ZMP
terf1
Ensembl ID:
ZFIN ID:
Description:
LOC566954 protein [Source:UniProtKB/TrEMBL;Acc:A7MD83]
Human Orthologues:
TERF1, TERF1P2
Human Descriptions:
telomeric repeat binding factor (NIMA-interacting) 1 [Source:HGNC Symbol;Acc:11728]
telomeric repeat binding factor (NIMA-interacting) 1 pseudogene 2 [Source:HGNC Symbol;Acc:38110]
telomeric repeat binding factor (NIMA-interacting) 1 pseudogene 2 [Source:HGNC Symbol;Acc:38110]
Mouse Orthologue:
Terf1
Mouse Description:
telomeric repeat binding factor 1 Gene [Source:MGI Symbol;Acc:MGI:109634]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32480 | Essential Splice Site | Available for shipment | Available now |
sa24459 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32480
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106008 | Essential Splice Site | 278 | 386 | 8 | 10 |
ENSDART00000134482 | Essential Splice Site | 257 | 365 | 8 | 10 |
ENSDART00000139212 | Essential Splice Site | 253 | 303 | 8 | 9 |
The following transcripts of ENSDARG00000058710 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 13245293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 13196741 |
GRCz11 | 24 | 13341160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTACTTTCATTATAATTGCTTTAATAACTGAAGTGATTCTGTTATGCA[G/A]ACCCAAAAGAAGACTTCTTCCAAAACAAAATGATCCATGGAAGCCAGAAA
Long Flanking Sequence:
GGTGGTTTAGATCCCTCACTCTGCAATTTAGTGACATTTAAAACAAAAAGGGAATGAAAAACTAAACAAATTATAGTGCATTTCGCTATAAACAGCATTTATCAATCTGACAAGGCACATTTCAGATGATAAATGACATTTCATTCTAGTCACTTATGAATGTAATAGCCCTTTTTAATTATTGAACATCTTTATTTATAGATATGATTAAGGTTTTATTTATAAATATTATGTGCACTTGAGCTAATGATGTCTTTATTTTCTGCTTTTGTTTCCATACAGAAATGAGGAACATGAGGATCCACTTGTGGTAAATATCAGGTGAGGTCTTAAAGTGGTTTCTGCACCAGAATAAACTTCCAAATGTATGAATATTAAGAGTCACTGTAATGACTCACTTTTAATTATGATTAGTGAAACTCTCCTCTCCTATATTTAAAGACTTTATTCCATTACTTTCATTATAATTGCTTTAATAACTGAAGTGATTCTGTTATGCA[G/A]ACCCAAAAGAAGACTTCTTCCAAAACAAAATGATCCATGGAAGCCAGAAACTGCAAAGAAAGCTCACGCCACACTCAAGAGAACCTCTATTTGCAGTAAGTTAACTCCAGTAAGGGAGTGCTTTCCCTGGTTGAACTTTTAATTTTTAGTATTGATCCTTTGAGTCTATTTCCCAATAAGTGATTATTTTATTCTCAATTCAAGTGATGCAAATTATGCTTTATTAGCAAATTATTCATATCATTTTTTAATTTGAAACTTGGTTAGTGGTTTCCATGTCTAATAAACAATGCGTACTATACACAGTTCTTTAGAGAGTCCCTACCTTCCATGTAGTGTGTCATTTTGCTGTTTTAAAATGTGAAAGTGTATCAAATCTCAAGAAAGAATCAGTTGAATCTCAACTGCTTAAATTAGTCAACAGCAATTCCAGTTTCACTTTCATAACTGGTCTGCATAGTCTAAATAAACCCTTTATTTATTTATGGAGCTTATTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24459
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106008 | Nonsense | 335 | 386 | 10 | 10 |
ENSDART00000134482 | Nonsense | 314 | 365 | 10 | 10 |
ENSDART00000139212 | None | None | 303 | None | 9 |
The following transcripts of ENSDARG00000058710 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 13241948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 13193396 |
GRCz11 | 24 | 13337815 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAGAATCAATGTGTTGTTGTTTTTTGTTTGTTTGTTTTTTCAGAAAT[G/A]GACTGATGTAGAAGACAAGAAGCTGAAAGCAGGTGTGAAGAAACATGGGG
Long Flanking Sequence:
CCTTCAAACCTCAAAAAAAAACATTAATATTGTCAAGATAATGGTCTTTAAAATGTGGATCACAACATCAATGAAGTCTTTCTTTGTGCAATTATTCATATTTAACCATTGATGAATATTGGTCTTATTCACACAGAGGTTTCCAGGAGAAGTAATACCCCTTCCGAATTACACAGCAATATTACTGTGTCACGCCATTCCAGGAAGGTGAGTTACTTCTCATTGTCTTCCTTTCTAGTGCAAGCATGCATTTAACATTTTTTTCATCTTTATTTCTATAGCGCTTTTACAATGTAGATTGTATCAAAGCAGAAGTTCTAGTCAATTGCAATTGAAATTATCGGGCCAGTTTTCAGAGCTGAAGTTCAGTTTAGTTTAGTTCAGTTCAGTGTGGTTTAAATTTCACTGCTGAAAGTCCAAACACAGAAGAGCAAATCCATCAAAACATATAAAGAGAATCAATGTGTTGTTGTTTTTTGTTTGTTTGTTTTTTCAGAAAT[G/A]GACTGATGTAGAAGACAAGAAGCTGAAAGCAGGTGTGAAGAAACATGGGGTTGGCAAATGGAGCAAAATCCTTAATGACTTTGATTTTGACAATCGCACCACTGTTAATTTGAAAGACAGATGGAGAGTCCTAAAGAAACAGAATCTTGTCTCTTGAGCTACAGCTGCCTTCTGCTTTTAATATTTAAAGACATTTCTTGTATTTCAGTTCTCAGCTGTGCATAGTGCTTGTGCAATATATATTTATATTTTAATGGTAGATGTTTTTTATTTCTTTAAACCAATTTACTTTATTTAGTTTACAACATAACCAACATTTTTTTACGATGTCACAGAATTTCAGCAGTTATACATGTCATTTCACACAGCAAGTAAAAAATGTTAGTATTTTTTCTGAATTGATTAAAAGCTTTCAGCATTATGTTGCCATTTATTTAAACTGTAAGACCAACATTTGTCCAGTAGAGGATGCAGATGAGTCTAGAGTAAGCTTTGTTTTG
Associated Phenotype:
Not determined