NTF4 neurotrophin 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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32 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | GLC10 |
SYNONYM | GLC1O |
SYNONYM | NT-4 |
SYNONYM | NT-4/5 |
SYNONYM | NT-5 |
SYNONYM | NT4 |
SYNONYM | NT5 |
SYNONYM | NTF5 |
MIM | 162662 OMIM |
HGNC | HGNC:8024 HGNC |
Ensembl | ENSG00000225950 Ensembl |
AllianceGenome | HGNC:8024 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000696089.1 | hg38 | chr19 | 49,061,066 | 49,064,855 | 3,790 |
ENST00000593537.2 | hg38 | chr19 | 49,061,128 | 49,064,818 | 3,691 |
ENST00000696088.1 | hg38 | chr19 | 49,061,066 | 49,062,671 | 1,606 |
ENST00000696091.1 | hg38 | chr19 | 49,061,066 | 49,065,076 | 4,011 |
ENST00000696090.1 | hg38 | chr19 | 49,061,066 | 49,064,855 | 3,790 |
ENST00000594938.2 | hg38 | chr19 | 49,061,066 | 49,064,855 | 3,790 |
ENST00000696088.1 | hg19 | chr19 | 49,564,323 | 49,565,928 | 1,606 |
ENST00000696089.1 | hg19 | chr19 | 49,564,323 | 49,568,112 | 3,790 |
ENST00000696090.1 | hg19 | chr19 | 49,564,323 | 49,568,112 | 3,790 |
ENST00000594938.2 | hg19 | chr19 | 49,564,323 | 49,568,112 | 3,790 |
ENST00000696091.1 | hg19 | chr19 | 49,564,323 | 49,568,333 | 4,011 |
ENST00000593537.2 | hg19 | chr19 | 49,564,385 | 49,568,075 | 3,691 |
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