FAM90A23
gene geneOn this page
Summary
FAM90A23 (family with sequence similarity 90 member A23, HGNC:32271) is a protein-coding gene on chromosome 8p23.1, encoding Protein FAM90A23 (A8MXZ1).
At a glance
- Clinical variants (ClinVar): 1 total
- MANE Select transcript:
NM_001397380
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:32271 |
| Approved symbol | FAM90A23 |
| Name | family with sequence similarity 90 member A23 |
| Location | 8p23.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000285765 |
| Ensembl biotype | protein_coding |
| Entrez | 645572 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000648435
RefSeq mRNA: 1 — MANE Select: NM_001397380
NM_001397380
CCDS: CCDS94252
Canonical transcript exons
ENST00000627994 — 0 exons
Expression profiles
Bgee: expression breadth tissue_specific, 4 present calls, max score 63.76.
Top tissues by expression
117 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 63.76 | gold quality |
| colonic epithelium | UBERON:0000397 | 41.51 | gold quality |
| ganglionic eminence | UBERON:0004023 | 38.70 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 35.32 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 35.23 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 33.57 | gold quality |
| muscle tissue | UBERON:0002385 | 32.42 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| sural nerve | UBERON:0015488 | 30.93 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.66 | gold quality |
| monocyte | CL:0000576 | 29.64 | silver quality |
| leukocyte | CL:0000738 | 29.45 | silver quality |
| liver | UBERON:0002107 | 28.25 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| urinary bladder | UBERON:0001255 | 28.05 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| blood | UBERON:0000178 | 26.99 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.88 | gold quality |
| muscle of leg | UBERON:0001383 | 26.43 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| endocervix | UBERON:0000458 | 26.29 | silver quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| placenta | UBERON:0001987 | 25.81 | gold quality |
| kidney | UBERON:0002113 | 25.39 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.04 |
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), FAM90A3 (ENSG00000233132), FAM90A20 (ENSG00000233295), FAM90A12 (ENSG00000254229), FAM90A9 (ENSG00000285607), FAM90A16 (ENSG00000285620), FAM90A19 (ENSG00000285657), FAM90A22 (ENSG00000285687), FAM90A17 (ENSG00000285720), FAM90A14 (ENSG00000285814), FAM90A18 (ENSG00000285913), FAM90A8 (ENSG00000285937), FAM90A10 (ENSG00000285950), FAM90A7 (ENSG00000285975)
Protein
Protein identifiers
Protein FAM90A23 — A8MXZ1 (reviewed: A8MXZ1)
All UniProt accessions (1): A8MXZ1
UniProt curated annotations — full annotation on UniProt →
Similarity. Belongs to the FAM90 family.
RefSeq proteins (1): NP_001384309* (*=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-A8MXZ1-F1 | 50.51 | 0.05 |
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, A6NDY2, A6NIJ5, A6NJQ4, A6NKC0, A6NNH2, A6NNJ1, A8MUA0, A8MWA6, A8MX19, A8MXJ8, A8MXZ1, A8MYA2, B1ASB6, D6RGX4, P0C7V4, P0C7W8, P0C7W9, P0C7X0, P0DV73, P0DV74, P0DV75, P0DV76, Q0VDD7, Q2KIS6, Q3UHD3, Q4R736, Q5SZB4, Q5T8A7, Q5VZ46, Q5XIK6, Q658T7, Q6A025, Q6NTE8, Q6PIX9, Q6ZMY3, Q86Y26, Q86YD7
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
1 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 1 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS113564423 (8:7579928 G>A,T), RS1156723528 (8:7583621 A>G,T), RS1157448880 (8:7579849 C>A,T), RS1157495477 (8:7580259 G>C,T), RS1157496539 (8:7584079 T>TTTTG), RS1157719019 (8:7583109 G>C), RS1159492783 (8:7579807 G>C,T), RS1159650439 (8:7580594 G>A,T), RS1159882615 (8:7584060 GTTGTTTTGTT>G,GTTGTT,GTTGTTTTGTTTTGTT,GTTGTTTTGTTTTGTTTTGTT,GTTGTTTTGTTTTGTTTTGTTTTGTT), RS1159957703 (8:7583570 A>C), RS1160586531 (8:7580176 G>A,C,T), RS1160712020 (8:7583047 C>T), RS1161418895 (8:7579961 C>G,T), RS1162550166 (8:7580505 G>A,C), RS1162836378 (8:7580790 G>A)
Disease associations
OMIM: gene `` | 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.