Incidental Mutation 'IGL01673:Lgals7'
ID 103570
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Lgals7
Ensembl Gene ENSMUSG00000053522
Gene Name lectin, galactose binding, soluble 7
Synonyms Galectin-7, Pig1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.126) question?
Stock # IGL01673
Quality Score
Status
Chromosome 7
Chromosomal Location 28563278-28565709 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 28565621 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000123110 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081457] [ENSMUST00000138272]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000081457
SMART Domains Protein: ENSMUSP00000080179
Gene: ENSMUSG00000053522

DomainStartEndE-ValueType
GLECT 4 136 3.91e-48 SMART
Gal-bind_lectin 10 135 1.68e-53 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128001
Predicted Effect probably benign
Transcript: ENSMUST00000138272
SMART Domains Protein: ENSMUSP00000123110
Gene: ENSMUSG00000053522

DomainStartEndE-ValueType
GLECT 4 86 1.92e-6 SMART
Gal-bind_lectin 10 86 7.37e-9 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207552
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cpz A T 5: 35,669,891 (GRCm39) V262E probably benign Het
Cyp4f14 A G 17: 33,130,125 (GRCm39) probably null Het
Ddx46 G T 13: 55,800,861 (GRCm39) V339F probably damaging Het
Gpn1 T G 5: 31,652,179 (GRCm39) C21W probably damaging Het
Gpr63 A T 4: 25,008,014 (GRCm39) Q246L probably benign Het
Hsp90b1 T A 10: 86,529,296 (GRCm39) M658L probably damaging Het
Immp2l T C 12: 41,118,320 (GRCm39) S4P probably benign Het
Krtap9-5 A T 11: 99,840,377 (GRCm39) *359C probably null Het
Mak G T 13: 41,201,699 (GRCm39) probably null Het
Mrps18c A G 5: 100,946,672 (GRCm39) R13G possibly damaging Het
Myo7a A G 7: 97,703,915 (GRCm39) V1946A probably benign Het
Nfyc T C 4: 120,636,307 (GRCm39) probably benign Het
Nkx2-4 C T 2: 146,925,834 (GRCm39) V343M possibly damaging Het
Or5be3 T C 2: 86,863,731 (GRCm39) Y278C probably damaging Het
Or8d2 T C 9: 38,760,316 (GRCm39) V302A probably benign Het
Rapgef4 G T 2: 72,071,781 (GRCm39) S743I probably damaging Het
Tcf7 A G 11: 52,147,823 (GRCm39) C210R probably damaging Het
Ubqln3 T A 7: 103,791,605 (GRCm39) I162F probably benign Het
Vmn1r216 A G 13: 23,283,641 (GRCm39) Q108R probably damaging Het
Vmn1r74 A T 7: 11,581,317 (GRCm39) I206F possibly damaging Het
Wdr64 T C 1: 175,627,922 (GRCm39) I872T possibly damaging Het
Other mutations in Lgals7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01323:Lgals7 APN 7 28,564,989 (GRCm39) missense probably benign 0.03
IGL02054:Lgals7 APN 7 28,565,614 (GRCm39) missense probably damaging 1.00
IGL02331:Lgals7 APN 7 28,565,143 (GRCm39) missense probably benign 0.36
R6833:Lgals7 UTSW 7 28,565,087 (GRCm39) missense probably damaging 1.00
Posted On 2014-01-21