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Sequence Detail
ID/Version
Q6IEE6 A0A0A0MQ93 Q5SUX0 B7ZN59 (UniProt | EBI) Last sequence update: 2019-04-10
Last annotation update: 2024-03-27
Sequence
description
from provider
RecName: Full=Transmembrane protein 132E;Flags: Precursor;
Provider SWISS-PROT
Sequence
Polypeptide 1074 aa
For this sequence
Source
Organism mouse
See UniProt | EBI for source
Annotated genes and markers Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.
Type Symbol Name GO Terms Expression
Assays
Orthologs Phenotypic
Alleles
Gene Tmem132e transmembrane protein 132E 3 98 3 8
Sequence references in MGI J:95648 Kehrer-Sawatzki H, et al., Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region. J Med Genet. 2003 Oct;40(10):e116
J:284992 Li J, et al., Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99. Hum Mutat. 2015 Jan;36(1):98-105
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory