ZMP
smarcd1
Ensembl ID:
ZFIN ID:
Description:
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1 [Sour
Human Orthologue:
SMARCD1
Human Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 [S
Mouse Orthologue:
Smarcd1
Mouse Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 Ge
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32372 | Nonsense | Available for shipment | Available now |
sa32371 | Nonsense | Available for shipment | Available now |
sa24071 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32372
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 |
---|---|---|---|---|---|
ENSDART00000003422 | Nonsense | 8 | 510 | 1 | 13 |
The following transcripts of ENSDARG00000019004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 6972141)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 6995469 |
GRCz11 | 22 | 7025315 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCTGTTTGCGGCTCGCGGAGAAGAAGATGGCGGCGCGGAGTGGTTTT[C/T]AGCCTTCGACACCCGGTGGCGGCGGAGCCCCGATGGGACCCGGGCCGCCG
Long Flanking Sequence:
TTTATTCTTCTTCTGGAAAAAAAATCGTCACGTAACATTTTTGTCCCAGACCCTTAAAAGTGGGGTAAATCATGCAGGCTAATCTGGCATTTCTGCATAAACTCACAGTATAAAACAGCAGCATTACAAAATAAACACATACTTTAACAGTTTAAAATAAAACTTAATAGAAAAATCGGTACTTACACTTTCCTTGTCATCCGTGTCGTCCATTAGCGCATCCATGATCCAATCCGACAGGTAACGCTGTCACAAAAAACTAGGGTCCTAAAGATGCGGTCCTAAAAATGCGGTCCTGAGAGTGCAGCCACTCCAGTTGTGCAGGATTACCCTTCTCATCGTCAGCGCAAGCGCGACGTCTCTTCACACCTCGCGAGACTCTACCTCAGCTCTGAACGCCTGTGCTCTTCAATTCTCGCGATACTAGTTTCAAGTCTCACCGGTGGTTCTCTGTCTGTTTGCGGCTCGCGGAGAAGAAGATGGCGGCGCGGAGTGGTTTT[C/T]AGCCTTCGACACCCGGTGGCGGCGGAGCCCCGATGGGACCCGGGCCGCCGGTAGCCGGAGCAGGACCCGGTATGGGTCCCGGTACACCCTCAGGAAGGATGGGACCAGGCGGCCCGCAGAACCACATGTACCGATCACCGATGCCCGGTTACCCGGTAAGGCGCGAGGAGAACAAAGAAGCAGCCGCGCATAAACCGAGGGCTTTAGTTTTAAAGTCTGAACGCAGAATTTGCTCGTTTATTTAAAGCGTCAACATTGAATCCGTTTAAAATGGTTTCTATAGTGTTAAATTGAGAATATACTCTATTATTATGCTCGACTGTGGTTGCGTTGCTTACCGTTTGGTTCAATGCTAAGCGTCAAACTTTATTTCAGTAAACCAGAAATTAGATTATTTGTTTGTGTTTCACTTGAGAATGACTTGAGGAATATTAACCTGCAGTTGGTTTTGATGGTGTAAACAGAGTTTCTGCGGAAGCTCTGTGTGTAACCGCGCGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32371
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 |
---|---|---|---|---|---|
ENSDART00000003422 | Nonsense | 235 | 510 | 6 | 13 |
The following transcripts of ENSDARG00000019004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 6965297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 6988625 |
GRCz11 | 22 | 7018471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGAAGCCACCAAGCAGAAGAGGAAGTTTTCTTCTTTTTTCAAGTCTT[T/A]AGTGATCGAGTTGGACAAAGACTTGTATGGACCTGACAATCATTTGGTTG
Long Flanking Sequence:
AGAAGATATATTAAAGAATGCTGTTTGCTGGCACCCAATGACTTCTATAGTAGACAAATAATGCTAAGGAAGCTAAGGGTTGTCAGGCACCAACATTTTTCAAAATGTCTTGTTCTGAACGAGTAAATGATGATTAATTGTTCATTTTTGGGTGAGCTATCCCATTAGGTCAAACCCCTTATCGTTTCTGTAGAAGTACACTATTTTTATTTGTAAAACTGAATTCTTTGTCACAGACTGAAACCATAAATTGTTTTAGATTTTTATCTTGTATATTATCATTATTATTGTTGTTCATTTATTTTTATCTTGTGTATTATTTACTGCTGGTGATGACTTCTAATTGCTATAATATTTTTATAATCATATGCCAATGCCATGACATAGCCAAAGAAGCTGATATGGCAATAAACTCAATTTCTTTCTCTTATCACAGACCGCTGTGTCCAAGTATGAAGCCACCAAGCAGAAGAGGAAGTTTTCTTCTTTTTTCAAGTCTT[T/A]AGTGATCGAGTTGGACAAAGACTTGTATGGACCTGACAATCATTTGGTTGAGGTGAGAATCAGAAATTGTGTTTCTCAAGTATAGTACTTTAAACTTAGTTTATTGCTGTGCTGTCCAGTAGATCCTCACTGCTGTCACTTATGTGCCATTTCTCACATCTTTGTCTTCATTACAGTGGCACAGAACAGCCACAACTCAGGAGACAGATGGATTTCAGGTCAAGAGGCCTGGGGATGTTGGGGTCCGCTGTACTGTACTGCTCATGCTGGACTACCAGGTAAACTTCAATTATAGTTGTGCACATGGTGTGTTTATTAGCATTTTTGTTCAAAAATCACCAGCAGATGGCGCCACCTCTTCTTGAGACATGCTTGAACTGGATATTATTTAGATTAAATGTGACTGATGGACGAAATCATTCTCTTTCTAGCCCCCTCAGTATAAGCTGGACCCCCGCCTGGCCCGGCTGCTGGGGATTCACACTCAGACCCGGCCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24071
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 |
---|---|---|---|---|---|
ENSDART00000003422 | Nonsense | 317 | 510 | 8 | 13 |
The following transcripts of ENSDARG00000019004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 6964773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 6988101 |
GRCz11 | 22 | 7017947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGATTCACACTCAGACCCGGCCTGTGATCATTCAGGCTTTGTGGCAGTA[T/A]GTGAAGACCCACAAACTCCAGGACCCTCATGAACGAGAGTTCATCAACTG
Long Flanking Sequence:
TGTATGGACCTGACAATCATTTGGTTGAGGTGAGAATCAGAAATTGTGTTTCTCAAGTATAGTACTTTAAACTTAGTTTATTGCTGTGCTGTCCAGTAGATCCTCACTGCTGTCACTTATGTGCCATTTCTCACATCTTTGTCTTCATTACAGTGGCACAGAACAGCCACAACTCAGGAGACAGATGGATTTCAGGTCAAGAGGCCTGGGGATGTTGGGGTCCGCTGTACTGTACTGCTCATGCTGGACTACCAGGTAAACTTCAATTATAGTTGTGCACATGGTGTGTTTATTAGCATTTTTGTTCAAAAATCACCAGCAGATGGCGCCACCTCTTCTTGAGACATGCTTGAACTGGATATTATTTAGATTAAATGTGACTGATGGACGAAATCATTCTCTTTCTAGCCCCCTCAGTATAAGCTGGACCCCCGCCTGGCCCGGCTGCTGGGGATTCACACTCAGACCCGGCCTGTGATCATTCAGGCTTTGTGGCAGTA[T/A]GTGAAGACCCACAAACTCCAGGACCCTCATGAACGAGAGTTCATCAACTGTGACAAATACCTCCAGCAGGTAACGAATGTCATGGACTTTATTTATGGGAACTAGTGAATGAAGACTTAAACTGGAAATACCCGTTTAGACAGAAGTGGTGACGTCTGACAATTATAAACTTCTTTAGTTGATAATTAAAGACTAGTAAAAAATTTCAGTATTATCAGAAAAAAACTACTGTGAAACTAAACTTTAAAATATTTGATCCTGAACGGCTATAGTTCAACTTAATTCATTTAATAATTGGCACTTCTACTTGGTGTAGGTCTTTGAAACAAACTCCTTTTACAATTCTTCTCATTCTAGATGTTTGAAATCCATTAATTGACTTATTTTATTTTAGATCTTCGTTTTAAGTTTTAATTCTTATTATAGATCGTACAACCAATAATAGATAGTTCTAGATTTTTGACAGCGGTTGGTTCTTCTCAGTGACTACGTTTACATGG
Associated Phenotype:
Not determined