RMND5B required for meiotic nuclear division 5 homolog B
Information
- Symbol
- RMND5B
- Type
- protein-coding
- Description
- required for meiotic nuclear division 5 homolog B
- Entrez Gene ID
- 64777
- Genome
- hg19
- Position
- chr5:177,557,997-177,577,566
- Genome
- hg38
- Position
- chr5:178,130,996-178,150,565
- HGNC
- HGNC:26181 HGNC
- Ensembl
- ENSG00000145916 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 6 |
| Benign | 0 | 10 |
| Likely benign | 0 | 32 |
| Uncertain significance | 0 | 96 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
18 |
 |
114 |
 |
4 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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| Category | : |
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| 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 | GID2 |
| SYNONYM | GID2B |
| HGNC | HGNC:26181 HGNC |
| Ensembl | ENSG00000145916 Ensembl |
| AllianceGenome | HGNC:26181 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000542098.2 | hg38 | chr5 | 178,135,213 | 178,148,570 | 13,358 |
| ENST00000515098.5 | hg38 | chr5 | 178,130,996 | 178,150,565 | 19,570 |
| ENST00000313386.9 | hg38 | chr5 | 178,131,014 | 178,150,568 | 19,555 |
| ENST00000515098.5 | hg19 | chr5 | 177,557,997 | 177,577,566 | 19,570 |
| ENST00000313386.9 | hg19 | chr5 | 177,558,015 | 177,577,569 | 19,555 |
| ENST00000542098.2 | hg19 | chr5 | 177,562,214 | 177,575,571 | 13,358 |
| Key | Value |
|---|---|
| strand | + |
| start | 177,557,961 |
| Gene Symbol | RMND5B |
| Entrez GeneId | 64,777 |
| Chr Band | 5q35.3 |
| end | 177,575,570 |
| chr | chr5 |
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