Incidental Mutation 'IGL01520:Inmt'
ID 90482
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Inmt
Ensembl Gene ENSMUSG00000003477
Gene Name indolethylamine N-methyltransferase
Synonyms Temt
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # IGL01520
Quality Score
Status
Chromosome 6
Chromosomal Location 55147612-55151975 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 55148213 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Phenylalanine at position 139 (V139F)
Ref Sequence ENSEMBL: ENSMUSP00000003569 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000003569]
AlphaFold P40936
Predicted Effect probably damaging
Transcript: ENSMUST00000003569
AA Change: V139F

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000003569
Gene: ENSMUSG00000003477
AA Change: V139F

DomainStartEndE-ValueType
Pfam:NNMT_PNMT_TEMT 1 260 4.9e-113 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152720
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204585
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] N-methylation of endogenous and xenobiotic compounds is a major method by which they are degraded. This gene encodes an enzyme that N-methylates indoles such as tryptamine. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream FAM188B (family with sequence similarity 188, member B) gene. [provided by RefSeq, Nov 2010]
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acan T A 7: 78,734,318 (GRCm39) H58Q probably damaging Het
Atp6v1c2 A T 12: 17,347,754 (GRCm39) L149Q probably damaging Het
Bltp1 T A 3: 37,027,409 (GRCm39) Y2265* probably null Het
Cd40lg A G X: 56,265,148 (GRCm39) N132D probably benign Het
Cemip G T 7: 83,597,830 (GRCm39) T1060K probably benign Het
Ces1a G T 8: 93,771,726 (GRCm39) P24T probably damaging Het
Ces5a A T 8: 94,246,206 (GRCm39) S328T probably benign Het
Cfap70 A G 14: 20,470,755 (GRCm39) C497R probably benign Het
Cndp2 T C 18: 84,686,732 (GRCm39) K430R probably benign Het
Cplane1 C A 15: 8,251,395 (GRCm39) T1889K probably damaging Het
Crlf3 T C 11: 79,950,972 (GRCm39) D126G probably benign Het
Cxcr1 A T 1: 74,231,434 (GRCm39) L196Q probably damaging Het
E330013P04Rik A G 19: 60,150,329 (GRCm39) noncoding transcript Het
Erbb2 C T 11: 98,324,835 (GRCm39) H810Y probably benign Het
Fmn1 C A 2: 113,274,713 (GRCm39) probably benign Het
Fpr3 A G 17: 18,191,325 (GRCm39) T199A possibly damaging Het
Gcsh A G 8: 117,710,688 (GRCm39) probably benign Het
Gm10073 T A 8: 107,299,901 (GRCm39) I28F probably benign Het
Gucy1a2 C A 9: 3,759,561 (GRCm39) Q456K probably damaging Het
Hgs C A 11: 120,369,174 (GRCm39) P317T probably damaging Het
Kcnma1 C A 14: 23,551,211 (GRCm39) M460I possibly damaging Het
Map9 A T 3: 82,286,272 (GRCm39) N359I probably damaging Het
Mavs T C 2: 131,087,263 (GRCm39) S254P probably benign Het
Mcts1 T A X: 37,700,636 (GRCm39) probably benign Het
Mecp2 C A X: 73,079,447 (GRCm39) R344L possibly damaging Het
Or1e32 T G 11: 73,705,612 (GRCm39) T99P probably damaging Het
Or4z4 A G 19: 12,077,000 (GRCm39) M1T probably null Het
Or5b3 G T 19: 13,388,114 (GRCm39) M60I probably damaging Het
Or8g36 T C 9: 39,422,342 (GRCm39) I225V possibly damaging Het
Or8g54 T G 9: 39,706,674 (GRCm39) M1R probably null Het
Or9g4 T C 2: 85,504,701 (GRCm39) T265A probably benign Het
Rasgrp1 T C 2: 117,119,144 (GRCm39) I498V probably damaging Het
Rbbp6 T A 7: 122,584,898 (GRCm39) S185T possibly damaging Het
Rd3 A T 1: 191,717,283 (GRCm39) H251L possibly damaging Het
Rnf180 T A 13: 105,386,864 (GRCm39) D148V probably damaging Het
Rnf43 C A 11: 87,555,542 (GRCm39) A34E probably damaging Het
Rslcan18 A G 13: 67,250,172 (GRCm39) V21A probably benign Het
Septin9 T C 11: 117,243,469 (GRCm39) V128A probably damaging Het
Slc36a1 A G 11: 55,110,482 (GRCm39) H103R probably benign Het
Spata6l A T 19: 28,873,532 (GRCm39) probably null Het
Ssh2 A G 11: 77,340,732 (GRCm39) D628G probably damaging Het
Tlcd3a T C 11: 76,098,051 (GRCm39) probably null Het
Tmem119 A G 5: 113,933,546 (GRCm39) F85S probably damaging Het
Tpp1 A T 7: 105,396,936 (GRCm39) I398N probably benign Het
Ttc3 T C 16: 94,191,066 (GRCm39) Y203H probably benign Het
Vars1 G T 17: 35,232,849 (GRCm39) V898L probably benign Het
Vmn1r85 A C 7: 12,819,081 (GRCm39) V21G probably damaging Het
Zfp521 T C 18: 14,072,045 (GRCm39) H65R possibly damaging Het
Other mutations in Inmt
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02404:Inmt APN 6 55,148,095 (GRCm39) missense possibly damaging 0.67
IGL02478:Inmt APN 6 55,150,355 (GRCm39) missense probably damaging 1.00
IGL02585:Inmt APN 6 55,150,431 (GRCm39) missense probably damaging 1.00
R0639:Inmt UTSW 6 55,148,212 (GRCm39) missense probably damaging 1.00
R0673:Inmt UTSW 6 55,148,212 (GRCm39) missense probably damaging 1.00
R1818:Inmt UTSW 6 55,150,404 (GRCm39) missense possibly damaging 0.92
R1862:Inmt UTSW 6 55,151,868 (GRCm39) missense probably damaging 1.00
R4383:Inmt UTSW 6 55,148,203 (GRCm39) missense probably damaging 1.00
R4529:Inmt UTSW 6 55,148,012 (GRCm39) missense probably benign 0.01
R5057:Inmt UTSW 6 55,151,883 (GRCm39) missense probably benign 0.00
R5999:Inmt UTSW 6 55,151,933 (GRCm39) nonsense probably null
R7135:Inmt UTSW 6 55,148,013 (GRCm39) nonsense probably null
R9242:Inmt UTSW 6 55,150,270 (GRCm39) critical splice donor site probably null
R9353:Inmt UTSW 6 55,151,984 (GRCm39) start gained probably benign
R9476:Inmt UTSW 6 55,147,990 (GRCm39) missense possibly damaging 0.95
R9510:Inmt UTSW 6 55,147,990 (GRCm39) missense possibly damaging 0.95
X0021:Inmt UTSW 6 55,150,281 (GRCm39) missense probably damaging 0.98
X0022:Inmt UTSW 6 55,150,460 (GRCm39) missense probably benign 0.40
Posted On 2013-12-09