Incidental Mutation 'IGL01594:Gm10305'
ID 91685
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10305
Ensembl Gene ENSMUSG00000104479
Gene Name predicted gene 10305
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.215) question?
Stock # IGL01594
Quality Score
Status
Chromosome 4
Chromosomal Location 99160908-99163382 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 99161414 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Asparagine at position 108 (D108N)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000094956
AA Change: D108N
Predicted Effect noncoding transcript
Transcript: ENSMUST00000195331
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 A T 5: 8,996,071 (GRCm39) probably null Het
Acss1 A T 2: 150,463,450 (GRCm39) V618E probably damaging Het
Adgrg6 T C 10: 14,310,084 (GRCm39) N774D probably damaging Het
Atp9a A G 2: 168,532,932 (GRCm39) V134A probably damaging Het
Csmd3 T A 15: 47,492,635 (GRCm39) T3169S probably benign Het
D030068K23Rik T A 8: 109,978,009 (GRCm39) Q52L unknown Het
Dnah5 T C 15: 28,311,480 (GRCm39) S1820P possibly damaging Het
Fem1c A C 18: 46,639,343 (GRCm39) S220A probably benign Het
Gtdc1 A G 2: 44,481,891 (GRCm39) probably null Het
Il2ra T C 2: 11,685,207 (GRCm39) V181A possibly damaging Het
Lrrn1 T C 6: 107,544,454 (GRCm39) I84T probably damaging Het
Map3k1 T A 13: 111,894,723 (GRCm39) probably null Het
Mical1 T G 10: 41,356,325 (GRCm39) Y293D probably damaging Het
Mpzl1 T C 1: 165,421,161 (GRCm39) D266G probably damaging Het
Or55b4 C A 7: 102,134,254 (GRCm39) M24I probably benign Het
Pabpc4l A T 3: 46,401,581 (GRCm39) V21D probably damaging Het
Prdm10 T C 9: 31,258,149 (GRCm39) C525R probably damaging Het
Ptprj C A 2: 90,271,139 (GRCm39) probably benign Het
Rgs3 T C 4: 62,537,981 (GRCm39) F4S probably damaging Het
Ryr3 G A 2: 112,603,073 (GRCm39) T2457I probably damaging Het
Scn3a A G 2: 65,291,775 (GRCm39) I1657T probably damaging Het
Sema6a A G 18: 47,381,884 (GRCm39) S888P probably damaging Het
Slc37a1 T A 17: 31,538,122 (GRCm39) Y148* probably null Het
Tex10 T C 4: 48,469,906 (GRCm39) N53S possibly damaging Het
Tyr A T 7: 87,133,022 (GRCm39) probably benign Het
Vmn2r100 A G 17: 19,751,495 (GRCm39) S513G possibly damaging Het
Other mutations in Gm10305
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0631:Gm10305 UTSW 4 99,161,313 (GRCm39) missense unknown
R1833:Gm10305 UTSW 4 99,161,363 (GRCm39) missense unknown
R4808:Gm10305 UTSW 4 99,161,481 (GRCm39) exon noncoding transcript
Posted On 2013-12-09