ZMP
si:dkey-228d14.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate tet oncogene family member 3 (TET3) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
TET1
Human Description:
tet oncogene 1 [Source:HGNC Symbol;Acc:29484]
Mouse Orthologue:
Tet1
Mouse Description:
tet oncogene 1 Gene [Source:MGI Symbol;Acc:MGI:1098693]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42172 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6292 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11214 | Nonsense | Available for shipment | Available now |
sa22265 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42172
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 |
---|---|---|---|---|---|
ENSDART00000109642 | Nonsense | 133 | 1855 | 1 | 10 |
ENSDART00000141009 | None | None | 559 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 18252073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18072108 |
GRCz11 | 13 | 18203100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAAAATATCCAGACACACGACTAGTTCTTTGAACCAAAATGGCTTAT[T/A]GTTGGAATGTAATGGGAAGGGGAAGTCACCTAGAAAGAGTGTCTCATGTC
Long Flanking Sequence:
ATTCACAACCCCCATATATTTCAAGTGATCTTTAATGAGATGCTACATCTTGCTACACAATTCAGTAATAAATGGTTCTTTCCACAGGTACCCATATGTACATATGTCAACATTGATTTTACTTCAAACAGGGAGCATTACATTAAAAGTACAGTTTCTCAGACGGCCTCAATACTGTTTCTCATGCCGGCTATCCCAAACTCCTCCTCCCTCACCCTCACTCACTTCAGCTATGCCTCGTACTGCCAAAGCACCCAAGAAGTCAACTCGCGCATCCACAAAGCGAAATGTTAAGAGGGTGAAGGCTTCCATGACAAGGAGGCAAACAATTAACTCACTGAAAGCCAGTGGTGAGATCAAGAAGGGCATAGACAAGAAACAGGCGGCCAAGAGGGCCCAGAGGACTGTTGTCAGCAAGCCTAACAAGAAGACTGTTGAGGATGTTCTACCTGTTAAAATATCCAGACACACGACTAGTTCTTTGAACCAAAATGGCTTAT[T/A]GTTGGAATGTAATGGGAAGGGGAAGTCACCTAGAAAGAGTGTCTCATGTCCGAGCATCCAAAGGGATGTTCAGAAAAAGGGAGCTCAGGAGATCAGGGAACAGGAGACTGAGACTAAAAGGTCAGAAGTGAATGATCCTAATGGTGATGCTGAACAACAAAAAGGTGCTGAAATTCCCACTGGAGAGGGACAGAGCGTCAACATAAGCTCTAAAGAATCTGGGGAGGAGCACAGAGAGACTGTTGTTAATGACACTTTAGTGGCAGAGAAGAAGAAGGTAAAAGTGAACACAGAAACTGTACAAAGTGAAAGCTATTCTGCTGTTGTTGAGCAGCCAAACACGGTGTTTGTGGATCAGCAAGATCCTCTGAAGCACAACCCTGTCAATAATGTGGACTTTGCCTACAACAATAATACCTCAGGCCCACCAACTCCCTCCCCTTCAGATCAGGTTGAGGCCATTCAACCCACACTTCCACCAGTGGACTTACAAGACATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6292
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109642 | Nonsense | 145 | 1855 | 1 | 10 |
ENSDART00000141009 | None | None | 559 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 18252108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18072143 |
GRCz11 | 13 | 18203135 |
KASP Assay ID:
554-5213.1 (used for ordering genotyping assays)
KASP Sequence:
ACCAAAATGGCTTATTGTTKGAATGTAATGGGAAGGGGAAGTCACCTAGA[A/T]AGAGTKTCTCATGTCCRAGCATCCAAAGGRATGTTCRGAAAAAGGGAGCT
Long Flanking Sequence:
TGAGATGCTACATCTTGCTACACAATTCAGTAATAAATGGTTCTTTCCACAGGTACCCATATGTACATATGTCAACATTGATTTTACTTCAAACAGGGAGCATTACATTAAAAGTACAGTTTCTCAGACGGCCTCAATACTGTTTCTCATGCCGGCTATCCCAAACTCCTCCTCCCTCACCCTCACTCACTTCAGCTATGCCTCGTACTGCCAAAGCACCCAAGAAGTCAACTCGCGCATCCACAAAGCGAAATGTTAAGAGGGTGAAGGCTTCCATGACAAGGAGGCAAACAATTAACTCACTGAAAGCCAGTGGTGAGATCAAGAAGGGCATAGACAAGAAACAGGCGGCCAAGAGGGCCCAGAGGACTGTTGTCAGCAAGCCTAACAAGAAGACTGTTGAGGATGTTCTACCTGTTAAAATATCCAGACACACGACTAGTTCTTTGAACCAAAATGGCTTATTGTTGGAATGTAATGGGAAGGGGAAGTCACCTAGA[A/T]AGAGTGTCTCATGTCCGAGCATCCAAAGGGATGTTCAGAAAAAGGGAGCTCAGGAGATCAGGGAACAGGAGACTGAGACTAAAAGGTCAGAAGTGAATGATCCTAATGGTGATGCTGAACAACAAAAAGGTGCTGAAATTCCCACTGGAGAGGGACAGAGCGTCAACATAAGCTCTAAAGAATCTGGGGAGGAGCACAGAGAGACTGTTGTTAATGACACTTTAGTGGCAGAGAAGAAGAAGGTAAAAGTGAACACAGAAACTGTACAAAGTGAAAGCTATTCTGCTGTTGTTGAGCAGCCAAACACGGTGTTTGTGGATCAGCAAGATCCTCTGAAGCACAACCCTGTCAATAATGTGGACTTTGCCTACAACAATAATACCTCAGGCCCACCAACTCCCTCCCCTTCAGATCAGGTTGAGGCCATTCAACCCACACTTCCACCAGTGGACTTACAAGACATCTCTCTTCAGACCACTCGAGGAAACTCTACAGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11214
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109642 | Nonsense | 911 | 1855 | 2 | 10 |
ENSDART00000141009 | None | None | 559 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 18324965)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18145000 |
GRCz11 | 13 | 18275992 |
KASP Assay ID:
2260-6241.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCCACCAAATGGCATGGCTAMTCAGAGTTTGAAATACAATCAAAATTA[T/G]TTGGGGCAGCATTTGAAAAAGCAGAGGAAACCGAAGATGACACCATCAAA
Long Flanking Sequence:
CAGATTCAGGACGCCCAGCAAGAAACATCTACATACTCTGCTCCAAGCAACCACATACCTATTCGGGAGGCTAAACCAGCTACAGATGTTGTCTCCAACAAAGTCTCGGTAATTAGTTCATCTTTGCACCAGACTTCTGTCATCCGCAGCTCTCTGAACACACCTACCAACTTTACCCAAAGTCAGCGCTGTGCACCTCCTCCCAGAAAACTATCCCTGAAGGACCTTCTGATGGCCAGCTCAGAATGTGAAAAGCTATCGTATACCACAGAGAACCGAAGAAACGGTCAAGCACTTTGTAAATCGGACCGGTTAGAAGGCACTTTTAAGATGTATAGGCATGGAGAAGCGACTCCCATCTACAGAAAGAAGGATGAAGAGGAAGTTGCGGCTCAGTTGGTACAGCTTGCTTTTATGATTGAATCGAGGCAGGCGCAAGTCTCTGAAAACAGTCCACCAAATGGCATGGCTACTCAGAGTTTGAAATACAATCAAAATTA[T/G]TTGGGGCAGCATTTGAAAAAGCAGAGGAAACCGAAGATGACACCATCAAATCCTAGGATGTCCAAGAAGAAAGTTGCTGAGATTGATGACAACCATTGTAGGATTCTTTTGGCCAAGAAGACACCCAATAAGAAAACCCCTCTCAAAGCCACCATTCAGAAAGCCATTTCACAACATAAAATGAGGTTCCAGCACAAAAGAAATCCTTTTCTTCCCCAGGCCCAGATAGACCTGAAAAAATACATTGCAGAGGCTCAACACGAGAACAGGCAGCTCTTATACTACAACACAAAGAAAGAGCACTTGGAAACATTCATTGGTTCTGGTAGGCAGAATGGCTTTCACGTTAAATATGAACATGGAGGTCATTCTTTACCACCACAAAATGGACACTTTTACAATCATACAAATGACCATCTAGGTGCTAGCCAGTGCCCAAGGCATGAATGTGAACAAAAGGTTTCTCAGGTATCAAAAACCTACGATGTGCTAAATCCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22265
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109642 | Essential Splice Site | 1556 | 1855 | 10 | 10 |
ENSDART00000141009 | None | None | 559 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 18343999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18164034 |
GRCz11 | 13 | 18295026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACATTCTCTATGGCACCTTTAAATATTATACATTTCTTCTGTTTGCA[G/T]GTTTTAAACAAACCTCTACTGAGAATTCCTCCTTTTCGGAAAAGAATTCG
Long Flanking Sequence:
CCAGGAACAGATTGGAAAGCCCTGCTTTACGTGTTATGTTTTTGTAATGTTTTTTGACAAGGTGAGGCAGAGTGAATCTTTTGCTTTTCATAAATATTTCAGACGGTAATCCAAAGAGTAAGCCCCTGTCCTCACGGCAGCAGATTGAAGCATTGAAGATGCCATAGATTAAAATCTGGATATATCTAGGCATAGCTGAATAATATAAGTTAAAAACCTGAAACCAATAAACTCCTCTGTTTATGTAGAGGTTATTATTAATCATATACTTTAACGCTTCAAAGCCTCAGAGCAGTGCTCAATAATATTTACAGCCCTACCAAATATGGCCAAGTCCAAGCTTTTCATTGTAGGGGTAATTCTTGTGGTTATGAATGAGCATATGAAACCATTTCTGGAGAATATTTGCACTAACCTAAGCCGCATACCTACTATGTAGAGATCAGACATTCAACATTCTCTATGGCACCTTTAAATATTATACATTTCTTCTGTTTGCA[G/T]GTTTTAAACAAACCTCTACTGAGAATTCCTCCTTTTCGGAAAAGAATTCGCCTAATTTAAGTTCAACCATGCGCGTTCCTGACATCGGAGGCCAATATTCACCCTTGCACTCTGGAGGCTCGTACAACCAGAGTAACAGCTGCCGCACACCTCCTGTGGGCTCCAGCTTTGGCACATCCACACTCCCAAAGTTCCCTCATGATCCCTCTGGAGGAACCACCCACTTCAATGGTTCCCCTCCTTTTAGACATGGAACTATCAAACAGGAACCATTCAGAAATGACCCTGTAAGGACGAATCCAAAATTCAAATCCGAGCCTGAGGAAATGCGGTGCTTCCAAGGAGGAGCTGCTCCCACCCCACTGTCCCCGCCGATGGCCGAGGGTCTCCACAGCCGTTTGAACATTACCGCACAACCGGTCACCCCAGAGGTGGCCAAAGCAGAGGAAGTGTGGTCAGACAGCGAGCACAATTTCCTTGACAAAAACATCGGCGGGGTC
Associated Phenotype:
Not determined