Incidental Mutation 'IGL03032:Mettl21e'
ID 408508
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mettl21e
Ensembl Gene ENSMUSG00000046828
Gene Name methyltransferase like 21E
Synonyms 4832428D23Rik, LOC381340
Accession Numbers
Essential gene? Probably non essential (E-score: 0.143) question?
Stock # IGL03032
Quality Score
Status
Chromosome 1
Chromosomal Location 44243230-44258121 bp(-) (GRCm39)
Type of Mutation splice site (5 bp from exon)
DNA Base Change (assembly) C to A at 44249319 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000056481 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054801]
AlphaFold Q8CDZ2
Predicted Effect probably null
Transcript: ENSMUST00000054801
SMART Domains Protein: ENSMUSP00000056481
Gene: ENSMUSG00000046828

DomainStartEndE-ValueType
Pfam:Methyltransf_16 49 217 3.9e-35 PFAM
Pfam:PrmA 74 225 7.1e-7 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150062
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161563
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310003L06Rik A T 5: 88,119,774 (GRCm39) Y177F possibly damaging Het
Als2 C A 1: 59,255,189 (GRCm39) probably benign Het
Arhgap44 A G 11: 64,915,038 (GRCm39) L410P probably damaging Het
Atp13a2 C T 4: 140,727,666 (GRCm39) A481V possibly damaging Het
Bod1l C A 5: 41,988,927 (GRCm39) L393F probably benign Het
Cflar T A 1: 58,780,179 (GRCm39) I258N probably damaging Het
Col24a1 T C 3: 145,244,458 (GRCm39) probably null Het
Csmd2 A T 4: 128,412,834 (GRCm39) N2542I probably benign Het
Cyp2b9 T C 7: 25,898,025 (GRCm39) probably benign Het
Dip2c A T 13: 9,601,814 (GRCm39) I258F probably damaging Het
Dock7 A G 4: 98,854,585 (GRCm39) S1560P probably benign Het
Drc7 C T 8: 95,802,875 (GRCm39) probably benign Het
Gm3667 T A 14: 18,269,522 (GRCm39) S203C probably null Het
Gramd2a A G 9: 59,619,410 (GRCm39) E190G probably benign Het
Gstm4 T C 3: 107,951,263 (GRCm39) D8G probably damaging Het
Heatr5b A T 17: 79,067,928 (GRCm39) M1820K probably benign Het
Irs4 A G X: 140,505,794 (GRCm39) Y801H unknown Het
Loxhd1 C T 18: 77,374,169 (GRCm39) T80I possibly damaging Het
Lrrc40 G A 3: 157,747,302 (GRCm39) probably benign Het
Mapk8ip1 T G 2: 92,216,958 (GRCm39) K446Q probably damaging Het
Mmp8 T A 9: 7,558,530 (GRCm39) probably benign Het
Muc19 A T 15: 91,808,424 (GRCm39) noncoding transcript Het
Nipsnap3b T A 4: 53,015,016 (GRCm39) V21E possibly damaging Het
Or1j15 C A 2: 36,458,716 (GRCm39) Y35* probably null Het
Or5al6 A G 2: 85,977,043 (GRCm39) F12L probably damaging Het
Or7a38 A T 10: 78,753,471 (GRCm39) I266F probably benign Het
Parp12 G A 6: 39,064,520 (GRCm39) probably null Het
Pramel14 C A 4: 143,719,815 (GRCm39) L183F probably damaging Het
Rgsl1 T A 1: 153,701,948 (GRCm39) T169S possibly damaging Het
Rnf38 T C 4: 44,152,529 (GRCm39) R12G probably damaging Het
Slc9c1 T C 16: 45,363,624 (GRCm39) probably benign Het
Slpi T C 2: 164,197,367 (GRCm39) probably benign Het
Snx17 G A 5: 31,353,355 (GRCm39) V165I probably benign Het
Tnfaip3 A G 10: 18,880,357 (GRCm39) V570A probably benign Het
Vmn1r63 A G 7: 5,806,350 (GRCm39) M94T probably benign Het
Vmn2r95 A G 17: 18,672,575 (GRCm39) I771V probably benign Het
Wiz A G 17: 32,575,532 (GRCm39) V868A probably benign Het
Other mutations in Mettl21e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00660:Mettl21e APN 1 44,245,530 (GRCm39) missense possibly damaging 0.80
IGL01878:Mettl21e APN 1 44,250,193 (GRCm39) missense probably null 1.00
IGL02194:Mettl21e APN 1 44,250,343 (GRCm39) missense probably benign
IGL03396:Mettl21e APN 1 44,245,759 (GRCm39) missense possibly damaging 0.67
R0165:Mettl21e UTSW 1 44,250,283 (GRCm39) missense probably damaging 1.00
R0363:Mettl21e UTSW 1 44,250,190 (GRCm39) critical splice donor site probably null
R0525:Mettl21e UTSW 1 44,245,542 (GRCm39) missense probably damaging 0.98
R2078:Mettl21e UTSW 1 44,245,662 (GRCm39) missense possibly damaging 0.80
R2143:Mettl21e UTSW 1 44,249,398 (GRCm39) missense probably benign 0.06
R3623:Mettl21e UTSW 1 44,245,857 (GRCm39) missense probably damaging 0.99
R3870:Mettl21e UTSW 1 44,245,524 (GRCm39) missense probably benign 0.01
R4780:Mettl21e UTSW 1 44,250,303 (GRCm39) missense probably benign
R5488:Mettl21e UTSW 1 44,257,276 (GRCm39) missense probably benign
R5654:Mettl21e UTSW 1 44,250,255 (GRCm39) missense probably damaging 1.00
R6490:Mettl21e UTSW 1 44,249,425 (GRCm39) missense probably damaging 0.97
R6697:Mettl21e UTSW 1 44,249,327 (GRCm39) missense probably damaging 1.00
R6804:Mettl21e UTSW 1 44,257,295 (GRCm39) missense probably benign 0.01
R6862:Mettl21e UTSW 1 44,245,526 (GRCm39) missense probably benign 0.00
R7282:Mettl21e UTSW 1 44,249,399 (GRCm39) missense probably damaging 0.98
R7870:Mettl21e UTSW 1 44,249,371 (GRCm39) missense probably damaging 1.00
R8054:Mettl21e UTSW 1 44,245,815 (GRCm39) missense probably damaging 1.00
R8492:Mettl21e UTSW 1 44,245,553 (GRCm39) missense probably damaging 1.00
R9481:Mettl21e UTSW 1 44,245,857 (GRCm39) missense probably benign 0.01
R9507:Mettl21e UTSW 1 44,245,536 (GRCm39) missense probably benign 0.05
R9641:Mettl21e UTSW 1 44,250,351 (GRCm39) missense probably benign 0.01
Z1177:Mettl21e UTSW 1 44,245,710 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02