Incidental Mutation 'IGL02971:Gm21976'
ID 365819
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm21976
Ensembl Gene ENSMUSG00000096330
Gene Name predicted gene 21976
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # IGL02971
Quality Score
Status
Chromosome 13
Chromosomal Location 98279887-98307154 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to A at 98302549 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glycine to Arginine at position 16 (G16R)
Ref Sequence ENSEMBL: ENSMUSP00000139945 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000180066] [ENSMUST00000180188] [ENSMUST00000186911]
AlphaFold J3QNN2
Predicted Effect probably null
Transcript: ENSMUST00000180066
AA Change: G90R

PolyPhen 2 Score 0.086 (Sensitivity: 0.93; Specificity: 0.85)
Predicted Effect probably benign
Transcript: ENSMUST00000180188
Predicted Effect probably null
Transcript: ENSMUST00000186911
AA Change: G16R

PolyPhen 2 Score 0.354 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000139945
Gene: ENSMUSG00000096330
AA Change: G16R

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
LDLa 52 91 1.4e-9 SMART
LDLa 98 136 3.4e-4 SMART
LDLa 141 175 9.2e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930018P22Rik C T 2: 104,123,219 T130I probably benign Het
Ahi1 T C 10: 21,000,551 L787P possibly damaging Het
Atf3 A G 1: 191,177,443 S10P probably benign Het
Cdr2l A G 11: 115,390,900 N77S probably damaging Het
Cnp A G 11: 100,576,699 D156G probably benign Het
Cntn3 A T 6: 102,168,933 D982E probably damaging Het
Col22a1 A G 15: 72,006,738 L190S probably damaging Het
Csmd3 C T 15: 47,913,929 probably benign Het
Dnah5 A G 15: 28,384,461 D3117G probably damaging Het
Dock5 T C 14: 67,757,109 E1834G probably null Het
Eea1 A G 10: 96,041,527 T1368A probably benign Het
Fam83f T C 15: 80,672,149 V78A probably benign Het
Fcgbp G A 7: 28,101,473 V1315I probably damaging Het
Fsd2 A T 7: 81,548,923 Y364* probably null Het
Guca2b A G 4: 119,657,688 S59P probably damaging Het
Hars2 A G 18: 36,786,178 E123G probably damaging Het
Hdac2 A T 10: 37,000,374 K462* probably null Het
Huwe1 T A X: 151,927,626 probably benign Het
Iqgap3 T A 3: 88,090,304 N262K probably benign Het
Kat6b A G 14: 21,669,758 S1502G probably damaging Het
Mapkapk3 A T 9: 107,257,080 D328E probably benign Het
Mgea5 A G 19: 45,762,243 F671S probably damaging Het
Naca C T 10: 128,041,568 probably benign Het
Npffr1 T C 10: 61,614,139 V64A probably damaging Het
Olfr331 A G 11: 58,502,385 L57P probably damaging Het
Olfr918 T A 9: 38,673,268 M72L probably damaging Het
Pcca A G 14: 122,889,533 D718G probably damaging Het
Pde6a A C 18: 61,264,255 D670A probably damaging Het
Pramel7 T A 2: 87,490,073 E292V probably benign Het
Prmt9 A C 8: 77,565,069 M357L probably benign Het
Ptgfr A T 3: 151,835,326 S182T probably benign Het
Rtraf A T 14: 19,816,192 M152K possibly damaging Het
Satb1 T C 17: 51,742,689 D579G possibly damaging Het
Serpinb6a A G 13: 33,931,470 probably null Het
Slc5a9 T C 4: 111,890,300 I297V possibly damaging Het
Slf1 T A 13: 77,047,104 probably benign Het
St8sia2 C T 7: 73,966,811 V139M probably damaging Het
Tas2r114 T C 6: 131,689,280 M262V probably benign Het
Tmem147 A G 7: 30,729,422 probably benign Het
Tmem220 A G 11: 67,034,107 probably null Het
Uspl1 A G 5: 149,188,346 N35S possibly damaging Het
Vmn1r170 A T 7: 23,606,334 I54F possibly damaging Het
Vmn2r121 T G X: 124,127,894 I810L probably damaging Het
Wbp2nl A T 15: 82,305,744 T46S possibly damaging Het
Zfp955b T A 17: 33,300,966 M57K probably benign Het
Other mutations in Gm21976
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Gm21976 APN 13 98302561 missense probably benign 0.15
IGL01921:Gm21976 APN 13 98305321 nonsense probably null
PIT4468001:Gm21976 UTSW 13 98307027 nonsense probably null
R2969:Gm21976 UTSW 13 98287282 missense unknown
R4510:Gm21976 UTSW 13 98305331 missense probably benign 0.25
R4511:Gm21976 UTSW 13 98305331 missense probably benign 0.25
R4595:Gm21976 UTSW 13 98305810 missense probably damaging 0.98
R6126:Gm21976 UTSW 13 98287313 missense unknown
R8962:Gm21976 UTSW 13 98287313 synonymous silent
Posted On 2015-12-18