FAM90A11

gene
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Summary

FAM90A11 (family with sequence similarity 90 member A11, HGNC:32259) is a protein-coding gene on chromosome 8p23.1, encoding Protein FAM90A11 (A0A8V8TNH8).

At a glance

  • MANE Select transcript: NM_001423539

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:32259
Approved symbolFAM90A11
Namefamily with sequence similarity 90 member A11
Location8p23.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000233115
Ensembl biotypeprotein_coding
Entrez441331

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000518378

RefSeq mRNA: 1 — MANE Select: NM_001423539 NM_001423539

Canonical transcript exons

ENST00000518378 — 4 exons

ExonStartEnd
ENSE0000209417580152308015352
ENSE0000210054880123428013304
ENSE0000219241580145368014735
ENSE0000219768180139698014077

Expression profiles

Bgee: expression breadth broad, 83 present calls, max score 78.34.

Top tissues by expression

108 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099178.34gold quality
stromal cell of endometriumCL:000225554.14gold quality
superior frontal gyrusUBERON:000266152.05gold quality
mucosa of stomachUBERON:000119949.89gold quality
primary visual cortexUBERON:000243649.81gold quality
right uterine tubeUBERON:000130249.66gold quality
cortical plateUBERON:000534349.10gold quality
ventricular zoneUBERON:000305348.82gold quality
right coronary arteryUBERON:000162547.32gold quality
left ovaryUBERON:000211946.10gold quality
right hemisphere of cerebellumUBERON:001489045.64silver quality
ovaryUBERON:000099245.39gold quality
cerebellar cortexUBERON:000212945.05silver quality
cerebellumUBERON:000203744.98silver quality
right frontal lobeUBERON:000281044.96gold quality
C1 segment of cervical spinal cordUBERON:000646944.88gold quality
cerebellar hemisphereUBERON:000224544.77silver quality
substantia nigraUBERON:000203844.34gold quality
descending thoracic aortaUBERON:000234544.30silver quality
body of uterusUBERON:000985344.21gold quality
myometriumUBERON:000129643.99silver quality
Ammon’s hornUBERON:000195443.64gold quality
right ovaryUBERON:000211843.31silver quality
Brodmann (1909) area 9UBERON:001354043.12gold quality
skeletal muscle tissueUBERON:000113443.11silver quality
frontal cortexUBERON:000187043.03gold quality
cortex of kidneyUBERON:000122543.00silver quality
hindlimb stylopod muscleUBERON:000425242.71gold quality
cerebral cortexUBERON:000095642.62gold quality
pituitary glandUBERON:000000742.61gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.24

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), FAM90A3 (ENSG00000233132), 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 FAM90A11A0A8V8TNH8 (reviewed: A0A8V8TNH8)

All UniProt accessions (1): A0A8V8TNH8

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_001410468* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR039213FAM90Family
IPR041670Znf-CCHC_6Domain

Pfam: PF15288

UniProt features (8 total): compositionally biased region 4, region of interest 3, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A8V8TNH8-F150.820.05

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, 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 `` | 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.