ZMP
smarce1
Ensembl ID:
ZFIN ID:
Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [
Human Orthologue:
SMARCE1
Human Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [S
Mouse Orthologue:
Smarce1
Mouse Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 Ge
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12565 | Nonsense | Available for shipment | Available now |
sa12524 | Nonsense | Available for shipment | Available now |
sa20071 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12565
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 |
---|---|---|---|---|---|
ENSDART00000011319 | Nonsense | 161 | 424 | 6 | 10 |
ENSDART00000121981 | Nonsense | 157 | 420 | 7 | 11 |
ENSDART00000011319 | Nonsense | 161 | 424 | 6 | 10 |
ENSDART00000121981 | Nonsense | 157 | 420 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 35076210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34861406 |
GRCz11 | 3 | 34990914 |
KASP Assay ID:
2259-3756.1 (used for ordering genotyping assays)
KASP Sequence:
ACGTTAATGCAAAGAACCGCGCAGAAGCAGCTCYAGAGGAAGAAAGCCGG[C/T]AGAGACAGTCACGTTTAGACAAAGGGGAGCCCTACATGAGCATCCAACCC
Long Flanking Sequence:
TTTTATTTAAAAATAGCATTTTTAACTATTTACCTTCATTTTTAATTACTTGCCTTACAGTCACATTTGTTTAAAAGTTTCCATTTATTTATTGCTAAGAATACTGACCTGACCTATATATTTTATTATTAAATTATTGTTATTGTAATAATATATTAAATTAAAATAATTTTTGATAGGGCAGGTGGGATATTCAACTGGGATATTAAAAAAAAAAAATCCTTAGCCTTTAACCTTGTATGAGTCTAAAATTTCCTTCATAATGGTCCTAAAAAAGTCTAAAGTCGTAAATGTAACTTGGTGAAAACTTGGTAACTTGGTGAAACCTGCAGAAACCCTGAATTCAATTTGAAGGCTATTCCTTAAGGCACTAAGCACAACTTCTATCCCCGCAGATTGAGTATAATGACTCTCTGAAGGCCTACCACAACTCTCCAGCCTACCTTGCGTACGTTAATGCAAAGAACCGCGCAGAAGCAGCTCTAGAGGAAGAAAGCCGG[C/T]AGAGACAGTCACGTTTAGACAAAGGGGAGCCCTACATGAGCATCCAACCCGCTGAGGACCCCGATGGTGAGATGCATGTCACGATTTCAAGTTTGAATAACAAGAACATAACACAGTGTTAATATGAATCATACATTATTTATAAATGATGTCAAGTTTTGTAAGCTTGTAAATGTTATCTGTTTTTCTCATTGAATATCTATTGAAGCTGATATGGAAATAAATTAAATGAAAAGGTCAATAAATAAGATATTGATGCATACAGTGTAAAGAAAATCTCACAGGCTAAATATTTTCATATACTTGATCTCAACTCACATCAGTCAAACCCTCAAAAATATTGAATTAAACATGAGTAACTTATTGAAATAAAGTACCATTAAAAAACATTGTCGTGACTTTTTGCCATATTTTTTACAGTATATAAAGTAATGCCTACTGTATTTTAATAGATGGTTATAACATGCTTGGGTAAGGTTAGATGTGAACAACTCAATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12524
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 |
---|---|---|---|---|---|
ENSDART00000011319 | Nonsense | 161 | 424 | 6 | 10 |
ENSDART00000121981 | Nonsense | 157 | 420 | 7 | 11 |
ENSDART00000011319 | Nonsense | 161 | 424 | 6 | 10 |
ENSDART00000121981 | Nonsense | 157 | 420 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 35076210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34861406 |
GRCz11 | 3 | 34990914 |
KASP Assay ID:
2259-3756.1 (used for ordering genotyping assays)
KASP Sequence:
ACGTTAATGCAAAGAACCGCGCAGAAGCAGCTCYAGAGGAAGAAAGCCGG[C/T]AGAGACAGTCACGTTTAGACAAAGGGGAGCCCTACATGAGCATCCAACCC
Long Flanking Sequence:
TTTTATTTAAAAATAGCATTTTTAACTATTTACCTTCATTTTTAATTACTTGCCTTACAGTCACATTTGTTTAAAAGTTTCCATTTATTTATTGCTAAGAATACTGACCTGACCTATATATTTTATTATTAAATTATTGTTATTGTAATAATATATTAAATTAAAATAATTTTTGATAGGGCAGGTGGGATATTCAACTGGGATATTAAAAAAAAAAAATCCTTAGCCTTTAACCTTGTATGAGTCTAAAATTTCCTTCATAATGGTCCTAAAAAAGTCTAAAGTCGTAAATGTAACTTGGTGAAAACTTGGTAACTTGGTGAAACCTGCAGAAACCCTGAATTCAATTTGAAGGCTATTCCTTAAGGCACTAAGCACAACTTCTATCCCCGCAGATTGAGTATAATGACTCTCTGAAGGCCTACCACAACTCTCCAGCCTACCTTGCGTACGTTAATGCAAAGAACCGCGCAGAAGCAGCTCTAGAGGAAGAAAGCCGG[C/T]AGAGACAGTCACGTTTAGACAAAGGGGAGCCCTACATGAGCATCCAACCCGCTGAGGACCCCGATGGTGAGATGCATGTCACGATTTCAAGTTTGAATAACAAGAACATAACACAGTGTTAATATGAATCATACATTATTTATAAATGATGTCAAGTTTTGTAAGCTTGTAAATGTTATCTGTTTTTCTCATTGAATATCTATTGAAGCTGATATGGAAATAAATTAAATGAAAAGGTCAATAAATAAGATATTGATGCATACAGTGTAAAGAAAATCTCACAGGCTAAATATTTTCATATACTTGATCTCAACTCACATCAGTCAAACCCTCAAAAATATTGAATTAAACATGAGTAACTTATTGAAATAAAGTACCATTAAAAAACATTGTCGTGACTTTTTGCCATATTTTTTACAGTATATAAAGTAATGCCTACTGTATTTTAATAGATGGTTATAACATGCTTGGGTAAGGTTAGATGTGAACAACTCAATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20071
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 |
---|---|---|---|---|---|
ENSDART00000011319 | Nonsense | 424 | 424 | 10 | 10 |
ENSDART00000121981 | Nonsense | 420 | 420 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 35079579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34864775 |
GRCz11 | 3 | 34994283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGACCGCATCAGACAACACCCCTGAGGAGCGCCTGCCCACCCAGCCA[C/T]AATAACACATCCACACACTCTCACCTCGCTCTGCGTAGAGTCATGTGTCC
Long Flanking Sequence:
TAGAATTTTGAGGAAATAAATAATTCCATTTTGCAATAAGTCTGTAACAAAGAAATGTGGCATTTCTGCCATTAATACTTTCCAGATGCAGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATGTGTGTATATATATATATATATATATATATATGTGTGTGTATATATATATATATATATATATATATATATATATATATATATACATACACAAATGAATTTTAAAAATGGCAGAATTGCAAAGGTTTGACAGGCCCTTTTGCCTGTTGTGCAGAGTCTCTTGCTGAAACTTCTGAAGGATCTCAGGAGGCTGAGCAAGGCACACCTGCAGCAGGAGAGAAAGCAGCCCAGCCTGAGCCTGCAGAGGGCGCAACAGACGAGGGCACCAGCGACAGCACGGCTCCATCTGAGAGCAGCTCCGGACCCCCAGCAGAACACCAGACCGCATCAGACAACACCCCTGAGGAGCGCCTGCCCACCCAGCCA[C/T]AATAACACATCCACACACTCTCACCTCGCTCTGCGTAGAGTCATGTGTCCTCTAGGATTTACCGGTTAATCCTGTGACCTGGCAGTGCATGAGAGTGAGAACAGTGAAAATTACTTTTCTCCCCCTCATAATCATCTACAGTGACAATGACAGCAAATTCTTAATTGCCGTTTCACAGAGATTCACCTGTTCACTTGAACTGAAGCCTGATGTTACAAGCCCCCTTCAGTCATCTTAAGCTTTATGGCCATTTAAACGTCATTTTATCTTTTTAAAGCAGAAATAAATTAAGCAGATGTTGTGTAAAATGTAACTTTTTCATCTTGTAGACACCAAATGGGTTGCGAAAGCAGAACGGCAAGGTTATTTGCTGTTGCCTTACCATTTATCTACCTGTGGCATGGCCATTTTATGCTGTATCTTTGTTTCTGATATTTTTTTCACTATTTAGTTGAGTAGTTTGTGGATTTAGTGCTTCTCTTTCTCTCACTTTATTCAAG
Associated Phenotype:
Not determined