ZMP
si:ch211-256m12.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
TTC29
Human Description:
tetratricopeptide repeat domain 29 [Source:HGNC Symbol;Acc:29936]
Mouse Orthologue:
Ttc29
Mouse Description:
tetratricopeptide repeat domain 29 Gene [Source:MGI Symbol;Acc:MGI:1920551]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22741 | Essential Splice Site | Available for shipment | Available now |
| sa45560 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22741
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081826 | Essential Splice Site | 13 | 409 | 2 | 10 |
| ENSDART00000148096 | None | None | 440 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 5441679)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 4668232 |
| GRCz11 | 16 | 4497521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACCAACAGGACAACACCGACATCCAAGTAAACTCGTATTTTTCTCTC[A/T]TACTGAACGTTTTGCCTTCAAACAAAATGCGTGAATGTTTTTTTTTTTTT
Long Flanking Sequence:
CTGTGTAAATTGTATATGTGCTCTATAAATAAAACTAAATATAAACAAAATCATAAATAACACTACAGCGACCTCGTATGGTCACCAGGGAAGCTCTTCAGCTTTTGTGGACTTGAAGTATCAACAAAGCTTATATAACAGGTTATTTATTACTCGTCACTACATACCATCCCATTACTTTCAGTCATTTAAATTGAGTGGCAAATTTCTATATAAGTTTTGCACGAATTCATCTCACAGTAGTTAGTTGTCAGCTTGGTCGCTATGGCAACATTTTGTTAACGCTGACAAATCTGACAACCAGGTAACGTTAAATCGCATCTTCATACAAAGTAACGTGTCTTGTTATATCTGTCGTTTTTAGCTAAATTATAACTTCTTTTTTGTTATTTAAACTTACTCAGCAGCATGTCTTCGAAAACTCGGTTTTCTATGATCCACAGTCCTCAGAAAACCAACAGGACAACACCGACATCCAAGTAAACTCGTATTTTTCTCTC[A/T]TACTGAACGTTTTGCCTTCAAACAAAATGCGTGAATGTTTTTTTTTTTTTTGTTTGTTTTTTTTTTTTTTTTTTGTATGTTTAGGTCTTTCCCTCGGTGTAATAAGAAGAATTCCGGCAGTCCTGTTGGAGAGGAACCAAACAAAATGACTGAGACCGAAATAGCACAGTAAGACAGATACAGTTGATTATCTATTGTTTATTTTGATCGTCATTAGCCTCTATCAGTGTAGTAGCTATTCTTCCTGGGGTCCAACGAATTAAAATAATGATAAAAATAATAATAATTAAGCTCAACAGTCAAGACTAGAAGACAAATTTACATTGTATTAAAACATTTGAAAGCTATAACCAAATTTCATACAAAACATAACAAAAGACAATGATGCTAAAACCATTTTAAAAGACAAATTTAAACCATAATAATAAAAAAACTAACACCAAACATATGATACTTAAACATCAAACATATGACTTTACTGATTACTCATTCATTCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45560
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 |
|---|---|---|---|---|---|
| ENSDART00000081826 | Nonsense | 227 | 409 | 6 | 10 |
| ENSDART00000148096 | Nonsense | 224 | 440 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 5445345)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 4671898 |
| GRCz11 | 16 | 4501187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCCAGACGGTCTACACGCTGATGGCACAGAGATCTCTGCAGGATCAA[C/T]AATATGAGCAGGCCATTAAGATGTCTAGAAAGGCCTATACTATTGCTAAA
Long Flanking Sequence:
TGCTCACATCATCCAATCAGATAAGAAGAACCGAGAAGGTAGCATTTGAAGGCTTGAAAATACAAACTGTTTCTCAATTCTAAAACTGTATTTGCACGCAATTGACAAATAGTCACAGGCAAATTAAACTTTAGTAACAAGGCAACAGTGGCCCGATCGGGCCAGTAACGATCCTGTCTACTGTCCCGAGCATCTCACACGCTGGCCCCGGGCCATCAGGCAGTCCTTATTGTTGAGCCCTGGATAGAATATAGTTTGTACAGTATAACAATTATTATGTCTATGCGAAGTCCCCAAAAAGATTGCTGTAAAAGTGTCTGTGTGTGTCTGCATGTTTTACAGGTGATCTTGAGCTTGCACAAGAGCATTTGGAGGTGTTTTATCAGCTAACCGCAGGCCGAACTTGGCAGGACAGCAACGGCCGGATGCAGCACTCTCGCTCATGTGAAGAGCTCCAGACGGTCTACACGCTGATGGCACAGAGATCTCTGCAGGATCAA[C/T]AATATGAGCAGGCCATTAAGATGTCTAGAAAGGCCTATACTATTGCTAAAGAGTGTATGCACACACTGTTCACTCTTAAGGCTGATTTATACTTCTGCGTCAAGAGCACGCGTATGCTATGGCGCAACCTACACATAGACTCATAGCCCTCTCCGTGGCCGTCGCGACATTGACGCACACCTCAAAAGAATGTAACTACGCATTGCAACAACGCATAGCGCAAGTTCTGTGATTGGTCGGCTTGGTAGCACTGACGAGTGTGAGCGGGACCTCACTGCTAGCTAGTGTTTAGGAAGTGTTATTACAGAGGAACACAAACAGTGCTCAGAGTTATAAATGCACGGCAACGAGCAAGGCTTGTGCCGTGGGTCACGCCGATCTTTTGACGCAGAAGTATAAACCAGACTTGACAGTGATTTACATTAGCTATAGGTTCACAGTTGGCCATGCACCCTAACTCAACTACACTGTAAAAAAATTCTGTATTCCACTCAATCGAT
Associated Phenotype:
Not determined