ZMP
smarcd3b
Ensembl ID:
ZFIN ID:
Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b
Human Orthologue:
SMARCD3
Human Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 [S
Mouse Orthologue:
Smarcd3
Mouse Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 Ge
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12626 | Essential Splice Site | Available for shipment | Available now |
sa12191 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12626
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006724 | Essential Splice Site | 90 | 476 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 44187812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41178112 |
GRCz11 | 7 | 41458185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCACAGCAGCAGATCCAGCAGCAGGCCGTACAGAACCGAAACAGAAAG[T/A]GAGTATAATACGACATGCTCAAGAAGATCCTATAAAGATACAGTAAATTT
Long Flanking Sequence:
GTACAAAAATTTACAATTTTAAAAAGGAGGTGTGGCACCCAACCTCACCATTTGAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGCTGCTTCTTCTGTACTAGTCTGTAAGAGGAGTTTTAACAGAAATCTTTAATTCTTAATCTTAAATTGAACTCTGAACCTTCAACGTGACATTTATTTGAAGGCAAATATGCACTGTTAGTTCTCTACTAGTGATCTTGTGTTAGGTATTAGTGATCAGTATGTTAATTATATAAATATCTCCACCTCACCTTCTTATTTTTTGTCATTTTTTTTTCAGCGACCTGGCATGCCATCAGGAGCACGAATGCCACATCAAGGGGCTCCAATGGGGCCTCCAGGACCACCATATGGAGGAAGTCCTGCTGTCCGGCCTGGACTTACCAATCAGTCCATGGAGGCCAGTCGCAAACGGCCCAATCCTTCACAGCAGCAGATCCAGCAGCAGGCCGTACAGAACCGAAACAGAAAG[T/A]GAGTATAATACGACATGCTCAAGAAGATCCTATAAAGATACAGTAAATTTAAGCATATTGTGCCTTGTTTGACTGAGCTACAGTACAGTATAGTAATGTATGATTCGGTATGGGTCACCCTGATCTGGCTTGTGTACCCTTAAGGCTGATTTATACTTCTGCTTCTGCAGCCTGCGCGTGGACGCATTGCCCTCGCCGTGGCTGACACTGACACGCACTCTTTTTAAAATGTAACTACATGTTGCAACGACATGTAACCCAAGCTCTGTTATTGGTAGGCTTGGTAGTGCTGACGAGTGTGGGTGGGACCGAGAGCTGTGGGAAACCGTTTGAGTGAGTGTTTACAAGTTTTGAGTTCTATGTAGGAGCATCACGTGGAAAGTTTTGTTTTGTGTTTACCTTATTATTAAAGCTGTTGCACGTTCCCTGGTTCCTGCTTCAAAATGAGCGAGTTTAAGCTACTTCTACAAGAAGGTAGCGTTCAGAAAAAACAACACCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12191
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 |
---|---|---|---|---|---|
ENSDART00000006724 | Nonsense | 310 | 476 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 44174953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41165253 |
GRCz11 | 7 | 41445326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAWTGAARARCTGTNNTTTTGCCTTCATCTCCTCTCATAGATCTTTGACTG[T/A]CCACGTCTGAARTTCTCTGAAATTCCCCAGCGCCTCACCAACCTTTTACT
Long Flanking Sequence:
CTCCACTTACTTTATATTGCTTTAAATTCAATGTTTGCAGAATCAATGAAATTCAGCTTTTTAGTGATTGAAAGTGGGACTTTGACATTTGGTTTCGATTGTGAATCCTGATTAACTGAGTAATGTAAGCATGTGTCAATGGTGGTGTGTCCTGTGTGCAGCCTCCTCAGTTTAAGCTGGATCCGCGTCTGGCTCGTCTGCTGGGCATTCACACACAGACCCGCTCCAGTATTATACAGGCCCTCTGGCAGTACGTCAAAACCAACAAGCTGCAGGACTCGCATGACAAAGAGTACATCAACTGTGACAAGTACTTTCAACAGGTACGCCTGATTGCAAGCATTCATTCACATTCATAAATAGCATTCATAAAAGATATTTGATATGAATTTAACATGCACGGAGATTATGCATGGTGGACTTATTTATATAAAGCCAGTTAACTAGATTTTATTGAAGAACTGTTTTTGCCTTCATCTCCTCTCATAGATCTTTGACTG[T/A]CCACGTCTGAAGTTCTCTGAAATTCCCCAGCGCCTCACCAACCTTTTACTGCCCCCCGACCCTATTGTCATCAACCACATCATCAGGTTTGTGTGCTTATCAGTCAAAATACACTGTTCTTCACTTGATATGCTCCTCGTCCAAAGTGTGAAGTCAGTAAAGTTTGTGTTTTAGAGAAAAAAATAATAAAACTTTTATTTATTTCTTTAAGACTTTTCATACAAAAAAATGCAACTCAAAGTGCTTCACAAGCATAAATCAGATATTAAAAAAAACATCATCAACATAAGGTAATCAAAGATTTGAATGATTTGAAAAATCAGTGCTGTCAAAATTATTGCTTTAAAGCATGCGATTAATTTGAAATATTTAATGCATTAAGAAAAAATTAACGCAGTTGCAGTTTTTTTTTCTGTTGTGGTCGACGTGTGTTCAACATGCAAAAAAATATGGATAAGACCAAGGAAGCACTTTTTTAAGGCAAGTTTCAGTATGAAACA
Associated Phenotype:
Not determined