KREMEN2 kringle containing transmembrane protein 2
Information
- Symbol
- KREMEN2
- Type
- protein-coding
- Description
- kringle containing transmembrane protein 2
- Entrez Gene ID
- 79412
- Genome
- hg19
- Position
- chr16:3,014,276-3,018,381
- Genome
- hg38
- Position
- chr16:2,964,275-2,968,380
- MIM
- 609899 OMIM
- HGNC
- HGNC:18797 HGNC
- Ensembl
- ENSG00000131650 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
62 |
![]() |
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
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
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
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 | KRM2 |
MIM | 609899 OMIM |
HGNC | HGNC:18797 HGNC |
Ensembl | ENSG00000131650 Ensembl |
AllianceGenome | HGNC:18797 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000303746.10 | hg38 | chr16 | 2,964,275 | 2,968,380 | 4,106 |
ENST00000572045.5 | hg38 | chr16 | 2,964,216 | 2,968,380 | 4,165 |
ENST00000575885.5 | hg38 | chr16 | 2,964,275 | 2,968,379 | 4,105 |
ENST00000319500.11 | hg38 | chr16 | 2,964,275 | 2,968,380 | 4,106 |
ENST00000571007.5 | hg38 | chr16 | 2,964,275 | 2,968,379 | 4,105 |
ENST00000575769.1 | hg38 | chr16 | 2,964,521 | 2,968,348 | 3,828 |
ENST00000572045.5 | hg19 | chr16 | 3,014,217 | 3,018,381 | 4,165 |
ENST00000571007.5 | hg19 | chr16 | 3,014,276 | 3,018,380 | 4,105 |
ENST00000575885.5 | hg19 | chr16 | 3,014,276 | 3,018,380 | 4,105 |
ENST00000303746.10 | hg19 | chr16 | 3,014,276 | 3,018,381 | 4,106 |
ENST00000319500.11 | hg19 | chr16 | 3,014,276 | 3,018,381 | 4,106 |
ENST00000575769.1 | hg19 | chr16 | 3,014,522 | 3,018,349 | 3,828 |
Genome browser