Incidental Mutation 'R6003:Lax1'
ID 478447
Institutional Source Beutler Lab
Gene Symbol Lax1
Ensembl Gene ENSMUSG00000051998
Gene Name lymphocyte transmembrane adaptor 1
Synonyms E430019B13Rik
MMRRC Submission 043252-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.048) question?
Stock # R6003 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 133606829-133617846 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 133611834 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 34 (I34F)
Ref Sequence ENSEMBL: ENSMUSP00000131126 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000169295] [ENSMUST00000189524]
AlphaFold Q8BHB3
Predicted Effect probably benign
Transcript: ENSMUST00000169295
AA Change: I34F

PolyPhen 2 Score 0.239 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000131126
Gene: ENSMUSG00000051998
AA Change: I34F

DomainStartEndE-ValueType
Pfam:LAX 27 378 2.4e-172 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000189524
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.4%
  • 10x: 97.2%
  • 20x: 90.9%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous null mice exhibit spontaneous germinal center formation and increased IgG1, IgG2a, and IgE levels. T and B cells are hyperresponsive upon engagement of T or B AgRs. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A4galt T C 15: 83,112,312 (GRCm39) E157G probably benign Het
Abcb11 T C 2: 69,073,811 (GRCm39) K1238R probably benign Het
Ankar T A 1: 72,738,046 (GRCm39) E45D probably damaging Het
Antxrl G T 14: 33,797,592 (GRCm39) K522N possibly damaging Het
Ap1m1 A G 8: 73,003,011 (GRCm39) Y93C probably damaging Het
As3mt C T 19: 46,696,567 (GRCm39) T35M possibly damaging Het
Aspg T C 12: 112,079,476 (GRCm39) S85P probably damaging Het
Cachd1 T C 4: 100,809,216 (GRCm39) S234P possibly damaging Het
Ccdc3 T C 2: 5,146,218 (GRCm39) probably null Het
Cnpy1 T C 5: 28,450,759 (GRCm39) T16A probably benign Het
Cope T C 8: 70,757,285 (GRCm39) L43P probably benign Het
E2f8 T C 7: 48,520,525 (GRCm39) M599V probably benign Het
Eif3a A T 19: 60,755,319 (GRCm39) D954E unknown Het
Gfpt1 T A 6: 87,065,230 (GRCm39) probably null Het
Ggps1 T G 13: 14,228,587 (GRCm39) S145R probably benign Het
Gon4l A G 3: 88,803,400 (GRCm39) D1337G probably damaging Het
Gtf2a1l G T 17: 89,001,531 (GRCm39) G82V probably damaging Het
Gucy1b1 C A 3: 81,965,584 (GRCm39) L87F probably damaging Het
Hoxc9 T C 15: 102,890,311 (GRCm39) V76A probably benign Het
Ints2 T C 11: 86,129,294 (GRCm39) E460G probably damaging Het
Kdm4b C T 17: 56,703,916 (GRCm39) R756W probably damaging Het
Marveld3 A T 8: 110,680,960 (GRCm39) C312S probably damaging Het
Ncoa2 T C 1: 13,237,254 (GRCm39) D824G possibly damaging Het
Nrxn2 C A 19: 6,548,358 (GRCm39) A17D possibly damaging Het
Nup133 A T 8: 124,665,031 (GRCm39) I220N probably damaging Het
Nup205 T C 6: 35,189,751 (GRCm39) V984A probably benign Het
Nup54 A T 5: 92,570,853 (GRCm39) D318E probably damaging Het
Obp2a A T 2: 25,591,151 (GRCm39) K94N probably damaging Het
Or2ak5 A T 11: 58,611,196 (GRCm39) I226N probably benign Het
Or5b3 T C 19: 13,388,403 (GRCm39) S157P probably benign Het
Pappa2 T C 1: 158,763,820 (GRCm39) I564V probably benign Het
Parpbp A G 10: 87,969,020 (GRCm39) V142A possibly damaging Het
Rdh16f2 A T 10: 127,712,201 (GRCm39) R219S probably benign Het
Rfx6 C T 10: 51,584,683 (GRCm39) R228C probably damaging Het
Rpap2 A G 5: 107,749,767 (GRCm39) probably null Het
Rskr T G 11: 78,183,846 (GRCm39) probably null Het
Slc15a2 T C 16: 36,574,910 (GRCm39) I531V probably benign Het
Srebf1 T C 11: 60,097,930 (GRCm39) E58G possibly damaging Het
Tmem214 C A 5: 31,028,068 (GRCm39) T96K possibly damaging Het
Usp19 T C 9: 108,373,579 (GRCm39) Y691H probably damaging Het
Vmn1r86 C T 7: 12,836,125 (GRCm39) W200* probably null Het
Vmn2r8 A T 5: 108,945,248 (GRCm39) S786R probably damaging Het
Vps52 T A 17: 34,175,068 (GRCm39) M1K probably null Het
Zzef1 T A 11: 72,714,891 (GRCm39) probably null Het
Other mutations in Lax1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01433:Lax1 APN 1 133,608,137 (GRCm39) missense probably benign 0.09
IGL01568:Lax1 APN 1 133,608,038 (GRCm39) missense probably benign 0.00
IGL02352:Lax1 APN 1 133,608,208 (GRCm39) missense possibly damaging 0.95
IGL02359:Lax1 APN 1 133,608,208 (GRCm39) missense possibly damaging 0.95
IGL02449:Lax1 APN 1 133,607,874 (GRCm39) missense probably damaging 0.98
yon UTSW 1 133,610,774 (GRCm39) missense probably benign 0.20
R0391:Lax1 UTSW 1 133,607,804 (GRCm39) missense probably benign 0.24
R1728:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1728:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1728:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1729:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1729:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1729:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1730:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1730:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1730:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1739:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1739:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1739:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1762:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1762:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1762:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1783:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1783:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1783:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1784:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1784:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1784:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R1785:Lax1 UTSW 1 133,611,372 (GRCm39) missense probably damaging 1.00
R1785:Lax1 UTSW 1 133,608,307 (GRCm39) missense probably benign 0.00
R1785:Lax1 UTSW 1 133,607,716 (GRCm39) missense probably benign
R2254:Lax1 UTSW 1 133,607,971 (GRCm39) missense probably damaging 0.99
R2906:Lax1 UTSW 1 133,616,643 (GRCm39) start codon destroyed probably null 0.53
R2912:Lax1 UTSW 1 133,611,791 (GRCm39) missense possibly damaging 0.77
R4022:Lax1 UTSW 1 133,610,774 (GRCm39) missense probably benign 0.20
R5234:Lax1 UTSW 1 133,608,321 (GRCm39) missense probably benign 0.02
R5686:Lax1 UTSW 1 133,607,914 (GRCm39) missense probably damaging 1.00
R5695:Lax1 UTSW 1 133,608,316 (GRCm39) missense probably damaging 1.00
R6362:Lax1 UTSW 1 133,608,334 (GRCm39) missense possibly damaging 0.92
R6493:Lax1 UTSW 1 133,607,530 (GRCm39) missense probably benign
R6494:Lax1 UTSW 1 133,608,186 (GRCm39) missense probably damaging 0.99
R6932:Lax1 UTSW 1 133,607,896 (GRCm39) missense probably benign 0.39
R7938:Lax1 UTSW 1 133,607,896 (GRCm39) missense probably benign 0.00
R8054:Lax1 UTSW 1 133,611,345 (GRCm39) missense probably benign 0.00
R8476:Lax1 UTSW 1 133,611,326 (GRCm39) missense probably benign 0.00
R9201:Lax1 UTSW 1 133,608,205 (GRCm39) missense possibly damaging 0.95
R9287:Lax1 UTSW 1 133,607,931 (GRCm39) missense probably benign 0.00
R9416:Lax1 UTSW 1 133,611,752 (GRCm39) missense probably benign 0.12
Predicted Primers PCR Primer
(F):5'- ATCAGACTCCAGAGCGATGG -3'
(R):5'- ACCATGGTGGAGCATATGAC -3'

Sequencing Primer
(F):5'- GCTTAACTGGAGACACAC -3'
(R):5'- TATGACCACCAGGGGAATCATCTG -3'
Posted On 2017-06-26