ZMP
hlx1
Ensembl ID:
ZFIN ID:
Description:
H2.0-like homeobox protein [Source:RefSeq peptide;Acc:NP_997866]
Human Orthologue:
HLX
Human Description:
H2.0-like homeobox [Source:HGNC Symbol;Acc:4978]
Mouse Orthologue:
Hlx
Mouse Description:
H2.0-like homeobox Gene [Source:MGI Symbol;Acc:MGI:96109]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11010 | Nonsense | Available for shipment | Available now |
| sa19249 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11010
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 |
|---|---|---|---|---|---|
| ENSDART00000004652 | Nonsense | 183 | 327 | 3 | 4 |
| ENSDART00000131806 | Nonsense | 212 | 356 | 3 | 4 |
| ENSDART00000143668 | Nonsense | 156 | 280 | 2 | 3 |
| ENSDART00000004652 | Nonsense | 183 | 327 | 3 | 4 |
| ENSDART00000131806 | Nonsense | 212 | 356 | 3 | 4 |
| ENSDART00000143668 | Nonsense | 156 | 280 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 52537440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 52385897 |
| GRCz11 | 20 | 52197802 |
KASP Assay ID:
2261-5004.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCCAAAGACACAATGCCACAGACKTACAAGAGGAAAAGATCCTGGTCC[A/T]GAGCTGTGTTTTCCAACCTGCAGCGGAAAGGCCTGGAGAAACGCTTCGAG
Long Flanking Sequence:
ATGCATAAATGCACGGGGTTAATGGGAACTCTTTGTGTTTTTCTGTAACAGATCTCACGTCGATTGTTAGTCCGAATCGGCAGTCTGCAGTCCATGTGTCTGCCAGCCCGTACTTCGCGTCCATAGACCCGACCATGAGCGAAACCTCCTCCCTGATGGGTTCGATAGGCAATGCCGCCAGACAATCAGGGCAACATCAGTTTCAAGACACCTTCCCAGGTAGTGTAGAAACTCCCCAGTTGAGCCAAAATAAGTAACTAAATCAGACAGAACGTGTGTGGACGAAATGTCCTTCTTTTGACTCTGACTGCACGTGTATAAGTGATTATTTTGCACATGCATAATTAAATAGCATGCATTTAAGACAAAGTTGGTGCATTGTGCAATGCATTTCTGCTCCGTTCTAATGGCGATTGTGTGGTTTGAACCAAACAGGGCCGTATGCGGTGCTTTCCAAAGACACAATGCCACAGACGTACAAGAGGAAAAGATCCTGGTCC[A/T]GAGCTGTGTTTTCCAACCTGCAGCGGAAAGGCCTGGAGAAACGCTTCGAGATACAAAAGTACGTCACAAAACCGGACAGAAAACAACTGGCTGCGATGCTGGGACTCACTGACGCACAGGTGAGCGTAACTTACAATTTGGTGTATTTTATGAAATGCGTGGTGATATTAATTCAGATAATTAGCAGATCTAGTGTATTTTTCATGGTGTTATTTATTTGTGCATTTACAGGTAATGTTCTCGCACTTAAATGATAAGCACATGCCATCTGGAGTGCTTTGTAAAAAAAAATAAAAAGCTGCAGCATTGCGACACCACACATTTCTAGAGAAATGAAAGTCAATTATAACGAATTATTGCAAACGCGGGAGGGGTTCAAGTTGTTTCGTTTCAAAACGTCCTAATTTAGGACATTGGGCAAGAGCTTGTGTTTTATTTGATATCGAAAATGACAGGACACCAGCATTAGGAAGGCGATAAGAGAGTTTCAAAACTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19249
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 |
|---|---|---|---|---|---|
| ENSDART00000004652 | Nonsense | 183 | 327 | 3 | 4 |
| ENSDART00000131806 | Nonsense | 212 | 356 | 3 | 4 |
| ENSDART00000143668 | Nonsense | 156 | 280 | 2 | 3 |
| ENSDART00000004652 | Nonsense | 183 | 327 | 3 | 4 |
| ENSDART00000131806 | Nonsense | 212 | 356 | 3 | 4 |
| ENSDART00000143668 | Nonsense | 156 | 280 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 52537440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 52385897 |
| GRCz11 | 20 | 52197802 |
KASP Assay ID:
2261-5004.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCCAAAGACACAATGCCACAGACGTACAAGAGGAAAAGATCCTGGTCC[A/T]GAGCTGTGTTTTCCAACCTGCAGCGGAAAGGCCTGGAGAAACGCTTCGAG
Long Flanking Sequence:
ATGCATAAATGCACGGGGTTAATGGGAACTCTTTGTGTTTTTCTGTAACAGATCTCACGTCGATTGTTAGTCCGAATCGGCAGTCTGCAGTCCATGTGTCTGCCAGCCCGTACTTCGCGTCCATAGACCCGACCATGAGCGAAACCTCCTCCCTGATGGGTTCGATAGGCAATGCCGCCAGACAATCAGGGCAACATCAGTTTCAAGACACCTTCCCAGGTAGTGTAGAAACTCCCCAGTTGAGCCAAAATAAGTAACTAAATCAGACAGAACGTGTGTGGACGAAATGTCCTTCTTTTGACTCTGACTGCACGTGTATAAGTGATTATTTTGCACATGCATAATTAAATAGCATGCATTTAAGACAAAGTTGGTGCATTGTGCAATGCATTTCTGCTCCGTTCTAATGGCGATTGTGTGGTTTGAACCAAACAGGGCCGTATGCGGTGCTTTCCAAAGACACAATGCCACAGACGTACAAGAGGAAAAGATCCTGGTCC[A/T]GAGCTGTGTTTTCCAACCTGCAGCGGAAAGGCCTGGAGAAACGCTTCGAGATACAAAAGTACGTCACAAAACCGGACAGAAAACAACTGGCTGCGATGCTGGGACTCACTGACGCACAGGTGAGCGTAACTTACAATTTGGTGTATTTTATGAAATGCGTGGTGATATTAATTCAGATAATTAGCAGATCTAGTGTATTTTTCATGGTGTTATTTATTTGTGCATTTACAGGTAATGTTCTCGCACTTAAATGATAAGCACATGCCATCTGGAGTGCTTTGTAAAAAAAAATAAAAAGCTGCAGCATTGCGACACCACACATTTCTAGAGAAATGAAAGTCAATTATAACGAATTATTGCAAACGCGGGAGGGGTTCAAGTTGTTTCGTTTCAAAACGTCCTAATTTAGGACATTGGGCAAGAGCTTGTGTTTTATTTGATATCGAAAATGACAGGACACCAGCATTAGGAAGGCGATAAGAGAGTTTCAAAACTTTACA
Associated Phenotype:
Not determined