Incidental Mutation 'IGL01083:Tmem182'
ID 50214
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmem182
Ensembl Gene ENSMUSG00000079588
Gene Name transmembrane protein 182
Synonyms 2310079P10Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.109) question?
Stock # IGL01083
Quality Score
Status
Chromosome 1
Chromosomal Location 40844761-40896047 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 40844977 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Tyrosine at position 21 (F21Y)
Ref Sequence ENSEMBL: ENSMUSP00000110413 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114765]
AlphaFold B2RVY9
Predicted Effect probably damaging
Transcript: ENSMUST00000114765
AA Change: F21Y

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000110413
Gene: ENSMUSG00000079588
AA Change: F21Y

DomainStartEndE-ValueType
Pfam:Claudin_2 15 220 1.2e-64 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy8 T C 15: 64,659,191 (GRCm39) D533G probably benign Het
Adgb A G 10: 10,283,298 (GRCm39) V136A possibly damaging Het
Aggf1 A G 13: 95,492,917 (GRCm39) V564A probably damaging Het
Atp1a2 T C 1: 172,112,186 (GRCm39) T570A probably benign Het
Bicdl2 A G 17: 23,887,105 (GRCm39) Q464R probably damaging Het
Cacng5 C T 11: 107,772,531 (GRCm39) V106I probably benign Het
Chd8 C A 14: 52,458,877 (GRCm39) R792L probably damaging Het
Crybg2 A T 4: 133,802,755 (GRCm39) I844F possibly damaging Het
Dock4 G A 12: 40,838,380 (GRCm39) probably benign Het
Ergic2 T C 6: 148,096,769 (GRCm39) T166A probably benign Het
Flrt2 A T 12: 95,747,121 (GRCm39) R486S probably benign Het
Flt3 T C 5: 147,291,680 (GRCm39) Y590C probably damaging Het
Fubp1 A G 3: 151,927,871 (GRCm39) E441G probably damaging Het
Gfpt1 A G 6: 87,031,678 (GRCm39) S107G probably damaging Het
Klra9 A G 6: 130,166,729 (GRCm39) L45P possibly damaging Het
Mfsd5 A G 15: 102,189,525 (GRCm39) Y299C probably damaging Het
Myo5b T A 18: 74,866,974 (GRCm39) probably benign Het
Obscn G A 11: 58,926,919 (GRCm39) T5532M probably damaging Het
Or5ac25 G A 16: 59,182,198 (GRCm39) P128S probably damaging Het
Palld A G 8: 61,991,841 (GRCm39) S165P probably benign Het
Pramel17 T A 4: 101,692,729 (GRCm39) M424L probably benign Het
Prokr1 A T 6: 87,565,766 (GRCm39) H26Q probably benign Het
Prrc2a G T 17: 35,375,177 (GRCm39) R1158S possibly damaging Het
Rasgrp1 A G 2: 117,115,549 (GRCm39) W680R probably benign Het
Ryr3 A G 2: 112,582,191 (GRCm39) probably benign Het
Sars1 A G 3: 108,334,174 (GRCm39) L528P probably damaging Het
Serpinb3b T A 1: 107,085,473 (GRCm39) L89F possibly damaging Het
Slc38a6 T C 12: 73,335,267 (GRCm39) V70A possibly damaging Het
Son G A 16: 91,454,279 (GRCm39) E1009K probably damaging Het
Thoc3 A C 13: 54,615,633 (GRCm39) probably benign Het
Tlk2 T A 11: 105,112,050 (GRCm39) C88S probably benign Het
Tmem214 G A 5: 31,033,437 (GRCm39) V557M probably benign Het
Zfp507 T C 7: 35,493,463 (GRCm39) T527A probably benign Het
Other mutations in Tmem182
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2002:Tmem182 UTSW 1 40,845,355 (GRCm39) missense probably damaging 1.00
R4282:Tmem182 UTSW 1 40,877,530 (GRCm39) missense probably damaging 0.96
R5120:Tmem182 UTSW 1 40,894,061 (GRCm39) missense possibly damaging 0.51
R5152:Tmem182 UTSW 1 40,877,460 (GRCm39) missense probably damaging 1.00
R5537:Tmem182 UTSW 1 40,894,069 (GRCm39) missense probably benign 0.09
R8745:Tmem182 UTSW 1 40,877,536 (GRCm39) missense probably damaging 1.00
Z1176:Tmem182 UTSW 1 40,844,982 (GRCm39) missense possibly damaging 0.94
Posted On 2013-06-21