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Spatial pattern gene: Ammecr1 (spascer ID:56068) |
Gene summary for Ammecr1 |
 Gene summary |
| Gene information | |
| Species | Mouse | Gene symbol | Ammecr1 | Gene ID | 56068 |
| Gene name | AMMECR nuclear protein 1 |
| Synonyms | 6230420G18Rik |
| Cytomap | X|X F2 |
| Type of gene | protein-coding |
| Description | AMME syndrome candidate gene 1 protein homolog |
| Modification date | 20220424 |
| UniProtAcc | Q9JHT5 |
| Gene ontology with evidence Inferred from Direct Assay (IDA) and Biological aspect of Ancestor (IBA). |
| Gene | GO ID | GO term | PubMed ID | Category |
| Ammecr1 | GO:0005634 | nucleus | 21873635 | Component |
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Spatial pattern events for Ammecr1 |
| spatial pattern gene list. |
| Gene symbol | Species | Tissue | Replication | PMID | Adj p-value |
| Ammecr1 | Mouse | Embryo | rep_3 | 33188776 | 1.13e-14 |
| Ammecr1 | Mouse | Embryo | rep_13 | 33188776 | 7.92e-09 |
| Ammecr1 | Mouse | Lymph | B1 | 0 | 6.64e-10 |
| Ammecr1 | Mouse | Lung | rep_4 | 35290801 | 1.03e-11 |
| spatial pattern gene map.(click to enlarge the image in a new window) |
| H&E staining (if available) | Singel gene map |
Lung_rep_4_H&E  |  |
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Spatial pattern pathway has Ammecr1 envolved |
| Symbol | Pathway | Species | Tissue type | Replication | P-value |
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Ammecr1 function as liang/receptor in single cell data |
| Tissue | Source | SourceCell | Target | TargetCell | PMID | Group |
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Ammecr1 function as liang/receptor across spatial transcriptomics tissue |
| Interactions using deconvoluted spatial data. |
| Ligand | Receptor | LR pair | Tissue | Replication |
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Transcription factor for Ammecr1 envolved |
| Transcription factor analysis using single cell data. |
| TF | Tissue | Group | Cell types | Target genes | Rss score |
| Motif information. |
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Related Drugs for Ammecr1 |
| Approved drugs targeting this gene. (DrugBank Version 5.1.9 2022-01-04) |
| Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for Ammecr1 |
| Diseases associated with this gene. (DisGeNet 7.0) |
| Gene | Disease ID | Disease name | Pubmeds | Source |
| Ammecr1 | C1846242 | Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis | 2 | ORPHANET |
| Ammecr1 | C4310810 | MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS | 2 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
| Ammecr1 | C0013336 | Dwarfism | 1 | GENOMICS_ENGLAND |
| Ammecr1 | C0349588 | Short stature | 1 | GENOMICS_ENGLAND |
| Ammecr1 | C2919142 | Short Stature, CTCAE | 1 | GENOMICS_ENGLAND |
