Incidental Mutation 'IGL02146:Fcrl6'
ID 281764
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 # IGL02146
Quality Score
Status
Chromosome 1
Chromosomal Location 172424209-172430118 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 172426264 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 178 (T178A)
Ref Sequence ENSEMBL: ENSMUSP00000091861 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094303]
AlphaFold A1YIY0
Predicted Effect probably benign
Transcript: ENSMUST00000094303
AA Change: T178A

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000091861
Gene: ENSMUSG00000070504
AA Change: T178A

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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik A G 9: 57,164,023 (GRCm39) C784R possibly damaging Het
Akp3 A T 1: 87,054,297 (GRCm39) D278V probably benign Het
Atxn7l1 G T 12: 33,418,030 (GRCm39) R730S probably benign Het
Bag6 A G 17: 35,355,191 (GRCm39) T30A probably damaging Het
Blk G T 14: 63,611,648 (GRCm39) P429H probably damaging Het
Bmp2k T A 5: 97,212,689 (GRCm39) M524K unknown Het
Bst1 T A 5: 43,983,678 (GRCm39) H221Q probably damaging Het
Ces2g T C 8: 105,693,576 (GRCm39) I419T possibly damaging Het
Cnep1r1 T C 8: 88,856,326 (GRCm39) V34A probably benign Het
Ctnnbl1 A G 2: 157,661,414 (GRCm39) E308G probably damaging Het
Cyp20a1 A T 1: 60,410,410 (GRCm39) K237I possibly damaging Het
Dlg5 T C 14: 24,252,429 (GRCm39) T104A probably damaging Het
Dnaaf11 C T 15: 66,361,374 (GRCm39) W42* probably null Het
Dnaaf11 C A 15: 66,361,375 (GRCm39) W42L probably benign Het
Dnah9 C T 11: 65,818,526 (GRCm39) V3271M probably damaging Het
Eed T A 7: 89,618,803 (GRCm39) N204Y possibly damaging Het
Fat3 A G 9: 15,910,878 (GRCm39) V1708A probably benign Het
Galnt4 A C 10: 98,945,563 (GRCm39) K429N possibly damaging Het
Ints6 T A 14: 62,996,709 (GRCm39) T94S possibly damaging Het
Iqsec3 A T 6: 121,360,916 (GRCm39) S981T probably damaging Het
Itga9 T A 9: 118,663,400 (GRCm39) S146T possibly damaging Het
Itpr3 A G 17: 27,336,249 (GRCm39) Y2325C probably damaging Het
Kng2 T A 16: 22,806,582 (GRCm39) Q539L probably damaging Het
Lmtk3 T A 7: 45,444,371 (GRCm39) probably benign Het
Map1a T C 2: 121,129,927 (GRCm39) Y248H probably damaging Het
Mroh1 A G 15: 76,318,879 (GRCm39) probably benign Het
Mroh2b T C 15: 4,980,776 (GRCm39) probably null Het
Myo18b A T 5: 112,991,151 (GRCm39) M942K probably damaging Het
Myzap T A 9: 71,471,730 (GRCm39) T94S probably benign Het
Nebl C A 2: 17,353,679 (GRCm39) R957S probably damaging Het
Nexn A T 3: 151,952,885 (GRCm39) D278E probably benign Het
Nlgn1 A T 3: 25,966,846 (GRCm39) N222K probably damaging Het
Or6c76 T A 10: 129,612,727 (GRCm39) probably benign Het
Or8d1 G A 9: 38,766,654 (GRCm39) A99T probably benign Het
Osbpl6 A T 2: 76,380,094 (GRCm39) R79S possibly damaging Het
Phip T C 9: 82,763,771 (GRCm39) I1268M probably benign Het
Pkd2 G T 5: 104,637,157 (GRCm39) R590L probably damaging Het
Reg2 G A 6: 78,382,568 (GRCm39) probably benign Het
Scaf1 A T 7: 44,662,934 (GRCm39) D26E probably damaging Het
Ska1 A G 18: 74,329,981 (GRCm39) I253T possibly damaging Het
Slc11a2 T C 15: 100,299,169 (GRCm39) N443D probably damaging Het
Slc6a12 A T 6: 121,330,460 (GRCm39) T155S probably benign Het
Slit3 A G 11: 35,125,675 (GRCm39) K118R possibly damaging Het
Snap23 T G 2: 120,429,792 (GRCm39) N212K probably damaging Het
Snx13 T A 12: 35,151,078 (GRCm39) D346E probably benign Het
Sumf1 C A 6: 108,150,392 (GRCm39) probably null Het
Susd2 T C 10: 75,474,267 (GRCm39) N479S possibly damaging Het
Tiam1 A G 16: 89,646,569 (GRCm39) I821T probably benign Het
Tll2 C A 19: 41,086,276 (GRCm39) V651L probably benign Het
Vmn2r1 A G 3: 64,012,104 (GRCm39) D655G probably benign Het
Vmn2r72 T C 7: 85,387,170 (GRCm39) Y798C probably damaging Het
Vps13b A C 15: 35,646,479 (GRCm39) I1528L probably benign Het
Wdtc1 G A 4: 133,029,076 (GRCm39) L337F probably benign Het
Zfp128 A C 7: 12,623,959 (GRCm39) K109T possibly 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
IGL02277:Fcrl6 APN 1 172,426,686 (GRCm39) missense probably damaging 1.00
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