Incidental Mutation 'IGL01735:Chil6'
ID 105679
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Chil6
Ensembl Gene ENSMUSG00000027902
Gene Name chitinase-like 6
Synonyms BYm, BC051070
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL01735
Quality Score
Status
Chromosome 3
Chromosomal Location 106294700-106313498 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to T at 106296004 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000029510 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029510]
AlphaFold Q80W26
Predicted Effect probably null
Transcript: ENSMUST00000029510
SMART Domains Protein: ENSMUSP00000029510
Gene: ENSMUSG00000027902

DomainStartEndE-ValueType
Glyco_18 39 382 3.04e-122 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy3 A T 12: 4,251,213 (GRCm39) M612L probably benign Het
Adhfe1 C A 1: 9,618,373 (GRCm39) T19K possibly damaging Het
Atxn1 C T 13: 45,720,198 (GRCm39) V566M probably damaging Het
Bag6 T C 17: 35,364,737 (GRCm39) probably benign Het
Cdkl1 T G 12: 69,797,514 (GRCm39) Y258S probably benign Het
Clcn7 T C 17: 25,370,090 (GRCm39) F326L probably benign Het
Cngb3 A G 4: 19,415,648 (GRCm39) Y386C probably damaging Het
Dnah6 C A 6: 73,053,643 (GRCm39) E2916* probably null Het
Dnhd1 A G 7: 105,362,961 (GRCm39) E3841G probably benign Het
Fat1 G T 8: 45,489,276 (GRCm39) V3493L probably benign Het
Irx5 A T 8: 93,087,331 (GRCm39) H421L probably damaging Het
Kbtbd6 T C 14: 79,690,889 (GRCm39) V465A probably damaging Het
Kcp T A 6: 29,498,878 (GRCm39) N340I probably damaging Het
Klhdc2 A G 12: 69,347,053 (GRCm39) M73V probably benign Het
Lpar1 A G 4: 58,437,407 (GRCm39) S341P probably damaging Het
Lrba G A 3: 86,234,968 (GRCm39) V838I probably benign Het
Med12l A G 3: 59,170,675 (GRCm39) I1652V probably damaging Het
Myo5c A T 9: 75,208,720 (GRCm39) D1677V probably damaging Het
Ncoa2 A T 1: 13,235,127 (GRCm39) N935K probably benign Het
Nfrkb T C 9: 31,321,435 (GRCm39) S711P possibly damaging Het
Or1j20 C A 2: 36,759,698 (GRCm39) T40K possibly damaging Het
Or52ae7 T C 7: 103,119,530 (GRCm39) F95L probably damaging Het
Or5w16 A G 2: 87,576,650 (GRCm39) I37V probably benign Het
Pramel27 A G 4: 143,578,401 (GRCm39) I220M probably damaging Het
Prl7d1 A G 13: 27,898,372 (GRCm39) F47L possibly damaging Het
Ptprd A C 4: 76,055,057 (GRCm39) probably null Het
Rsph14 C A 10: 74,860,992 (GRCm39) G103C probably damaging Het
Slco1a4 A G 6: 141,763,477 (GRCm39) F413S probably benign Het
Slfn9 A G 11: 82,873,158 (GRCm39) Y582H probably damaging Het
Tcirg1 A T 19: 3,954,210 (GRCm39) probably benign Het
Trac G A 14: 54,460,438 (GRCm39) probably benign Het
Wbp2nl G T 15: 82,198,017 (GRCm39) V185L probably benign Het
Other mutations in Chil6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01411:Chil6 APN 3 106,296,141 (GRCm39) missense probably damaging 1.00
IGL01795:Chil6 APN 3 106,296,108 (GRCm39) missense probably damaging 0.96
IGL02505:Chil6 APN 3 106,313,278 (GRCm39) missense probably benign
IGL03164:Chil6 APN 3 106,301,714 (GRCm39) missense probably benign 0.04
cold_cut UTSW 3 106,297,290 (GRCm39) missense probably damaging 1.00
R0409:Chil6 UTSW 3 106,311,492 (GRCm39) missense probably benign 0.44
R1761:Chil6 UTSW 3 106,301,654 (GRCm39) missense probably damaging 1.00
R1967:Chil6 UTSW 3 106,298,470 (GRCm39) missense possibly damaging 0.84
R2571:Chil6 UTSW 3 106,297,709 (GRCm39) nonsense probably null
R3024:Chil6 UTSW 3 106,296,086 (GRCm39) missense probably damaging 1.00
R3829:Chil6 UTSW 3 106,313,274 (GRCm39) missense probably benign 0.00
R4835:Chil6 UTSW 3 106,313,290 (GRCm39) nonsense probably null
R4851:Chil6 UTSW 3 106,297,244 (GRCm39) missense possibly damaging 0.61
R4948:Chil6 UTSW 3 106,295,988 (GRCm39) intron probably benign
R5056:Chil6 UTSW 3 106,301,659 (GRCm39) missense probably damaging 1.00
R5244:Chil6 UTSW 3 106,297,290 (GRCm39) missense probably damaging 1.00
R5555:Chil6 UTSW 3 106,297,268 (GRCm39) missense possibly damaging 0.87
R5594:Chil6 UTSW 3 106,301,745 (GRCm39) splice site probably null
R5633:Chil6 UTSW 3 106,296,068 (GRCm39) missense probably damaging 1.00
R6194:Chil6 UTSW 3 106,312,192 (GRCm39) critical splice donor site probably null
R6587:Chil6 UTSW 3 106,312,197 (GRCm39) missense probably benign
R6613:Chil6 UTSW 3 106,297,191 (GRCm39) missense probably benign 0.25
R6641:Chil6 UTSW 3 106,296,240 (GRCm39) missense possibly damaging 0.61
R6651:Chil6 UTSW 3 106,311,576 (GRCm39) missense probably damaging 1.00
R7094:Chil6 UTSW 3 106,311,486 (GRCm39) missense probably damaging 0.96
R7161:Chil6 UTSW 3 106,301,728 (GRCm39) missense probably benign 0.01
R7653:Chil6 UTSW 3 106,301,641 (GRCm39) missense possibly damaging 0.82
R8802:Chil6 UTSW 3 106,312,208 (GRCm39) missense probably damaging 1.00
R9217:Chil6 UTSW 3 106,313,411 (GRCm39) start gained probably benign
R9584:Chil6 UTSW 3 106,301,672 (GRCm39) missense probably damaging 1.00
R9782:Chil6 UTSW 3 106,296,121 (GRCm39) nonsense probably null
X0026:Chil6 UTSW 3 106,296,284 (GRCm39) missense probably benign 0.02
X0064:Chil6 UTSW 3 106,311,635 (GRCm39) nonsense probably null
Posted On 2014-01-21