STMP1

protein-coding

short transmembrane mitochondrial protein 1

Gene summary

Involved in mitochondrial respirasome assembly and mitochondrial respiratory chain complex IV assembly. Located in mitochondrion. Is active in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Jun 2026]

Previous symbols:
  • C7orf73

MANE transcript

NM_001130929.2

Inheritance

—

ClinVar variants

U:2

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 0

Max pathogenic AF

—

Genomic locus

chr7:135,662,496-135,693,418

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~30.9 kb
Loading mutation effect viewer...

GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to STMP1 variants in ClinVar

1 Conditions Cataloged
not specifiedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001130929.2. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
1
clinvar
1
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
1
clinvar
1
Total002002
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 17 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001130929.2RefSeqNP_001124401.13MANE Select
ENST00000507606.3EnsemblENSP00000425996.13MANE Select
ENST00000509448.5EnsemblENSP00000485469.13Standard
ENST00000873095.1EnsemblENSP00000543154.12Standard

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Cellular Component

  • mitochondrial respirasome
  • integral component of membrane
  • mitochondrial membrane

gnomAD Constraint

Source: gnomAD

Gene type
protein_coding
Transcript type
protein_coding
Transcript
ENST00000507606
Coding exons
3
Length
30923
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense0.8631021.20.4729.92e-7303
Missense (PolyPhen)24.08110.4900649
Synonymous0.47367.670.7834.26e-781
Loss of Function1.4402.400.001.01e-734

Population LoF Frequency

PopulationCAFp-valueStatus
African00.0absent
Latino/Admixed American00.0absent
Ashkenazi Jewish00.0absent
East Asian00.0absent
Finnish00.0absent
European (Non-Finnish)00.0absent
South Asian00.0absent
Other00.0absent

dbNSFP Gene Annotations

Source: dbNSFP

Intolerance Scores

RVIS EVS
0.19
RVIS percentile EVS
66.32

Essentials

Essential (gene trap)
E
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