Incidental Mutation 'R3703:Bcap29'
ID 258623
Institutional Source Beutler Lab
Gene Symbol Bcap29
Ensembl Gene ENSMUSG00000020650
Gene Name B cell receptor associated protein 29
Synonyms Bap29
MMRRC Submission 040696-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.143) question?
Stock # R3703 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 31645353-31684657 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 31667151 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 170 (H170R)
Ref Sequence ENSEMBL: ENSMUSP00000137260 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020979] [ENSMUST00000177962]
AlphaFold Q61334
Predicted Effect probably benign
Transcript: ENSMUST00000020979
AA Change: H170R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000020979
Gene: ENSMUSG00000020650
AA Change: H170R

DomainStartEndE-ValueType
Pfam:Bap31 1 219 9.2e-62 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000177962
AA Change: H170R

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000137260
Gene: ENSMUSG00000020650
AA Change: H170R

DomainStartEndE-ValueType
Pfam:Bap31 1 219 4.3e-70 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 93.7%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap10 C T 8: 77,985,685 (GRCm39) probably null Het
Asap3 TGAGGAGGAGGAGGAGGA TGAGGAGGAGGAGGAGGAGGA 4: 135,968,552 (GRCm39) probably benign Het
Bltp1 T A 3: 37,041,730 (GRCm39) C2703S probably damaging Het
Brf1 T C 12: 112,932,991 (GRCm39) probably null Het
Btnl7-ps T A 17: 34,752,941 (GRCm39) noncoding transcript Het
Cdh12 C A 15: 21,583,912 (GRCm39) T584K probably damaging Het
Col13a1 A G 10: 61,703,608 (GRCm39) probably null Het
Col25a1 A G 3: 130,343,682 (GRCm39) probably null Het
Csrp2 G A 10: 110,773,735 (GRCm39) probably benign Het
Ctla2a T A 13: 61,083,821 (GRCm39) D37V probably damaging Het
Cubn T A 2: 13,355,754 (GRCm39) H1826L probably damaging Het
Dnajc19 A G 3: 34,134,378 (GRCm39) probably null Het
Dxo T C 17: 35,057,745 (GRCm39) probably benign Het
Edil3 A T 13: 89,325,417 (GRCm39) M269L probably benign Het
Fbxl7 C A 15: 26,543,841 (GRCm39) G269C probably damaging Het
Gpnmb T A 6: 49,028,799 (GRCm39) I439N possibly damaging Het
Grm7 G T 6: 110,623,309 (GRCm39) V161F probably damaging Het
Gtpbp3 T G 8: 71,944,779 (GRCm39) S345A probably benign Het
Hnrnpul2 A G 19: 8,801,773 (GRCm39) E327G probably damaging Het
Ifi207 A T 1: 173,555,029 (GRCm39) Y884* probably null Het
Ifi47 T C 11: 48,986,352 (GRCm39) S40P probably benign Het
Kcnq3 A G 15: 65,893,588 (GRCm39) probably null Het
Kifc3 G A 8: 95,830,656 (GRCm39) probably benign Het
Muc4 G C 16: 32,753,919 (GRCm38) R1265P probably benign Het
Mug1 C T 6: 121,865,515 (GRCm39) probably benign Het
Myh2 A G 11: 67,080,427 (GRCm39) I1214V probably benign Het
Naa30 A G 14: 49,425,059 (GRCm39) N337S probably benign Het
Nap1l3 A T X: 121,305,221 (GRCm39) I499N possibly damaging Het
Nfat5 T A 8: 108,078,053 (GRCm39) probably benign Het
Nisch A G 14: 30,898,702 (GRCm39) probably benign Het
Nt5c3 A G 6: 56,860,652 (GRCm39) probably benign Het
Pklr C T 3: 89,050,008 (GRCm39) R328C probably damaging Het
Prrc2c G A 1: 162,538,260 (GRCm39) R457C probably damaging Het
Rab1a T G 11: 20,174,506 (GRCm39) probably benign Het
Rasa3 A T 8: 13,638,972 (GRCm39) D278E probably benign Het
Rdh8 C T 9: 20,734,629 (GRCm39) P99S probably damaging Het
Snx9 T A 17: 5,978,475 (GRCm39) probably null Het
Spns3 C T 11: 72,390,356 (GRCm39) probably benign Het
Sympk A G 7: 18,774,486 (GRCm39) Y421C probably damaging Het
Tas1r2 G A 4: 139,394,729 (GRCm39) C495Y probably damaging Het
Tmem63a G A 1: 180,790,679 (GRCm39) D446N possibly damaging Het
Tmprss15 T C 16: 78,851,030 (GRCm39) probably null Het
Tox3 G T 8: 90,975,533 (GRCm39) T366K possibly damaging Het
Trdmt1 T A 2: 13,526,108 (GRCm39) Q170L probably benign Het
Ttn A T 2: 76,565,752 (GRCm39) V28200D probably damaging Het
Zfp616 G A 11: 73,974,145 (GRCm39) W138* probably null Het
Zfr2 T G 10: 81,081,913 (GRCm39) V493G probably benign Het
Other mutations in Bcap29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00419:Bcap29 APN 12 31,680,871 (GRCm39) missense probably benign 0.02
IGL00537:Bcap29 APN 12 31,667,095 (GRCm39) nonsense probably null
R1328:Bcap29 UTSW 12 31,680,807 (GRCm39) missense probably benign 0.02
R1735:Bcap29 UTSW 12 31,680,839 (GRCm39) missense probably damaging 1.00
R3704:Bcap29 UTSW 12 31,667,151 (GRCm39) missense probably benign 0.00
R3705:Bcap29 UTSW 12 31,667,151 (GRCm39) missense probably benign 0.00
R3871:Bcap29 UTSW 12 31,667,080 (GRCm39) missense probably benign 0.07
R4628:Bcap29 UTSW 12 31,676,806 (GRCm39) missense probably benign
R4832:Bcap29 UTSW 12 31,674,202 (GRCm39) missense probably benign 0.11
R7399:Bcap29 UTSW 12 31,680,881 (GRCm39) missense probably damaging 0.99
R8942:Bcap29 UTSW 12 31,684,353 (GRCm39) start codon destroyed probably damaging 0.99
R9515:Bcap29 UTSW 12 31,676,756 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AACCTATGAATAAGTCATCCTCAGTGC -3'
(R):5'- GTGTGTTTGCTAGCTATCAAGTTCC -3'

Sequencing Primer
(F):5'- GAATAAGTCATCCTCAGTGCTTGGC -3'
(R):5'- TTGCTAGCTATCAAGTTCCTTTTAG -3'
Posted On 2015-01-23