Incidental Mutation 'IGL03246:Prr9'
ID 414422
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prr9
Ensembl Gene ENSMUSG00000056270
Gene Name proline rich 9
Synonyms A030004J04Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03246
Quality Score
Status
Chromosome 3
Chromosomal Location 92029511-92031254 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 92030286 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000068470 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070284]
AlphaFold Q8BV84
Predicted Effect probably benign
Transcript: ENSMUST00000070284
SMART Domains Protein: ENSMUSP00000068470
Gene: ENSMUSG00000056270

DomainStartEndE-ValueType
low complexity region 6 19 N/A INTRINSIC
low complexity region 37 50 N/A INTRINSIC
internal_repeat_1 53 78 2e-5 PROSPERO
internal_repeat_1 85 114 2e-5 PROSPERO
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197811
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198245
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921511C20Rik T A X: 126,303,238 (GRCm39) H392Q probably benign Het
Alox8 T A 11: 69,076,841 (GRCm39) I547L probably damaging Het
Capn13 T C 17: 73,689,855 (GRCm39) H52R probably benign Het
Cfap57 T A 4: 118,433,842 (GRCm39) I979L probably benign Het
Ctdnep1 T C 11: 69,875,156 (GRCm39) probably benign Het
Ercc5 C A 1: 44,206,241 (GRCm39) P385T probably damaging Het
Fam98a C T 17: 75,845,848 (GRCm39) M299I probably damaging Het
Flcn A T 11: 59,684,936 (GRCm39) I505N possibly damaging Het
Fn1 G A 1: 71,663,455 (GRCm39) T1011I possibly damaging Het
Klhl28 T C 12: 65,004,060 (GRCm39) D151G probably benign Het
Klk13 T A 7: 43,370,422 (GRCm39) N28K probably damaging Het
Macc1 T C 12: 119,410,420 (GRCm39) V396A probably benign Het
Mageb11 C A X: 89,936,008 (GRCm39) H87Q probably benign Het
Magi2 T A 5: 20,563,948 (GRCm39) I360K probably damaging Het
Myh7b T C 2: 155,459,792 (GRCm39) I251T probably damaging Het
Naalad2 A T 9: 18,296,395 (GRCm39) I85K possibly damaging Het
Or5ae1 T C 7: 84,565,919 (GRCm39) C311R probably benign Het
Pbrm1 A T 14: 30,832,506 (GRCm39) M1490L probably benign Het
Pclo C T 5: 14,727,631 (GRCm39) probably benign Het
Pdcd6ip T C 9: 113,507,485 (GRCm39) K357R possibly damaging Het
Pnpla6 C T 8: 3,581,530 (GRCm39) T601I probably benign Het
Pof1b A T X: 111,557,817 (GRCm39) N366K probably benign Het
Ptprz1 G T 6: 22,986,159 (GRCm39) A320S probably damaging Het
Ripor1 A G 8: 106,342,490 (GRCm39) Y187C possibly damaging Het
Rnf13 A G 3: 57,676,471 (GRCm39) E42G probably damaging Het
Sdf4 T C 4: 156,085,154 (GRCm39) V163A probably benign Het
Smc2 C T 4: 52,440,301 (GRCm39) Q16* probably null Het
Srsf3-ps T A 11: 98,516,119 (GRCm39) R85* probably null Het
Tbck T A 3: 132,480,331 (GRCm39) C737S probably benign Het
Tra2a A T 6: 49,226,019 (GRCm39) Y140* probably null Het
Vcpip1 A C 1: 9,816,182 (GRCm39) L734V probably benign Het
Vmn1r87 G A 7: 12,866,288 (GRCm39) probably benign Het
Other mutations in Prr9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01146:Prr9 APN 3 92,030,504 (GRCm39) nonsense probably null
R2850:Prr9 UTSW 3 92,030,476 (GRCm39) missense probably benign
R5155:Prr9 UTSW 3 92,030,356 (GRCm39) missense possibly damaging 0.66
R8401:Prr9 UTSW 3 92,030,356 (GRCm39) missense possibly damaging 0.92
Posted On 2016-08-02