Incidental Mutation 'IGL01785:Clec2e'
ID153789
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Clec2e
Ensembl Gene ENSMUSG00000030155
Gene NameC-type lectin domain family 2, member e
SynonymsClra
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.014) question?
Stock #IGL01785
Quality Score
Status
Chromosome6
Chromosomal Location129091998-129100913 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) A to T at 129093401 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000032258 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032258]
Predicted Effect probably benign
Transcript: ENSMUST00000032258
SMART Domains Protein: ENSMUSP00000032258
Gene: ENSMUSG00000030155

DomainStartEndE-ValueType
transmembrane domain 49 71 N/A INTRINSIC
CLECT 89 200 1.03e-21 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 T A 5: 8,915,058 Y309* probably null Het
Abhd18 G A 3: 40,905,904 R42Q 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
Clec1b A G 6: 129,403,562 D115G probably damaging Het
Corin T C 5: 72,339,876 N532S probably damaging Het
Csn1s2b A G 5: 87,809,913 K2R possibly damaging Het
Mcm8 A G 2: 132,827,948 D314G probably benign Het
Mga T A 2: 119,902,912 D80E probably damaging Het
Msh4 A G 3: 153,857,507 L744P probably damaging Het
Myof A T 19: 37,980,423 L348* probably null Het
Olfr1348 T C 7: 6,501,900 I109V probably benign Het
Olfr530 T A 7: 140,373,125 M162L probably benign Het
Otud3 T C 4: 138,896,897 D278G probably benign Het
Pdpr C A 8: 111,129,656 H670Q probably damaging Het
Phf21b C A 15: 84,808,061 probably benign Het
Polr3a G A 14: 24,484,120 Q106* probably null Het
Ptprm G T 17: 66,685,623 N1366K probably damaging Het
Slc10a5 G A 3: 10,335,199 P134S probably benign Het
Slc30a9 A G 5: 67,346,238 probably benign Het
Stat6 T A 10: 127,657,227 V576D probably damaging Het
Tmem132d T C 5: 127,984,315 I408V probably benign Het
Tmem50a T C 4: 134,898,447 E153G probably damaging Het
Tmod4 A G 3: 95,125,618 T22A probably benign Het
Tmprss7 C T 16: 45,680,634 G268D probably damaging Het
Tor1a A G 2: 30,963,703 probably null Het
Ttc29 T C 8: 78,282,341 L280P probably damaging Het
Tusc5 G A 11: 76,680,466 V103I probably benign Het
Usp20 A G 2: 31,017,163 E594G probably benign Het
Vmn1r31 A C 6: 58,472,724 M3R possibly damaging Het
Other mutations in Clec2e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02529:Clec2e APN 6 129098496 splice site probably benign
IGL03242:Clec2e APN 6 129095026 missense probably damaging 1.00
IGL03289:Clec2e APN 6 129098455 missense probably damaging 0.97
R0090:Clec2e UTSW 6 129095218 intron probably null
R0390:Clec2e UTSW 6 129093468 missense probably damaging 0.99
R1468:Clec2e UTSW 6 129093496 nonsense probably null
R1468:Clec2e UTSW 6 129093496 nonsense probably null
R1477:Clec2e UTSW 6 129095200 missense probably benign 0.03
R3721:Clec2e UTSW 6 129094410 nonsense probably null
R4769:Clec2e UTSW 6 129100827 missense probably benign 0.08
R5589:Clec2e UTSW 6 129098428 missense probably benign 0.01
R6056:Clec2e UTSW 6 129100809 missense probably benign 0.00
R6156:Clec2e UTSW 6 129095098 missense possibly damaging 0.94
Posted On2014-02-04