Gene
GIPC1
GIPC PDZ domain containing family member 1
- HGNC 1226↗(opens in a new tab)
- Ensembl gene ENSG00000123159↗(opens in a new tab)
- NCBI Gene 10755↗(opens in a new tab)
Summary
- Cytogenetic location
- 19p13.12
- Coordinates
- Chromosome 19: 14,477,762–14,496,127 (GRCh38)
- Exons
- 9 exons across 18.4 kb
- Protein
- 333 amino acids
- Also known as
- TIP-2, Hs.6454, GIPC, SEMCAP, GLUT1CBP, SYNECTIN, NIP
- Previous symbols
- C19orf3, RGS19IP1
- MANE Select transcript
- ENST00000393033.9NM_005716.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Distal Myopathies
- Distal myopathy
A group of inherited muscle disorders in which weakness starts in the hands, forearms, lower legs or feet, caused by genes such as TTN, DYSF, FLNC, MYH7, ADSS1, SMPX and MATR3.
- 1 GenCC submitter rates it definitive or strong
How GIPC1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.9 kb of the gene's 18.4 kb; 1,002 of those bases code for the protein.
Genes linked to the same conditions
- ADSS1adenylosuccinate synthase 1Shares 1 condition
- ANO5anoctamin 5Shares 1 condition
- CRYABcrystallin alpha BShares 1 condition
- DNAJB4DnaJ heat shock protein family (Hsp40) member B4Shares 1 condition
- DYSFdysferlinShares 1 condition
- FLNCfilamin CShares 1 condition
- GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinaseShares 1 condition
- LDB3LIM domain binding 3Shares 1 condition
- LRP12LDL receptor related protein 12Shares 1 condition
- MATR3matrin 3Shares 1 condition
- MYH7myosin heavy chain 7Shares 1 condition
- MYOTmyotilinShares 1 condition
Traits linked to GIPC1
The Human Phenotype Ontology lists these as features of the rare conditions GIPC1 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). GIPC1 gene: GIPC PDZ domain containing family member 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/gipc1
Dante Labs. GIPC1 gene: GIPC PDZ domain containing family member 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/gipc1
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