ZMP
si:ch211-227i14.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate E1A binding protein p400 (EP400) [Source:UniProtKB/TrEMBL;Acc:B0
Human Orthologues:
EP400, EP400NL
Human Descriptions:
E1A binding protein p400 [Source:HGNC Symbol;Acc:11958]
EP400 N-terminal like [Source:HGNC Symbol;Acc:26602]
EP400 N-terminal like [Source:HGNC Symbol;Acc:26602]
Mouse Orthologue:
Ep400
Mouse Description:
E1A binding protein p400 Gene [Source:MGI Symbol;Acc:MGI:1276124]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21364 | Nonsense | Available for shipment | Available now |
| sa21365 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21364
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111655 | Nonsense | 1667 | 3108 | 29 | 63 |
| ENSDART00000138261 | None | None | 184 | None | 3 |
| ENSDART00000145142 | None | None | 1616 | None | 24 |
The following transcripts of ENSDARG00000074040 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 46441714)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 43701775 |
| GRCz11 | 8 | 43695194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACACCACCACAAGGTGAGGCACTGCTCCGTTCTGAAGCTGATTTTTA[T/G]CTTCATGTGGGTTGGCCAACAAGGTTTTTGAAAACTAGGCCCAGCAATAT
Long Flanking Sequence:
ATTGTAAACCACTGTCATTTAACGATAGTTTTTGTTCTCTGCTGAAAGGTGGAGATGTGGTGAAGGTTGCTCAGCTGGTGGGTCAGAGTCGGATCGCTCAGCCGGAGACTCCAGTGACCCTGCAGTTTCAGGGAAACAAGTTCACCTTGTCCCAGAGTCAGCTGCGTCAGCTCACCACCGGCCAACCCCTGCAGCTTCAAGGTACACTCGGTAATGTCCAGCTCATATTCATCTTCTCTCTGTCATTTCACCTCCATATATAGTCAGAATTGTGCGTTTATTTATTTATAATGCTCATGTCTATAAATGTCTGCTTTAGGTAACATCCTGCAGATTGTGTCAGCTCCTGGACAGCCTCTTCTCAGGCCTCAGGGGCCACCTATGGTGATGCCTACTGTCCCTCAGGCTGTGCCTGCGCAGAACTCCTCAGGCACGCCACCTCCTGCAACCTCCACACCACCACAAGGTGAGGCACTGCTCCGTTCTGAAGCTGATTTTTA[T/G]CTTCATGTGGGTTGGCCAACAAGGTTTTTGAAAACTAGGCCCAGCAATATTATTATTCATTCATTTTCTTGTCGGCTTAGTCCCTTAATTAATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTTTTACGCAGCAGATGTCCTTCCAGCCGCAACCCATCTCTGGGAAAGCAATATTATTCATTAAAAATAATTTAATTAATTACAAATAAAAATAATTATTAAAATGTGCAATTATATAAAAATTTGTGCTGGTCAAAGAGTAATCACATAATAAAAGTTTGCTTTTATATAATATATATTGCCTTGTTTCCAATGAATGGTATGGTTTAGTTCAGTACGGGTCACCTTTATCAGGCTTGTGTCCACTGCCAAATGGTACCAATGGAACCCTTTTTGTGGGCATGGTGTATGACAGTTGCAGACGATGTCATTCTCATTGGAGGAATATAAAAGTAAAGCTATACTGGCTAGAGGTGTGAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21365
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111655 | Essential Splice Site | 2200 | 3108 | 39 | 63 |
| ENSDART00000138261 | None | None | 184 | None | 3 |
| ENSDART00000145142 | None | None | 1616 | None | 24 |
The following transcripts of ENSDARG00000074040 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 46453268)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 43690627 |
| GRCz11 | 8 | 43684046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACGAAGAGGATCTGCTCTCCTATACTAGAGAGGATGCATACAACATG[G/A]TACAAATATATTTTAGCTAGTTGTTGTGTAAAATATGATGTGGCATAGTA
Long Flanking Sequence:
AAGGTGAACCACAATATGCCGAGAGACTACTGTGCATATATAAATGACTTGAAATCTTTTTTTGATTAATCGAAAGAAAGGCATTCATGGAAGAAACAGAAGAACAGAATTATTAATTTGTTGAAAAACAAGACAAAAAAAACTTACCAATAATATGTGATATGTTGATTTGTGATTAAAGTTTGTGTTGTGTCATCTAGCTGACTCCAATTGAAAGATACGCTCTGCACTATCTGGAATACCTGCACATCAGTGAAGATGAACAAGTTGTAAAGGTAAGGGATAGACTTTGAGTACAGCAATAGAGATATTTTGCCTGCCCTGCAAATACAGACTGCTTAATTGTTAAATTGTTTGCTTTACAGGAACGCATGGAGACTACTAAGAGAGGCTGGGAACTGCAACTACAACAAAAACTGAAGGTGGAGAAAGAGGAACAAATGATTCAAGAAGACGAAGAGGATCTGCTCTCCTATACTAGAGAGGATGCATACAACATG[G/A]TACAAATATATTTTAGCTAGTTGTTGTGTAAAATATGATGTGGCATAGTACTGTAACACTCTCCACACCTTCTTTATAGGAGTATGTGTTTGAGAATGAGGATGGACAAACAGAAATAATGCCGGTGAGTTTACTCTAAAAGTAGATTTCCTATTGCAAGTATGTTTTAGAATTGTTACATTTATTGCAACCTACTTTATAGAAAAGGTTTAAACTCCAAGCAGTAATATTAATTCCTTGATGTATACCATTTTAAACTTGATTACATTTGTTTTGATGGATTTATATTAATAACTTATTAAAAAAATGTCAATTAGGTTTGAGTTTATCTAAGTTTATTATTAATACATTACAGTTATTACAATTTATTCATTTATTTTTTCATGCTGGTATGAAGTTGTTGGTAAGCTTTATGAAATACACCCCAATATTTAACAAAAATGCCTTATCGTTTCTAACTCAATGTTGCTCTTTTCTGTAGCTGTGGACTCCGCCAACTC
Associated Phenotype:
Not determined