Pituitary hormone deficiency, combined or isolated, 8

disease
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Summary

Pituitary hormone deficiency, combined or isolated, 8 (MONDO:0957208) is a disease caused by ROBO1 (GenCC Strong), with 1 cohort gene.

At a glance

  • Causal gene: ROBO1 (GenCC Strong)
  • Cohort genes: 1
  • ClinVar variants: 4

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namepituitary hormone deficiency, combined or isolated, 8
Mondo IDMONDO:0957208
OMIM620303
DOIDDOID:0061018
UMLSC5830375
MedGen1841011
GARD0026788
Is cancer (heuristic)no

Data availability: 4 ClinVar variants · 3 GenCC gene-disease records.

Disease family

Classification path: disease › human disease › disease by body system or component › nervous system disordercongenital nervous system disordercombined pituitary hormone deficiencies, genetic formpituitary hormone deficiency, combined or isolated, 8

Related subtypes (8): isolated congenital growth hormone deficiency, septooptic dysplasia, congenital isolated adrenocorticotropic hormone deficiency, non-acquired combined pituitary hormone deficiency with spine abnormalities, short stature-pituitary and cerebellar defects-small sella turcica syndrome, pituitary hormone deficiency, combined, 6, panhypopituitarism, pituitary hormone deficiency, combined, 1

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

ClinVar germline variants

4 retrieved; paginated sample, class counts are floors:

1 likely pathogenic, 1 pathogenic, 1 conflicting classifications of pathogenicity, 1 uncertain significance

ClinVarVariant (HGVS)GeneClassificationReview
4081917NM_002941.4(ROBO1):c.4615C>T (p.Gln1539Ter)ROBO1Pathogenicno assertion criteria provided
2692578NM_002941.4(ROBO1):c.2440_2442+4delROBO1Likely pathogeniccriteria provided, single submitter
978578NM_002941.4(ROBO1):c.719G>C (p.Cys240Ser)ROBO1Conflicting classifications of pathogenicitycriteria provided, conflicting classifications
995978NM_002941.4(ROBO1):c.1690C>T (p.Pro564Ser)ROBO1Uncertain significancecriteria provided, single submitter

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 10 · Orphanet: 1 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0

GenCC gene–disease validity (cohort genes)

the Disease column is the GenCC-asserted condition — a cohort gene’s strongest validity may be for a related predisposition syndrome.

GeneClassificationInheritanceDiseaseRecords
ROBO1StrongAutosomal dominantpituitary hormone deficiency, combined or isolated, 810

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
ROBO1Orphanet:95496Pituitary stalk interruption syndrome

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
multi_evidence1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
ROBO1HGNC:10249ENSG00000169855Q9Y6N7Roundabout homolog 1gencc,clinvar

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
ROBO1Roundabout homolog 1Receptor for SLIT1 and SLIT2 that mediates cellular responses to molecular guidance cues in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuro…

Protein-family classification

Druggable: 1 · Difficult: 0 · Unknown: 0 · Druggable fraction: 1.0

Family distribution

Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.

FamilyGenesFoldFDR
Antibody/Immunoglobulin129.2×0.034

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
ROBO1Antibody/ImmunoglobulinyesIg_sub2, Ig_sub, FN3_dom

Expression context

Cohort genes with no expression data: 0.

1 cohort gene are a single-cell marker in ≥1 SCXA experiment.

Breadth distribution (Bgee present_calls)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)1
unknown0

Top tissues across cohort

TissueCohort genes
ganglionic eminence1
tibia1
ventricular zone1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
ROBO1287ubiquitousmarkerventricular zone, ganglionic eminence, tibia

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
ROBO12,359

Structural data

PDB: 1 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
ROBO1Q9Y6N712

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 12. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).

Pathways by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
SLIT2:ROBO1 increases RHOA activity12855.0×0.002ROBO1
Regulation of cortical dendrite branching12284.0×0.002ROBO1
Inactivation of CDC42 and RAC111427.5×0.002ROBO1
Role of ABL in ROBO-SLIT signaling11268.9×0.002ROBO1
Regulation of commissural axon pathfinding by SLIT and ROBO1951.7×0.002ROBO1
Activation of RAC11815.7×0.002ROBO1
Netrin-1 signaling1439.2×0.004ROBO1
Signaling by ROBO receptors1124.1×0.012ROBO1
Regulation of expression of SLITs and ROBOs169.2×0.019ROBO1
Axon guidance145.1×0.025ROBO1
Nervous system development142.9×0.025ROBO1
Developmental Biology114.5×0.069ROBO1

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
chemorepulsion involved in postnatal olfactory bulb interneuron migration18426.0×0.002ROBO1
negative regulation of negative chemotaxis15617.3×0.002ROBO1
axon midline choice point recognition13370.4×0.002ROBO1
negative regulation of mammary gland epithelial cell proliferation13370.4×0.002ROBO1
Roundabout signaling pathway12808.7×0.002ROBO1
negative regulation of chemokine-mediated signaling pathway12407.4×0.002ROBO1
heart induction12106.5×0.002ROBO1
endocardial cushion formation11404.3×0.002ROBO1
positive regulation of vascular endothelial growth factor signaling pathway11123.5×0.002ROBO1
positive regulation of vascular endothelial growth factor receptor signaling pathway11053.2×0.002ROBO1
pulmonary valve morphogenesis1936.2×0.003ROBO1
cell migration involved in sprouting angiogenesis1648.1×0.003ROBO1
outflow tract septum morphogenesis1648.1×0.003ROBO1
positive regulation of Rho protein signal transduction1581.1×0.003ROBO1
positive regulation of axonogenesis1581.1×0.003ROBO1
aorta development1561.7×0.003ROBO1
aortic valve morphogenesis1432.1×0.003ROBO1
ventricular septum morphogenesis1432.1×0.003ROBO1
positive regulation of Notch signaling pathway1351.1×0.004ROBO1
homophilic cell-cell adhesion1140.4×0.009ROBO1
negative regulation of cell migration1111.6×0.011ROBO1
positive regulation of MAPK cascade180.6×0.015ROBO1
negative regulation of gene expression169.1×0.016ROBO1
nervous system development145.9×0.024ROBO1
positive regulation of gene expression138.7×0.027ROBO1
cell adhesion137.5×0.027ROBO1

Therapeutics

Drug target analysis

Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 0 · Undrugged: 1

Druggability breadth: 0 of 1 evidence-associated genes (0%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Top cohort targets by molecule count

SymbolMoleculesMax phase
ROBO100

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Pharmacogenomics

Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.

No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).

Chemical tractability of cohort targets

0 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)0
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug1ROBO1
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

Undrugged target profiles

1 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

SymbolChEMBL assaysDrugged partners (top 3)
ROBO10

Clinical trials & evidence

Clinical trials

Clinical trials: 0.