Incidental Mutation 'IGL01828:RP24-77E13.10'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol RP24-77E13.10
Ensembl Gene ENSMUSG00000110105
Gene Name
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.425) question?
Stock #IGL01828
Quality Score
Chromosomal Location (GRCm38)
Type of Mutationunclassified (4 bp from exon)
DNA Base Change (assembly) T to C at 7231323 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131990 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170922] [ENSMUST00000173842] [ENSMUST00000209325] [ENSMUST00000209833] [ENSMUST00000210333]
Predicted Effect probably null
Transcript: ENSMUST00000170922
SMART Domains Protein: ENSMUSP00000131990
Gene: ENSMUSG00000095730

signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 469 2e-34 PFAM
Pfam:NCD3G 512 565 1.4e-20 PFAM
Pfam:7tm_3 598 833 2e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000173842
Predicted Effect probably benign
Transcript: ENSMUST00000209325
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209788
Predicted Effect probably benign
Transcript: ENSMUST00000209833
Predicted Effect probably benign
Transcript: ENSMUST00000210333
Predicted Effect probably benign
Transcript: ENSMUST00000211433
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 T C 11: 110,287,695 I1151V probably benign Het
Abcc4 C T 14: 118,553,279 probably benign Het
Asxl3 T A 18: 22,525,558 probably benign Het
Car4 C A 11: 84,964,745 Q198K probably benign Het
Ces1a T C 8: 93,025,201 H435R probably damaging Het
Chdh T A 14: 30,036,608 F503L probably damaging Het
Dennd4a C T 9: 64,842,561 R145* probably null Het
Dse T A 10: 34,152,776 T773S probably damaging Het
Fbxw11 T A 11: 32,720,505 L123H probably damaging Het
Gigyf2 A G 1: 87,419,098 D550G probably damaging Het
Krcc1 T A 6: 71,284,367 Y128N probably damaging Het
Myh8 T C 11: 67,303,826 M1621T possibly damaging Het
Notch2 T A 3: 98,072,613 C148S probably damaging Het
Plcg2 C A 8: 117,590,233 H616Q probably damaging Het
Plec T C 15: 76,183,755 E1218G probably damaging Het
Plekhm2 T C 4: 141,629,585 E749G probably benign Het
Slco1a6 C T 6: 142,096,411 V480M probably damaging Het
Vmn1r88 C T 7: 13,177,735 T6I probably damaging Het
Vmn2r14 A G 5: 109,224,577 F16L possibly damaging Het
Ywhab G A 2: 164,011,774 R57H possibly damaging Het
Other mutations in RP24-77E13.10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02746:RP24-77E13.10 APN 7 7240179 missense probably damaging 1.00
Posted On2014-02-04