Incidental Mutation 'IGL00903:Fcrl6'
ID 26605
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 # IGL00903
Quality Score
Status
Chromosome 1
Chromosomal Location 172424209-172430118 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 172426674 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 91 (T91S)
Ref Sequence ENSEMBL: ENSMUSP00000091861 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094303]
AlphaFold A1YIY0
Predicted Effect probably benign
Transcript: ENSMUST00000094303
AA Change: T91S

PolyPhen 2 Score 0.077 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000091861
Gene: ENSMUSG00000070504
AA Change: T91S

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: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arsk A G 13: 76,246,487 (GRCm39) probably null Het
As3mt A G 19: 46,700,673 (GRCm39) I159V probably benign Het
Atpsckmt T C 15: 31,606,261 (GRCm39) V73A possibly damaging Het
Ctsll3 C A 13: 60,948,075 (GRCm39) V201L probably benign Het
Dapk1 T C 13: 60,909,211 (GRCm39) Y1275H probably damaging Het
Erap1 G A 13: 74,821,826 (GRCm39) R727H probably benign Het
Gvin1 T C 7: 105,757,377 (GRCm39) E2364G probably benign Het
Hacd3 T C 9: 64,911,535 (GRCm39) probably benign Het
Hcls1 T A 16: 36,776,383 (GRCm39) probably null Het
Igf2r C T 17: 12,902,754 (GRCm39) R2432H possibly damaging Het
Kif27 C A 13: 58,492,486 (GRCm39) V218F possibly damaging Het
Klhl20 T C 1: 160,918,076 (GRCm39) Y70C probably benign Het
Krt86 C T 15: 101,371,741 (GRCm39) H104Y probably benign Het
Lcn12 G T 2: 25,383,332 (GRCm39) N15K possibly damaging Het
Mrgpra1 T C 7: 46,985,326 (GRCm39) M118V probably benign Het
Nacad G T 11: 6,550,632 (GRCm39) T853K probably damaging Het
Nos3 A T 5: 24,574,860 (GRCm39) Q293L probably damaging Het
Prkca C T 11: 107,874,800 (GRCm39) V381M probably damaging Het
Ptcd3 A G 6: 71,884,828 (GRCm39) F37S possibly damaging Het
Ptgs2 A G 1: 149,980,175 (GRCm39) Y371C probably damaging Het
Pygl T C 12: 70,254,516 (GRCm39) Y143C probably damaging Het
Samhd1 A G 2: 156,949,343 (GRCm39) probably benign Het
Scube1 T A 15: 83,587,702 (GRCm39) H89L probably damaging Het
Tmem59l G A 8: 70,938,315 (GRCm39) probably benign Het
Vmn2r108 A G 17: 20,682,774 (GRCm39) V810A probably damaging Het
Vmn2r61 T G 7: 41,949,935 (GRCm39) F785C probably damaging Het
Zfas1 G T 2: 166,907,406 (GRCm39) probably benign Het
Other mutations in Fcrl6
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
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 2013-04-17