Incidental Mutation 'R6582:Klri2'
ID 524144
Institutional Source Beutler Lab
Gene Symbol Klri2
Ensembl Gene ENSMUSG00000043932
Gene Name killer cell lectin-like receptor family I member 2
Synonyms A530090P03Rik
MMRRC Submission 044706-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R6582 (G1)
Quality Score 225.009
Status Validated
Chromosome 6
Chromosomal Location 129706004-129717447 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 129716096 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Lysine at position 81 (I81K)
Ref Sequence ENSEMBL: ENSMUSP00000052805 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050385]
AlphaFold Q5DT36
Predicted Effect possibly damaging
Transcript: ENSMUST00000050385
AA Change: I81K

PolyPhen 2 Score 0.655 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000052805
Gene: ENSMUSG00000043932
AA Change: I81K

DomainStartEndE-ValueType
transmembrane domain 82 104 N/A INTRINSIC
CLECT 132 245 7.01e-6 SMART
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.1%
Validation Efficiency 100% (40/40)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 T C 1: 71,297,384 (GRCm39) T2369A probably benign Het
Abhd6 T G 14: 8,042,828 (GRCm38) probably null Het
Abhd6 G T 14: 8,042,826 (GRCm38) G128C probably damaging Het
Acsm3 A G 7: 119,378,896 (GRCm39) E426G probably benign Het
Ankrd11 T C 8: 123,618,368 (GRCm39) D1828G probably benign Het
Asmt T A X: 169,108,766 (GRCm39) probably null Het
Casp4 A G 9: 5,324,884 (GRCm39) Q232R probably benign Het
Cenpt A T 8: 106,575,833 (GRCm39) L171* probably null Het
Chd3 AGCGGCGGCGGCGGCGGCGG AGCGGCGGCGGCGGCGG 11: 69,259,982 (GRCm39) probably benign Het
Col5a2 G T 1: 45,429,275 (GRCm39) H948N possibly damaging Het
Dnah9 G T 11: 65,951,923 (GRCm39) H1859N probably damaging Het
Dscaml1 G A 9: 45,664,104 (GRCm39) R1993Q probably benign Het
Fbxw8 C A 5: 118,263,028 (GRCm39) R217L probably benign Het
Flnb T G 14: 7,892,275 (GRCm38) probably null Het
Fyb2 A G 4: 104,802,739 (GRCm39) N214D probably benign Het
Gbp2b A G 3: 142,316,801 (GRCm39) E484G possibly damaging Het
Gzmk A G 13: 113,317,045 (GRCm39) Y45H probably damaging Het
Ivl CCTGCTGCTGCTGCT CCTGCTGCTGCT 3: 92,479,217 (GRCm39) probably benign Het
Kcnj6 A G 16: 94,633,685 (GRCm39) V142A possibly damaging Het
Lama3 T A 18: 12,710,897 (GRCm39) V3144E probably damaging Het
Mark1 G A 1: 184,644,786 (GRCm39) S390L possibly damaging Het
Mbd3l1 T C 9: 18,396,024 (GRCm39) Y50H probably benign Het
Mcat T C 15: 83,433,383 (GRCm39) N220S probably benign Het
Muc2 A G 7: 141,282,941 (GRCm39) E81G probably benign Het
Neto1 A T 18: 86,512,985 (GRCm39) K327* probably null Het
Or10j3 G T 1: 173,031,847 (GRCm39) R308L probably benign Het
Or4a67 A T 2: 88,598,587 (GRCm39) L24Q probably damaging Het
Or52p1 A T 7: 104,267,648 (GRCm39) Y254F probably damaging Het
Or52u1 T C 7: 104,237,218 (GRCm39) L69P probably damaging Het
Pidd1 A T 7: 141,019,494 (GRCm39) V722D probably damaging Het
Ppp2r2a G T 14: 67,257,253 (GRCm39) H326N probably damaging Het
Smarca5 G A 8: 81,446,281 (GRCm39) T473I probably damaging Het
Spg11 C A 2: 121,922,773 (GRCm39) W892L probably damaging Het
Tas2r110 T A 6: 132,845,248 (GRCm39) I93N possibly damaging Het
Tiam2 CGGG CGGGG 17: 3,464,897 (GRCm39) probably null Het
Vmn1r71 T A 7: 10,482,608 (GRCm39) I27F probably benign Het
Vsnl1 A G 12: 11,376,489 (GRCm39) V132A probably benign Het
Wdsub1 T C 2: 59,708,652 (GRCm39) T74A probably damaging Het
Ywhaz T C 15: 36,791,166 (GRCm39) Y19C probably damaging Het
Other mutations in Klri2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00672:Klri2 APN 6 129,710,034 (GRCm39) missense probably damaging 1.00
R0137:Klri2 UTSW 6 129,709,171 (GRCm39) missense possibly damaging 0.95
R0371:Klri2 UTSW 6 129,709,106 (GRCm39) makesense probably null
R0396:Klri2 UTSW 6 129,717,251 (GRCm39) missense possibly damaging 0.77
R0671:Klri2 UTSW 6 129,717,171 (GRCm39) missense probably benign
R0903:Klri2 UTSW 6 129,710,739 (GRCm39) missense possibly damaging 0.46
R1353:Klri2 UTSW 6 129,716,049 (GRCm39) missense probably damaging 1.00
R1557:Klri2 UTSW 6 129,709,174 (GRCm39) missense probably damaging 0.99
R1642:Klri2 UTSW 6 129,715,837 (GRCm39) missense probably benign 0.00
R2221:Klri2 UTSW 6 129,717,272 (GRCm39) missense probably damaging 0.99
R6044:Klri2 UTSW 6 129,717,247 (GRCm39) missense probably damaging 0.98
R6236:Klri2 UTSW 6 129,715,858 (GRCm39) missense probably benign
R6640:Klri2 UTSW 6 129,709,158 (GRCm39) missense probably benign 0.01
R6883:Klri2 UTSW 6 129,709,985 (GRCm39) missense probably benign
R8330:Klri2 UTSW 6 129,710,694 (GRCm39) missense probably damaging 0.99
R8947:Klri2 UTSW 6 129,710,742 (GRCm39) critical splice acceptor site probably null
R9268:Klri2 UTSW 6 129,710,037 (GRCm39) missense probably damaging 1.00
RF009:Klri2 UTSW 6 129,710,737 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- TCCTGTCACATAGAGGATCAAGAAGG -3'
(R):5'- TGGTAAGGCCACCAAGAAAC -3'

Sequencing Primer
(F):5'- CAAGAAGGGAGAACTTTCTGCTTTG -3'
(R):5'- GGCCACCAAGAAACTTCAGGATTG -3'
Posted On 2018-06-22