ZMP
zgc:162976
Ensembl ID:
ZFIN ID:
Description:
Protein HEXIM [Source:UniProtKB/Swiss-Prot;Acc:A5D8S8]
Human Orthologues:
HEXIM1, HEXIM2
Human Descriptions:
hexamethylene bis-acetamide inducible 1 [Source:HGNC Symbol;Acc:24953]
hexamthylene bis-acetamide inducible 2 [Source:HGNC Symbol;Acc:28591]
hexamthylene bis-acetamide inducible 2 [Source:HGNC Symbol;Acc:28591]
Mouse Orthologues:
Hexim1, Hexim2
Mouse Descriptions:
hexamethylene bis-acetamide inducible 1 Gene [Source:MGI Symbol;Acc:MGI:2385923]
hexamthylene bis-acetamide inducible 2 Gene [Source:MGI Symbol;Acc:MGI:1918309]
hexamthylene bis-acetamide inducible 2 Gene [Source:MGI Symbol;Acc:MGI:1918309]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22060 | Nonsense | Available for shipment | Available now |
| sa35236 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22060
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000053003 | Nonsense | 58 | 319 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 16413108)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 15524073 |
| GRCz11 | 12 | 15566380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGGTGTCAGGAGATGTGCATCCAATGTGTCGGGATCGGAGTGATCCT[G/T]AGCCCAGGACTGGCGATGCAGCAAGTGACGACGGGTTTCCTGCAGACAAA
Long Flanking Sequence:
TTCGTTGAGACAGCGTTAAATAGTAGAGGGAACGTAAATAGTTAAAATCAACAGTATCATATAGCATATCAACTCAAACACGAGATTTGAGTTAAACGGTAAGTTAACTGAAATATAACTTGTGCGTGTTTGTTAATGCTGTTTCTTATGTTTAAACAGTGCACTTTATGAGTAAACACTGACTTTTTCCCTCTTGGGTGTTTTGTGCGTTGTTTAAAATGATAGTGTTTATAAAGTTTCTTTTCTTTCATATCACAGTTTAACATACGATTGTATCCCCATCTGACTGATCAGAAACTTGTATCTCCTTCAGGTGGGAGTGTGCAGTTATGGAGCTTATTAAAGAAGAAACTGCACCGGAGGATGACAGCAGGGGGCGGCAGAGAGATTATCGGACGAGTGTTGTCTCCTCGAAACAAGTGCAAAGAAATCAGTTTGAGATTTGTCCTGGTTTGGTGTCAGGAGATGTGCATCCAATGTGTCGGGATCGGAGTGATCCT[G/T]AGCCCAGGACTGGCGATGCAGCAAGTGACGACGGGTTTCCTGCAGACAAAACGAGTAGTAAGAGAGACTCTGAATGCGCGGCAGTAAACACCGATGGGGTGTCTGATGGCCGCCAGGGCAAAAAGAAACACAGACGGCGACCCTCCAAGAAGAAGCGCCGCTGGAAGCCGTATTTTAAACTGACATGGGAGGAGAAAAAAGAGCTGGATGAACGCGAGACCGCGCGGGCGTCGCGAGTGCGCGCCGAAATGTTCGCTAAAGGTCTCCCCGTCGCACCGTACAACACCACCCAGTTCTTAATGGAGGAGCACGACCGTGAAGAACCCGATCTCAACACTGAGCTGGGAGGTCGAAAATCCGGGGCAATCCGCTCCGAGGACACGGCCAGTGAGGACGAGAATTTCGAGGCTGAAGAGGACGACGAGGAGGAAGGCGGCGGAGGTAGCGACGGTATGGGAAGACCAGGGCAAGCAGGTGGGGAGTTTTTGCAGAAGGACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35236
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 |
|---|---|---|---|---|---|
| ENSDART00000053003 | Nonsense | 96 | 319 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 16412994)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 15523959 |
| GRCz11 | 12 | 15566266 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACTCTGAATGCGCGGCAGTAAACACCGATGGGGTGTCTGATGGCCGC[C/T]AGGGCAAAAAGAAACACAGACGGCGACCCTCCAAGAAGAAGCGCCGCTGG
Long Flanking Sequence:
ATAACTTGTGCGTGTTTGTTAATGCTGTTTCTTATGTTTAAACAGTGCACTTTATGAGTAAACACTGACTTTTTCCCTCTTGGGTGTTTTGTGCGTTGTTTAAAATGATAGTGTTTATAAAGTTTCTTTTCTTTCATATCACAGTTTAACATACGATTGTATCCCCATCTGACTGATCAGAAACTTGTATCTCCTTCAGGTGGGAGTGTGCAGTTATGGAGCTTATTAAAGAAGAAACTGCACCGGAGGATGACAGCAGGGGGCGGCAGAGAGATTATCGGACGAGTGTTGTCTCCTCGAAACAAGTGCAAAGAAATCAGTTTGAGATTTGTCCTGGTTTGGTGTCAGGAGATGTGCATCCAATGTGTCGGGATCGGAGTGATCCTGAGCCCAGGACTGGCGATGCAGCAAGTGACGACGGGTTTCCTGCAGACAAAACGAGTAGTAAGAGAGACTCTGAATGCGCGGCAGTAAACACCGATGGGGTGTCTGATGGCCGC[C/T]AGGGCAAAAAGAAACACAGACGGCGACCCTCCAAGAAGAAGCGCCGCTGGAAGCCGTATTTTAAACTGACATGGGAGGAGAAAAAAGAGCTGGATGAACGCGAGACCGCGCGGGCGTCGCGAGTGCGCGCCGAAATGTTCGCTAAAGGTCTCCCCGTCGCACCGTACAACACCACCCAGTTCTTAATGGAGGAGCACGACCGTGAAGAACCCGATCTCAACACTGAGCTGGGAGGTCGAAAATCCGGGGCAATCCGCTCCGAGGACACGGCCAGTGAGGACGAGAATTTCGAGGCTGAAGAGGACGACGAGGAGGAAGGCGGCGGAGGTAGCGACGGTATGGGAAGACCAGGGCAAGCAGGTGGGGAGTTTTTGCAGAAGGACTTTTCTGAGACCTATGAGAAGTACCATGTAGAGGCGCTTCAGAATATGTCTAAACAAGAACTAGTTCGGGAATACCTGGAGCTGGAGAAGTGCATGTCGCGGTTAGAAGAGGAGAAC
Associated Phenotype:
Not determined