ZMP
heg
Ensembl ID:
ZFIN ID:
Description:
Protein HEG [Source:UniProtKB/Swiss-Prot;Acc:Q6R8J2]
Human Orthologue:
HEG1
Human Description:
HEG homolog 1 (zebrafish) [Source:HGNC Symbol;Acc:29227]
Mouse Orthologue:
Heg1
Mouse Description:
HEG homolog 1 (zebrafish) Gene [Source:MGI Symbol;Acc:MGI:1924696]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14693 | Nonsense | Available for shipment | Available now |
| sa14122 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14693
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 |
|---|---|---|---|---|---|
| ENSDART00000004462 | Nonsense | 95 | 977 | 2 | 13 |
| ENSDART00000140325 | Nonsense | 95 | 841 | 2 | 12 |
| ENSDART00000147938 | Nonsense | 95 | 935 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 39744537)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38882433 |
| GRCz11 | 9 | 38692228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCGTTCTTCTTTAAYTATCCAATMCAGGACATTCACCAAAACCTTTA[C/T]AAACCTCTACAAATGCAGCGGATTGGAAGACCAGTATGACCTCAGATGAG
Long Flanking Sequence:
TATCCAAGGACGATTTGTCTACCATGAAGGTAATTTTACGCCATCTGACTCATTAAACTTATTGGACTCACATATACAGTATTCCTCCTATCCAGTCAGCAGTCCTGCTGATTATAACTTTGCCTGTGTATGAACTCCATGCAGGCAGCGACAACGCTGTGATATGGACTTTGCTAGGTCAGCTGAAGGAAGGAAACAGCAGGTCCCAATGGGTCAGATCCCCTCCATTTTTAGGGCTCAAGCTTTTGTTAGGTTAGACGAGCTTGGCTGCCAATTGTTCTCCACCCAAAATCATTACATCCGCAGTCACTTCTGAAAACATCTCACATGGTTCATGAGGTTTCCCAAGACTCACTCGATATGAAGCGCACCCTAGTGGCCATCTAAAATCCCCCCTACCTCAGTTTCAGTATTATTTGCAGTTTGACTGATTTACAGTACACATTTTCTAACTCGTTCTTCTTTAATTATCCAATACAGGACATTCACCAAAACCTTTA[C/T]AAACCTCTACAAATGCAGCGGATTGGAAGACCAGTATGACCTCAGATGAGACAACAGAACATCTTCAATCTGACACTGAGCTTACCCATAATGCGACCGCCCAATGGGAGAGTCCATCATCAGCATCTCACAGCATTACCAGCCACCATCCAGTAACAGAGACACGAACCGTGCGAGATGTAACAGATCTGATAGACATGGACACCACAGACTCAGTCTCCCACACTGATAGCACCTACATTTCCACAACCAACCGAGTTGGAGAACGCACACTGCTCTCAGTGATCTCCAACAGCACCTTTGCGTACACCCAGAACTCAAGCATCTCTGATGCAGAGTCTCAAACGTCCCCATGGGAGGAGAAGACATCAGGAGCCACCCAAGTCAATGAGGAAACTGAAGAAACTGTGTCAACAGTGTCCGAACAGACTGATCCCACTTTTGAAGACCGCAATATCACCAGTGCAACTCTGGAGACTGGGCGGTCAACATTATTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14122
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 |
|---|---|---|---|---|---|
| ENSDART00000004462 | Nonsense | 671 | 977 | 5 | 13 |
| ENSDART00000140325 | Nonsense | 671 | 841 | 5 | 12 |
| ENSDART00000147938 | Nonsense | 671 | 935 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 39748890)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38886786 |
| GRCz11 | 9 | 38696581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATAAGATAACTCTGTCTGCTTTGGTTTTACCTTGCAGTCAAGACATTTT[T/A]GGGCACTTTCACAGTCAACAACTCTCTTCATCTCAGAAATTTAGGTCTGC
Long Flanking Sequence:
TGTGCACAATTACAACAACACTTTTTCCTTTTAGGTCATGTATGTGGACCTAAAACCTGTGCAAATGGAGGTCATTGTGTTAGATCAGCTGAAGGAAGTTACTACTGTCAGTGTCTCTCCGCATGGACCGGACCCTTCTGCACTGAAGGTAAGAATAAGCCCATTACATATCATTTGTTCACATATTACAACATGCCACAATATTCAGACTTTTGAATTTGTTCTGCTTGCATCAGTGCATGGGATAAAAACAAATTGATTGGTCTATGTTCATTTCTCTAGATGTGGACGAGTGTGTGAACAGTCCATGTCCTCAGGGTTCAGTGTGTGTCAACACAGGTGGTTCTTTCAGCTGTGAATGTGACCTGGGCTTTGACCTGGAGGATGGCCGCAGTTGTACACAAGGTATGTGGTCAGTATTTTAGAATAATTTCTGGAGAAGATAACAAACATAAGATAACTCTGTCTGCTTTGGTTTTACCTTGCAGTCAAGACATTTT[T/A]GGGCACTTTCACAGTCAACAACTCTCTTCATCTCAGAAATTTAGGTCTGCACGAGCTACACAGAGAGATCCAACAGCTGGTACGCAACAATATGCTGCAACTTGCATTATAAGCTCATCTAATGCTGTATAGCAACCATTATGGAAATGGGTTGAAGATGATAAATTGATGTTGATGGAGTTTGGGTTAATTTGATACATTTGTGTATTGGTTTTTCAGCTCAATGCTTCTCTCTCCATCTTCCATGGTTATAGACGCTTTACCCTGGGTAAAAGGTGAGTTTCATAAATGATCATAAACATAAATAGCATAAAAGTTATTTGATCTCTTCATATTGTGCCATGCAATTACTGTCTGCCTGTCCATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGCCTGTCTGTCTATCTATTGTTTGTTTGTTTGTTCGAACTATCATTTGTTCTATCGTTCTATCTATCGTTTGTTATCATTATATTGTTTGTTCTAT
Associated Phenotype:
Not determined