Incidental Mutation 'IGL02054:Lgals7'
ID 185159
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 # IGL02054
Quality Score
Status
Chromosome 7
Chromosomal Location 28563278-28565709 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 28565614 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 136 (F136S)
Ref Sequence ENSEMBL: ENSMUSP00000080179 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081457] [ENSMUST00000138272]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000081457
AA Change: F136S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000080179
Gene: ENSMUSG00000053522
AA Change: F136S

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: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 G T 11: 110,182,949 (GRCm39) P1036Q probably damaging Het
Bag4 T C 8: 26,261,253 (GRCm39) S163G probably benign Het
Camkk1 G A 11: 72,916,708 (GRCm39) R102Q probably damaging Het
Caprin1 A C 2: 103,602,143 (GRCm39) probably null Het
Cct8 A T 16: 87,287,364 (GRCm39) probably benign Het
Dlgap2 A G 8: 14,893,552 (GRCm39) M941V probably damaging Het
Dock7 C T 4: 98,861,646 (GRCm39) R1327Q probably damaging Het
Fhip1b A G 7: 105,033,630 (GRCm39) S529P probably damaging Het
Gbp9 T C 5: 105,230,673 (GRCm39) D417G probably benign Het
Gemin2 G A 12: 59,068,523 (GRCm39) probably null Het
Grk6 G T 13: 55,602,210 (GRCm39) A346S probably benign Het
Gtf2h1 A G 7: 46,464,849 (GRCm39) probably benign Het
Irak3 T A 10: 120,012,164 (GRCm39) Q200L probably benign Het
Irx4 A G 13: 73,416,947 (GRCm39) T448A probably damaging Het
Iws1 T C 18: 32,223,595 (GRCm39) probably null Het
Kcnk18 G A 19: 59,224,045 (GRCm39) probably benign Het
Klk1b11 C A 7: 43,648,251 (GRCm39) S86Y possibly damaging Het
Luc7l T A 17: 26,498,314 (GRCm39) probably benign Het
Mta2 T A 19: 8,928,276 (GRCm39) V525E probably benign Het
Mtnr1b G T 9: 15,785,536 (GRCm39) A74E possibly damaging Het
Myo1c A G 11: 75,551,962 (GRCm39) T354A probably benign Het
Nat1 T C 8: 67,944,074 (GRCm39) F153S probably damaging Het
Oasl2 T C 5: 115,035,867 (GRCm39) C48R probably damaging Het
Or4f60 T G 2: 111,902,269 (GRCm39) I220L probably benign Het
Pkm C A 9: 59,585,484 (GRCm39) R489S probably damaging Het
Pth2r T A 1: 65,375,940 (GRCm39) I66N probably damaging Het
Slc25a18 T C 6: 120,769,358 (GRCm39) probably null Het
Tnip3 T C 6: 65,567,595 (GRCm39) S2P possibly damaging Het
Vmn2r61 T C 7: 41,926,158 (GRCm39) probably null Het
Other mutations in Lgals7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01323:Lgals7 APN 7 28,564,989 (GRCm39) missense probably benign 0.03
IGL01673:Lgals7 APN 7 28,565,621 (GRCm39) unclassified probably benign
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 2014-05-07