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 |
---|---|---|---|
sa27100 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1148 | Essential Splice Site | Available for shipment | Available now |
sa34238 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13110 | Essential Splice Site | Available for shipment | Available now |
sa31619 | Essential Splice Site | Available for shipment | Available now |
sa41083 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9531 | Nonsense | Available for shipment | Available now |
sa41084 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27100
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090165 | Nonsense | 218 | 1684 | 5 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72394154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69438889 |
GRCz11 | 7 | 69675037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTAAAATCCCCCCCCCCCTCCCCCTCCCCCATGCAGATAATAAAGCC[A/T]GAGCTCACTGTAAGACTGATGACTGCCTGAAGGGTCTCAAACTGCTGAAA
Long Flanking Sequence:
GCATGAATAGTCCTCACTTTCGATTAGGTCACAAAACTAGGTGAAGTTGAGTTAATAAAGCATTTATTAATATACATATATGCCTGAATAATAAGACATATAAACTTTGATTTCAATAGTTTTTTTTAATCATTTACTAACTCATTCTGAATGATCCTAAAAACCCTCATCTACTCTTAAATACCAATGGTTTGTAAATAATGCGGGACTTAATTTAGTAATGAAAAATAAATCATTAACAGAGTATGAAAATACAATCATTAATCACATTATATAGGTGCTTATAAGAATACAGCATTTGTAGCTGCAGTTATAAACTGCTTACTAACGCTTATTAATGTAGAGTTAACGCTTAACAAATAATGAGTTCACTATTTGCTAATGCTTAATAAATGATTTATAGTGTGTAGTTATTATAAAGTGTTACCAATATTACTGCAAATATACAGTTGAGTAAAATCCCCCCCCCCCTCCCCCTCCCCCATGCAGATAATAAAGCC[A/T]GAGCTCACTGTAAGACTGATGACTGCCTGAAGGGTCTCAAACTGCTGAAAATCACCAAAGTGCCATGCAATGACTTCCTGATGATGGGCATCCGCTACCAGCACACCGACCCTCCGTCTCCACATACAGACTACATCTCCATCAGACTGGACCTCACAGACACCCGGAGCAGGAGCATAATACAGGTGTTAATCCTAAATTCACATTACATTCACATTACTGTGTTGTCTCCATGCCAGATAAAGGTTTGGTATTAAAACAACAGGTAACTCTTTATTTGAAGGGGAAAATGAGGAGAGGAAAACCATGTCAGTCTGCTTCTTTATTCTTAATATAAAGTACAGATATTACTAGGGATGTAACGGTATCAGAATTTCACGGTTCGGTAATACCTCGGTATGAATGTCACGGTACGGTATTTATTGAATCATTTACAGGAAAAAACAAAACTTATGAAAATACTCCAAAAAAGTGCCAAAAGTGTCAATGACATACAAATT
Associated Phenotype:
Not determined
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:
sa34238
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090165 | Essential Splice Site | 782 | 1684 | 13 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72407549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69452284 |
GRCz11 | 7 | 69687527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCTGCTTTAACGTAACTGTTCTGCCAGTGGATAACCAGGCACCAGAG[G/T]TACAAGAACCCTTAATTACAAGAGTTAAAAAGTACTCACCCACACTTTGG
Long Flanking Sequence:
CACGTGCACACATAGGGCTCAACCTGTGCAGTGCACATGCCCTTTTTAGTCTTGGATAGAAAGTGCCCTTACAAAATGATCAAAAGTGCCCCCGCGACGCGACACACCCTCCGTCCCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCTCCAGGAACAAGTTTGGCTCCAGGAACAAGTTTGGTGACCCCTGCTTTAGAAGAATCAAAACGTTCACCAGAAGCAACTGACGCTGTACACTATCCTCTTGGATGTGTCTGTAGCACGCAGTCAACTACATGAAAGTAGCTTACATGCCCCCCATCCCGGACATCGGACCGTACCCTCAGCACATCCAGTTTGTCCTGTCAGTGACCAACCAGCAAGGCAGCACGACCACCGGGATCTGCTTTAACGTAACTGTTCTGCCAGTGGATAACCAGGCACCAGAG[G/T]TACAAGAACCCTTAATTACAAGAGTTAAAAAGTACTCACCCACACTTTGGTCCAATTCCCTGAGACCTTTGTTCATCCTCAAAACACAAGTTAAGATATTTTAGATGAAATTCGAGAGCTCTCTTATCCTCCATATAGACAGAAATGCTCCGGAGATGCTTAAAGTCCTAAAAAGGAACCAAAACATTCAGTGTGACTTCAGCGGTTGAACAATAATTATATGAAGCTCCAAGAACACTTTTGTGCACCCTCCAAAAGAAAAAAACTATAAATAAACTTTGTTCGTCAGTCACATTTTTTTTTTCGTCAAGTGGTCAATGTGTTTAATGCGGGCTGCATGACATTCCTATTAGGGCCTACTCACACTATCCCATCCGTACCGTGCCCAGGCCCGTTTCCCGGATCGTTTGAGTGCGCTGAATCGGGCTCAAGCACAGTTCACTTGGCCGGCCCTGGCTCGGTTGGAAGAGGTGCGCCTGAGCGCGGTTCACTTGGGCTTT
Associated Phenotype:
Not determined
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:
sa41083
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 |
---|---|---|---|---|---|
ENSDART00000090165 | Essential Splice Site | 1229 | 1684 | 20 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72418604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69463339 |
GRCz11 | 7 | 69698376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGAGGAGCCTGTCCAGCATTTTTGCATGGATGACCTCAAGAGCGGCAA[G/A]TCTCAAATTTAAACATAAATATAAGCTTGCCAACTTTTTTTTTTTGACTC
Long Flanking Sequence:
AGAAAAAATAAAAGCAATACGAAGCAATTACTTGATCAGTGCGAATCATTATCTTATTGAATAAAGACAATAAACTAACAAAATTTTCTTTCGAATTGTGGTTTAGCAAAAGCATTAAATAAAGGGAACAATAAATGAAACTGGCTTTGACAAAATCGAAGAGTACCAACACATTTTTCCACATAAGAAATTGAATAAAGTGTTGTGTTTATAGCCTAGAGTTGGCTATCTGTATGCAGAAACATTGCAGTAGTTACTGTAAATGTGATCACAGGTTTTTGTCTTTAGGTTTTTGAAGGAGACAGGACAGAGTTAAACTCGTCTGTAATCAGTGCGGTGGATTTGGATGTTCCCCAAGAGCGTCTGATGTTCAGCATCGTCCAGAATCCTCAGCACGGCTCTATCATCAGTCTGCCACACAGAAATCAAGTCTCACATTACAAGCGTGGAGCTGAGGAGCCTGTCCAGCATTTTTGCATGGATGACCTCAAGAGCGGCAA[G/A]TCTCAAATTTAAACATAAATATAAGCTTGCCAACTTTTTTTTTTTGACTCGTACGTTATTAAATTTATAGTAAATACTGTAATGAAGTACTTGAGTAGTTAATGTGTTGTTGTAATTCTATAGTTACTGTAATATACTTAAGTTTATAATGTGTCTCTGTCCACAGGCATGACTCTGATGTATGTACACGATGACTCTGAGAGTGAGCAGGATGAATTCATCCTTCAGCTCTCTGATGGAAAACACAAGCTCCAGAAACACGTGCAGGTGAAAATACTGCCTGTCAACGACGAGGAGCCGCAAATCATCCGGTAACTGCAGATGAATATCAGTAAAATAAATCATGCTGTGTTTTTATCCGTGCCATATAAATACCATAACCTTCTCTCTCCCTCAAAACGACTTTTCTTCACTTCCTGGTCATATGGATTGCCTTTAGGGTGGGGCTATCAGTGCTTTAGGGCAAGGCTATCAGTTAGTGTCTTGTTTCTGCTTTGAAT
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
Mutation Details
Allele Name:
sa41084
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 |
---|---|---|---|---|---|
ENSDART00000090165 | Essential Splice Site | None | 1684 | 29 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 72431335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69476070 |
GRCz11 | 7 | 69717425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGGAAAGACTTTATACCAGCTTCATCTCTGATTCAGTTTGACCCAGG[T/C]AAACAAAAATATGCTGAATATTGCATGATAGTGGGTGACATTGCGGAAAT
Long Flanking Sequence:
TAGCATCTAGTAAGAGCTTGATTAGCTGGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTCTCAAGGACACCGTCAGTCCAGGACCAGGTTTGGACACCCCTGGTCTATACTGTAATAGAGCATTGGAGTATATTAAGATATATTGAAGTGTATTAGGATGTGTAATGTACTTTCTCTGTCAGATTGAACTTCAGCTGGGCCGGTGTTGAGCTGACCAGGACTCAGTATACAGTATGTGAAAGTCAAGGCTCAGTTTCACTAACCATCCAGAGGAAAGGAAACATGCAGGACTCCTCTTATGTGACCGTACAGGTGGGTAGGACAGAATTTGACAGCTTTAAAAAAATATTTCCATGCAGAAATGTGTATAATACGTCTATGTGTTCTACTAAAAACAGATTTGTAAAGTATATAATTCCTCACAGGTGAAAGAGCTCACCGCATCTGCTGGGAAAGACTTTATACCAGCTTCATCTCTGATTCAGTTTGACCCAGG[T/C]AAACAAAAATATGCTGAATATTGCATGATAGTGGGTGACATTGCGGAAATATAAACACAAATTCATTGAGATGTCACTGCAGGATAATGCAAAATTAGCTCATTCGCTAAAGCTAATTTGCTAAAGCTAAGCTAATTCGCAGCTTATATCACTGCTAGCAAAACTTAGACCTGTTTTTTTTCCAGGGGTGGCCAGTCGAGTTTGGAAAGTGGAGATTGTTCAGGACTCATTGGAGGAAGCGGATGAGAAATTTGAGGTTAGCTTGGCGTCTCCTGTAGCTGCGGTGCTGAAGGACAATTCAAGAGCCACAATCTCCATTAAAGACTCAAATGGTTTGTGTTTAAGTTGTCAAGAAAGCTAAACATTTATAGTCAGTGTTTATTTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTGTAAAGGGCAGTGT
Associated Phenotype:
Not determined