ZMP
fstl1b
Ensembl ID:
ZFIN ID:
Description:
follistatin-like 1b [Source:RefSeq peptide;Acc:NP_001034710]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34567 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21439 | Nonsense | Available for shipment | Available now |
sa44701 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1267 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34567
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 |
---|---|---|---|---|---|
ENSDART00000083326 | Essential Splice Site | 19 | 309 | 2 | 11 |
ENSDART00000121456 | Essential Splice Site | 20 | 310 | 2 | 11 |
The following transcripts of ENSDARG00000039576 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 10063268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9863819 |
GRCz11 | 9 | 9841856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTTACCCGTGTTTTTCCTCCTGGCTGTAGTCTGCTGTCATGCCGAG[G/A]TAAGTTACACCAAACCCGCTTTTAATAAGGAGAAGAGCTCGTGTTTTTGG
Long Flanking Sequence:
TTTTCTAACATTCCACTAATATTTGTTATGTCTCACACTAGCAAAAGCTGCAATTTTCTGCAAGTGTAGGCTAATATATGCACTAATATGGACTTATTGGTCTCGCAAACCTCTAGCACTTTTATCCGAGCTTGTGCTCATTATCTGGATCTGCTCCACGGCTTTTCACGGGCCACGTCACGTCACGGAGGGGGAAGAAACGGATTCCTGAGCGCTGCTCGAGTTTCCTGCGATCACATCCTCAGACCTACAGCGGACCGAGACGTCGCGCTTTTCCTCCTCACAGACACCCAGGCGGCGTTTTTTTGCAAAAAATGGTGAGAAACCTGAATTATATTTACAACATTTTACAGCGTCAAAACAACTTGTGTCGTTTTGCCTTGCGTTTTCTCCTTTTGTAATGTCTTTTCCTCCGTTCTCCCTCTTCTCTCTGCCCGTTACAGATGTTTCGGTGTTTACCCGTGTTTTTCCTCCTGGCTGTAGTCTGCTGTCATGCCGAG[G/A]TAAGTTACACCAAACCCGCTTTTAATAAGGAGAAGAGCTCGTGTTTTTGGAAAAGAATGTTTATTGTGGATCCTGATAATAGTTTCTCTGATATCCGACTTGGCCAGAATGAACTGTTGAAGAAATGAGTGCACTAACTAACTAACATTACTTACAACAAAACAATGGATAATTATGATTAATGTTAAAACTGCGGCCAGTGTTGTTGTTTTTCCCAATTGAAAATGTTTTGTACATAAAGAAAAGCAACTTCAATGAGGTTGACTAACATTAGATCATTCCAGACGCCTTCGAGGAAAAAATAGAGAGGGGGAGAGACAAAAAAAGGTTTATTTTACATGCATAGAGCGGGTCGCACCTCATGTTGATATCACATGATCATGTGTGCACGTGACCGAATTGGCACTTAAACTAATATGCATATTTTACTTTAAAATTAGTATCAAGTCAGAAAGCATTTATGCATTCTGATAGAGAGCTCAGTATAATATGAAACTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21439
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083326 | Nonsense | 56 | 309 | 4 | 11 |
ENSDART00000121456 | Nonsense | 57 | 310 | 4 | 11 |
The following transcripts of ENSDARG00000039576 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 9992835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9793386 |
GRCz11 | 9 | 9771423 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATGTGGCAGTGGTGATGTTTTCATTGTTGTGTTCTCCTGCAGCAATG[C/A]AAGACTCATAAGCGCTCGGTGTGTGGCAGTAATGGAAAGACATACCGGAA
Long Flanking Sequence:
ATGTCAACAGAGCAGAGATCAAAGTCTCATAATGCAATTTACAACAATAAATAAACTGAAAATACTTGTGAATCACAACATACAGAAACTGTTAATGAACAGATATTTATGTACCGTGTATCATCATGCCAGGTCTGATGCTATATTATTAGGATTATTTATCTCAAAATTATAGTCTCATAAACTTTTGCTCAATAACAGTACTGTATGTGTGGGATTGGGGTCATGTGTGATGTATAGACTTTGCTATGTGTCTACACAGCTCAGCAGATTATACAATCATACTATTGTGGTACCACCAGCCTGCTCTCCATACTTATATTTTATTACAGGCTTAGTGTCAGCTTTAAAGCAGAGGAAAATTAAATTAGAGTCACAGTGTCACAGAGCATTTAAACACCAGCCTTTGTTTATTTCATGCATTTTATTGTTGTTTGCAAGATAGATATTGTAATGTGGCAGTGGTGATGTTTTCATTGTTGTGTTCTCCTGCAGCAATG[C/A]AAGACTCATAAGCGCTCGGTGTGTGGCAGTAATGGAAAGACATACCGGAACCACTGCGAACTGCATCGTGATGCCTGTCTCACTGGACTGAAGATCCAAGTGGCTCATGATGGACACTGCAAAGGTGAGCATACAGAAGAACTTGAATCAGTAACAGCAGACTGATTAGGGATGATACAGACTAGAAATCAAATTTGCTGCTAATATAAAGTTCTATCATAAAACTCATTTGGGTGCACAGGATGATGGGTCCTATGCAATCTGCTTTCAACCACAGGAAGTGTGATGCAGGAGGACCTCAGCAGCCAATACGCTTGCTTCTCAACATTTACTGAACCACATCTCAGTGTTCCAATCTGCAGCACATTTACGGATACTCTTCTCCACCACAGCTCCAACTGTGTATTCAGTTTCAGTCTTCGCAGTTGCAATATTATAGTTAAATAAAATCGGCTATCAAAGTGGTCACTAGATAATGGCTTAAACTATATTGTAATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44701
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083326 | Essential Splice Site | 98 | 309 | None | 11 |
ENSDART00000121456 | Essential Splice Site | 99 | 310 | None | 11 |
The following transcripts of ENSDARG00000039576 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 9992709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9793260 |
GRCz11 | 9 | 9771297 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTCACTGGACTGAAGATCCAAGTGGCTCATGATGGACACTGCAAAGG[T/C]GAGCATACAGAAGAACTTGAATCAGTAACAGCAGACTGATTAGGGATGAT
Long Flanking Sequence:
TGCCAGGTCTGATGCTATATTATTAGGATTATTTATCTCAAAATTATAGTCTCATAAACTTTTGCTCAATAACAGTACTGTATGTGTGGGATTGGGGTCATGTGTGATGTATAGACTTTGCTATGTGTCTACACAGCTCAGCAGATTATACAATCATACTATTGTGGTACCACCAGCCTGCTCTCCATACTTATATTTTATTACAGGCTTAGTGTCAGCTTTAAAGCAGAGGAAAATTAAATTAGAGTCACAGTGTCACAGAGCATTTAAACACCAGCCTTTGTTTATTTCATGCATTTTATTGTTGTTTGCAAGATAGATATTGTAATGTGGCAGTGGTGATGTTTTCATTGTTGTGTTCTCCTGCAGCAATGCAAGACTCATAAGCGCTCGGTGTGTGGCAGTAATGGAAAGACATACCGGAACCACTGCGAACTGCATCGTGATGCCTGTCTCACTGGACTGAAGATCCAAGTGGCTCATGATGGACACTGCAAAGG[T/C]GAGCATACAGAAGAACTTGAATCAGTAACAGCAGACTGATTAGGGATGATACAGACTAGAAATCAAATTTGCTGCTAATATAAAGTTCTATCATAAAACTCATTTGGGTGCACAGGATGATGGGTCCTATGCAATCTGCTTTCAACCACAGGAAGTGTGATGCAGGAGGACCTCAGCAGCCAATACGCTTGCTTCTCAACATTTACTGAACCACATCTCAGTGTTCCAATCTGCAGCACATTTACGGATACTCTTCTCCACCACAGCTCCAACTGTGTATTCAGTTTCAGTCTTCGCAGTTGCAATATTATAGTTAAATAAAATCGGCTATCAAAGTGGTCACTAGATAATGGCTTAAACTATATTGTAATGGTGCCATAGAATAAAAATCAGGATATACAGTACATAGGCAAAGCTGAGTGATAAGAGTACAGTACCTTGATTGAAATGACCATTGTTCCACTCCTTGTGAAAAACGGGCCAAAACACAGACTATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1267
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 |
---|---|---|---|---|---|
ENSDART00000083326 | Essential Splice Site | 266 | 309 | 9 | 11 |
ENSDART00000121456 | Essential Splice Site | 267 | 310 | 9 | 11 |
The following transcripts of ENSDARG00000039576 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 9964902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9765453 |
GRCz11 | 9 | 9743490 |
KASP Assay ID:
554-1182.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCGTCTGCGCTTGTGGAAACTGGGTCTGCACCGCCATGACTTGTGATG[G/A]TGAGCTTTAATTTGCAMATCTGTTATCATCTTATTTTGATAAATGACAGG
Long Flanking Sequence:
GCAATTATGAAAATTAGCAGGGGTGGCCAAACTTTTGCATAAGACTGTACATCACATTTATACAATATACTGACAGCACACTTCAATCTTATTCATATGTTCTATCTTTCCCTTTGTAGCAACACAGTCATTCCAAAGTAATTTCCTGTTTTGTATTTGGGAATCTGGGACACAGGCTTATTCAGTTGCAGACTCAGCTGCATAAAAAAGCATGCACACAAAATGGCCTGTTTGGACGGCTTTTGTTGGTTTTAGCTTAGTTTATAGAGAAAAGCAGATCTCGTTTCGGCAGTCCTCTGTTAACTCATGTAAGAAAACTATGGCATATTTTTGGAGAACTAATTTTATTTTCCTGAGCATGGGTTAACATATGTTTTGTATCATTTCAGAGTGTGCTCTAGAAGATGAGACATATGAGGATGGTGCAGAGACGCAGGTGGAGTGCAATCGCTGCGTCTGCGCTTGTGGAAACTGGGTCTGCACCGCCATGACTTGTGATG[G/A]TGAGCTTTAATTTGCAAATCTGTTATCATCTTATTTTGATAAATGACAGGAGAGTGGCATAAAATAAGCACTTTGCTCTGGAAGTGTTAGGAGACTAAGATAAAAAAAAAGGTATATCTAATTATATTTCAGCATGTCAAGATATATTCAAAGTTCTATTCAGGCGGCATGGCGCCACACTGGTTAACACTGTCGCCTTACAGCAAGAAGGTTGCTGTTTCAAGTCCCGGCTGGTTCAGTTGGCATTTCTGTATGGAGTTTGCTTGTTCTTCCTGTGTTGGAGTGGGTTTCATCCGGGTGCTCCAGTTTCCCCCACAGTTCAAATACATTCTCTCTAGGTGAATTAGGAAAAAACTAAATTGACCATAGTGTATGATTGTGGGAGTGTATGGGTGTTTTCCAATACTGGGTTGCAGCTGGAAGGGCATCAGCTGTGTAAAACATATACCATAATAGTTGGCGGTGAAACCCCTGATAAATAAAGGGACTAAGCTGAAGGA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |