ZMP
ttc23
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LX69]
Human Orthologues:
TTC23, TTC23L
Human Descriptions:
tetratricopeptide repeat domain 23 [Source:HGNC Symbol;Acc:25730]
tetratricopeptide repeat domain 23-like [Source:HGNC Symbol;Acc:26355]
tetratricopeptide repeat domain 23-like [Source:HGNC Symbol;Acc:26355]
Mouse Orthologues:
Ttc23, Ttc23l
Mouse Descriptions:
tetratricopeptide repeat domain 23 Gene [Source:MGI Symbol;Acc:MGI:1914259]
tetratricopeptide repeat domain 23-like Gene [Source:MGI Symbol;Acc:MGI:1923027]
tetratricopeptide repeat domain 23-like Gene [Source:MGI Symbol;Acc:MGI:1923027]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17911 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17911
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090100 | Essential Splice Site | 171 | 463 | 5 | 11 |
ENSDART00000138692 | None | None | 251 | None | 6 |
ENSDART00000141686 | Essential Splice Site | 171 | 212 | 5 | 5 |
ENSDART00000146751 | None | None | 140 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 20609034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20839257 |
GRCz11 | 18 | 20828323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WAGTTYAGTTATAGGTTAATWGACCTSTTATGAGTTCTTAACTATGTGAA[C/T]TTTAGCAGAAGCSGAGTCAAGCTTTCAGARGGCAGAGATCGTCTTAGGAG
Long Flanking Sequence:
ATAGCATTTTTTACATGAGTGTGAGTAAATTAATAGCCAAAAAAAGTCTGAACCTTTATTTATGTAATGCATTTAAATACATATAAATAAGAATAATGAACATCAAACATATTATCATTGAAACAAAACTACTCTGTTTGTCCTTCTCGTTTTCCAGGATGGGCACATCAAGCACAGGAACATGCATCGCAAGCACATGAAGTACTCAGTTTGTGTCAGCAGGAGGAGAGATTGAGCTGCCTTAACTGCTTTCTTTCCATACATCAAACTCATGGAAGTGCTGCTCTGCATCTTGGAAAATATCCTTGTTTACAAAAGCATTCATATTCATATATTATATTCTTAAGAGCATCTTTTAGGGATATAATATGTGTATTTGACATTATTAAACTTTGCCTTTGGAGTAGAAAAGAGTGGATAATTTGTCAAATGGACTGTTGTTCCAGATAAAAGTTCAGTTATAGGTTAATTGACCTGTTATGAGTTCTTAACTATGTGAA[C/T]TTTAGCAGAAGCCGAGTCAAGCTTTCAGAAGGCAGAGATCGTCTTAGGAGACATAGTAGCACAAGAAGCCACTGGAAAGGAGGACAGACTGGCCACGGAGTATGAAATATTTACAAATTTAGCAAGGTAATTGAGCACTTTTATTTGGATTATTGTTTTGTCCGGCTGTAATATCATAGCTGAAATACCAAAAGGCACAATATAACAAAAAATTATTGCATTTTTTGAGAAGTACTGAAGTGTTTGCCTTTCTTTTAATCCTTTTATTTTCTTTCTTTTATTTTGATACCCTGCATAAATGTTCAAATCTAAAACTAAAACAAAAGAGACTAATTTTGTATTTGTCCTTAGAGACATCATAATCACTTTGCACTGTCTGTTTATGAAATAATAAACACATGAAGTTAGTTGTCTACAGGCTTAAAATATAGCATTGAAGTCGAGTCTACATTGATATTTTCACAAAGCTCTACAGTGAATCACATGCTGTGGTCTATTTA
Associated Phenotype:
Not determined