Incidental Mutation 'IGL01602:Rbpj-ps3'
ID 278757
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rbpj-ps3
Ensembl Gene ENSMUSG00000079575
Gene Name recombination signal binding protein for immunoglobulin kappa J region, pseudogene 3
Synonyms Rbpsuh-rs3, Igkrsbp-rs3
Accession Numbers
Essential gene? Not available question?
Stock # IGL01602
Quality Score
Status
Chromosome 6
Chromosomal Location 46506288-46507728 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 46507025 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000110288 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114641]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000114641
SMART Domains Protein: ENSMUSP00000110288
Gene: ENSMUSG00000039419

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
FA58C 34 181 3.99e-22 SMART
LamG 208 345 5.5e-34 SMART
LamG 393 529 3.31e-28 SMART
EGF 557 591 5.04e-2 SMART
Blast:FBG 594 777 7e-68 BLAST
LamG 819 945 5.58e-35 SMART
EGF 966 1002 2.11e1 SMART
LamG 1048 1188 3.55e-28 SMART
low complexity region 1263 1273 N/A INTRINSIC
4.1m 1283 1301 4.21e-7 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182751
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts17 A T 7: 66,538,159 (GRCm39) M242L probably benign Het
Brip1 T A 11: 85,952,830 (GRCm39) T984S possibly damaging Het
Cdh17 T C 4: 11,795,670 (GRCm39) Y417H probably damaging Het
Chd7 T A 4: 8,833,834 (GRCm39) I1196N probably damaging Het
Cyp3a57 T C 5: 145,323,854 (GRCm39) F447S probably damaging Het
Dnah12 C T 14: 26,431,430 (GRCm39) probably benign Het
Dock8 C T 19: 25,067,252 (GRCm39) probably benign Het
Eif1ad5 A T 12: 87,940,530 (GRCm39) noncoding transcript Het
Fam163b A G 2: 27,002,688 (GRCm39) F103S probably damaging Het
G0s2 A G 1: 192,954,964 (GRCm39) L40P probably damaging Het
Gucy1b1 C T 3: 81,942,660 (GRCm39) R494Q probably benign Het
Hsd17b1 T C 11: 100,969,755 (GRCm39) V89A probably damaging Het
Iqcg T C 16: 32,837,348 (GRCm39) probably benign Het
Lmo7 T C 14: 102,148,192 (GRCm39) probably benign Het
Mmp17 A G 5: 129,679,008 (GRCm39) D331G probably benign Het
Mnx1 T C 5: 29,682,591 (GRCm39) D228G unknown Het
Msantd2 A G 9: 37,428,736 (GRCm39) E101G probably benign Het
Msh2 T C 17: 88,003,917 (GRCm39) probably benign Het
Pabpc1 A G 15: 36,599,550 (GRCm39) Y382H probably benign Het
Prl7b1 A G 13: 27,786,027 (GRCm39) S214P possibly damaging Het
Sgsm1 A T 5: 113,433,531 (GRCm39) M162K possibly damaging Het
Skint2 A G 4: 112,483,191 (GRCm39) T199A probably benign Het
Slc24a1 T A 9: 64,833,463 (GRCm39) D1044V probably damaging Het
Stim1 A G 7: 102,035,322 (GRCm39) D100G possibly damaging Het
Taar5 C T 10: 23,846,962 (GRCm39) T120I probably benign Het
Trhde A G 10: 114,623,848 (GRCm39) V352A probably benign Het
Ubap2 T A 4: 41,227,237 (GRCm39) D160V probably damaging Het
Vmn2r18 A G 5: 151,510,106 (GRCm39) V89A possibly damaging Het
Wbp1l A G 19: 46,642,839 (GRCm39) D264G possibly damaging Het
Other mutations in Rbpj-ps3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01605:Rbpj-ps3 APN 6 46,507,025 (GRCm39) intron probably benign
IGL01739:Rbpj-ps3 APN 6 46,507,694 (GRCm39) missense probably benign 0.03
IGL02216:Rbpj-ps3 APN 6 46,506,641 (GRCm39) intron probably benign
Posted On 2015-04-16