TMEM164 - transmembrane protein 164 Gene

Homo sapiens

Also known as bB360B22.3

Gene ID: 84187 | Gene type: protein coding

About TMEM164

This gene has 8 transcripts (splice variants) and 206 orthologues. Ubiquitous expression in lung (RPKM 5.4), fat (RPKM 5.2) and 25 other tissues.

Summary

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

TMEM164 Products(6)

mRNA	Protein	Name
NM_001353849.2	NP_001340778.1	transmembrane protein 164 isoform b
NM_001353850.2	NP_001340779.1	transmembrane protein 164 isoform c
NM_001353851.2	NP_001340780.1	transmembrane protein 164 isoform c
NM_001410717.1	NP_001397646.1	transmembrane protein 164 isoform d
NM_017698.3	NP_060168.2	transmembrane protein 164 isoform a precursor
NM_032227.4	NP_115603.2	transmembrane protein 164 isoform b

Gene Ontology

Biological Process

Biological Process GO Annotation	Evidence	Reference	Source
involved in positive regulation of ferroptosis	IDA IDA: Inferred from direct assay	35947500	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TMEM164 Protein Structure

TMEM164

0
100
200
297 a.a.

Protein Preferred Names

Protein Names

transmembrane protein 164

RP13-360B22.2

Related Diseases

Diseases

Alias

Amme Complex

Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis	ATS-MR
Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome	Chromosome Xq22.3 Telomeric Deletion Syndrome
Amme Syndrome	Alport Syndrome With Intellectual Disability, Midface Hypoplasia And Elliptocytosis

X-Linked Alport Syndrome

Nephropathy And Deafness, X-Linked

Alport Syndrome

Hereditary Nephritis	Alport Syndrome, X-Linked
Hemorrhagic Hereditary Nephritis	Congenital Hereditary Hematuria
Hemorrhagic Familial Nephritis	Familial Nephritis
Thin Basement Membrane Disease	Thin Basement Membrane Nephropathy
Hematuria-Nephropathy-Deafness Syndrome	Hematuric Hereditary Nephritis
Hereditary Familial Congenital Hemorrhagic Nephritis	Hereditary Hematuria Syndrome
Hereditary Interstitial Pyelonephritis	Alport Deafness-Nephropathy
Alport Hearing Loss-Nephropathy	Alports Syndrome
Nephritis, Hereditary

Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability	Non-Specific X-Linked Mental Retardation
X-Linked Non-Specific Intellectual Disability

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS14678	TMEM164 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	TMEM164	MGD	MGI:2148020
Canis familiaris	TMEM164	VGNC	VGNC:47491
Macaca mulatta	TMEM164	VGNC	VGNC:79589
Bos taurus	TMEM164	VGNC	VGNC:35989
Rattus norvegicus	TMEM164	RGD	RGD:1563286

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