Incidental Mutation 'IGL01149:Gm13941'
ID50642
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: 0.156) question?
Stock #IGL01149
Quality Score
Status
Chromosome2
Chromosomal Location111088372-111105982 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 111101137 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Valine at position 50 (E50V)
Ref Sequence ENSEMBL: ENSMUSP00000115383 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000127918]
Predicted Effect unknown
Transcript: ENSMUST00000127918
AA Change: E50V
SMART Domains Protein: ENSMUSP00000115383
Gene: ENSMUSG00000079170
AA Change: E50V

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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4632415L05Rik A G 3: 19,895,112 noncoding transcript Het
Adcy1 A C 11: 7,137,385 N420H probably damaging Het
Avp T C 2: 130,580,673 probably benign Het
B3galnt2 A T 13: 13,980,685 I216F probably benign Het
Cdc42bpa T C 1: 180,074,572 S465P probably damaging Het
Cdc42bpg T A 19: 6,312,205 probably benign Het
Cdcp2 T C 4: 107,107,111 F386S probably benign Het
Cdh4 A G 2: 179,874,144 T372A probably damaging Het
Clspn T G 4: 126,573,178 M612R probably damaging Het
Dll4 T C 2: 119,331,109 C391R probably damaging Het
Dll4 T C 2: 119,332,745 Y616H probably damaging Het
Exoc1 A G 5: 76,542,244 probably benign Het
F830045P16Rik A G 2: 129,460,312 probably null Het
Fhod1 A G 8: 105,347,807 V16A probably benign Het
Fign T C 2: 63,979,760 R389G possibly damaging Het
Gm436 T C 4: 144,673,779 D143G probably benign Het
Kit C T 5: 75,610,876 T231M probably damaging Het
Neu3 T C 7: 99,813,880 H212R probably benign Het
Nup214 G T 2: 32,034,700 S1747I probably damaging Het
Olfr1289 T C 2: 111,484,101 S252P probably damaging Het
Olfr735 G T 14: 50,345,614 A276E probably damaging Het
Olfr870 G T 9: 20,171,530 L14I probably damaging Het
Secisbp2 T C 13: 51,676,455 probably null Het
Slc26a10 G A 10: 127,174,177 probably benign Het
Slc7a6 T C 8: 106,179,600 S155P probably damaging Het
Slf1 A T 13: 77,112,648 I173N probably damaging Het
Tedc1 C T 12: 113,163,188 R357* probably null Het
Tkfc A G 19: 10,600,651 L38P probably damaging Het
Tubgcp4 A G 2: 121,184,783 D324G probably null Het
Zfyve16 T C 13: 92,508,283 H1137R probably damaging Het
Other mutations in Gm13941
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00323:Gm13941 APN 2 111104853 missense unknown
IGL00420:Gm13941 APN 2 111091848 unclassified probably benign
IGL01319:Gm13941 APN 2 111094805 unclassified probably null
IGL02557:Gm13941 APN 2 111101156 missense unknown
IGL03163:Gm13941 APN 2 111098416 missense unknown
R0067:Gm13941 UTSW 2 111059416 missense 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
Posted OnJun 21, 2013