ZMP
fstl1a
Ensembl ID:
ZFIN ID:
Description:
follistatin-like 1a [Source:RefSeq peptide;Acc:NP_001017860]
Human Orthologue:
FSTL1
Human Description:
follistatin-like 1 [Source:HGNC Symbol;Acc:3972]
Mouse Orthologue:
Fstl1
Mouse Description:
follistatin-like 1 Gene [Source:MGI Symbol;Acc:MGI:102793]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12164 | Essential Splice Site | Available for shipment | Available now |
| sa32756 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12164
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015046 | Essential Splice Site | 54 | 314 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 47967713)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46779374 |
| GRCz11 | 1 | 47470606 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAATGTTCGGTCACAGAGAAAGGCGAACCAACTTGTCTGTGTATCGAG[G/A]TGAGTCATGTCTATTTGTTTRCTTTAGCCACACGTTCACAGTGAYCCAGA
Long Flanking Sequence:
TCGCAAGACTTTTTGTATTCCATTCTTCATTAAATAAAAAAAACTTTTTTGTCAATTATTAGACGTCAATCTTTTCAAGTAAGATATCTGAAGTAAAGTCCGCCATCTTGTGGTTCAACTAAAATCTGCATGTTTGTCAACATTACCAATAAAAACAGGATTTTTTAACGGTTTGAGTTAAGTATTCTGACTAAATCAACTATTAGCTTCTATCAAACTCAAAAAGGGTCCTAAAAGAGTACTTAGAAAGTACTAAAGCTTATACTTCAGTTTGATAGTACTTATGTTTACCATCCTTCACCGCAATATGGAGCCAAAGTTCCAAACGTCATGCTTAAAAAACTAAGGATCTGGTTTCTTTCAGTAAATATTCAAATGTATTGTTTTGTTTTGTGCAGGGGGTGAGGAGCAAAAGTAAAGTTTGTGCTAATGTGTTCTGTGGAGCTGGGAGAGAATGTTCGGTCACAGAGAAAGGCGAACCAACTTGTCTGTGTATCGAG[G/A]TGAGTCATGTCTATTTGTTTACTTTAGCCACACGTTCACAGTGACCCAGAAAATACCCTAAACCACATGTGTTGTGAATTAAACACATGCTGCGTTCCCAATAGGGGTTGCCAGATCTTTACAGTTTGGCATACCTTTTAAACACAACTTTCATTTGATACTACACTAAAAAATGACATGATCAATTAGTCCTGACAGCATATGTTTTAGGTCATTGTTACTTATAAAATAAAGTTAGAACTTGATTAACTTAGTTTAATAAGTTATGCCAGCTATTTTAAAAGTCAGTTTACCATAATATAAGTTCAGTGGACTCATAAGGTTAGTTTGATTCATCTTATTTTTTTACAGTGTAGTTCTTATTTATTTGGCACGAGTATACTTGCGGTAATACCAATTAAATATATACTAGTGCACATGTTTTGTTAGATATTTGTACATATTATAGATAGATATTCCATACTCAACCATTACATTAAACATACTCAAATACGCTACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32756
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 |
|---|---|---|---|---|---|
| ENSDART00000015046 | Essential Splice Site | 267 | 314 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 47980576)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46792237 |
| GRCz11 | 1 | 47483469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCATTTGTGCCTGCGGCAACTGGGTCTGCACTGCTGTGATTTGTGATG[G/A]TGAGCCCCAAATATTAAAGTTTTTTTTTCTGCAGATCGAGGCTAAAGCAG
Long Flanking Sequence:
CTTGAAATGTCCACCCTGGTTTCTTCTTTATCATACTGATAATGTAGATGTTGGACTAAAGCAGCCAATATTAATTCACAATGAAGAAGGGAAGAGGGTGGCTGAATAACTACCGAGAGATGTCAGCTACTGTCTGGGCTTTCACTGCCTTTCTACACCTCCCTTTGTTCATGTGTTCAATACTTTTTGCCTGCGTCATTTTATTTTATTACACATAACTTCATTTGTAAACTAATTAGATTTGTTTTCTTTGCATATATTGTTTTCTTTGGTTGTTACCAACATCCGTTGAAAATTTCAGGTCAACAGCAAAGAAATATGTTTTCTGAGATAAATGGTGACGTGCTCAATACTTATTTATCCTGTAAGATAAATGTGTATGTTTTTAGAGTGTGCCTTAGAAGATGAGACGTATGAGGATGGTGCTGAGACTCAGATGGAATGTAACCGCTGCATTTGTGCCTGCGGCAACTGGGTCTGCACTGCTGTGATTTGTGATG[G/A]TGAGCCCCAAATATTAAAGTTTTTTTTTCTGCAGATCGAGGCTAAAGCAGGGATTTGGACATAAAAGCTTTTTTTTTCAATGGAATGTGCTCTGAATAGCTGTGCTCTTCATCTCGACAGGTTCAAATAAGTTACAAGCTCTTGAGGAAATGGAGGGAAATAATCAAGAAATGACAGAAGAGGAGTGGGTTCAAAGAGTGGCTGAACTCAATAAGCATCAGGTTGGTATAAATTTTCATTGTAGATGTTATAATTAATATATAATTTACATTGTAGGTGTTTTTTTCTCATAGTGCTTGTAACAGTTCATTCGAATATTTGGGCTATCATTTATAAATGTGGTGTAGACAAAATGGCGGTAGAAATCTGCGTACACTAAAATCTATCGATTAGTTTACAGTTTTTGTATTTTGTGATTCACAGGTGTTTTTCCATTTATTTATGGTTGTGAATTGCAATATGTGATGTTGATCTCTGCACTGTCGACTTCTGATATCAAA
Associated Phenotype:
Not determined