ARMC9 - armadillo repeat containing 9 Gene

Homo sapiens

Also known as ARM; NS21; JBTS30; KU-MEL-1

Gene ID: 80210 | Gene type: protein coding

About ARMC9

Cytogenetic location: 2q37.1 Genomic coordinates (GRCh38): 2:231,198,631-231,376,848 (from NCBI)

This gene has 45 transcripts (splice variants), 198 orthologues and is associated with 3 phenotypes. Broad expression in endometrium (RPKM 2.3), ovary (RPKM 1.9) and 22 other tissues.

Summary

Predicted to be involved in cilium assembly and positive regulation of smoothened signaling pathway. Located in centriole and ciliary basal body. Implicated in Joubert syndrome 30. [provided by Alliance of Genome Resources, Apr 2022]

ARMC9 Products(9)

mRNA	Protein	Name
NM_001271466.4	NP_001258395.2	lisH domain-containing protein ARMC9 isoform 1
NM_001291656.2	NP_001278585.2	lisH domain-containing protein ARMC9 isoform 2
NM_001352754.2	NP_001339683.2	lisH domain-containing protein ARMC9 isoform 1
NM_001352755.2	NP_001339684.2	lisH domain-containing protein ARMC9 isoform 2
NM_001352756.2	NP_001339685.2	lisH domain-containing protein ARMC9 isoform 2
NM_001352757.2	NP_001339686.2	lisH domain-containing protein ARMC9 isoform 3
NM_001352758.2	NP_001339687.2	lisH domain-containing protein ARMC9 isoform 3
NM_001352759.2	NP_001339688.2	lisH domain-containing protein ARMC9 isoform 4
NM_025139.6	NP_079415.4	lisH domain-containing protein ARMC9 isoform 2

Protein Preferred Names

Protein Names

lisH domain-containing protein ARMC9

armadillo repeat-containing protein 9

Related Diseases

Diseases

Alias

Joubert Syndrome 30

JBTS30

Joubert Syndrome, Type 30

Joubert Syndrome 1

Joubert Syndrome	Jbts
Cerebellooculorenal Syndrome 1	JBTS1
Joubert-Boltshauser Syndrome	Cerebelloparenchymal Disorder Iv
Cpd4	Cors1
Joubert Syndrome And Related Disorders	Jsrd
Familial Aplasia Of The Vermis	Joubert Syndrome Related Disorders
Js	Cerebellar Vermis Agenesis
Cerebelloparenchymal Disorder 4	Agenesis Of Cerebellar Vermis
Cerebello-Oculo-Renal Syndrome	Cors
Joubert-Bolthauser Syndrome	Cpd Iv
Classic Joubert Syndrome	Joubert Syndrome Type A
Pure Joubert Syndrome	Cerebello-Oculo-Renal Syndrome 1
Joubert Syndrome-1	Joubert Syndrome, Type 1
Joubert'S Syndrome

Dandy-Walker Syndrome

Dandy-Walker Malformation	DWS
Atresia Of Foramina Of Magendie And Luschka	Dandy-Walker Complex
Dandy-Walker Cyst	Dandy-Walker Deformity
Dandy Walker Cyst	Dw Complex
Dandy-Walker Syndrome Or Malformation	Dandy-Walker Variant
Mega Cisterna Magna	Dwm
Hydrocephalus, Internal, Dandy-Walker Type	Hydrocephalus, Noncommunicating, Dandy-Walker Type
Luschka-Magendie Foramina Atresia	Isolated Dandy-Walker Malformation
Mega-Cisterna Magna	Dandy Walker Variant
Atresia Of Foramen Of Luschka	Atresia Of Foramen Of Magendie
Congenital Blockage Of Foramen Magendie

Macular Degeneration, Age-Related, 8

Age Related Macular Degeneration 8	ARMD8
Macular Degeneration, Age-Related, Type 8

Noonan Syndrome 11

NS11

Noonan Syndrome 12

NS12

Polydactyly

Non-Syndromic Polydactyly	Polydactyly, Postaxial
Postaxial Polydactyly	Supernumerary Digit
Extra Digits	Hyperdactyly
Polydactylia	Polydactylism
Supernumerary Digits

Joubert Syndrome 23

JBTS23

Joubert Syndrome, Type 23

Argyll Robertson Pupil

Atypical Argyll-Robertson Pupil	Argyll Robertson Phenomenon Or Pupil, Nonsyphilitic
Argyll Robertson Pupil, Atypical

Abnormal Pupillary Function

Pupil Disease

Pupil Disorders

Pupillary Disorder

Pseudoretinitis Pigmentosa

Secondary Pigmentary Retinal Degeneration

Secondary Pigmentary Degeneration Of Retina

Vogt-Koyanagi-Harada Disease

Uveomeningoencephalitic Syndrome	Uveomenigitic Syndrome
Vogt-Koyanagi-Harada Syndrome	Harada'S Disease
Vogt-Koyanagi Syndrome	Vkh Disease
Vkh Syndrome	Vkh

Bardet-Biedl Syndrome

Bbs	Biedl-Bardet Syndrome

Melanoma

Malignant Melanoma	Cutaneous Melanoma
Naevocarcinoma	Malignant Melanomas

Fundus Dystrophy

Retinal Dystrophy	Retinal Dystrophies
Dystrophy, Retinal

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-RS01006	ARMC9 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	ARMC9	VGNC	VGNC:59938
Rattus norvegicus	ARMC9	RGD	RGD:1305615
Bos taurus	ARMC9	VGNC	VGNC:26163
Macaca mulatta	ARMC9	VGNC	VGNC:69870
Canis familiaris	ARMC9	VGNC	VGNC:38129
Mus musculus	ARMC9	MGD	MGI:1926045

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