Incidental Mutation 'IGL03132:Scgb2b21'
ID 410374
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Scgb2b21
Ensembl Gene ENSMUSG00000099900
Gene Name secretoglobin, family 2B, member 21
Synonyms Abpbg21, Gm6725
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # IGL03132
Quality Score
Status
Chromosome 7
Chromosomal Location 33217913-33219880 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 33219299 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 35 (V35A)
Ref Sequence ENSEMBL: ENSMUSP00000140117 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000185407]
AlphaFold A0A087WQA9
Predicted Effect possibly damaging
Transcript: ENSMUST00000185407
AA Change: V35A

PolyPhen 2 Score 0.462 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000140117
Gene: ENSMUSG00000099900
AA Change: V35A

DomainStartEndE-ValueType
low complexity region 3 16 N/A INTRINSIC
Pfam:Feld-I_B 24 90 8.3e-33 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb1 G A 6: 88,815,941 (GRCm39) R177C probably benign Het
Adam21 C A 12: 81,607,148 (GRCm39) G205* probably null Het
Baz2b T A 2: 59,738,097 (GRCm39) probably benign Het
Col6a3 C T 1: 90,731,615 (GRCm39) G939D probably damaging Het
Csf1r A G 18: 61,261,171 (GRCm39) E749G probably benign Het
Dnm3 C T 1: 161,838,674 (GRCm39) probably null Het
Dsg3 A G 18: 20,657,653 (GRCm39) D241G probably damaging Het
Dst T C 1: 34,295,722 (GRCm39) S6015P probably benign Het
Dvl2 T C 11: 69,896,514 (GRCm39) S183P probably benign Het
Exoc6b T C 6: 84,768,246 (GRCm39) N699S possibly damaging Het
Fat2 T C 11: 55,144,746 (GRCm39) R4043G probably benign Het
Gbp9 T A 5: 105,232,819 (GRCm39) T278S possibly damaging Het
Gm2a T A 11: 54,994,474 (GRCm39) I48N probably damaging Het
Gorasp2 T C 2: 70,514,379 (GRCm39) V232A probably benign Het
Gpa33 G A 1: 165,980,218 (GRCm39) D94N probably benign Het
Il1rap A T 16: 26,498,869 (GRCm39) S123C probably damaging Het
Kctd17 T C 15: 78,319,887 (GRCm39) S102P probably damaging Het
Lamb1 A G 12: 31,350,333 (GRCm39) probably null Het
Mfsd1 T A 3: 67,495,273 (GRCm39) I131K possibly damaging Het
Pkhd1l1 G A 15: 44,438,013 (GRCm39) C3576Y probably damaging Het
Pla2g4a A T 1: 149,778,035 (GRCm39) probably benign Het
Ptpn11 T A 5: 121,272,878 (GRCm39) D575V possibly damaging Het
Reck A T 4: 43,938,898 (GRCm39) R755* probably null Het
Srpra G A 9: 35,125,574 (GRCm39) probably null Het
Stk11ip T C 1: 75,512,733 (GRCm39) S1025P probably benign Het
Tmprss9 G A 10: 80,730,699 (GRCm39) V742M probably damaging Het
Trh T C 6: 92,220,755 (GRCm39) T36A probably benign Het
Trim35 A G 14: 66,546,595 (GRCm39) E454G probably damaging Het
Vmn2r99 C T 17: 19,598,485 (GRCm39) Q170* probably null Het
Other mutations in Scgb2b21
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4296:Scgb2b21 UTSW 7 33,219,233 (GRCm39) missense probably benign 0.06
R7327:Scgb2b21 UTSW 7 33,219,330 (GRCm39) missense probably benign 0.08
R9001:Scgb2b21 UTSW 7 33,218,956 (GRCm39) intron probably benign
Posted On 2016-08-02