ZMP
ttc17
Ensembl ID:
Human Orthologue:
TTC17
Human Description:
tetratricopeptide repeat domain 17 [Source:HGNC Symbol;Acc:25596]
Mouse Orthologue:
Ttc17
Mouse Description:
tetratricopeptide repeat domain 17 Gene [Source:MGI Symbol;Acc:MGI:1921819]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38640 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41006 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38640
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 |
|---|---|---|---|---|---|
| ENSDART00000065864 | Essential Splice Site | 100 | 1198 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 51805404)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50075640 |
| GRCz11 | 7 | 50348416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTCATGCAGCAAGAAACCCGTGTGAACTACCTCAAGAAGTTAGAGG[T/C]GATTTTAACCCTCATGTTCATCATAATATCGTTGTAGAAACTTGGATAAT
Long Flanking Sequence:
ATGATATTGAGGTAAAGTTGGTTTGTTTTTGATCAGTGACACGGTGACTATATTGTTTACCATGCTACTTTGAATATTTGGTCTGAAATCGAATGTAAGTATGACTTCAACACAACATTAGCACTATTGAATTGACTGAACAATCTTGTACTTTGAACGTCATTGGCTGCTTAACATTGTATGATTTCCCTGTTTAGGGTTTGCCAATAATACTTTTCTGAAATTATATTATTAAGGAGAAATTCTGAATATGAAACCAGCTTTACCTCAGTAGCGTGATTTGTCTTCTTGATGTCATTTAACCTCTGACCTGATTCCTGTCAGACAGAGTGACTCTTGCTCTTAGCATGTGTGTGTGTGCGCGCATTGATTTTACACTTTGCCTTTTGTGTGTTCTTTGGTTTTTTAGGTGGACTCTCCTCTTAACTTGAAACATCCCCACCATTTAGTTCTTTTCATGCAGCAAGAAACCCGTGTGAACTACCTCAAGAAGTTAGAGG[T/C]GATTTTAACCCTCATGTTCATCATAATATCGTTGTAGAAACTTGGATAATGTGCAGTGTTATGTTAAAGACTAATGATGTTTATACTTTGCTAAACTATCCTGACAGCGAGGTATTGTACATTTTTGCAGAAACAACTAGTTGCTCAGAAGATTCACATCGAAGAGAACGAGGACCGGGATACTGGTCTAGAGCAGCGACACTACAAAGAAGATGCGGACTGTGTCACAGCTAAAGTTCCTCTGGGAGACTTGGATCTTTACGATGGCACGTTTATATCCTTGGAAAGCAAAGATATAAAGTAAGTGTCATTTGTTTTACGGAGGTGTTTTTTTCATGATAAAATTAAGATTTCACATGTTCGTTCAGTATTAATTGCTCACCGTCATGCCGTTCCAAAGCCCTGAGATCTTTGTACGTTTTTGGAATAAGAGTAAAGATATTTAAGATCAAATCTGAGAACTCCCTCATCCTTCATAGACCTCAAGGGTCCCGACTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41006
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000065864 | Nonsense | 948 | 1198 | 20 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 51762049)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50032285 |
| GRCz11 | 7 | 50305061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACGAACACAGATGTTTCATCCTAATATTGGGTGTTTACAGAGAGGTG[G/A]AAGGACTACAGCAGTCTTGGTTGGCCTGGTCCTGAGGAGTGCCAGCGCAC
Long Flanking Sequence:
ACGATATGTTACTGAAAACCATTGCATCCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATATATATATATATATATTTATTTATTTATTTATTAAATATATGTGTATCAGTATTGTCAGTTTTTAGGATATCTATAATCTAGCGTTTAATATTATATATATATATATATATATACATACACATTTTAATTGAACTTTATTGTGGTTTTTATTTTGTTTAAAGTACTTATTTTGGTTTGTTGAAAAGGTAATCTTTCTATTTAGCTTCATTTTTATTTTTATTTTATTGTTAATGTTCACAGTTATATTATTTTAGTCTGTTGACATGACAATATCTATGTGTTTCATCAAATATTTGATCATTTTTGTATTAATGTTTTATTTTATCGTAATAGTTTTAGTACCAGTACGAACACAGATGTTTCATCCTAATATTGGGTGTTTACAGAGAGGTG[G/A]AAGGACTACAGCAGTCTTGGTTGGCCTGGTCCTGAGGAGTGCCAGCGCACCCGCCGTGTGGACCTCACCACTGTGGCGAGCACCTGGCTGGCAGTTTCTGCAAAAAACATAGAGTAGGACATCATTCATAGCTTCATTCTCTATCCTCAAACACATTTAAAATACTATCATGCTTGTGTTTTGTCTTACACTTACTTGTGATTCTGATTTTTTTACAGTATCACAGAGCACATCGACTTTGCCACTCCGCTCCAGGAGCCAGCAGTGGAGCCTGTGTGTAATGCCAACCTCCCTGCCAGCATGCACACACTGGACCACCTGAGCGGGGTCGCCAACCGCGGAGGCATTCACTACACTGGAGAAAGTCAGCTCAGAGAGGTGCGCATTTCTCCTCTTTACAGCCATCACAAGGCCTGTTGCCATTATTAAAGGTTGCATGAAGTGCTTAGAAATATGCATTTTTATTCGATGTTTGATGTAATCTCAACATGAAGAGAGTG
Associated Phenotype:
Not determined