DNLZ DNL-type zinc finger
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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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 |
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SYNONYM | C9orf151 |
SYNONYM | HEP |
SYNONYM | HEP1 |
SYNONYM | TIMM15 |
SYNONYM | ZIM17 |
SYNONYM | bA413M3.2 |
MIM | 620797 OMIM |
HGNC | HGNC:33879 HGNC |
Ensembl | ENSG00000213221 Ensembl |
AllianceGenome | HGNC:33879 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000371738.4 | hg38 | chr9 | 136,359,483 | 136,363,744 | 4,262 |
ENST00000371739.3 | hg38 | chr9 | 136,359,480 | 136,363,719 | 4,240 |
ENST00000371739.3 | hg19 | chr9 | 139,253,932 | 139,258,171 | 4,240 |
ENST00000371738.4 | hg19 | chr9 | 139,253,935 | 139,258,196 | 4,262 |
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