Human GRCh38.p14
WHSC1L2P
Wolf-Hirschhorn syndrome candidate 1-like 2, pseudogene
- Locus tag
- gene-WHSC1L2P
- Reference assembly
- GCF_000001405.40
- Sequence
- NC_000017.11
- Gene interval
- 43,718,314–43,720,436 · - strand
- Coordinate system
- 1-based, inclusive
This reference annotates this locus as a pseudogene. Do not assume it produces a functional protein.
Published evidence
No curated experimental phenotype evidence is attached to this locus. Its annotated product describes a reference annotation, not a measured editing outcome.
Nearby genes
- MEOX1 · gene-MEOX1 — mesenchyme homeobox 1
- LINC02594 · gene-LINC02594 — long intergenic non-protein coding RNA 2594
- LOC107985085 · gene-LOC107985085 — uncharacterized LOC107985085
- WHSC1L2P · gene-WHSC1L2P — Wolf-Hirschhorn syndrome candidate 1-like 2, pseudogene
- SOST · gene-SOST — sclerostin
- DUSP3 · gene-DUSP3 — dual specificity phosphatase 3
- CFAP97D1 · gene-CFAP97D1 — CFAP97 domain containing 1
Reference and sequence
NCBI reference annotation · Reference gene interval · Download gene DNA (FASTA)
Gene-level evidence does not identify a validated nucleotide edit. Evaluate the study’s strain and conditions before applying an observation to another background.