Incidental Mutation 'IGL00323:Gm13941'
ID 332247
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm13941
Ensembl Gene ENSMUSG00000079170
Gene Name predicted gene 13941
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # IGL00323
Quality Score
Status
Chromosome 2
Chromosomal Location 110885009-110935204 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 110935198 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 11 (M11L)
Ref Sequence ENSEMBL: ENSMUSP00000115383 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000127918]
AlphaFold A2AJ38
Predicted Effect unknown
Transcript: ENSMUST00000127918
AA Change: M11L
SMART Domains Protein: ENSMUSP00000115383
Gene: ENSMUSG00000079170
AA Change: M11L

DomainStartEndE-ValueType
low complexity region 225 244 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap5m1 T C 14: 49,311,247 (GRCm39) Y106H probably damaging Het
Atrnl1 C A 19: 57,680,249 (GRCm39) N716K probably benign Het
Ccnq A G 11: 78,641,782 (GRCm39) V236A probably benign Het
Cdk13 A T 13: 17,895,683 (GRCm39) N1075K possibly damaging Het
Daam1 G A 12: 72,005,517 (GRCm39) probably benign Het
Exd2 T C 12: 80,522,940 (GRCm39) V133A probably damaging Het
Glrb T C 3: 80,769,262 (GRCm39) D155G probably damaging Het
Gm4553 T C 7: 141,718,964 (GRCm39) S155G unknown Het
Inpp5d G T 1: 87,611,537 (GRCm39) V329F probably benign Het
Lilrb4b A T 10: 51,357,347 (GRCm39) D61V probably benign Het
Malt1 T A 18: 65,582,034 (GRCm39) C299* probably null Het
Or10j27 G A 1: 172,957,978 (GRCm39) Q269* probably null Het
Or4f14 A T 2: 111,742,381 (GRCm39) M298K possibly damaging Het
Pigk C A 3: 152,453,269 (GRCm39) S282* probably null Het
Pik3r1 T A 13: 101,827,044 (GRCm39) M1L probably benign Het
Pnpla1 A G 17: 29,096,416 (GRCm39) Y165C probably damaging Het
Rfx7 A G 9: 72,524,702 (GRCm39) N631D probably damaging Het
Rp1 T A 1: 4,416,969 (GRCm39) D1381V probably damaging Het
Rrp8 T C 7: 105,382,223 (GRCm39) probably benign Het
Scn4a A T 11: 106,210,745 (GRCm39) D1757E probably benign Het
Sec62 T C 3: 30,864,591 (GRCm39) probably benign Het
Smarca5 G A 8: 81,440,670 (GRCm39) T598M probably benign Het
Sptbn5 T C 2: 119,884,948 (GRCm39) probably benign Het
Srcap T C 7: 127,141,885 (GRCm39) probably benign Het
Stab1 T A 14: 30,861,263 (GRCm39) E71D probably benign Het
Trhde A T 10: 114,322,652 (GRCm39) S716R possibly damaging Het
Ttn T C 2: 76,726,859 (GRCm39) probably benign Het
Wscd2 A C 5: 113,689,236 (GRCm39) T81P possibly damaging Het
Zfp335 G A 2: 164,734,302 (GRCm39) T1295I probably damaging Het
Other mutations in Gm13941
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00420:Gm13941 APN 2 110,922,193 (GRCm39) splice site probably benign
IGL01149:Gm13941 APN 2 110,931,482 (GRCm39) missense unknown
IGL01319:Gm13941 APN 2 110,925,150 (GRCm39) critical splice acceptor site probably null
IGL02557:Gm13941 APN 2 110,931,501 (GRCm39) missense unknown
IGL03163:Gm13941 APN 2 110,928,761 (GRCm39) missense unknown
R0067:Gm13941 UTSW 2 110,889,761 (GRCm39) unclassified noncoding transcript
R0918:Gm13941 UTSW 2 110,930,945 (GRCm39) missense unknown
R2315:Gm13941 UTSW 2 110,935,162 (GRCm39) missense unknown
R3847:Gm13941 UTSW 2 110,935,198 (GRCm39) missense unknown
R3848:Gm13941 UTSW 2 110,935,198 (GRCm39) missense unknown
R5416:Gm13941 UTSW 2 110,925,079 (GRCm39) missense unknown
R5574:Gm13941 UTSW 2 110,930,951 (GRCm39) missense unknown
R6389:Gm13941 UTSW 2 110,928,734 (GRCm39) missense unknown
R6616:Gm13941 UTSW 2 110,931,520 (GRCm39) missense unknown
R7056:Gm13941 UTSW 2 110,927,147 (GRCm39) missense unknown
R7455:Gm13941 UTSW 2 110,925,085 (GRCm39) missense unknown
R8197:Gm13941 UTSW 2 110,926,921 (GRCm39) splice site probably null
R9116:Gm13941 UTSW 2 110,935,146 (GRCm39) missense unknown
R9164:Gm13941 UTSW 2 110,936,324 (GRCm39) missense unknown
R9536:Gm13941 UTSW 2 110,918,861 (GRCm39) missense unknown
R9763:Gm13941 UTSW 2 110,931,518 (GRCm39) missense unknown
Z1177:Gm13941 UTSW 2 110,925,123 (GRCm39) missense unknown
Posted On 2015-08-05