ZMP
frem2a
Ensembl ID:
ZFIN ID:
Description:
Fras1 related extracellular matrix protein 2a [Source:RefSeq peptide;Acc:NP_001131129]
Human Orthologue:
FREM2
Human Description:
FRAS1 related extracellular matrix protein 2 [Source:HGNC Symbol;Acc:25396]
Mouse Orthologue:
Frem2
Mouse Description:
Fras1 related extracellular matrix protein 2 Gene [Source:MGI Symbol;Acc:MGI:2444465]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16135 | Nonsense | Available for shipment | Available now |
sa17334 | Essential Splice Site | Available for shipment | Available now |
sa21742 | Nonsense | Available for shipment | Available now |
sa14672 | Nonsense | Available for shipment | Available now |
sa21743 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16135
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 |
---|---|---|---|---|---|
ENSDART00000108808 | Nonsense | 1112 | 3119 | 1 | 25 |
ENSDART00000128292 | Nonsense | 1112 | 3113 | 1 | 25 |
ENSDART00000143255 | None | None | 1427 | None | 23 |
Genomic Location (Zv9):
Chromosome 10 (position 26620264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26024121 |
GRCz11 | 10 | 25985834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGACAGGTTMACGTTCAGATGTTCKGAWGGTGTRAATTTCTCAGAGAGA[C/T]AGTTCTTTCCCATTGTCATTATYCCCACAAATGATGAAAAACCAGAAATC
Long Flanking Sequence:
TCAGTGGTCTTGTTGTGTATGCGCACACCAGTGGTGAGATTGGTCTTACTTCAATTGAAGATTTTTTCAGTTTGACCCTCTCTGACATGTCTGATGAGTGGAATGTAGGGGGTAACCGAGTACACGGAGTCCGTGTTCATGTCACCATTCTCCCTGTAGATAACCAGACTCCATTGGTCACAGTTGGCCCTACTTTTAATGTCTTTGAAGCAGATAAAAACATTATCGGGAGCCATCAGATTAAAGTCGAGGATGCCGACACACCAAACGAGGACATCCTGTGCACCATTATCGTTCAGCCCACATCAGGATATGTGGAGAACATTTCTCCAGCTCCAGGCTCTGAAAAGTCAAGAGCAGGAACGGCAGTGAGTGCTTTCACCATCAGTGATGTGAATGAAGGTCATATTTATTATGTCCAAAGCATACACAAAGGAGTTGAGCCAGTGGAGGACAGGTTCACGTTCAGATGTTCTGATGGTGTGAATTTCTCAGAGAGA[C/T]AGTTCTTTCCCATTGTCATTATCCCCACAAATGATGAAAAACCAGAAATCTTCATGCGAGAGGTTGTTGTAATGGAGGGTATGAATGTTATTATTGACACGCCACTCTTGAATGGAGTCGATGCTGATGTTCCTGCTCAAGAGTTGATGTTTATTATCACCAAACTTCCCAATCATGGGTTCATTCTCAATCAGCTCGCCAGTGGCTCTGTCCCAGTCACAAACTTCACTCTGGAACAAATCAAAGAAGCCTCTAGCATAATTTACGAACATGATGATTCTGAAACCACCGAAGACAAGTTTGATGTTCTTCTTACAGATGGGAAACATAAAGCTGAAGGCACAGTCATGATCATGATTATTCCAGTGGATGATGAAACACCAAGGCTTGCCATAAATGACGGGCTTGAAATTGAGATTGGTGAAACAAAAGAGATAAATGCTAAAGTGCTGAAAGCTACTGATTTGGACTCAGACGACGAGTCCCTTACTTTCATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17334
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 |
---|---|---|---|---|---|
ENSDART00000108808 | Essential Splice Site | 1748 | 3119 | None | 25 |
ENSDART00000128292 | Essential Splice Site | 1748 | 3113 | None | 25 |
ENSDART00000143255 | Essential Splice Site | 56 | 1427 | None | 23 |
Genomic Location (Zv9):
Chromosome 10 (position 26653965)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26057822 |
GRCz11 | 10 | 26019535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGTGACCCTCAGACGGAGAGGTTTCCTGGGTGAAACGTCTTTTGTTGG[T/C]GAGTATCTTTATATGCAATTTAGCTTTGCCTGCATTTTCCACTCATTAAC
Long Flanking Sequence:
CCCCTTCAAGAAGCTTCTTATTTGCTTTCCATTTGATGTGCTTGAGCTCAAGAACTCTCACTGGCAGAGCGTTGATAAAACAAAACGCTATTGGCTGTTTTTTTAAAGGGGAGGAGTTGCACTATGTCTCACCCTCTTTTAATGTTTAATGTTTTAATGTTTCTGAAAACTTGACTGACATTGGACTGTCTATGTTGATCTGTTTTGACACAATCTACAGTGTAAACTCATTATAGAAATAAAGATGAATTAAGTTTAATGGAATATTTCAAACACTTTAAAAGACCTTTAATATTGCGTTCAACTTCTGATAGCTGTAAAATTCATTGTATGTTTTTACTGTTGTTCTTAGGAGGGAACAAACTGAAGAACCAACCGTTTCATCTGAACTGGTCTTGGATCTCTCTGGAGAAGCCAAACTATGTGGTGGATGAGCACGACAAAGTTCTGGAGGTGACCCTCAGACGGAGAGGTTTCCTGGGTGAAACGTCTTTTGTTGG[T/C]GAGTATCTTTATATGCAATTTAGCTTTGCCTGCATTTTCCACTCATTAACACATTTCCACAAAAACAAGCTGTTATCCAGAATTGATTAAACTTGACAAGAAGTCACCAGCACACGCATTAACAGGGGATCATTAGCATTCAGTAGCGTCTGTGTTTCACAGAGAGAGCTGTTATTAGTTAAGCTTATCAACGGGAAGCTGTTAGAGATGTTTTTCTAAGTGGTTTTGGCTTCTTTGTGTCTAAGATGAAAGCCCTCGCTCTCTCTGACATCCGTAGAACAGTCTGAACAGTTTTTTTTTTTTCAAGCGTACACCTGCTTATCTTGCCTTGCACTCTGCTCAGCTCAGCCCCACATGTGGTCAGTATTCAAGAAACCAAGGGTCTTTGTTCATGCGGCTGTGGGTTTGTGGATGTGTGTTGGCTTTGAGGGATGTTCGGGTTGAAAAAAGAAGCGGTAAGCAGAAGGCAGCAAGAGAGATGAGAAAGAAAAGGCTGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21742
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 |
---|---|---|---|---|---|
ENSDART00000108808 | Nonsense | 2663 | 3119 | 17 | 25 |
ENSDART00000128292 | Nonsense | 2663 | 3113 | 17 | 25 |
ENSDART00000143255 | Nonsense | 971 | 1427 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 10 (position 26733166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26137023 |
GRCz11 | 10 | 26098736 |
KASP Assay ID:
2260-3297.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCTTTGTTTATGACACTGCCATCTTGTGGAAGGACGGAGTCGGCAGC[C/T]AAACACAGGCTGATCTACAAGGCAAGTCATGAGTTTCAGAAACAAGTTTA
Long Flanking Sequence:
ATTCCGCTGTGGCAACTCTGATTAATCAAGGGTCTAAGCCAAAAAGAAAATGAATGAATGAGTGATAATAAAAATAATAATCATTTAATAATAATAATAATAATAATAAGTTTTGATGAGTAGCAAATCATATTAGAATGGATTTTGAAGGATGATGGTAAACTGAAGACATTAATCACAGTGATAAACCTAAACACATTCAAATAGGAAATAATTCTTTTAGATTGTGATCAAACTTGACAATATGACTGATAGCAGCCTCTAGTGGAGAAGTGGGCTTGTTAAAAGTGTTTTTCCTCAGTCTGTGTGTTGTGAATGTGTTGTGGCAGGTGCTGAACCTGGTGCAGTCATACGTGACCCTGCGTGTTCCTCTTCACGTCTCATACGTGTTTCATTCCCCTGTGGGTGCTGGAGGCTGGCAGCATTTCGACCTGCACTCCGAGCTCCGGCTCACCTTTGTTTATGACACTGCCATCTTGTGGAAGGACGGAGTCGGCAGC[C/T]AAACACAGGCTGATCTACAAGGCAAGTCATGAGTTTCAGAAACAAGTTTAGTTTGCATTATCTCAAGTCTTAGCATTTAGATTCTGGACATTTTTATGCGCTGTTATTCAATTGGTTGGCGGCCAATAATTGTTTTTTAGTGTTTAATTGCAATTACAATTTACTAACAATGACGTATTAAAGCAGGGATGTCAAACTCAGTTCCTGGAGGTCGCAGCTCTGCAGTTTAGTTTCAACCCTGTTTCAGCACACTTACCTGGAGTTTTAAAACAAACCTAAAGGACTCAATTAGTCTGTTCAGGTGTGTAAAATTAGGGTTAAAGCTGAACTGTGTGGATCTAGGATTTGAAACCTGTGTATTAAAGAGACAGAGAAGACCTTTATAGTGTCATAAAAGATTTCAGTTTGAAATATGTGATGTTATTTTGAACTTGATAGTAATTTTAAAAATCCAAAAAATGTGTTGCTGTTAAGAATAAAATACTAAGCCGCACAACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14672
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 |
---|---|---|---|---|---|
ENSDART00000108808 | Nonsense | 2878 | 3119 | 23 | 25 |
ENSDART00000128292 | Nonsense | 2872 | 3113 | 23 | 25 |
ENSDART00000143255 | Nonsense | 1186 | 1427 | 21 | 23 |
ENSDART00000108808 | Nonsense | 2878 | 3119 | 23 | 25 |
ENSDART00000128292 | Nonsense | 2872 | 3113 | 23 | 25 |
ENSDART00000143255 | Nonsense | 1186 | 1427 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 10 (position 26742243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26146100 |
GRCz11 | 10 | 26107813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTACTGTAACATTGAGAAGGTGTATCTGTGCACTGGAGCTGATGGATA[T/A]GTTCCTAAATACAACCCCAGCAAGTCTGAGTTTGGATGCCTTGCTGACTC
Long Flanking Sequence:
CACAGGCATCATCTTTTTTGATAGGTCCATATGAAATGTATAACTGCAGGTGTACCATGTTTATATATAATATCCGCCCGTTATACAACTCCTGCTTTGAAACAATTATTGTGAAAAGTGCAATACAAAATAAACTTGAATTGAATTGAATAACTATTGCAGATTCGTTTACCCTATTTATCTGCAGTGTCTTGCCTTAACCAACAAAATTACACCTTAGAAATCACATATCAACACTCTTGCACAAACAACATTTCCAAAAATGTAAGTTTGTTTCAGCTATGTTTCCACACGAGTTGTGAGATCTGTCATAGTCAAGTAAGTCATAGTCATGTAATTGCAGTGAGAGATGTTTGCTGTCTCAGTTTCCAACACTGAGCTTGTTCTCCTCAAGGTGACGTGATCTATGGACGTGTGATGGTGGACCCGGTACAGAATTTGGGCGACTCTTTCTACTGTAACATTGAGAAGGTGTATCTGTGCACTGGAGCTGATGGATA[T/A]GTTCCTAAATACAACCCCAGCAAGTCTGAGTTTGGATGCCTTGCTGACTCTCCGTCTCTGCTCTACCAATTCAAGATTATTGTAAGTACGATAGTAATGTTGCTAGTGATAAATACAACTAAACTTAGTTATTCAATAATTCCATTAACTGAAATGAAGCTGAAAACATATTATTAAACTAAAAACTCTCATTAAAAATAAATATAAATCAAAATATGAGTAATTGTGAGGAGTGTGAGGAAAAAACAAACTATTTCAGTACAGGGATTTCTTTGTGATGTTTACTGATGCAATCCTTATACACATTATAATCACAAAATCTGAAATCACACTGGAGCCTATTGCGTACACAGTGATTTATCAACACAGCCCTCCATTATCAATGTATTATTTACATTCATTGACAAATGCCTCTGCTGGATTTAAATGCTCAGTTGTTAAAAAAAATCTAGAATATTAATATCTGATGTAATTAGTGATAGGAGAAATAAAGCTTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21743
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108808 | Nonsense | 2890 | 3119 | 23 | 25 |
ENSDART00000128292 | Nonsense | 2884 | 3113 | 23 | 25 |
ENSDART00000143255 | Nonsense | 1198 | 1427 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 10 (position 26742277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26146134 |
GRCz11 | 10 | 26107847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGCTGATGGATATGTTCCTAAATACAACCCCAGCAAGTCTGAGTTT[G/T]GATGCCTTGCTGACTCTCCGTCTCTGCTCTACCAATTCAAGATTATTGTA
Long Flanking Sequence:
AATGTATAACTGCAGGTGTACCATGTTTATATATAATATCCGCCCGTTATACAACTCCTGCTTTGAAACAATTATTGTGAAAAGTGCAATACAAAATAAACTTGAATTGAATTGAATAACTATTGCAGATTCGTTTACCCTATTTATCTGCAGTGTCTTGCCTTAACCAACAAAATTACACCTTAGAAATCACATATCAACACTCTTGCACAAACAACATTTCCAAAAATGTAAGTTTGTTTCAGCTATGTTTCCACACGAGTTGTGAGATCTGTCATAGTCAAGTAAGTCATAGTCATGTAATTGCAGTGAGAGATGTTTGCTGTCTCAGTTTCCAACACTGAGCTTGTTCTCCTCAAGGTGACGTGATCTATGGACGTGTGATGGTGGACCCGGTACAGAATTTGGGCGACTCTTTCTACTGTAACATTGAGAAGGTGTATCTGTGCACTGGAGCTGATGGATATGTTCCTAAATACAACCCCAGCAAGTCTGAGTTT[G/T]GATGCCTTGCTGACTCTCCGTCTCTGCTCTACCAATTCAAGATTATTGTAAGTACGATAGTAATGTTGCTAGTGATAAATACAACTAAACTTAGTTATTCAATAATTCCATTAACTGAAATGAAGCTGAAAACATATTATTAAACTAAAAACTCTCATTAAAAATAAATATAAATCAAAATATGAGTAATTGTGAGGAGTGTGAGGAAAAAACAAACTATTTCAGTACAGGGATTTCTTTGTGATGTTTACTGATGCAATCCTTATACACATTATAATCACAAAATCTGAAATCACACTGGAGCCTATTGCGTACACAGTGATTTATCAACACAGCCCTCCATTATCAATGTATTATTTACATTCATTGACAAATGCCTCTGCTGGATTTAAATGCTCAGTTGTTAAAAAAAATCTAGAATATTAATATCTGATGTAATTAGTGATAGGAGAAATAAAGCTTTTCAAAGCTTTTGAGTCAATTCTTTCTCAAAATATGTA
Associated Phenotype:
Not determined