Incidental Mutation 'IGL01526:S100a7l2'
ID 89584
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol S100a7l2
Ensembl Gene ENSMUSG00000091175
Gene Name S100 calcium binding protein A7 like 2
Synonyms 9130204L05Rik, LOC229550
Accession Numbers
Essential gene? Probably non essential (E-score: 0.125) question?
Stock # IGL01526
Quality Score
Status
Chromosome 3
Chromosomal Location 90995444-90998110 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) T to A at 90995612 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130512 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166173]
AlphaFold G3UWB8
Predicted Effect probably benign
Transcript: ENSMUST00000166173
SMART Domains Protein: ENSMUSP00000130512
Gene: ENSMUSG00000091175

DomainStartEndE-ValueType
Pfam:S_100 9 48 4.4e-10 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500002C15Rik G T 4: 155,818,628 (GRCm39) probably benign Het
4933430I17Rik G T 4: 62,450,858 (GRCm39) R107L possibly damaging Het
Acvr1 A T 2: 58,348,997 (GRCm39) D388E probably benign Het
Art3 T C 5: 92,562,199 (GRCm39) S354P probably damaging Het
Bpnt1 C A 1: 185,077,591 (GRCm39) S102* probably null Het
Ces1a G T 8: 93,771,726 (GRCm39) P24T probably damaging Het
Cfap65 A T 1: 74,950,237 (GRCm39) S1171T probably damaging Het
Cracd T A 5: 77,005,478 (GRCm39) M613K unknown Het
Csn2 T C 5: 87,842,838 (GRCm39) H47R possibly damaging Het
Gm14496 T A 2: 181,637,458 (GRCm39) D177E probably benign Het
Hmbs A G 9: 44,250,845 (GRCm39) V126A possibly damaging Het
Ica1l A G 1: 60,054,916 (GRCm39) M105T probably damaging Het
Morc2a G A 11: 3,600,428 (GRCm39) E17K probably benign Het
Mroh8 T C 2: 157,080,232 (GRCm39) probably benign Het
Mroh9 G T 1: 162,883,172 (GRCm39) L436I probably damaging Het
Nup54 T C 5: 92,565,334 (GRCm39) D461G probably benign Het
Or10ag2 A T 2: 87,249,319 (GRCm39) D309V probably damaging Het
Or2t45 A G 11: 58,669,123 (GRCm39) T57A probably benign Het
Pcid2 G A 8: 13,135,319 (GRCm39) probably benign Het
Ppp1r3b G T 8: 35,851,872 (GRCm39) R237L probably benign Het
Prdm11 A G 2: 92,843,102 (GRCm39) V119A probably damaging Het
Serpina5 T A 12: 104,068,149 (GRCm39) V70E probably damaging Het
Skap2 C T 6: 51,884,894 (GRCm39) D249N probably benign Het
Slc22a29 A T 19: 8,184,542 (GRCm39) probably benign Het
Slc4a1ap C A 5: 31,685,571 (GRCm39) T283K possibly damaging Het
Slc6a21 T G 7: 44,937,220 (GRCm39) I575S probably damaging Het
Smpd1 T G 7: 105,203,982 (GRCm39) W82G probably benign Het
Snx14 T A 9: 88,263,553 (GRCm39) M897L probably damaging Het
Tjp1 A G 7: 64,972,406 (GRCm39) V586A probably damaging Het
Tmc8 T C 11: 117,682,910 (GRCm39) probably benign Het
Trim34a A G 7: 103,909,706 (GRCm39) Y298C probably damaging Het
Ube3c T C 5: 29,872,960 (GRCm39) V1000A probably damaging Het
Other mutations in S100a7l2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:S100a7l2 APN 3 90,995,665 (GRCm39) missense probably benign 0.01
IGL01372:S100a7l2 APN 3 90,995,616 (GRCm39) utr 3 prime probably benign
IGL02894:S100a7l2 APN 3 90,995,700 (GRCm39) missense probably benign 0.18
IGL03110:S100a7l2 APN 3 90,995,626 (GRCm39) missense unknown
IGL03250:S100a7l2 APN 3 90,997,715 (GRCm39) utr 5 prime probably benign
R2357:S100a7l2 UTSW 3 90,995,733 (GRCm39) missense probably benign 0.35
R3795:S100a7l2 UTSW 3 90,995,730 (GRCm39) missense possibly damaging 0.73
R5315:S100a7l2 UTSW 3 90,997,637 (GRCm39) missense possibly damaging 0.56
R5495:S100a7l2 UTSW 3 90,997,602 (GRCm39) missense possibly damaging 0.93
R6314:S100a7l2 UTSW 3 90,995,683 (GRCm39) missense possibly damaging 0.56
R8351:S100a7l2 UTSW 3 90,995,671 (GRCm39) missense probably benign 0.01
R8451:S100a7l2 UTSW 3 90,995,671 (GRCm39) missense probably benign 0.01
R9371:S100a7l2 UTSW 3 90,997,698 (GRCm39) missense unknown
Z1177:S100a7l2 UTSW 3 90,995,663 (GRCm39) missense probably benign 0.01
Posted On 2013-12-03