ZMP
smc1al
Ensembl ID:
ZFIN ID:
Description:
structural maintenance of chromosomes 1A, like [Source:RefSeq peptide;Acc:NP_997975]
Human Orthologue:
SMC1A
Human Description:
structural maintenance of chromosomes 1A [Source:HGNC Symbol;Acc:11111]
Mouse Orthologue:
Smc1a
Mouse Description:
structural maintenance of chromosomes 1A Gene [Source:MGI Symbol;Acc:MGI:1344345]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11612 | Nonsense | Available for shipment | Available now |
sa32430 | Nonsense | Available for shipment | Available now |
sa18059 | Nonsense | Available for shipment | Available now |
sa37639 | Nonsense | Available for shipment | Available now |
sa24270 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11612
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 |
---|---|---|---|---|---|
ENSDART00000081016 | Nonsense | 200 | 1233 | 4 | 26 |
ENSDART00000121697 | Nonsense | 200 | 285 | 4 | 5 |
The following transcripts of ENSDARG00000058203 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12974472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 13106405 |
GRCz11 | 23 | 12862482 |
KASP Assay ID:
2261-7426.1 (used for ordering genotyping assays)
KASP Sequence:
AGTTTAACTACCATCGCAAGAAAAACATAGCTGCTGAACGAAAAGAAGCC[A/T]AACAGGAAAAAGAGGAGGTGGGCTCCTAGTATTGTAATATGTTATCATGC
Long Flanking Sequence:
TCGACAACAGTAATAGTTGAAAGATGTTAAAAGAAAATAATATAGATTTAAACTGAAATTTCAAAACTGTCAATATGTGACTGTTTATACACATCACTTGCTGACCGGAAGTTCTTACCATTCTCCTTGCGCATACACGCAAAGCATAATGGATAGTTTTGCATTCTAAGAAAAAGGTCTATAGTACTAATTAACTATAATTTGAGTAGTTTGAAAAACAGCATTATAATTTTGCTAGTAAGAACTCAATGACCTGTTTGTCTGTTAGGGGTCTCTTAATTGTTCTGGAATAAAAAAGGTTTTCTTTTTCCCAGGGTGCTGTAGAGTCAATTGCAATGAAGAACCCCAAAGAGAGAACAGCTCTGTTTGAAGAGATTTCTCGCTCTGGAGAGCTTGCCCAAGAATATGACAGATGCAAAAAAGAAATGGTCAAGGCTGAAGAGGACACGCAGTTTAACTACCATCGCAAGAAAAACATAGCTGCTGAACGAAAAGAAGCC[A/T]AACAGGAAAAAGAGGAGGTGGGCTCCTAGTATTGTAATATGTTATCATGCAAATAAATCACTTTTCCTCAGTGTAGAAATAGATGCATTTAGGTGCTAAAAAAGCCTGAAGGCAGAAATGCTAATTATGTTTTCTCCTCCTGTCATATGCAGGCAGAGCGTTATCAACGCCTGAAGGATGAGGTGGTGCGAGCTCATGTACAGTTACAGCTGTTTAAACTGTACCACAATGAATCAGAGATTGAGAAACTTAACAGAGAGCTGGCCCACCGCAATAAAGAGATTGATAAAGACAGAAAGCGCATGGACCGTGTGGAGGAAGAGTTAAAAGACAAAAAGAAGGAGCTTGGCAGAATGATGAGAGACCAACAGATGATTGAGAAAGAGATCAAGTGAGTTTAAACCTTCTAAAAATCTCCCAATTAATCTTAAGAACAAAATAACAATTTTTAATTGTTTAATAAATTTTGTAGTGTTTGGCCTCAATTCATTGTTGTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32430
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 |
---|---|---|---|---|---|
ENSDART00000081016 | Nonsense | 272 | 1233 | 5 | 26 |
ENSDART00000121697 | Nonsense | 272 | 285 | 5 | 5 |
The following transcripts of ENSDARG00000058203 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12974823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 13106756 |
GRCz11 | 23 | 12862833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGGACCGTGTGGAGGAAGAGTTAAAAGACAAAAAGAAGGAGCTTGGC[A/T]GAATGATGAGAGACCAACAGATGATTGAGAAAGAGATCAAGTGAGTTTAA
Long Flanking Sequence:
AGAGAACAGCTCTGTTTGAAGAGATTTCTCGCTCTGGAGAGCTTGCCCAAGAATATGACAGATGCAAAAAAGAAATGGTCAAGGCTGAAGAGGACACGCAGTTTAACTACCATCGCAAGAAAAACATAGCTGCTGAACGAAAAGAAGCCAAACAGGAAAAAGAGGAGGTGGGCTCCTAGTATTGTAATATGTTATCATGCAAATAAATCACTTTTCCTCAGTGTAGAAATAGATGCATTTAGGTGCTAAAAAAGCCTGAAGGCAGAAATGCTAATTATGTTTTCTCCTCCTGTCATATGCAGGCAGAGCGTTATCAACGCCTGAAGGATGAGGTGGTGCGAGCTCATGTACAGTTACAGCTGTTTAAACTGTACCACAATGAATCAGAGATTGAGAAACTTAACAGAGAGCTGGCCCACCGCAATAAAGAGATTGATAAAGACAGAAAGCGCATGGACCGTGTGGAGGAAGAGTTAAAAGACAAAAAGAAGGAGCTTGGC[A/T]GAATGATGAGAGACCAACAGATGATTGAGAAAGAGATCAAGTGAGTTTAAACCTTCTAAAAATCTCCCAATTAATCTTAAGAACAAAATAACAATTTTTAATTGTTTAATAAATTTTGTAGTGTTTGGCCTCAATTCATTGTTGTATTTTACATATTAAAGGGGTTACAAAAGGCAGTGCCTTACAACAGTGTGTGTAAGTAAAAAAACAAACAAACAAAAAAACATTGAGCATGTGGAAGAAAACAAAGTGTATCAATTTGTGTAAAGTATGTTTAAACATCACTCTACTGAACTGCTGACAACAAAATAAACAATTTAAATAGAGTTGTGTTGCGTCAAACTGAGTGCTCATAAGAATTTTCACTTGATTTAGTAGTTAATATTATAGCCTACATAACTAAATGATAAAGTGTAATATTAAACGATAGCTTCATTTTGTCTATATAATACATATTTTCATTTGCACAGCCATAATAAACAGCAATTAATGCATTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18059
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 |
---|---|---|---|---|---|
ENSDART00000081016 | Nonsense | 465 | 1233 | 9 | 26 |
ENSDART00000121697 | None | None | 285 | None | 5 |
The following transcripts of ENSDARG00000058203 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12981150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 13113083 |
GRCz11 | 23 | 12869160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGGATGAACAGAAAAGAATGGAAGAGGAACTCACAGAAGAAGTAGAA[C/T]AGGCCAAACGAAGAATAGATGAGATCAACATGGAAYTTAACCAGGTAAAC
Long Flanking Sequence:
ACTACATTAGTAAAGACTGGATGTGTGGTGTAATTTATGGCTTTTTTGTGTTTAGGTTAAGGCATATCACCGTTTGAAGGAGGAGGCGAGTAAGCGAGCAGCTACCCTGGCTCAAGAGCTAGAGAAATTCAACAGAGACCAGAAAGCTGACCAGGACCGTCTGGACCTGGAGGAGAGGAAGAAAATAGAAACAGAGGTAAATAAAGTTTGACCATTTTTATTTTAAAATATAATTAGCAAACAATGTTAATTTGTTCTAATTGTTATTGATAGGCCAAGATCAAGCAAAAAATCAGAGAGATTGAGGAGAACCAAAAACGCATTGAGAAGCTAGAGGACTATATCACTACTAGCAGGTACAAATGCATCACAAAGCCACGCTTTATCCTGTGAACAACTGTTGATGGCTGTAGATCATGACTCTTTTTCTGTTTCTCTTCTCCAGGCAGTCTTTGGATGAACAGAAAAGAATGGAAGAGGAACTCACAGAAGAAGTAGAA[C/T]AGGCCAAACGAAGAATAGATGAGATCAACATGGAACTTAACCAGGTAAACATCAGAAAATACTTTATATAGGGTTGGATGTTAAGCATTTGTGATGTTTATCTCAATATAGTTTAATCCTTATGTAGAGCTGGGTGATATGGCAAAAAATTATCACAATAATTTTTTTCATATCAGTCGATTTTGATATCACGATAAACGTAAAATCTTTATATCTATCAATTTTTATAAGATTTTCAGTATGCTAATGGCTTTGTGCAGCTGATTTAACACATTTAGTGAAATGTTTTAGCTGACTGACAATATAAATAACAAAATAATAAACAAAAGAACTATCCTAATTCAGCATTTACTGTTCAAGTTTTCAGCAACCAAAGACATTACAAGTTATTGGATATTATTGCTCAACATCAGAAAAAAATAATAAACCCGTTTTGGAACAAGTAAAATGTGAGTTAATGGTCACAGAATTTTCAGTTTTGGATGAACTCTCTTTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37639
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 |
---|---|---|---|---|---|
ENSDART00000081016 | Nonsense | 675 | 1233 | 13 | 26 |
ENSDART00000121697 | None | None | 285 | None | 5 |
The following transcripts of ENSDARG00000058203 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12990424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 13122357 |
GRCz11 | 23 | 12878434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTAAAGGCCAAAGCTCGACGTTGGGATGAAAAAGCTGTTGATAAGCTG[A/T]AAGACAGAAAGGAAAAACTCACAGATGAACTTAAAGTAAGTTGTTGAATC
Long Flanking Sequence:
TAATTTTGTTAGGCTTGAGCATCGTGACTTATATTATAATGTGCTCAAACATAACAGGTCAAGCCCACAGATGAGAAGCTACGTGAGCTGCGTGGTGCTAAATTGGTGATTGATGTAATTCGATATGAGCCACCACAGATTAAGAAAGCCCTGCAATATGCTTGTGGAAATGCCCTGGTCTGTGATAATGTGGAGGATGCTCGCAGGATTGCCTTTGGAGGACCATACAGACACAAGGTACAAAGGATAAAACAATGTCAAGAGATTATGCTTTAGATCATAGGTAAACAGACTACTACAGTAAGGCTGTCTAAGACCTGTAGTATGACTGTGTGTTACTTATTGCTTATGCAGACACTAATGTATAGGACATGTTATGTATTCTGTAGACTGTGGCTCTAGATGGGACGTTATTCCAGAAGTCTGGAGTGATCTCTGGTGGTGCCAGTGATCTAAAGGCCAAAGCTCGACGTTGGGATGAAAAAGCTGTTGATAAGCTG[A/T]AAGACAGAAAGGAAAAACTCACAGATGAACTTAAAGTAAGTTGTTGAATCAAGTTTGTTCTATCGACAAATAGATTTGTCAATGAACCGTTTGCTGAGTGTTTGTGTGTAAATGACAGGAACAAATGAAGGCCAAAAGAAAGGAAGCAGAGCTGCGTCAGGTTCAGTCTCAAGCTCATGGTTTGCAGATGAGGCTCAAGTACTCCCAGAGTGATCTGGAGCAAACCAAGACCAGACACCTGTCCCTTAACATGCAGGTACCCAACACTTACTTATCTTGAATCATTTCAGACATTTGTGGTTGCCACAGACTACAGCTCTGCGCAGGACTGTTTATTTTTTAGATAAATAAACCTGCATCTGCCCCATTCCAGTGAACTTATGTGCAGGACCACCCGTTCACGCAACTTACGTGTTCAACAATAACAAAAGCCTACTAACAATAAAGAAAGAAAGGAACAGCCTATTTGCCTAGTCAAAGAAATGTGATCACTGGACCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24270
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 |
---|---|---|---|---|---|
ENSDART00000081016 | Essential Splice Site | 954 | 1233 | 19 | 26 |
ENSDART00000121697 | None | None | 285 | None | 5 |
The following transcripts of ENSDARG00000058203 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12992720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 13124653 |
GRCz11 | 23 | 12880730 |
KASP Assay ID:
2261-7428.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACTTCCTCTCCGATCGGGAACTATGGATGACATCAGCCAGGAAGAGG[T/A]GTGTGTATATGTGCTAGTCTTGCAGCTTAATTTTACCTTTGCTGTTGAAT
Long Flanking Sequence:
CAAGAAAGATGAAAATGAGATTGAAAAGCTTAAGAAGGTAGAAAACATTCAGATGATCTCTTGATGTTTGAGTCTGGAAAATTTTCTGATTTTAGTGGTTTTGTTTAATATTTTTAACAGGAAGAGCAGAGGAATATGAAGATAATTGATGAGACCATGGCACAATTGCAGGATCTGAAAAACCAGCACTTGACTAAGAAATCTGAGGTTAATGATAAAAACCATGAAATGGAGGAGATCCGCAAGAAACTAGGGGGTGCCAACAAGTAGGATCAACATGTGATTTACTTCAGACATGCTCCGAGATTTTCAAGAAATTAAGTATGATGTAATGTGTGTGACTAGGGAGTTGACGCAGCTGCAGAAGGAAGTGACTGCTATCGAGACCAAGCTGGAGCAAAAACGCAGTGACAGACACAATCTACTGCAGGCTTGTAAGATGCAGGACATCAAACTTCCTCTCCGATCGGGAACTATGGATGACATCAGCCAGGAAGAGG[T/A]GTGTGTATATGTGCTAGTCTTGCAGCTTAATTTTACCTTTGCTGTTGAATCGCTAGACTGGTGTGTTTTTAGATATATATTGATTCAAGAGTTTGTTTTAAATTAGTTGTGTAGATACTCTACGTCTGCAATCAATGAAGCTTCAGTACTTTTAGAAACATTGTTGCCATTTTTTCGCACAAAAATGGCCAGTCAAAAATAGCCCAATGCTATCAGAACTTAAAATATGCCACCACCCATGTGGTATATAGTATTTATTTTTATCACTGAATGCTTTGTTATCATTATCAACTCAAAATAAGTGTAAAAATCATATTGCCTTAAAGGGTGGCCAAAAATTATGGCCAAAGATTTACTTTTACTTTTCCCCCGTTTTGTTACAAACGCCTTAAACTTTTGTTCACCTTAGCACTACAAATAGAACAAATATTTTTGTTCAACAAAAAAATTAAAATAAATTGTTCTATACTGACATTGAGAATGGAGAGCAAACGTACAAG
Associated Phenotype:
Not determined