FAM90A23

gene
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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

FieldValue
HGNC IDHGNC:32271
Approved symbolFAM90A23
Namefamily with sequence similarity 90 member A23
Location8p23.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000285765
Ensembl biotypeprotein_coding
Entrez645572

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):

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099163.76gold quality
colonic epitheliumUBERON:000039741.51gold quality
ganglionic eminenceUBERON:000402338.70gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
hindlimb stylopod muscleUBERON:000425235.32gold quality
skeletal muscle tissueUBERON:000113435.23gold quality
mucosa of transverse colonUBERON:000499133.57gold quality
muscle tissueUBERON:000238532.42gold quality
bone marrowUBERON:000237131.74gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.66gold quality
monocyteCL:000057629.64silver quality
leukocyteCL:000073829.45silver quality
liverUBERON:000210728.25gold quality
duodenumUBERON:000211428.14gold quality
urinary bladderUBERON:000125528.05gold quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
bloodUBERON:000017826.99gold quality
islet of LangerhansUBERON:000000626.88gold quality
muscle of legUBERON:000138326.43gold quality
vermiform appendixUBERON:000115426.42gold quality
endocervixUBERON:000045826.29silver quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
kidneyUBERON:000211325.39gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.04

Regulation

Is transcription factor: no

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
mus_musculusFam90a1bENSMUSG00000043549
mus_musculusFam90a1aENSMUSG00000079112
rattus_norvegicusFam90a1l1ENSRNOG00000064072

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 FAM90A23A8MXZ1 (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)

IDNameType
IPR039213FAM90Family
IPR041670Znf-CCHC_6Domain

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)

ModelpLDDTFraction very-high
AF-A8MXZ1-F150.510.05

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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign1
Benign0

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.