ZMP
ttll7
Ensembl ID:
ZFIN ID:
Description:
tubulin polyglutamylase TTLL7 [Source:RefSeq peptide;Acc:NP_001074064]
Human Orthologue:
TTLL7
Human Description:
tubulin tyrosine ligase-like family, member 7 [Source:HGNC Symbol;Acc:26242]
Mouse Orthologue:
Ttll7
Mouse Description:
tubulin tyrosine ligase-like family, member 7 Gene [Source:MGI Symbol;Acc:MGI:1918142]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38825 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35024 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41784 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38825
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000091617 | Essential Splice Site | 457 | 505 | None | 13 |
| ENSDART00000101561 | Essential Splice Site | 457 | 917 | None | 20 |
Genomic Location (Zv9):
Chromosome 11 (position 8192963)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 8037066 |
| GRCz11 | 11 | 8046905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATAATCAGATAAAACCCTTTTTTCTCCTCTCTCTCTTTCTCTCCATAC[A/T]GACGTATTTACCCCCCAGATGACAAGCTGCTCTTGGAGAAATATGAGAGT
Long Flanking Sequence:
CAAAGTATTATTTGTTGTTCCTAAAACTTGGATAGCGACAAGACTTTTGTCAGGTAGTGTCGAATAATAAGTCCACCATTAGTGAACAATACCTTCTGAAAATGTGTTTGTTTCAGTGTGACTGAAAATATGAATACATTCAAAGCACAATTTTGTGCCGTAGGGGGTCTCCGTCTGATGCCTTTTGTTCAACCTGGGGCTGAAGCAAAGCCAGTTGCTGGTTTTGATTATATACATGACCCAAAACGGAGCTGATCTGAAGATCCATCACTGAGATATAGGCAGATGTTTACACATCTTTGGCTTTTGTTTAGTCTTAACGTCTAATACAAAGACAAGTTTATTAATCATTAGAATATACACAGCATAAATGGACAAACGTATGTGTGAAAAGAACGATCGAGGTTTGTTTAAGTGATTAGAAAAGCAGGCAGACCAGGCTGCTAAATCAGATAATCAGATAAAACCCTTTTTTCTCCTCTCTCTCTTTCTCTCCATAC[A/T]GACGTATTTACCCCCCAGATGACAAGCTGCTCTTGGAGAAATATGAGAGTCTCCTTTCAGCTGCCTTTCAGACATTCCTCGCTGGGCGAGCAGCTTCACTTCAAAAGGAAATGAATAATCCACTGAAACGAATGAAGGCATGTACCTGAGACGCAACCCAACAATCTTTTGCTCTTTTTCCCCTCTTTCTCTCCCCTTTACTACAACTGCTTCCTACTATTTAATCTTTTGAATTTAAAATAAGAAATGTGGAAAAGAAACTATTTTGCTTCCTAACTCTTTTTGTGGCCATCTGTTTTTCTTTACCGCAGCTTAAGGCAGCCATCAGTAATACTGCTCATTCAAAGGGTTAGGGATTTAGACTAACCGTTTGTGCTACAGACATGAATGATACCTCAAATCATGTGGTTAGTTGAGGAGAGGTGTGCAATTACTTTTCAAAGCACTGATAGAATTTTTTTTTTCTGGCACTCAATACTGCTCACCCATTGACTGACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35024
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 |
|---|---|---|---|---|---|
| ENSDART00000091617 | None | None | 505 | None | 13 |
| ENSDART00000101561 | Nonsense | 605 | 917 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 11 (position 8158603)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 8002706 |
| GRCz11 | 11 | 8012545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTGGAAACCTGCCCCTAAACCAGTGCGGGGTCCTTCCTCCTCACCCTA[T/A]CTTTCTGGATTCATCCGCCGCTCTATGTCCTGTCCCCGCTCCATATCCTC
Long Flanking Sequence:
TGCGAGTGATCACCGGTGATTGGGTTTCTGCCAATCGGGGCATTAGGCCGTTCTGCGGTGACATTGTTTGCCCCCTTTGCCCCACACTACCCTGAGGCCATCTGCAATATTCCAAGCTAAGCTTCTATAATACCACATTTGGCAGGTTCTTCCCTCAAGATTCATGGATGAAGCAGCGATGCCTCTGGCCAGCTCACAAGCTGGAGGTCATTCAAAATCACAGATTTTGCTCGATGTGTGTTTCGGTTCACTGTTCGCCTTGAGTTTGGAAACTTGACAGCCACTCGGGCCTGCAGTATGATCACATGGTGGAGTGATTCATTAAAGCTTTTGGTTATTGGATTTGAAATGCTAGATTTAATATCCACAGCGATCCAGGAGAGGGTGTGGGAATGAATGTGCCTTAAATTGAAGTCAAATGCTCTGTTTTATTTTGTCTTAGGTCGTGTTCATTGGAAACCTGCCCCTAAACCAGTGCGGGGTCCTTCCTCCTCACCCTA[T/A]CTTTCTGGATTCATCCGCCGCTCTATGTCCTGTCCCCGCTCCATATCCTCTCTGACTGCGCAGTCACCTACCAACGAGACCAGGCAGCCAAAAACAGCCACTCAAATGGCCAACACGATGACTGCTGCAGCCACTCAAACTGCAGCCACCATGATGCAGATGACCCCAGTTCGACCCCACACAGCATCTCGTTCCCAGTCGCTCAGTCGCAACTGCTCTACAAATAGAGTTCCACACAGCAGCAGTCTAGGTGCCATTCACCCCAATTCGGCAAGTATTGAATCTGTCACACTGGAGCTATTTGAAAATGTGCGTTGATTACCTTGAGCCACCATCACACACTTCTCCTTAGAGCTCGACAGAACTGAACTGAGTTCCCATGTATGTTTGCTTACATCTCGAGGTAAAACAACCACAGAAGAAGTCATCTGAAAAGGGACATGACGTTTATATACAATGCATGTCAAACATTAAGTGACCATTACAATATCACAATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41784
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 |
|---|---|---|---|---|---|
| ENSDART00000091617 | None | None | 505 | None | 13 |
| ENSDART00000101561 | Nonsense | 806 | 917 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 11 (position 8147213)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 7991316 |
| GRCz11 | 11 | 8001155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTACGTCTGTATCGCCTCTTCAATCGTGTGTTTAACCGTCTGCTCTG[G/A]AGCCATGGTCAGGGGCTCTGGAACTGCCTCTCCACCTCTGGGTAAGAGAT
Long Flanking Sequence:
AAAATATTGCAATGTCTGATTTTTCCAATATCATGCAACCCTACCATTTCCGCCTTGTAATGCAAAACCCACACAAAGCATGGTGGGAACTACACCTTTTTTTAACCAGGTAGTTACACCAACACAAAACAATTAAATTAACTTTTACATATGTAAGTGGATTAAATGGAAATAAATAAAGTGTTCATTGTTTCAGCTTATTTTAAACAAGTGATTTAAACAAGCAGCAACAATCGTTTTTCTGAGTGTAGCCTACTTTTTTGAAGTGCTTAAAATCCCCATTTCTAGACATGAGTAGATTCTAGCTTTTTAAATTACAGTTTTTCCCCAACATACTCTTGTATTTTTAGTTATTTTTATCTATCTGATCCTTTTATGTAGGTTTTGGATATTGTCCGTACCAACATCCGCTCAGTTCTGCAGAGGATTTGGAGTGAACCAGATGTGGAGAGTCTACGTCTGTATCGCCTCTTCAATCGTGTGTTTAACCGTCTGCTCTG[G/A]AGCCATGGTCAGGGGCTCTGGAACTGCCTCTCCACCTCTGGGTAAGAGATTGAAATGATGATATCCTGAAGTCAATGTAAAACTGCCATTGCAATTACCTACAGCCAATGAGAGAGCAGCATCCACTAGTATGGGTATCTGCCAGCCAGCAGGAGGTTGGGAGAGAAGTGTAAAGGGCTTCTTTTAGGTCTACTTAGACCCAAGAAATGAATGAAAAGCAAGTGTAAATTTGGCAGGAGAACTTGTGTTTGTTTAACGTGTCATCTGAGGAATACCACAACCAGGGCGCAAAAGGAAAAGTTCAAGAGAAATTGCTAATTCCCTTCAAAGCCCAGATGAGCAAAATAAGTACAATTTCTACCCCACTTAAATAATAACAAAAAATATACTACATGACCTTGTGTTGTTGCCATGTCATTTTTCGCGCATTTGTGGCTGCAAGATGTAGTTTGCGGACCAAGATACAGTTGTCAGTGATTTTTCCTTTTGTAAAGACATTC
Associated Phenotype:
Not determined