FAM90A3
gene geneOn this page
Summary
FAM90A3 (family with sequence similarity 90 member A3, HGNC:32251) is a protein-coding gene on chromosome 8p23.1, encoding Protein FAM90A3 (A0A8V8TPE2).
FAM90A3 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).
Source: NCBI Gene 389611 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001423528
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:32251 |
| Approved symbol | FAM90A3 |
| Name | family with sequence similarity 90 member A3 |
| Location | 8p23.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000233132 |
| Ensembl biotype | protein_coding |
| OMIM | 613042 |
| Entrez | 389611 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000506444
RefSeq mRNA: 1 — MANE Select: NM_001423528
NM_001423528
Canonical transcript exons
ENST00000506444 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003516461 | 7265143 | 7265342 |
| ENSE00003664821 | 7265801 | 7265909 |
| ENSE00003671106 | 7264526 | 7264648 |
| ENSE00003681319 | 7266574 | 7267536 |
Expression profiles
Bgee: expression breadth broad, 23 present calls, max score 39.83.
Top tissues by expression
95 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| cortical plate | UBERON:0005343 | 39.83 | gold quality |
| ganglionic eminence | UBERON:0004023 | 38.85 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| mucosa of stomach | UBERON:0001199 | 35.59 | silver quality |
| sural nerve | UBERON:0015488 | 35.56 | gold quality |
| left uterine tube | UBERON:0001303 | 35.07 | gold quality |
| tonsil | UBERON:0002372 | 34.76 | gold quality |
| apex of heart | UBERON:0002098 | 34.45 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 33.38 | gold quality |
| muscle tissue | UBERON:0002385 | 33.34 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 33.02 | gold quality |
| duodenum | UBERON:0002114 | 32.79 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| gall bladder | UBERON:0002110 | 31.13 | gold quality |
| urinary bladder | UBERON:0001255 | 30.35 | silver quality |
| islet of Langerhans | UBERON:0000006 | 30.22 | gold quality |
| prefrontal cortex | UBERON:0000451 | 30.09 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| lymph node | UBERON:0000029 | 29.84 | gold quality |
| liver | UBERON:0002107 | 29.01 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 28.71 | gold quality |
| fallopian tube | UBERON:0003889 | 27.78 | silver quality |
| placenta | UBERON:0001987 | 27.51 | gold quality |
| blood | UBERON:0000178 | 27.37 | gold quality |
| leukocyte | CL:0000738 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| right lung | UBERON:0002167 | 26.17 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Cross-species orthologs
3 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Fam90a1b | ENSMUSG00000043549 |
| mus_musculus | Fam90a1a | ENSMUSG00000079112 |
| rattus_norvegicus | Fam90a1l1 | ENSRNOG00000064072 |
Paralogs (21): FAM90A1 (ENSG00000171847), FAM90A27P (ENSG00000189348), FAM90A24 (ENSG00000215354), FAM90A5 (ENSG00000215373), FAM90A13 (ENSG00000223885), FAM90A26 (ENSG00000229924), FAM90A15 (ENSG00000230045), FAM90A11 (ENSG00000233115), FAM90A20 (ENSG00000233295), FAM90A12 (ENSG00000254229), FAM90A9 (ENSG00000285607), FAM90A16 (ENSG00000285620), FAM90A19 (ENSG00000285657), FAM90A22 (ENSG00000285687), FAM90A17 (ENSG00000285720), FAM90A23 (ENSG00000285765), FAM90A14 (ENSG00000285814), FAM90A18 (ENSG00000285913), FAM90A8 (ENSG00000285937), FAM90A10 (ENSG00000285950), FAM90A7 (ENSG00000285975)
Protein
Protein identifiers
Protein FAM90A3 — A0A8V8TPE2 (reviewed: A0A8V8TPE2)
All UniProt accessions (1): A0A8V8TPE2
UniProt curated annotations — full annotation on UniProt →
Miscellaneous. Primate-specific FAM90A gene family, thought to have arisen during multiple duplication and rearrangement events.
Similarity. Belongs to the FAM90 family.
RefSeq proteins (1): NP_001410457* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR039213 | FAM90 | Family |
| IPR041670 | Znf-CCHC_6 | Domain |
Pfam: PF15288
UniProt features (7 total): region of interest 3, compositionally biased region 3, chain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A0A8V8TPE2-F1 | 50.40 | 0.04 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 1 (showing top):
chr8p23
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (0):
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A096LP49, A0A8V8TNH8, A0A8V8TPE2, A2VE02, A5D7I0, A6NDY2, A6NGG8, A6NIJ5, A6NNJ1, A8MXJ8, A8MYA2, B1ASB6, B2RW88, D6RGX4, O60269, P0C7V4, P0C7W8, P0C7W9, P0C7X0, P0DV75, P0DV76, Q2KIS6, Q2NL68, Q3SY00, Q4R736, Q4V8B5, Q5RCQ2, Q5SZB4, Q5VZ46, Q5XIK6, Q658T7, Q66JV7, Q6NS69, Q6PAC4, Q6ZMY3, Q76N32, Q7TSA6, Q7Z591, Q80VW7, Q80X53
Diamond homologs: A0A8V8TNH8, A0A8V8TPE2, A6NDY2, A6NIJ5, A6NJQ4, A6NKC0, A6NNH2, A6NNJ1, A8MWA6, A8MX19, A8MXJ8, A8MXZ1, D6RGX4, P0C7V4, P0C7W8, P0C7W9, P0C7X0, P0DV73, P0DV74, P0DV75, P0DV76, Q658T7, Q86YD7
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
Disease associations
OMIM: gene MIM:613042 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.