Incidental Mutation 'IGL01621:Bpifb9b'
ID 92624
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Bpifb9b
Ensembl Gene ENSMUSG00000067996
Gene Name BPI fold containing family B, member 9B
Synonyms 5430413K10Rik, OTTMUSG00000015915
Accession Numbers
Essential gene? Probably non essential (E-score: 0.131) question?
Stock # IGL01621
Quality Score
Status
Chromosome 2
Chromosomal Location 154149164-154162564 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 154158871 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000086311 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088921]
AlphaFold A2AJD1
Predicted Effect probably null
Transcript: ENSMUST00000088921
SMART Domains Protein: ENSMUSP00000086311
Gene: ENSMUSG00000067996

DomainStartEndE-ValueType
low complexity region 29 42 N/A INTRINSIC
low complexity region 60 77 N/A INTRINSIC
low complexity region 122 157 N/A INTRINSIC
low complexity region 167 181 N/A INTRINSIC
low complexity region 184 203 N/A INTRINSIC
Pfam:LBP_BPI_CETP 216 377 1.7e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik C T 5: 64,055,726 (GRCm39) T154I possibly damaging Het
4933434E20Rik T A 3: 89,971,809 (GRCm39) M56K possibly damaging Het
Abca6 A G 11: 110,075,534 (GRCm39) L1319S probably damaging Het
Adh4 C T 3: 138,134,788 (GRCm39) probably benign Het
Aloxe3 A G 11: 69,020,839 (GRCm39) N188S probably benign Het
Ap1s1 G A 5: 137,070,658 (GRCm39) R119* probably null Het
Apc2 T G 10: 80,142,035 (GRCm39) L318R probably damaging Het
Atg101 A G 15: 101,184,976 (GRCm39) S33G possibly damaging Het
Atp8a2 A T 14: 60,253,317 (GRCm39) probably benign Het
Braf A T 6: 39,623,787 (GRCm39) probably benign Het
Cabp5 A G 7: 13,135,189 (GRCm39) D43G probably damaging Het
Cfap46 T C 7: 139,186,523 (GRCm39) N2462S unknown Het
Cit C T 5: 116,130,662 (GRCm39) probably benign Het
Cpa4 T C 6: 30,574,415 (GRCm39) V68A probably damaging Het
Cyp2j5 T C 4: 96,517,791 (GRCm39) I474V probably benign Het
Dennd1a C A 2: 37,734,821 (GRCm39) D49Y probably damaging Het
Dlg5 T C 14: 24,198,289 (GRCm39) D1525G probably damaging Het
Dnajc18 C T 18: 35,813,893 (GRCm39) R292H probably benign Het
Dync2h1 A G 9: 7,140,897 (GRCm39) probably null Het
E2f6 A G 12: 16,875,369 (GRCm39) D268G probably benign Het
Evi2b T A 11: 79,407,126 (GRCm39) T150S probably damaging Het
F13b A G 1: 139,431,589 (GRCm39) D53G probably benign Het
Fbxo38 G A 18: 62,655,595 (GRCm39) probably benign Het
Flnb C T 14: 7,950,470 (GRCm38) P2596L probably damaging Het
Fyco1 A G 9: 123,656,247 (GRCm39) probably benign Het
Gm21759 A G 5: 8,229,775 (GRCm39) probably benign Het
Gtse1 A G 15: 85,759,283 (GRCm39) N597S probably benign Het
Hcn3 G T 3: 89,055,030 (GRCm39) S739Y probably damaging Het
Ighv9-4 T A 12: 114,263,612 (GRCm39) N107I probably damaging Het
Inava C A 1: 136,147,513 (GRCm39) A402S probably damaging Het
Iqub T C 6: 24,446,211 (GRCm39) K738E probably benign Het
Itga6 A T 2: 71,656,000 (GRCm39) D308V probably benign Het
Klf12 T C 14: 100,260,585 (GRCm39) Y48C probably damaging Het
Klhdc9 A G 1: 171,186,384 (GRCm39) *351Q probably null Het
Krt40 A T 11: 99,433,694 (GRCm39) N97K probably damaging Het
Lrit1 A C 14: 36,782,112 (GRCm39) T262P probably damaging Het
Mcoln1 T C 8: 3,560,910 (GRCm39) Y411H probably damaging Het
Mfsd4a A G 1: 131,981,881 (GRCm39) S149P probably benign Het
Minar2 A G 18: 59,195,458 (GRCm39) M1V probably null Het
Mipep A G 14: 61,033,614 (GRCm39) probably benign Het
Mslnl A G 17: 25,962,641 (GRCm39) probably benign Het
N4bp2 A T 5: 65,948,267 (GRCm39) H299L probably damaging Het
Nbn C T 4: 15,965,221 (GRCm39) P190S probably benign Het
Nos1 T A 5: 118,083,949 (GRCm39) I1253N probably damaging Het
Nup210 G T 6: 91,007,099 (GRCm39) F572L probably damaging Het
Or10k2 T C 8: 84,268,247 (GRCm39) V158A probably benign Het
Or1e30 T C 11: 73,678,103 (GRCm39) F113S probably damaging Het
Or2y11 T C 11: 49,442,964 (GRCm39) L130P probably damaging Het
P4htm T A 9: 108,460,935 (GRCm39) E106V probably damaging Het
Pcdhb20 C T 18: 37,637,860 (GRCm39) H129Y possibly damaging Het
Pdcd6ip T C 9: 113,514,490 (GRCm39) E240G probably benign Het
Pex5l T C 3: 33,069,110 (GRCm39) probably null Het
Plcd1 T C 9: 118,905,246 (GRCm39) N181S probably damaging Het
Plekhg6 G T 6: 125,349,062 (GRCm39) L412M probably damaging Het
Ppp1r13b T A 12: 111,801,526 (GRCm39) Q386L possibly damaging Het
Pramel25 T C 4: 143,520,502 (GRCm39) F85L probably benign Het
Prpf40b A G 15: 99,207,926 (GRCm39) probably benign Het
Rdh11 C T 12: 79,233,187 (GRCm39) probably null Het
Ripor3 A T 2: 167,839,172 (GRCm39) S110T probably damaging Het
Sec24d G A 3: 123,087,807 (GRCm39) probably null Het
Secisbp2l T C 2: 125,615,131 (GRCm39) S165G probably benign Het
Shank1 C T 7: 43,991,889 (GRCm39) A698V unknown Het
Shank1 T C 7: 44,001,023 (GRCm39) M914T unknown Het
Slc22a3 T C 17: 12,677,379 (GRCm39) Q263R probably benign Het
Smc1a C A X: 150,819,125 (GRCm39) Q647K probably damaging Het
Sohlh1 A G 2: 25,736,873 (GRCm39) probably benign Het
Tacc2 C A 7: 130,331,498 (GRCm39) T484K probably damaging Het
Ubr4 G T 4: 139,168,094 (GRCm39) E2825* probably null Het
Wbp2nl G A 15: 82,192,806 (GRCm39) M163I probably benign Het
Zfp69 T A 4: 120,788,697 (GRCm39) K206M probably damaging Het
Zswim3 G A 2: 164,663,440 (GRCm39) R640H probably damaging Het
Other mutations in Bpifb9b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02119:Bpifb9b APN 2 154,155,544 (GRCm39) missense possibly damaging 0.84
IGL02658:Bpifb9b APN 2 154,153,201 (GRCm39) missense probably benign 0.00
R0230:Bpifb9b UTSW 2 154,158,995 (GRCm39) missense probably damaging 1.00
R0269:Bpifb9b UTSW 2 154,161,545 (GRCm39) missense probably benign 0.00
R0617:Bpifb9b UTSW 2 154,161,545 (GRCm39) missense probably benign 0.00
R1953:Bpifb9b UTSW 2 154,153,234 (GRCm39) missense probably damaging 0.99
R2050:Bpifb9b UTSW 2 154,151,524 (GRCm39) missense possibly damaging 0.93
R2160:Bpifb9b UTSW 2 154,161,595 (GRCm39) missense possibly damaging 0.53
R2200:Bpifb9b UTSW 2 154,155,574 (GRCm39) missense probably benign 0.00
R2354:Bpifb9b UTSW 2 154,153,662 (GRCm39) missense probably benign
R4755:Bpifb9b UTSW 2 154,161,614 (GRCm39) missense probably benign 0.01
R4872:Bpifb9b UTSW 2 154,155,551 (GRCm39) missense probably damaging 0.99
R4914:Bpifb9b UTSW 2 154,156,026 (GRCm39) splice site probably null
R4915:Bpifb9b UTSW 2 154,156,026 (GRCm39) splice site probably null
R4917:Bpifb9b UTSW 2 154,156,026 (GRCm39) splice site probably null
R4918:Bpifb9b UTSW 2 154,156,026 (GRCm39) splice site probably null
R4950:Bpifb9b UTSW 2 154,153,579 (GRCm39) missense probably damaging 1.00
R5438:Bpifb9b UTSW 2 154,151,288 (GRCm39) missense possibly damaging 0.65
R5507:Bpifb9b UTSW 2 154,158,947 (GRCm39) missense possibly damaging 0.91
R6255:Bpifb9b UTSW 2 154,151,284 (GRCm39) missense probably damaging 0.98
R7130:Bpifb9b UTSW 2 154,153,592 (GRCm39) missense probably damaging 0.98
R7161:Bpifb9b UTSW 2 154,155,535 (GRCm39) missense possibly damaging 0.95
R7736:Bpifb9b UTSW 2 154,154,025 (GRCm39) missense probably benign 0.00
R8536:Bpifb9b UTSW 2 154,158,197 (GRCm39) missense probably benign 0.00
R9134:Bpifb9b UTSW 2 154,151,441 (GRCm39) missense probably benign
R9348:Bpifb9b UTSW 2 154,160,766 (GRCm39) missense probably benign 0.28
R9528:Bpifb9b UTSW 2 154,153,297 (GRCm39) missense probably benign 0.02
Posted On 2013-12-09