RMND5A required for meiotic nuclear division 5 homolog A
Information
- Symbol
- RMND5A
- Type
- protein-coding
- Description
- required for meiotic nuclear division 5 homolog A
- Entrez Gene ID
- 64795
- Genome
- hg19
- Position
- chr2:86,947,414-87,005,164
- Genome
- hg38
- Position
- chr2:86,720,291-86,778,041
- MIM
- 618964 OMIM
- HGNC
- HGNC:25850 HGNC
- Ensembl
- ENSG00000153561 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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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
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CTLH |
SYNONYM | GID2 |
SYNONYM | GID2A |
SYNONYM | RMD5 |
SYNONYM | p44CTLH |
MIM | 618964 OMIM |
HGNC | HGNC:25850 HGNC |
Ensembl | ENSG00000153561 Ensembl |
AllianceGenome | HGNC:25850 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000283632.5 | hg38 | chr2 | 86,720,291 | 86,778,041 | 57,751 |
ENST00000283632.5 | hg19 | chr2 | 86,947,414 | 87,005,164 | 57,751 |
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