ZMP
ncoa1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate nuclear receptor coactivator 1 (NCOA1) [Source:UniProtKB/TrEMBL;
Human Orthologue:
NCOA1
Human Description:
nuclear receptor coactivator 1 [Source:HGNC Symbol;Acc:7668]
Mouse Orthologue:
Ncoa1
Mouse Description:
nuclear receptor coactivator 1 Gene [Source:MGI Symbol;Acc:MGI:1276523]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23769 | Nonsense | Available for shipment | Available now |
sa17222 | Nonsense | Available for shipment | Available now |
sa12342 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23769
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 |
---|---|---|---|---|---|
ENSDART00000045948 | Nonsense | 440 | 1367 | 9 | 27 |
ENSDART00000130513 | Nonsense | 436 | 738 | 9 | 10 |
ENSDART00000147515 | None | None | 466 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 36798236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 36870749 |
GRCz11 | 20 | 36773628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCCACTCCACCAGGCTACCTGACGCCCAGCCGCGTCGGGCCGTCACAG[C/T]AGGTCAGCAGCCCCTCTCCACTAGGCAGCCCTCTTACAGCAACCCCTACC
Long Flanking Sequence:
TTTAAATAAGTGGAGAATAAAGTAAACAATAAAAATTCTTAAGTTTTATATATACAGTATATACACACAGTTAGGTACATAAATGTTTAGACATCGACAGAATTCTAACATTTTTGGCTCAGTACACTAACACAATGGATTTTAAATGAAACTAACAAGATTTTTAACTTTAAAGGTATTTACATCGAAATCAGGTGAATGCTGTAGGATTACTACAGTTTGCATATGTGTCACACTTGTGTCACACTTCTGAATGGGTACATAGCTAATAACTATTTTTTAAATTGTGTTGCAGGGAACACAACACTGCTAGCTCTCAGGAAAACACTACCCCCAGCCTTTCGTCTCCTGCTGCTCCCCCTTCCCGCTCGCCTGCCCTGCAACCCTCCAGTGACCTCAGCATCCATCTCAACAACACCAACGGCACCTGTGCCACTCCCGGCCCCCTCACGCCCACTCCACCAGGCTACCTGACGCCCAGCCGCGTCGGGCCGTCACAG[C/T]AGGTCAGCAGCCCCTCTCCACTAGGCAGCCCTCTTACAGCAACCCCTACCTCATTCATGTCGCCCCGACCTCCACGGGGCAGCCCGGGCCTGGCCAGCAGCCCACGAGTGCCCGGACATCCATTCTCCCCCTCAACGCCCAGCATCCACTCGCCAGCTGGTGGACTAACCAGGCAGCAATCTGGCGGCGATGGTGTTGGTTTCTCGCTCCCTTCTCCTTTGCCCCCCAGACAGACTCCAACTCCCAGCAGCTCGCCGGCAAGGCAGCCTCCTGCCAAACCGCCAGAAGCATCCAACGATGAGCCTAAAAGCAATCAAGTCGGCAACCCCAAGCTCAGCCAGCTTTTAGATGGCGCAAGCGCCCCCGAACAAGACTCACAACCCCGTCCTTCACCCACGTCCCAATGCCCGGCCTCGCACAGCAGCCTGACAGAGCGGCATAAGATTCTGCATCGGCTGCTTCAGGACAATAGCCCTGCAGATGCGGGCAAGGAGCCGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17222
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 |
---|---|---|---|---|---|
ENSDART00000045948 | Nonsense | 856 | 1367 | 16 | 27 |
ENSDART00000130513 | None | None | 738 | None | 10 |
ENSDART00000147515 | Nonsense | 6 | 466 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 36808037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 36880550 |
GRCz11 | 20 | 36783429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACCATCTCTGTCATTTGTGTTTKTCTCTGAGCAGGCAKTGTGTCCCGTG[T/A]CCGCTGGATGAGATGCTRTGTCCTCCCACCACCCCAGAGGGAYGAAACGA
Long Flanking Sequence:
GCAGAGTTGGATTCAAACTGCAGGGCAGCAGCCCTCCAGGAACTAAATTTGACACCACTGAGCTAGGCGTTCCTTACAATTAAAGCTAGCAAATGCTAATGTTGTCTTTTTTTAATGTGTTGAACATCAGTTATGTTAAAATCTTATTTTTCATGACTCTAATATACGTTTGTCACTTTGATGTATAAAACAGTTAATGAGAAGAAAAGATACAAAGAACATTGTTGTACACCTACTTTGATTAGCATCTGAAAGTAAGTGTTGCTGTTCTGAAAGTGTTGGCTGGTAAAATGTTTTGTCTGGTCCCTCAAGAATCAATTACCACTATAAACATCACCCGGGTCGGAAGGAAACAGATGTGTGCTTTCACCCAAATTCTACTAAAAGTGTTAGCCAAATCAGCTAGAGTACCTGTCAAATTCTCCATCTCCAGTAGCAGTCAGAATCTCAGACCATCTCTGTCATTTGTGTTTGTCTCTGAGCAGGCAGTGTGTCCCGTG[T/A]CCGCTGGATGAGATGCTGTGTCCTCCCACCACCCCAGAGGGACGAAACGACGAGAAGGCCCTGCTGGAGCAACTGGTCACTTTCTTGAGCCACACTGACGAGAGCGAGCTGGCAGAGCTGGACCGAGCGCTGGGCATCGATAAGATTGTTCAAGTTCGTATCATATTTTCGTCAATGTTCTTTGCTGACCTTTTATTGTATAGTTTTGACACAATAATTAACTTTTGTTTCATATTTGCAGGAATTCACTAAATACCAGTTAGCAAGATTAAATAGTGGGTGTAATGAGTTAAAGTTAAAGGTGCAGTAGGTGATCTGCCTACATGCTATCCATTAGCATAATATCTTTAAATATCATTAAATCTTTAAAAATCATTTAAGATGACCCACTTGATCATGTCATTCACCAGTTAGAAAACTTTATAGTACTTTATAATACTACAATTCTGAACTGAAAACTGTATTGAATCTAGCACGTTTTCAGTTGTGTAGCAAGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12342
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045948 | Essential Splice Site | 1161 | 1367 | None | 27 |
ENSDART00000130513 | None | None | 738 | None | 10 |
ENSDART00000147515 | Essential Splice Site | 291 | 466 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 36812009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 36884522 |
GRCz11 | 20 | 36787401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAACACTCCTGTTCAACAGGGGCTTTTCCAGCAATTTGGGGGGTCTGG[T/G]ATGTGTCATTTGTATGTTTTATTTATTTTTTAAAAGAGAGCAACCMTTTT
Long Flanking Sequence:
CCTATGCTTCTGTGCATTTTCACACTCTTTCCCTCTTTTTCCACATGTTTTTTGTGTGATTCTGACAGTCTTGTGATTTCTCCATGTGTCTCTCAGCCTCCGCTGAATGCTCAAATGATGGCCCAGCGGCAGCGTGAGGTCTACAGTTACCAGCACCGCCAGCGGCAGCTTCTGCAGCAAAAGGTCATGCTAATGAGGCAGGGAATAAACACAGGGCCCCTGGGGGCTCAGAGACTTCCTAAGGGCCCCCAGCAGCAGCAGCAGCCGCCACCGCAGCAGCAGCAGCAATTTGGCTTTCCTCCAGGATACAACGCTGTGCCTGGAAACACCCCTACCTCCCCGAGCCACTTTAACCCCATGGGAGGACCTCTGGACCCAAAGCTGTCCGTCAGGGCAGGCCTGGGGAACCAAGGCATTATGGGAGCCATTCAAGGGCAGTTTGGGGGGCCTGTGAACACTCCTGTTCAACAGGGGCTTTTCCAGCAATTTGGGGGGTCTGG[T/G]ATGTGTCATTTGTATGTTTTATTTATTTTTTAAAAGAGAGCAACCATTTTCATTTAGTTTATTTGATGTAGTAGAGTAACTAAACTAAAACAGAAAAAATAATAACTTTATTGACCTATTGAAAAAAAATAAAACTATTAATTATTATGTATTTAATTATGTATTTAACTTAAACCATAAAAATTGTTACTAAAATAAATATTTTAATTTAGCTTAATAAATAATTAAGAAATATTATTTATAACTAAAAAAAAACATTTAAATAAATGTATTTATTATTTTATTTAACCTAAATAATTTTTCAGTTAGTTTACGTAATTGGAAAAAAAACCTAATTATTTAAAAACACTTTACAATTATATAAAATTATATAAACGTACAGAATTACTAAAACTATTATTTCAAATTAAAATGCAAAGTGTACAAATAAACACTGAAAAATGTCATTTAAAAATTTTAATATATTTTATTAATGCTAAATATCACACTGATTATGATAT
Associated Phenotype:
Not determined