NECAP1 NECAP endocytosis associated 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 8 |
Likely benign | 0 | 164 |
Uncertain significance | 0 | 186 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
36 |
![]() |
322 |
![]() |
4 |
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 | DEE21 |
SYNONYM | EIEE21 |
MIM | 611623 OMIM |
HGNC | HGNC:24539 HGNC |
Ensembl | ENSG00000089818 Ensembl |
AllianceGenome | HGNC:24539 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000639955.1 | hg38 | chr12 | 8,076,939 | 8,097,859 | 20,921 |
ENST00000639811.1 | hg38 | chr12 | 8,082,280 | 8,097,531 | 15,252 |
ENST00000339754.11 | hg38 | chr12 | 8,082,274 | 8,097,881 | 15,608 |
ENST00000639167.1 | hg38 | chr12 | 8,082,280 | 8,097,738 | 15,459 |
ENST00000638237.1 | hg38 | chr12 | 8,082,266 | 8,097,768 | 15,503 |
ENST00000638237.1 | hg19 | chr12 | 8,234,862 | 8,250,364 | 15,503 |
ENST00000339754.11 | hg19 | chr12 | 8,234,870 | 8,250,477 | 15,608 |
ENST00000639167.1 | hg19 | chr12 | 8,234,876 | 8,250,334 | 15,459 |
ENST00000639811.1 | hg19 | chr12 | 8,234,876 | 8,250,127 | 15,252 |
ENST00000639955.1 | hg19 | chr12 | 8,229,535 | 8,250,455 | 20,921 |
Genome browser