ZMP
htatsf1
Ensembl ID:
ZFIN ID:
Description:
HIV TAT specific factor 1 [Source:RefSeq peptide;Acc:NP_957497]
Human Orthologue:
HTATSF1
Human Description:
HIV-1 Tat specific factor 1 [Source:HGNC Symbol;Acc:5276]
Mouse Orthologue:
Htatsf1
Mouse Description:
HIV TAT specific factor 1 Gene [Source:MGI Symbol;Acc:MGI:1919709]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44725 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13523 | Essential Splice Site | Available for shipment | Available now |
sa13135 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34918
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 |
---|---|---|---|---|---|
ENSDART00000079174 | Nonsense | 173 | 450 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 27291706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26694500 |
GRCz11 | 10 | 26656213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATGTCCAAATGTGGAATTGTCATGCGTGATCCCATCACAGAGGAATA[T/A]AAAATCAAAATATACAAGGACAAAGACGGGAACCAAAAAGGAGATGGACT
Long Flanking Sequence:
AACACAAATGTTTATGTGACCGGTAAATAATTTATCATTTATTAAATTCAATAAGATTGTTACTATTAAGACACTGACGTCTAGTTATTATGTTGTAATAACTGGTCCCTCTAGTGACTCCCTCTAGTGGTCACACAAATCAGTTGCTTAGTTTAAAGAGAAGTTTGTCTTCTCTGCATGACTTGTTTCACTGAGTGCAGTTACTAAAATGAAGCAATAGCCCTTACACTCAACATGCACTTTACTTTTTTTAGAAAGATAAACCAATAAATGGCATTTGATTATAGTCTGAACCGTCTTGAGAGAATTTTGTTTTACATTACGAAAATCTTCAATGATTACCCTGACAATACAATCTAAAATTCAGTATAACACATTTAAAGAAATGTATTTTCACACATGTTTTTGCTAGGCCTTCCTCCAGACATCACTCCTGATGAGTTTGTGGAGGTGATGTCCAAATGTGGAATTGTCATGCGTGATCCCATCACAGAGGAATA[T/A]AAAATCAAAATATACAAGGACAAAGACGGGAACCAAAAAGGAGATGGACTGTGCTGCTACTTAAAGGTTTGTCATTGTTTTTGTTTAGTTTTTTTTGGTGTAATACTACATTTTATTTTTATTTAAAGTAATTAAAATGTATCTGAGTAATATTTCTTCATATAATTTGTATCTGTAGACATATTTATTTAATATTTTTGTTATTTGTTCTACAGAAAGAGTCTGTCGCTCTAGCTAAGCAGCTCTTGGATGAGACAGAGATTCGGGGCTACCGGCTGCATGTGGAGGAAGCACGATTTGAACTTAAAGGGCAATTTGATGCCAGCAAGAAGAAGAAAAAGAACAAAGAGTACCGCAAAAAACTACAGCAGCAACAAAAGTAAGAACATGTTCAGACTTGTTAAGTCAAATCTTACACACGGTGTAACAATGCTCTCCTTCATCACCATATTACTAGTGTTGCTTGAGGGGGGATGGGGTAAATTAAATTAGCTATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44725
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079174 | Essential Splice Site | 282 | 450 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 27294776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26697570 |
GRCz11 | 10 | 26659283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAAAAGTTATCATCATCCAAAACATGTTTCATCCCACTGACTTTGAGG[T/G]AAGAATTTACCTCGAAACACACCCATAAGAACATGCTGCAGGTGTTATTC
Long Flanking Sequence:
TTCTTTTAGTGAACAGATCATTAAATCATTGACTCAGATGATTTGTTGGAAAACAGATTCATTCAGAGATACTGCAGTGTTGCTCAGAGATGCACAAATGCTCTGTTGTTTAGCTAGCAAAACAAAAGTCAGAGACACACTGTTGGGTCTGAAATGTGACTCGCTCCATATATTTTTTTTTTATGTTTGTTGAAATGTTGTATAAAGTTCATAATAAATGTACTTTTCTACATTTTATTTCATCTTTTTATCAACTGTCTTTTATCAACAAAAAGTGAGTGACAACAATAACAAACTCGTACATCATTAAAACAACTATTACAACATATGATCAAAGACAACAAATAATGGCCACCCTGAAGATCGCCGTAGACTGACAGTTTTGCTATTTATTTTGATCAGGCAGCTGGATTGGAGGCCTGAGAAGAGCGGAGAAGTGCGCAAAAGACACGAAAAAGTTATCATCATCCAAAACATGTTTCATCCCACTGACTTTGAGG[T/G]AAGAATTTACCTCGAAACACACCCATAAGAACATGCTGCAGGTGTTATTCAATAGAAGAATGTCTTGTTGGCAACACTTCACATCGAGTGCCAGATGAATGATAGAAATGCCTGAAAAGAGATTCACCGCAGATGAAACCAGAATTTAGCTTTTACAGCTCAGATGAAGCTCAGCCCTGTGCTGGTATTTCTGAAGTGCTAGTTAATTGGAATAATGCTTTTGATTAGCACTAGTTTAGCATCGCTGTGGAATTGTTTGTTTTCTCTTCACCGGTGTCAAGAGCTCACGGCGGGTTTTTCTGCATTCCTTAAGTAGGTGCAACTGTAGGGTCAGATCAGAGCAGGAATGCAGGTGTGGATCTGCAGTTGAAGTATCATAAGGTTTTTTTACGATGTTAATTGCGTTTAATGAATGAGATAGATGCTTTATTAGAAACTATGTTTGTGAGTTCTTTATAAAAAATATTGCGTTTAAATATCAGTGATATGACTGGTTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13523
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079174 | Essential Splice Site | 312 | 450 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 27297027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26699821 |
GRCz11 | 10 | 26661534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAGAATGTGAGAAATTCGGGCAAGTGAAGAAAGTGATCATTTTTGATG[T/A]AAGTCCTCTTYTACTCCTGCAACATATTGACCTTATTCTTCAYGWACRAG
Long Flanking Sequence:
ACGTATCTGCAGCTCAAACCAGGTCCGAATTATTTGCATACGGAGTTGATTAAAACTCCACGCACCTCCTGGACTACTCTCCATTGGAAATTAACGACTTCCGGTCTGTCGCTTGTTGTTTGTAGTGTTCAGTGGAAAGGCGGCTTTATTTATTTATACATGTTTATAAAAAATATTCCAATGTATGTCTATTTCCAGAATTCATTAAAATGTAATAATTTTTATTATGATTTTTAAAATTGCATTTAAAGTTTAATTACATTTATTCATTGAGTAATTTGGTTTATTTACTTTTTATTTAGTTTGTTTTCAAAGTTTAACAAAGCAAATTTATGCATTAAAAACACTTAACGAATGCAAACTTTTGACTCGTAATGTATTTAAAAGCTGCCCGTGTAATCTCCTGCAGGAGGATCCTCTGGTCCTCAACGAGTATAGAGATGATCTGCGGACAGAATGTGAGAAATTCGGGCAAGTGAAGAAAGTGATCATTTTTGATG[T/A]AAGTCCTCTTTTACTCCTGCAACATATTGACCTTATTCTTCACGAACGAGCGGGCACAGCCATTGGAATTTTTGGCTCAAGACTTCCGGTCTCATTCACTTCCATTGATTATTATATGTTAAAAACATTTGTTGTGCTGCTTCATGTTGCAAACAGATTTTTTCTTTTTATATTATTCTACTTTTTATATATAGTTATGAACACACTTGCTAGTATAGCAAGTAGTCTGACTGTTTTCTGCTGTGTTATTATTCCTAGTCATTTCTTCCATAGGCAGCTTAATCAGAACTACTAAAACAATCGCAAAAACAAGTGCATTTTCACATTGAAGAATAAGGTCAACACTGCTCATTTAAATGTGTCTTATTTACTCTGCTGTGTGCTTTCTGCATGGACATCAGAGGCACCCTGATGGAGTGGCGTCAGTGGCATTTAAGGAGCCTGAAGAGGCAGACGCGTGTCAGGTGGCTTTGAACGGACGCTGGTTTGGAGGAAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13135
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 |
---|---|---|---|---|---|
ENSDART00000079174 | Nonsense | 364 | 450 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 27302285)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26705079 |
GRCz11 | 10 | 26666792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTCTTCATTATCTCTGTKTGTTTGGTCACCCAGRTTGAGGAAACGTCA[C/T]GAGAGCGAGAAGAGAGACTGAAAGGCTGGTYGTCTTTTCTGGGCGAYGAA
Long Flanking Sequence:
TTACTTCCATTGTATCTGTTCAGCTGAGGGAACGGAGCCAACCTCATGACGTCAGACACAGTGACATTCCGAGATGTCAGCACCCTAGCTCTAAAAGCTATAATAAAATGTTGTTTTCTTCTAAATGGTTTCATTAATCGAGTTTGTTTAATATATTTTCAATAAGGTGGAAACCAGTTTGTCTGCGCAATAGCCTAGTGGTTAGTGGTCGACATATGGTGCTGTAGCACTTCAGGGAGTCCCGAGTTCAAATCCCGGCTCGAGGACATTTCCCGTCCCTAACCCCTCTCTCTCCCACTTCGCTTCCTGTCTGAAATACTGTCCTATCCACTTAATAAAGGCAAAAAGGCCAAAAATAAATCTAAAAAAAAAAAGAAACCAGTTTACAAAATAATGTAAACTTGACTGACTGCTTCACTTCCACTTTAATTTAGCTGCAGTAGCCTGCTTTATTCTTCATTATCTCTGTTTGTTTGGTCACCCAGGTTGAGGAAACGTCA[C/T]GAGAGCGAGAAGAGAGACTGAAAGGCTGGTCGTCTTTTCTGGGCGATGAAAAAGGATCTGGCGAAGCTAAAGCTAACTCCACAAAAACAGACGAACAACAGAATTCCAGCACACAAGAAGCAGCAGCAGCAGAACAGACCCAGCAGGAGCCACATGTAAACGAAAGCAGCACAAAACCACAGGAGGAGAAAAATGAGGAGGAAGGAGGAGGAATGGCATCGACTGATAGCAGTTTAGCAGGAAGTGATGATGAAGATGCGTAACTTCTTTAATGTCTCACTCATACATCTCAACACCAACAGTGTTTTCATTTTAAATGCCTGTTAATGAATCGCATCATATTCCAATTTGACTGTAAATAATAATTTGTGATCTGTTTTCTCTCACTTCCCCGTGTTATGATGTGTGATCCATTTGAACTTCTGTCAATATAGTTTTATAGTAAAAATCATATTTTGTGACCTCATCATTGTTTCTTGCTTTCATGAAAAAACAAACAA
Associated Phenotype:
Not determined