Incidental Mutation 'IGL03031:Chgb'
ID408466
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Chgb
Ensembl Gene ENSMUSG00000027350
Gene Namechromogranin B
Synonymssecretogranin I, Scg-1
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.075) question?
Stock #IGL03031
Quality Score
Status
Chromosome2
Chromosomal Location132781278-132795079 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 132793514 bp
ZygosityHeterozygous
Amino Acid Change Glutamine to Lysine at position 459 (Q459K)
Ref Sequence ENSEMBL: ENSMUSP00000028826 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028826]
Predicted Effect probably benign
Transcript: ENSMUST00000028826
AA Change: Q459K

PolyPhen 2 Score 0.029 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000028826
Gene: ENSMUSG00000027350
AA Change: Q459K

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:Granin 26 677 8.1e-238 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a tyrosine-sulfated secretory protein abundant in peptidergic endocrine cells and neurons. This protein may serve as a precursor for regulatory peptides. [provided by RefSeq, Jan 2009]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced catecholamine secretion from adrenal chromaffin cells. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 T C 1: 71,314,024 D753G probably benign Het
Adat2 T C 10: 13,556,846 probably benign Het
Ahsa2 A G 11: 23,490,426 L275S probably benign Het
Arhgef38 C T 3: 133,132,067 D118N possibly damaging Het
Bicra A T 7: 15,975,801 H1097Q probably benign Het
C4b T C 17: 34,731,130 T1389A possibly damaging Het
Cd180 A G 13: 102,705,027 S194G probably benign Het
Clvs1 G T 4: 9,449,385 probably benign Het
Cpox G A 16: 58,672,560 G186R probably damaging Het
Cul5 A G 9: 53,642,675 probably benign Het
Epsti1 G A 14: 77,974,581 R249K probably benign Het
Gabrg1 A T 5: 70,794,682 Y90* probably null Het
Gabrp T C 11: 33,554,980 R274G probably damaging Het
Gm597 A G 1: 28,778,583 F123L probably benign Het
Gm6401 C T 14: 41,966,894 E73K possibly damaging Het
Gm9825 T C 6: 7,982,857 noncoding transcript Het
Hectd4 C T 5: 121,348,794 T3284M possibly damaging Het
Hoxc9 T C 15: 102,984,090 M245T probably damaging Het
Lpar6 T C 14: 73,239,442 V281A possibly damaging Het
Med18 G T 4: 132,459,613 Q192K possibly damaging Het
Mis18bp1 A G 12: 65,161,930 V3A probably benign Het
Mpped2 G T 2: 106,783,623 probably benign Het
Ms4a10 A G 19: 10,968,671 V32A probably benign Het
Mthfd1l T A 10: 4,018,601 probably null Het
Myh1 A T 11: 67,206,387 Q422L possibly damaging Het
Myo3b A T 2: 70,255,377 Q819L possibly damaging Het
Ncoa1 G A 12: 4,274,818 T921I possibly damaging Het
Olfr807 A G 10: 129,755,369 L27P possibly damaging Het
Olfr894 A C 9: 38,219,065 T81P probably damaging Het
Olfr960 A G 9: 39,623,398 I92V probably damaging Het
Phf3 A G 1: 30,804,653 S1742P probably benign Het
Plxdc2 G A 2: 16,650,232 probably null Het
Poc5 A G 13: 96,401,615 T263A probably benign Het
Prss41 T A 17: 23,842,422 I132F probably damaging Het
Pxylp1 A G 9: 96,825,142 I329T probably benign Het
Rbm27 T C 18: 42,333,399 probably null Het
Rpgrip1l A T 8: 91,260,783 V882E probably damaging Het
Sec16b T C 1: 157,560,799 S579P probably benign Het
Senp7 A G 16: 56,175,886 E776G probably damaging Het
Smc2 A G 4: 52,449,638 I207V probably benign Het
Spats2 A G 15: 99,180,688 T211A probably benign Het
Sphkap A T 1: 83,276,831 S779T probably damaging Het
Syt11 A T 3: 88,748,841 M1K probably null Het
Tacc2 A G 7: 130,623,855 T757A possibly damaging Het
Tecta A C 9: 42,345,493 M1629R probably benign Het
Ufsp2 T A 8: 45,984,100 I101N probably damaging Het
Unc13b T A 4: 43,235,368 C892S probably damaging Het
Ush1c A G 7: 46,224,937 probably benign Het
Vwde A T 6: 13,208,382 V167E probably benign Het
Wdfy4 A G 14: 33,140,651 L588P probably damaging Het
Zfyve1 T C 12: 83,574,821 T267A probably damaging Het
Other mutations in Chgb
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01601:Chgb APN 2 132793491 missense probably benign 0.00
R0317:Chgb UTSW 2 132793811 missense probably benign 0.06
R0513:Chgb UTSW 2 132785977 splice site probably benign
R0607:Chgb UTSW 2 132793335 missense probably benign
R1177:Chgb UTSW 2 132793470 missense possibly damaging 0.55
R1468:Chgb UTSW 2 132792800 missense probably benign 0.00
R1468:Chgb UTSW 2 132792800 missense probably benign 0.00
R1595:Chgb UTSW 2 132793737 missense probably benign 0.22
R1994:Chgb UTSW 2 132786498 missense possibly damaging 0.93
R3861:Chgb UTSW 2 132793144 missense probably damaging 0.99
R4074:Chgb UTSW 2 132793927 missense possibly damaging 0.48
R4354:Chgb UTSW 2 132793944 missense probably damaging 1.00
R4815:Chgb UTSW 2 132793299 missense probably benign 0.27
R4983:Chgb UTSW 2 132793682 missense probably damaging 1.00
R5426:Chgb UTSW 2 132793533 missense possibly damaging 0.63
R5711:Chgb UTSW 2 132792698 missense probably benign 0.00
R5946:Chgb UTSW 2 132792596 missense probably benign
R7116:Chgb UTSW 2 132781317 start gained probably benign
Posted On2016-08-02