Incidental Mutation 'IGL03286:Gm21834'
ID 415722
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm21834
Ensembl Gene ENSMUSG00000095330
Gene Name predicted gene, 21834
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.218) question?
Stock # IGL03286
Quality Score
Status
Chromosome 17
Chromosomal Location 58048762-58049214 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 58048922 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 98 (V98A)
Ref Sequence ENSEMBL: ENSMUSP00000136534 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178907]
AlphaFold J3QN05
Predicted Effect possibly damaging
Transcript: ENSMUST00000178907
AA Change: V98A

PolyPhen 2 Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox1 G A 1: 58,088,543 (GRCm39) G110S probably benign Het
Arhgap32 T C 9: 32,170,816 (GRCm39) S1548P probably benign Het
Cacna1s A G 1: 136,005,397 (GRCm39) D147G probably benign Het
Calcoco2 A G 11: 95,994,098 (GRCm39) V116A possibly damaging Het
Chd5 A T 4: 152,469,952 (GRCm39) M1842L probably benign Het
Comt T C 16: 18,230,490 (GRCm39) D73G probably damaging Het
Ctnna1 A G 18: 35,308,206 (GRCm39) I175M probably benign Het
Dnah6 A T 6: 73,060,068 (GRCm39) Y2839N probably damaging Het
Dph7 T A 2: 24,856,628 (GRCm39) H193Q probably damaging Het
Eif2b5 A G 16: 20,321,012 (GRCm39) D258G probably damaging Het
Eml5 T C 12: 98,826,762 (GRCm39) D630G probably damaging Het
Ext2 C T 2: 93,537,617 (GRCm39) V590M probably damaging Het
Fchsd2 T C 7: 100,908,982 (GRCm39) probably null Het
Gm13272 A G 4: 88,698,586 (GRCm39) Q167R probably benign Het
Grid1 T A 14: 35,242,642 (GRCm39) probably benign Het
H2-DMa T A 17: 34,356,083 (GRCm39) probably null Het
Ighv5-17 T G 12: 113,822,797 (GRCm39) E108A possibly damaging Het
Invs A G 4: 48,382,261 (GRCm39) T144A probably benign Het
Ipo9 A G 1: 135,334,816 (GRCm39) probably benign Het
Itga4 A T 2: 79,119,706 (GRCm39) Y504F probably damaging Het
Krt5 A G 15: 101,615,983 (GRCm39) F544S unknown Het
Larp4 A G 15: 99,883,967 (GRCm39) Y67C probably damaging Het
Msh2 T C 17: 87,990,095 (GRCm39) M261T possibly damaging Het
Nav1 A T 1: 135,382,274 (GRCm39) C1367S probably benign Het
Nox4 T A 7: 87,019,349 (GRCm39) probably benign Het
Noxa1 A G 2: 24,975,732 (GRCm39) probably null Het
Or5b98 A C 19: 12,931,532 (GRCm39) Y193S probably benign Het
Or6p1 A C 1: 174,258,743 (GRCm39) I250L probably benign Het
Pde4d T A 13: 110,091,040 (GRCm39) probably benign Het
Pdlim2 C T 14: 70,411,925 (GRCm39) G36S possibly damaging Het
Plekhm2 A G 4: 141,361,658 (GRCm39) S262P possibly damaging Het
Pnpla6 C A 8: 3,581,473 (GRCm39) T582K probably damaging Het
Rap1b A T 10: 117,654,480 (GRCm39) L120* probably null Het
Rft1 C T 14: 30,383,323 (GRCm39) T121I probably benign Het
Scn1a A G 2: 66,107,920 (GRCm39) I1613T probably damaging Het
Slc47a2 T G 11: 61,233,293 (GRCm39) E79A possibly damaging Het
Slc9a4 A G 1: 40,619,928 (GRCm39) I85V probably null Het
Slfn8 A T 11: 82,904,294 (GRCm39) F365L probably damaging Het
Smcr8 T A 11: 60,668,853 (GRCm39) probably benign Het
Sntb1 T C 15: 55,655,442 (GRCm39) D258G possibly damaging Het
Sorbs1 A G 19: 40,332,858 (GRCm39) I520T probably damaging Het
Sptbn2 T C 19: 4,797,860 (GRCm39) S1896P probably damaging Het
Sptlc3 G A 2: 139,431,579 (GRCm39) G367D probably damaging Het
Stab1 C T 14: 30,881,283 (GRCm39) probably benign Het
Tars2 T C 3: 95,662,067 (GRCm39) probably benign Het
Tchhl1 C T 3: 93,378,430 (GRCm39) A378V probably benign Het
Tet3 A T 6: 83,352,760 (GRCm39) F1012Y probably damaging Het
Tuba8 A G 6: 121,199,913 (GRCm39) D199G possibly damaging Het
Vmn2r110 T A 17: 20,804,468 (GRCm39) T151S possibly damaging Het
Xirp2 T C 2: 67,346,654 (GRCm39) I2965T probably damaging Het
Zfp688 T A 7: 127,018,703 (GRCm39) M141L probably benign Het
Other mutations in Gm21834
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0440:Gm21834 UTSW 17 58,049,121 (GRCm39) missense possibly damaging 0.66
R0624:Gm21834 UTSW 17 58,049,015 (GRCm39) missense possibly damaging 0.82
R1542:Gm21834 UTSW 17 58,048,946 (GRCm39) missense possibly damaging 0.66
R2051:Gm21834 UTSW 17 58,048,763 (GRCm39) missense possibly damaging 0.46
R2314:Gm21834 UTSW 17 58,049,210 (GRCm39) missense possibly damaging 0.92
R4591:Gm21834 UTSW 17 58,048,880 (GRCm39) missense possibly damaging 0.66
R9012:Gm21834 UTSW 17 58,049,162 (GRCm39) missense probably null 0.00
R9049:Gm21834 UTSW 17 58,048,826 (GRCm39) missense possibly damaging 0.92
R9407:Gm21834 UTSW 17 58,048,863 (GRCm39) missense probably benign 0.00
Z1088:Gm21834 UTSW 17 58,049,116 (GRCm39) missense possibly damaging 0.46
Posted On 2016-08-02