ZMP
nfya
Ensembl ID:
ZFIN ID:
Description:
nuclear transcription factor Y, alpha [Source:RefSeq peptide;Acc:NP_001076264]
Human Orthologue:
NFYA
Human Description:
nuclear transcription factor Y, alpha [Source:HGNC Symbol;Acc:7804]
Mouse Orthologue:
Nfya
Mouse Description:
nuclear transcription factor-Y alpha Gene [Source:MGI Symbol;Acc:MGI:97316]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10216 | Nonsense | Available for shipment | Available now |
sa15592 | Nonsense | Available for shipment | Available now |
sa2607 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa10216
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 |
---|---|---|---|---|---|
ENSDART00000099571 | Nonsense | 59 | 265 | 3 | 8 |
ENSDART00000103064 | Nonsense | 59 | 321 | 3 | 8 |
ENSDART00000122531 | Nonsense | 72 | 167 | 4 | 6 |
ENSDART00000125616 | Nonsense | 83 | 316 | 4 | 9 |
ENSDART00000140397 | None | None | 218 | None | 6 |
Genomic Location (Zv9):
Chromosome 11 (position 37106509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36003737 |
GRCz11 | 11 | 36265720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATCACTTCCTCTGGGCAGCCCATAATGGTTCAGGCCATGACARGAGGA[C/T]AAGRTCAAACCATTATGCAAGTACCGGTATCTGGTACACAGGGGCTGCAG
Long Flanking Sequence:
ACCTTGTATCTCATGCATTGCTATCCTTATTTGTATTATTATTATTATTTTTTTATCTTTCTCAGTACTATTACAGTATTATGAATATCATTTGCTATGATTTTCAAAAAATATCCAAATAATTCCCACAGGAATGACTTTAAAGCATGCTTTTTTTTGTGCAAATTGCATTATCAAACCCCCAGCAAGTCCAGTGCCACCAACTTCTTGCATTTCACATGCACTGCATTTTCTTGCATGCATCTACGTTTTGCATCATCTCAGTGTCTATCATAATGTCATCATGAAATTAGCATTTAAAAGTTACTATTATTCTCATTATAACGTAAGTAATGGAAGCCTGAGAAGTCTAAGAAGTAAATTGTGTTTTAGTACTGACATTTTTTTTTCATGTATTTTCTTCAAAGGTCCAAGGGCAGCCTCTTATGGTTCAAGTCAGCGGCGGTCAGCTCATCACTTCCTCTGGGCAGCCCATAATGGTTCAGGCCATGACAGGAGGA[C/T]AAGGTCAAACCATTATGCAAGTACCGGTATCTGGTACACAGGGGCTGCAGCAGGTGAGTGAAGCTAATTTCAAATTCAGTTACTTGATAAAAATGCAGTATTTACTTTTTTTTTTTTACTTTATGCACTTTAATACTTCAAGGCAGTGTTGGGGGTAATACATTACAAATAACGCAAGTTATAAATAACGCAACCAATAAAGTATTACTTTTAAAAAATAAGTCATATTTGAGTTTTTTTTTTTTTTTTGAAAATGTAACATGGGTTACTTTTTAGTTTATGTATTGAGTTTTTAAAAAAATAAATTGCTGAATTAAAATGAAAGTAATCACGATGAATCACGTTGGATCAATGAGGGAATGTCTTTATTATTTTGAACACATTGAAGAAAAAGAAAATGGCATTGTCTTAATGGGCAGTGATTTTACTTAAGACAAATAGTACAAAAGTAGCAAACACATTGCATTACATTTTCATTAATCTGTATATATGGCATGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15592
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 |
---|---|---|---|---|---|
ENSDART00000099571 | Nonsense | 79 | 265 | 4 | 8 |
ENSDART00000103064 | Nonsense | 79 | 321 | 4 | 8 |
ENSDART00000122531 | Nonsense | 92 | 167 | 5 | 6 |
ENSDART00000125616 | Nonsense | 103 | 316 | 5 | 9 |
ENSDART00000140397 | None | None | 218 | None | 6 |
Genomic Location (Zv9):
Chromosome 11 (position 37104747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36001975 |
GRCz11 | 11 | 36263958 |
KASP Assay ID:
2260-4556.1 (used for ordering genotyping assays)
KASP Sequence:
NNNNTACTGGGGATGAAGTTATAATGAAAANCCTCTATGTTACACAGATTCAGT[T/A]GGTYCAGCCTGGTCAGATTSAGCTTCCTGGTGGACAGACTTTACAGCTAC
Long Flanking Sequence:
GACTAGGTTTAAACAGGCCCTAACAAACAACTTGACAGTCAGTCATTGTGAGCATGGAGTCACAAAAGTTAAGAACCCCTCAGTATAAAACTCCAGCAAGATACTGGGGATAGGTGGCACGGTGGCTTAGCGGTTAGCACACCTCACAGCAAGAAGGTCAATGGCTGAGTCCTCCCTGTGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCTCTGTTTGCTTGGGTTTCCTCCAGGTGCTCCGATTTCCCCCACAGTCCAAAGATGAGGTATAAGTGAATTGGATTCATTAAATTGGCCGTTGTTTGCATGAATGAGCGTGTATGGCTGTTTCCCAGTATGGGTTGCGGCTGGAAAGGCACCCACTGCATAAAAGATATGCTGGAATAGTTGGTGGTTCATTCTGCTGTGGACCAAGCTAAAGAAAAATGAATGAATGAATGATACTGGGGATGAAGTTATAATGAAAAACCTCTATGTTACACAGATTCAGT[T/A]GGTTCAGCCTGGTCAGATTCAGCTTCCTGGTGGACAGACTTTACAGCTACAGGGTCAGCAGGGTCAAACTCAACAGATCATCATTCAACAGCCACAGACCGCAGTCACTGCAGGACAAAACCAGGTATTGTACTTATGCAGATTTTTTAATTTTATCATAAATATGAAAGCACAACAATCTATTTAAATACCCATTATCAATGAAGTGCATAATAAATCCTGGTGCTTTCTGATTTTTTTAGGGTCAACAGCAGATTACAGTACAAGGTCAGCAAGTGGCTCAAACCGCTGAAGGACAGACCATCGTATACCAGCCTGTAAATGCAGACGGGACCATCCTACAGCAGGGTAAACCCAGAAAAACTAAATTAACAACGATAAAATGTGTTTATATCAGTCGATACTGATAATTATCTAGCTAAATTTTACATTTCTATTTCTTTTAAGTTTAAAGGGGATTTTTGCTGCTGAATGAATGTTTTAGAAAGCAGTCTGTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2607
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 |
---|---|---|---|---|---|
ENSDART00000099571 | Nonsense | 239 | 265 | 7 | 8 |
ENSDART00000103064 | Nonsense | 239 | 321 | 7 | 8 |
ENSDART00000122531 | None | None | 167 | None | 6 |
ENSDART00000125616 | Nonsense | 263 | 316 | 8 | 9 |
ENSDART00000140397 | Nonsense | 137 | 218 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 11 (position 37101670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35998898 |
GRCz11 | 11 | 36260881 |
KASP Assay ID:
554-3133.1 (used for ordering genotyping assays)
KASP Sequence:
TTCCTGGAGCAGAGATGTTGGAGGAGGAACCTTTGTATGTTAATGCAAAA[C/T]AGTATCACCGGATACTCAAGAGGAGACAAGCTCGCGCCAAACTGGAGGCT
Long Flanking Sequence:
CTACCCTGATCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTTTAAAAGCGCTATACAAATAAAGCTGAATTGAATTGGATTGAATTGAATATATTGCTGATTAATTTTGTGATTGTTGTTTTTTCCCCATCCAGGAATGATCACCATTCCTGCTGCATCTTTAGCAGGAGCTCAGTTAGTCTCAGCTGGATCCAACACAAACACCACCAACACCGGTCAGGGCACAGTTACAGTCACTCTCCCCATGGCTGGAAACATGGTCAATGCTGGAGGAATGGTCATGGTGAGCTCATGTGGTCATTTTTTTCCATCCAACATGACTTCTGGCCATAAACATGTGCTTTTTTAACCTTAGTATGTGTGCGTGTTTGTAATTGAATCAGATGGTGCCAGGCGGTAGCAATTCAGTTCCCACCATGCAGCGCATTCCTCTTCCTGGAGCAGAGATGTTGGAGGAGGAACCTTTGTATGTTAATGCAAAA[C/T]AGTATCACCGGATACTCAAGAGGAGACAAGCTCGCGCCAAACTGGAGGCTGAAGGCAAAATACCCAAAGAGAGAAGAGTATGTGTGATTTTTTTTTTTACTGCGCTAACAATGACATTTCAGTCACTTAAGTATTATTTTTGCTCGCTTTATTAAATATATATTGTTAATTTATAGTTAATTCACATTTGACTGCGTTAAAATATCAGAATATATTTTTAATTAAATATATTTTCATTAAATATACTGTTATTGTCACATTTTGGCCAGTCGCATCTTTTTAAAAATAACATTTGCCGTTTTTAAAATTCTTTTAAAGCACAGGTGTCAAACTCAGTTCCTGGAGTGCCTCAGCTCTGTGCAGTTTAGTTTCAAGCCTAATTAAACACACCTGATCTAACTAAATAAATGCTTCAGGCTTGTTTGAAACGTTCAGGTTATGCTGCTGTCAAACCACAGTTGTGCATGTGAAATTCTGTTGTACGGCGCTGCGAAAAGGGG
Associated Phenotype:
Not determined