ZMP
TTLL5
Ensembl ID:
Description:
tubulin tyrosine ligase-like family, member 5 [Source:HGNC Symbol;Acc:19963]
Human Orthologue:
TTLL5
Human Description:
tubulin tyrosine ligase-like family, member 5 [Source:HGNC Symbol;Acc:19963]
Mouse Orthologue:
Ttll5
Mouse Description:
tubulin tyrosine ligase-like family, member 5 Gene [Source:MGI Symbol;Acc:MGI:2443657]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31017 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43017 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13692 | Nonsense | Available for shipment | Available now |
sa12240 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31017
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103339 | Nonsense | 16 | 343 | 1 | 11 |
ENSDART00000103339 | Nonsense | 16 | 343 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 52467565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51852220 |
GRCz11 | 17 | 51941255 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGATGCCAGACGCTAGAGAGCAGAAGGACGAATCCAAGTCATCGTCT[G/T]AAGATGAGCTGGAGTAAGTGTCTTTACCACTTTAAGACTTTTGATCATGC
Long Flanking Sequence:
CACTGAGGTGCCACCTATTGCGCGCATGCGCATCTCAGCGGCTGTCAGCTGGTTGTTATAGTAACAAGCGTCAGGAGTTTAGCACCGGTGAACAGTGGAGCTAACAGTTAATAATTACACTAAGAGCTCTCACATTACACAACCAGGTATGTTACTAATAACACATTTACTAACAAACTAACTGCACTGTGAGGCCGAAGATCTAATGGAATGTTAGACATTCAAGTGGCTGCATCTGGTTAGCTCGGGCTAGCTAACAGCTAGTGAACTCTCTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCTTACTATTTTGCAGCTGCATTAAGAAGATTGGAGAAGAGAGCTGTCATGCACATGCTGAGCTGACACACACAGACGGAGATGCCAGACGCTAGAGAGCAGAAGGACGAATCCAAGTCATCGTCT[G/T]AAGATGAGCTGGAGTAAGTGTCTTTACCACTTTAAGACTTTTGATCATGCAGAATAAGTTCAGATAACGAGTGAGCAAGACTTGTGACTTTACCATCACCACTACACACAAAACTACAGCAGAGACACCCCATGGTGCACATCCACAGACGGATGACTTCACAAGGGTTATTGTGACTTGACAGGGGTGCGTTTATCAATCAACAACGTAACTGGCGTAACTAACATAGTACGATGCATCATTTGGGAAAAGAACGATGTAGTGATGAGTGTTTCCCAAAACCTGTACTTACTCTATCTCAGATTCATCGTTAGTTATAACGTAAAACGGCCATAGTGATGCTCTAAACTGGCTGAAGTAACAACTTCTTTGGAGATGAACCCCATCATTTCTTTGTGTAAATTATATTGTTTTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGTAGAAAAAAATCCAATGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43017
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103339 | Nonsense | 16 | 343 | 1 | 11 |
ENSDART00000103339 | Nonsense | 16 | 343 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 52467565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51852220 |
GRCz11 | 17 | 51941255 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGATGCCAGACGCTAGAGAGCAGAAGGACGAATCCAAGTCATCGTCT[G/T]AAGATGAGCTGGAGTAAGTGTCTTTACCACTTTAAGACTTTTGATCATGC
Long Flanking Sequence:
CACTGAGGTGCCACCTATTGCGCGCATGCGCATCTCAGCGGCTGTCAGCTGGTTGTTATAGTAACAAGCGTCAGGAGTTTAGCACCGGTGAACAGTGGAGCTAACAGTTAATAATTACACTAAGAGCTCTCACATTACACAACCAGGTATGTTACTAATAACACATTTACTAACAAACTAACTGCACTGTGAGGCCGAAGATCTAATGGAATGTTAGACATTCAAGTGGCTGCATCTGGTTAGCTCGGGCTAGCTAACAGCTAGTGAACTCTCTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCTTACTATTTTGCAGCTGCATTAAGAAGATTGGAGAAGAGAGCTGTCATGCACATGCTGAGCTGACACACACAGACGGAGATGCCAGACGCTAGAGAGCAGAAGGACGAATCCAAGTCATCGTCT[G/T]AAGATGAGCTGGAGTAAGTGTCTTTACCACTTTAAGACTTTTGATCATGCAGAATAAGTTCAGATAACGAGTGAGCAAGACTTGTGACTTTACCATCACCACTACACACAAAACTACAGCAGAGACACCCCATGGTGCACATCCACAGACGGATGACTTCACAAGGGTTATTGTGACTTGACAGGGGTGCGTTTATCAATCAACAACGTAACTGGCGTAACTAACATAGTACGATGCATCATTTGGGAAAAGAACGATGTAGTGATGAGTGTTTCCCAAAACCTGTACTTACTCTATCTCAGATTCATCGTTAGTTATAACGTAAAACGGCCATAGTGATGCTCTAAACTGGCTGAAGTAACAACTTCTTTGGAGATGAACCCCATCATTTCTTTGTGTAAATTATATTGTTTTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGTAGAAAAAAATCCAATGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13692
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103339 | Nonsense | 22 | 343 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 52468910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51853565 |
GRCz11 | 17 | 51942600 |
KASP Assay ID:
554-7932.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTTGGTACCACARAAGAATTATCCGTACACKCTTTGTCYRACAGGAAA[C/T]AGCCGTGTATCGCCTGGAGTGGTGTCAGTAAACGCATTCCTGTGCTGCTA
Long Flanking Sequence:
TGCTCACGTGGACTTCCCCTGAATCCCCCGGTTTCCTCCCACCATCCAAAAACATGCAGCTTAAGTTAATTGACTAATCCAAATCGCCACCATAGACATGCTCCTAGTCAGTAGTTATCTCTTAAGAGCGATCACTGTCTGTTCATTAGCTACTACAGCAGGGGAGTTCTCAAGATCTACCTAAGCTCAAACTCCCCTCTCGCCTTGCAAACAGTAGGGAGCCCCAGACTCGAGGATCTTATGAGCTCAGGGCTCTCTCCCGGGACAGCATGCCAAACAAGCTTTAAAATCAGTCATCAGCTAAGTGTGAACTCTTGAATTGGAATATGTGTAAACGGCACATTTAGGGCCTGTGTTTACAAATATTATTTGATTAAGTGCAATTAAGATGATTAAATGCAATGAATGGCTCTTGCCAACACACTGGTGAACTGACTTTCCTTGGAAGAGACTTTGGTACCACAGAAGAATTATCCGTACACTCTTTGTCCAACAGGAAA[C/T]AGCCGTGTATCGCCTGGAGTGGTGTCAGTAAACGCATTCCTGTGCTGCTATTCTGTGCTGAAGCCATTGTGTCTAAAGATGTGGCCATCCGCTCTGTTGGAGGTATACAGACACCAATTATTCATAATACAGAGGAATTTATTTAATCATAGTTCTGCACAATGGAGAAATTTAAAGGTGACTTTTGTTGACATTTTCAGTTTTGTCGATTTTTTTATTTATTATTTTATTATTTTTTTATTTTATTTGATTTGTGTTGTGTCAAACTCGTGCAGACATTTTGTTATAAACTGTCTGAGTTTCTTTACGTATGATAATTTGAGCCGTTTGAATCACCTACCAGTTTCGACGTAATAAGCTAGTTCTTTACATGCACGTACAAAATGGTGTATTTAGTATTTCTGCATTTGTACACCAAAGTGGTTCTTTATTAATTTATTACTATAGCCGTTTTAACGGTGTGCACTGCCTGACAAAAGTCTTGTCGTTGATGCCAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12240
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 |
---|---|---|---|---|---|
ENSDART00000103339 | Nonsense | 248 | 343 | 9 | 11 |
ENSDART00000103339 | Nonsense | 248 | 343 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 52481747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51866402 |
GRCz11 | 17 | 51955437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGTTTTCCTGCTCGGTTGTGYGTGTTGTAGGTTTGCCACRGTGAAGTA[T/A]GACCACGCCACTGCAAACATCAAGAACCAGTTCATGCATCTGACCAACTA
Long Flanking Sequence:
CTGTTGACTAGTGAGTAGATGAGTTTACTGTGTGCTCATACACACCAATTTTATGAAATCTAAAAAAAATAGATGAAAAATGAACTCTAGCCGCCACCAAACAATTATTCAGAAGAGTTAGCAACCCCAAACACCCCTCCAGTGCGCAAGATAATTAGTCATATACTTTTAGTTAATAGTTTTAAATGTAAACTTTTTCATATGTCATCCAGTGAAATAACACTGGATGGATTCATCAGTTTCCCATCATACTGCCCTCATGACCACAGTGCTGGTGTTGTGTGTTTTAGTTGGATGGCTTTTACAAAATCTCTGTTAATGTAATGTGTCACTTTAATATTAGATAGATGTATGGCCGGAATTGAAGGCCGTCTCGAGTTTACACGAGACTGCTTGCTTTGGTTCTGTACCTGTTTATTCTTTTCAGCAGGTCATAATCGCTATTAAGCTCATGTTTTCCTGCTCGGTTGTGTGTGTTGTAGGTTTGCCACGGTGAAGTA[T/A]GACCACGCCACTGCAAACATCAAGAACCAGTTCATGCATCTGACCAACTACAGCGTCAACAAGAAGAGCAGCGACTACGTCAGGTGGCTTTTCACAGCGTTCATCTATTTTTGTGTATATCGATATGTACAGTTTTACATTTTTGTCTGCTTATATTTTATTCATGTCATTTAAAATGTTAAGCCTTTAAATTGCACTTTAAGCTGAATTTAAGTTACTTGCTAAATAACTAGTACAATATTATGTGCTGTCATCATAGCAAAAATAAAATAGAGGTATTAGAAATATTATGTTTAAAAATGTGTTGATAAAGTCATTTGGGAAATATGCAAAAATTTAATGTACATTTCATAGTAAGGTAAAAAAAAAAAATGTCTTAAACTATACGTTATGTGTTCAAGTAGACAGTCCAGAATCAATATTAAACCATAAAATGCTCATTTTTAAATAAATGCGCAGACTGTAAACCGTAGAATGTATTGTGATCATTGACACCTTTT
Associated Phenotype:
Not determined