ZMP
si:ch211-284o19.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
TEP1
Human Description:
telomerase-associated protein 1 [Source:HGNC Symbol;Acc:11726]
Mouse Orthologue:
Tep1
Mouse Description:
telomerase associated protein 1 Gene [Source:MGI Symbol;Acc:MGI:109573]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38344 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6856 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32973 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32974 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38344
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 |
---|---|---|---|---|---|
ENSDART00000056536 | Essential Splice Site | 287 | 1036 | 3 | 19 |
ENSDART00000141784 | Essential Splice Site | 287 | 561 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 37641637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37920769 |
GRCz11 | 2 | 37903226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACTAGCTACCGAGATTACCACAGAAGATCCTGAGTTTGTCCTCAAGG[T/C]TTGTGCATTTGCGTGTGTGAGTGTATGCTTGTTGTGATTTTTGTAGTTGA
Long Flanking Sequence:
CTGTGGAACGAACCGCCAACTATTCCAGCATATGTTTTGCAGAGTAGATGCCCTTTCAACCGCAACCCAGTACACAGTCATACACTATGGCCAATTTAGTTCATCCAATTCACCTATATCGCATGTTTTTATGCTGAACATGGGGAGAACATGCAAACTCCACACAGAAATTCCAACTTGCCAAGCCCGGACTCGAACCAGTGACCTTCTTGCTGTGAGGAGACAGTGCTAACCTCTGAGCCACAATGCTACCCTTTTAATAATTTAAATAATAATAATAAATAATTACTTCAATCATTATTCTGCCAGATAATGGATGTTGTTTTTGTTGTTTTTGCAAATCCTTCAGAACAACCTGTTGAATATGGTGTGCTGCTCGCTGATTCAGAAGGGCTGTGCCCCAGGCCAGAAGGACTGGGATAACAAGAAGAGTGTGTGGAGCATTATCAAGAAACTAGCTACCGAGATTACCACAGAAGATCCTGAGTTTGTCCTCAAGG[T/C]TTGTGCATTTGCGTGTGTGAGTGTATGCTTGTTGTGATTTTTGTAGTTGATGCTAATGATTTTATATTTGCATTGGTTTTAGGTTGCAGTCTACACTAGGCAGGAACTGAACATTCGTATCACAGCCAACTACCTGCTGGCGTTGGCTGCTCATCTGCCTGCGTCTAAACAACACCTGAGAAGATACTTTTGTCCTGCTGTGCAGCTGCCATCTGATTGGCTGGAAGTGGCACGTCTCTATAGCATGGTATGTTCGCCTGTCATATGATATTTACACGGTATTATATATCATATTGGCTCTTCAAGGTATTTCAAAGAATATTAGCACTGTAGATTTACAAATAAGGTCTTTATTTTTCTTGTGTGGTATTATTTCAATGTTGTTTTGCTTTTTTCCTGCTCTTTCAGTGTTTCAGTAAATCTTTACCCTCTTGCCTGAAAAAAGCTCTTGTGGATAAATTTAAGCAGTTCAGCGAATATCAGCTGGCTAAATACAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6856
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056536 | Essential Splice Site | 542 | 1036 | 9 | 19 |
ENSDART00000141784 | Essential Splice Site | 538 | 561 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 37644366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37923498 |
GRCz11 | 2 | 37905955 |
KASP Assay ID:
554-4388.1 (used for ordering genotyping assays)
KASP Sequence:
GCATCAGCGAGAAACATCACTCTAAGATTCTTAACAGACTGTCCTCGAAG[G/A]TGAGCTAGATTTCTTTCAKTCTTTTGCTCACYGAAAAGTGTGCGTGTATG
Long Flanking Sequence:
ACTGTGGATGGGTGTAAACGTATCGTAGGAGGGTGTAAAACAAAATTAAAAACCTTAAGAAAAGCAAAATGGGGACACTTTAATATGTTTTACATTGGTTAACTGCTATCTTCAACTTTCTATTTTTTTATGTATTTTTTTTTTATTCTGCAGATACCCGAGTGATCTGAAGGCGTTCTCTCGCAGTGGTCTTAGTGGGGTCTGGGACAGAGAGAGAGCCGGAAAGCAGATGAAACTTAAGCAACCTGACACATGGGAGCGCAAAGTTAGTCAGGAGGGAAACAAAGCTGCCACCTGGGAGAAACTCATCGGTGTGTGAAGGAGGGACATACTGCATCTGAAACGGACATTATTTTTGAACGTCTACTTATTTAGGTTTTTAATTTGCAGATGGGAAGTCTCTTCCTTTTATGGCCATGCTCAGGAACCTGAGGAACATGATCACTGTGGGCATCAGCGAGAAACATCACTCTAAGATTCTTAACAGACTGTCCTCGAAG[G/A]TGAGCTAGATTTCTTTCATTCTTTTGCTCACCGAAAAGTGTGCGTGTATGTGTATACAGTATTATTTCATTTTTGAGTCTGAATTTTTCTTACAGAATGCTGTAATCCAGAGCAGGCAGTTTCCCTTCCGCTTCCTGTCTGCTTATAAAGTCATTTTGGAGCTCTTTAAGTTTGGTAAGTTCCTGATTTTAAAGGGCATTCAATTTAAGAGTTGGGTCCAGATGAATGCAAAAACCCAAGCTGTAAAAACTGAGTGCAAAACTTTGAGACCCTCATACATGCTTTATTTAAAATGAATATGTTCTATTGCTTTATTGCATTGTGTGTTCATGGAGGGCATTACTTTTTATGTGCAGAAGCCCTTTGCTGGAGATTAGGAAAATAATGTTGCAGACACCATTAGCAAATCCATGATTATACTATCAATACAGTTTTACTTGCATTAATTAGGGAGGCAGTAATAAAAAGTAATTATTAATATGTAACTAAATAAATTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32973
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 |
---|---|---|---|---|---|
ENSDART00000056536 | Essential Splice Site | 635 | 1036 | 11 | 19 |
ENSDART00000141784 | None | None | 561 | None | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 37646608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37925740 |
GRCz11 | 2 | 37908197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCTACCGCCTGTTCAACGTCAAACGCAGTCTCATGATAAAAGCAAAG[T/C]GTGTATTGCTCAATATTTTGTTTAAAAAAACTTTACCATAGTTTAAAGGT
Long Flanking Sequence:
TTGCGCCATGCTCTTTAGACTTTGCACCTAGATCAATAAAATAGGGCCTAAACTATGTAAAGCGAGCTATTTCCACCTTTATTTTTTTATCATATTAATGTATCTTTTGGTTAACACAAATTATTAAAAAACAGATACCCCAAACCTTTGTACAGTTGTGTATATTTAACTCGTACATTAGGTTTAAGTGTTTTAATCTACAAAACTGTTTATTATTGAAACAGCACATTTCCATAGAAACTTTTTATATTTTTATAGATGTGCTCTTGATGTTTGAGTGACATGTTTTCCCTCTTTCAGCCAGAGGAGCTGCGGTAAAAACGAAGAGCTCTACGGACATCATTCGAGACATTCTAAAGAAACTGCCAAAGACCAGACGATACAACCGAAACTGCTTGGACTGGGATAAAGCAGAACGCAAGAAACTGCGGGTTACATTGCGTGTGCCCTTTGTCTACCGCCTGTTCAACGTCAAACGCAGTCTCATGATAAAAGCAAAG[T/C]GTGTATTGCTCAATATTTTGTTTAAAAAAACTTTACCATAGTTTAAAGGTGCTTTATGTAAGTTTTTAACTGTTATTAAGCATTAAAAAAACATAATATGTTTGCAGATATTTAAGAAACATGGTAAGTGAACATTTTTGTTTATGTGAAAAACAATGCTAGGATCAGATATTATGCTTTGAAAATATGAGCTACATGCTGGAACGGCTGTCTTTGTTTTTGTTTTTTTAACCCGCCCAATGCCAGTTTAGCCAATTATATTTCAGCACCCTGCGTTGCCTTGAAGGAAAGCTGAGTAATTCATTCATTCATTCATTCATTCATTCATTCATTCAGTCAGTCAGAAAGGCTCTCAAAGTGTTTGACCACAACCAAAATGCAACCTCTTGTGGACAGTAGCAGCCTCCGAAATGAGACTCAGATTCAGAGTTCCACATGAGGTTGTAAATTAGCAAATAATATAAGTATAACGAGCGTAAACATTGGGTGAGAAGGTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32974
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 |
---|---|---|---|---|---|
ENSDART00000056536 | Nonsense | 878 | 1036 | 17 | 19 |
ENSDART00000141784 | None | None | 561 | None | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 37652954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37932086 |
GRCz11 | 2 | 37914543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTGGAGAACATGGACAGAGTCTATAACATCCCACCACCACAAGGATG[C/A]CAAAAGGAGCCTGAGAGATCTGCTGACGTCATGCCACTTCAAGCAACACC
Long Flanking Sequence:
AACCTGCTGAATTAGCTAGATTTAATAGATTTTTATTCAGTATATGAATAATCTTTTAGTTTTGAATTAGTTTTTTTACATTAATATTTAGTAAATATACTAACATATACTAAATTTAGTTATTCAAGTAAAATATCGCCAGTGTTTCCAGTTAAAAAGTAGTTATAAGGTCTTAAAATGTATGGAAAGAGTCATTAAAAAGATCTTCAAAAGGTATTAAATTTTACTCTTTAATTCCTGTATATACTCTGATTATAGACATGAGCTGCTGCATCTGTGTGCTTTAATATGTACATTGTAGATGTTTTTTATGCATTTATGCTTGAGCCGATTGCATGACTACATTTGGATGTACGTTCTCTCAGTGGCTGGAGTTGTTTTAAATGCTCATTCAAATGTGTTCTGGGATGTAGGTTTGTTTCTGAGAGAGGCTCTTCAAGGATGCTGCAGCATGTGGAGAACATGGACAGAGTCTATAACATCCCACCACCACAAGGATG[C/A]CAAAAGGAGCCTGAGAGATCTGCTGACGTCATGCCACTTCAAGCAACACCAAAGTTCAGGTATGACTATTAAAAAAGAATATATAAAAGATAAATAGATCAGTAACTTTGTCCAATTTGTGTCTAGAATAAGTTCCAGTGTAGAACAAAATAAGCTGTGAATACGAAGTTCTGAAAAATGGTTGTCATTTAGAGCATGCTTTTTCTCAGAAAAGTACAATTATTCAGCATTGGAATTATGTTTGTCTAAAAAAATAAATACAAAATTACACACTTTTTTTGTATTTTATGCAAAAAATGCTCTAAATAATTTTTTTATTTCAAATGAGGAAAAATGTTATCAGTAGTTTAACTCAAGCACACAACAATTAAGTGTTTTTTTTCTCCATAGCTCTGTAAATGTATTGTTAGAAGGTCAAATATATTTCCCACCCTAGATAAAAAAAAAGAAAAAAAAAACATGAATTGAGTGTTATTCTGAGATAACAACCACTGAATAAC
Associated Phenotype:
Not determined