LMTK3 lemur tyrosine kinase 3
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 10 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 152 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
172 |
 |
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 | |||||||||||
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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 | AATYK3 |
| SYNONYM | LMR3 |
| SYNONYM | PPP1R101 |
| SYNONYM | TYKLM3 |
| MIM | 619624 OMIM |
| HGNC | HGNC:19295 HGNC |
| Ensembl | ENSG00000142235 Ensembl |
| AllianceGenome | HGNC:19295 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000598924.1 | hg38 | chr19 | 48,513,207 | 48,513,660 | 454 |
| ENST00000650440.1 | hg38 | chr19 | 48,485,773 | 48,513,935 | 28,163 |
| ENST00000673139.1 | hg38 | chr19 | 48,485,271 | 48,513,189 | 27,919 |
| ENST00000672160.1 | hg38 | chr19 | 48,485,271 | 48,501,837 | 16,567 |
| ENST00000600059.6 | hg38 | chr19 | 48,485,271 | 48,511,835 | 26,565 |
| ENST00000672160.1 | hg19 | chr19 | 48,988,528 | 49,005,094 | 16,567 |
| ENST00000600059.6 | hg19 | chr19 | 48,988,528 | 49,015,092 | 26,565 |
| ENST00000673139.1 | hg19 | chr19 | 48,988,528 | 49,016,446 | 27,919 |
| ENST00000650440.1 | hg19 | chr19 | 48,989,030 | 49,017,192 | 28,163 |
| ENST00000598924.1 | hg19 | chr19 | 49,016,464 | 49,016,917 | 454 |
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