Incidental Mutation 'IGL02316:Klrb1-ps1'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Klrb1-ps1
Ensembl Gene ENSMUSG00000079295
Gene Namekiller cell lectin-like receptor subfamily B member 1, pseudogene 1
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.063) question?
Stock #IGL02316
Quality Score
Chromosomal Location129116518-129129446 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) G to A at 129116569 bp
Amino Acid Change
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184388
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203057
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c13 G T 13: 4,203,459 probably benign Het
Arhgap26 C T 18: 38,642,546 noncoding transcript Het
Atp5b T C 10: 128,084,309 V108A probably benign Het
B230307C23Rik G A 16: 98,008,650 V9M probably damaging Het
Ccdc85c T A 12: 108,211,570 H321L probably damaging Het
Diaph3 A T 14: 86,986,115 M321K possibly damaging Het
Dicer1 G A 12: 104,702,553 A1290V probably damaging Het
Dnah6 G A 6: 73,168,911 T839M probably benign Het
Eif3a G A 19: 60,771,638 probably benign Het
Eml1 T C 12: 108,534,759 probably benign Het
Exoc4 A G 6: 33,910,584 Q769R probably damaging Het
Fam184a T G 10: 53,638,239 T426P probably damaging Het
Fsip2 C A 2: 82,978,793 H1819N probably benign Het
Gm6686 T A 17: 15,566,238 probably benign Het
Hadha T C 5: 30,126,567 S464G probably benign Het
Ighv5-17 A T 12: 113,859,155 C115* probably null Het
Jmjd6 T C 11: 116,843,102 Y31C possibly damaging Het
Mgat1 T C 11: 49,261,358 Y223H probably damaging Het
Muc4 T C 16: 32,750,850 S243P possibly damaging Het
Numa1 T C 7: 102,001,370 L69P probably damaging Het
Olfr1198 A G 2: 88,746,843 F15S probably damaging Het
Olfr350 C A 2: 36,850,282 P79T probably damaging Het
Olfr50 A T 2: 36,793,620 H128L probably damaging Het
Olfr745 T C 14: 50,642,287 I2T probably benign Het
Pde1c A T 6: 56,151,351 D332E possibly damaging Het
Pitpnm1 A G 19: 4,112,835 I1143V probably benign Het
Rsl1 T A 13: 67,177,056 probably null Het
Scg2 A C 1: 79,435,681 L442V probably damaging Het
Sez6l A T 5: 112,462,962 V530E probably damaging Het
Ubr4 T C 4: 139,473,178 I4655T possibly damaging Het
Zcwpw1 T C 5: 137,810,010 probably benign Het
Other mutations in Klrb1-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01319:Klrb1-ps1 APN 6 129116585 missense possibly damaging 0.91
IGL02067:Klrb1-ps1 APN 6 129129388 missense probably damaging 1.00
IGL02218:Klrb1-ps1 APN 6 129129306 splice site noncoding transcript
R0035:Klrb1-ps1 UTSW 6 129129343 missense possibly damaging 0.80
R2972:Klrb1-ps1 UTSW 6 129119756 splice site noncoding transcript
R2993:Klrb1-ps1 UTSW 6 129121029 missense probably benign 0.19
R5076:Klrb1-ps1 UTSW 6 129119788 exon noncoding transcript
Posted On2015-04-16