ZMP
ncoa3
Ensembl ID:
ZFIN ID:
Description:
SRC3 [Source:UniProtKB/TrEMBL;Acc:Q1L661]
Human Orthologue:
NCOA3
Human Description:
nuclear receptor coactivator 3 [Source:HGNC Symbol;Acc:7670]
Mouse Orthologue:
Ncoa3
Mouse Description:
nuclear receptor coactivator 3 Gene [Source:MGI Symbol;Acc:MGI:1276535]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21881 | Nonsense | Available for shipment | Available now |
sa35062 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10250 | Nonsense | Available for shipment | Available now |
sa35063 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21881
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 |
---|---|---|---|---|---|
ENSDART00000110621 | Nonsense | 28 | 1497 | 1 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19085896)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18503210 |
GRCz11 | 11 | 18665552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTGTGCTCGGACAGGAAGCGCAAACTCTCCACATGTGACACACCAGGA[C/T]AAGGGTGAGACTTTTTTTTTTGTTTGAATGAATGCATTATTGTTGGTGTT
Long Flanking Sequence:
CCACACGCGCACACACACACACACTGAGGGTTGATCCATTTCCCCTGGGGCCCCGTTTCACTCCATCATAATCAGTGTCTCTTCTCAGACACACTGTCACACAAACACACACACACACACACATACACACACAGAGCACTGCTGCTGAGGCATGGAACATTCCGCGCATTCAGCTGTATGTGGGAACACTTCAAAATAAGCGATAGACACGTGCACACACACATGCAGATTTTGACCAAAACCTTTCGGAGAGAGATGAAGCCTTCAAGTGCATTGTGTACAATTGCAAATGATTTGTTTGTAAAGGAAAGGAAGTGCTTGTTTTGTTGTCCTTTCGTTTTAAGCTCTTGGATGGATGTACACCCAGTCTAAACTTTGTGTGTTTTATGTGTTTTTTTAGGTGCTGATATGTTTTAAGCATGAGTGGAGTGGGTGAGAACTCACTTGAGCCGTTGTGCTCGGACAGGAAGCGCAAACTCTCCACATGTGACACACCAGGA[C/T]AAGGGTGAGACTTTTTTTTTTGTTTGAATGAATGCATTATTGTTGGTGTTTAGGTGCGTTTCATCTTCTTAAATTGTGTGTTTTTGTTTGTCTCCAGATGTGATAAGCGCAGGAGGGAACAGGAGAGCAAGTATATCGAGGAACTGGCTGAGCTGATTTCAGCCAACCTTAGTGACATCGACAGCTTCAATGTCAAACCAGACAAATGTGCCATCCTTAAAGAGACAGTGCGCCAGATACGCCAGATCAAAGAGCAAGGTACACATCTGCTCGAGCTGCCCTTTTACATATCAGTCTGTGAAAATATTTACTAAGCCCACAGTGTGTGGAAACTGATGAATTTCTTTGGTTCTTTAAAACGCTGCCACCTGGTGGCTGGTGGAATGTTGTGTTGATGCAGTTTTTGCCATTTAAATTGAGTGATTCTTAGTCATTTTTAACACATTTACTACATTTTCTGGTGATCAAAAATATTATGTACTTTTTTAAACGCTGTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35062
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110621 | Essential Splice Site | 116 | 1497 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19089442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18506756 |
GRCz11 | 11 | 18669098 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCAAGGGGTCATCGACAAGGACCATCTGGGCCCTCTGTTGCTGCAG[G/A]TTAGATTAGAGACCTAAGGGTCACCAGAAGAACATTTGCTCATTTCTCAT
Long Flanking Sequence:
GCTGGCCCATAATGCATTCTCAGATGCACATTATAAATGATTCAGACTCGCGTTTAAAGAAATGGACTTGGTGTTGAGTAGCATTTACTGTAAACCGAGACTGTGAAAACACTGTTTTCATGAGCTGCCTCTGTGAAAAGATCACAGTGCTGCACATCTGAATATATATTCATGTAGTTGTGATTTTTACAATTGTCTTTTTACCTGCATTAAAACTTGCCAAATGTTAGACCCTTTACATGATCTTTTAGTAATTGTTCTAATATGCCAATTCTTTCATGACTCTCTTGTTACTATTATAATAGTTTTATTATCATCAGTGTTAATCAGTGCTAATATATTCTCTGCTATTTTTCTAAACCACTTCTAATACATGCTTTACATTTCCACGTGACACAGGTAAAAGCTCATGTGGTGATGATGATGTCCAGAAGGCGGATGTGTCCTCCACTGGTCAAGGGGTCATCGACAAGGACCATCTGGGCCCTCTGTTGCTGCAG[G/A]TTAGATTAGAGACCTAAGGGTCACCAGAAGAACATTTGCTCATTTCTCATACTAGCATCCCGAGCAATTATGATAACTGTGTTTTGTAAAGCACCAGTGGCATTTTAGAGGTTTATATAAATAAATAAATAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTACAGTTAAAGTCAGAATATAGCCCCCCCCCCCCCCCCCCCCATTTTTTCCTCAATTTCTGTTTAACGGAGAGAAGATTTTTTTTTTTTTTTTTTAACGTAATAGTTTTAATAACTAATTTCTAATAACTATTTTCTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAAACAAGTTATTGTAAATCGATGGTTTGTTCTGTAGACTATCAAAAATATATATTGCTTAAAGGGGCTAATAATTTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10250
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 |
---|---|---|---|---|---|
ENSDART00000110621 | Nonsense | 311 | 1497 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19096028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18513342 |
GRCz11 | 11 | 18675684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTTCCTGCATCGCAGYGAGGGTCAGCCCTGGTCATACAAGAGACATTA[T/A]CATGAAGGTATGTGGACAGACACTTGCAGGGATTTTCTTCTCATTTCCAG
Long Flanking Sequence:
TTTGAATCGTTCAGTTGTCTATGTTGTTATCTTTTCAATAAATGCATTGTAATATAGCACTGATATATTTTGTTTTTGATATAAATATGTAAAAAAAAATTTAAATAGTTAGAAATGTAGTGATATACGAATAATTATGAATAAATGAATAAAACACTGCTAAACAGCAATACCCTCATCAAATAAATCATATTTTAGTTCATGTTTTATAATAATTCAACACATTTATTATTTTATTTAACAAAAAAAATATCATAGAATATTACTTGCTGAAACAAAAAATTGTATAGCTATTATATCACAGTATATACAGAAGTGTAAAACCAGTCTAGTAGTATATCTGAGTGTGTGTATTTGTCCACAGGTAAACTGATTGAGATCGAGCAGCAGAGTCTTCTGCATACCACCATGCGTCCTGGCTGGGAGGATTTAGTGCGCCGCTGTATGCAGATGTTCCTGCATCGCAGTGAGGGTCAGCCCTGGTCATACAAGAGACATTA[T/A]CATGAAGGTATGTGGACAGACACTTGCAGGGATTTTCTTCTCATTTCCAGGGTTCTCAGATGTGGAACCTTATATTTGGTGAGATGTTGTTTTTGCATTCCTGTTTGCTCCAGTAGCAAAAGCAGCTATCAATGTTTGTGGCTTAAAGAAGAAAATGTATCTAGAGATTGATTATGGTTGTCAGATGAGATAAAGAAGCAGGTTTGCAATTTAACATCTCTTCTTTTGTTGTACTTTTCTGAAATGTGGTGCCAAGGTAATTTATTAAAGCAACAAAAATGTTTTAGATGTTCATTAAACAAACAAACAACACATTTAAATTCCAGTCAAAATAAATATAAAGTATTACATAGTACACTAGGACATTAAATCATTTTTGACATTGTGCAATACAGTCTTCATTATGTGTATTTTATTGTATCCATTTGTGACCAAATACACAAAATTATTTGCAATAAATACACTCACACACCCATTATCCACATATATACAAACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35063
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 |
---|---|---|---|---|---|
ENSDART00000110621 | Nonsense | 844 | 1497 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 11 (position 19101910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18519224 |
GRCz11 | 11 | 18681566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCAAGCCAAAGCTGGAGGAGCTTGAAGCAAGAGGGGCATCTGGAGGG[C/T]AGGGGGCAGGGGTCACGACCTCCAGTTCTAGTAACCAGGAGAGCAAGGTC
Long Flanking Sequence:
TCGGGACTGCGACTAGTGGACCTGTTCCAGGTCGTGCGTCCACTCCGATGGGATCTGACCCGAAGGAGACTGGAAGTGGCATGATGAGTCCTTCCTCCACAGGGGTGTCCTCTTCATCCGGTTCATCATCCGGGAATAACGTTAATCAGCAAAGCTCGGGTGGAGTGTCGTCCACTGCTTGTCCTAGTGGACATCACAGCACTCACACCTTACAGGAGAAACACAAGATACTCCACAAGCTTCTTCAGAATGGAAACACACCCGATGACGTGGCTCGCATTACAGCTGAAGCCACCGGCAAGTCCTCGCTTAGTTCAGAACACCCGGGTGCTGAGGGGAGGAATCTGGAGCTCAAACAGGAGCAGCACAGTCCGAAAGAAGGAAAAAAGCCACAAGCCCTCCTTCACTACCTCCTCAATAAGGATGACTCCAAAGAGCCCGGTGCTACAGAGGTCAAGCCAAAGCTGGAGGAGCTTGAAGCAAGAGGGGCATCTGGAGGG[C/T]AGGGGGCAGGGGTCACGACCTCCAGTTCTAGTAACCAGGAGAGCAAGGTCAAGCTCGAACAACCGGATGAGGTATGTGGTTGTTTCTTGACGCATGTCAACATCACATTGGTTCTATATTTTAGAATATATTTCAGTTAATAAGTAGATATTTAAATAGATGTAATATTCATTGTTTTTTGTGTTCATTAAGTAGATTCAAGTCTCATAAGATGCATTTGTAATGTTACTAAACATGTATATTAAAAAGGTTTGTTTTATTTTAATATTTTCTCTTCATCAAAAATTTTTTCTACAAAATGTGTAAAGTAGCACAGCTGTTTTTATAGACGTTTCTCAAGCACCATATCGTCATATGATTGATTTATCATGGATGGATAGATAAAAATGAACATGCCTTTTTTTAAATAGTCATCGCTTAAGAATCTGAACAACAATGTTTCTCTAAACCAGGGATGTTCAATCCTGTTCCTGGGAATCTACCTTCCTGCAGATTGCAGT
Associated Phenotype:
Not determined