ZMP
smarcc1b
Ensembl ID:
ZFIN ID:
Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1b
Human Orthologue:
SMARCC1
Human Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 [S
Mouse Orthologue:
Smarcc1
Mouse Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 Ge
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1718 | Nonsense | Available for shipment | Available now |
sa23497 | Essential Splice Site | Available for shipment | Available now |
sa17040 | Nonsense | Available for shipment | Available now |
sa14091 | Nonsense | Available for shipment | Available now |
sa29186 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1718
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 |
---|---|---|---|---|---|
ENSDART00000085619 | Nonsense | 186 | 961 | 5 | 29 |
ENSDART00000104385 | Nonsense | 184 | 959 | 5 | 27 |
ENSDART00000130233 | Nonsense | 184 | 322 | 5 | 11 |
ENSDART00000133978 | None | None | 410 | None | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 18956598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19801799 |
GRCz11 | 19 | 19374752 |
KASP Assay ID:
554-1664.1 (used for ordering genotyping assays)
KASP Sequence:
CCCCGGATCTGGAACAAAAGCAAACTTCTAAACTTAAAGACATCATCCTG[C/T]GACACAATGWAAGTAAAAAATAAAATAAAAAAAATACTGACTAGACAGTA
Long Flanking Sequence:
TATCTGAAATGTTAAACTTTTGTAAGGGTGTCTTTGCTTTCACCTTTGATTTTAAGTTAATGCATGCAATAGTATATGTGAATGTTTTTACATTTGATATTAAGATATTAATGTCAGTTTTACAGAGATGCAATATTTTGGTCAACACACTAGCCCTCACTAATAATAAATTTAAGCTTTCAATAAATATGATGTCTCTTTTATCTCATACTCTGTGTATGTGTGTTTTTTTTTTTTAAAGGAGGCGCTTCGATCTGCAGAATCCATCCAGACTGGATCGCAATACAGAGATGCTGGGCTGTGTGGAGAAAACGCTGATGCAGGTATTTGTGTTTGGATCTTTAGCTAAGACAAACATCATGAGCAAATCTGTGTGTGGTGCAGTATCTGACATTTGTCTTCTGTGTTTGTGTTAGAATAACTTATTAAGCAGACCTGTGGTGTACCTTTCCCCGGATCTGGAACAAAAGCAAACTTCTAAACTTAAAGACATCATCCTG[C/T]GACACAATGTAAGTAAAAAATAAAATAAAAAAAATACTGACTAGACAGTAGTGATGGGTATTTAGAGATATTTTAATTTAAGTTACATGTACTAGTTAAAAGAATCGTAATATTTAGCAATAGGTGTGACATTTTATATTAGATTTTAATTATTTCAAAAATCTAATATAAGTTCAAATATCCCCTTAAAAGTTATATTGTTTATTAAAAGTTACTTAAAAGTTATTATTGTTTATTTTGTATTATTACAATTACTGGCCACTTTATTTGGTACACCTTACTTGTACCCGGTTAGACCCCCTTCAGAACTGCTTTCATCCATTGTGGCATAGATTCAGCAAGGTACTGAAAATATTCCTCAGAGATTTTGGTCCATATTGACATGAGGGCATCATGCAGTTGCTGGAGATTTGACAGCTGCACACCCATGATGCAAATCTCCCATTCCACCACATCTCAATCTAATAGAGCACCTTTGGAATCTGGTGAAAATGGGGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23497
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 |
---|---|---|---|---|---|
ENSDART00000085619 | Essential Splice Site | 300 | 961 | 9 | 29 |
ENSDART00000104385 | Essential Splice Site | 298 | 959 | 9 | 27 |
ENSDART00000130233 | Essential Splice Site | 298 | 322 | 9 | 11 |
ENSDART00000133978 | None | None | 410 | None | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 18954143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19799344 |
GRCz11 | 19 | 19372297 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACGGGAATAGTTTGCGTTTTCGGCGACGGATCTACCAAAATACTGAAG[T/C]ATGTTTATCTAATAATTTGATTACATACCATGTTTAACCCTTTCACATTT
Long Flanking Sequence:
TGGTTTAGACCAGTCATGCGATTGGATCAGCAAGTGATGGTGCACTGGGGCATGTGTCCAGACAGGTAGTGAAGGATTGCACAAACATTTTCTCACGCACTAAATGTTTGCATTGTAAATTGCGGCATTTTGCTTTGTGTTCTAATGATTGTATATGCTTTCCATATTTAATTTTTTTAGTTATGATTCGCTTATATCAGCAAGTGATGTAGATGCAGATGTTGAGGAACCTCCTAACCCTGACAGATGCTTGAAGGTGATATAATACTTTTAAAAACAATACTTTGATTTCCCATGATCCTCCAAAACGGATCATTAAACAATTGAGATTAGCTTTTCCTGATGACATTAAAACGTTAAATTTTTTTCCCCTCAGGTTAGTTCCAGATGGGTTCTCGACACGGATACATATAACGAGTGGATGAATGAAGAAGACTATGAGATTGACGAGAACGGGAATAGTTTGCGTTTTCGGCGACGGATCTACCAAAATACTGAAG[T/C]ATGTTTATCTAATAATTTGATTACATACCATGTTTAACCCTTTCACATTTACCTATTAAATACTCCTGCTCATTCCAATGGGAGTTTTTTTTAATGTAACCATTATTTAGAACAAATCGTTTTAATGCTTTCGTGGTGATGCATAAAGTTTATCATGTGACACACCACTACTCCAATGACATGCATATATACCCGATTTTGTTTATTTTTTAACTTCTTTGCCAATATTGACAAATGTCCCTGTACAAATGTAATTATATTGTGAGATATTTGGTATTCTGACTTTCAAAAATGAGTTAAAAATATTAATAATGGTCGAATTAGTTGACGGGGTAGTCACGATACTGAAAGTCAGTACCAATCGATACTGAAATTTTAAAAAAGCCCATTTTCTGCTAACATTTGAGCGCTATTGAGCACGTTCTTAAACTGTTGATTTTCCATTGGCTTCATGTGCTCAACAGAAATGACTGTGATTGGCTGTGAAGGTCATAAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17040
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 |
---|---|---|---|---|---|
ENSDART00000085619 | Nonsense | 514 | 961 | 17 | 29 |
ENSDART00000104385 | Nonsense | 512 | 959 | 17 | 27 |
ENSDART00000130233 | None | None | 322 | None | 11 |
ENSDART00000133978 | None | None | 410 | None | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 18940172)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19785407 |
GRCz11 | 19 | 19358360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTACTGTAGGGTTCATTCTTTTTTGGAGCAGTGGGGATTGATAAATTAT[C/T]AGGTTGAYGCGGAGAGTCGCCCCCTCCCRATGGGCCCACCCCCAACACCA
Long Flanking Sequence:
TTTTACTCTGTGAAAGGACACCCATGAGCCCATACATCTGAACAGAGAGCAGGCTACACGCCTCGTTGTTCAAACAGAAAAACATAAGGCACCTTTGTTAGCAACATTTGCCATATTTTTACAAAAGGGACAGGAATAAGGTGGAGTGCATATTTTGTTTTGAGGCAGCAACAATGAAAGAACTAGTAATTAATAGTTTACATTAACACAAACATGAAAATATATTGGGTCAAATGATGGCACATTTAATAACAAATGTTGCATATTTTTTGAGAAAGTAGACACAGCAAAAACAAAATACAAAAAATACAAAAACAAAAAGTGCAAAAAAGTTAGTTTCATCTGATGTCACCTTTAAACCCCAAAGTCATGATTCTCAATTTATCCAGAACTTTGCTACTCTACTATGCATATTATATCATTTGTAAATAATTTATTAACCTTGTTATATGTACTGTAGGGTTCATTCTTTTTTGGAGCAGTGGGGATTGATAAATTAT[C/T]AGGTTGACGCGGAGAGTCGCCCCCTCCCGATGGGCCCACCCCCAACACCACACTTTAATGTTCTTACAGATGCACCCTCTGGACTAGTCCCACTACAGCACAGACCACTACAGGTGATGTATACAACTTTGACTGCACGTTGAGAAGCTTCAGTTTAGCTATTATAAAACAAAATGTTAAATCAAATTATGTGTGTTTGAAGGTTTCAGCTTCTCAGCATATGCTGCATTTCCCTGAGAAATCAAGAGAAAAACCATCTGACCTGCAGAACTTTGGTTTACGAAGTGACATTTATGCTAAGAAACATCCAAAGGTAAAAAAAAAAAATGCAAATTGTTTTATTTTAGAAGTGTTTAACACAGCTGTCTTGAATCTATTTGTTCAGCTGAACTTTGTGTTCTTATTTTCTGTTTTACTTTTTTTTTTATCTTTTAGAGTAAAGGTGCAAGTGCAGGGAGAGAATGGACAGAACAGGAAACACTCTTGCTGTTGGAGGTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14091
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 |
---|---|---|---|---|---|
ENSDART00000085619 | Nonsense | 551 | 961 | 17 | 29 |
ENSDART00000104385 | Nonsense | 549 | 959 | 17 | 27 |
ENSDART00000130233 | None | None | 322 | None | 11 |
ENSDART00000133978 | None | None | 410 | None | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 18940061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19785296 |
GRCz11 | 19 | 19358249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTACAGATGCACCCTCTGGACTAGTCCCACTACAGCACAGACCACTA[C/T]AGGTGATGTATACAACTTTGACTGCACGTTGAGAAGCWTCAGTTTAGCTA
Long Flanking Sequence:
CATATTTTTACAAAAGGGACAGGAATAAGGTGGAGTGCATATTTTGTTTTGAGGCAGCAACAATGAAAGAACTAGTAATTAATAGTTTACATTAACACAAACATGAAAATATATTGGGTCAAATGATGGCACATTTAATAACAAATGTTGCATATTTTTTGAGAAAGTAGACACAGCAAAAACAAAATACAAAAAATACAAAAACAAAAAGTGCAAAAAAGTTAGTTTCATCTGATGTCACCTTTAAACCCCAAAGTCATGATTCTCAATTTATCCAGAACTTTGCTACTCTACTATGCATATTATATCATTTGTAAATAATTTATTAACCTTGTTATATGTACTGTAGGGTTCATTCTTTTTTGGAGCAGTGGGGATTGATAAATTATCAGGTTGACGCGGAGAGTCGCCCCCTCCCGATGGGCCCACCCCCAACACCACACTTTAATGTTCTTACAGATGCACCCTCTGGACTAGTCCCACTACAGCACAGACCACTA[C/T]AGGTGATGTATACAACTTTGACTGCACGTTGAGAAGCTTCAGTTTAGCTATTATAAAACAAAATGTTAAATCAAATTATGTGTGTTTGAAGGTTTCAGCTTCTCAGCATATGCTGCATTTCCCTGAGAAATCAAGAGAAAAACCATCTGACCTGCAGAACTTTGGTTTACGAAGTGACATTTATGCTAAGAAACATCCAAAGGTAAAAAAAAAAAATGCAAATTGTTTTATTTTAGAAGTGTTTAACACAGCTGTCTTGAATCTATTTGTTCAGCTGAACTTTGTGTTCTTATTTTCTGTTTTACTTTTTTTTTTATCTTTTAGAGTAAAGGTGCAAGTGCAGGGAGAGAATGGACAGAACAGGAAACACTCTTGCTGTTGGAGGTAATCCAGTCAAACGGTTTAAAGATTTATTAAATTTTTATGTACGTAAATTAAAGATTTGTAATCTAGACTTCAGCAGCAATAGTACTGGATGCATTTGACAATTATTTTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29186
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 |
---|---|---|---|---|---|
ENSDART00000085619 | Nonsense | 911 | 961 | 28 | 29 |
ENSDART00000104385 | Nonsense | 909 | 959 | 26 | 27 |
ENSDART00000130233 | None | None | 322 | None | 11 |
ENSDART00000133978 | Nonsense | 360 | 410 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 18927810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19773045 |
GRCz11 | 19 | 19345998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGCAGACCTTCCACCTGGAGCAGGTGAAATATGCAGAGCAGAAAGTG[C/T]GACAGAATGTGGAACAACAGCAGCCGCAGCAGCAAACTGGAGGCTCTCAG
Long Flanking Sequence:
ATCTTCATTGCAGTTGTTGTCTTAAATCGGTTCACTGTTTGAAGTGAATAGGATGATTGTCAAGAATGGTCTGTGGTCTGCAGTAATATGTATGGGGCTAATTTTATTTTAAATTTTTAACTTGGGTTGTTGTCTTGATGAGTGCTGCTATTGTGTGATTGTTGTGTGTATATAGTTGTTGTCTTAAATCCAGTGTTAAAGACAAATTTCCTTTCTGTGCAAATCAGAACAGACAAAAGTTTAAACTAAACTAATTTATATGATGAAAAACATAACATCAACTTAACCATAGCACTGGTGTATTGTTACACACCTTTTATTTACTCAAATTCCTAATTATTTAAGTTATGAAAGATCTTGTTGACTGTTAACTGCATTTTCAGTGTATTTAAATGTAATTTGATTTCTGTCTCTTGTAGCTTGAGCAGCAAAGACAGCAGTTACTCTCTGAGAGGCAGACCTTCCACCTGGAGCAGGTGAAATATGCAGAGCAGAAAGTG[C/T]GACAGAATGTGGAACAACAGCAGCCGCAGCAGCAAACTGGAGGCTCTCAGAGCAGCCCTACATTCAACCCTCTTCACCAAGGTACAGTTTATGTGCACTCACACATTGTATTAACTGGAAAAGAAGTCATCACACTGTCATAATTGCAGAAGAAAACATAAGAACATGCTTCGGGTGTCTGTCCACTGACTTAAAGCAGCACACTTTTTGATTGAGTTTTATTATATAAAAATAATTATATAATTATATGAGCGCAATGTTACCAAATTCTGTGAATCGTTACACCCCTATTCATAAGTAATTTAAAATAGGCAAATCAACCACAGTAAACATTTGCAATAAAGCATTATAAATTGTCTTCTAGTCACTCCACGGTCAGTCTTTGACAATTAATGGTATTCATGACGATAAAGCAACTGCAAAAAGTATCGACTACAAATATACACCTTGGTCCTACACCCTATGATGCTTTACCTGGTTTATCTGGAGGAACAGAACAC
Associated Phenotype:
Not determined