NDUFB11 NADH:ubiquinone oxidoreductase subunit B11
Information
- Symbol
- NDUFB11
- Type
- protein-coding
- Description
- NADH:ubiquinone oxidoreductase subunit B11
- Entrez Gene ID
- 54539
- Genome
- hg19
- Position
- chrX:47,001,470-47,004,865
- Genome
- hg38
- Position
- chrX:47,142,071-47,145,466
- MIM
- 300403 OMIM
- HGNC
- HGNC:20372 HGNC
- Ensembl
- ENSG00000147123 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 6 |
Likely pathogenic | 0 | 12 |
Benign | 0 | 18 |
Likely benign | 0 | 44 |
Conflicting classifications of pathogenicity | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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24 |
![]() |
94 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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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
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Category | : |
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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 | CI-ESSS |
SYNONYM | ESSS |
SYNONYM | MC1DN30 |
SYNONYM | NP17.3 |
SYNONYM | Np15 |
SYNONYM | P17.3 |
MIM | 300403 OMIM |
HGNC | HGNC:20372 HGNC |
Ensembl | ENSG00000147123 Ensembl |
AllianceGenome | HGNC:20372 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000690053.1 | hg38 | chrX | 47,142,216 | 47,144,688 | 2,473 |
ENST00000687244.1 | hg38 | chrX | 47,142,071 | 47,145,466 | 3,396 |
ENST00000377811.4 | hg38 | chrX | 47,142,216 | 47,144,702 | 2,487 |
ENST00000276062.9 | hg38 | chrX | 47,142,216 | 47,144,710 | 2,495 |
ENST00000692649.1 | hg38 | chrX | 47,142,216 | 47,144,707 | 2,492 |
ENST00000687244.1 | hg19 | chrX | 47,001,470 | 47,004,865 | 3,396 |
ENST00000690053.1 | hg19 | chrX | 47,001,615 | 47,004,087 | 2,473 |
ENST00000377811.4 | hg19 | chrX | 47,001,615 | 47,004,101 | 2,487 |
ENST00000692649.1 | hg19 | chrX | 47,001,615 | 47,004,106 | 2,492 |
ENST00000276062.9 | hg19 | chrX | 47,001,615 | 47,004,109 | 2,495 |
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