Incidental Mutation 'IGL01653:Scgb2b19'
ID 102873
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Scgb2b19
Ensembl Gene ENSMUSG00000096467
Gene Name secretoglobin, family 2B, member 19
Synonyms Gm5894, Abpbg19
Accession Numbers
Essential gene? Probably non essential (E-score: 0.033) question?
Stock # IGL01653
Quality Score
Status
Chromosome 7
Chromosomal Location 32977795-32979763 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 32979153 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 43 (Y43F)
Ref Sequence ENSEMBL: ENSMUSP00000136155 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000179688]
AlphaFold J3QM75
Predicted Effect probably damaging
Transcript: ENSMUST00000179688
AA Change: Y43F

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000136155
Gene: ENSMUSG00000096467
AA Change: Y43F

DomainStartEndE-ValueType
low complexity region 3 16 N/A INTRINSIC
Pfam:Feld-I_B 24 90 2.4e-31 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933421I07Rik T C 7: 42,096,398 (GRCm39) D119G probably damaging Het
Apol7c A G 15: 77,410,500 (GRCm39) C149R probably damaging Het
Arfgef1 G A 1: 10,230,133 (GRCm39) R1235* probably null Het
Bpifb4 A G 2: 153,786,703 (GRCm39) D285G probably damaging Het
Cep192 T A 18: 67,986,043 (GRCm39) H1682Q possibly damaging Het
Cerk G T 15: 86,033,552 (GRCm39) Y290* probably null Het
Cyld A T 8: 89,467,998 (GRCm39) I544F probably damaging Het
Dcp1a T C 14: 30,227,528 (GRCm39) S134P possibly damaging Het
Epha6 A C 16: 59,659,666 (GRCm39) N817K probably benign Het
Ephb4 A G 5: 137,364,003 (GRCm39) probably benign Het
Fcgr3 A T 1: 170,886,849 (GRCm39) L25Q probably damaging Het
Heatr3 A G 8: 88,871,245 (GRCm39) I83V probably benign Het
Hormad1 T A 3: 95,485,608 (GRCm39) N265K possibly damaging Het
Kpna1 A G 16: 35,840,562 (GRCm39) T201A probably benign Het
Krt6b T A 15: 101,587,549 (GRCm39) T182S probably damaging Het
Macc1 A G 12: 119,414,088 (GRCm39) K755E probably damaging Het
Med12l C T 3: 59,169,314 (GRCm39) T1568M probably damaging Het
Muc4 G T 16: 32,581,722 (GRCm39) probably null Het
Myt1l T C 12: 29,960,770 (GRCm39) S1028P unknown Het
Nhlrc2 C T 19: 56,559,282 (GRCm39) R256C probably benign Het
Or4c123 T A 2: 89,127,471 (GRCm39) T48S probably benign Het
Or5a3 G A 19: 12,399,736 (GRCm39) R21H probably benign Het
Pfkfb4 G A 9: 108,828,202 (GRCm39) R79H probably damaging Het
Piezo2 T C 18: 63,315,904 (GRCm39) probably benign Het
Pramel5 C T 4: 144,000,429 (GRCm39) R49H probably benign Het
Ralgapb T A 2: 158,304,079 (GRCm39) S613T possibly damaging Het
Ryr1 T C 7: 28,778,022 (GRCm39) E2158G probably damaging Het
Slc17a6 A G 7: 51,317,770 (GRCm39) T468A possibly damaging Het
Slc36a1 A G 11: 55,119,147 (GRCm39) D374G possibly damaging Het
Wdtc1 T C 4: 133,022,543 (GRCm39) D601G probably damaging Het
Zfp1007 A C 5: 109,825,182 (GRCm39) Y89* probably null Het
Other mutations in Scgb2b19
AlleleSourceChrCoordTypePredicted EffectPPH Score
PIT4515001:Scgb2b19 UTSW 7 32,979,036 (GRCm39) critical splice donor site probably null
R0580:Scgb2b19 UTSW 7 32,977,995 (GRCm39) missense probably benign 0.15
R1437:Scgb2b19 UTSW 7 32,977,980 (GRCm39) missense probably benign 0.08
R1445:Scgb2b19 UTSW 7 32,979,037 (GRCm39) critical splice donor site probably null
R5332:Scgb2b19 UTSW 7 32,978,006 (GRCm39) missense probably benign 0.07
R6424:Scgb2b19 UTSW 7 32,978,022 (GRCm39) missense possibly damaging 0.91
R7102:Scgb2b19 UTSW 7 32,979,711 (GRCm39) missense probably null
R7576:Scgb2b19 UTSW 7 32,979,211 (GRCm39) missense possibly damaging 0.92
R9551:Scgb2b19 UTSW 7 32,979,198 (GRCm39) missense probably damaging 1.00
R9552:Scgb2b19 UTSW 7 32,979,198 (GRCm39) missense probably damaging 1.00
R9561:Scgb2b19 UTSW 7 32,978,039 (GRCm39) missense probably benign 0.04
Posted On 2014-01-21