WHSC1L1 Back

Wolf-Hirschhorn syndrome candidate 1-like 1

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NCBI Description of WHSC1L1
This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. The function of the protein has not been determined. Two alternatively spliced variants have been described. Transcript variant: This variant (long) contains an alternative 3' end sequence. The longer protein encoded has a different carboxy terminus than the protein encoded by variant short. ;This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. The function of the protein has not been determined. Two alternatively spliced variants have been described. Transcript variant: This variant (short) contains an alternative 3' end sequence. The shorter protein encoded has a different carboxy terminus than the protein encoded by variant long.

Community Annotation of WHSC1L1 Add / Edit WHSC1L1: Annotations

No community annotations yet for WHSC1L1.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

WHSC1L1 is highly significantly mutated in
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WHSC1L1 is significantly mutated in
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WHSC1L1 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for WHSC1L1