ZMP
ttc6
Ensembl ID:
ZFIN ID:
Human Orthologue:
TTC6
Human Description:
tetratricopeptide repeat domain 6 [Source:HGNC Symbol;Acc:19739]
Mouse Orthologue:
Ttc6
Mouse Description:
tetratricopeptide repeat domain 6 Gene [Source:MGI Symbol;Acc:MGI:2684915]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36337 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5900 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36338 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25035 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17451 | Nonsense | Available for shipment | Available now |
sa42874 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36337
Status:
Mutation detected in F1 DNA
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081247 | Nonsense | 129 | 612 | 4 | 13 |
ENSDART00000081247 | Nonsense | 129 | 612 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 10323366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10121958 |
GRCz11 | 17 | 10277992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTCTCTTCTCCTTCAGGCTTTGGATGCTTTTAACAGCACTGTGAGCT[T/A]AAACCCAGACCATGCCGAGGCTCACCATCAGCGAGGCCTTTGTCGCATTC
Long Flanking Sequence:
CTAATAAAATACAAAATACAAGGGAATTAGGATGGTAAAATAAATAAACAAAAAAAACTGCATTTTTTTTTTGCATATTGAATGTTTTATACTGTGTCAAACACAGGAAGCAGTGGAAACTTTTAAGAAGGCCTTGTCATTTCTGGGTAGCACTAAAGCTAAACTCAGTCCTGCAAAAGAAACTGCAGAGGTCTTCTATTTAATCGGTGTATGCTACGTGACGCAAAGGCTTTTGTTTCAGGTAATAAATTAATTTATATTAGTTAATATCATAACTCCCAAAAAATATTGATTTATGAATGTTATGTGTGATCCAGATATGAAATGTAGAAATGTAGCATTTTATCAGATTCCCAAGATGTGATGATAATTTAAAAAAAAGAAGCAGATGGAAACGCAGCCATATCTGTCACTACTCTATCATCACCTTTTTTTAATATAGGAGAGTGGAGATTCTCTTCTCCTTCAGGCTTTGGATGCTTTTAACAGCACTGTGAGCT[T/A]AAACCCAGACCATGCCGAGGCTCACCATCAGCGAGGCCTTTGTCGCATTCATTTACAAGACTCCACAGGCGTGCAAGACTTTAATAGAGCTCTCAAAATCAACCCCAAGTTCTATCAGGTACACCCTGATGCTCTGTCAGGTACACTCTAAATACTATTATTTAGAGAAATGAAATTATTTATTCCATATTCCAAGTTTCAGATTTGAAATGGTTTTTCATTTTTCCCAAGGTGCATCTAAGCCGAGCTGCCCTTTATGGGGCTGAAGGACGACATGCAAAGGCCATACTCGACTGTAATGAGGCTATCAGGATCCAGCCGAAGAGCCTCAGAGCACACTTGTATAAAGGGGCTCTTAAATTCTATTTGAAAGTTAGTAAAAATAGCACCATTTTGAGCATAATTATCGTACACTTGAGGCTGATGCTCTCTGAAATATGTTGTATGTTCATCATCTTGTTTTAGGCATACAAGAGTGCAGTGGAGGATCTAACAATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5900
Status:
Mutation detected in F1 DNA
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081247 | Nonsense | 129 | 612 | 4 | 13 |
ENSDART00000081247 | Nonsense | 129 | 612 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 10323366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10121958 |
GRCz11 | 17 | 10277992 |
KASP Assay ID:
554-3715.1 (used for ordering genotyping assays)
KASP Sequence:
AGATTCTCTTCTCCTTCAGGCTTTGGATGCTTTTAACAGCACTGTGAGCT[T/G]RAACCCAGACCATGCCGAGGCTCACCATCAGCGAGGCCTTTGTCGCATTC
Long Flanking Sequence:
CTAATAAAATACAAAATACAAGGGAATTAGGATGGTAAAATAAATAAACAAAAAAAACTGCATTTTTTTTTTGCATATTGAATGTTTTATACTGTGTCAAACACAGGAAGCAGTGGAAACTTTTAAGAAGGCCTTGTCATTTCTGGGTAGCACTAAAGCTAAACTCAGTCCTGCAAAAGAAACTGCAGAGGTCTTCTATTTAATCGGTGTATGCTACGTGACGCAAAGGCTTTTGTTTCAGGTAATAAATTAATTTATATTAGTTAATATCATAACTCCCAAAAAATATTGATTTATGAATGTTATGTGTGATCCAGATATGAAATGTAGAAATGTAGCATTTTATCAGATTCCCAAGATGTGATGATAATTTAAAAAAAAGAAGCAGATGGAAACGCAGCCATATCTGTCACTACTCTATCATCACCTTTTTTTAATATAGGAGAGTGGAGATTCTCTTCTCCTTCAGGCTTTGGATGCTTTTAACAGCACTGTGAGCT[T/G]AAACCCAGACCATGCCGAGGCTCACCATCAGCGAGGCCTTTGTCGCATTCATTTACAAGACTCCACAGGCGTGCAAGACTTTAATAGAGCTCTCAAAATCAACCCCAAGTTCTATCAGGTACACCCTGATGCTCTGTCAGGTACACTCTAAATACTATTATTTAGAGAAATGAAATTATTTATTCCATATTCCAAGTTTCAGATTTGAAATGGTTTTTCATTTTTCCCAAGGTGCATCTAAGCCGAGCTGCCCTTTATGGGGCTGAAGGACGACATGCAAAGGCCATACTCGACTGTAATGAGGCTATCAGGATCCAGCCGAAGAGCCTCAGAGCACACTTGTATAAAGGGGCTCTTAAATTCTATTTGAAAGTTAGTAAAAATAGCACCATTTTGAGCATAATTATCGTACACTTGAGGCTGATGCTCTCTGAAATATGTTGTATGTTCATCATCTTGTTTTAGGCATACAAGAGTGCAGTGGAGGATCTAACAATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36338
Status:
Mutation detected in F1 DNA
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081247 | Nonsense | 140 | 612 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 10323398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10121926 |
GRCz11 | 17 | 10277960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACAGCACTGTGAGCTTAAACCCAGACCATGCCGAGGCTCACCATCAG[C/T]GAGGCCTTTGTCGCATTCATTTACAAGACTCCACAGGCGTGCAAGACTTT
Long Flanking Sequence:
TGGTAAAATAAATAAACAAAAAAAACTGCATTTTTTTTTTGCATATTGAATGTTTTATACTGTGTCAAACACAGGAAGCAGTGGAAACTTTTAAGAAGGCCTTGTCATTTCTGGGTAGCACTAAAGCTAAACTCAGTCCTGCAAAAGAAACTGCAGAGGTCTTCTATTTAATCGGTGTATGCTACGTGACGCAAAGGCTTTTGTTTCAGGTAATAAATTAATTTATATTAGTTAATATCATAACTCCCAAAAAATATTGATTTATGAATGTTATGTGTGATCCAGATATGAAATGTAGAAATGTAGCATTTTATCAGATTCCCAAGATGTGATGATAATTTAAAAAAAAGAAGCAGATGGAAACGCAGCCATATCTGTCACTACTCTATCATCACCTTTTTTTAATATAGGAGAGTGGAGATTCTCTTCTCCTTCAGGCTTTGGATGCTTTTAACAGCACTGTGAGCTTAAACCCAGACCATGCCGAGGCTCACCATCAG[C/T]GAGGCCTTTGTCGCATTCATTTACAAGACTCCACAGGCGTGCAAGACTTTAATAGAGCTCTCAAAATCAACCCCAAGTTCTATCAGGTACACCCTGATGCTCTGTCAGGTACACTCTAAATACTATTATTTAGAGAAATGAAATTATTTATTCCATATTCCAAGTTTCAGATTTGAAATGGTTTTTCATTTTTCCCAAGGTGCATCTAAGCCGAGCTGCCCTTTATGGGGCTGAAGGACGACATGCAAAGGCCATACTCGACTGTAATGAGGCTATCAGGATCCAGCCGAAGAGCCTCAGAGCACACTTGTATAAAGGGGCTCTTAAATTCTATTTGAAAGTTAGTAAAAATAGCACCATTTTGAGCATAATTATCGTACACTTGAGGCTGATGCTCTCTGAAATATGTTGTATGTTCATCATCTTGTTTTAGGCATACAAGAGTGCAGTGGAGGATCTAACAATGGCAGTCCAAATCGATCCTGCATGTTCATTCGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25035
Status:
Mutation detected in F1 DNA
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 |
---|---|---|---|---|---|
ENSDART00000081247 | Essential Splice Site | 215 | 612 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 10323740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10121584 |
GRCz11 | 17 | 10277618 |
KASP Assay ID:
554-7351.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCTCAGAGCACACTTGTATAAAGGGGCTCTTAAATTCTATTTGAAAG[T/C]TAGTAAAAATAGCACCATTTTGAGCATAATTATCGTACACTTGAGGCTGA
Long Flanking Sequence:
AAAAAAAGAAGCAGATGGAAACGCAGCCATATCTGTCACTACTCTATCATCACCTTTTTTTAATATAGGAGAGTGGAGATTCTCTTCTCCTTCAGGCTTTGGATGCTTTTAACAGCACTGTGAGCTTAAACCCAGACCATGCCGAGGCTCACCATCAGCGAGGCCTTTGTCGCATTCATTTACAAGACTCCACAGGCGTGCAAGACTTTAATAGAGCTCTCAAAATCAACCCCAAGTTCTATCAGGTACACCCTGATGCTCTGTCAGGTACACTCTAAATACTATTATTTAGAGAAATGAAATTATTTATTCCATATTCCAAGTTTCAGATTTGAAATGGTTTTTCATTTTTCCCAAGGTGCATCTAAGCCGAGCTGCCCTTTATGGGGCTGAAGGACGACATGCAAAGGCCATACTCGACTGTAATGAGGCTATCAGGATCCAGCCGAAGAGCCTCAGAGCACACTTGTATAAAGGGGCTCTTAAATTCTATTTGAAAG[T/C]TAGTAAAAATAGCACCATTTTGAGCATAATTATCGTACACTTGAGGCTGATGCTCTCTGAAATATGTTGTATGTTCATCATCTTGTTTTAGGCATACAAGAGTGCAGTGGAGGATCTAACAATGGCAGTCCAAATCGATCCTGCATGTTCATTCGCTTACTACAACCGTGGCATATGTTTTCAGGAACTGCAACATTATGAGATGGTGAGGTTTTTTTTTTCAGCAGTGTATGCGGGATCATATATACAGAAACGTATACAAATGCAGGATATCTTTTCATCACAATTGCACTTCTGCATTTGCATTTTAATGCATGCCTGTTCTCTTCCTCCACATTATTTCTTTTTTATCTTCAAGGCTCTCAGAGACTACAGCGTGACGCTGCTCTTGGGCTGTAAGACAGAGCTTGAACTGAAAGTCTTGATAAATCGTGGCCTGCTCTATGTGGAGCTAAATGACTACAGCAGTGCCCTTCAGGTAAGCCAGAGATGTAAAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17451
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081247 | Nonsense | 377 | 612 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 10329497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10115827 |
GRCz11 | 17 | 10271861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGCCCAGAGGGACTTCCTCTCAGCCCTCCATCTCAATCCACTCTGCT[T/A]GAGTGCCCGCATTAGCCTGGCAYACAATTTACAGGTAGAGTCAAAATAAT
Long Flanking Sequence:
TGTTTTCAGATCCTTGTAAGCTGGCATTTTTATTGCTTTAAAGAAGCACTCTCAGATAAATGCGTCTTCACAAGACCACTACAGAAAAGCTGTAATTGCAGGGTGGGTTTTTTCTCCTCTTTTATATGGCATCTTTTGGGTGAATTCAATGTTTGCACTGGCAATGTCGCACAGCTTGTCATTTAATATTTCAAAAGTGGAAATTAAAGCGTTTTGAGATATTAGAACAGATGGTTCGAGCAAGAGTTATGTAATTAAACAGATATCTAATTTTGCAAGCACATCATTGAGTCTGATGATCTACTTCCTTTGTCTGTGATCAAGGCTCGGCCAGTTGCAGGAAGCTGTGGATGCTTACAGTGAAGCTGCAAGACTTGATCCCTTCTTGCAAGATTGTCTTGTGGGTAGAGGCAACGTTTTCATGGATTATGGGCACAATCAGGCCAGGAAAAAAGCCCAGAGGGACTTCCTCTCAGCCCTCCATCTCAATCCACTCTGCT[T/A]GAGTGCCCGCATTAGCCTGGCATACAATTTACAGGTAGAGTCAAAATAATTGTCTTGCTTCTTCTTGTTTCTGGCAGGTTGATCCTTCACAGCTTAACGGGTTTAGAAAGATTCCCAAGTGCTTCATTTAAGTATCTAGTTTGATACTTCTACTACAAGTAAAATAAAAAAGGGTGTGAATAATTTGTTCTTGGGAGAATTTGATCTGAAATGTTTTTTTTTTTAATTTCGACCGCATACATTTTGTTTCTTGGCAAATCTGTGCACAATTGTGATTTCCTCTGAATCTTTAGACGAGACACATATGAGATTACTTTTTCCCCTCAGGAGAAACATCTAAGAAGCAGGAGATTTACTCGGTTTCCATTTAATCTCTTTGCTGTCTAGAGGATACACTTGAGATAGTAGAAAGATTTTATTTGTGATTTGGTTTTATACTGGTAACAGAAAATGTTAGCATGGTACTTGTTGTGGGTTAGAAATTACATTTGTTGCTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42874
Status:
Mutation detected in F1 DNA
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081247 | Nonsense | 385 | 612 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 10329522)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10115802 |
GRCz11 | 17 | 10271836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCTCCATCTCAATCCACTCTGCTTGAGTGCCCGCATTAGCCTGGCATA[C/A]AATTTACAGGTAGAGTCAAAATAATTGTCTTGCTTCTTCTTGTTTCTGGC
Long Flanking Sequence:
ATTTTTATTGCTTTAAAGAAGCACTCTCAGATAAATGCGTCTTCACAAGACCACTACAGAAAAGCTGTAATTGCAGGGTGGGTTTTTTCTCCTCTTTTATATGGCATCTTTTGGGTGAATTCAATGTTTGCACTGGCAATGTCGCACAGCTTGTCATTTAATATTTCAAAAGTGGAAATTAAAGCGTTTTGAGATATTAGAACAGATGGTTCGAGCAAGAGTTATGTAATTAAACAGATATCTAATTTTGCAAGCACATCATTGAGTCTGATGATCTACTTCCTTTGTCTGTGATCAAGGCTCGGCCAGTTGCAGGAAGCTGTGGATGCTTACAGTGAAGCTGCAAGACTTGATCCCTTCTTGCAAGATTGTCTTGTGGGTAGAGGCAACGTTTTCATGGATTATGGGCACAATCAGGCCAGGAAAAAAGCCCAGAGGGACTTCCTCTCAGCCCTCCATCTCAATCCACTCTGCTTGAGTGCCCGCATTAGCCTGGCATA[C/A]AATTTACAGGTAGAGTCAAAATAATTGTCTTGCTTCTTCTTGTTTCTGGCAGGTTGATCCTTCACAGCTTAACGGGTTTAGAAAGATTCCCAAGTGCTTCATTTAAGTATCTAGTTTGATACTTCTACTACAAGTAAAATAAAAAAGGGTGTGAATAATTTGTTCTTGGGAGAATTTGATCTGAAATGTTTTTTTTTTTAATTTCGACCGCATACATTTTGTTTCTTGGCAAATCTGTGCACAATTGTGATTTCCTCTGAATCTTTAGACGAGACACATATGAGATTACTTTTTCCCCTCAGGAGAAACATCTAAGAAGCAGGAGATTTACTCGGTTTCCATTTAATCTCTTTGCTGTCTAGAGGATACACTTGAGATAGTAGAAAGATTTTATTTGTGATTTGGTTTTATACTGGTAACAGAAAATGTTAGCATGGTACTTGTTGTGGGTTAGAAATTACATTTGTTGCTGTTGTAATTGTGGCAGATGCAGTTATATT
Associated Phenotype:
Not determined