ZMP
zgc:171784
Ensembl ID:
ZFIN ID:
Description:
transcriptional enhancer factor TEF-5 [Source:RefSeq peptide;Acc:NP_001103194]
Human Orthologue:
TEAD3
Human Description:
TEA domain family member 3 [Source:HGNC Symbol;Acc:11716]
Mouse Orthologue:
Tead3
Mouse Description:
TEA domain family member 3 Gene [Source:MGI Symbol;Acc:MGI:109241]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15971 | Essential Splice Site | Available for shipment | Available now |
sa33977 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20825 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15971
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093199 | Essential Splice Site | 42 | 402 | None | 13 |
ENSDART00000127519 | Essential Splice Site | 68 | 453 | None | 13 |
Genomic Location (Zv9):
Chromosome 6 (position 54580275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 54617009 |
GRCz11 | 6 | 54625117 |
KASP Assay ID:
2259-8215.1 (used for ordering genotyping assays)
KASP Sequence:
CCCTGTGGTCGCCGCAAAATCATCCTGTCAGATGAGGGGAAGATGTACGG[T/C]AAGTGAGCTGAAGGGGAAGTTRTGATGCAGAGATGAGCACAAAATTGTCA
Long Flanking Sequence:
CTTTTGGTGCACACTCGAGTACGATTATTACATTCACACCTGCCCAAACGAACCCCACCAAAGGGGAAAATGAACTCTAGTGCGATTCAATCAAACTAAATAAGGCAGGTGTGAAAGCACCCTTAGGCGATTTTGGATGCAGCCTTATTCTTCTGTTCAGCACTTTGGGAGTTTTAAAGTGCTTTATATATAAAGTTTGATTGATTGGTTGAAGTAATGATCTCTTTCCTCTGCTTCTGTCTTGCAGTACCTGTGTAGCGTGGGGGCTCGTGGCAGGGCCCGGTAGGAGCCGGCACCATTGCGTCCAACAAGTGGAGTGCCAACGGCAGCCCGGAGCAGGGGCTGGAGGATGGGGCCGATGAACTGGACAAGGCCATGGACGGAGATGCAGAGGGCGTGTGGAGCCCCGACATCGAGCAGAGCTTTCAGGAGGCACTGGCCATCTACCCGCCCTGTGGTCGCCGCAAAATCATCCTGTCAGATGAGGGGAAGATGTACGG[T/C]AAGTGAGCTGAAGGGGAAGTTGTGATGCAGAGATGAGCACAAAATTGTCATCCACTTTAGATCATATTATTTAAATTCCTATATACATCACAGGATAGTACCATTCTGTAAATTCAATCAATTAACAGTCTATATACAGTTGAATTCAGAATTCTTAGCTCCCTTTGAATTATTATTATTTTTTTTCATTTTTAAATATTTCCCAAATGATGTTTAACAGCAAGGCAATTTCCATAGTATTTCCTATAATATTTTTTTCTCTTGAGAAAGTCTTATTTGTTTATTTCGGCTAGAATAAAAGCCCTTTTTCAAACCATTTTAAGGTCTATATTATTAGCCCCCTTAGCCGATATATATATTTTTAAAAATTCTACAGAATTAAACACTGTTATACAATGATTTGCCAAGTTCATTACCCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATACTTGTATCTTGAAAAATATCTAGTCAAAAATAATGTACTGTCATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33977
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 |
---|---|---|---|---|---|
ENSDART00000093199 | Nonsense | 337 | 402 | 12 | 13 |
ENSDART00000127519 | Nonsense | 388 | 453 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 6 (position 54623992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 54660726 |
GRCz11 | 6 | 54668834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGAGGAAAGTGTTTGTATCGCATCCATCGCTCTCCCATGTGCGAATA[C/A]ATGATCAACTTCATCCACAAGCTCAAGCACCTGCCGGAGAAATACATGAT
Long Flanking Sequence:
GTGGATGGAGATCAGTTCAGAAATGCTAGGTAAAGCGCTAGTGTGGACGCGGATCGTTTTCATTCTAAAATGCTGTTTTAAAACTAAAACGCTCTAGTGTAAAAGGGGCCTTAGTCTTTAAAACACTATGAGTGAGTAAACATCATTTTTCATTACTAATAATTTTCCTGCCATTTAGCTCTGGGTTCATCTTTTACCCAATAGCAGAACAGCTACTGCTGGAGAGGCGGGGATAAAGATCGTACAGCTCCATCTGATTGGTCAAATTTAGATATACAACCAAATCTGTCAAATAACTGTAATTTATAACGTGTCTGCGATATGTACATTGCAGATACTTTTATCGCGATGACAATGATTTTGCGATTCATTTATTATGCAGCCCTTTTCTCCATGTAAAACTGCATCTGACTGCGTTTTCTGCACTTCCAGACGGAGTACGCTCATGTTGATGGAGGAAAGTGTTTGTATCGCATCCATCGCTCTCCCATGTGCGAATA[C/A]ATGATCAACTTCATCCACAAGCTCAAGCACCTGCCGGAGAAATACATGATGAACAGCGTATTAGAAAACTTCACCATCTTACAGGTCAGATGCCAACCAGTATTTCAGTCCATTTACAAAGCACTCATTTGTAGCTGCATAAAATGAGAAGTACTTGGTGGTCTAGAATAGAATAATTGAATTGAAAAGTTGTCAGATTTTTTTGTCTTTGTAGTTTATGTGAGTCGTGGAGTATATAGTGGATTGCAAAAGTATTCATACCCCTTAAAATTTTTACACATTTTTTCACATTATGACCACAAACATATATATTATTGGAATGTTTTGTGAAAGACCAAAACAAAGTGGCATACAATTGTGAAGTAGAAAGAAAATTATACAGGAGTTTATACTTTATACAGAAGGGATATTTTACGAGTAAAAACTGTGTGCAAAAGTATTCATCCCCCTTTTATCTGAGTACATCCAATTGCCTTCAGAGGTTGCCAGATGATTACGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20825
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 |
---|---|---|---|---|---|
ENSDART00000093199 | Nonsense | 393 | 402 | 13 | 13 |
ENSDART00000127519 | Nonsense | 444 | 453 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 6 (position 54626574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 54663308 |
GRCz11 | 6 | 54671416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGTGTATAGCGTTTGTATTTGAAGTGTCGACGAGTGAACACGGGGCA[C/T]AATACCACGTCTATAGGCTCATCAAGGACTAGCAGCGCATCGGTCAACAG
Long Flanking Sequence:
TAACTCATGAAAGATTAAAGTTATGTTAAAACCAAGCGCACCATTGTTTTTCATGTGAAATTCCTTATAGGTTTGATGTGTCACATGACCCTCTTCCTATTGAAAAAGACAAAAGTTGAATCCAAGATGGCCGACTTCAAAATGGCCACCATGGTCACCACCCATCTTGAAAAGTTTGCTCCCTTACATATACTAATGTGCCACAAACAGGACGTTAATATCACCAGCCATTCCCTTTTTTAAAAAGGTGTATCCATATAAATGGCCCACCCTGTATATAAGACAACTGATATGATTCCTAGCAGAGGTGTATCATTCATTTATTGACAATTAATTGAGAAAAAAGTATATATGTATTTTTATACGCATGTTTCTTTGTTTTTAAAGAATAAAATAGTAATATTTGTCCCTCTCTTCAGGTGGTGACCAACAGGGAAACCCAGGAGACTCTACTGTGTATAGCGTTTGTATTTGAAGTGTCGACGAGTGAACACGGGGCA[C/T]AATACCACGTCTATAGGCTCATCAAGGACTAGCAGCGCATCGGTCAACAGACACCTGTTGCTTTGCACAGACGCTCCAGCACACGCTTGGAGGAAAACGCCAAATTGTCCAAACATCGGAGGAAAACGCCTAAATGTTACAAAAAATACCAAATGTTTTGATCCTGGTGCCGAATTTGAGTCTTTGAGGACGTAAAAAGATATAGTATTACTCTGTTTAAAAAGAAAAGAACGTGTTTTTTTGTATTTGTTTTTAAATGCCTTAAATACAGAATGGGTCATGTTGGTTTTGTTGCATATACAGAAATGGTAGATGTTTTTAAGCTTTGTTGTGTCTCCACAGAGGGAATGTGAAGGTGTTGATGGAAGAGAACGTCATAAAAAAGACAATGTGTGCTGTTTATACGCAGCGCACGCAGCATTTTACAGTTATATAATGGTGAATCTCGAAAAAATCTCATTTTACCCCTGAAATTAAAAGAAAATGAAACATTTATTTTA
Associated Phenotype:
Not determined