ZMP
helb
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0UYS3]
Human Orthologue:
HELB
Human Description:
helicase (DNA) B [Source:HGNC Symbol;Acc:17196]
Mouse Orthologue:
Helb
Mouse Description:
helicase (DNA) B Gene [Source:MGI Symbol;Acc:MGI:2152895]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20235 | Nonsense | Available for shipment | Available now |
| sa15508 | Nonsense | Available for shipment | Available now |
| sa30607 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20235
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 |
|---|---|---|---|---|---|
| ENSDART00000058020 | Nonsense | 663 | 1176 | 5 | 13 |
The following transcripts of ENSDARG00000053127 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 11839403)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 12776030 |
| GRCz11 | 4 | 12774879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCTTAGCATGCTTACCAAACACGCACAACTCCAGAAGTTCATCATTT[T/A]GGGTATAGACATAATTCATGTAGTTCTGTAGTATTCTGTAGATCATACTT
Long Flanking Sequence:
CACAAAACATAACATTACACTTCATGATGAATCAGAATTGATGTATAATTTTGCACTCGGCCACCTCAAACAACAAAACATTTTAAAACATGACCAACAATTTACATGATGCTACACTTTACAATTTAAAAAACGATAAAGCTAAACTTGACTTTAAATCATATTTTGTAATGTTAGGTCTTAAAATGTGTATTATTCTAATGAGATTGTTGATAATAGTTAGTATTTATAATAATGCAAACTTGACTTTGCACAATATTTCATTGAATATTTAAACATTATTATTTGACTAGTTAAGATAACTTTCTTCATTTCCATTTTGCAGGTGTTATGGAGTTTCATGACTGTAGATAAGGATCGAAGTGGGAATCCACAGGACTGGAAGTTCTCAAAGGTTCGGGTGCTGGTGGTTGACGAGGGAAGCTTGGTTTCTGTTCAGATCCTTCACTCCATTCTTAGCATGCTTACCAAACACGCACAACTCCAGAAGTTCATCATTT[T/A]GGGTATAGACATAATTCATGTAGTTCTGTAGTATTCTGTAGATCATACTTGCTAAATAAAATGTAACTAAATGATTATATATTTTCTGTCTGCAGGTGATGTGCGGCAGTTGCCCAGCATTGAGCCTGGAAACACACTATATGATCTGTTTGAAGGTCTCAGAAGAGTCCGCTGGGCTATTGAGATGAGGACCAATCATCGAGCCGAGTCTGAGCTCATCGTCAGAAATGCTGGACTGTGAGTTGATGGTTTATTCTCTTAAACATTTAGTTCCTTAGTGGGTTGTATGTATATGTTTTAATCTAATACAACTAAATAATAATTTATTAATCGCTATTTTCATAATCTTTTAGCATCTCTGAGATGGGTAAAAAAAAGTATTACAAGCCTCTGGACTTTGATGCCACCATAGACATGACAAACCCCTCTGCAGTGCCATCCGACAAAAGATTCATTTTTATCAAAATCAGTTCGGACAATTTTTCTTTTGGTAAGTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15508
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 |
|---|---|---|---|---|---|
| ENSDART00000058020 | Nonsense | 721 | 1176 | 7 | 13 |
The following transcripts of ENSDARG00000053127 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 11839019)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 12775646 |
| GRCz11 | 4 | 12774495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATTTTCATAATCTTTTAGCATCTCTGAGATGGGYAAAAAAAAGTATTA[C/A]AAGCCTCTGGACTTTGATGCCAYCATAGACATGACAAACCCCTCTGCAGT
Long Flanking Sequence:
GTTCTCAAAGGTTCGGGTGCTGGTGGTTGACGAGGGAAGCTTGGTTTCTGTTCAGATCCTTCACTCCATTCTTAGCATGCTTACCAAACACGCACAACTCCAGAAGTTCATCATTTTGGGTATAGACATAATTCATGTAGTTCTGTAGTATTCTGTAGATCATACTTGCTAAATAAAATGTAACTAAATGATTATATATTTTCTGTCTGCAGGTGATGTGCGGCAGTTGCCCAGCATTGAGCCTGGAAACACACTATATGATCTGTTTGAAGGTCTCAGAAGAGTCCGCTGGGCTATTGAGATGAGGACCAATCATCGAGCCGAGTCTGAGCTCATCGTCAGAAATGCTGGACTGTGAGTTGATGGTTTATTCTCTTAAACATTTAGTTCCTTAGTGGGTTGTATGTATATGTTTTAATCTAATACAACTAAATAATAATTTATTAATCGCTATTTTCATAATCTTTTAGCATCTCTGAGATGGGTAAAAAAAAGTATTA[C/A]AAGCCTCTGGACTTTGATGCCACCATAGACATGACAAACCCCTCTGCAGTGCCATCCGACAAAAGATTCATTTTTATCAAAATCAGTTCGGACAATTTTTCTTTTGGTAAGTGAGCAGTCTTTAAATGGTATCTTTTTTTCACAACACTTACAATGATAATGCATGCTAGAAATGGAAGAATTATTACAGTATACAGGGGTCGGGAACCTTTTTTCAACAAAGATTTTTTTAGCAAATATCTTTTTTTTTTTAAAGAGTCATTTGGATGTATATTTATCTCAAAATGCCTCTTTAAAGTGCATTTGCTACTGTATTACTACTATAAATAATGCAGGTTTCCATGAATGAAAAAAGAGCGTCCTTTTATTGAAAGGAGTTCTTATTCATTTTGCTGTAAAAATTACAATAAAGAGGGAACTGTAATTGTATTTTCGATAGGAAAATGATTTCTAGTGATGGTTATCATTTTTAAACTGTAAAATATTATTGAAGGAAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30607
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058020 | Nonsense | 891 | 1176 | 11 | 13 |
The following transcripts of ENSDARG00000053127 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 11837405)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 12774032 |
| GRCz11 | 4 | 12772881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGGATGTGACTAAATCTGTCGAGAATGAAAAAAATAAAATGGTGCGT[C/T]AACTGACACTCGATGATAAAAGCGACCGCCAGGTGACTTGTAACTACAAA
Long Flanking Sequence:
GGATTGTGAGTTAATCAATGAGCTTTGCTGCAGACATTATTCAAACCATACCACAAAGTGAGAAAACAAGTTATTTTCACAGATATACTAGCATCACAACATAAATGTAATGCTTTTTTTAATTAATTCGTTTCAGAACTGCCAAGAAAACATTCAACTTTCAGGTAGGTGATAAAGTCTGCTGCACTAAGAATGGCTACGTCACAGACTATGATAAGAAGGAGACGTCTTTGGCGGACATCAGAGCTTCACATAATCGTGCTGAAAGTCAACAAGATGATCAGAAGAAAGAAAAGAAAGAGAAGAAAGAGCGATTGTGCAATGGCGAAATTTTCTTCATTAAAGATGTACTTTTATTTACTGATTTATGATCATCTTTATATTTTGATTCGAAATGTAAGAAGTCATTTGATCTATTTATTGATTGATTTAACTTATTTCTGGACCAATCACAGGATGTGACTAAATCTGTCGAGAATGAAAAAAATAAAATGGTGCGT[C/T]AACTGACACTCGATGATAAAAGCGACCGCCAGGTGACTTGTAACTACAAAGAGCTACAGAGAGAGTGTAAACTGCGCCATTCTTGGGCAAGAACCATTCACACCTTTCAGGTATTGATGCTCTTTGTTCATCTAGGGCTCTATTAACACCCAGCATCACCATTTGTCCTAAGGCCCTGTTTGACATCTGGCATTAACATGTGTTTTTAGTGACCCGGAGACAAGATTATCACTTACACCTGGTATTGAGATGCTTTTTCTTTGATCTAATCACAAGTTGGCAATGCTAAATACTGACGTCAATGAGGTGTAAAATGTTCAGCCACTTCCACAGGTGTAAACAACTTTTTCTGTTGTCTCCTATAAATACCAGATTAATATGCTACTTAGCGAAATATTTCAGTGTCAGCTAGATGATGTGGATAAAGAAGAAAGAGTAGGGTTTTTTTTGTTTGAAATGCAGTGATATACATCAAAAACAAATGTGTTAGACCCCAGATG
Associated Phenotype:
Not determined