NEDD1 NEDD1 gamma-tubulin ring complex targeting factor
Information
- Symbol
- NEDD1
- Type
- protein-coding
- Description
- NEDD1 gamma-tubulin ring complex targeting factor
- Entrez Gene ID
- 121441
- Genome
- hg19
- Position
- chr12:97,301,244-97,346,048
- Genome
- hg38
- Position
- chr12:96,907,466-96,952,270
- MIM
- 600372 OMIM
- HGNC
- HGNC:7723 HGNC
- Ensembl
- ENSG00000139350 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 68 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
74 |
 |
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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| Category | : |
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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
| Target data | : |
MGeND data only
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| 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 | GCP-WD |
| SYNONYM | TUBGCP7 |
| MIM | 600372 OMIM |
| HGNC | HGNC:7723 HGNC |
| Ensembl | ENSG00000139350 Ensembl |
| AllianceGenome | HGNC:7723 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000411739.6 | hg38 | chr12 | 96,907,238 | 96,952,475 | 45,238 |
| ENST00000429527.6 | hg38 | chr12 | 96,907,224 | 96,953,351 | 46,128 |
| ENST00000266742.9 | hg38 | chr12 | 96,907,257 | 96,953,780 | 46,524 |
| ENST00000557644.5 | hg38 | chr12 | 96,907,466 | 96,952,270 | 44,805 |
| ENST00000457368.2 | hg38 | chr12 | 96,912,576 | 96,953,221 | 40,646 |
| ENST00000429527.6 | hg19 | chr12 | 97,301,002 | 97,347,129 | 46,128 |
| ENST00000411739.6 | hg19 | chr12 | 97,301,016 | 97,346,253 | 45,238 |
| ENST00000266742.9 | hg19 | chr12 | 97,301,035 | 97,347,558 | 46,524 |
| ENST00000557644.5 | hg19 | chr12 | 97,301,244 | 97,346,048 | 44,805 |
| ENST00000457368.2 | hg19 | chr12 | 97,306,354 | 97,346,999 | 40,646 |
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