ZMP
ncor1
Ensembl ID:
ZFIN ID:
Description:
nuclear receptor corepressor 1 [Source:RefSeq peptide;Acc:NP_956570]
Human Orthologues:
AC144838.1, AL391119.1, NCOR1
Human Descriptions:
Putative nuclear receptor corepressor 1-like protein C20orf191 [Source:UniProtKB/Swiss-Prot;Acc:Q9H4
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A6NGY8]
nuclear receptor corepressor 1 [Source:HGNC Symbol;Acc:7672]
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A6NGY8]
nuclear receptor corepressor 1 [Source:HGNC Symbol;Acc:7672]
Mouse Orthologue:
Ncor1
Mouse Description:
nuclear receptor co-repressor 1 Gene [Source:MGI Symbol;Acc:MGI:1349717]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18033 | Nonsense | Available for shipment | Available now |
sa17067 | Nonsense | Available for shipment | Available now |
sa20512 | Essential Splice Site | Available for shipment | Available now |
sa13384 | Nonsense | Available for shipment | Available now |
sa13203 | Nonsense | Available for shipment | Available now |
sa17231 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18033
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 |
---|---|---|---|---|---|
ENSDART00000097574 | Nonsense | 492 | 2409 | 15 | 48 |
ENSDART00000143573 | Nonsense | 454 | 2398 | 14 | 47 |
Genomic Location (Zv9):
Chromosome 5 (position 43553265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41334530 |
GRCz11 | 5 | 41934683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGTCAKCTGTCTAAATGCTTCTGGTATTGTGCTTCTTTTCTTKAAAAG[C/T]AGATAACACGACCTTCACAGGAAGAGAAGACAGAAGACAAGAACGAAGAG
Long Flanking Sequence:
TGGAGCCAACGCACACCTCCCACTAGTGCCAGTATATCGCACTGCTACTCGTGCTGTATTTAAATGTGCGTATATATGTAAATGTGTATATGTATGCGTGTGTGTCCAAAATGGTTTACCTTCATAGCTTCTAACCTGATATTTAATGCTCTGTAAATCTATAAATGACCGTCTGTAATTCTTGCCGGATTTCCAGTTTATTTAGATTCTAATCATCATTCATTTTAAGAAAATTCAGTGAACAAGGTACATTTAAAAGTGAGCTTAATAAATGTAACTTAGATATTTATTTTTGTTAAATATTTGTTTTCCTTGATTTAAAGGAACTAGCGATATTGCCCATTTGATGCTTGATGGTGTGTGTAATCAATCCTTCTTAGCTGGTCTGACACAAATAAAGGTGAAATGTTTTTTGTGATGGGAACCTGGTCACAGATCTGTGCTCTTGAAAAGGTCAGCTGTCTAAATGCTTCTGGTATTGTGCTTCTTTTCTTTAAAAG[C/T]AGATAACACGACCTTCACAGGAAGAGAAGACAGAAGACAAGAACGAAGAGGACAAATCCGAGAAAACCGAGAAGAAAGAGGACGAGGAGAAAAAGGAAGAGGAGGAGAAAGATGAAAAAGAGGACTCTAAGTAAGTCTCATGATTTTCCCCTCTTGCTTTGAACTGGCCTCACTTCACCCTATTGCCCCAACTCCACTGTGAAATCCCTGAGCCACACACACACACACACACACACAATAATCTGTTGAGAGCGATATCAGCACAGTTATTGGTCTGTTGAAACGATGTGGGATTCACTCTTAAGTTGCAGTGTTTGCAAAAAATGTTTCTCTTAATTCAGAAAGAGCCCAGACGATGAAGAGCAAACAGATATATTGGATTGCTCTCTCAATGAGAATGCAGTAGGTTAAAGTAGGTGAGATGATCTGGTTTCTGTGAGGTGAGCCTTATTGTAACAGAGGCTTAAGATTAACCTCATTAACTCATTTGCTCTGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17067
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097574 | Nonsense | 1071 | 2409 | 25 | 48 |
ENSDART00000143573 | Nonsense | 1060 | 2398 | 24 | 47 |
Genomic Location (Zv9):
Chromosome 5 (position 43522163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41303428 |
GRCz11 | 5 | 41903581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCACAGGCCGCCAAACATTCCCTCTCCTCCACCCCTCATTCACACCTCC[A/T]AACCYACAGACAAGCCCTCCTTCATTCAAGGCGGCTCCATTTCGCAGGTA
Long Flanking Sequence:
GTTGAAGATGAAAGAAGGTTGACAGATAAAAATCCTAGGTGATTTAACTAAAGTAATGAGGAAGTATGAGTGTCTGTTTTACTCTTGTCTGTTAAATAGTGGATTAGAGGTTTGCCACCTTGTGGAGAAACGAGTCAAATCACATTTGCAAGCTGAGCATACGGAGTAAACATGGTTAAAAAAAAAAACAGTTTGTTGTTTTTCCACACTGTAATGACTTTTTAAGTTATGCCACATGCATTGTGCACATTCCCAAGCATTGCACTTTTAAACTAAATTACATTTAGGCTTTAGAGAGAAAGACTTGTCAGCTGTGGGGATAAAGAGTGATCCTCTTTTGCCCGCCTCCTTTCATCCCTTGTTCTTCTTATCCTTTCATTCCCACAGTTCTTCAGCCGGCACCAAACCAGGCAGTCCAGACTGTTTCAGATGTCCGCATGACGTTCTCTCGGCACAGGCCGCCAAACATTCCCTCTCCTCCACCCCTCATTCACACCTCC[A/T]AACCCACAGACAAGCCCTCCTTCATTCAAGGCGGCTCCATTTCGCAGGTAAGAGAATCAGTTTTTTGTTGTTGTTGTTTTTTTCTCTCAGTTCGACTTTTATAACAGTGATTTCTCATCCATGGATAATGTTTTTAGCTTCTTCAGGCTGTTAGTTGTTATTTAAGACTCGTGGTGCTTCTGCTGAGTTTAAATGCTTCCTTCATCTAATGGGATCAAGGCAGGGGATCAGGGGTTTTCCTGGTATTCAGTTCTGAAATGCTGTTTTCTTCTCACCATGTCCTGCAGGGTACGCCAGGAACATACCTTCCTCCTCAATCACACGCGGTGTACATACCCGAGGTGGTCAAGACCACAGGAGGGTCAATCTCACTCGGCTTGCCAAGACAGCAAGACCCTGCCAAACCTGGTGAGAGAGAGAGATTTGAGAGTATAAATAAACAGTCGAGCTCAGCTGAATGAAACACAATCCTTCCAAGTGCTTGTTTTGGTCGAGTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20512
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097574 | Essential Splice Site | 1310 | 2409 | 31 | 48 |
ENSDART00000143573 | Essential Splice Site | 1299 | 2398 | 30 | 47 |
Genomic Location (Zv9):
Chromosome 5 (position 43518932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41300197 |
GRCz11 | 5 | 41900350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACATGAGTCGAAGGATCGACCCATGCTTGCAGGATCCATAATGCAAGG[T/C]AATTTGTGGACCCATTTTGAAAATTCATATTGTATTTTTTTTAAAAAAGA
Long Flanking Sequence:
GACAGATTTTGAAAATGTGCTTTACTTTAAAGGCTAAATTACATGTTTGTTAGCAGTGTGACAAGGGCAGTCGCTATTTTTATAGAGCGCCACAGCAAGATGTTAGCCAGGAGTCTTTTGGACATGGTCTGTTGGTATTTTTAGTTCATATTATTATAATAATATGTCTCTCTCATTTTGTATTCCCACAGCCATTAAGAACCCTAGAGAGGGCACAAGAAGCCCACGTATGGGGCACGATCTTAAGCGCACATATGACATCATGGAGGGATCACGGGGACACACACCACGTGAGACTACACCTTATGAAGGTTAGTCACATTTTCATTTTCTTTCTAATTAAAAGAATAATGAGGCACAAAAAAAAGTTGAAGATGCTTGCAAGGAAGAAATGTTTTCACGAGTTGTTTCTGTCTGCCAGGTTTGATTTGCAGAACATTGAGGGAAAGTCCACATGAGTCGAAGGATCGACCCATGCTTGCAGGATCCATAATGCAAGG[T/C]AATTTGTGGACCCATTTTGAAAATTCATATTGTATTTTTTTTAAAAAAGAAAAAAGTTTGCTTAAAGATGTTGTTTCTCAGTAAATGTTTACTACATCATGCTCAGTTTTTCCTCTGTTTCAGGAACACCAAGAGCCTCTACTGAAGTCTATGATGAAGCCTCCAAATATGGTAAACAGATCAAGAGGGAGAGTCCACCCATACGCTCTTTTGAAGGTGGCATCACAAAGGGTAAACCATATGAAGGTGTTAACACCATAAAGGAAATGGGCCGCTCTATTCATGAAATCCCCCGCAAGGAAACCCAAGATAGCCGCAAAACTCCTGTTTTAGAAGGTTCTATTACTCAGGTACGACCTTTACAGTTGTTGTTATTTTCTGCACTGTGATTTGTCTGAGTAACATTTACACTACCGGTCAAAAGTTTGGGGTTAGTCTGATTTTAAAATAAGCTTCTCCTGCTCACCAAGGCTGAATTTATTTCATTCAAAATACAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13384
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 |
---|---|---|---|---|---|
ENSDART00000097574 | Nonsense | 1610 | 2409 | 35 | 48 |
ENSDART00000143573 | Nonsense | 1599 | 2398 | 34 | 47 |
Genomic Location (Zv9):
Chromosome 5 (position 43514973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41296238 |
GRCz11 | 5 | 41896391 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATACCATGGARAACACTCGGCAAACCATCCTAAACGATTACATMACGTCA[C/T]AACAGATGCAGGTCATACCACGGCCTGATCTCGCAAGGGGACTATCGCCA
Long Flanking Sequence:
GTAGTAGTCCTGTGTGAACAGAATAGCAGCTCTAGTACATGTTTATTTGTGGATGAAATATCTCTTTAATTAGCCTCAGCAAACACAAGTGGGTACTCTTGCCTGGGTCTGGAAAATTTGTGAATTATGAATTAGTTCTGTTCAAACAGGCCTGCAGGAAAAACAGTTCATGCGTCATGCACAAAATTGATTGATGCTCTGAATAATGACTCTCTCTAAAAGCACTACTTCTGTCTCATTTGTAAACATCATGTTTTGGTTTTTCATGCATTTGATAATGGCACTTCCTGGTTGACTCTCCACTACTGTGGCAAACCTGCACTATTGACGTCAAGACAAGAACAGCTGTCTTTTCACCTGTCATTGTTGTTTTTCCTCTGTATATCGCAGCAGCGTATATGTTCCCACGGCAACCATCGCCAACTGGATACCCCAACACTTACCAGCTGTATACCATGGAAAACACTCGGCAAACCATCCTAAACGATTACATCACGTCA[C/T]AACAGATGCAGGTCATACCACGGCCTGATCTCGCAAGGGGACTATCGCCACGTGAACAGTCTATTGCCATCCCGTACCCGCCACCTAGAGGTAAAGGGCATGATTGTCTGAGAATGTGTGTGTGTGTATGTTTGTAAAAGTGAATGAAAGGATCAAAGAAAGAATGTGGTGTTTGGATACCGTGTTTGTGTGAACAAGTGGCAACCTTTTCCAGACCACCAGAAGCAAATGACCCTAAAGCAAATTGTGTCAGTTCACAGAGTTCAAAACTATTTTAAATCCAGGGCTGGGGCTGTTTCTCACATGTCCATGATACCTGTCTATAAAGAGGCCTGCAGGTTTTGTTGTTTGTTTGTTTGTTTGTTGCAAGATCACTCTTCACCCCATTGTAACTCAAGTAACATCATTCATTTTACTGGGCAAATTAACCTAGGTCTTAGAAGACATAATGTTACACAAATGAGAGGATGGCTTTAAAGCAAGAGCATGATTTAGGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13203
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 |
---|---|---|---|---|---|
ENSDART00000097574 | Nonsense | 1741 | 2409 | 38 | 48 |
ENSDART00000143573 | Nonsense | 1730 | 2398 | 37 | 47 |
Genomic Location (Zv9):
Chromosome 5 (position 43510034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41291299 |
GRCz11 | 5 | 41891452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCYTCCAGCATTTTCAAGACATGACACTTTTYTCTTTCAGGTCCCGAG[C/T]AGCCTGTTCGACCAGGCAGCCGTAGTTTCCTGCGCTCCACCTCTCCATCT
Long Flanking Sequence:
TTTATATATTTTTTTGGACTAAACCAAGACTATGCAGCTTGCAGTTTTTCCCACTCGCATGAACCAGCACCATTTGTGCAAAAGGGGTCAAATCAAAATTGCTAATGTGTGTTAACAAGAATGGCACCATGAATGGATTAATGCTTGAGGTTTACTGTGAATCTGTCAGCTGGCCCTGTCAAACTACAGCAAGTGAAATGAGCTGGTTTGCTTGTAACTCCACACTGTTTGTTTTTGTGTGTTGCCTGTTCTTCGCTCCCTGCAGGACATCCGGCTCATCACAGTGCCGCTGCAGCCATAGTGGAGCGGGAGACTCAGAGAGAAAAGGAGCGCGAGAGGGAAAGGGAAAGAGAGCGAGAAAGAGAGCAGAGAGAACGGGAGCGTGCAGCAGTAGAATATATGCGTGGGGGTAAGATTATTCAACAGGTGTAACAATAGTTAAACTACTCATTTCTTCCAGCATTTTCAAGACATGACACTTTTCTCTTTCAGGTCCCGAG[C/T]AGCCTGTTCGACCAGGCAGCCGTAGTTTCCTGCGCTCCACCTCTCCATCTGTAAGGGCACAGGAAGGTGTCCTCCAGCAGCGGCCGAGCATCTTTCAGGGCACTAACTCCAAAAGCGTCATTACCCCACTCATGTGAGTAATATGCTAATCATTTATGAAAATTATACTTGACCTGTTAAATAAAAGTATGAAAAAAGCAAGTTTGGATGTAAAGGACATAAGGGATGTAAATGACTGAAAAAAGCAGCGGGTGAAGTATATTGATCACAAGTGCTTAGTTTGTGATCATATCTCTGCTTTTGTTTAGTTGATATGTTATCCAAATATTCAGAGCTTGAAACTAAAGGACATGTGACTGGATTGTGCTGCTTTTAATGCCCCTCACACAGCTTGATCCACGCTGGCATTTTCCCCCTTGGGTTTTAGGTTTTCATTCAAACTTTTAGAATACCGGTGTCAGATTTGCACAATCCATATGCACAACGCTGGCAGACCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17231
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 |
---|---|---|---|---|---|
ENSDART00000097574 | Nonsense | 2009 | 2409 | 41 | 48 |
ENSDART00000143573 | Nonsense | 1998 | 2398 | 40 | 47 |
Genomic Location (Zv9):
Chromosome 5 (position 43504372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 41285637 |
GRCz11 | 5 | 41885790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAGCCCGGGGATTCAGGACCATCTGCACCCCAGCCGCCCCCCTCCTCA[C/T]AATCAGACAGTTATGGCTCTGTCCCWAAAACACACCGCATCATGACYCTC
Long Flanking Sequence:
ATGCAGTCTGAACTTGGCATTAGAAACACCGACCGGATGCATTTTTAAACCTCAAAAAGGCTGCCAATCTCTTTGAGTACATGAGACTGTATGAGGAAGTGTTGTTGACAGTTCTCCTGCACACGCAATGAACAGTACGAAATTTGTAGGGCGAGAGAAGATTTTCCACTGGTTAATCGAACGCTGATGTTTAGTTATGTCAGCCAAATACAAAAAAGTTTTAAAGGATAATAATATTGGTCAAAAAAATCAAATATGATTGGGCAGCCTTAATATACCTGGGTGATCTGCCCAAGTAAAGTCTATGTGTGGAAAGCACTGTAAATATAAATAAGCTAGCGCTTTTTCTCAGATGTTTTTTGCATTGAAAAAGCCTAGACAGATTTACCATTGTGTAATAATTTTTTTACCTGATCTTTTATTTTGCAGGAATGTCATTTGGCCGGTACAGACAGCCCGGGGATTCAGGACCATCTGCACCCCAGCCGCCCCCCTCCTCA[C/T]AATCAGACAGTTATGGCTCTGTCCCAAAAACACACCGCATCATGACCCTCGCTGACCACATTTCGGTAAGACACACTCAAACTCCTGATGCTTTATCACAGATCCTGCTTCCTCTAATTCCCTCATCTCTCTCTCGCAGCATATCATTACCCAGGACTTTGCCAAGAGCCAGGACACTCCCCCATCGTCCACTTCACTGCCTTCCTCCTCTTCCTCGCTCTCCTCCACATTCCAGAGCTCTGGTGTTGGAGGTGGTGTGGGTCGAGTAAAAGCCCTGAACCGCTACAGCCCAGAAAACCCAACTTCTGCTCACCATCAGAGACCAGCAAGAGTATCTCCTGAAAACTCTTCCGATAAATCAAGAGCCAGGTAAAAATGCACTGTTTGTAAAAACATTTAAAGGGATAATTGGCCCAAAAACAATGAGGTGTGCACACTTAAGGGATTCCAATCCTCAATGAGTTTCTTACATCTGTTGAAAACAGAAAGATTTTAAAGAA
Associated Phenotype:
Not determined