ZMP
fras1
Ensembl ID:
ZFIN ID:
Description:
extracellular matrix protein FRAS1 [Source:RefSeq peptide;Acc:NP_001124312]
Human Orthologue:
FRAS1
Human Description:
Fraser syndrome 1 [Source:HGNC Symbol;Acc:19185]
Mouse Orthologue:
Fras1
Mouse Description:
Fraser syndrome 1 homolog (human) Gene [Source:MGI Symbol;Acc:MGI:2385368]
Alleles
There are 15 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17510 | Nonsense | Available for shipment | Available now |
sa20491 | Nonsense | Available for shipment | Available now |
sa14516 | Nonsense | Available for shipment | Available now |
sa20492 | Nonsense | Available for shipment | Available now |
sa20493 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17510
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 |
---|---|---|---|---|---|
ENSDART00000076845 | Nonsense | 537 | 3970 | 14 | 72 |
ENSDART00000097856 | Nonsense | 548 | 3989 | 15 | 74 |
ENSDART00000137112 | Nonsense | 503 | 3936 | 13 | 71 |
The following transcripts of ENSDARG00000054619 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40557425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 38356815 |
GRCz11 | 5 | 38956968 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATATTTGATTTATTTATTTGTAGCTTGTGACCCTTCCTGTGCAACCTGC[C/T]AACCTGACAGCCCCAGCTGTATGAGCTGCCCTGCAGAACAWGCACTGCAT
Long Flanking Sequence:
ACCATTCCTTGTACTGTAATGACAAAGCCTGCTTCCCAAACATCCCCCTGTCAACACTACAGCAAATGCAGAATGACACTCTACATGTCTTCTTTATAGTGGAGAACTTAAGCTGCCACACATCCAGCTTGTCTGTTTATCAGAAGTAGAAGTGTGCTGATGGGAGTTTGTTGGGTTTCTGACTGTGGGTAAAAATAGCTTGTGGTTTGAGCATTTATACTGTATTTTGTATTGATATGCTGACTTGAAGGTTCTTAGGCTTTTCTATATTTGTTTGTTCTATTTTTAATTGAGGTTTCTCATAAGTGTTTCTCACAAAACCTCAAATTATTTTAGTCATATGAGGTTATACTAAATTAAAAAATAAAGAAATCTTGTAAAACACGTTTCTATAAAAATAAAAGTGCGTTTTATTTACAGCATTGCAGTGTAGCTGTTTTATTTATATCAGATATTTGATTTATTTATTTGTAGCTTGTGACCCTTCCTGTGCAACCTGC[C/T]AACCTGACAGCCCCAGCTGTATGAGCTGCCCTGCAGAACATGCACTGCATCAAGGGAAATGTGCACCACAATGTCCAGCGCAGTATTACAAGGATGACCACGGCCGATGCCAAGGTGAAAAATTATCTATTACTGTTTTTATATTTTGTGCAACACGTAGGCTTACTGGCAACCAGAGGCTCATAAATCTCTTTTGTAGCGAATTGAAAACATATTCTTCATTCTGAAACCCATTTTCTCTGCCAGAGACGCTGCTTTGGAAAGTTTCCCTGTCATTTGGACTCGATCCGTTGAAATGTCTTACCTAGGTTTTTTCCGCAAAACCGCAGGGCCTAGAAAATGATCATTGTAGTGCTATGCTCGATTAATTTTAAAATCACATTTAATACCCTGTCAAAACCTAATCCTGTGGTGTTTAGTCAATTAGCATTTTTTTTGCCAGGCACCTTTATCCTTCTAGCTGATAAAAACAGCATAGAGTGCAGTAGCTAGAAAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20491
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 |
---|---|---|---|---|---|
ENSDART00000076845 | Nonsense | 1394 | 3970 | 29 | 72 |
ENSDART00000097856 | Nonsense | 1406 | 3989 | 31 | 74 |
ENSDART00000137112 | Nonsense | 1360 | 3936 | 28 | 71 |
The following transcripts of ENSDARG00000054619 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40613255)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 38412645 |
GRCz11 | 5 | 39012798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTAAATGAAGGCACTGTCTGGTACCGACATTATGGATCTGGAACACAG[A/T]GAGACACTTTTCAGTTTCAGGTGAGACATGAATAGATTTAACCCAAGGCA
Long Flanking Sequence:
AGATAGGTCTTTTACACTGACACAGACGCAGCGTTAATAATGATGATGATGTTTTATGCTTTCTCTGTAGGTTGGATTGACTCCGCACCTGCGTTCAGTGCCCAAAACTTGGGTGAAGGAGGGAGGAATGGTGCAGCTTTCTAAAAAGTGTCTCAATGCTCAATTCAAAGGAGCCAGTGACTCTGAGATCCTGTACAGCATCCATTCTGAGAGCGGACAGCCCAAATACGGTAACCTCAGCATATTCTACCTTTATTATTTCTCACACATTATCTGCCTTTTGTTCTGAACTCATTTTAGTGCAATGAACTAGGCAAAATGTTTCTTGTGTTTGTGTGTGTCTAGGAGAGATTGTGCTGGTGTCTATGCCCGCTGACGGTCCTGTGGAAGCGTGGCAAGCCTTTTCTGATGGTCAAGACTCTACACCCACCAGCTCATTTACACAGCAAGATGTAAATGAAGGCACTGTCTGGTACCGACATTATGGATCTGGAACACAG[A/T]GAGACACTTTTCAGTTTCAGGTGAGACATGAATAGATTTAACCCAAGGCAAATACTGTCACTTCAGCACGAGCCCCGAGGCTCTGTGTGTAGAGCTAAAGGTGCCACTTAACGTTTGACTTGTTAAAACATGTCTACTCCTATAGCTCTTTGTTTTTTTATTGATTTGGTACTTAATTGGAGCAATACTAACTTAAACGCTCATCATAAACACATCGAGTAATTACTGTTAAACTTTTTGCCGTGCTCAAAGGAGCAGATTCTTCTGGCTTCTGCTTTGTGTTCTGCCAAAATAATGCTCCTGACAAAACATGACACTTCGGCAGATAATATAAAAGGGTAGATTGCAACTACTTTGACTTGTTTTTTTAGTTCAAATTAGCAATGATCTAACATATGATACATTACTTATTAAACATTTACTATTTAATGCCTAGTAATGTGGCTGCAAGAAATGAATACTTTAATACTTTCTTTTCTATGATTTATTAATCTAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14516
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 |
---|---|---|---|---|---|
ENSDART00000076845 | Nonsense | 3010 | 3970 | 59 | 72 |
ENSDART00000097856 | Nonsense | 3029 | 3989 | 61 | 74 |
ENSDART00000137112 | Nonsense | 2976 | 3936 | 58 | 71 |
The following transcripts of ENSDARG00000054619 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40666717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 38466107 |
GRCz11 | 5 | 39066260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAAAAACAGTGCATGTCCTGCTTTTCAGCACCTACGATCGAGTTTGAA[C/T]AAGCCACATATCAAGTTCGTGAGCCACCTGGTCCCGATGGCATTGAGGTT
Long Flanking Sequence:
TCTGTGGCCAAAGCTCTTTTGAAATGCCAGTTTTGTTTCTTTATTTATATTTTTTTCTTTGTTGTCCCTAATTACAGTATTATTTAAGACGCCCATAATGATTGTTTACAGTTTAATGCAAGTTACTGCCATAATTCACACAAAGCTTCATGGGGTGTAGGAATAACGTAGATAAAAGGAAGAGTTCAGATGCAAAAGCTTGTAAGTGCCACCTGAAATGTTCTAAAATGAGCATTTTTCTTATGCTCATATGTTTCTGTGCAGTTATTTCAATTTAAAGTCAATAAAAAAAACTATCGATGGCCATAAAAGTGAAAAAAATGATTCAAGACACAGGACTCTTACAGAAATGCAAAATTTTAGAGGGAAATTTCAGATAGACTTTTGCATTTGAAGTCTTCAAACATATAGCCTGAATAGATTGAAAGTCAATTTTCATAAACGCATGAATGTAAAAACAGTGCATGTCCTGCTTTTCAGCACCTACGATCGAGTTTGAA[C/T]AAGCCACATATCAAGTTCGTGAGCCACCTGGTCCCGATGGCATTGAGGTTTTGAATATCAAGGTAATTCGTAAAGGAGACCTCGACCGCACCTCCAAAATTCGATGCAGCACGAGGGATGGATCGGCCCAGTCAGGTGTGGACTATAACCCAAAGAGTCGAGTGCTGAAGTACAGCCCTGGTAAGTTGTTGATTTACTTTCATTTATTTTACATTTGTAAACAAGAGCTTTGTTCTAATCTATGACTAATGTGTTGAAAAGGTGTGGACCACATCATGTTTAAGGTGGAGATTCTGTCCAATGAGGACAGAGAGTGGCATGAGTCTTTCTCTTTGGTCCTTGGTCCTGACGACCCAGTTGAAGCTGTTCTTGGAGAGATCATCATTGCAACAGTCACTATTCTGGATCAGGAGGCTGCAGGAAGTCTTATCCTTCCGGCTCCACCCATTGTAAGAATCGTACACTAGAAAAAAACAAGAAATACTTTATATTTCATTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20492
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 |
---|---|---|---|---|---|
ENSDART00000076845 | Nonsense | 3691 | 3970 | 70 | 72 |
ENSDART00000097856 | Nonsense | 3710 | 3989 | 72 | 74 |
ENSDART00000137112 | Nonsense | 3657 | 3936 | 69 | 71 |
The following transcripts of ENSDARG00000054619 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40683477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 38482867 |
GRCz11 | 5 | 39083020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAACCTGAATTCAGCCTACAAGCTGCAGCTGGAGAAAGTGTATTTGTG[T/A]ACGGGACGGGATGGATATGTTCCCTTCTTTGACCCTACAGGCACACTGTA
Long Flanking Sequence:
TGGCCCAGTAGAGCTTTATGTCTAGCAACACCCCTGCTTGAATGGCTTTGCTGTTGTCATTGACTTTCAGTGGACTTGTTTTACTCGTTTCATCAGATCGTTTGTGTGAATCAGCAAGAGTATTTATAATATCCAAGGACTTCTAACAATCTCTTTCAATCAATAGATTCCTGCTGCCCATCGCCTTCCAGCAGACCAACCGCCCTGTCCCTGTTGTCTACTCTCTGAATACTGAGTTCCAGCTTTGTAATAATGAGAAAGTTTTTCTAATGGATCCTGCTCTCGCAGACATGTCTGTGGCTGAGATGGATTACAAAGGAGCCTTTTCAATGGGTAAAATGAGCAAATTAGTGAAAATGATGAGATGCGTCACTATTGTGCTTTTGTTCATTCAATATTTGATGTTATGCAGGTCAAACCCTGTATGGCAGAGTCCTGTGGAATCCTGACCAGAACCTGAATTCAGCCTACAAGCTGCAGCTGGAGAAAGTGTATTTGTG[T/A]ACGGGACGGGATGGATATGTTCCCTTCTTTGACCCTACAGGCACACTGTATAATGAGGGCCCTCAGTATGGCTGCATTCAACCAAACAAGCACCTTAAACACAGGTTCTTACTTCTGGTAGGTGCATATTGTAACAAGTCCAGACCAGTTTAACTAGCCTAACAAGATCGGCTTGATGTGGTTAAGTTTTAACTGAAATACTTTTGTGGAGTGGAATTTTTCAGTGGGCACTGCAAAGATCAAGCTGGTTTTGTTTACCTTGAAAAAATATCAAATTTAATTCTTGTTTATTTCTGTAGTGTTTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATAGTTTTAGTAAAGTCCAGTTTTTAGTGTTAAAGTTTAGTTAAGTTCAGTGTGGTTTAAGTTTCACTGCTGAAAGTTCAAACACTGACAAGCAAATCCGAGAAAAGCAATGCAATATAATATGCAGTTCTTAAAGGAAAGTTTTTTTAATAATTGTTATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20493
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 |
---|---|---|---|---|---|
ENSDART00000076845 | Nonsense | 3810 | 3970 | 72 | 72 |
ENSDART00000097856 | Nonsense | 3829 | 3989 | 74 | 74 |
ENSDART00000137112 | Nonsense | 3776 | 3936 | 71 | 71 |
The following transcripts of ENSDARG00000054619 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40685554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 38484944 |
GRCz11 | 5 | 39085097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGACCCGAGTCTATTTCGTCTCCCAGAATCCAGCGCTCAGTGACTTA[T/A]GAGCTGAAGCGAAGCCGCCGAGATCTAGTAGACCGATCAGGTCGCCTAAT
Long Flanking Sequence:
CTAATAATTCTGACTTCAACTGTATTTATGTGTGTTACCTAGGACCGAAAGCAGCCTGATGTATGTGATCGCTACTTCCATGATGTTCCCTTTGAGGCCAGCTTTGCATCTGACATTCCTGACCTCCTGTCTTTGTCTGCGATGCCCGGTGTAGACGGATTCACAATGAAGGTTGATGCCCTTTATAAGGTCAGTGACTTCAACAACCACATACTCAAACGTTCTAACTGAAACATGCTCCAAATCCTGGCATATGCCAGTGCCAAAGCATTTCAGATGTACCCTTCAAGCAATTGCCTAGATCTGTTTGTTTAAGAAAAGATGCCAGACTAACAGTCTGCCATGACTATAGGCAGCTTGGGGAGCTCTTTTGTTGGCATCTCATTCGTTGTGTTTGCTCTTCTTTAGGTTGAAGCAGGGCACCAATGGTACCTCCAGGTCATCTACGTTATTGGACCCGAGTCTATTTCGTCTCCCAGAATCCAGCGCTCAGTGACTTA[T/A]GAGCTGAAGCGAAGCCGCCGAGATCTAGTAGACCGATCAGGTCGCCTAATGCTTGATGAATCATTGATCTACGACAATGAAGGTGACCAGGTAAAGAATGGCACCAACATGAAGACCTTGAAGCTTGAGATGGAACCATCAGGCACCTTCAACCCCCAAATGGGAGGATCCATTGGGGGTGGCGTGGCAGCCATCCTCCTGCTTTTCTTAGTCCTTCTAGCGTTCTGTTTCATGGTCAGGAAGTGCCGCAGGGTTGTCAAAAAGAGGCCTTCAAAGACGGTGGAGGATTATCCTCTGAACACAAAGGTGGAGGTCTGCATTGAACGTCTGGAGAAAAACCTCAACAGCAAGCACTGCTCTGTAAGAAACATCAACGTTCTCAACAAGAACCCCGACACCTACAAAGTCAATGGGGTGAAAGTCAAACAGGTCAATCTGGAGGTCAAACTCCACAACAATCTAAATGACGGCACTGAAGTCTGACCTTCTAGAGTATTTAA
Associated Phenotype:
Not determined