Incidental Mutation 'IGL02529:Clec2e'
ID297252
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: 0.050) question?
Stock #IGL02529
Quality Score
Status
Chromosome6
Chromosomal Location129091998-129100913 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 129098496 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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik T A 14: 32,661,233 H925L probably benign Het
Agpat5 T A 8: 18,881,754 Y297N possibly damaging Het
Apobec3 C T 15: 79,897,687 probably benign Het
Atpaf1 C A 4: 115,791,269 A161E probably damaging Het
Bnc1 A T 7: 81,977,368 D91E probably damaging Het
Capg G A 6: 72,555,846 V98I probably benign Het
Ccdc7b C T 8: 129,178,225 L115F possibly damaging Het
Ces2a T A 8: 104,737,219 probably benign Het
Cldn6 T G 17: 23,681,317 V85G probably damaging Het
Csgalnact1 C A 8: 68,401,492 G219V probably damaging Het
Dhx38 T C 8: 109,559,013 E396G probably benign Het
Dock8 A T 19: 25,100,926 K532* probably null Het
Efr3b C T 12: 3,983,391 V139I probably benign Het
Gmip G A 8: 69,816,789 G537E probably damaging Het
Hacd1 T C 2: 14,045,202 H64R probably damaging Het
Hdac3 G T 18: 37,944,132 Q230K probably benign Het
Htt C T 5: 34,819,043 probably benign Het
Il18r1 A G 1: 40,487,059 D255G possibly damaging Het
Krt82 T A 15: 101,550,396 R70* probably null Het
Krt9 G T 11: 100,189,966 H353Q probably damaging Het
Kyat3 T C 3: 142,720,474 I57T probably benign Het
L1td1 A G 4: 98,737,421 K618E probably benign Het
Limch1 C A 5: 67,002,613 N617K possibly damaging Het
Lsm8 T C 6: 18,851,652 F34S probably damaging Het
Man2a2 G A 7: 80,359,640 A822V probably damaging Het
Mmrn2 C A 14: 34,398,613 A480E possibly damaging Het
Mthfd1 A G 12: 76,303,709 I474V probably benign Het
Mycl A G 4: 122,996,977 K152R probably damaging Het
Numa1 A G 7: 101,999,953 probably null Het
Olfr474 G T 7: 107,955,216 V192F possibly damaging Het
Otog A C 7: 46,259,957 D617A probably damaging Het
Ppef2 A G 5: 92,244,737 I267T probably damaging Het
Ptprq A G 10: 107,635,365 Y1392H probably benign Het
Rasgrp3 G T 17: 75,525,102 K639N possibly damaging Het
Rgs19 C T 2: 181,689,150 R203H probably benign Het
Scnn1g C A 7: 121,742,446 probably benign Het
Tmem181b-ps T C 17: 6,466,921 noncoding transcript Het
Vmn2r118 A G 17: 55,610,870 V214A possibly damaging Het
Zfp811 T C 17: 32,797,815 Y417C probably damaging Het
Other mutations in Clec2e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01785:Clec2e APN 6 129093401 utr 3 prime 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 splice site 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
R7762:Clec2e UTSW 6 129095128 missense possibly damaging 0.92
R8024:Clec2e UTSW 6 129094425 missense possibly damaging 0.83
Posted On2015-04-16