TAMALIN trafficking regulator and scaffold protein tamalin
Information
- Symbol
- TAMALIN
- Type
- protein-coding
- Description
- trafficking regulator and scaffold protein tamalin
- Entrez Gene ID
- 160622
- Genome
- hg19
- Position
- chr12:52,400,730-52,409,673
- Genome
- hg38
- Position
- chr12:52,006,946-52,015,889
- MIM
- 612027 OMIM
- HGNC
- HGNC:18707 HGNC
- Ensembl
- ENSG00000161835 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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66 |
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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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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 |
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SYNONYM | GRASP |
MIM | 612027 OMIM |
HGNC | HGNC:18707 HGNC |
Ensembl | ENSG00000161835 Ensembl |
AllianceGenome | HGNC:18707 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000552049.5 | hg38 | chr12 | 52,010,521 | 52,015,887 | 5,367 |
ENST00000293662.9 | hg38 | chr12 | 52,006,946 | 52,015,889 | 8,944 |
ENST00000293662.9 | hg19 | chr12 | 52,400,730 | 52,409,673 | 8,944 |
ENST00000552049.5 | hg19 | chr12 | 52,404,305 | 52,409,671 | 5,367 |
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