SPIN3 spindlin family member 3
Information
- Symbol
- SPIN3
- Type
- protein-coding
- Description
- spindlin family member 3
- Entrez Gene ID
- 169981
- Genome
- hg19
- Position
- chrX:57,017,296-57,022,239
- Genome
- hg38
- Position
- chrX:56,990,863-56,995,806
- HGNC
- HGNC:27272 HGNC
- Ensembl
- ENSG00000204271 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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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Search word | : | |
Filtering | : |
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 | SPIN-3 |
SYNONYM | TDRD27 |
SYNONYM | bA445O16.1 |
HGNC | HGNC:27272 HGNC |
Ensembl | ENSG00000204271 Ensembl |
AllianceGenome | HGNC:27272 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000638289.1 | hg38 | chrX | 56,990,942 | 56,995,555 | 4,614 |
ENST00000639007.1 | hg38 | chrX | 56,990,946 | 56,995,553 | 4,608 |
ENST00000640768.1 | hg38 | chrX | 56,990,954 | 56,995,426 | 4,473 |
ENST00000639525.1 | hg38 | chrX | 56,991,003 | 56,995,555 | 4,553 |
ENST00000638386.1 | hg38 | chrX | 56,990,895 | 56,995,647 | 4,753 |
ENST00000374919.6 | hg38 | chrX | 56,990,831 | 56,995,541 | 4,711 |
ENST00000638712.1 | hg38 | chrX | 56,990,864 | 56,995,827 | 4,964 |
ENST00000639583.1 | hg38 | chrX | 56,990,906 | 56,995,555 | 4,650 |
ENST00000638257.1 | hg38 | chrX | 56,990,863 | 56,995,806 | 4,944 |
ENST00000374919.6 | hg19 | chrX | 57,017,264 | 57,021,974 | 4,711 |
ENST00000638257.1 | hg19 | chrX | 57,017,296 | 57,022,239 | 4,944 |
ENST00000638712.1 | hg19 | chrX | 57,017,297 | 57,022,260 | 4,964 |
ENST00000638386.1 | hg19 | chrX | 57,017,328 | 57,022,080 | 4,753 |
ENST00000639583.1 | hg19 | chrX | 57,017,339 | 57,021,988 | 4,650 |
ENST00000638289.1 | hg19 | chrX | 57,017,375 | 57,021,988 | 4,614 |
ENST00000639007.1 | hg19 | chrX | 57,017,379 | 57,021,986 | 4,608 |
ENST00000640768.1 | hg19 | chrX | 57,017,387 | 57,021,859 | 4,473 |
ENST00000639525.1 | hg19 | chrX | 57,017,436 | 57,021,988 | 4,553 |
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