Pituitary hormone deficiency, combined or isolated, 8
diseaseOn this page
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
| Field | Value |
|---|---|
| Canonical name | pituitary hormone deficiency, combined or isolated, 8 |
| Mondo ID | MONDO:0957208 |
| OMIM | 620303 |
| DOID | DOID:0061018 |
| UMLS | C5830375 |
| MedGen | 1841011 |
| GARD | 0026788 |
| 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 disorder › congenital nervous system disorder › combined pituitary hormone deficiencies, genetic form › pituitary 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
| ClinVar | Variant (HGVS) | Gene | Classification | Review |
|---|---|---|---|---|
| 4081917 | NM_002941.4(ROBO1):c.4615C>T (p.Gln1539Ter) | ROBO1 | Pathogenic | no assertion criteria provided |
| 2692578 | NM_002941.4(ROBO1):c.2440_2442+4del | ROBO1 | Likely pathogenic | criteria provided, single submitter |
| 978578 | NM_002941.4(ROBO1):c.719G>C (p.Cys240Ser) | ROBO1 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications |
| 995978 | NM_002941.4(ROBO1):c.1690C>T (p.Pro564Ser) | ROBO1 | Uncertain significance | criteria 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.
| Gene | Classification | Inheritance | Disease | Records |
|---|---|---|---|---|
| ROBO1 | Strong | Autosomal dominant | pituitary hormone deficiency, combined or isolated, 8 | 10 |
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| ROBO1 | Orphanet:95496 | Pituitary stalk interruption syndrome |
Cohort genes → proteins
1 cohort genes, 1 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| multi_evidence | 1 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| ROBO1 | HGNC:10249 | ENSG00000169855 | Q9Y6N7 | Roundabout homolog 1 | gencc,clinvar |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| ROBO1 | Roundabout homolog 1 | Receptor 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.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Antibody/Immunoglobulin | 1 | 29.2× | 0.034 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| ROBO1 | Antibody/Immunoglobulin | yes | Ig_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)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 1 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| ganglionic eminence | 1 |
| tibia | 1 |
| ventricular zone | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| ROBO1 | 287 | ubiquitous | marker | ventricular zone, ganglionic eminence, tibia |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| ROBO1 | 2,359 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| ROBO1 | Q9Y6N7 | 12 |
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.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| SLIT2:ROBO1 increases RHOA activity | 1 | 2855.0× | 0.002 | ROBO1 |
| Regulation of cortical dendrite branching | 1 | 2284.0× | 0.002 | ROBO1 |
| Inactivation of CDC42 and RAC1 | 1 | 1427.5× | 0.002 | ROBO1 |
| Role of ABL in ROBO-SLIT signaling | 1 | 1268.9× | 0.002 | ROBO1 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | 1 | 951.7× | 0.002 | ROBO1 |
| Activation of RAC1 | 1 | 815.7× | 0.002 | ROBO1 |
| Netrin-1 signaling | 1 | 439.2× | 0.004 | ROBO1 |
| Signaling by ROBO receptors | 1 | 124.1× | 0.012 | ROBO1 |
| Regulation of expression of SLITs and ROBOs | 1 | 69.2× | 0.019 | ROBO1 |
| Axon guidance | 1 | 45.1× | 0.025 | ROBO1 |
| Nervous system development | 1 | 42.9× | 0.025 | ROBO1 |
| Developmental Biology | 1 | 14.5× | 0.069 | ROBO1 |
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 term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| chemorepulsion involved in postnatal olfactory bulb interneuron migration | 1 | 8426.0× | 0.002 | ROBO1 |
| negative regulation of negative chemotaxis | 1 | 5617.3× | 0.002 | ROBO1 |
| axon midline choice point recognition | 1 | 3370.4× | 0.002 | ROBO1 |
| negative regulation of mammary gland epithelial cell proliferation | 1 | 3370.4× | 0.002 | ROBO1 |
| Roundabout signaling pathway | 1 | 2808.7× | 0.002 | ROBO1 |
| negative regulation of chemokine-mediated signaling pathway | 1 | 2407.4× | 0.002 | ROBO1 |
| heart induction | 1 | 2106.5× | 0.002 | ROBO1 |
| endocardial cushion formation | 1 | 1404.3× | 0.002 | ROBO1 |
| positive regulation of vascular endothelial growth factor signaling pathway | 1 | 1123.5× | 0.002 | ROBO1 |
| positive regulation of vascular endothelial growth factor receptor signaling pathway | 1 | 1053.2× | 0.002 | ROBO1 |
| pulmonary valve morphogenesis | 1 | 936.2× | 0.003 | ROBO1 |
| cell migration involved in sprouting angiogenesis | 1 | 648.1× | 0.003 | ROBO1 |
| outflow tract septum morphogenesis | 1 | 648.1× | 0.003 | ROBO1 |
| positive regulation of Rho protein signal transduction | 1 | 581.1× | 0.003 | ROBO1 |
| positive regulation of axonogenesis | 1 | 581.1× | 0.003 | ROBO1 |
| aorta development | 1 | 561.7× | 0.003 | ROBO1 |
| aortic valve morphogenesis | 1 | 432.1× | 0.003 | ROBO1 |
| ventricular septum morphogenesis | 1 | 432.1× | 0.003 | ROBO1 |
| positive regulation of Notch signaling pathway | 1 | 351.1× | 0.004 | ROBO1 |
| homophilic cell-cell adhesion | 1 | 140.4× | 0.009 | ROBO1 |
| negative regulation of cell migration | 1 | 111.6× | 0.011 | ROBO1 |
| positive regulation of MAPK cascade | 1 | 80.6× | 0.015 | ROBO1 |
| negative regulation of gene expression | 1 | 69.1× | 0.016 | ROBO1 |
| nervous system development | 1 | 45.9× | 0.024 | ROBO1 |
| positive regulation of gene expression | 1 | 38.7× | 0.027 | ROBO1 |
| cell adhesion | 1 | 37.5× | 0.027 | ROBO1 |
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
| Symbol | Molecules | Max phase |
|---|---|---|
| ROBO1 | 0 | 0 |
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):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 0 | |
| B | Phased (≥1) drug, not yet approved | 0 | |
| C | Druggable family + PDB, no drug | 1 | ROBO1 |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
Undrugged target profiles
1 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
| Symbol | ChEMBL assays | Drugged partners (top 3) |
|---|---|---|
| ROBO1 | 0 | — |
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
- Cohort genes: ROBO1