Incidental Mutation 'R2972:Klrb1-ps1'
ID 255242
Institutional Source Beutler Lab
Gene Symbol Klrb1-ps1
Ensembl Gene ENSMUSG00000079295
Gene Name killer cell lectin-like receptor subfamily B member 1, pseudogene 1
Synonyms Nkrp1e
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R2972 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 129093481-129106409 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 129096719 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000071342
Gene: ENSMUSG00000079295

DomainStartEndE-ValueType
transmembrane domain 43 65 N/A INTRINSIC
CLECT 94 170 1.28e-1 SMART
Predicted Effect
SMART Domains Protein: ENSMUSP00000071342
Gene: ENSMUSG00000079295

DomainStartEndE-ValueType
transmembrane domain 43 65 N/A INTRINSIC
CLECT 94 170 1.28e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184388
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203057
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
BC048507 T C 13: 68,011,749 (GRCm39) I42T probably benign Het
Card9 C T 2: 26,247,222 (GRCm39) R309H probably damaging Het
Clec14a T A 12: 58,314,360 (GRCm39) R421W probably damaging Het
Crnkl1 A G 2: 145,774,181 (GRCm39) L94P probably benign Het
D930007J09Rik C T 13: 32,986,742 (GRCm39) probably benign Het
Dhrs7c T A 11: 67,706,697 (GRCm39) I285N possibly damaging Het
Golga2 A G 2: 32,195,671 (GRCm39) N752S probably benign Het
Nin G A 12: 70,109,487 (GRCm39) R151C probably damaging Het
Nsun6 A C 2: 15,042,883 (GRCm39) probably null Het
Nyap2 C T 1: 81,169,485 (GRCm39) R81* probably null Het
Or1n2 G A 2: 36,797,416 (GRCm39) V153M probably benign Het
Or4a69 G T 2: 89,313,120 (GRCm39) R120S possibly damaging Het
Pkhd1l1 T A 15: 44,410,644 (GRCm39) M2717K possibly damaging Het
Ralgapa1 T C 12: 55,867,540 (GRCm39) K5E possibly damaging Het
Rnf130 T A 11: 49,984,627 (GRCm39) L309* probably null Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Rxrg G A 1: 167,466,715 (GRCm39) R422H probably damaging Het
Serpinb9e T A 13: 33,439,126 (GRCm39) V184E probably benign Het
Slc10a5 A T 3: 10,399,517 (GRCm39) I381N probably damaging Het
Slit1 G A 19: 41,599,455 (GRCm39) P1032L probably benign Het
Sptlc3 A G 2: 139,431,581 (GRCm39) T368A probably damaging Het
Ubr4 T C 4: 139,133,847 (GRCm39) Y748H probably benign Het
Ugt8a T C 3: 125,708,957 (GRCm39) H51R probably benign Het
Vmn2r117 A G 17: 23,678,830 (GRCm39) V798A probably damaging Het
Vmn2r77 T C 7: 86,452,893 (GRCm39) Y537H probably benign Het
Other mutations in Klrb1-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01319:Klrb1-ps1 APN 6 129,093,548 (GRCm39) missense possibly damaging 0.91
IGL02067:Klrb1-ps1 APN 6 129,106,351 (GRCm39) missense probably damaging 1.00
IGL02218:Klrb1-ps1 APN 6 129,106,269 (GRCm39) splice site noncoding transcript
IGL02316:Klrb1-ps1 APN 6 129,093,532 (GRCm39) exon noncoding transcript
R0035:Klrb1-ps1 UTSW 6 129,106,306 (GRCm39) missense possibly damaging 0.80
R2993:Klrb1-ps1 UTSW 6 129,097,992 (GRCm39) missense probably benign 0.19
R5076:Klrb1-ps1 UTSW 6 129,096,751 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- AGCTGAACCTAATGGAGAGTTC -3'
(R):5'- TGGACATGGGATACTGTCCTG -3'

Sequencing Primer
(F):5'- CTGAACCTAATGGAGAGTTCATTTCG -3'
(R):5'- CATGTGAAGAGGCACCGATATTTATG -3'
Posted On 2014-12-29