39) missense probably benign
R9019:Prr23a3 UTSW 9 98,747,213 (GRCm39) missense probably damaging 1.00
R9257:Prr23a3 UTSW 9 98,747,298 (GRCm39) missense probably benign 0.14
Posted On 2015-04-16