KLHL36 kelch like family member 36
Information
- Symbol
- KLHL36
- Type
- protein-coding
- Description
- kelch like family member 36
- Entrez Gene ID
- 79786
- Genome
- hg19
- Position
- chr16:84,682,117-84,701,292
- Genome
- hg38
- Position
- chr16:84,648,511-84,667,686
- HGNC
- HGNC:17844 HGNC
- Ensembl
- ENSG00000135686 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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90 |
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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 |
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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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Category | : |
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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 | C16orf44 |
HGNC | HGNC:17844 HGNC |
Ensembl | ENSG00000135686 Ensembl |
AllianceGenome | HGNC:17844 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000258157.9 | hg38 | chr16 | 84,648,535 | 84,662,314 | 13,780 |
ENST00000564996.6 | hg38 | chr16 | 84,648,511 | 84,667,686 | 19,176 |
ENST00000564996.6 | hg19 | chr16 | 84,682,117 | 84,701,292 | 19,176 |
ENST00000258157.9 | hg19 | chr16 | 84,682,141 | 84,695,920 | 13,780 |
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