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Gene Info
| Gene Information For: | Hs. AMMECR1, Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 | | Sequence ID: | NM_015365
NM_001025580
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- This gene is found in these
cDNA libraries
from the following tissue types:
b-cell, bone, brain, cartilage, cerebellum, cerebrum, cervix, colon, embryonic tissue, endocrine, esophagus, eye, fetus, gastrointestinal tract, kidney, liver, lung, lymph node, lymphoreticular, mammary gland, muscle, nervous, ovary, placenta, pooled tissue, prostate, skin, soft tissue, spleen, stem cell, synovium, t-cell, testis, thymus, uncharacterized tissue, uterus, vascular
- SAGE Anatomic Viewer
- SAGE Digital Northern
- Monochromatic SAGE/cDNA Virtual Northern
- Two-dimensional array displays (similar expression pattern in NCI60 microarray data or SAGE data)
| Cytogenetic Location (from UniGene) |
| Chromosomal Position (from UCSC) |
| Chromosomal Position: | X: 109328273 - 109448123 |
| Full-Length MGC Clones for This Gene |
| IMAGE Id | Status | Accession |
GenBank Def Line |
|---|
| 30344824 | Full Length | BC060813 | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 |
| 5140448 | Incomplete | BC024762 | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 |
| 5405764 | Incomplete | BC037983 | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 |
| 6168870 | Incomplete | BC051895 | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 |
| Protein Similarities Based on Shared Motif Content |
Find gene products sharing protein motifs with: NP_001020751 NP_056180
RefSeq
Related Sequences
| Homologs (from HomoloGene) |
Note: Both orthologs and
paralogs are included.
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)
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