Busch Lab

ZMP

ttc35

Ensembl ID:
ENSDARG00000003308
ZFIN ID:
ZDB-GENE-040625-82
Description:
Tetratricopeptide repeat protein 35 [Source:UniProtKB/Swiss-Prot;Acc:Q6TGY8]
Human Orthologue:
TTC35
Human Description:
tetratricopeptide repeat domain 35 [Source:HGNC Symbol;Acc:28963]
Mouse Orthologue:
Ttc35
Mouse Description:
tetratricopeptide repeat domain 35 Gene [Source:MGI Symbol;Acc:MGI:1913986]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17192 Essential Splice Site Available for shipment Available now
sa36218 Nonsense Mutation detected in F1 DNA Not yet available
sa17729 Essential Splice Site Available for shipment Available now
sa42787 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17192
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023238 Essential Splice Site 14 297 1 11
Genomic Location (Zv9):
Chromosome 16 (position 41325335)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 38709559
GRCz11 16 38659591
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAAAAACATGTCGTCCATATCGGAGCTGTACGATGTCACTTGGGAAGG[T/C]AAATKACTTTATTTTCGTTAACAGCGCTTATTACGTGATTTACTTACAAT
Long Flanking Sequence:
TTTATTTACTTATTGTTTTATTTATGCAAAAATGTATGGATTTACTTACTCATTTAAATATTTATCTGTGTGTTTATGTATTTATTTATTGTTTTTGCAGTTTTCGTCCTTCATAGGCTCTAGTATACTAATACACATTATAAATGGCTATGTTTTACATAAGCTTTCTTTTAATAATAATGTCCATATTAAAGCTCTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTATTTCTCAATATAATATACCTGCATGAATAAATAAAAACCTCATTGGGTTTGGCTTTTGCCCTTCAATGACCCTTCTCACAGCGTTGACTGTCAACGTCACTGCCCTCCACCAATCCGTTCACAAGGGGCGGAGCTCAAAAAACATGTCGTCCATATCGGAGCTGTACGATGTCACTTGGGAAGG[T/C]AAATGACTTTATTTTCGTTAACAGCGCTTATTACGTGATTTACTTACAATATGTAGTGATTCAATAGTCACCAGAGTTCTAGATTTTGTAAAGGTTATCGCCTAAAGTTTCTTATTTGTTGTGCTTTTCATTAAAGACAAAATGCTAGCCAGTTAGCATATGTAGGCAGAGCTTAGTAACAGAACCTGTGTTTTTACGACTGTCGTTTACAAATATTACAATGTGTTTTGTATTTGAATGTCATGTTGTACATGTATAATGCTAAAAATGATTAATCTGTTGATGTCTGGTCTGTTTTCGGTAAAATGAGGATTTGCAAAGACCAGATATGCAATACTAATGTATCCCAAGTAATATTTGTATGTACAATCAATAAGAATGAGTCAGTTTACTTGATAAGATCCCCATCAGCATCATCATCTCCTGTTGTTTTTGTGATTAACCTGACAAAATCTAATATTTTAATTCAGTTCAATAATCTTCAGATTTAGATAATTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36218
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023238 Nonsense 39 297 2 11
Genomic Location (Zv9):
Chromosome 16 (position 41328887)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 38713111
GRCz11 16 38663143
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGGAAGAGAATTACAGGAACAGTGAGCAGATTGTGGATGTCGGTGAA[G/T]AGCTGATTAATGAGCATGCGTCTAAACTGGGAGATGACAGTAAGTACAAT
Long Flanking Sequence:
TGCTTTTTTTTTTGGTGGGGCCAGTGAAAATTTTGGCAGGGCGCGTAAAAATCAGAACCACTGGTCCAATCAGGCCAGTAGAAAAAATCCTTAGCGTTGAACTCTGTATGTTATTGAGGAGAAAGTCTGAATGTGTGACTATAACACCAACTTTACGTTAATATTTATGCTTTCATATTTTTTTGACACCATTATCAGAATTACTCTGATCATCAAGGTGCTTTATAGATCATATATCACAAGTTTTTTTATGTTGTTTTATTGATTAAGCATGTCAATCTAATACAGCATTATATATATGTTTAAAACAAAGCAGGAAAGTGAATAAAGCACCAGTTAAAATAACAAGTTATTATTGATAAAGAAAATAAATTGCTGCTAATAAATTTCCGCCAATTGCTAATGCATTTCTTTATTGCATTTCAGAGATGCGTGACAAACTCCGTAAGTGGAGGGAAGAGAATTACAGGAACAGTGAGCAGATTGTGGATGTCGGTGAA[G/T]AGCTGATTAATGAGCATGCGTCTAAACTGGGAGATGACAGTAAGTACAATTACAGTAAACAAAAGCGTTATATCAAAACAAAGAACATTCTGCCTCTGTAACACTAGAGTGCTTTATATTAATGCATTTCGTAATTGAAGCAGTTCAAGATGATGCCCACCTGACAATTATCGGATGTGTTTTTATGCACACATGGACACTAAGTAGTAGGATAACTGACAGATATTTAATATATAAATAGGCTGTATGGCTATAACTTTTTATTGCATGGAACCATCATAGTGCTCGCAAAACAGCGAGCCCATATTCCCATTACACAAATAATAGGAACATTTCCCACAGCAGTCCAACTGAAGCTTGACAGTAATTGTCCTGAAATTTATTAAAGGTGGTTATTTTGTTATGAAAGCCATGTTTTGATGGCAGCAGCACTAGTGATTTAAAGAGGATGAATTTAGAGTGCTGCTTCTTGGAAAGGGTTTGCTTTGAAAATGAGAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17729
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023238 Essential Splice Site 170 297 7 11
Genomic Location (Zv9):
Chromosome 16 (position 41361315)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 38745539
GRCz11 16 38695571
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAGGAAGCCTGGCATGAGCTGTCCGAACTCTACATCAATGAGCATGAG[T/A]AATTCTTACCNNNNNNCTTNNNNNNNNTTTCTTTCTTTCTAAACATGCAATTTGATAG
Long Flanking Sequence:
TTGGCTGTAGTTCTTCTTCCATCCCGTAGTCTCCAAAGTCCCAGGGGATTGTGGAGATTCCTTCAGCTCTTACAATACTGCGATCATTTACACATCCCTCTTTCTTTTACTCTTTGCTCTTTTCTGTTGCTAACAAACACTTGAAACACTAAAGCCCTAATCCTCTGTTGATGTCCCAACAGGCAGCGAGGAAGCGCAAGATCTGCATCCTCCGAGCGCAGGGCAAAAGCAGCGAGGCCATCCGCGAACTCAACGAATATCTGGAGCAGTGAGTGTTTTACTAGAGGATTTAGACCCCCCTTACTGTTCCCTTCCTCTCCACTTTTTAATTAAAAGGGGTTTTGCATTTGATTGCATTGGCCCCCAAGCCTTTCCCTAACCCCCCTTTTGTCCACAGTGGCCTTTCTGATGAACTAACTACCACTGCTGTGTGTTGCAGGTTTGTGGGAGACCAGGAAGCCTGGCATGAGCTGTCCGAACTCTACATCAATGAGCATGAG[T/A]AATTCTTACCCTTTTTCTTTTTCTTTCTTTCTAAACATGCAATTTGATAGAACGGGGGTTAATAAAACTGTCTGGGGTCAGTCTGACCCAATACAAAAGCCACAGATCATAAACCAGTCACTTTTTGAATTTTTTAAAAACTTTTTTATGGCAGAAATGGGAACAGATTTCAGTAAAATCCAGTGTGGTGGCTTTTAGTGAGCTCTGAAGGATTTATTTAAAGAATTAGTATGAAGATGCTATATTCTTTGACAGCCAATGATTGAACTAGGTAATGCACTTCTGGATCAAAACAAATGCAAGTGTAGGTTGTTAGATTGAGGACCAACAGGATCAAGTTTGACGATCGAGTCTAAAGGATGATTTACGACGTGTTGTATATAAAAGCAACTGCATGCGATAGAAGAAATGTTTTCCACATTAAAAGGAATTTCTGTTCCAACCAACGCCTCGAATTGATATATCAAATCAAATCACTTTTATTGTCACATCATCAGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42787
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023238 Essential Splice Site 170 297 8 11
Genomic Location (Zv9):
Chromosome 16 (position 41370912)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 38755136
GRCz11 16 38705168
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCATTAAAGTTTTTTTCTCTCTCTCTCTTTTCTTGTTTGATTCTCAC[A/T]GTTATGCAAAAGCAGCTTTTTGTCTTGAAGAGCTGATGATGACAAACCCA
Long Flanking Sequence:
TTCCATGTCAACAGCTCCTTTAGAAATATTATTCCCAGGGAAAAAAACATGACGTGTTTAATACTTATTTTCCCCGCTGTATAAGGAAGAGAGTGTCTGAAACTGTCAATTTAGTGTGAGGTCAGTGGCTCAGCAGTGATCTCATTTGGGAACGGCTCTCTAAAATGACCTCAGGACAGACTGAGATGTCAATGAAGAACCCAGGGACAGATTGGCAGAGCAGACTGTCATTCATCTTTGAATCTAAGGCAGGATTGCCACCTCTGTTGCAATGATTTGTTCATCCCTTGACCAAATGGGCATTTTTACACGGATTTCCATTAACCCTCTGAAAAGCTAATAAACGAGAAACCTCAGACTGTCCCGTCTCCCAACTGTCAACGAGATTGAGCCGCGCTATGCATAATCAGCCACAAAGCTACCAGGAGATGTATTGTTGTATATGTGTGATATCCATTAAAGTTTTTTTCTCTCTCTCTCTTTTCTTGTTTGATTCTCAC[A/T]GTTATGCAAAAGCAGCTTTTTGTCTTGAAGAGCTGATGATGACAAACCCACACAATCACCTGTATTGCGAACAGTACGCAGAGGTACAGTACATTTTTTTTGTTCATCTTGAAACCATGTTCTCTTTAATTTAATTGTGATAAAATGACAATTAAAAATGAGGAAATTCAAACTCCAAATATACTGATTTCACACGGTCACCATTTAAAAAGCGGAATCGAGGCTGCGGTGGGAAGAAACCTGGAAATATCACCTGAGTCACACAGGAATGTTCAGTACTGGCTGTATATCTTATCAGCGAAGAGAAAGCGACACAAATGTATAATTTCACCTCCTTCCGAGTAACCCGAAGGTCTGTTCTGAATGGAAAGTGAAATAAAAAGGATTTTAGACCTCATTTTTAGCTAAGTTAAGGGAAATGGTACTAGTTAGCTTTCGTTTTCTTTTCTACACAAACGTTTTGGATGCCATTTATCAATCTCAAGTTATTGAACTGTTTT
Associated Phenotype:
Not determined