RTL9 - retrotransposon Gag like 9 Gene

GLP-1 and Obesity Research

2026-08-18

Also Known as MAR9; MART9; RGAG1; SIRH10

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 57529

About RTL9

Cytogenetic location: Xq23 Genomic coordinates (GRCh38): X:110,358,848-110,456,334 (from NCBI)

This gene has 3 transcripts (splice variants), 99 orthologues and 2 paralogues. Restricted expression toward testis (RPKM 5.0).

RTL9 Products (2)

mRNA	Protein	Name
NM_001385449.1	NP_001372378.1	retrotransposon Gag-like protein 9
NM_020769.2	NP_065820.1	retrotransposon Gag-like protein 9

Protein Preferred Names	Protein Names
retrotransposon Gag-like protein 9	Sushi-Ichi retrotransposon homolog 10

Protein Preferred Names

Protein Names

retrotransposon Gag-like protein 9

Sushi-Ichi retrotransposon homolog 10

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
Embryonal Testis Carcinoma	Testicular Embryonal Carcinoma Embryonal Carcinoma Of Testis Embryonal Carcinoma Of The Testis
X-Linked Alport Syndrome	Nephropathy And Deafness, X-Linked
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

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

Embryonal Testis Carcinoma

Testicular Embryonal Carcinoma
Embryonal Carcinoma Of Testis
Embryonal Carcinoma Of The Testis

X-Linked Alport Syndrome

Nephropathy And Deafness, X-Linked

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

Diseases

Alias

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS12328	RTL9 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	RTL9	VGNC	VGNC:34202
Mus musculus	RTL9	MGD	MGI:2685231
Canis familiaris	RTL9	VGNC	VGNC:45795
Macaca mulatta	RTL9	VGNC	VGNC:77125
Rattus norvegicus	RTL9	RGD	RGD:6486824
Others	RTL9	NCBI

Species

Symbol

Source

Bos taurus

RTL9

VGNC

VGNC:34202

Mus musculus

RTL9

MGD

MGI:2685231

Canis familiaris