Busch Lab

ZMP

zgc:153460

Ensembl ID:
ENSDARG00000061207
ZFIN ID:
ZDB-GENE-070105-3
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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