Incidental Mutation 'R1475:Fcamr'
ID 163972
Institutional Source Beutler Lab
Gene Symbol Fcamr
Ensembl Gene ENSMUSG00000026415
Gene Name Fc receptor, IgA, IgM, high affinity
Synonyms
MMRRC Submission 039528-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.048) question?
Stock # R1475 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 130728639-130742477 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 130742221 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000108096 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000027670] [ENSMUST00000112477]
AlphaFold Q2TB54
Predicted Effect probably null
Transcript: ENSMUST00000027670
SMART Domains Protein: ENSMUSP00000027670
Gene: ENSMUSG00000026415

DomainStartEndE-ValueType
signal peptide 1 36 N/A INTRINSIC
IG 87 191 1.19e-5 SMART
low complexity region 208 220 N/A INTRINSIC
low complexity region 241 253 N/A INTRINSIC
transmembrane domain 456 475 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000112477
SMART Domains Protein: ENSMUSP00000108096
Gene: ENSMUSG00000026415

DomainStartEndE-ValueType
low complexity region 80 87 N/A INTRINSIC
IG 143 247 1.19e-5 SMART
low complexity region 264 276 N/A INTRINSIC
low complexity region 297 309 N/A INTRINSIC
transmembrane domain 512 531 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000122968
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125056
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136015
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.8%
Validation Efficiency 96% (46/48)
MGI Phenotype PHENOTYPE: Homozygous null mice have enhanced germinal center formation, affinity maturation and memory induction of IgG3 producing B cells after immunization with T cell-independent antigens. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018B08Rik A T 8: 122,267,327 (GRCm39) probably benign Het
9230112D13Rik T A 14: 34,234,012 (GRCm39) D93V unknown Het
Aatk G A 11: 119,901,714 (GRCm39) T894M probably damaging Het
Acacb T C 5: 114,333,313 (GRCm39) I479T possibly damaging Het
Acap3 T C 4: 155,987,278 (GRCm39) I431T probably damaging Het
Adgrl1 A G 8: 84,664,979 (GRCm39) K1267R possibly damaging Het
Bphl A C 13: 34,244,507 (GRCm39) D208A probably benign Het
C2cd5 T C 6: 143,018,298 (GRCm39) D308G possibly damaging Het
Camsap3 C T 8: 3,654,708 (GRCm39) R782C probably damaging Het
Cdk11b G A 4: 155,718,674 (GRCm39) R208H probably damaging Het
Cfap44 T C 16: 44,254,175 (GRCm39) probably benign Het
Chrna4 T C 2: 180,671,172 (GRCm39) S195G probably benign Het
Cpsf2 T C 12: 101,951,495 (GRCm39) L144S probably damaging Het
Creld2 G A 15: 88,704,834 (GRCm39) W103* probably null Het
Dffa T A 4: 149,201,935 (GRCm39) L171Q probably damaging Het
Emcn C T 3: 137,085,668 (GRCm39) H89Y possibly damaging Het
Espn G A 4: 152,218,728 (GRCm39) P452S probably damaging Het
Fam78b T A 1: 166,829,346 (GRCm39) I71N probably damaging Het
Fam89b A G 19: 5,779,447 (GRCm39) S37P probably damaging Het
Fat4 G A 3: 38,942,472 (GRCm39) R455H probably damaging Het
Fbxo6 A G 4: 148,230,567 (GRCm39) F232L probably benign Het
Fermt3 T C 19: 6,996,242 (GRCm39) probably null Het
Fsip2 A T 2: 82,817,539 (GRCm39) D4424V probably damaging Het
Gaa G A 11: 119,165,142 (GRCm39) probably null Het
Glce T C 9: 61,968,210 (GRCm39) T314A possibly damaging Het
Hdac5 T C 11: 102,093,012 (GRCm39) Q575R possibly damaging Het
Il23r C A 6: 67,429,280 (GRCm39) probably null Het
Kcnj4 T A 15: 79,368,831 (GRCm39) E383V probably damaging Het
Lrsam1 G T 2: 32,844,277 (GRCm39) Q115K possibly damaging Het
Lyst T A 13: 13,882,797 (GRCm39) probably null Het
Myf5 A G 10: 107,320,515 (GRCm39) V190A probably benign Het
Nmnat2 G A 1: 152,950,441 (GRCm39) R42H probably damaging Het
Or8b42 T A 9: 38,342,160 (GRCm39) V194D probably benign Het
Or8k20 A T 2: 86,105,905 (GRCm39) *309R probably null Het
Osbpl1a T A 18: 12,890,737 (GRCm39) K380M probably damaging Het
Pgd T C 4: 149,241,232 (GRCm39) T226A probably benign Het
Pitpnm3 T C 11: 71,965,453 (GRCm39) T127A probably damaging Het
Plekhm2 T C 4: 141,355,165 (GRCm39) D954G possibly damaging Het
Pramel14 T C 4: 143,720,882 (GRCm39) K20E probably benign Het
Rasal1 T A 5: 120,801,047 (GRCm39) F236I possibly damaging Het
Stab1 T C 14: 30,885,785 (GRCm39) N63S probably benign Het
Syf2 T A 4: 134,662,745 (GRCm39) M145K possibly damaging Het
Usp34 C A 11: 23,423,253 (GRCm39) L3152I probably damaging Het
Usp50 T C 2: 126,611,787 (GRCm39) probably null Het
Wdfy4 A T 14: 32,830,645 (GRCm39) I929N probably benign Het
Zfp874b A T 13: 67,622,211 (GRCm39) probably null Het
Other mutations in Fcamr
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00840:Fcamr APN 1 130,740,951 (GRCm39) missense probably benign 0.01
IGL02880:Fcamr APN 1 130,741,071 (GRCm39) missense probably benign 0.00
IGL03199:Fcamr APN 1 130,740,655 (GRCm39) missense probably damaging 1.00
IGL03392:Fcamr APN 1 130,728,685 (GRCm39) utr 5 prime probably benign
IGL03398:Fcamr APN 1 130,730,985 (GRCm39) missense probably damaging 0.97
R1101:Fcamr UTSW 1 130,742,223 (GRCm39) splice site probably null
R1312:Fcamr UTSW 1 130,739,224 (GRCm39) missense probably damaging 1.00
R1351:Fcamr UTSW 1 130,740,757 (GRCm39) missense possibly damaging 0.83
R1387:Fcamr UTSW 1 130,732,379 (GRCm39) missense possibly damaging 0.85
R1728:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1728:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1728:Fcamr UTSW 1 130,732,306 (GRCm39) missense probably benign 0.06
R1728:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1728:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1728:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1728:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1728:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1728:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1729:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1729:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1729:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1729:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1729:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1729:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1729:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1729:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1730:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1730:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1730:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1730:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1730:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1730:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1730:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1739:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1739:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1739:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1739:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1739:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1739:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1739:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1739:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1762:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1762:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1762:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1762:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1762:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1762:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1762:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1762:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1783:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1783:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1783:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1783:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1783:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1783:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1783:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1783:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1784:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1784:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1784:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1784:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1784:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1784:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1784:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1784:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1785:Fcamr UTSW 1 130,740,546 (GRCm39) missense probably benign 0.02
R1785:Fcamr UTSW 1 130,740,475 (GRCm39) missense probably benign 0.00
R1785:Fcamr UTSW 1 130,740,429 (GRCm39) missense probably benign
R1785:Fcamr UTSW 1 130,740,366 (GRCm39) missense probably benign 0.38
R1785:Fcamr UTSW 1 130,739,317 (GRCm39) missense probably benign
R1785:Fcamr UTSW 1 130,732,364 (GRCm39) missense probably benign 0.00
R1785:Fcamr UTSW 1 130,732,306 (GRCm39) missense probably benign 0.06
R1785:Fcamr UTSW 1 130,742,334 (GRCm39) missense probably benign
R1785:Fcamr UTSW 1 130,740,553 (GRCm39) missense probably benign 0.41
R1793:Fcamr UTSW 1 130,739,284 (GRCm39) missense probably benign 0.03
R2085:Fcamr UTSW 1 130,739,335 (GRCm39) missense probably damaging 1.00
R3937:Fcamr UTSW 1 130,732,313 (GRCm39) missense probably damaging 0.97
R4529:Fcamr UTSW 1 130,732,313 (GRCm39) missense probably damaging 0.99
R4624:Fcamr UTSW 1 130,730,999 (GRCm39) missense probably damaging 0.99
R4822:Fcamr UTSW 1 130,740,423 (GRCm39) missense possibly damaging 0.82
R5055:Fcamr UTSW 1 130,739,174 (GRCm39) missense probably damaging 1.00
R5514:Fcamr UTSW 1 130,741,793 (GRCm39) missense probably damaging 1.00
R5807:Fcamr UTSW 1 130,739,263 (GRCm39) missense probably damaging 1.00
R6077:Fcamr UTSW 1 130,740,663 (GRCm39) missense probably damaging 1.00
R6200:Fcamr UTSW 1 130,730,927 (GRCm39) missense probably benign 0.16
R6653:Fcamr UTSW 1 130,740,939 (GRCm39) missense possibly damaging 0.89
R7081:Fcamr UTSW 1 130,740,949 (GRCm39) missense probably damaging 1.00
R7362:Fcamr UTSW 1 130,741,760 (GRCm39) missense possibly damaging 0.52
R7828:Fcamr UTSW 1 130,739,443 (GRCm39) missense probably damaging 1.00
R7861:Fcamr UTSW 1 130,742,375 (GRCm39) missense probably benign
R8188:Fcamr UTSW 1 130,730,665 (GRCm39) splice site probably null
R8869:Fcamr UTSW 1 130,739,335 (GRCm39) missense probably damaging 1.00
R8907:Fcamr UTSW 1 130,740,328 (GRCm39) missense probably damaging 1.00
R9568:Fcamr UTSW 1 130,732,356 (GRCm39) missense probably damaging 0.99
X0012:Fcamr UTSW 1 130,740,471 (GRCm39) missense probably benign 0.09
Predicted Primers
Posted On 2014-03-28