Incidental Mutation 'IGL01786:Klra8'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Klra8
Ensembl Gene ENSMUSG00000089727
Gene Namekiller cell lectin-like receptor, subfamily A, member 8
SynonymsLy49u<129>, Cmv1, Cmv-1, Ly49h
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.050) question?
Stock #IGL01786
Quality Score
Chromosomal Location130115226-130129898 bp(-) (GRCm38)
Type of Mutationcritical splice acceptor site
DNA Base Change (assembly) T to A at 130119068 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000014476 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000014476]
PDB Structure Crystal structure of the activating Ly49H receptor in complex with m157 (G1F strain) [X-RAY DIFFRACTION]
Predicted Effect probably null
Transcript: ENSMUST00000014476
SMART Domains Protein: ENSMUSP00000014476
Gene: ENSMUSG00000089727

Blast:CLECT 73 124 9e-8 BLAST
CLECT 143 258 6.53e-15 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Most mouse strains other than C57BL/6 and C57BL/10 lack this gene and this correlates with an increased susceptiblity to CMV infection. A congenic strain in which the CMV resistant allele from C57BL/6 mice has been introduced in the BALB/c background shows high susceptibility to malarial infection. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam9 T A 8: 24,996,839 H20L probably damaging Het
Ano3 T A 2: 110,682,715 Q645L probably damaging Het
Clasp1 T A 1: 118,497,736 L272Q possibly damaging Het
Corin T C 5: 72,339,876 N532S probably damaging Het
Ddx1 A T 12: 13,229,136 D468E probably benign Het
Hk2 A G 6: 82,739,553 S333P probably benign Het
Kctd19 T C 8: 105,390,304 T398A probably benign Het
Mcm8 A G 2: 132,827,948 D314G probably benign Het
Mga T A 2: 119,902,912 D80E probably damaging Het
Mylk3 T C 8: 85,359,317 Q36R probably benign Het
Myom2 T C 8: 15,106,330 S726P probably damaging Het
Nuf2 T C 1: 169,510,483 S242G possibly damaging Het
Nup210l T A 3: 90,122,776 Y265* probably null Het
Olfr1445 C T 19: 12,884,277 T132I probably damaging Het
Olfr530 T A 7: 140,373,125 M162L probably benign Het
Otud3 T C 4: 138,896,897 D278G probably benign Het
Papolg A G 11: 23,874,488 V298A probably damaging Het
Phc1 T C 6: 122,319,520 D847G possibly damaging Het
Pkd2l1 A G 19: 44,191,442 F110L probably damaging Het
Plxnd1 T A 6: 115,959,935 T1638S probably damaging Het
Polr3a G A 14: 24,484,120 Q106* probably null Het
Rnf32 T C 5: 29,206,814 probably benign Het
Slc30a9 A G 5: 67,346,238 probably benign Het
Slc44a2 A G 9: 21,352,486 Y650C probably damaging Het
Sv2a A T 3: 96,188,209 Y306F probably benign Het
Tmem50a T C 4: 134,898,447 E153G probably damaging Het
Tor1a A G 2: 30,963,703 probably null Het
Tusc5 G A 11: 76,680,466 V103I probably benign Het
Usp20 A G 2: 31,017,163 E594G probably benign Het
Other mutations in Klra8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01363:Klra8 APN 6 130115598 missense probably benign
IGL02145:Klra8 APN 6 130125236 missense probably benign 0.01
IGL02531:Klra8 APN 6 130118970 missense possibly damaging 0.67
P4748:Klra8 UTSW 6 130122044 missense possibly damaging 0.51
R0082:Klra8 UTSW 6 130125055 missense probably benign 0.00
R0853:Klra8 UTSW 6 130119014 missense probably damaging 1.00
R1517:Klra8 UTSW 6 130115640 missense probably benign 0.02
R1610:Klra8 UTSW 6 130119018 missense probably damaging 1.00
R1669:Klra8 UTSW 6 130115629 nonsense probably null
R2015:Klra8 UTSW 6 130115573 missense probably damaging 1.00
R3784:Klra8 UTSW 6 130125055 missense probably benign 0.02
R6909:Klra8 UTSW 6 130125160 missense probably benign 0.03
R7009:Klra8 UTSW 6 130125184 missense probably benign 0.02
R8443:Klra8 UTSW 6 130128093 missense probably damaging 0.98
X0013:Klra8 UTSW 6 130125119 missense probably benign 0.01
Posted On2014-02-04