Incidental Mutation 'IGL02277:Fcrl6'
ID 287381
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fcrl6
Ensembl Gene ENSMUSG00000070504
Gene Name Fc receptor-like 6
Synonyms FcRH6, moFcRH6, mIFGP6, ENSMUSG00000070504
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02277
Quality Score
Status
Chromosome 1
Chromosomal Location 172424209-172430118 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 172426686 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 87 (C87R)
Ref Sequence ENSEMBL: ENSMUSP00000091861 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094303]
AlphaFold A1YIY0
Predicted Effect probably damaging
Transcript: ENSMUST00000094303
AA Change: C87R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000091861
Gene: ENSMUSG00000070504
AA Change: C87R

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
Pfam:Ig_3 19 91 1.2e-4 PFAM
Pfam:Ig_2 20 106 8e-9 PFAM
Pfam:Ig_3 113 187 1.9e-9 PFAM
transmembrane domain 215 237 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000193431
Predicted Effect noncoding transcript
Transcript: ENSMUST00000193566
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik C T 9: 57,165,708 (GRCm39) G222D probably benign Het
Abcc6 T C 7: 45,650,485 (GRCm39) D625G probably benign Het
Akr1c12 C T 13: 4,322,268 (GRCm39) R258Q probably damaging Het
Akr1c20 T A 13: 4,564,404 (GRCm39) E36D probably benign Het
Csn2 A G 5: 87,845,881 (GRCm39) probably benign Het
Dennd5a T C 7: 109,497,176 (GRCm39) I1084V possibly damaging Het
Dlg1 A G 16: 31,609,082 (GRCm39) I259V probably damaging Het
Dpysl5 A G 5: 30,946,125 (GRCm39) I344V probably damaging Het
Fras1 A G 5: 96,735,977 (GRCm39) E524G probably benign Het
Gabpb2 A G 3: 95,096,595 (GRCm39) V270A probably benign Het
Gm5591 T A 7: 38,218,462 (GRCm39) I804F possibly damaging Het
Gm5591 T C 7: 38,219,856 (GRCm39) D339G probably damaging Het
Ighv2-5 T A 12: 113,649,127 (GRCm39) T109S possibly damaging Het
Ints4 T A 7: 97,136,665 (GRCm39) L119Q probably damaging Het
Kansl3 A T 1: 36,388,028 (GRCm39) D386E possibly damaging Het
Kdm3b A T 18: 34,956,717 (GRCm39) H1224L probably damaging Het
Macf1 C A 4: 123,380,497 (GRCm39) R1523L probably damaging Het
Myo1f A G 17: 33,798,835 (GRCm39) probably null Het
Nup188 A G 2: 30,216,523 (GRCm39) T776A possibly damaging Het
Or1q1 G A 2: 36,887,196 (GRCm39) probably null Het
Or2y8 T A 11: 52,036,189 (GRCm39) H56L probably damaging Het
Or4f56 T A 2: 111,703,925 (GRCm39) I92F possibly damaging Het
Plxnb1 T A 9: 108,941,201 (GRCm39) L1660Q probably damaging Het
Ppp1r17 A G 6: 56,003,123 (GRCm39) D71G probably damaging Het
Ptprt T C 2: 161,389,301 (GRCm39) Q1264R probably damaging Het
Rgl3 C T 9: 21,885,405 (GRCm39) V642M probably damaging Het
Slc26a2 T C 18: 61,332,052 (GRCm39) T460A probably damaging Het
Smtnl2 T A 11: 72,282,199 (GRCm39) M395L probably damaging Het
St3gal5 A T 6: 72,119,184 (GRCm39) T99S possibly damaging Het
Unc5b T C 10: 60,610,521 (GRCm39) N421S probably benign Het
Zcchc17 G A 4: 130,221,014 (GRCm39) T179M probably benign Het
Zfp369 T C 13: 65,432,746 (GRCm39) S79P probably damaging Het
Other mutations in Fcrl6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00903:Fcrl6 APN 1 172,426,674 (GRCm39) missense probably benign 0.08
IGL01074:Fcrl6 APN 1 172,426,680 (GRCm39) missense possibly damaging 0.89
IGL02146:Fcrl6 APN 1 172,426,264 (GRCm39) missense probably benign 0.01
IGL03162:Fcrl6 APN 1 172,425,820 (GRCm39) missense probably damaging 1.00
IGL03303:Fcrl6 APN 1 172,425,255 (GRCm39) missense probably damaging 0.99
K3955:Fcrl6 UTSW 1 172,425,251 (GRCm39) missense probably benign 0.00
R0051:Fcrl6 UTSW 1 172,426,320 (GRCm39) missense probably benign 0.24
R0051:Fcrl6 UTSW 1 172,426,320 (GRCm39) missense probably benign 0.24
R1336:Fcrl6 UTSW 1 172,426,791 (GRCm39) nonsense probably null
R2125:Fcrl6 UTSW 1 172,426,815 (GRCm39) missense probably benign 0.41
R2126:Fcrl6 UTSW 1 172,426,815 (GRCm39) missense probably benign 0.41
R5376:Fcrl6 UTSW 1 172,426,847 (GRCm39) missense probably damaging 1.00
R5395:Fcrl6 UTSW 1 172,426,287 (GRCm39) missense possibly damaging 0.55
R6314:Fcrl6 UTSW 1 172,426,186 (GRCm39) splice site probably null
R7525:Fcrl6 UTSW 1 172,425,239 (GRCm39) missense probably benign 0.25
R7690:Fcrl6 UTSW 1 172,426,223 (GRCm39) missense probably damaging 0.97
R8033:Fcrl6 UTSW 1 172,426,748 (GRCm39) missense probably benign 0.03
R8894:Fcrl6 UTSW 1 172,426,856 (GRCm39) missense probably benign 0.05
U24488:Fcrl6 UTSW 1 172,426,437 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16