Incidental Mutation 'IGL02029:Fcrl1'
ID 184320
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fcrl1
Ensembl Gene ENSMUSG00000059994
Gene Name Fc receptor-like 1
Synonyms mBXMH1, A230020G22Rik, IFGP1, moFcRH1L, moFcRH1, Fcrh1, BXMAS1-like, moFcRH1S, mIFGP1
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02029
Quality Score
Status
Chromosome 3
Chromosomal Location 87283694-87310241 bp(+) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) T to A at 87283794 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142286 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072480] [ENSMUST00000163661] [ENSMUST00000167200] [ENSMUST00000191666] [ENSMUST00000194786]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000072480
SMART Domains Protein: ENSMUSP00000072300
Gene: ENSMUSG00000059994

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
IG 28 113 4.03e-8 SMART
IG 123 204 1.35e0 SMART
transmembrane domain 221 243 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000163661
SMART Domains Protein: ENSMUSP00000130936
Gene: ENSMUSG00000059994

DomainStartEndE-ValueType
IG 48 133 4.03e-8 SMART
IG 143 224 1.35e0 SMART
transmembrane domain 241 263 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000167200
SMART Domains Protein: ENSMUSP00000128235
Gene: ENSMUSG00000059994

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
IG 28 113 4.03e-8 SMART
IG 123 204 1.35e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000191666
SMART Domains Protein: ENSMUSP00000141916
Gene: ENSMUSG00000059994

DomainStartEndE-ValueType
IG_like 9 94 4.5e-2 SMART
IG 28 113 1.7e-10 SMART
IG 123 204 5.5e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000194786
SMART Domains Protein: ENSMUSP00000142286
Gene: ENSMUSG00000059994

DomainStartEndE-ValueType
IG_like 9 94 4.5e-2 SMART
IG 28 113 1.7e-10 SMART
IG 123 204 5.5e-3 SMART
transmembrane domain 221 243 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein contains three extracellular C2-like immunoglobulin domains, a transmembrane domain and a cytoplasmic domain with two immunoreceptor-tyrosine activation motifs. This protein may play a role in the regulation of cancer cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agap2 T C 10: 126,916,152 (GRCm39) V221A unknown Het
Akr1c13 T A 13: 4,255,361 (GRCm39) Y317* probably null Het
Bicd2 T A 13: 49,522,975 (GRCm39) I30N probably damaging Het
Cadm2 G T 16: 66,544,182 (GRCm39) N291K probably damaging Het
Ccdc61 C T 7: 18,637,423 (GRCm39) C68Y probably damaging Het
Ccnl2 A G 4: 155,906,319 (GRCm39) S351G probably benign Het
Cdcp1 A G 9: 123,012,899 (GRCm39) probably benign Het
Clhc1 T C 11: 29,510,798 (GRCm39) S256P probably benign Het
Fam83h T C 15: 75,878,287 (GRCm39) E37G probably damaging Het
Fancd2 C T 6: 113,547,936 (GRCm39) L938F probably benign Het
Fbn2 G T 18: 58,342,675 (GRCm39) A68E probably benign Het
Ganc A G 2: 120,290,338 (GRCm39) T892A probably benign Het
Gramd1a C T 7: 30,832,249 (GRCm39) R596H possibly damaging Het
Limk1 A T 5: 134,686,808 (GRCm39) Y518* probably null Het
Map1a A G 2: 121,133,779 (GRCm39) T1294A possibly damaging Het
Marchf3 G A 18: 56,940,753 (GRCm39) P126S probably benign Het
Ntn5 A G 7: 45,336,015 (GRCm39) I149V probably benign Het
Nup43 T C 10: 7,543,347 (GRCm39) F8L possibly damaging Het
Or5b122 A T 19: 13,563,468 (GRCm39) M267L probably benign Het
Or5be3 A G 2: 86,864,245 (GRCm39) F107L probably benign Het
P2rx6 C T 16: 17,385,959 (GRCm39) S236F probably benign Het
Peg10 G T 6: 4,754,473 (GRCm39) probably benign Het
Runx2 T A 17: 44,969,574 (GRCm39) R238* probably null Het
Serpinb9d A T 13: 33,380,512 (GRCm39) I133L possibly damaging Het
Snph A G 2: 151,435,527 (GRCm39) V434A probably damaging Het
Trp53rkb C A 2: 166,637,314 (GRCm39) P90Q probably damaging Het
Ttn C A 2: 76,580,148 (GRCm39) E21836* probably null Het
Tut7 A G 13: 59,932,702 (GRCm39) probably benign Het
Ube3c T A 5: 29,824,326 (GRCm39) F507I probably damaging Het
Ugt1a6a T C 1: 88,066,403 (GRCm39) S70P probably benign Het
Zfp354b C T 11: 50,814,664 (GRCm39) C87Y probably benign Het
Zfp462 G T 4: 55,079,395 (GRCm39) probably benign Het
Other mutations in Fcrl1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00321:Fcrl1 APN 3 87,296,942 (GRCm39) missense probably damaging 0.99
IGL01884:Fcrl1 APN 3 87,292,044 (GRCm39) missense probably damaging 1.00
IGL02231:Fcrl1 APN 3 87,292,470 (GRCm39) missense probably damaging 1.00
IGL02231:Fcrl1 APN 3 87,292,469 (GRCm39) missense possibly damaging 0.94
IGL02405:Fcrl1 APN 3 87,293,074 (GRCm39) missense probably damaging 0.99
IGL02858:Fcrl1 APN 3 87,292,012 (GRCm39) missense probably damaging 1.00
IGL03133:Fcrl1 APN 3 87,296,699 (GRCm39) missense probably benign 0.00
IGL03176:Fcrl1 APN 3 87,298,564 (GRCm39) missense probably damaging 1.00
IGL03352:Fcrl1 APN 3 87,292,398 (GRCm39) missense probably benign 0.01
R1497:Fcrl1 UTSW 3 87,292,109 (GRCm39) missense probably damaging 1.00
R1569:Fcrl1 UTSW 3 87,292,012 (GRCm39) missense probably damaging 1.00
R1581:Fcrl1 UTSW 3 87,293,030 (GRCm39) missense possibly damaging 0.94
R1778:Fcrl1 UTSW 3 87,292,626 (GRCm39) splice site probably benign
R1959:Fcrl1 UTSW 3 87,283,827 (GRCm39) missense possibly damaging 0.92
R2928:Fcrl1 UTSW 3 87,298,564 (GRCm39) missense probably benign 0.19
R4677:Fcrl1 UTSW 3 87,297,563 (GRCm39) missense possibly damaging 0.61
R5122:Fcrl1 UTSW 3 87,293,081 (GRCm39) missense probably benign 0.35
R5507:Fcrl1 UTSW 3 87,298,549 (GRCm39) missense probably benign 0.16
R6363:Fcrl1 UTSW 3 87,292,475 (GRCm39) missense probably damaging 0.96
R6478:Fcrl1 UTSW 3 87,296,946 (GRCm39) missense probably benign 0.41
R6559:Fcrl1 UTSW 3 87,298,560 (GRCm39) missense probably benign 0.33
R6985:Fcrl1 UTSW 3 87,296,957 (GRCm39) missense probably benign
R7291:Fcrl1 UTSW 3 87,293,088 (GRCm39) critical splice donor site probably null
R9649:Fcrl1 UTSW 3 87,291,918 (GRCm39) missense possibly damaging 0.68
Z1177:Fcrl1 UTSW 3 87,296,670 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07