Incidental Mutation 'IGL00323:Gm13941'
ID332247
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm13941
Ensembl Gene ENSMUSG00000079170
Gene Namepredicted gene 13941
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.119) question?
Stock #IGL00323
Quality Score
Status
Chromosome2
Chromosomal Location111088372-111105982 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 111104853 bp
ZygosityHeterozygous
Amino Acid Change Methionine to Leucine at position 11 (M11L)
Ref Sequence ENSEMBL: ENSMUSP00000115383 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000127918]
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: 49,073,790 Y106H probably damaging Het
Atrnl1 C A 19: 57,691,817 N716K probably benign Het
Cdk13 A T 13: 17,721,098 N1075K possibly damaging Het
Daam1 G A 12: 71,958,743 probably benign Het
Exd2 T C 12: 80,476,166 V133A probably damaging Het
Fam58b A G 11: 78,750,956 V236A probably benign Het
Glrb T C 3: 80,861,955 D155G probably damaging Het
Gm4553 T C 7: 142,165,227 S155G unknown Het
Inpp5d G T 1: 87,683,815 V329F probably benign Het
Lilr4b A T 10: 51,481,251 D61V probably benign Het
Malt1 T A 18: 65,448,963 C299* probably null Het
Olfr1306 A T 2: 111,912,036 M298K possibly damaging Het
Olfr1408 G A 1: 173,130,411 Q269* probably null Het
Pigk C A 3: 152,747,632 S282* probably null Het
Pik3r1 T A 13: 101,690,536 M1L probably benign Het
Pnpla1 A G 17: 28,877,442 Y165C probably damaging Het
Rfx7 A G 9: 72,617,420 N631D probably damaging Het
Rp1 T A 1: 4,346,746 D1381V probably damaging Het
Rrp8 T C 7: 105,733,016 probably benign Het
Scn4a A T 11: 106,319,919 D1757E probably benign Het
Sec62 T C 3: 30,810,442 probably benign Het
Smarca5 G A 8: 80,714,041 T598M probably benign Het
Sptbn5 T C 2: 120,054,467 probably benign Het
Srcap T C 7: 127,542,713 probably benign Het
Stab1 T A 14: 31,139,306 E71D probably benign Het
Trhde A T 10: 114,486,747 S716R possibly damaging Het
Ttn T C 2: 76,896,515 probably benign Het
Wscd2 A C 5: 113,551,175 T81P possibly damaging Het
Zfp335 G A 2: 164,892,382 T1295I probably damaging Het
Other mutations in Gm13941
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00420:Gm13941 APN 2 111091848 splice site probably benign
IGL01149:Gm13941 APN 2 111101137 missense unknown
IGL01319:Gm13941 APN 2 111094805 critical splice acceptor site probably null
IGL02557:Gm13941 APN 2 111101156 missense unknown
IGL03163:Gm13941 APN 2 111098416 missense unknown
R0067:Gm13941 UTSW 2 111059416 unclassified noncoding transcript
R0918:Gm13941 UTSW 2 111100600 missense unknown
R2315:Gm13941 UTSW 2 111104817 missense unknown
R3847:Gm13941 UTSW 2 111104853 missense unknown
R3848:Gm13941 UTSW 2 111104853 missense unknown
R5416:Gm13941 UTSW 2 111094734 missense unknown
R5574:Gm13941 UTSW 2 111100606 missense unknown
R6389:Gm13941 UTSW 2 111098389 missense unknown
R6616:Gm13941 UTSW 2 111101175 missense unknown
R7056:Gm13941 UTSW 2 111096802 missense unknown
R7455:Gm13941 UTSW 2 111094740 missense unknown
Z1177:Gm13941 UTSW 2 111094778 missense unknown
Posted On2015-08-05