ZMP
si:dkey-69h6.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to autism susceptibility candidate 2 (Auts2) [Source:UniProtKB/TrEMBL;Acc:A5WW
Human Orthologue:
FBRSL1
Human Description:
fibrosin-like 1 [Source:HGNC Symbol;Acc:29308]
Mouse Orthologue:
Fbrsl1
Mouse Description:
fibrosin-like 1 Gene [Source:MGI Symbol;Acc:MGI:1920907]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40381 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1316 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40381
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 |
|---|---|---|---|---|---|
| ENSDART00000081064 | Essential Splice Site | 261 | 937 | 3 | 15 |
| ENSDART00000147657 | Essential Splice Site | 170 | 867 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 19510142)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17227634 |
| GRCz11 | 5 | 17731630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTCTGCCCCCGGCAGCCATCATTGGGCCGCCCACTGCACCTCCCATG[G/A]TGCGTACCCCAGCCAGAAATGTGAGGATAAGTAAAAACAGATAGATTTTA
Long Flanking Sequence:
GCCAGCCTCATTCGGGGATTCTGATTGGCACATTGTCACAGGCAACTCTCTTACCTCCACCAATGAGTCCTCACGTAGAAAACCCTCACACCTTGAATTGGAGAAACAGAGAAAGCCAGGTGACTACCCTCTTTCGCTTCTTCCAACCACTGTTGTGAAAACTCACTGGCCGCCCGTGCCTTTTTTTTCTTTTCCCTCCCGTGTCTTCCCCCTCTCCCCCTTTCCCTCCTTTTCCCCCTTCACTCTCCTATCTTGCAGAGCATGATCTTCTGAGGCAGGAGCTGAACAACCGCTTCCTGGTTCAGAGCTCGGAGCGAGGCCGGGGGACGGCGCCAGGGGCCACAGGGTCGCCGTTGGCCCCTGTGTCGCTCCTCCGGGCCGAATTTCACCAACATCAGCATATGCACCAGCACCAACACACGCATCAGCACACCTTCACGCCTTTCCCTGCCAGTCTGCCCCCGGCAGCCATCATTGGGCCGCCCACTGCACCTCCCATG[G/A]TGCGTACCCCAGCCAGAAATGTGAGGATAAGTAAAAACAGATAGATTTTACTCCCTTCCTACCTCCCTGATCCCCCCTTAAAAAACACCAACCTATTTAAAACAAGCGGCCATCGCATTCTTCAAACAATATCGCACTCACAATTGCGTTGACATACTGATTTTCAGCATGGCTGCATCATTCTGATGTTCAGACAGATTTTAATTTTAAAAATAGGATCATCTGTCGTTTGGTCTGTTGTTGTTCCATTGGCGAAGATAGTTCCAAACGAAGAGAACAAGCAGACTGGCAGCCAATCAAAAAAAACTGTTGTAGTGTATAGTGACACCAACAAATCACAACAGACCTCTAGAATGAACTATTGCATTATAAATTCTGATTAATTTACACCATTTAATTGAAACATTGAATTTCAGTTAGCTGTTAACATTATAACATCGAAACATCTCTATCATTCTTCCTTTCTTCTCAGATGGGATGGAGGGCAAAATCAAAGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1316
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081064 | Essential Splice Site | 365 | 937 | 8 | 15 |
| ENSDART00000147657 | Essential Splice Site | 279 | 867 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 19522372)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17239864 |
| GRCz11 | 5 | 17743860 |
KASP Assay ID:
554-1230.1 (used for ordering genotyping assays)
KASP Sequence:
ACATGTTCAAATCGCCTGGCAGATCTACCATCATCAGCAGAAGATGAAAG[T/C]AAGTTCTCTCAGAAGCCAAGAAAAGATTCTTTCTGAAATATAGTGTAGTC
Long Flanking Sequence:
CAAATGCTGGATAAGTTAGCGGTTCATTGCCTGAAAATGAATGTATGAATGTTTCATTATTTGTATCTAAAAAGGTCTTAATCTTCCCTCCAGGCCTCAAACCCTATTGATGTTGCAGCACGACCAGGAACAGTCCCACACACTCTCCTTCAGAAGGACCCAAGGGTAAGCTGTCCACTCTGGAGAAACACTTAAGCCGTTAGAAACGCATCAGGATTGTGATGTTTTCAGCATTTCATGAAGTTGAACTTCTGCCTTTGTCCTTTTCTCTATTTCTTTCTTAACTCCTCACAGATAACAGATCCTTTTAGGACTTCAGTAAGAGTAAGAATCATATTTCCATTCTCTTTCAAATCCCTACATTTTCCACCTTAAATGCCCGTGCCTTTGTGCTAATGCTTTGAAATTTCTTCTGTTCTCATGTCAGAAGCCAGGTAAATGGTGCGCAGTACATGTTCAAATCGCCTGGCAGATCTACCATCATCAGCAGAAGATGAAAG[T/C]AAGTTCTCTCAGAAGCCAAGAAAAGATTCTTTCTGAAATATAGTGTAGTCTTTAGTGTAAGTGAAATACAAGAATATGTAGGTGCAAAGTGGAATGTTTCATGCATTAAACATTATTGCTGGGTTCAGGCTACACAATATCAGCTTGATTTTTGGCACAGATCATCTGAATCAAAGTTGTAGTTTTTTCGTAAAAGGGGACATCTCAACAGAAAGACATGTTTAATTTTGTTGTGGACTTTTCACATACTTATTTTCTGATGCCAGTAGAAAACATTCCAATTCATTAGCCATTGTTTCTTTACACTTTTGTTTCCAGAACTCGTTTGTTATTGCCACCTTCTTAGTCATTAAAGATGGCAAGAAATGATTGGCTCTGGAAGAAACATCTTTCTTGCTCATGACATAAAAAGTACTTACGAGTCAAAATAACAATCTCACAGCAAATTTTTGTAAGAGATAAAAAAAATATTGTGTAATAAAAACCTGAAACTAATTAGT
Associated Phenotype:
Not determined