Incidental Mutation 'R2348:Klra13-ps'
ID 323527
Institutional Source Beutler Lab
Gene Symbol Klra13-ps
Ensembl Gene ENSMUSG00000030178
Gene Name killer cell lectin-like receptor subfamily A, member 13, pseudogene
Synonyms Ly49M
MMRRC Submission 040330-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.133) question?
Stock # R2348 (G1)
Quality Score 225
Status Validated
Chromosome 6
Chromosomal Location 130268124-130283391 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 130268271 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125813
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144414
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204367
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205252
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.3%
Validation Efficiency 100% (31/31)
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcyap1 A G 17: 93,509,702 (GRCm39) D51G possibly damaging Het
Ano3 A G 2: 110,614,088 (GRCm39) I205T possibly damaging Het
Arhgap10 A T 8: 78,177,555 (GRCm39) probably benign Het
Asb18 T G 1: 89,942,256 (GRCm39) D15A probably damaging Het
Atm C A 9: 53,403,568 (GRCm39) S1368I possibly damaging Het
Atp9a A T 2: 168,552,746 (GRCm39) probably benign Het
C2cd3 T C 7: 100,062,573 (GRCm39) V653A probably damaging Het
Ctc1 T A 11: 68,917,017 (GRCm39) S304T probably benign Het
Dennd4c G A 4: 86,729,764 (GRCm39) V789I probably benign Het
Dlgap4 C A 2: 156,543,126 (GRCm39) D176E possibly damaging Het
Hdac5 T C 11: 102,090,840 (GRCm39) T747A probably benign Het
Htr2a A T 14: 74,882,550 (GRCm39) N179Y probably damaging Het
Ift52 T C 2: 162,887,177 (GRCm39) V393A probably damaging Het
Itch T C 2: 155,050,998 (GRCm39) S562P possibly damaging Het
Khdc4 T C 3: 88,616,183 (GRCm39) S457P probably benign Het
Kiss1r G T 10: 79,757,654 (GRCm39) R336L probably benign Het
Krt8 T C 15: 101,907,300 (GRCm39) D261G probably benign Het
Mycl A T 4: 122,890,745 (GRCm39) T144S probably benign Het
Naip5 C T 13: 100,356,246 (GRCm39) R1123K probably benign Het
Or5b122 A T 19: 13,563,553 (GRCm39) E295V probably damaging Het
Rasip1 T G 7: 45,278,507 (GRCm39) probably null Het
Rc3h1 C A 1: 160,778,430 (GRCm39) R452S probably damaging Het
Shroom3 G T 5: 93,090,945 (GRCm39) V1151F probably damaging Het
Tpk1 A G 6: 43,323,778 (GRCm39) S224P probably damaging Het
Vmn2r88 A T 14: 51,651,461 (GRCm39) K258N probably benign Het
Vps37c T C 19: 10,683,664 (GRCm39) S29P probably damaging Het
Zfp457 T A 13: 67,441,468 (GRCm39) D369V probably benign Het
Other mutations in Klra13-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4545:Klra13-ps UTSW 6 130,268,232 (GRCm39) exon noncoding transcript
R4633:Klra13-ps UTSW 6 130,268,136 (GRCm39) exon noncoding transcript
R5668:Klra13-ps UTSW 6 130,281,246 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- CTGCAATAAGTCCAATGGTCAAAAC -3'
(R):5'- ATTGGGAGAGCAGGTTCAGC -3'

Sequencing Primer
(F):5'- AGTCCAATGGTCAAAACACTTG -3'
(R):5'- GCAGGTTCAGCATAAAATAACTTCC -3'
Posted On 2015-06-22