PABIR3 PABIR family member 3
Information
- Symbol
- PABIR3
- Type
- protein-coding
- Description
- PABIR family member 3
- Entrez Gene ID
- 159091
- Genome
- hg19
- Position
- chrX:133,941,267-133,988,862
- Genome
- hg38
- Position
- chrX:134,807,237-134,854,832
- HGNC
- HGNC:25202 HGNC
- Ensembl
- ENSG00000156500 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Conflicting classifications of pathogenicity | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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2 |
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | FAM122C |
HGNC | HGNC:25202 HGNC |
Ensembl | ENSG00000156500 Ensembl |
AllianceGenome | HGNC:25202 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000645288.1 | hg38 | chrX | 134,796,395 | 134,810,975 | 14,581 |
ENST00000414371.6 | hg38 | chrX | 134,796,789 | 134,822,975 | 26,187 |
ENST00000647516.1 | hg38 | chrX | 134,796,409 | 134,811,150 | 14,742 |
ENST00000623326.4 | hg38 | chrX | 134,807,191 | 134,822,990 | 15,800 |
ENST00000370784.8 | hg38 | chrX | 134,807,193 | 134,854,610 | 47,418 |
ENST00000370785.4 | hg38 | chrX | 134,807,194 | 134,854,591 | 47,398 |
ENST00000475361.1 | hg38 | chrX | 134,807,223 | 134,811,183 | 3,961 |
ENST00000646004.1 | hg38 | chrX | 134,807,169 | 134,854,835 | 47,667 |
ENST00000645433.2 | hg38 | chrX | 134,807,237 | 134,854,832 | 47,596 |
ENST00000482240.5 | hg38 | chrX | 134,807,217 | 134,809,557 | 2,341 |
ENST00000643150.1 | hg38 | chrX | 134,807,281 | 134,854,591 | 47,311 |
ENST00000494709.1 | hg38 | chrX | 134,807,239 | 134,808,180 | 942 |
ENST00000414371.6 | hg19 | chrX | 133,930,819 | 133,957,005 | 26,187 |
ENST00000482240.5 | hg19 | chrX | 133,941,247 | 133,943,587 | 2,341 |
ENST00000475361.1 | hg19 | chrX | 133,941,253 | 133,945,213 | 3,961 |
ENST00000645288.1 | hg19 | chrX | 133,930,425 | 133,945,005 | 14,581 |
ENST00000370784.8 | hg19 | chrX | 133,941,223 | 133,988,640 | 47,418 |
ENST00000370785.4 | hg19 | chrX | 133,941,224 | 133,988,621 | 47,398 |
ENST00000623326.4 | hg19 | chrX | 133,941,221 | 133,957,020 | 15,800 |
ENST00000645433.2 | hg19 | chrX | 133,941,267 | 133,988,862 | 47,596 |
ENST00000494709.1 | hg19 | chrX | 133,941,269 | 133,942,210 | 942 |
ENST00000646004.1 | hg19 | chrX | 133,941,199 | 133,988,865 | 47,667 |
ENST00000643150.1 | hg19 | chrX | 133,941,311 | 133,988,621 | 47,311 |
ENST00000647516.1 | hg19 | chrX | 133,930,439 | 133,945,180 | 14,742 |
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