Incidental Mutation 'IGL02529:Tmem181b-ps'
ID 297233
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmem181b-ps
Ensembl Gene ENSMUSG00000096780
Gene Name transmembrane protein 181B, pseudogene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02529
Quality Score
Status
Chromosome 17
Chromosomal Location 6706401-6718393 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 6734320 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000167717
SMART Domains Protein: ENSMUSP00000130420
Gene: ENSMUSG00000079733

DomainStartEndE-ValueType
transmembrane domain 17 36 N/A INTRINSIC
Pfam:MIG-14_Wnt-bd 127 190 1.3e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181052
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188746
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik T A 14: 32,383,190 (GRCm39) H925L probably benign Het
Agpat5 T A 8: 18,931,770 (GRCm39) Y297N possibly damaging Het
Apobec3 C T 15: 79,781,888 (GRCm39) probably benign Het
Atpaf1 C A 4: 115,648,466 (GRCm39) A161E probably damaging Het
Bnc1 A T 7: 81,627,116 (GRCm39) D91E probably damaging Het
Capg G A 6: 72,532,829 (GRCm39) V98I probably benign Het
Ccdc7b C T 8: 129,904,706 (GRCm39) L115F possibly damaging Het
Ces2a T A 8: 105,463,851 (GRCm39) probably benign Het
Cldn6 T G 17: 23,900,291 (GRCm39) V85G probably damaging Het
Clec2e T C 6: 129,075,459 (GRCm39) probably benign Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Dhx38 T C 8: 110,285,645 (GRCm39) E396G probably benign Het
Dock8 A T 19: 25,078,290 (GRCm39) K532* probably null Het
Efr3b C T 12: 4,033,391 (GRCm39) V139I probably benign Het
Gmip G A 8: 70,269,439 (GRCm39) G537E probably damaging Het
Hacd1 T C 2: 14,050,013 (GRCm39) H64R probably damaging Het
Hdac3 G T 18: 38,077,185 (GRCm39) Q230K probably benign Het
Htt C T 5: 34,976,387 (GRCm39) probably benign Het
Il18r1 A G 1: 40,526,219 (GRCm39) D255G possibly damaging Het
Krt82 T A 15: 101,458,831 (GRCm39) R70* probably null Het
Krt9 G T 11: 100,080,792 (GRCm39) H353Q probably damaging Het
Kyat3 T C 3: 142,426,235 (GRCm39) I57T probably benign Het
L1td1 A G 4: 98,625,658 (GRCm39) K618E probably benign Het
Limch1 C A 5: 67,159,956 (GRCm39) N617K possibly damaging Het
Lsm8 T C 6: 18,851,651 (GRCm39) F34S probably damaging Het
Man2a2 G A 7: 80,009,388 (GRCm39) A822V probably damaging Het
Mmrn2 C A 14: 34,120,570 (GRCm39) A480E possibly damaging Het
Mthfd1 A G 12: 76,350,483 (GRCm39) I474V probably benign Het
Mycl A G 4: 122,890,770 (GRCm39) K152R probably damaging Het
Numa1 A G 7: 101,649,160 (GRCm39) probably null Het
Or5p54 G T 7: 107,554,423 (GRCm39) V192F possibly damaging Het
Otog A C 7: 45,909,381 (GRCm39) D617A probably damaging Het
Ppef2 A G 5: 92,392,596 (GRCm39) I267T probably damaging Het
Ptprq A G 10: 107,471,226 (GRCm39) Y1392H probably benign Het
Rasgrp3 G T 17: 75,832,097 (GRCm39) K639N possibly damaging Het
Rgs19 C T 2: 181,330,943 (GRCm39) R203H probably benign Het
Scnn1g C A 7: 121,341,669 (GRCm39) probably benign Het
Vmn2r118 A G 17: 55,917,870 (GRCm39) V214A possibly damaging Het
Zfp811 T C 17: 33,016,789 (GRCm39) Y417C probably damaging Het
Posted On 2015-04-16