ZMP
tert
Ensembl ID:
ZFIN IDs:
Description:
telomerase reverse transcriptase [Source:RefSeq peptide;Acc:NP_001077335]
Human Orthologue:
TERT
Human Description:
telomerase reverse transcriptase [Source:HGNC Symbol;Acc:11730]
Mouse Orthologue:
Tert
Mouse Description:
telomerase reverse transcriptase Gene [Source:MGI Symbol;Acc:MGI:1202709]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3430 | Nonsense | Available for shipment | Available now |
sa25076 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6541 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu3430
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 |
---|---|---|---|---|---|
ENSDART00000098884 | Nonsense | 156 | 1088 | 3 | 19 |
ENSDART00000098893 | Nonsense | 164 | 1098 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 608257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 629744 |
GRCz11 | 19 | 629553 |
KASP Assay ID:
554-0052.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTACCTGCTGCAGGACTGTGCCGTTTTCACCACCGTCCCGCCATCGTG[T/A]GTTCTGCAGGTGTGCGGAGAACCTGTTTACGACTTGCTGATGCCGCGCTC
Long Flanking Sequence:
AAAATGTTATGCAAATAAAATCAACTTAATAGTTAATTTAGTGTTAACCAGGAATTTTTTTTTACCGTAGCAGTTTACTATATATATATATTTTTTAATCAATTTTCATCATTACTGCCCTACTAAACATTGCACATCCATAACTGAGTTACGGCCAATGTTCTTCTATGTTTTCAGGATTTAAAAATATTTATGTATGTTTTTCTCTACAAATAAAAGAAATGTGTGTTATTTCAGCTCAGCACCCTGCCGGAGGTCTTGGCGTTCACTCTGAACCACATTAAACGTAAGAAACTGAGGAACGTCCTGGGCTTCGGTTATCAATGCAGCGACGTGACGACCAGTTCGGATCCCTTCCGTTTCCATGGTGACGTTTCGCAGACGGCTGCTTCCATCAGCACCAGCGAGGTCTGGAAGCGTATCAACCAGCGTCTGGGCACGGAGGTAACGCGGTACCTGCTGCAGGACTGTGCCGTTTTCACCACCGTCCCGCCATCGTG[T/A]GTTCTGCAGGTGTGCGGAGAACCTGTTTACGACTTGCTGATGCCGCGCTCATGGTCTGGCTTTTTCCTCAGTAACTCAGATAATGAACGAATCAGCGGCGCGATGCGGAAATCCCCTGCTGTCCAGAAGACAGTCGCAATTTCCAAAAAGAGAACAAGAGATAACGAAAAATATATTTCGGTAAAGCGGCGGAGGGTAAAGGAAACTGTGAATAATAATAACGGAAATTACAGATCTCGGTGTTTTGCAATTTCTAAAAAGAGAGCGAGAGATAATGAAGAAAATATTTCGTTAAAGCGACGGAGGATGGAGGAAACTGACCAAGAAGCGAAAATACGTAATGAAAATCACGGATCTCAGAGTTTCACAATTTCTAAAAAGAGAGCGAGAGATAACGAAGAAAATATTTCGTTAAAGCGACAAAGGATGGAGGAAATTGACCAAGTAGCGAAAATACGTAACGAAAATCACGGATCTCAGAGTTGGAAACCAGCGGATCA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa25076
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 |
---|---|---|---|---|---|
ENSDART00000098884 | Nonsense | 231 | 1088 | 3 | 19 |
ENSDART00000098893 | Nonsense | 239 | 1098 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 608480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 629967 |
GRCz11 | 19 | 629776 |
KASP Assay ID:
554-7560.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTCGGTAAAGCGGCGGAGGGTAAAGGAAACTGTGAATAATAATAAC[G/T]GAAATTACAGATCTCGGTGTTTTGCAATTTCTAAAAAGAGAGCGAGAGAT
Long Flanking Sequence:
GTGTGTTATTTCAGCTCAGCACCCTGCCGGAGGTCTTGGCGTTCACTCTGAACCACATTAAACGTAAGAAACTGAGGAACGTCCTGGGCTTCGGTTATCAATGCAGCGACGTGACGACCAGTTCGGATCCCTTCCGTTTCCATGGTGACGTTTCGCAGACGGCTGCTTCCATCAGCACCAGCGAGGTCTGGAAGCGTATCAACCAGCGTCTGGGCACGGAGGTAACGCGGTACCTGCTGCAGGACTGTGCCGTTTTCACCACCGTCCCGCCATCGTGTGTTCTGCAGGTGTGCGGAGAACCTGTTTACGACTTGCTGATGCCGCGCTCATGGTCTGGCTTTTTCCTCAGTAACTCAGATAATGAACGAATCAGCGGCGCGATGCGGAAATCCCCTGCTGTCCAGAAGACAGTCGCAATTTCCAAAAAGAGAACAAGAGATAACGAAAAATATATTTCGGTAAAGCGGCGGAGGGTAAAGGAAACTGTGAATAATAATAAC[G/T]GAAATTACAGATCTCGGTGTTTTGCAATTTCTAAAAAGAGAGCGAGAGATAATGAAGAAAATATTTCGTTAAAGCGACGGAGGATGGAGGAAACTGACCAAGAAGCGAAAATACGTAATGAAAATCACGGATCTCAGAGTTTCACAATTTCTAAAAAGAGAGCGAGAGATAACGAAGAAAATATTTCGTTAAAGCGACAAAGGATGGAGGAAATTGACCAAGTAGCGAAAATACGTAACGAAAATCACGGATCTCAGAGTTGGAAACCAGCGGATCAGCGTCCTCCTCGACCCTCGCAATGTTCAATACGCGTTCTGAGCATGCTCTACAATGGGCGGGGCATGAAGAACTTCCTGCTCAACAGGAAGTTGAAAGGAGTGGGCGGGGCCAGGCGCATGCAAGGGGAGGATCTTGTCCGCATGATTTTCCTCCAATCAGAATCCAACGATAGCAAACCGAAAAAACTTCCTAAACGATTCTTCGCAATGGTGCCGCTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6541
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 |
---|---|---|---|---|---|
ENSDART00000098884 | Nonsense | 440 | 1088 | 3 | 19 |
ENSDART00000098893 | Nonsense | 448 | 1098 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 609109)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 630596 |
GRCz11 | 19 | 630405 |
KASP Assay ID:
554-4929.1 (used for ordering genotyping assays)
KASP Sequence:
RAGGATATGGAGTCTCTGCTGAAGTCACACTCGTCTCCWTATAGAGTTTA[T/A]CTGTTYGTCAGGGAGTGTCTGCGCYATATTATTCCCCACGAGCTCTGGGG
Long Flanking Sequence:
GGATCTCAGAGTTTCACAATTTCTAAAAAGAGAGCGAGAGATAACGAAGAAAATATTTCGTTAAAGCGACAAAGGATGGAGGAAATTGACCAAGTAGCGAAAATACGTAACGAAAATCACGGATCTCAGAGTTGGAAACCAGCGGATCAGCGTCCTCCTCGACCCTCGCAATGTTCAATACGCGTTCTGAGCATGCTCTACAATGGGCGGGGCATGAAGAACTTCCTGCTCAACAGGAAGTTGAAAGGAGTGGGCGGGGCCAGGCGCATGCAAGGGGAGGATCTTGTCCGCATGATTTTCCTCCAATCAGAATCCAACGATAGCAAACCGAAAAAACTTCCTAAACGATTCTTCGCAATGGTGCCGCTATTCAGTCGGCTGTTGCGGCAGCACAGGAAGTGTCCGTATCGGCTGTTCCTGCAAAGAAAGTGTGCAGGAAATCCAGACGTGGAGGATATGGAGTCTCTGCTGAAGTCACACTCGTCTCCATATAGAGTTTA[T/A]CTGTTCGTCAGGGAGTGTCTGCGCCATATTATTCCCCACGAGCTCTGGGGCTGCCAGGAAAACCAGCTCCACTTCCTGTCTAATGTAAAGAACTTCCTGCTTCTGGGGAAGTTTGAGCGCCTCACGCTGGTCCAGCTGATGTGGAGGATGAAGGTTCAGGCCTGCCATTGGCTGGGGCCCAAGAAACGTGAGTGTGTGTGTGTGCATTTAAATGTGTGTATGTTCATATATATATATATATATATATATGAGTGTGTGTGTGTGTGCTTCTGCAGGTCAGTGTGCGAGCGAGCACCGCTACCGTGAGTGGATGTTGGGTCAGTGTATGGGCTGGGTGTTGAGTGGTTTTGTGGTCGGTCTGGTCAGAGCTCAGTTCTACATCACGGAGAGTATGGGCCACAAACACACACTGCGCTTCTACAGGGGAGATGTCTGGAGCAGACTGCAGGACCAGGCCTTCAGGTGACACACAGCTCACCAACACACACTTTCCACATTTC
Associated Phenotype:
Not determined