ZMP
zgc:153460
Ensembl ID:
ZFIN ID:
Description:
tetratricopeptide repeat protein 7B [Source:RefSeq peptide;Acc:NP_001074072]
Human Orthologue:
TTC7B
Human Description:
tetratricopeptide repeat domain 7B [Source:HGNC Symbol;Acc:19858]
Mouse Orthologue:
Ttc7b
Mouse Description:
tetratricopeptide repeat domain 7B Gene [Source:MGI Symbol;Acc:MGI:2144724]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2911 | Essential Splice Site | F2 line generated | Not yet available |
sa16905 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2911
Status:
F2 line generated
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:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087023 | Essential Splice Site | 41 | 844 | 1 | 20 |
The following transcripts of ENSDARG00000061207 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 26453850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26593769 |
GRCz11 | 17 | 26612160 |
KASP Assay ID:
554-2921.1 (used for ordering genotyping assays)
KASP Sequence:
AAAATACCAGAGCTCGTGCGGCAGCTGTCGGCRAAACTCATCTCCAACGG[T/C]GAGAGTGATTTATCTTTATTTTCTCATGGCTAACGCGTTAGCTCGGACAG
Long Flanking Sequence:
CATTTAAGTATTTAGTATTTATTTGTAGTTATTTTTGATTTTTATTTTTATTTTTTTGCATTTATTTCCAAACATTTTCACAGCTTCGTCTCCTCCTGACACTAGATCATTTGCAGAACTCATTATTCAGAAATAATAACTACTGTATGCCATGATTGCCCAGTCAAAACAAATAATATAAAAATAAGTAAATATAAAAAAGCAAATCAAAACCATGTTTTATAGTTAAAAAGATCACCTGACAGGAATCTATCCAATCAGCGTTCAGTTTTGTGGCCCGGAAGCGTACTCCCGTTCATGTTTTTGTCGTCCTCTCCAGGTCTTTGATGTTTCTGTGCTGCGGCTCTGGTCGTGTTTTGGTCAGGAGGTGGTGGAAAGATGACAGCCAGAAAGTCCGGGTCGCGATTAGAGACTGAAATAGAGCGCTGTAGATCTGAGGGACAATGGGACAAAATACCAGAGCTCGTGCGGCAGCTGTCGGCGAAACTCATCTCCAACGG[T/C]GAGAGTGATTTATCTTTATTTTCTCATGGCTAACGCGTTAGCTCGGACAGTCTGTCTCTCTCTCTGTGTGTGTGTCTCAGGCCTGATGGCAGATCAGTCTGATTCATTCATGGACATTTTTCTACATGTGTAATGTTTCACTCAATGAATACTTTAATCTTAGGTTGACGGAGCTGCGATATTGATGTCCTTTAAGTAGCATCCCGTTCATCTGCCCAGCACACTTCCTGATTGCTCATAGCTGTGTCCATTCATCTTCACAAGTGATAATCATTCACATTTTTGTCAACTCTATAAAGTTATACAGAGTTGCTGTTTGGTTTATTTTCTTGAGAGGATGTGTTGTGGTTTTATTTGTGTTTTCTGTGTTATCATTGCTGAAAACAGTGATTCAGATAGATAGTTAAATAATTGATTGTTGCATTTTCACACTTTAAAAAAAATCAACAACATTAACAAACAGATGAAGAAAAGGATAAAGAAAGAAGTGGAAATGGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16905
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087023 | Nonsense | 541 | 844 | 15 | 20 |
The following transcripts of ENSDARG00000061207 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 26499519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26639438 |
GRCz11 | 17 | 26657829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTANNTGTRTGTGTGTGTCAGATTCCAGAAGCGCTCGGTTAKGTACGA[C/T]AGGCGTTACAGCTGCAGGGTGAYGATGTTCACTCGCTGCACCTGCTGGCC
Long Flanking Sequence:
AAGTCTTATCATCAGTTTTGTTTTCCTGTAAATTATTCAATAAATACCGTACGGTGCCATTCATACCGAGGTATTATCGTACCGTGAAATTATGATACCGTTACATCCCTACTGTTCAGCGTTTCTCATTTTGGCCGATTTAAACAATTATAAACAACATAATCAGAAATATTTTGATGTTCTAATCACTTCTCCATCTAAATTCCGCGCATCATCAATGACGTACGTGTGAAAACAACCTATCATAGTTGATGCCTTGTTTTGTATAATAATTATCTTTACTTATGCTTCACCCAATTCTAGCCACATCTGACTCTGCTCACTAAAGGAACTTAGTTCTGTCCTTATTTTCTTTCTAGCCTGTCTCTCCCACCAAATGACAGTCTGTTATTTTTTCTCCTCATTTTTCTCTTGTCTTATTTAAACAGTCGTCTAATAAAAGCATCTCTTGTGTATGTGTGTGTGTGTGTCAGATTCCAGAAGCGCTCGGTTATGTACGA[C/T]AGGCGTTACAGCTGCAGGGTGATGATGTTCACTCGCTGCACCTGCTGGCCTTGCTGCTGTCAGCTCAGAAACACTACCACGATGCTCTCAACATCATCGAGATGGCCCTCAGCGAATACCCAGAGAACTTCATGTGAGTCCAACAAAACCACTGTCACACTAAATCTAACCTATCGAGCCTTACTCTAAAGTAGCCTTGTTGTTTGAAACGGATGTCACCAGCTAATCAGAGAAAAGGAAAACACCTTTTCTTGGCTCAGAGAACCAATTAGATGATTCCGTGTTCCTCTGCACAGCATTTATAAAGCTACAAACACACACACACACACACACACACACACAGCAGTAGGCAGTGTTTAGACAGTTAGAGGCATGCCACAGTGCCCACTTTAATGAGAATGTTTGTGTTTGCTGTCGCAGCTGGGATAGATGGGTACATATCTGCTTCTGGCATCATCAATTAGACAACTTAGAAGTGTGTGAGTGTGTGTGTTGGATGT
Associated Phenotype:
Not determined