Incidental Mutation 'IGL02061:Scgb2b26'
ID 185394
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Scgb2b26
Ensembl Gene ENSMUSG00000066586
Gene Name secretoglobin, family 2B, member 26
Synonyms Abpbg4, Abpbg26, C2d, Abpg, Scgb2b4
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL02061
Quality Score
Status
Chromosome 7
Chromosomal Location 33642422-33644410 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 33642610 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 107 (N107S)
Ref Sequence ENSEMBL: ENSMUSP00000082763 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085623]
AlphaFold Q8JZX1
Predicted Effect probably benign
Transcript: ENSMUST00000085623
AA Change: N107S

PolyPhen 2 Score 0.162 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000082763
Gene: ENSMUSG00000066586
AA Change: N107S

DomainStartEndE-ValueType
low complexity region 5 11 N/A INTRINSIC
Pfam:Feld-I_B 24 90 2.9e-29 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000117273
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arl15 T A 13: 113,931,193 (GRCm39) D3E probably benign Het
Atp4a A G 7: 30,414,454 (GRCm39) Y159C probably damaging Het
Card10 A G 15: 78,662,415 (GRCm39) F861S probably damaging Het
Ccdc85c A G 12: 108,188,002 (GRCm39) V279A probably damaging Het
Cndp1 G A 18: 84,652,751 (GRCm39) R136W probably damaging Het
Eif2b3 A G 4: 116,885,608 (GRCm39) E50G possibly damaging Het
Entrep3 C T 3: 89,095,903 (GRCm39) R545* probably null Het
Eva1c C T 16: 90,663,163 (GRCm39) Q67* probably null Het
Exoc1 A G 5: 76,689,967 (GRCm39) E169G probably damaging Het
Fsd2 T A 7: 81,190,172 (GRCm39) K537* probably null Het
Gbf1 T G 19: 46,267,697 (GRCm39) S1236A possibly damaging Het
Gpt C A 15: 76,583,617 (GRCm39) probably benign Het
Gsap A G 5: 21,486,609 (GRCm39) probably benign Het
Hdac6 A C X: 7,809,878 (GRCm39) probably null Het
Ivns1abp T A 1: 151,227,324 (GRCm39) L44Q probably damaging Het
Kcnt1 T A 2: 25,790,494 (GRCm39) probably null Het
Kdm2b A G 5: 123,021,404 (GRCm39) I58T probably damaging Het
Mrpl23 C T 7: 142,094,319 (GRCm39) P76S probably benign Het
Nbea A G 3: 55,625,308 (GRCm39) I2261T possibly damaging Het
Oasl1 G A 5: 115,061,651 (GRCm39) V61M probably damaging Het
Or4g7 T A 2: 111,309,614 (GRCm39) F162I possibly damaging Het
Pabpc2 A G 18: 39,908,046 (GRCm39) Q437R probably benign Het
Ppp1r26 T A 2: 28,340,639 (GRCm39) C90S possibly damaging Het
Ppp3ca A G 3: 136,503,624 (GRCm39) T66A probably benign Het
Prss55 A G 14: 64,313,192 (GRCm39) Y231H possibly damaging Het
Psmb10 T C 8: 106,664,343 (GRCm39) T38A probably damaging Het
Rfx5 A G 3: 94,865,792 (GRCm39) T364A probably benign Het
Seh1l A G 18: 67,920,328 (GRCm39) probably benign Het
Skic3 T A 13: 76,277,660 (GRCm39) probably null Het
Sod1 T A 16: 90,022,126 (GRCm39) H111Q probably benign Het
Thbs2 A T 17: 14,900,176 (GRCm39) D592E probably benign Het
Tmem67 G A 4: 12,053,526 (GRCm39) A740V probably damaging Het
Tra2a A G 6: 49,226,032 (GRCm39) V136A possibly damaging Het
Utp18 T C 11: 93,772,967 (GRCm39) D158G probably benign Het
Zfp524 A G 7: 5,020,871 (GRCm39) E133G probably damaging Het
Other mutations in Scgb2b26
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0010:Scgb2b26 UTSW 7 33,643,774 (GRCm39) missense probably damaging 0.98
R0010:Scgb2b26 UTSW 7 33,643,774 (GRCm39) missense probably damaging 0.98
R6768:Scgb2b26 UTSW 7 33,644,379 (GRCm39) missense probably damaging 1.00
R7188:Scgb2b26 UTSW 7 33,644,379 (GRCm39) missense probably damaging 1.00
R7325:Scgb2b26 UTSW 7 33,643,782 (GRCm39) missense probably benign 0.14
R8205:Scgb2b26 UTSW 7 33,643,833 (GRCm39) missense probably benign 0.03
R8679:Scgb2b26 UTSW 7 33,643,784 (GRCm39) missense probably damaging 0.99
Z1088:Scgb2b26 UTSW 7 33,643,792 (GRCm39) missense probably benign 0.00
Posted On 2014-05-07