ZMP
zgc:175264
Ensembl ID:
ZFIN ID:
Description:
putative homeodomain transcription factor 1 [Source:RefSeq peptide;Acc:NP_001107901]
Human Orthologue:
PHTF1
Human Description:
putative homeodomain transcription factor 1 [Source:HGNC Symbol;Acc:8939]
Mouse Orthologue:
Phtf1
Mouse Description:
putative homeodomain transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:1332671]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21884 | Nonsense | Available for shipment | Available now |
sa933 | Nonsense | F2 line generated | Not yet available |
sa676 | Essential Splice Site | Available for shipment | Available now |
sa21883 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21884
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 |
---|---|---|---|---|---|
ENSDART00000080355 | None | 257 | 691 | 8 | 17 |
ENSDART00000124369 | Nonsense | 334 | 779 | 13 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19234535)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18651849 |
GRCz11 | 11 | 18814191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCATCAGCGCCTCCCAAATATGCCAGCGCGCTGAGAAACAGACTTCA[C/T]AACGTTCCCAAGAACAATGTACAACCCCAGGCTCAGGTGGATATCTGACT
Long Flanking Sequence:
ACATTTCAATTAAAAAATGATCTGGTCAAAAACGTTTATTGTTATTATTATATATTACAAAACAGTTAGGTCCTGTCTTCTGATTGATCAAAACTTTTTATGTTTCCTGTTTATACATTTTGTTGTTGTTTTTTTATTCACAGACAGAGGAAGAGTAGAAAAGCCAAGAGGTCTGGGGATGAAGGAAGTCGAGTAGCAGGGATAGTAGAACTCAAACCCTGGCAACTTGAAGACAACCATCGGCTCTACAGATCAGAGAAGACTCTGGTAAAACGCTTTCCAAAAAATCTGTTCTTTCAAGACTCTTAATCATTCATGTTTATGTTGATGGAGATTGTGTGGGCTTTACAGAACTCCCTGAGGAGGCCTCCATATGGGGCATCTGAAGATCTGTCCAGTGAAGAAGAAGAAGAAGAAGCAGAAGAAGCAGAACTACAAAAAGAGAGGCTCTTTTCATCAGCGCCTCCCAAATATGCCAGCGCGCTGAGAAACAGACTTCA[C/T]AACGTTCCCAAGAACAATGTACAACCCCAGGCTCAGGTGGATATCTGACTGAATCCAAGAGAGATGTGTGTAGGAGAGTTCAGGATATTCATTAGCATTTTGTGATCTGATACAGGGAGAGAGCAATGGCATGCCAACAGAAATCCCAGGGCTGCCACGTGAAGTTGAGCATCTACGGCCTTCAGAGGGATCGCATCCTGCTTCTGATACAGATGATATGTTGTGGGAGGAGCTTTTACAAGATTCTGACTCCGCCTCCACAGGAAGTAGTGAGATTGGGGAGGACGAGCCTCACAGTCAAAGCCACTCCCTTCCTGTGCCCACTATTGCTTTAACAAGTGATGAGGATGAGGATGAGAATGAGGCCTTACCGCAGGTGGGAAGCAATTTTGCTGGAAAAAATATTTTAAGTTGTGGTTTTATATGCACTTAATGTTTGTTTGTTTTTTTAAGTTTAGAAAAAGCTCATTGTATCTCCTCCATTAGAATTAAGATTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa933
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080355 | Nonsense | 306 | 691 | 9 | 17 |
ENSDART00000124369 | Nonsense | 394 | 779 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19234309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18651623 |
GRCz11 | 11 | 18813965 |
KASP Assay ID:
554-0838.1 (used for ordering genotyping assays)
KASP Sequence:
CGGCCTTCAGAGGGATCGCATCCTGCTTCTGATACAGATGATATGTTGTG[G/A]GAGGAGCTTTTACAAGATTCTGACTCCGCCTCCACAGGAAGTAGTGAGAT
Long Flanking Sequence:
TTGAAGACAACCATCGGCTCTACAGATCAGAGAAGACTCTGGTAAAACGCTTTCCAAAAAATCTGTTCTTTCAAGACTCTTAATCATTCATGTTTATGTTGATGGAGATTGTGTGGGCTTTACAGAACTCCCTGAGGAGGCCTCCATATGGGGCATCTGAAGATCTGTCCAGTGAAGAAGAAGAAGAAGAAGCAGAAGAAGCAGAACTACAAAAAGAGAGGCTCTTTTCATCAGCGCCTCCCAAATATGCCAGCGCGCTGAGAAACAGACTTCACAACGTTCCCAAGAACAATGTACAACCCCAGGCTCAGGTGGATATCTGACTGAATCCAAGAGAGATGTGTGTAGGAGAGTTCAGGATATTCATTAGCATTTTGTGATCTGATACAGGGAGAGAGCAATGGCATGCCAACAGAAATCCCAGGGCTGCCACGTGAAGTTGAGCATCTACGGCCTTCAGAGGGATCGCATCCTGCTTCTGATACAGATGATATGTTGTG[G/A]GAGGAGCTTTTACAAGATTCTGACTCCGCCTCCACAGGAAGTAGTGAGATTGGGGAGGACGAGCCTCACAGTCAAAGCCACTCCCTTCCTGTGCCCACTATTGCTTTAACAAGTGATGAGGATGAGGATGAGAATGAGGCCTTACCGCAGGTGGGAAGCAATTTTGCTGGAAAAAATATTTTAAGTTGTGGTTTTATATGCACTTAATGTTTGTTTGTTTTTTTAAGTTTAGAAAAAGCTCATTGTATCTCCTCCATTAGAATTAAGATTAATATATAAAAAGTTTTGCTGTCAGTGTTCATTGTGCATTTGATTGTGCAGGTAAAAAATGGCATAGGTGGGTTGACAAATTTGGGCAGTTTTGAAACATTTTATATACAACTTATATAATAAAACATAACTGTGTGCTCCTACTGACTGATTGATTCACCTGCAACAGGAGGTGAGGGAAAGTTACATCAAAATCTGACTCCCTGGACAAATCTGACTCCCCTTCGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa676
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 |
---|---|---|---|---|---|
ENSDART00000080355 | Essential Splice Site | 559 | 691 | 13 | 17 |
ENSDART00000124369 | Essential Splice Site | 647 | 779 | 18 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19229688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18647002 |
GRCz11 | 11 | 18809344 |
KASP Assay ID:
554-0584.1 (used for ordering genotyping assays)
KASP Sequence:
CATCAATTTTCCTCTTGGCTTTGTCTATTGCCTTTATCATCTGTGCACAG[G/A]TTAGCTGTTTCTTCTACTAAACACTTTTTTTNCTGGCACACCCTTTAGACA
Long Flanking Sequence:
TTTATACTGTACATTACACTACTGTGATACCTACATTTACTTGTAGCATTAAATGTTTTCATTTATGTAGGTTTATTTTTTTACACTTTTATAAAATAGTATCGAATTGTAATCTCAGCCACAGCTAGAACATTTTTGTCTTTGTTTTACCATCAAGTGCAATGGAAAAATGCTTTACAGTCTTTCCTATCAAAAAGCTATTTGGCTGTTGTTACAAGTGCAATGGAAAAATGCTTTACAGTCTTTCCTGTCTAAAAGCTATTTGGCTGTTGTTACAAGTTAAGCCTACTAGTTTAACTGGTATGTTGTTTTTTTGTCAGACATCTCTCTAGTCCTTTTATAATATATACCTAGGTTTCATTATATGAAAATACAGTATCAATTTAATCATTTCTTTGTTTTGTTTTTAACAGAGACGAGGCCCTCAGCGGTCTGTCGATGTCATTGTATCATCAATTTTCCTCTTGGCTTTGTCTATTGCCTTTATCATCTGTGCACAG[G/A]TTAGCTGTTTCTTCTACTAAACACTTTTTTTCTGGCACACCCTTTAGACATTTCTTTTCATGGTTTCTTCCTTCTGAAGAAAATCAATGCTATTTACATAAATGCTTTACCGTAAAGGGCATTCATTCTGAAGCACAGAAACACCCTCTATTTCTACAAATATACCACTAAGAGTCAGGAGAGCAGCTACATGTTGTTTCACGGCCAAACTTGTTTAAACTAATAGCAAAAATTGTCTTTTTCTGCTTGCCAAATCAACAACTTAGACCTGATTGTGAAAGCACTTTTTTAAAGCCTTTGCTTTATTAAGCACTAATATTCAGATTAGTCTGCTTTTTGAATTGTGGGAATTTTTTTTGCACTGATCTGCACCTTAAATAATAACAAAAATATTAAGTTATTATAGATACAACTTTGACCCGCCCATATAATCATTGATAGCATTGTCAGTGCATGGTCATATACAGTTCACTGATATATTCAGTCGGTGGTCTTAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21883
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 |
---|---|---|---|---|---|
ENSDART00000080355 | Essential Splice Site | 643 | 691 | 15 | 17 |
ENSDART00000124369 | Essential Splice Site | 731 | 779 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19223934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18641248 |
GRCz11 | 11 | 18803590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGAACATAGTGAACAATGTGCTGAGGCTGGCCACCAAATTACTGAAA[G/A]TAAGACCAGTATAAAAACATCACTCTTTGGGGAAAAAAACAAAACACGTT
Long Flanking Sequence:
ATCACTACAAAATCTTTGACTTATCAATTGCAGCCTGAGACGTGCATATTAATGATTTCAGAGCTTTTTTTTATCATCTCAGTAATCTCTCGATGACATAGCGTCTCGTCATAGTTTGTTTTGTCCTCTGATTGGCCTGTTCTTCACTGGGTTTTTACACTAGTGGAATTTTCATGATAACAAGAAAACAGTGTCTGAGGCGCACATTATGCTCATTTCCATATCCTTGTCTTTTATTTTTCTTTTATTATGTCTTGGTATACCCAAATTTTCATTCTAGGGCACCTTTAAATTTTTCTTTGCATTATTGATTTTATTTATATGCATAAATATCGTTAGCTGCCAGTTATCTGGAATAAAATACATTGTTTTACTTCTAATTAATTGCAACAACTCTGTTTCAGATCAACTTGTATCTTAAAATGGAGAAGAAACCCAACAAAAAGGATCAGTTGAACATAGTGAACAATGTGCTGAGGCTGGCCACCAAATTACTGAAA[G/A]TAAGACCAGTATAAAAACATCACTCTTTGGGGAAAAAAACAAAACACGTTTTCTCGTATTGACCGCGATTTGCTTGTTTCAGGAATTGGACACTCCATTTCGTCTGCTAGGCCTGACGGTGAACCCGCTCATCTACAATATCACACGAGTGCTCATCCTGTCTGCCGTTTCTGCTGCTGTCAGCGATTTATTAGGGTTCAACATCCGGGTGAGAGAAACATTTGCACTTTAACTACTGTGCTTATCTGCACCTGTATCCTGGGCCTGTTTTATTGTCCCGCTGAAATGCACCTTTATTGATCGTGATGATCTGTGTTTTTATGACACACTGCTTCCTGTTATCAGGACAGAGAGTTTTGCTCACTCTTTGTAGAGCATGACTTTTATCATAATGGTGTTTAACAGTCCTTCAACTAACCGCTTTAACAATATCCATCATGTGCTTTTTTAACAGCTCTGGAAGATCAAACCATGATGACTTTTACACTGCCAGCGTCTTA
Associated Phenotype:
Not determined