FAM90A3

gene
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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

FieldValue
HGNC IDHGNC:32251
Approved symbolFAM90A3
Namefamily with sequence similarity 90 member A3
Location8p23.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000233132
Ensembl biotypeprotein_coding
OMIM613042
Entrez389611

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

ExonStartEnd
ENSE0000351646172651437265342
ENSE0000366482172658017265909
ENSE0000367110672645267264648
ENSE0000368131972665747267536

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):

TissueAnatomy IDExpression scoreQuality
cortical plateUBERON:000534339.83gold quality
ganglionic eminenceUBERON:000402338.85gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
bone marrow cellCL:000209236.16gold quality
mucosa of stomachUBERON:000119935.59silver quality
sural nerveUBERON:001548835.56gold quality
left uterine tubeUBERON:000130335.07gold quality
tonsilUBERON:000237234.76gold quality
apex of heartUBERON:000209834.45gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
muscle tissueUBERON:000238533.34gold quality
smooth muscle tissueUBERON:000113533.02gold quality
duodenumUBERON:000211432.79gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
gall bladderUBERON:000211031.13gold quality
urinary bladderUBERON:000125530.35silver quality
islet of LangerhansUBERON:000000630.22gold quality
prefrontal cortexUBERON:000045130.09gold quality
stromal cell of endometriumCL:000225529.87gold quality
lymph nodeUBERON:000002929.84gold quality
liverUBERON:000210729.01gold quality
olfactory segment of nasal mucosaUBERON:000538628.71gold quality
fallopian tubeUBERON:000388927.78silver quality
placentaUBERON:000198727.51gold quality
bloodUBERON:000017827.37gold quality
leukocyteCL:000073826.55gold quality
vermiform appendixUBERON:000115426.42gold quality
right lungUBERON:000216726.17gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.00

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), 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 FAM90A3A0A8V8TPE2 (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)

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-A0A8V8TPE2-F150.400.04

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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

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.

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