LRRC23 leucine rich repeat containing 23
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
34 |
 |
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
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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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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 | LRPB7 |
| SYNONYM | SPGF92 |
| MIM | 620708 OMIM |
| HGNC | HGNC:19138 HGNC |
| Ensembl | ENSG00000010626 Ensembl |
| AllianceGenome | HGNC:19138 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000323702.9 | hg38 | chr12 | 6,904,841 | 6,914,228 | 9,388 |
| ENST00000622489.4 | hg38 | chr12 | 6,904,733 | 6,914,241 | 9,509 |
| ENST00000429740.1 | hg38 | chr12 | 6,905,634 | 6,914,071 | 8,438 |
| ENST00000433346.5 | hg38 | chr12 | 6,873,569 | 6,907,733 | 34,165 |
| ENST00000436789.5 | hg38 | chr12 | 6,905,028 | 6,913,968 | 8,941 |
| ENST00000443597.7 | hg38 | chr12 | 6,904,822 | 6,914,229 | 9,408 |
| ENST00000007969.12 | hg38 | chr12 | 6,904,733 | 6,914,229 | 9,497 |
| ENST00000433346.5 | hg19 | chr12 | 6,982,733 | 7,016,897 | 34,165 |
| ENST00000007969.12 | hg19 | chr12 | 7,013,897 | 7,023,393 | 9,497 |
| ENST00000622489.4 | hg19 | chr12 | 7,013,897 | 7,023,405 | 9,509 |
| ENST00000443597.7 | hg19 | chr12 | 7,013,986 | 7,023,393 | 9,408 |
| ENST00000323702.9 | hg19 | chr12 | 7,014,005 | 7,023,392 | 9,388 |
| ENST00000436789.5 | hg19 | chr12 | 7,014,192 | 7,023,132 | 8,941 |
| ENST00000429740.1 | hg19 | chr12 | 7,014,798 | 7,023,235 | 8,438 |
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