Incidental Mutation 'R6047:Antxrl'
ID 483355
Institutional Source Beutler Lab
Gene Symbol Antxrl
Ensembl Gene ENSMUSG00000047441
Gene Name anthrax toxin receptor-like
Synonyms 1700112N15Rik
MMRRC Submission 044215-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6047 (G1)
Quality Score 151.008
Status Not validated
Chromosome 14
Chromosomal Location 33774625-33798280 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 33775433 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153806 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058725] [ENSMUST00000178958] [ENSMUST00000226211] [ENSMUST00000227979]
AlphaFold Q8BVM2
Predicted Effect probably benign
Transcript: ENSMUST00000058725
SMART Domains Protein: ENSMUSP00000052816
Gene: ENSMUSG00000047441

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
VWA 74 248 2.9e-19 SMART
Pfam:Anth_Ig 249 351 6.7e-41 PFAM
low complexity region 370 381 N/A INTRINSIC
low complexity region 392 461 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000178958
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215823
Predicted Effect probably benign
Transcript: ENSMUST00000226211
Predicted Effect probably benign
Transcript: ENSMUST00000227979
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.6%
Validation Efficiency 100% (36/36)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1b T C 5: 8,856,066 (GRCm39) I58T probably damaging Het
Adgrb2 G T 4: 129,912,498 (GRCm39) G1208C probably damaging Het
Appl2 C T 10: 83,448,765 (GRCm39) probably null Het
Bloc1s2 T C 19: 44,130,629 (GRCm39) I112V possibly damaging Het
Cblb G T 16: 51,932,611 (GRCm39) probably null Het
Cdk9 T C 2: 32,598,285 (GRCm39) probably null Het
Dok7 G A 5: 35,236,651 (GRCm39) G206D probably damaging Het
Ftsj3 C T 11: 106,143,144 (GRCm39) R390H probably damaging Het
Gpr179 G T 11: 97,229,242 (GRCm39) P971Q probably damaging Het
Hic1 A T 11: 75,057,675 (GRCm39) S405T possibly damaging Het
Ifngr1 T C 10: 19,482,061 (GRCm39) L217P probably damaging Het
Insrr A G 3: 87,711,483 (GRCm39) K468E probably damaging Het
Lce1j G C 3: 92,696,503 (GRCm39) R92G unknown Het
Lrp12 T C 15: 39,735,463 (GRCm39) E823G probably damaging Het
Lrp1b A G 2: 40,527,787 (GRCm39) I98T probably benign Het
Mbd3l2 A T 9: 18,356,212 (GRCm39) H179L possibly damaging Het
Med24 A T 11: 98,598,591 (GRCm39) C691* probably null Het
Mical1 T C 10: 41,357,703 (GRCm39) probably null Het
Msantd2 A T 9: 37,434,738 (GRCm39) Y326F probably damaging Het
Nfyc T A 4: 120,636,314 (GRCm39) probably null Het
Nrg3 T A 14: 38,119,309 (GRCm39) probably null Het
Nt5c3 G A 6: 56,859,964 (GRCm39) S291L probably damaging Het
Pak4 A G 7: 28,262,461 (GRCm39) Y384H probably benign Het
Pdia5 T C 16: 35,217,848 (GRCm39) K512E probably damaging Het
Pfpl T C 19: 12,406,597 (GRCm39) F283L probably damaging Het
Pick1 A G 15: 79,139,895 (GRCm39) probably benign Het
Pkd1 T C 17: 24,814,059 (GRCm39) V4143A probably damaging Het
Ptprc C T 1: 138,028,779 (GRCm39) probably null Het
Scn10a A G 9: 119,451,897 (GRCm39) F1342S probably benign Het
Slc17a7 A T 7: 44,822,830 (GRCm39) I436F probably benign Het
Slc34a1 G T 13: 55,559,884 (GRCm39) A403S probably damaging Het
Stmn3 A T 2: 180,950,952 (GRCm39) Y35N possibly damaging Het
Tldc2 A G 2: 156,938,382 (GRCm39) E207G probably damaging Het
Unc79 A G 12: 103,027,717 (GRCm39) N436S probably damaging Het
Uty G T Y: 1,158,288 (GRCm39) P538Q probably damaging Het
Zzef1 A G 11: 72,756,921 (GRCm39) D1142G probably damaging Het
Other mutations in Antxrl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01344:Antxrl APN 14 33,797,554 (GRCm39) missense probably benign 0.01
IGL01632:Antxrl APN 14 33,789,904 (GRCm39) missense probably damaging 0.99
IGL02379:Antxrl APN 14 33,778,492 (GRCm39) splice site probably null
IGL02381:Antxrl APN 14 33,778,568 (GRCm39) splice site probably null
IGL02736:Antxrl APN 14 33,778,575 (GRCm39) unclassified probably benign
R0631:Antxrl UTSW 14 33,780,758 (GRCm39) critical splice donor site probably null
R1190:Antxrl UTSW 14 33,791,207 (GRCm39) missense probably benign 0.00
R1406:Antxrl UTSW 14 33,794,999 (GRCm39) missense possibly damaging 0.53
R1406:Antxrl UTSW 14 33,794,999 (GRCm39) missense possibly damaging 0.53
R1454:Antxrl UTSW 14 33,782,906 (GRCm39) missense probably damaging 0.99
R1469:Antxrl UTSW 14 33,789,388 (GRCm39) intron probably benign
R1638:Antxrl UTSW 14 33,792,453 (GRCm39) critical splice donor site probably null
R1996:Antxrl UTSW 14 33,797,786 (GRCm39) missense probably benign 0.01
R2174:Antxrl UTSW 14 33,782,357 (GRCm39) missense probably damaging 1.00
R2421:Antxrl UTSW 14 33,793,646 (GRCm39) intron probably benign
R3850:Antxrl UTSW 14 33,789,338 (GRCm39) missense probably benign 0.00
R4178:Antxrl UTSW 14 33,776,928 (GRCm39) splice site probably null
R4434:Antxrl UTSW 14 33,793,574 (GRCm39) intron probably benign
R4603:Antxrl UTSW 14 33,797,792 (GRCm39) missense possibly damaging 0.72
R4769:Antxrl UTSW 14 33,795,027 (GRCm39) missense possibly damaging 0.53
R6003:Antxrl UTSW 14 33,797,592 (GRCm39) missense possibly damaging 0.72
R6228:Antxrl UTSW 14 33,778,556 (GRCm39) missense probably damaging 1.00
R6363:Antxrl UTSW 14 33,791,244 (GRCm39) missense probably damaging 1.00
R6525:Antxrl UTSW 14 33,782,363 (GRCm39) missense probably damaging 1.00
R6800:Antxrl UTSW 14 33,787,864 (GRCm39) missense probably damaging 1.00
R6933:Antxrl UTSW 14 33,797,728 (GRCm39) missense possibly damaging 0.53
R7086:Antxrl UTSW 14 33,787,873 (GRCm39) missense probably benign 0.26
R7257:Antxrl UTSW 14 33,787,806 (GRCm39) missense probably benign 0.03
R7315:Antxrl UTSW 14 33,793,504 (GRCm39) missense unknown
R7981:Antxrl UTSW 14 33,787,838 (GRCm39) missense probably damaging 0.99
R9070:Antxrl UTSW 14 33,793,671 (GRCm39) nonsense probably null
R9097:Antxrl UTSW 14 33,793,660 (GRCm39) missense probably benign 0.33
X0028:Antxrl UTSW 14 33,775,872 (GRCm39) critical splice donor site probably null
Z1088:Antxrl UTSW 14 33,789,928 (GRCm39) missense probably damaging 1.00
Z1177:Antxrl UTSW 14 33,789,887 (GRCm39) frame shift probably null
Predicted Primers
Posted On 2017-07-14