ZMP
ahctf1
Ensembl ID:
ZFIN ID:
Description:
Ahctf1 protein [Source:UniProtKB/TrEMBL;Acc:A5D6S7]
Human Orthologue:
AHCTF1
Human Description:
AT hook containing transcription factor 1 [Source:HGNC Symbol;Acc:24618]
Mouse Orthologue:
Ahctf1
Mouse Description:
AT hook containing transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:1915033]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23014 | Nonsense | Available for shipment | Available now |
sa9115 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa664 | Nonsense | F2 line generated | Not yet available |
sa32129 | Nonsense | Available for shipment | Available now |
sa28817 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23014
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 |
---|---|---|---|---|---|
ENSDART00000115321 | Nonsense | 416 | 2527 | 8 | 35 |
Genomic Location (Zv9):
Chromosome 17 (position 12100512)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12083034 |
GRCz11 | 17 | 12237100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGTATTTGACATAAACAGATGGTACCACGCTCAGATGCCAGATTCAT[T/A]GAGGTCAGTATGCTATTAGTAATGCACTCAGATTTGATGGAAGGACATGT
Long Flanking Sequence:
GGAGAGGAAGTGCTTGGCTTCAGGAAAAATTATTTATGAGGTACAGTGGCATGCAGAATTCTGAATGCTGCAAGTCTTTATGTTTGTTATGTTCTTGCAGAAAAAGATTCATTCTCAATGTGCTGACTTTTAGGGTCTGGAGTATTGTGAAGAACGTTACAGTCAGGACTTGAACGGTACATCATTTCCTCTAAGAGCTCAGGCCACCAATACCCGTCTGATCAGCTGTCAGACCATAGAGAAGTTTCGTCACCATCCTGACCGTGACGACAGCATGAATGAAGGTATTTACATGTCAAACACCACATGCTTTGCAGAGATTGATTGACTGATGTCACATTACCTTTAACTTTCAATTTGATTCTTTTTAGTGGCGTCTCCTGATACAAGTGTGTCAGTTTTCAGCTGGCAAGTGAAATCATATGGACAAGGCCAGCCATCAACATTCATAGGTGTATTTGACATAAACAGATGGTACCACGCTCAGATGCCAGATTCAT[T/A]GAGGTCAGTATGCTATTAGTAATGCACTCAGATTTGATGGAAGGACATGTTGCATGTTGATGCATGTAAATAAATGCAAGCTTGCATCAAAGGCGTTTTTTCTTGTACAGAACGGGTGAATCCTTACGGAACTGTCCCTATCTGGCGGTCTGGTCTCTTGACTGTGTGATTGAGATGACAGCGCCCTGTGCTTTGTTGGACATCTTGGTTCATGAGCGCAGTCTAAGCAGAGGTCTCCCCTATACATGTCCTCCACCAGAACAGTTCTTCAATCCCACCACATACAACTTTGGCAAGACCTTTTCTTTATTTCATAATTTGCATGTTTGTGTTGTATAATTCCATTTGAATTCTAATAATATTACTCTTTCTATTCTAGATGGAAGTTGTTTGTTTAATGCTGGAATTGTGCACTTTACTTGCTCTGGCTATCAGAAAGAGGTTCGATTTTGGCCCATTCTGTACTAAATTGTGTTGAATTTTTATTTATTGTTTAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9115
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 |
---|---|---|---|---|---|
ENSDART00000115321 | Essential Splice Site | 417 | 2527 | 8 | 35 |
Genomic Location (Zv9):
Chromosome 17 (position 12100507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12083029 |
GRCz11 | 17 | 12237095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTGACATAAACAGATGGTACCACGCTCAGATGCCAGATTCATTGAGG[T/G]CAGTATGCTATTAGTAATGCACTCAGATTTGATGGAAGGAYATGTTGCAT
Long Flanking Sequence:
GGAAGTGCTTGGCTTCAGGAAAAATTATTTATGAGGTACAGTGGCATGCAGAATTCTGAATGCTGCAAGTCTTTATGTTTGTTATGTTCTTGCAGAAAAAGATTCATTCTCAATGTGCTGACTTTTAGGGTCTGGAGTATTGTGAAGAACGTTACAGTCAGGACTTGAACGGTACATCATTTCCTCTAAGAGCTCAGGCCACCAATACCCGTCTGATCAGCTGTCAGACCATAGAGAAGTTTCGTCACCATCCTGACCGTGACGACAGCATGAATGAAGGTATTTACATGTCAAACACCACATGCTTTGCAGAGATTGATTGACTGATGTCACATTACCTTTAACTTTCAATTTGATTCTTTTTAGTGGCGTCTCCTGATACAAGTGTGTCAGTTTTCAGCTGGCAAGTGAAATCATATGGACAAGGCCAGCCATCAACATTCATAGGTGTATTTGACATAAACAGATGGTACCACGCTCAGATGCCAGATTCATTGAGG[T/G]CAGTATGCTATTAGTAATGCACTCAGATTTGATGGAAGGACATGTTGCATGTTGATGCATGTAAATAAATGCAAGCTTGCATCAAAGGCGTTTTTTCTTGTACAGAACGGGTGAATCCTTACGGAACTGTCCCTATCTGGCGGTCTGGTCTCTTGACTGTGTGATTGAGATGACAGCGCCCTGTGCTTTGTTGGACATCTTGGTTCATGAGCGCAGTCTAAGCAGAGGTCTCCCCTATACATGTCCTCCACCAGAACAGTTCTTCAATCCCACCACATACAACTTTGGCAAGACCTTTTCTTTATTTCATAATTTGCATGTTTGTGTTGTATAATTCCATTTGAATTCTAATAATATTACTCTTTCTATTCTAGATGGAAGTTGTTTGTTTAATGCTGGAATTGTGCACTTTACTTGCTCTGGCTATCAGAAAGAGGTTCGATTTTGGCCCATTCTGTACTAAATTGTGTTGAATTTTTATTTATTGTTTAGTTAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa664
Status:
F2 line generated
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115321 | Nonsense | 468 | 2527 | 9 | 35 |
Genomic Location (Zv9):
Chromosome 17 (position 12100250)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12082772 |
GRCz11 | 17 | 12236838 |
KASP Assay ID:
554-0572.1 (used for ordering genotyping assays)
KASP Sequence:
ATGAGCGCAGTCTAAGCAGAGGTCTCCCCTATACATGTCCTCCACCAGAA[C/T]AGTTCTTCAATCCCACCACATACAACTTTGGCAAGACCTTTTCTTTATTT
Long Flanking Sequence:
CGTGACGACAGCATGAATGAAGGTATTTACATGTCAAACACCACATGCTTTGCAGAGATTGATTGACTGATGTCACATTACCTTTAACTTTCAATTTGATTCTTTTTAGTGGCGTCTCCTGATACAAGTGTGTCAGTTTTCAGCTGGCAAGTGAAATCATATGGACAAGGCCAGCCATCAACATTCATAGGTGTATTTGACATAAACAGATGGTACCACGCTCAGATGCCAGATTCATTGAGGTCAGTATGCTATTAGTAATGCACTCAGATTTGATGGAAGGACATGTTGCATGTTGATGCATGTAAATAAATGCAAGCTTGCATCAAAGGCGTTTTTTCTTGTACAGAACGGGTGAATCCTTACGGAACTGTCCCTATCTGGCGGTCTGGTCTCTTGACTGTGTGATTGAGATGACAGCGCCCTGTGCTTTGTTGGACATCTTGGTTCATGAGCGCAGTCTAAGCAGAGGTCTCCCCTATACATGTCCTCCACCAGAA[C/T]AGTTCTTCAATCCCACCACATACAACTTTGGCAAGACCTTTTCTTTATTTCATAATTTGCATGTTTGTGTTGTATAATTCCATTTGAATTCTAATAATATTACTCTTTCTATTCTAGATGGAAGTTGTTTGTTTAATGCTGGAATTGTGCACTTTACTTGCTCTGGCTATCAGAAAGAGGTTCGATTTTGGCCCATTCTGTACTAAATTGTGTTGAATTTTTATTTATTGTTTAGTTAATTTCTTTCTCTTTCAGACCCTTTGCTACCTAAAGAAGGTGGCACCAAGTTTGGGGGACAGTATTTCTAATGGATACTCTCGCTGTCTCATGTCTGGCCTTCTGTCTTCTCGTCTGGCTGATGTCCAGCCCTCCAGTCTCTCCCAGGTAACACTTCCTTATTTAACATGATGCAAGTTTGCTTCATAGATTTCACTCGTATGCATCAGAATTTTGTAGTCACTTTATTTTAATGTGGAATTTTCATTTATTAACCAACTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32129
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115321 | Nonsense | 1030 | 2527 | 23 | 35 |
Genomic Location (Zv9):
Chromosome 17 (position 12092877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12075399 |
GRCz11 | 17 | 12229465 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTAGCCATCGAACGAGCAAAACCGTACCAACACCCTACTTTGATTCAC[A/T]GAGGTAATGAAAGCTGTCATAAGCACTGGAAACTATTCGTAAAAAGTGCA
Long Flanking Sequence:
TAAAGTTACACAATTTTGCTTTTTTACTGTATTTTGGGTCATAAATACAGCCTTAGTGAGTAAAAAAAAGACATGAAATAGAAACAAACAGGATCACTAATTTGTTTTCATTTGAGTGCGTGTGTGTCTGTGTGTGCAGGAGTGTTTGCAACGGTTCCTTCAAAGCAACGGAGGTTTCCAGAATCGGGAGCTGCTCATGGTCCACTACCTCCAGCAGGCAAATTACGTGCCTGCTCTACAACTCAACCAGACACTCAAATTGAACTTAGCTGTATGTTCAGTATTTAGGTTCACTTATCATTGTATAAATGTTTACTTTCATCTGTTGTAATTGGCTATTTAAAACATTTCTAATTCAGGCTGATCGGGATCCTAAAATGAAGGAAAGGTCAAACACGAGGAACTCTATTCTCAATCAGTATGGAAAGGTTCTTCCACGGGTACAGCGAAAGTTAGCCATCGAACGAGCAAAACCGTACCAACACCCTACTTTGATTCAC[A/T]GAGGTAATGAAAGCTGTCATAAGCACTGGAAACTATTCGTAAAAAGTGCAACATGAGAGATACCCTTAATCTTCTTTCCACTAGTGAAAAGACCCCAGCCTCTTTCAACCGTAACCAAACGTTCAGCTTCTGAAAACGTGATGACCAGGGCAGCGTTTATTAATAATGTATACTCGAAGATTGAGGAAGTGTGGGCTGGCAATAACACCACTCCAGAGTCATCTCCTTTCAAAAGGTAGTATGCTTTCTTTTATCCACTTTGCCTTCATTTTCAGTTCATAAGTCTTAGTTTTATCCCCCAAACAAATGTCTTTTAATCTAAATCATTTTGTTTGGCTTTGCTATTCAGCCCCAAAGAGTCTGAGATGCAAGTGCCTAGCCGACATCCATCCTCTCCAGATCTGCCTGAGGCCTTTGTAGGAACTCCCATCAACAAGCTAACCAAGAGAATGTCCAGGTAAAATTGTTCCAAGAGAGGTTTTGGGGTGTTGTGATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28817
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 |
---|---|---|---|---|---|
ENSDART00000115321 | Nonsense | 1303 | 2527 | 28 | 35 |
Genomic Location (Zv9):
Chromosome 17 (position 12091165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12073687 |
GRCz11 | 17 | 12227753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAGAGCAGGAGAATCCTGACGTAGAATCTGAGACTGGATCCTCTATT[A/T]AAGAAATCCCCTTAGCAGAGTCCACAAAAGTGCTTCCCACTCTCGTGCGA
Long Flanking Sequence:
ACGATCAATCACTCCTCCTCTCCGGCCCAAAGAGAGCCGCATTACCTTCATAGAGGATGCTGATTCTCCAGAAGCTCCCAAAGGCTCTGTTCACTGGAACAATGGGGTAATGTGCCTTTTCTACAATCAAATGTCTATCTAAAATCAGATCAATTGCATTTATTATCACTGTAAATATAATAATGTAAATAGTTATATACCTTTACATTTGTCAATTTGTATCTTGCATATTATAGAAGTCATACTCCATGAGCCCTACTTATTAAAACATTGGAACAATTTTAGCAAGAGTGATTAATGCTTTTGGTTCTCCACAGATTTCAGTTAACAGGGAGCACAATACTCCTAAGCGATCTTCTCCTCCTGCTAAAGCAAGCATTGGGGTCTGGAGTGAACATTCAGATGCTGAAGAGGAAGATGTAGATATGAAAATGACATGCATGCCCTCTCTGGGAGAGCAGGAGAATCCTGACGTAGAATCTGAGACTGGATCCTCTATT[A/T]AAGAAATCCCCTTAGCAGAGTCCACAAAAGTGCTTCCCACTCTCGTGCGACGGCCTAGTTTGGGGCAAGAAGCAAGTCTTGTATCCAACCAATCCGATACCACCCTTGAGTTTCATGATGCTCCTGCTCCCGAGGATCTTTTGATTACTCTGAAAGAGCAGCAAGCAAACAATAGTGTGGATCGAGAGGTGACAGTAAGACTTCCAAACACTTTTGAGGAACATACAGCTCCTGTAGAAAGGAACACAACTGTGGACTTGCCTTCTCTTATGCTGCCTGAGAAAGAAAAGGACAATTCAAGGGGAGACTTGTCCAATGCAGAGAGATCTTTAGGCATACAGGAAGCCCAAAATGAGGAGGAGTGTGTTAATATTACCAATGATGTTGTGGAGAACGTAAGCGAGGAGCAGCTAAAAGGAATTTCAGAGGCTCAGGTTCTCAAGATAGATGTGGTTATTAAACCAGAGTTGGTTGTTCCTGTTCAGGAACCAAGCTCTGAA
Associated Phenotype:
Not determined