ARMCX5 armadillo repeat containing X-linked 5
Information
- Symbol
- ARMCX5
- Type
- protein-coding
- Description
- armadillo repeat containing X-linked 5
- Entrez Gene ID
- 64860
- Genome
- hg19
- Position
- chrX:101,854,448-101,859,087
- Genome
- hg38
- Position
- chrX:102,599,520-102,604,159
- MIM
- 301047 OMIM
- HGNC
- HGNC:25772 HGNC
- Ensembl
- ENSG00000125962 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | GASP5 |
MIM | 301047 OMIM |
HGNC | HGNC:25772 HGNC |
Ensembl | ENSG00000125962 Ensembl |
AllianceGenome | HGNC:25772 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000473968.7 | hg38 | chrX | 102,599,515 | 102,604,159 | 4,645 |
ENST00000372742.1 | hg38 | chrX | 102,601,137 | 102,604,153 | 3,017 |
ENST00000246174.6 | hg38 | chrX | 102,599,168 | 102,604,159 | 4,992 |
ENST00000604957.1 | hg38 | chrX | 102,599,520 | 102,604,159 | 4,640 |
ENST00000246174.6 | hg19 | chrX | 101,854,096 | 101,859,087 | 4,992 |
ENST00000473968.7 | hg19 | chrX | 101,854,443 | 101,859,087 | 4,645 |
ENST00000604957.1 | hg19 | chrX | 101,854,448 | 101,859,087 | 4,640 |
ENST00000372742.1 | hg19 | chrX | 101,856,065 | 101,859,081 | 3,017 |
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