ZMP
smad1
Ensembl ID:
ZFIN ID:
Description:
Mothers against decapentaplegic homolog 1 [Source:UniProtKB/Swiss-Prot;Acc:Q9I8V2]
Human Orthologues:
SMAD1, SMAD9
Human Descriptions:
SMAD family member 1 [Source:HGNC Symbol;Acc:6767]
SMAD family member 9 [Source:HGNC Symbol;Acc:6774]
SMAD family member 9 [Source:HGNC Symbol;Acc:6774]
Mouse Orthologues:
Smad1, Smad5, Smad9
Mouse Descriptions:
MAD homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:109452]
MAD homolog 5 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1328787]
MAD homolog 9 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1859993]
MAD homolog 5 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1328787]
MAD homolog 9 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1859993]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32713 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32712 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32713
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033566 | Essential Splice Site | 134 | 472 | 3 | 7 |
ENSDART00000125043 | Essential Splice Site | 134 | 473 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 35616729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35176587 |
GRCz11 | 1 | 35908614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTCAGTTCTGATTCTCATGGTTGACATATTTCTCCCGTTTTCCTGCA[G/A]TGCTGCCACCCGTGCTGGTTCCACGAAACAGCGAGTTCAACGCTAAACTC
Long Flanking Sequence:
GAAGCAAATCTTTTCAAAGTTCGCAAAAAAAGACAAAATCCCAAATGGGAATTAGGTGCATTTCCATCAAGTTGTTGGAGAGGTCGACTGTACCAATACTACCAATACTACAGTCGACCTCTCCAACAACTTGATGAAAACACACCTAATTCCCATTTGGGATTTAACCAAGGGAAGCATAAAGGAGGCGACTGCAGTCACATTGGTGTAATTTATTCTCATTTCCGTCTCCCATTATTAACATTCAGCATTTTTTGCACAAACTCAAAACCATCTCAACCAAGCATAAAAACCTTTTTGCCAACTTTTATTCAGAATATCTTGTTTCTCATGCAAAAATGTGCATTAACGCAGTGTGATGGAAACTCAGCTACTGTGAAAACCTCTTTCATTAATAAGAGTGTGTATGATTATATTAAAATCTTCAATGGATTCTCTTCAATGGATCACCTATTCAGTTCTGATTCTCATGGTTGACATATTTCTCCCGTTTTCCTGCA[G/A]TGCTGCCACCCGTGCTGGTTCCACGAAACAGCGAGTTCAACGCTAAACTCTCCATGCTGCCACGCTTCCGTAACCCACTCCACCAGACGGAGCCCCCCATGCCTCAGAACGCCACCTTCCCCGACTCCTTCCCCCAGCAGCCAGCAAATGCCCTTCCCTTTACCCCGAACTCCCCAACCAACAGTTATCCCAGCTCGCCCAACAGCGGCACAGGCAGCACTGCCACCTTTCCACATTCGCCATCCAGCTCAGATCCAGGCAGCCCTTTTCAGATGCCAGGTGAGATCGCTCTTAACCTGCACGTTAATGGTGCACTAGAAACATTTATGAATATTATTAATGCATTATTACTGTGAGGAGTTCACCTACAGTATGTTTATAGTTGAAATGTATGTTAGTTAAATCTCATACCGAGCTTATTCACACACTCTTGTACTGGATTTAGCAAATTAAGTTTAGCAAATTCATATTAGTTTGATTTTACTGTTCTGGCATTAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32712
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 |
---|---|---|---|---|---|
ENSDART00000033566 | Nonsense | 259 | 472 | 4 | 7 |
ENSDART00000125043 | Nonsense | 259 | 473 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 35615927)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35175785 |
GRCz11 | 1 | 35907812 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTGTCCCCAGCCAATGGACACTAACCTATTAGCTCCAAACTTGCCAT[T/A]GGAGATCAGCAACCGAACAGGTACCCTTCATTTAAATGCTAAAAGACACC
Long Flanking Sequence:
CGTTAATGGTGCACTAGAAACATTTATGAATATTATTAATGCATTATTACTGTGAGGAGTTCACCTACAGTATGTTTATAGTTGAAATGTATGTTAGTTAAATCTCATACCGAGCTTATTCACACACTCTTGTACTGGATTTAGCAAATTAAGTTTAGCAAATTCATATTAGTTTGATTTTACTGTTCTGGCATTAAGCTATGCAAAACTTCTACAGCTTTTAAGGGAAAGACTGTACATTTGACATGTATCTTTTTTCTGACTGACTCTTTTTTTCCACTTAAGTTAATGTTTAACCCTCAATATTTCTAATGTGGAAATACAAAAATGTTAGTCATTTGTCAGTACATGTCGTCATTCACCTTTCACTGTGTTGCTTGTGTTTTTGGGTGTTGCTTCTAAAGAAACCCCTCCACCTGCGTATATGCCTCCAGAGGAGCCAATGACACAGGACTGTCCCCAGCCAATGGACACTAACCTATTAGCTCCAAACTTGCCAT[T/A]GGAGATCAGCAACCGAACAGGTACCCTTCATTTAAATGCTAAAAGACACCATAAAATAAGACACTACTCTAAGCTCCAGTCACTCCAGCAAAGATATTGCTCCTTCCTTACAGTCTGACATGGGCGTTTTATAGCTATCAGCAGCTGCCGACCCACACTGCAGGTGCAGGAAGTCCACACACAAACATACTCGTGCACAGCGTCACAGACAGTCTGAGTTTTTGTCCTTTAAATGTGTATGGGGGTTCTTGCAGTACAGCATGTGGCATGCAAATGAGCAAAACAGTTAGAAATTGGTAAATAATGGGGTTCTTTAAAAACTGTGTTTTAGTTGGAAAAAGGGAGTCCATATACAGTTGAAGTCAGAATTATTAGCCCCCCTTTGTATTTTTTTTTCTTTTTTTAATTAATTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGACAATATATTTTTCTTTTGGAGAAAGTCTTATTTGTTTTATT
Associated Phenotype:
Not determined