| Gene Symbol |
FAM161A
|
| Entrez Gene |
84140
|
| Alt Symbol |
RP28
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
family with sequence similarity 161, member A
|
| Other Description |
protein FAM161A|retinitis pigmentosa 28 (autosomal recessive)
|
| Swissprots |
Q9H8R2 B4DJV7 Q3B820
|
| Accessions |
EAW99988 EAW99989 EAW99990 EAW99991 Q3B820 AI690681 AK023367 BAB14544 AK091575 AK296255 BAG58969 AK310908 AM392542 CAL37420 AM392832 CAL37710 AM393518 CAL38395 BC036448 BC107162 BC107163 BX648834 BX649029 DC398889 XR_939724 NM_001201543 NP_001188472 NM_032180 NP_115556 NR_037710
|
| Function |
Involved in ciliogenesis. {ECO:0000269|PubMed:22940612}.
|
| Subcellular Location |
Cytoplasm, cytoskeleton, cilium basal body {ECO:0000269|PubMed:22940612}. Cell projection, cilium {ECO:0000269|PubMed:22940612}. Note=Localized to the region between the outer and inner photoreceptor segments, corresponding to the photoreceptor connecting cilium.
|
| Tissue Specificity |
Isoform 1 and isoform 3 are widely expressed with highest levels in retina and testis, with isoform 1 being the most abundant in all tissues tested. {ECO:0000269|PubMed:20705278, ECO:0000269|PubMed:20705279}.
|