ZMP
hfm1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2BIH3]
Human Orthologue:
HFM1
Human Description:
HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:20193]
Mouse Orthologue:
Hfm1
Mouse Description:
HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:3036246]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19742 | Nonsense | Available for shipment | Available now |
sa32909 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19742
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099851 | Nonsense | 408 | 1049 | 11 | 29 |
ENSDART00000141518 | Nonsense | 533 | 977 | 14 | 26 |
The following transcripts of ENSDARG00000068922 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23002243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22887671 |
GRCz11 | 2 | 22543322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAGCAACTGCAGTAATCATGACACGGCCTCAGACAAAGGACAAATA[C/A]ATGCATTTCTTGAGTGGCTTAGACTGCATAGAGAGCAGGTATACACCTAA
Long Flanking Sequence:
TGACTTGCCAGTTTTATGTAAGCTCTGCAACTTTATTTTCACTTATTTACTTCTGATTACACATTATTCAGTATGCATTATTATAGATATAATATATATATATATATATATATATATATATATATTTATTATTTTTTTTTTTTATATATATTTTTAGTTACAACAAGTACTCTAGCCATGGGTGTGAATATGCCAGCCCACCTTGTGGTAATCAAATCCACAATGCACTATGTTGGTGGTGCATGTGAGGAGTACAGTGAAGCTGACCTGTTACAAATGATTGGAAGAGCTGGCAGACCACAGGTACTATTAACAAATGTTAATATTATTACAAACACAAAGTGCCAGCTCTAAAAGCAGAGTTGTTAGTAGTAAAACACAAAATCTCAGCTAGTTACAGTATTCAGATTTGGACAATAATCACTTGCTTTGGTTTTTGTTTAGTTTGACACAACAGCAACTGCAGTAATCATGACACGGCCTCAGACAAAGGACAAATA[C/A]ATGCATTTCTTGAGTGGCTTAGACTGCATAGAGAGCAGGTATACACCTAATCACATTTTGTTCTGTTAGAAATTTTAGTTGCATTTTCTGTTCTTTTTAAATAGATCTTATTAACAGGTTGATTTATTTGTTACTTATGGATTTGACAAGTACAACAAAATAAACATTTTTCAGTTTGCATACAAATCTGGTGGAGCACTTGAATGCAGAAATAGTTCTTCACACCATATCTGATGTGAACATGGCTCTGGACTGGATCCGCTCTACTTTCCTGTACATCCGTGCTTTGAAAAACCCCAAACACTATGGTAAACCTTAAACCATGAGTACACTGAAGATACAGACATCAGCCAAAGCTCTTCTTTATTAGCCTCTCATTTCACAGGCTTTCCCCCTGAGGTTGACAAATGTGGAATTGAGACTAAATTACAAGGTATGAAAATTAATAAATTAAATCGTGAATCAGTTGTTGTTCAATGGCTAAAGGCTGATTTATACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32909
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 |
---|---|---|---|---|---|
ENSDART00000099851 | Nonsense | 905 | 1049 | 26 | 29 |
ENSDART00000141518 | None | None | 977 | None | 26 |
The following transcripts of ENSDARG00000068922 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 22987586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22904241 |
GRCz11 | 2 | 22559892 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGCCATTTCTTTTTTTAGGCAAAATTGGAGTCAAAAGGACTGTACTA[C/T]AGTCAAATGTCTCCTCATACCTTGACAACCTAAAAATGAGGAATGAGAAA
Long Flanking Sequence:
GAGCAGTGGGTGTTCCAAAGTTAGTGTACAGTGAGTAGCTACTGTCTGGTCTAATCATCACTTATTTAAACTCGCCTGACTCCCTTGATGTTCTGCTACCTTCTTTGCATTCTTTCTCACCTGTCATCCCCTTATCACCTCTCATCCATGGTCTCCCTCCTGCAAACAAAAGACTCTAAAATATATCCATATCACTGCCTTCTGGCATAATCAGTGCATTTCTAAATAAAACCATTAAGAATTACTAAATGGCTTAAATAACATAGTAATGTTCGACGGTTATATTCAAATTCATATAGACATTCTCTTCGTGGATCAAGTTGCTCCAAACATGGTTAAGAGAAATTGCCATCATCTCTGCAAAAACAAAGAGCTCTGTAGACATGACTGCTGTGAGTACAAGAGGTTTTAGGTGATCCTAGACTGCTCTCATTGTCTGTACTGGTTCATTCATGCCATTTCTTTTTTTAGGCAAAATTGGAGTCAAAAGGACTGTACTA[C/T]AGTCAAATGTCTCCTCATACCTTGACAACCTAAAAATGAGGAATGAGAAACTTTGTGAGACTCCTGTGAAGCGATTGAAGGTCAGAATTCTTATGATCAGGGTTACATTTACACAACGGTCAGAAAATGTAATTCATTATATCCTAATAGTTCAGCTGCATGGCAAGATTTTGTTTTGTAAGATATACTGTATTTTCAATTGAGTTTTGACTTTTTCTTTAGATGATGATGAATAATGGCACAGCAGCTGTAAGCATGCAGCAGTTCTCCTACAAACCCAAAGACACACATTCTGCTGCCAAGAGGTACTCCAGTGTTTCTATTATTAAACTTTAAGTTAACCTAAAAACAAAACTGACTCACTTTTAGTCGTTCCAAATCCCTGTGACCTTCGTTTAATATTTGAAACAAAAATTAACATATTTTAGGTGAAATAGCTGAGAGCTCCGTCATCCCCTATAGACAGCATGGATTCAGACTCAAAAAAAAAAAAACAACTT
Associated Phenotype:
Not determined