Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionacyltransferase activity

RNF121 ZDHHC23 SPTLC3 MARVELD3 RNF175

8.63e-05775135GO:0016746
GeneOntologyMolecularFunctionpalmitoyltransferase activity

ZDHHC23 SPTLC3

2.57e-0437132GO:0016409
GeneOntologyMolecularFunctionubiquitin protein ligase activity

RNF121 MARVELD3 RNF175

1.60e-03372133GO:0061630
GeneOntologyMolecularFunctionubiquitin-like protein ligase activity

RNF121 MARVELD3 RNF175

1.94e-03398133GO:0061659
GeneOntologyMolecularFunctionubiquitin-protein transferase activity

RNF121 MARVELD3 RNF175

3.16e-03473133GO:0004842
GeneOntologyMolecularFunctionubiquitin-like protein transferase activity

RNF121 MARVELD3 RNF175

3.96e-03512133GO:0019787
GeneOntologyMolecularFunctionaminoacyltransferase activity

RNF121 MARVELD3 RNF175

4.41e-03532133GO:0016755
GeneOntologyMolecularFunctionacyltransferase activity, transferring groups other than amino-acyl groups

ZDHHC23 SPTLC3

1.01e-02238132GO:0016747
GeneOntologyBiologicalProcessdolichol-linked oligosaccharide biosynthetic process

DPAGT1 ALG3

8.41e-0522132GO:0006488
GeneOntologyBiologicalProcessdolichol metabolic process

DPAGT1 ALG3

1.00e-0424132GO:0019348
GeneOntologyBiologicalProcesspolyprenol metabolic process

DPAGT1 ALG3

1.47e-0429132GO:0016093
GeneOntologyCellularComponentendoplasmic reticulum membrane

RNF121 FADS2B DPAGT1 SPTLC3 ALG3 RNF175

6.51e-051293136GO:0005789
GeneOntologyCellularComponentendoplasmic reticulum subcompartment

RNF121 FADS2B DPAGT1 SPTLC3 ALG3 RNF175

6.68e-051299136GO:0098827
GeneOntologyCellularComponentnuclear outer membrane-endoplasmic reticulum membrane network

RNF121 FADS2B DPAGT1 SPTLC3 ALG3 RNF175

7.53e-051327136GO:0042175
GeneOntologyCellularComponentGolgi membrane

RNF121 ZDHHC23 RNF175

9.02e-03721133GO:0000139
HumanPhenoPulmonary hypoplasia

DPAGT1 ALG3 ETFDH

7.30e-0513643HP:0002089
HumanPhenoType I transferrin isoform profile

DPAGT1 ALG3

1.06e-042242HP:0003642
HumanPhenoAplasia/Hypoplasia of the lungs

DPAGT1 ALG3 ETFDH

1.19e-0416043HP:0006703
HumanPhenoAbnormal lung development

DPAGT1 ALG3 ETFDH

4.19e-0424443HP:4000059
HumanPhenoAbnormal isoelectric focusing of serum transferrin

DPAGT1 ALG3

4.73e-044642HP:0003160
HumanPhenoAbnormal protein N-linked glycosylation

DPAGT1 ALG3

4.94e-044742HP:0012347
HumanPhenoAbnormal protein glycosylation

DPAGT1 ALG3

5.15e-044842HP:0012346
HumanPhenoInverted nipples

DPAGT1 ALG3

5.60e-045042HP:0003186
HumanPhenoAbnormal glycosylation

DPAGT1 ALG3

6.29e-045342HP:0012345
Domainzf-C3HC4

RNF121 RNF175

8.66e-03223122PF00097
DomainZF_RING_1

RNF121 RNF175

1.44e-02291122PS00518
DomainZF_RING_2

RNF121 RNF175

1.51e-02298122PS50089
DomainRING

RNF121 RNF175

1.57e-02305122SM00184
DomainZnf_RING

RNF121 RNF175

1.79e-02326122IPR001841
Domain-

RNF121 RNF175

3.25e-024491223.30.40.10
DomainZnf_RING/FYVE/PHD

RNF121 RNF175

3.38e-02459122IPR013083
PathwayREACTOME_DISEASES_ASSOCIATED_WITH_N_GLYCOSYLATION_OF_PROTEINS

DPAGT1 ALG3

2.86e-052062M27274
PathwayWP_GLYCOSYLATION_AND_RELATED_CONGENITAL_DEFECTS

DPAGT1 ALG3

4.51e-052562M39813
PathwayKEGG_N_GLYCAN_BIOSYNTHESIS

DPAGT1 ALG3

1.55e-044662M11079
PathwayWP_NGLYCAN_BIOSYNTHESIS

DPAGT1 ALG3

2.38e-045762M48051
PathwayREACTOME_BIOSYNTHESIS_OF_THE_N_GLYCAN_PRECURSOR_DOLICHOL_LIPID_LINKED_OLIGOSACCHARIDE_LLO_AND_TRANSFER_TO_A_NASCENT_PROTEIN

DPAGT1 ALG3

4.36e-047762MM15118
PathwayREACTOME_BIOSYNTHESIS_OF_THE_N_GLYCAN_PRECURSOR_DOLICHOL_LIPID_LINKED_OLIGOSACCHARIDE_LLO_AND_TRANSFER_TO_A_NASCENT_PROTEIN

DPAGT1 ALG3

4.58e-047962M897
PathwayREACTOME_DISEASES_OF_GLYCOSYLATION

DPAGT1 ALG3

1.49e-0314362M27275
PathwayREACTOME_DISEASES_OF_METABOLISM

DPAGT1 ALG3

4.48e-0325062M27554
PathwayREACTOME_ASPARAGINE_N_LINKED_GLYCOSYLATION

DPAGT1 ALG3

6.11e-0329362MM15120
PathwayREACTOME_ASPARAGINE_N_LINKED_GLYCOSYLATION

DPAGT1 ALG3

6.69e-0330762M894
Pubmed

A genome-wide perspective of genetic variation in human metabolism.

SPTLC3 ETFDH

4.64e-06913220037589
Pubmed

Genetic mapping of mouse transient receptor potential (Trrp) genes responsible for capacitative calcium entry channels to chromosomes 3, 7, 9, and X.

TRPC3 ETFDH

3.54e-05241329722956
Pubmed

Congenital Disorders of N-Linked Glycosylation and Multiple Pathway Overview

DPAGT1 ALG3

1.21e-044413220301507
GeneFamilyRing finger proteins

RNF121 RNF175

4.60e-032757258
CoexpressionGSE411_WT_VS_SOCS3_KO_MACROPHAGE_IL6_STIM_100MIN_UP

DPAGT1 TM9SF1 ETFDH

1.18e-04200133M5992
CoexpressionGSE40274_CTRL_VS_FOXP3_AND_HELIOS_TRANSDUCED_ACTIVATED_CD4_TCELL_DN

DPAGT1 ALG3 TM9SF1

1.18e-04200133M9120
CoexpressionGSE27786_LIN_NEG_VS_BCELL_UP

DPAGT1 LANCL1 ETFDH

1.18e-04200133M4766
CoexpressionAtlase10.5_Nasal_Pit_top-relative-expression-ranked_500_1

RNF121 MARVELD3

2.65e-0514122Facebase_ST1_e10.5_Nasal_Pit_500_1
DiseaseCongenital disorder of glycosylation

DPAGT1 ALG3

1.25e-0438132cv:C0282577
Diseasesphingomyelin measurement

SPTLC3 ETFDH

6.44e-03278132EFO_0010118
Diseasefree cholesterol measurement, high density lipoprotein cholesterol measurement

LANCL1 ETFDH

8.20e-03315132EFO_0004612, EFO_0008591
Diseasephospholipid measurement, high density lipoprotein cholesterol measurement

LANCL1 ETFDH

8.50e-03321132EFO_0004612, EFO_0004639
Diseaselipid measurement, high density lipoprotein cholesterol measurement

LANCL1 ETFDH

8.97e-03330132EFO_0004529, EFO_0004612

Protein segments in the cluster

PeptideGeneStartEntry
PAGFVYIFMGLYYAT

ALG3

101

Q92685
MLYGRIGYIYALLFV

LANCL1

151

O43813
GILYYVYMGLLAVFC

DPAGT1

166

Q9H3H5
FGLYYGIFGTMLLIY

FADS2B

351

A8MWK0
VLGVYGGMIYTGIFY

ETFDH

461

Q16134
MLIAGGYIPALYFYF

MARVELD3

311

Q96A59
FYIGKYFGGVLEYFM

RHOBTB3

181

O94955
FGGGYMGLMVFLIYL

MT-ND6

46

P03923
TYMGYGIGTLFGYLR

SPTLC3

66

Q9NUV7
SMDFGIVSLFYGLYY

RNF175

176

Q8N4F7
IVSLFYGLYYGVMGR

RNF175

181

Q8N4F7
MDFGISLLFYGLYYG

RNF121

176

Q9H920
FLSLGLFSLGYMYYV

ZDHHC23

141

Q8IYP9
GYSLLTGYVFFLMLG

TM9SF1

571

O15321
IGMFILYSYYLGAKV

TRPC3

581

Q13507