AAMDC adipogenesis associated Mth938 domain containing
Information
- Symbol
- AAMDC
- Type
- protein-coding
- Description
- adipogenesis associated Mth938 domain containing
- Entrez Gene ID
- 28971
- Genome
- hg19
- Position
- chr11:77,552,065-77,583,400
- Genome
- hg38
- Position
- chr11:77,841,019-77,872,354
- MIM
- 620474 OMIM
- HGNC
- HGNC:30205 HGNC
- Ensembl
- ENSG00000087884 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
![]() |
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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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 | |||||
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | C11orf67 |
SYNONYM | CK067 |
SYNONYM | PTD015 |
MIM | 620474 OMIM |
HGNC | HGNC:30205 HGNC |
Ensembl | ENSG00000087884 Ensembl |
AllianceGenome | HGNC:30205 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000527134.5 | hg38 | chr11 | 77,821,154 | 77,900,732 | 79,579 |
ENST00000525034.1 | hg38 | chr11 | 77,841,138 | 77,872,352 | 31,215 |
ENST00000526415.5 | hg38 | chr11 | 77,821,129 | 77,872,352 | 51,224 |
ENST00000304716.12 | hg38 | chr11 | 77,821,155 | 77,900,714 | 79,560 |
ENST00000533193.5 | hg38 | chr11 | 77,841,019 | 77,872,354 | 31,336 |
ENST00000532481.5 | hg38 | chr11 | 77,821,109 | 77,918,432 | 97,324 |
ENST00000525409.5 | hg38 | chr11 | 77,821,187 | 77,872,352 | 51,166 |
ENST00000393427.7 | hg38 | chr11 | 77,821,144 | 77,872,352 | 51,209 |
ENST00000532481.5 | hg19 | chr11 | 77,532,155 | 77,629,478 | 97,324 |
ENST00000526415.5 | hg19 | chr11 | 77,532,175 | 77,583,398 | 51,224 |
ENST00000393427.7 | hg19 | chr11 | 77,532,190 | 77,583,398 | 51,209 |
ENST00000527134.5 | hg19 | chr11 | 77,532,200 | 77,611,778 | 79,579 |
ENST00000304716.12 | hg19 | chr11 | 77,532,201 | 77,611,760 | 79,560 |
ENST00000525409.5 | hg19 | chr11 | 77,532,233 | 77,583,398 | 51,166 |
ENST00000533193.5 | hg19 | chr11 | 77,552,065 | 77,583,400 | 31,336 |
ENST00000525034.1 | hg19 | chr11 | 77,552,184 | 77,583,398 | 31,215 |
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