ZMP
frem1a
Ensembl ID:
ZFIN ID:
Description:
Fras1 related extracellular matrix 1a [Source:RefSeq peptide;Acc:NP_001177237]
Human Orthologue:
FREM1
Human Description:
FRAS1 related extracellular matrix 1 [Source:HGNC Symbol;Acc:23399]
Mouse Orthologue:
Frem1
Mouse Description:
Fras1 related extracellular matrix protein 1 Gene [Source:MGI Symbol;Acc:MGI:2670972]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1148 | Essential Splice Site | Available for shipment | Available now |
sa13110 | Essential Splice Site | Available for shipment | Available now |
sa31619 | Essential Splice Site | Available for shipment | Available now |
sa9531 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1148
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 |
---|---|---|---|---|---|
ENSDART00000090165 | Essential Splice Site | 387 | 1684 | 6 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72395866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69440601 |
GRCz11 | 7 | 69676749 |
KASP Assay ID:
554-1059.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCTTCCAGCCTCCCAACTCCAGCGCCACACATCGCAGGAACTACGAGG[T/C]GAAACACGAATGCTTTAACATACTGTTTGTTTTTTTTATTGTATTTTTTT
Long Flanking Sequence:
CGCTTCATTCGCCTGAGCAAATTTTCTCAGAAGACCTATAGTTTTACCGAGTCATGCGACTACGGTAATATCGAAAAAAATTAATATTGCGGTATTTACAATACCGTTACATCCCTAGATATTACACAACCCATTCTTTCATCTGAAGACTTAGTTCTGTCCATCTGTCCATCAGTCAGAGCAGGCCTGGATCCCGGTGACCATTACAGGCGCTCTCCCCAACCAGCCGCCCAAACCTGCCTTCATGTCCATGTTCATCCTGGAGGTGGATCAGTTCATCCTGACTCCTCTCTCCACTGCGACTGTGGACGCGGAGGACGACGAGACGCCCAAGCAGAGGCTGGTGTTCAACATCACTAAACCCCCCAGTGAAGGCTTCATTACTCACCTGTCGGACCACACCAAACCAGTGTCCTCCTTCAGCTGGACGGATCTGAATGGCATGCTGATCAGCTTCCAGCCTCCCAACTCCAGCGCCACACATCGCAGGAACTACGAGG[T/C]GAAACACGAATGCTTTAACATACTGTTTGTTTTTTTTATTGTATTTTTTTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCATCTCTGTTTAGGGGGGAGTGTCGGAGGAAGAAAAGTGGGATGGTGTGGGAGTGTCTATTTGGGCACGCGAGTTTCAGAGTCAAAACACACACACACACACAGTATAAAAGTGATGGTGTTTAACCCACATGGACATCTGTAGTCGAATTATTTGCCAAATTATTAAATGTTGGACTTTAACTGCAGTTTGGCTCTTTCATTCAGGGAACTCATTCATGCCCCTCGCGACAAACGAGATATTTGATTCGAGGATCTGCTCTAAGCGTGTATTTTTCATGCAATGTTTGATACCGCACGGCGAATGAGAGAAAAAAAACCTCAGTATTTTCCGGAAACTTAGATGCACACGACAGGTAGTGTCAGAAAGC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13110
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090165 | Essential Splice Site | 1093 | 1684 | 19 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72416387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69461122 |
GRCz11 | 7 | 69696159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTGATGTATATTGAATCCTGATATCCTAATGWTGYTGTTCCTCGTTC[A/G]GCCTCGTTCACCTAYAGGGRTGTGTTGGATGGACACATTAACTATGTCCA
Long Flanking Sequence:
AACGTGGGAATCAGTATTGGTCAGTCGGTTTTGTTACCCTGCTAAAATCAACCCAGACTCATTGCTGATATGCCCCCAGATTTACATTTCTGGGGACAGCGAAATGCGAAACTGGACGTACATCTCTCACATGTCCTCTTCTTTCGTAAATTCACCAGAGGGCGCAATATAACCTTCAGCTGACCAGGCTAGCTTGTTGTCGACTGACTGACTGACTGACCCACCCCGTCCCTAAACCCAACCGATAGTGTTTTTAAATACACTCTAGTAAAAGTAAAGCCGTCACCTTGTGATTTCGCCATGTTTTCAGCCTGTTGTTTATTTATTTATTTATTTGTTCTTTGTTTTACCTGATTTCCGGAACCATTCTCTGCCATACTCAAACCCCGTTGTCGCGGTCAACTCCATTTCAGAATGCTGTATAATATATGTATACAGTTTTGTATATTGATATTGATGTATATTGAATCCTGATATCCTAATGATGCTGTTCCTCGTTC[A/G]GCCTCGTTCACCTACAGGGATGTGTTGGATGGACACATTAACTATGTCCAGTCCAGACACCAGAGGATGGAGCCCACCACTGACCAGCTCATGCTGCAGGTGTCTGATGGGAAACAGCAGTCATCTCCAGTCCCGCTTTACATCATCATCAGTCCAACTAATGACGAGATTCCAGACTTCCAGACTCAAAACATCACGGTGGGTCACAGGGACATTCGGTAACTCTCAGCTAACTGAGAATATTATTGCCTAAAGAGATGTGGTGGTGCAAAAAATAACCGGGTGGGCAAAAAAAAAAGAGTGGGATGAAAAATATTTTTTGTACGTTTTTGCATTCTTAAGTGTTTGCATTCCCCTGAGAAACGTTGCTTTCGCTTACCCTTTAAAGGTCCAGTCAAATTAAAATAACATTTTTTAGATGTTAGAATCAGTATGTTAGTCTGTGTAAAACAATGACAAAATATGCGTTTAGAAAATATAACACTGATATTAACATGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31619
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090165 | Essential Splice Site | 1158 | 1684 | 19 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72416587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69461322 |
GRCz11 | 7 | 69696359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCCAACTAATGACGAGATTCCAGACTTCCAGACTCAAAACATCACGG[T/A]GGGTCACAGGGACATTCGGTAACTCTCAGCTAACTGAGAATATTATTGCC
Long Flanking Sequence:
CGACTGACTGACTGACTGACCCACCCCGTCCCTAAACCCAACCGATAGTGTTTTTAAATACACTCTAGTAAAAGTAAAGCCGTCACCTTGTGATTTCGCCATGTTTTCAGCCTGTTGTTTATTTATTTATTTATTTGTTCTTTGTTTTACCTGATTTCCGGAACCATTCTCTGCCATACTCAAACCCCGTTGTCGCGGTCAACTCCATTTCAGAATGCTGTATAATATATGTATACAGTTTTGTATATTGATATTGATGTATATTGAATCCTGATATCCTAATGATGCTGTTCCTCGTTCAGCCTCGTTCACCTACAGGGATGTGTTGGATGGACACATTAACTATGTCCAGTCCAGACACCAGAGGATGGAGCCCACCACTGACCAGCTCATGCTGCAGGTGTCTGATGGGAAACAGCAGTCATCTCCAGTCCCGCTTTACATCATCATCAGTCCAACTAATGACGAGATTCCAGACTTCCAGACTCAAAACATCACGG[T/A]GGGTCACAGGGACATTCGGTAACTCTCAGCTAACTGAGAATATTATTGCCTAAAGAGATGTGGTGGTGCAAAAAATAACCGGGTGGGCAAAAAAAAAAGAGTGGGATGAAAAATATTTTTTGTACGTTTTTGCATTCTTAAGTGTTTGCATTCCCCTGAGAAACGTTGCTTTCGCTTACCCTTTAAAGGTCCAGTCAAATTAAAATAACATTTTTTAGATGTTAGAATCAGTATGTTAGTCTGTGTAAAACAATGACAAAATATGCGTTTAGAAAATATAACACTGATATTAACATGTAGAGCTTGTGGTTTGTCACTTCCGCCTAAATGGATCAATGTTTTTTTTTTCACGTCACCTCATAATTCAGTTTCTCATCAAATCTTGAGCAATCAAATGCTCTCTAGTATCTGACATGCCCCGCCCCCTTCAAGATTCTTCTTATTTGCTTTTCAGTTGATGCGCTTGAGCTCAACCCCTCTCACTGGCAAACCTGTGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9531
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 |
---|---|---|---|---|---|
ENSDART00000090165 | Nonsense | 1234 | 1684 | 21 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72418787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69463522 |
GRCz11 | 7 | 69698559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YATACTTAAGTTTATAATGTGTCTCTGTCCACAGGCATGACTCTGATGTA[T/A]GTACACGATGACTCTGAGAGTGAGCAGGATGAATTCATCCTTCAGCTCTC
Long Flanking Sequence:
TAAGAAATTGAATAAAGTGTTGTGTTTATAGCCTAGAGTTGGCTATCTGTATGCAGAAACATTGCAGTAGTTACTGTAAATGTGATCACAGGTTTTTGTCTTTAGGTTTTTGAAGGAGACAGGACAGAGTTAAACTCGTCTGTAATCAGTGCGGTGGATTTGGATGTTCCCCAAGAGCGTCTGATGTTCAGCATCGTCCAGAATCCTCAGCACGGCTCTATCATCAGTCTGCCACACAGAAATCAAGTCTCACATTACAAGCGTGGAGCTGAGGAGCCTGTCCAGCATTTTTGCATGGATGACCTCAAGAGCGGCAAGTCTCAAATTTAAACATAAATATAAGCTTGCCAACTTTTTTTTTTTGACTCGTACGTTATTAAATTTATAGTAAATACTGTAATGAAGTACTTGAGTAGTTAATGTGTTGTTGTAATTCTATAGTTACTGTAATATACTTAAGTTTATAATGTGTCTCTGTCCACAGGCATGACTCTGATGTA[T/A]GTACACGATGACTCTGAGAGTGAGCAGGATGAATTCATCCTTCAGCTCTCTGATGGAAAACACAAGCTCCAGAAACACGTGCAGGTGAAAATACTGCCTGTCAACGACGAGGAGCCGCAAATCATCCGGTAACTGCAGATGAATATCAGTAAAATAAATCATGCTGTGTTTTTATCCGTGCCATATAAATACCATAACCTTCTCTCTCCCTCAAAACGACTTTTCTTCACTTCCTGGTCATATGGATTGCCTTTAGGGTGGGGCTATCAGTGCTTTAGGGCAAGGCTATCAGTTAGTGTCTTGTTTCTGCTTTGAATTGATCCAAGATTTACGTCACCATATAGCAGAAAAAAGGACAATCTTAACTTCCATTTCATCACAACTTTAAAGACCTTAAGATTTTTTGTTTAATTGTTTGTCATAAAGGTCATACATGTCAACCCAAGCTCATTCTGAAAACGTAGTCTCGTTGATGTTTCTGGAGACCGCAAAATACATCC
Associated Phenotype:
Not determined