zgc:163141

Ensembl ID:
ENSDARG00000074518
ZFIN ID:
ZDB-GENE-070615-15
Description:
transmembrane protein 17 [Source:RefSeq peptide;Acc:NP_001091861]
Human Orthologue:
TMEM17
Human Description:
transmembrane protein 17 [Source:HGNC Symbol;Acc:26623]
Mouse Orthologue:
Tmem17
Mouse Description:
transmembrane protein 17 Gene [Source:MGI Symbol;Acc:MGI:2144205]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa38097 Essential Splice Site Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa38097
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111738 Essential Splice Site 73 191 2 5
Genomic Location (Zv9):
Chromosome 25 (position 29457222)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 28147316
GRCz11 25 28590518
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGTTCTTTCCTTTCTGGTGGATCAGTGAGGTTGTGATGCTTGACCTAAAG[G/A]TGATTCTCGTCTTTGTCATTTTTAACATTTCAATATGATCTTATGGCTGT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

Short-link