NUTM1 NUT midline carcinoma family member 1
Information
- Symbol
- NUTM1
- Type
- protein-coding
- Description
- NUT midline carcinoma family member 1
- Entrez Gene ID
- 256646
- Genome
- hg19
- Position
- chr15:34,635,516-34,649,936
- Genome
- hg38
- Position
- chr15:34,343,315-34,357,735
- MIM
- 608963 OMIM
- HGNC
- HGNC:29919 HGNC
- Ensembl
- ENSG00000184507 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 10 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 102 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
116 |
 |
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
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
| Target data | : |
MGeND data only
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| 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
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| Category | : |
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| 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 | C15orf55 |
| SYNONYM | FAM22H |
| SYNONYM | NUT |
| MIM | 608963 OMIM |
| HGNC | HGNC:29919 HGNC |
| Ensembl | ENSG00000184507 Ensembl |
| AllianceGenome | HGNC:29919 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000333756.5 | hg38 | chr15 | 34,343,315 | 34,357,737 | 14,423 |
| ENST00000438749.7 | hg38 | chr15 | 34,343,410 | 34,357,737 | 14,328 |
| ENST00000537011.6 | hg38 | chr15 | 34,343,315 | 34,357,735 | 14,421 |
| ENST00000537011.6 | hg19 | chr15 | 34,635,516 | 34,649,936 | 14,421 |
| ENST00000333756.5 | hg19 | chr15 | 34,635,516 | 34,649,938 | 14,423 |
| ENST00000438749.7 | hg19 | chr15 | 34,635,611 | 34,649,938 | 14,328 |
| Key | Value |
|---|---|
| strand | + |
| start | 34,635,515 |
| Gene Symbol | NUTM1 |
| Entrez GeneId | 256,646 |
| Chr Band | 15q14 |
| end | 34,649,937 |
| chr | chr15 |
| Name | NUT midline carcinoma, family member 1 |
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