Incidental Mutation 'R1203:Tmem241'
ID 100304
Institutional Source Beutler Lab
Gene Symbol Tmem241
Ensembl Gene ENSMUSG00000049411
Gene Name transmembrane protein 241
Synonyms 6030446N20Rik
MMRRC Submission 039273-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1203 (G1)
Quality Score 225
Status Validated
Chromosome 18
Chromosomal Location 12113193-12254604 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to T at 12217035 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147954 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050228] [ENSMUST00000055447] [ENSMUST00000092075] [ENSMUST00000209859] [ENSMUST00000211298]
AlphaFold Q3UME2
Predicted Effect probably benign
Transcript: ENSMUST00000050228
SMART Domains Protein: ENSMUSP00000062148
Gene: ENSMUSG00000049411

DomainStartEndE-ValueType
transmembrane domain 119 136 N/A INTRINSIC
transmembrane domain 200 217 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000055447
SMART Domains Protein: ENSMUSP00000052001
Gene: ENSMUSG00000049411

DomainStartEndE-ValueType
transmembrane domain 32 54 N/A INTRINSIC
transmembrane domain 69 91 N/A INTRINSIC
transmembrane domain 121 140 N/A INTRINSIC
transmembrane domain 150 167 N/A INTRINSIC
transmembrane domain 184 201 N/A INTRINSIC
transmembrane domain 214 236 N/A INTRINSIC
transmembrane domain 248 270 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000092075
SMART Domains Protein: ENSMUSP00000089709
Gene: ENSMUSG00000049411

DomainStartEndE-ValueType
transmembrane domain 32 54 N/A INTRINSIC
transmembrane domain 69 91 N/A INTRINSIC
transmembrane domain 121 140 N/A INTRINSIC
transmembrane domain 150 167 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000209859
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210051
Predicted Effect probably benign
Transcript: ENSMUST00000211298
Predicted Effect noncoding transcript
Transcript: ENSMUST00000211480
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 98.4%
  • 10x: 95.6%
  • 20x: 89.3%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830018L16Rik A T 1: 11,588,818 (GRCm39) R78S probably damaging Het
Aadacl3 T C 4: 144,190,140 (GRCm39) T54A probably benign Het
Adcy8 A G 15: 64,618,780 (GRCm39) I791T probably damaging Het
Aldh1b1 A G 4: 45,803,359 (GRCm39) D299G probably damaging Het
Aoah A G 13: 21,000,764 (GRCm39) E66G probably damaging Het
Atl2 G T 17: 80,160,334 (GRCm39) H418N probably damaging Het
Atp6v1d A G 12: 78,908,214 (GRCm39) I7T possibly damaging Het
Calhm3 C T 19: 47,143,839 (GRCm39) V155M probably damaging Het
Carmil1 A T 13: 24,282,989 (GRCm39) I105K probably damaging Het
Csrp3 C A 7: 48,489,278 (GRCm39) M1I probably null Het
Dnah10 T A 5: 124,837,078 (GRCm39) probably null Het
Dnah11 T C 12: 117,897,547 (GRCm39) N3561S possibly damaging Het
Dzip3 A T 16: 48,772,180 (GRCm39) D496E probably damaging Het
Eif2ak1 T C 5: 143,820,797 (GRCm39) V246A probably benign Het
Fam171b T A 2: 83,643,313 (GRCm39) V74E probably benign Het
Gm14137 C T 2: 119,005,605 (GRCm39) R55W probably damaging Het
Gm4950 T C 18: 51,998,830 (GRCm39) I42V probably benign Het
Gpr35 T C 1: 92,910,870 (GRCm39) V194A probably damaging Het
Kdm5d C T Y: 941,011 (GRCm39) S1132F probably damaging Het
Muc4 C A 16: 32,754,529 (GRCm38) H1468N probably benign Het
Ncln A G 10: 81,332,027 (GRCm39) V24A possibly damaging Het
Nphp4 A G 4: 152,573,289 (GRCm39) K76E probably damaging Het
Nsf CAATAATAATAATAATA CAATAATAATAATAATAATA 11: 103,816,952 (GRCm39) probably benign Het
Nup155 A T 15: 8,187,244 (GRCm39) H1391L probably damaging Het
Or52h2 A T 7: 103,839,060 (GRCm39) L118* probably null Het
Pabpc1l G T 2: 163,879,091 (GRCm39) V313F possibly damaging Het
Pcbd2 G A 13: 55,880,881 (GRCm39) probably null Het
Rapgef6 T A 11: 54,582,525 (GRCm39) V1479D probably benign Het
Rnf43 T C 11: 87,618,301 (GRCm39) probably benign Het
Robo3 A G 9: 37,329,978 (GRCm39) W1113R probably damaging Het
Sall1 A T 8: 89,758,562 (GRCm39) V514E probably damaging Het
Sgpp1 A G 12: 75,763,056 (GRCm39) I375T probably benign Het
Strc T C 2: 121,202,604 (GRCm39) N1187S possibly damaging Het
Tbc1d17 G A 7: 44,492,895 (GRCm39) R363W probably damaging Het
Tbcd A G 11: 121,366,451 (GRCm39) Q242R probably benign Het
Tbcel A C 9: 42,362,947 (GRCm39) V50G probably damaging Het
Tead3 C T 17: 28,560,536 (GRCm39) A23T probably benign Het
Tedc2 T A 17: 24,435,291 (GRCm39) E366V probably damaging Het
Tedc2 C A 17: 24,435,292 (GRCm39) E366* probably null Het
Tlcd5 A G 9: 43,022,775 (GRCm39) V193A probably benign Het
Tmtc3 G T 10: 100,312,606 (GRCm39) T79K probably damaging Het
Utrn A G 10: 12,362,281 (GRCm39) V241A probably damaging Het
Vps8 A T 16: 21,330,307 (GRCm39) I729F probably damaging Het
Zfp407 C T 18: 84,577,898 (GRCm39) A1072T probably benign Het
Other mutations in Tmem241
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02256:Tmem241 APN 18 12,246,489 (GRCm39) missense probably damaging 1.00
R0106:Tmem241 UTSW 18 12,239,066 (GRCm39) intron probably benign
R1218:Tmem241 UTSW 18 12,197,271 (GRCm39) missense probably damaging 1.00
R1304:Tmem241 UTSW 18 12,203,135 (GRCm39) critical splice donor site probably null
R1416:Tmem241 UTSW 18 12,126,631 (GRCm39) missense probably benign 0.00
R1430:Tmem241 UTSW 18 12,126,651 (GRCm39) missense probably benign 0.01
R1539:Tmem241 UTSW 18 12,176,297 (GRCm39) missense possibly damaging 0.92
R1729:Tmem241 UTSW 18 12,201,369 (GRCm39) missense probably damaging 0.99
R1775:Tmem241 UTSW 18 12,251,469 (GRCm39) missense probably damaging 1.00
R3813:Tmem241 UTSW 18 12,200,167 (GRCm39) splice site probably benign
R4352:Tmem241 UTSW 18 12,246,496 (GRCm39) missense probably benign 0.35
R4903:Tmem241 UTSW 18 12,237,176 (GRCm39) missense probably damaging 1.00
R4966:Tmem241 UTSW 18 12,237,176 (GRCm39) missense probably damaging 1.00
R5490:Tmem241 UTSW 18 12,176,320 (GRCm39) missense probably benign 0.00
R5704:Tmem241 UTSW 18 12,197,263 (GRCm39) missense probably damaging 1.00
R6943:Tmem241 UTSW 18 12,180,641 (GRCm39) missense possibly damaging 0.92
R7037:Tmem241 UTSW 18 12,246,463 (GRCm39) missense probably benign 0.02
R7209:Tmem241 UTSW 18 12,237,229 (GRCm39) missense probably damaging 0.97
R8698:Tmem241 UTSW 18 12,197,288 (GRCm39) missense possibly damaging 0.93
R9562:Tmem241 UTSW 18 12,176,356 (GRCm39) nonsense probably null
RF013:Tmem241 UTSW 18 12,116,618 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2014-01-15