|
Gene Tools
SNP Tools
Transcriptome Analysis
CGAP Data
Purchase CGAP Reagents
Related Links
Quick Links:
|
Gene Info
| Gene Information For: | Mm. Ammecr1, Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human) | | Sequence ID: | NM_019496
|
- This gene is found in these
cDNA libraries
from the following tissue types:
bone marrow, brain, cerebrum, embryonic tissue, endocrine, eye, fetus, heart, lung, lymph node, lymphoreticular, mammary gland, nervous, ovary, pituitary gland, placenta, prostate, retina, skin, stem cell, testis, thyroid, uncharacterized tissue
- SAGE Expression Matrix
- SAGE Digital Northern
- Monochromatic SAGE/cDNA Virtual Northern
- Two-dimensional array displays (similar expression pattern in SAGE data)
| Cytogenetic Location (from UniGene) |
| Cytogenetic Location: | X F2 | |
| Chromosomal Position (from UCSC) |
| Chromosomal Position: | X: 139289355 - 139401271 |
| Full-Length MGC Clones for This Gene |
| IMAGE Id | Status | Accession |
GenBank Def Line |
|---|
| 100016345 | Full Length | BC153030 | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human) |
| Protein Similarities Based on Shared Motif Content |
Find gene products sharing protein motifs with: NP_062369
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)
|
