Incidental Mutation 'IGL01096:Tmem101'
ID 52277
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmem101
Ensembl Gene ENSMUSG00000020921
Gene Name transmembrane protein 101
Synonyms 2610511E22Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.163) question?
Stock # IGL01096
Quality Score
Status
Chromosome 11
Chromosomal Location 102043372-102047230 bp(-) (GRCm39)
Type of Mutation splice site (5 bp from exon)
DNA Base Change (assembly) C to A at 102045378 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000021296 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021296]
AlphaFold Q91VP7
Predicted Effect probably null
Transcript: ENSMUST00000021296
SMART Domains Protein: ENSMUSP00000021296
Gene: ENSMUSG00000020921

DomainStartEndE-ValueType
Pfam:TMEM101 8 256 9.9e-122 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136434
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143986
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg3 A T 8: 95,766,221 (GRCm39) M351L possibly damaging Het
Alk T C 17: 72,228,891 (GRCm39) K725E possibly damaging Het
Castor1 A C 11: 4,171,850 (GRCm39) E309A probably damaging Het
Dspp T A 5: 104,323,233 (GRCm39) H125Q possibly damaging Het
Elmo2 A T 2: 165,138,907 (GRCm39) probably benign Het
Erg A G 16: 95,190,912 (GRCm39) probably benign Het
Fam20c A G 5: 138,794,910 (GRCm39) E513G possibly damaging Het
Gm9839 G T 1: 32,559,917 (GRCm39) T55N possibly damaging Het
Gpd2 A T 2: 57,228,879 (GRCm39) M228L probably damaging Het
Hp A T 8: 110,302,033 (GRCm39) M305K probably benign Het
Ifng T A 10: 118,281,174 (GRCm39) probably benign Het
Igkv9-123 T C 6: 67,931,449 (GRCm39) D39G possibly damaging Het
Melk T A 4: 44,347,262 (GRCm39) F431I probably benign Het
Or10ak12 A G 4: 118,666,653 (GRCm39) V136A probably damaging Het
Or12j5 A T 7: 140,084,097 (GRCm39) S92T probably damaging Het
Or4p19 A G 2: 88,242,135 (GRCm39) M289T probably damaging Het
Or51k1 A C 7: 103,661,321 (GRCm39) L196W probably damaging Het
Or8g27 G A 9: 39,129,412 (GRCm39) G253D probably damaging Het
Pappa T C 4: 65,107,553 (GRCm39) Y655H probably damaging Het
Prss58 A T 6: 40,872,399 (GRCm39) I208N probably damaging Het
Ryr2 T A 13: 11,718,430 (GRCm39) I2720F probably damaging Het
Slc13a1 G T 6: 24,104,076 (GRCm39) T322K probably damaging Het
Spag17 T C 3: 99,970,691 (GRCm39) F1292L probably benign Het
Tbx5 A G 5: 120,021,091 (GRCm39) T366A probably benign Het
Tmeff2 G A 1: 50,969,705 (GRCm39) probably benign Het
Tpp2 C A 1: 44,000,048 (GRCm39) P389T probably damaging Het
Tyk2 A G 9: 21,020,159 (GRCm39) Y1000H probably damaging Het
Ush2a C A 1: 188,410,574 (GRCm39) N2407K probably damaging Het
Vmn1r94 C T 7: 19,901,561 (GRCm39) V248I probably damaging Het
Vmn2r12 T A 5: 109,234,125 (GRCm39) I696F probably damaging Het
Vmn2r83 A G 10: 79,313,662 (GRCm39) E90G probably damaging Het
Washc5 T C 15: 59,222,060 (GRCm39) probably benign Het
Wee2 A G 6: 40,440,187 (GRCm39) E445G probably benign Het
Zfp518b T C 5: 38,830,131 (GRCm39) T625A probably benign Het
Other mutations in Tmem101
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01085:Tmem101 APN 11 102,045,486 (GRCm39) missense probably damaging 0.99
IGL01593:Tmem101 APN 11 102,046,704 (GRCm39) missense probably damaging 1.00
IGL01814:Tmem101 APN 11 102,044,284 (GRCm39) missense possibly damaging 0.58
IGL02451:Tmem101 APN 11 102,044,119 (GRCm39) missense probably damaging 1.00
IGL03238:Tmem101 APN 11 102,046,611 (GRCm39) missense probably damaging 1.00
R0462:Tmem101 UTSW 11 102,046,693 (GRCm39) missense probably benign 0.08
R0848:Tmem101 UTSW 11 102,046,692 (GRCm39) missense possibly damaging 0.65
R1465:Tmem101 UTSW 11 102,044,155 (GRCm39) missense probably damaging 0.97
R1465:Tmem101 UTSW 11 102,044,155 (GRCm39) missense probably damaging 0.97
R1722:Tmem101 UTSW 11 102,045,519 (GRCm39) missense probably damaging 1.00
R1928:Tmem101 UTSW 11 102,044,222 (GRCm39) missense probably benign
R2082:Tmem101 UTSW 11 102,044,203 (GRCm39) missense probably benign 0.17
R4577:Tmem101 UTSW 11 102,046,663 (GRCm39) missense possibly damaging 0.48
R4724:Tmem101 UTSW 11 102,044,269 (GRCm39) missense probably benign 0.32
R4729:Tmem101 UTSW 11 102,047,155 (GRCm39) missense probably benign 0.25
R5146:Tmem101 UTSW 11 102,045,450 (GRCm39) missense probably benign
R5184:Tmem101 UTSW 11 102,047,059 (GRCm39) missense possibly damaging 0.78
R7381:Tmem101 UTSW 11 102,044,176 (GRCm39) missense possibly damaging 0.91
R8799:Tmem101 UTSW 11 102,044,336 (GRCm39) missense probably benign 0.08
R9612:Tmem101 UTSW 11 102,044,194 (GRCm39) missense probably damaging 1.00
Posted On 2013-06-21