LIN7C lin-7 homolog C, crumbs cell polarity complex component
Information
- Symbol
- LIN7C
- Type
- protein-coding
- Description
- lin-7 homolog C, crumbs cell polarity complex component
- Entrez Gene ID
- 55327
- Genome
- hg19
- Position
- chr11:27,515,965-27,528,316
- Genome
- hg38
- Position
- chr11:27,494,418-27,506,769
- MIM
- 612332 OMIM
- HGNC
- HGNC:17789 HGNC
- Ensembl
- ENSG00000148943 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | LIN-7-C |
| SYNONYM | LIN-7C |
| SYNONYM | MALS-3 |
| SYNONYM | MALS3 |
| SYNONYM | VELI3 |
| MIM | 612332 OMIM |
| HGNC | HGNC:17789 HGNC |
| Ensembl | ENSG00000148943 Ensembl |
| AllianceGenome | HGNC:17789 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000524596.1 | hg38 | chr11 | 27,494,898 | 27,506,769 | 11,872 |
| ENST00000278193.7 | hg38 | chr11 | 27,494,418 | 27,506,769 | 12,352 |
| ENST00000278193.7 | hg19 | chr11 | 27,515,965 | 27,528,316 | 12,352 |
| ENST00000524596.1 | hg19 | chr11 | 27,516,445 | 27,528,316 | 11,872 |
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