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Gene Info
- This gene is found in these
cDNA libraries
from the following tissue types:
b-cell, bone, bone marrow, brain, cartilage, cerebellum, cerebrum, cervix, colon, ear, embryonic tissue, endocrine, esophagus, eye, fetus, gastrointestinal tract, heart, kidney, liver, lung, lymph node, lymphoreticular, mammary gland, muscle, nervous, ovary, pancreas, pancreatic islet, parathyroid, peripheral nervous system, pituitary gland, placenta, pooled tissue, prostate, retina, skin, spleen, stem cell, stomach, synovium, t-cell, testis, thymus, thyroid, 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: | 3: 182113153 - 182177027 |
| Full-Length MGC Clones for This Gene |
| IMAGE Id | Status | Accession |
GenBank Def Line |
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| 5122574 | Full Length | BC028983 | fragile X mental retardation, autosomal homolog 1 |
| Protein Similarities Based on Shared Motif Content |
Find gene products sharing protein motifs with: NP_001013456 NP_001013457 NP_005078
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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