Incidental Mutation 'IGL02826:Tmem215'
ID 361195
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmem215
Ensembl Gene ENSMUSG00000046593
Gene Name transmembrane protein 215
Synonyms A930001M12Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # IGL02826
Quality Score
Status
Chromosome 4
Chromosomal Location 40472180-40475653 bp(+) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to G at 40474632 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Tryptophan at position 236 (*236W)
Ref Sequence ENSEMBL: ENSMUSP00000136595 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049655] [ENSMUST00000179526]
AlphaFold A7E1Z1
Predicted Effect probably null
Transcript: ENSMUST00000049655
AA Change: *236W
SMART Domains Protein: ENSMUSP00000052129
Gene: ENSMUSG00000046593
AA Change: *236W

DomainStartEndE-ValueType
transmembrane domain 13 32 N/A INTRINSIC
transmembrane domain 37 59 N/A INTRINSIC
low complexity region 168 179 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000179526
AA Change: *236W
SMART Domains Protein: ENSMUSP00000136595
Gene: ENSMUSG00000046593
AA Change: *236W

DomainStartEndE-ValueType
Pfam:TMEM215 1 235 2.5e-117 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A3galt2 T C 4: 128,655,302 (GRCm39) probably benign Het
Alk C T 17: 72,176,531 (GRCm39) G1591D probably damaging Het
Angptl2 T C 2: 33,118,327 (GRCm39) S34P probably benign Het
Atp2a2 A G 5: 122,627,354 (GRCm39) V137A probably benign Het
Atp8b5 A G 4: 43,366,770 (GRCm39) M845V probably damaging Het
Camk1d A G 2: 5,570,571 (GRCm39) V30A possibly damaging Het
Ceacam19 G A 7: 19,616,535 (GRCm39) T193I probably benign Het
Cfap298 A C 16: 90,722,950 (GRCm39) D261E probably benign Het
Chst15 T A 7: 131,868,475 (GRCm39) D315V probably damaging Het
Cux1 G T 5: 136,336,857 (GRCm39) P885Q probably damaging Het
Cyth1 C T 11: 118,076,307 (GRCm39) E88K possibly damaging Het
Dido1 A G 2: 180,325,751 (GRCm39) V479A probably benign Het
Dlc1 G T 8: 37,037,429 (GRCm39) probably benign Het
H2-Ab1 G A 17: 34,483,885 (GRCm39) R82Q probably damaging Het
Hps6 T A 19: 45,994,480 (GRCm39) *806K probably null Het
Ilf3 T C 9: 21,309,340 (GRCm39) S486P probably benign Het
Kdm1b C A 13: 47,233,943 (GRCm39) T759K probably damaging Het
Kirrel1 C A 3: 86,995,792 (GRCm39) V381F probably damaging Het
Kmt2b A T 7: 30,276,569 (GRCm39) V1701E probably damaging Het
Lrmda T C 14: 22,878,805 (GRCm39) Y100H probably damaging Het
Mastl T C 2: 23,035,421 (GRCm39) I169V probably damaging Het
Mroh2b A G 15: 4,991,630 (GRCm39) E1576G probably damaging Het
Nek3 A T 8: 22,650,384 (GRCm39) probably null Het
Nipal3 G T 4: 135,195,861 (GRCm39) Y247* probably null Het
Nt5e A C 9: 88,237,758 (GRCm39) K229N probably damaging Het
Opa1 A G 16: 29,429,705 (GRCm39) M290V probably null Het
Or2a14 A G 6: 43,130,511 (GRCm39) I91V possibly damaging Het
Or8d6 G T 9: 39,854,254 (GRCm39) G233C probably damaging Het
Parp2 T A 14: 51,052,872 (GRCm39) I155K probably benign Het
Pde4dip G T 3: 97,674,403 (GRCm39) A171E probably damaging Het
Prom2 C T 2: 127,373,036 (GRCm39) E678K probably benign Het
Rab12 A G 17: 66,805,111 (GRCm39) probably benign Het
Rgs8 A T 1: 153,546,545 (GRCm39) T13S probably damaging Het
Setd3 A G 12: 108,078,383 (GRCm39) probably benign Het
Shisal1 A G 15: 84,304,330 (GRCm39) probably benign Het
Slx4ip G A 2: 136,846,893 (GRCm39) V53I probably damaging Het
Stil A G 4: 114,881,295 (GRCm39) D613G probably benign Het
Tektip1 A G 10: 81,200,570 (GRCm39) probably benign Het
Tjp3 T A 10: 81,109,523 (GRCm39) S858C probably damaging Het
Ttbk1 A G 17: 46,781,586 (GRCm39) V389A probably benign Het
Wdfy4 A G 14: 32,693,707 (GRCm39) F2706S possibly damaging Het
Xpo4 C A 14: 57,866,877 (GRCm39) V222L possibly damaging Het
Zfc3h1 A G 10: 115,236,809 (GRCm39) S428G probably benign Het
Zfp286 T C 11: 62,678,786 (GRCm39) Q47R probably damaging Het
Zfp318 A G 17: 46,709,680 (GRCm39) K468E probably damaging Het
Other mutations in Tmem215
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02028:Tmem215 APN 4 40,473,940 (GRCm39) missense possibly damaging 0.75
IGL02380:Tmem215 APN 4 40,474,534 (GRCm39) missense probably benign 0.19
R1531:Tmem215 UTSW 4 40,473,965 (GRCm39) missense probably damaging 1.00
R4941:Tmem215 UTSW 4 40,474,520 (GRCm39) missense probably damaging 0.97
R5636:Tmem215 UTSW 4 40,474,394 (GRCm39) missense probably damaging 0.99
R6820:Tmem215 UTSW 4 40,473,926 (GRCm39) start codon destroyed probably null 0.88
R7767:Tmem215 UTSW 4 40,474,042 (GRCm39) missense possibly damaging 0.75
R8958:Tmem215 UTSW 4 40,474,376 (GRCm39) missense probably benign 0.03
R9035:Tmem215 UTSW 4 40,473,945 (GRCm39) missense probably damaging 0.99
Posted On 2015-12-18