ZMP
zgc:158288
Ensembl ID:
ZFIN ID:
Description:
cellular repressor of E1A-stimulated genes [Source:RefSeq peptide;Acc:NP_001074159]
Human Orthologue:
CREG1
Human Description:
cellular repressor of E1A-stimulated genes 1 [Source:HGNC Symbol;Acc:2351]
Mouse Orthologue:
Creg1
Mouse Description:
cellular repressor of E1A-stimulated genes 1 Gene [Source:MGI Symbol;Acc:MGI:1344382]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17479 | Nonsense | Available for shipment | Available now |
| sa32575 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17479
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 |
|---|---|---|---|---|---|
| ENSDART00000092502 | Nonsense | 58 | 207 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 776519)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150699.1 | 15957 |
| GRCz11 | KN150699.1 | 15957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGACTGGGCTTCAGTGGCGACGATCTCCAGCCGCGAGCCGGTGCGCGGA[C/T]AGCCCTTCTCCAACAGCTTCTCCATCAGCGACGGGCCGCCCGGGGCCAGC
Long Flanking Sequence:
GTGTTTGTGTTTCAGCTTTTGTTTCTCTGTGCAGTTCAGGATAGAGTCATCATCTCTCCTGTTTATAACTCTTAATCATCTTTACATCCATTATTTTCAGAGAGTGACTGAATGAATCGTGTGATTAACTCTTATGAACGAGTGAAAGTCAGTCTGGCAGCAGAGCGTCATCATCTGTTTACTAGCTTGTGCAAGTGAACACGTGCTGTGTTGAGGTCACATGACTGCGCTGGTCACGTGGCGCTGTGGACATCAGAGACGCCGCGGTGTTTATCTGACCCTCTGCAGTTGTTGTTGTTGTTGTTTTCTTCTTCTCCCGCTCGCTCGTGATGTTGCGCGCGCTGCTCCCCGTGATTCTGGCTCTCTCCGCCGCCGCTCCGGTGTTTCCGCTGGTTCTGGTTCCGCCGCACGAGCAGGTGGCGCGCATGGCCCGGTTTGTGGTCAGTAAGAGCGACTGGGCTTCAGTGGCGACGATCTCCAGCCGCGAGCCGGTGCGCGGA[C/T]AGCCCTTCTCCAACAGCTTCTCCATCAGCGACGGGCCGCCCGGGGCCAGCAGCGGGACACCATACCTGTACCTCACACACCTGGACATCTCTGTGCAGGACCTGCAGGTGAACACACACACACACACACACACACACACACAGACTGGAGATCTCTGTGCCAGAGCTGTACACTCTGATGATGATGATGATGATGATGATGATGATGAGGGGTGTTTGGAGGTGTATCACTGTAGTCTGAGTTTGTTTTTATTTATTTTGTCATAAAGCAGTGAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGTGTGCGTGAGTGAGTGAGTGAGTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTGTGTGTCTGTGCGCGCTGGTTTTGGTGGTTTGCAAAATTTGTATAATGACATGGGTTTGTCCTAGTTGGACTCTAATAAGTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32575
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092502 | Essential Splice Site | 94 | 207 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 778049)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150699.1 | 17487 |
| GRCz11 | KN150699.1 | 17487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAATAGACCTAATAATACAGTGTGTGTGTGTGTGTGTGTGTGTGTGC[A/G]GGTGAACCCGCAGGTCTCTCTCTCCATGTCTCTGGCTCAGAGCAGTTACT
Long Flanking Sequence:
ATACAATAATACACACTCTCTGACACACACATTCAAACTAACTCTCTCTCTCACACACACACACACACACACACTCCTGATGAGCGTCAGCACTATGTACGTTACGTCTGTAATCATCTGTGGCAGTGTGTGTTCATTGAACAGTAAGAATGATCATTAATCCAGATCAACCCGTCACGTCTCGTGGTCAGTTTCGGGCTCAGGCGTGTTTTGCACTCACACATAAGCGTACCGCACCAAACTGAACCATGCCAGAGCCCGATACAGAGCACTCACACTTCTCAAACCATCCGGGAAACGGGCCTGGGCAGGGTTCGGATAGCCTAGTGTGAGTGCACCCTTAAACCTCCTTCCTCATTAGAGGGTCACACACTCCTGCAGGAGACTATATATAGTGGAGTGAGGGCGGGGTCAACCTGTCACTCACATCAGATCTGCTGAAAGCCCCGCCTACAATAGACCTAATAATACAGTGTGTGTGTGTGTGTGTGTGTGTGTGC[A/G]GGTGAACCCGCAGGTCTCTCTCTCCATGTCTCTGGCTCAGAGCAGTTACTGCAGGAATCATGGGTACGACCCTCAGTCTCCTCTGTGTGCGCACGTCATCCTGTCCGGATCACTGCTGCAGGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTTAATCTGCGTGCATGTGAGATTCTGACCTGTGTGTGTGTGTGTGTGTGTGTTCAGCTGAATGACTCTGAGGAGGTGTGTGTGGCGAAGCGTGCTCTGTTCAGCAGACACCCGCAGATGCAGGACTGGCCCTCAGATCACGGCTGGTTCTTCTCGAAGATCAACATCACGCAGGTCTGGGTGCTCGATTACTTCGGCGGAGTCAAGACCGTCACACCGGACGAGTATTACAGAGCCCAGCCGTACCACACACACACACACAGAGGTGAGTCTGAGCACCACACACACACACATGTAAACACACTGATCTCTAGTTGACCATTCCTCAGTGAGTATGAAGGAGCAGTTGAC
Associated Phenotype:
Not determined