GLYATL2

gene
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Also known as BXMAS2-10MGC24009

Summary

GLYATL2 (glycine-N-acyltransferase like 2, HGNC:24178) is a protein-coding gene on chromosome 11q12.1, encoding Glycine N-acyltransferase-like protein 2 (Q8WU03). Mitochondrial acyltransferase which transfers the acyl group to the N-terminus of glycine.

Enables glycine N-acyltransferase activity. Involved in long-chain fatty acid catabolic process; medium-chain fatty acid catabolic process; and monounsaturated fatty acid catabolic process. Located in endoplasmic reticulum.

Source: NCBI Gene 219970 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 63 total
  • MANE Select transcript: NM_145016

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24178
Approved symbolGLYATL2
Nameglycine-N-acyltransferase like 2
Location11q12.1
Locus typegene with protein product
StatusApproved
AliasesBXMAS2-10, MGC24009
Ensembl geneENSG00000156689
Ensembl biotypeprotein_coding
OMIM614762
Entrez219970

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 2 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000287275, ENST00000532258, ENST00000533636

RefSeq mRNA: 1 — MANE Select: NM_145016 NM_145016

CCDS: CCDS41649

Canonical transcript exons

ENST00000287275 — 6 exons

ExonStartEnd
ENSE000011330845883406558834837
ENSE000011331325883953558839652
ENSE000012769345884443458844704
ENSE000035425995883826158838368
ENSE000035858665883701558837177
ENSE000036146235883727158837397

Expression profiles

Bgee: expression breadth ubiquitous, 146 present calls, max score 85.03.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.1242 / max 50.1416, expressed in 27 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1198330.091018
1198320.033310

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
minor salivary glandUBERON:000183085.03gold quality
saliva-secreting glandUBERON:000104479.92gold quality
gall bladderUBERON:000211079.88gold quality
mouth mucosaUBERON:000372979.53gold quality
ventricular zoneUBERON:000305378.45gold quality
ganglionic eminenceUBERON:000402374.77gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099174.62gold quality
olfactory segment of nasal mucosaUBERON:000538671.97gold quality
nasal cavity mucosaUBERON:000182669.43gold quality
calcaneal tendonUBERON:000370169.23gold quality
C1 segment of cervical spinal cordUBERON:000646968.76gold quality
monocyteCL:000057667.22gold quality
spinal cordUBERON:000224066.30gold quality
skin of hipUBERON:000155466.25gold quality
buccal mucosa cellCL:000233666.08gold quality
leukocyteCL:000073865.97gold quality
mammary ductUBERON:000176565.85silver quality
tendonUBERON:000004364.79gold quality
upper leg skinUBERON:000426261.93gold quality
mammary glandUBERON:000191161.15gold quality
thoracic mammary glandUBERON:000520061.06gold quality
stromal cell of endometriumCL:000225558.92gold quality
tonsilUBERON:000237257.86gold quality
tendon of biceps brachiiUBERON:000818857.62gold quality
lymph nodeUBERON:000002957.51gold quality
skin of abdomenUBERON:000141657.25gold quality
smooth muscle tissueUBERON:000113555.76gold quality
granulocyteCL:000009455.67gold quality
skin of legUBERON:000151155.65gold quality
hypothalamusUBERON:000189855.51gold quality

Single-cell (SCXA)

Detected in 3 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-CURD-114yes17.83
E-HCAD-1yes9.51
E-ANND-3yes4.23

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

38 targeting GLYATL2, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-569699.9872.364487
HSA-MIR-365899.9673.874379
HSA-MIR-651-3P99.9473.485177
HSA-MIR-335-3P99.9373.364958
HSA-MIR-218-5P99.9372.222103
HSA-MIR-548E-5P99.8972.734486
HSA-MIR-548AR-3P99.8571.263889
HSA-MIR-548AZ-5P99.8369.943230
HSA-MIR-548T-5P99.8369.913220
HSA-MIR-5010-3P99.8370.602357
HSA-MIR-548AZ-3P99.8270.563549
HSA-MIR-548BC99.8270.613524
HSA-MIR-548E-3P99.8270.593514
HSA-MIR-548F-3P99.8270.593540
HSA-MIR-548A-3P99.7670.583524
HSA-MIR-33A-3P99.7070.273362
HSA-MIR-7154-5P99.6970.521900
HSA-MIR-1212499.6869.172700
HSA-MIR-211399.5871.221521
HSA-MIR-360999.5269.892587
HSA-MIR-548AH-5P99.5269.732626
HSA-MIR-467299.5071.582893
HSA-MIR-203A-3P99.4970.562806
HSA-MIR-548G-3P99.4868.672159
HSA-MIR-4735-5P99.4368.491780
HSA-MIR-183-3P99.4169.411598
HSA-MIR-6770-5P98.9766.761853
HSA-MIR-126298.1766.52757
HSA-MIR-4701-3P98.1766.25788
HSA-MIR-6736-5P98.1766.43760

Literature-anchored findings (GeneRIF, showing 2)

  • report on the characterization of human glycine N-acyltransferase-like 2 (hGLYATL2) and show that it synthesizes various N-acyl glycines. (PMID:20305126)
  • acetylation of lysine(s) in hGLYATL2 regulates the enzyme activity, thus linking post-translational modification of proteins with the production of biological signaling molecules, the N-acyl glycines. (PMID:22408254)

Cross-species orthologs

6 orthologs

OrganismSymbolGene ID
danio_reriosi:dkey-76k16.5ENSDARG00000075561
danio_reriosi:dkey-76k16.6ENSDARG00000077481
danio_reriosi:ch73-106k19.2ENSDARG00000102568
caenorhabditis_elegansWBGENE00011681
caenorhabditis_elegansWBGENE00018400
caenorhabditis_elegansWBGENE00022683

Paralogs (4): GLYAT (ENSG00000149124), GLYATL1 (ENSG00000166840), GLYATL3 (ENSG00000203972), GLYATL1B (ENSG00000255151)

Protein

Protein identifiers

Glycine N-acyltransferase-like protein 2Q8WU03 (reviewed: Q8WU03)

Alternative names: Acyl-CoA:glycine N-acyltransferase-like protein 2

All UniProt accessions (1): Q8WU03

UniProt curated annotations — full annotation on UniProt →

Function. Mitochondrial acyltransferase which transfers the acyl group to the N-terminus of glycine. Conjugates numerous substrates, such as arachidonoyl-CoA and saturated medium and long-chain acyl-CoAs ranging from chain-length C8:0-CoA to C18:0-CoA, to form a variety of N-acylglycines. Shows a preference for monounsaturated fatty acid oleoyl-CoA (C18:1-CoA) as an acyl donor. Does not exhibit any activity toward C22:6-CoA and chenodeoxycholoyl-CoA, nor toward serine or alanine.

Subcellular location. Endoplasmic reticulum.

Tissue specificity. Expressed at highest levels in salivary gland and trachea. Also detected in thyroid gland, spinal cord, prostate, lung and fetal brain.

Post-translational modifications. Acetylation at Lys-19 drastically decreases the production of N-oleoyl and N-arachidonoyl glycines.

Similarity. Belongs to the glycine N-acyltransferase family.

RefSeq proteins (1): NP_659453* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR010313Glycine_N-acyltransferaseFamily
IPR013652Glycine_N-acyltransferase_CDomain
IPR015938Glycine_N-acyltransferase_NDomain
IPR016181Acyl_CoA_acyltransferaseHomologous_superfamily

Pfam: PF06021, PF08444

Enzyme classification (BRENDA):

  • EC 2.3.1.13 — glycine N-acyltransferase (BRENDA: 7 organisms, 40 substrates, 29 inhibitors, 71 Km, 14 kcat entries)

Substrate kinetics (BRENDA)

16 substrates with measured Km, best-characterized 15. Km ranges are aggregated across organisms/conditions.

SubstrateKm (mM)Measurements
BENZOYL-COA0.0094–99828
GLYCINE0.0016–7919
BUTYRYL-COA0.052–0.73
SALICYL-COA0.03–83.73
ACETYL-COA0.2092
ALANINE997–15732
HEXANOYL-COA0.045–4502
ISOVALERYL-COA73.3–1242
OCTANOYL-COA108.6–1982
ASPARAGINE1291
GLUTAMIC ACID11501
GLUTAMINE3531
GLYCINE ETHYL ESTER9.71
GLYCINE METHYL ESTER291
OLEOYL-COA0.00441

Catalyzed reactions (Rhea), 11 shown:

  • an acyl-CoA + glycine = an N-acylglycine + CoA + H(+) (RHEA:19869)
  • (9Z)-octadecenoyl-CoA + glycine = N-(9Z-octadecenoyl)glycine + CoA + H(+) (RHEA:51272)
  • (5Z,8Z,11Z,14Z)-eicosatetraenoyl-CoA + glycine = N-(5Z,8Z,11Z,14Z)-eicosatetraenoyl-glycine + CoA + H(+) (RHEA:51364)
  • octadecanoyl-CoA + glycine = N-octadecanoylglycine + CoA + H(+) (RHEA:51368)
  • (9Z)-hexadecenoyl-CoA + glycine = N-(9Z-hexadecenoyl)-glycine + CoA + H(+) (RHEA:51372)
  • octanoyl-CoA + glycine = N-octanoylglycine + CoA + H(+) (RHEA:64240)
  • a fatty acyl-CoA + glycine = an N-(fatty acyl)-glycine + CoA + H(+) (RHEA:64244)
  • decanoyl-CoA + glycine = N-decanoylglycine + CoA + H(+) (RHEA:64248)
  • tetradecanoyl-CoA + glycine = N-tetradecanoylglycine + CoA + H(+) (RHEA:64252)
  • dodecanoyl-CoA + glycine = N-dodecanoylglycine + CoA + H(+) (RHEA:64256)
  • (9Z,12Z)-octadecadienoyl-CoA + glycine = N-(9Z,12Z-octadecadienoyl)-glycine + CoA + H(+) (RHEA:64260)

UniProt features (7 total): sequence variant 3, sequence conflict 2, chain 1, modified residue 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8WU03-F189.920.78

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (1): 19

Function

Pathways and Gene Ontology

Reactome pathways

4 pathways

IDPathway
R-HSA-159424Conjugation of carboxylic acids
R-HSA-177128Conjugation of salicylate with glycine
R-HSA-177135Conjugation of benzoate with glycine
R-HSA-9749641Aspirin ADME

MSigDB gene sets: 55 (showing top): GOBP_FATTY_ACID_CATABOLIC_PROCESS, REACTOME_BIOLOGICAL_OXIDATIONS, GOBP_LONG_CHAIN_FATTY_ACID_METABOLIC_PROCESS, GOBP_MONOCARBOXYLIC_ACID_METABOLIC_PROCESS, GOBP_ORGANIC_ACID_CATABOLIC_PROCESS, GOBP_LIPID_METABOLIC_PROCESS, GOBP_ORGANIC_ACID_METABOLIC_PROCESS, GOBP_SMALL_MOLECULE_CATABOLIC_PROCESS, GOBP_MONOCARBOXYLIC_ACID_CATABOLIC_PROCESS, GOBP_LIPID_CATABOLIC_PROCESS, GOBP_FATTY_ACID_METABOLIC_PROCESS, GOMF_ACYLTRANSFERASE_ACTIVITY, TAKEDA_TARGETS_OF_NUP98_HOXA9_FUSION_6HR_UP, GOMF_N_ACYLTRANSFERASE_ACTIVITY, REACTOME_PHASE_II_CONJUGATION_OF_COMPOUNDS

GO Biological Process (4): long-chain fatty acid catabolic process (GO:0042758), medium-chain fatty acid catabolic process (GO:0051793), monounsaturated fatty acid catabolic process (GO:1903965), lipid metabolic process (GO:0006629)

GO Molecular Function (3): glycine N-acyltransferase activity (GO:0047961), transferase activity (GO:0016740), acyltransferase activity (GO:0016746)

GO Cellular Component (2): mitochondrion (GO:0005739), endoplasmic reticulum (GO:0005783)

Reactome top-level categories

Rollup of top-3 pathways:

CategoryPathways
Conjugation of carboxylic acids2
Amino Acid conjugation1
Drug ADME1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
fatty acid catabolic process3
cytoplasm2
intracellular membrane-bounded organelle2
long-chain fatty acid metabolic process1
medium-chain fatty acid metabolic process1
monounsaturated fatty acid metabolic process1
primary metabolic process1
amino acid acyltransferase activity1
catalytic activity1
transferase activity1
endomembrane system1

Protein interactions and networks

STRING

540 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
GLYATL2MUCL1Q96DR8477
GLYATL2SUSD3Q96L08398
GLYATL2ZNF772Q68DY9395
GLYATL2FAM43BQ6ZT52391
GLYATL2FBXW10BO95170387
GLYATL2LIPKQ5VXJ0382
GLYATL2TMBIM1Q969X1366
GLYATL2SUOXP51687350
GLYATL2PLA1AQ53H76327
GLYATL2GAL3ST3Q96A11320
GLYATL2ZNF418Q8TF45314
GLYATL2STOML1Q9UBI4312
GLYATL2FKBP10Q96AY3310
GLYATL2AGR3Q8TD06306
GLYATL2RAVER2Q9HCJ3303

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A0U1RQE8, F1S5L4, O43010, O77512, P06592, P13233, P14714, P42498, P49895, P55004, P97564, Q07071, Q09305, Q0P464, Q0P4Y1, Q1LYL8, Q2KHV5, Q2KIR7, Q3UW68, Q5BK10, Q5FW57, Q5GJ77, Q5PQT3, Q5RFP0, Q60462, Q61586, Q62240, Q64112, Q6IB77, Q6MZZ7, Q6P5U7, Q6QN13, Q6QR59, Q6V915, Q7L7V1, Q804E1, Q8CBA2, Q8T773, Q8WU03, Q91754

Diamond homologs: A0A0U1RQE8, E9Q5L8, O77512, Q2KIR7, Q5FW57, Q5PQT3, Q5RFP0, Q5SZD4, Q6IB77, Q8WU03, Q91XE0, Q969I3, Q9DCY0, Q9Z2Y0

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

63 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance56
Likely benign4
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

821 predictions. Top by Δscore:

VariantEffectΔscore
11:58837013:A:ACdonor_gain1.0000
11:58837014:C:CCdonor_gain1.0000
11:58837178:C:CCacceptor_gain1.0000
11:58838255:TCCTA:Tdonor_loss1.0000
11:58838256:CCTAC:Cdonor_loss1.0000
11:58838257:CTACC:Cdonor_loss1.0000
11:58837056:A:ACdonor_gain0.9900
11:58837057:C:CCdonor_gain0.9900
11:58837174:CAAC:Cacceptor_gain0.9900
11:58837178:C:CAacceptor_loss0.9900
11:58837179:T:Aacceptor_loss0.9900
11:58837401:A:Cacceptor_gain0.9900
11:58838364:TATAC:Tacceptor_gain0.9900
11:58838366:TACC:Tacceptor_loss0.9900
11:58838367:ACCT:Aacceptor_loss0.9900
11:58838369:C:CAacceptor_loss0.9900
11:58838370:T:Aacceptor_loss0.9900
11:58838372:CGA:Cacceptor_gain0.9900
11:58838374:A:ACacceptor_gain0.9900
11:58839529:CGTTA:Cdonor_loss0.9900
11:58839530:GTTA:Gdonor_loss0.9900
11:58839531:TTACC:Tdonor_loss0.9900
11:58839532:TACCT:Tdonor_loss0.9900
11:58839533:A:Tdonor_loss0.9900
11:58839534:CCTT:Cdonor_loss0.9900
11:58834833:CTTCC:Cacceptor_gain0.9800
11:58837053:A:ACdonor_gain0.9800
11:58837058:T:Cdonor_gain0.9800
11:58837398:C:CCacceptor_gain0.9800
11:58838366:TAC:Tacceptor_gain0.9800

AlphaMissense

1977 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:58838302:A:GW49R0.974
11:58838302:A:TW49R0.974
11:58838283:A:TV55D0.972
11:58837350:G:CF78L0.971
11:58837350:G:TF78L0.971
11:58837352:A:GF78L0.971
11:58834674:A:GW214R0.962
11:58834674:A:TW214R0.962
11:58838274:C:GR58P0.961
11:58834750:G:CS188R0.955
11:58834750:G:TS188R0.955
11:58834752:T:GS188R0.955
11:58834458:A:GW286R0.954
11:58834458:A:TW286R0.954
11:58838327:G:CF40L0.954
11:58838327:G:TF40L0.954
11:58838329:A:GF40L0.954
11:58834456:C:AW286C0.947
11:58834456:C:GW286C0.947
11:58837276:A:GI103T0.939
11:58839535:C:AK26N0.939
11:58839535:C:GK26N0.939
11:58837293:C:AW97C0.937
11:58837293:C:GW97C0.937
11:58837295:A:GW97R0.931
11:58837295:A:TW97R0.931
11:58834467:A:GW283R0.929
11:58834467:A:TW283R0.929
11:58839543:A:GS24P0.925
11:58838300:C:AW49C0.917

dbSNP variants (sampled 300 via entrez): RS1000138727 (11:58909709 C>T), RS1000168154 (11:58907261 C>T), RS1000222601 (11:58877959 A>G), RS1000273901 (11:58911753 C>T), RS1000313982 (11:58871027 A>G), RS1000321676 (11:58842597 C>T), RS1000405222 (11:58870717 C>T), RS1000406965 (11:58858257 C>A,T), RS1000421168 (11:58874698 T>C), RS1000465179 (11:58877697 T>A,C,G), RS1000513893 (11:58854290 T>C), RS1000559076 (11:58905728 T>A), RS1000608250 (11:58874413 C>T), RS1000614171 (11:58897918 C>T), RS1000621711 (11:58869065 G>C)

Disease associations

OMIM: gene MIM:614762 | 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)

CTD chemical–gene interactions

12 total (human), top 12 by PubMed support.

ChemicalActions (top 5)PubMed papers
nickel sulfatedecreases expression1
bisphenol Sincreases methylation1
theaflavin-3,3’-digallateaffects expression1
Benzo(a)pyreneincreases methylation1
Diethylhexyl Phthalatedecreases expression1
Folic Aciddecreases expression1
Tobacco Smoke Pollutionincreases expression1
Tretinoinincreases expression1
Vanadatesincreases expression1
Antirheumatic Agentsincreases expression1
Acrylamidedecreases expression1
Particulate Matterincreases expression1

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.