Busch Lab

ZMP

fmr1

Ensembl ID:
ENSDARG00000037433
ZFIN ID:
ZDB-GENE-020731-6
Description:
fragile X mental retardation 1 [Source:RefSeq peptide;Acc:NP_694495]
Human Orthologue:
FMR1
Human Description:
fragile X mental retardation 1 [Source:HGNC Symbol;Acc:3775]
Mouse Orthologue:
Fmr1
Mouse Description:
fragile X mental retardation syndrome 1 homolog Gene [Source:MGI Symbol;Acc:MGI:95564]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa992 Nonsense Available for shipment Available now
hu2787 Nonsense Available for shipment Available now
sa10402 Essential Splice Site Available for shipment Available now
sa19080 Essential Splice Site Mutation detected in F1 DNA Not yet available
hu2898 Essential Splice Site Confirmed mutation in F2 line Not yet available
sa22461 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa992
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054473 Nonsense 40 493 3 15
ENSDART00000054476 Nonsense 40 569 3 15
ENSDART00000123434 Nonsense 40 569 3 16
ENSDART00000129431 Nonsense 40 492 3 14
Genomic Location (Zv9):
Chromosome 14 (position 21160395)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 19861883
GRCz11 14 20159128
KASP Assay ID:
554-0896.1 (used for ordering genotyping assays)
KASP Sequence:
AAGGTAAAATATATTCCCATATTTTATCACTATGCAGTTGGCAGCCAGAA[C/T]GACAGATTTCTTTCCAGGATGTTCGGTTTCCACCTCCAACCGGTTTTCAG
Long Flanking Sequence:
AAACTCTTAATTTATTTATTTTCCTTTGTATTGCGATATAAATTTTCATATTTAGAAATTCAGTATAAATTTAGATGCCTTAATTCTCTTCTTATTTCATCTCAATTGTTTATTCAATTAATGAGTCTAGATATTCTAATATAAAAAAATGAACAGTGAGCATCACTTTATAAATGTTGAATTAAATGAATGAAGAGCTACAGACTCATTATTATTATTATTATTACTATTATTGTTATTATTATTGTTACTATTATTGTTATTATTATTGTTATTATTATTAAGCTCTTTTTATTTTATGTACACATTAATGCATTAAAACAAAACTCACTTCAATTTCAGATGCATACAATGAGTAGTCTAAATGTGTAATATATAAGAATATTGCATAGCGGACGTTGAATTGACCATGTTTATTTATATATTTTACACTTGCTCAGCCCTAATATAAAGGTAAAATATATTCCCATATTTTATCACTATGCAGTTGGCAGCCAGAA[C/T]GACAGATTTCTTTCCAGGATGTTCGGTTTCCACCTCCAACCGGTTTTCAGAAAGAAATAAATGAGAGCGATGAAGTGGAGGTATGTGATAGCTTCTTTAATCCTTTACCAAATGTTAAACAAATGCGCTGAAGTTTTAAACCTTTCTCTTCCGCAGGTGTACTCTAGGGCTAATGATAAGGAACCCTGTGGATGGTGGCTTGCCAAAGTTCGCATGGTGAAAGGAGAAGTAAGTGATTTAAACATTATTCACTTTAACAGAAGGACAAAATTGCATTATTACACTGGTAAAAAACAAAAAAACAAAAAAAAGGGTTTTACACAATTCATGAACACACAAATTATTAAGTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTTCTCTTATTTTTGGCAAATTAAAGTGGATTGAACATGAAACAATTAAGTTGTCCCAAAACAAATCTCAAAAATTGTGTTGTTTAAGCTATTTTTAAATAATTAGTTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
hu2787
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054473 Nonsense 113 493 5 15
ENSDART00000054476 Nonsense 113 569 5 15
ENSDART00000123434 Nonsense 113 569 5 16
ENSDART00000129431 Nonsense 113 492 5 14
Genomic Location (Zv9):
Chromosome 14 (position 21161310)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 19862798
GRCz11 14 20160043
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGCCTGTGATGCCACCCTAAATGAAATCGTCACATTAGAGAGGCTA[C/T]GACCTGTGAACCCCAACAAAGCAGCAACAAAGAACACCTTTCTCAAAACC
Long Flanking Sequence:
TGGATTGAACATGAAACAATTAAGTTGTCCCAAAACAAATCTCAAAAATTGTGTTGTTTAAGCTATTTTTAAATAATTAGTTTAAACAAGCAATTTTTTGAGTGTTCACTGTAAAAATGAAGGCTTCGACACTTATCAACATTTATTCATGTTTTGCCAATACAAATCGATTAAGGTAACTCTCTCTCTTTTTGGCAAATTTAAGTTGATTGAACATAAAAGAATTAAGTTGTCCCAAAACAAATCTCAATAATTATTATTTTTTTGTTTATTTAGCTTGTTTTAAATAAGTTTGAACAAGCCAGTTTTTTTTTCGTGTAGTAGATTAAAACATTAAACATTACATTGATTCAAATTTGTTTTATGCTTGCATGAAGTTGTATGTAAATTTATGTATTTGCTAATTATTTGTGTTCACTTTCCTGCTCTTTTAGTTTTACGTTATAGAATATGCAGCCTGTGATGCCACCCTAAATGAAATCGTCACATTAGAGAGGCTA[C/T]GACCTGTGAACCCCAACAAAGCAGCAACAAAGAACACCTTTCTCAAAACCAGACTAGATGTTCCTGAAGACTTGAGACAGATGTAAGTTGGTAGCTTTTTCATTATTTTAGTGGGGATTCCTGCAGCATTGGACAATACATTGAGAAATCCAGTCATAAAAAAATCATTAACTAATGCAGGATGTCATGGAGTTTGGCCAATTTTGGATAAATAAATCAAAAGCAGAGTTTTAAACTTAATCAAACTACAAAGCAGAATAGTGTATGTGAATATTAAACTGCAATGACAAAATGTGAACTTCTCTCCAGAGCTGCTTTAAAAATCCTTTATGATAATTTTTATGGTTTAATCCAGGACCACAAAACCATAAAAGTCATAAATGTCTTTTTTTTTTTTAACTGTGATTTTATATATCTTCTTAAAGCCAAATAAGTAAACTTTTCATTGATGTGTAATTTTTTAGGTTAAGACAATATTTAGCCCAGATACAACTAATTGA
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:
sa10402
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054473 Essential Splice Site 140 493 5 15
ENSDART00000054476 Essential Splice Site 140 569 5 15
ENSDART00000123434 Essential Splice Site 140 569 5 16
ENSDART00000129431 Essential Splice Site 140 492 5 14
ENSDART00000054473 Essential Splice Site 140 493 5 15
ENSDART00000054476 Essential Splice Site 140 569 5 15
ENSDART00000123434 Essential Splice Site 140 569 5 16
ENSDART00000129431 Essential Splice Site 140 492 5 14
Genomic Location (Zv9):
Chromosome 14 (position 21161394)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 19862882
GRCz11 14 20160127
KASP Assay ID:
2260-7454.1 (used for ordering genotyping assays)
KASP Sequence:
ACACCTTTCTCAAAACCAGACTAGATGTWCCTGAAGACTTGAGACAGATG[T/A]AAGTTGGTAGCTTTTTCATTATTTTAGTGGGGATTCCTGCAGCATTGGAC
Long Flanking Sequence:
AACAAGCAATTTTTTGAGTGTTCACTGTAAAAATGAAGGCTTCGACACTTATCAACATTTATTCATGTTTTGCCAATACAAATCGATTAAGGTAACTCTCTCTCTTTTTGGCAAATTTAAGTTGATTGAACATAAAAGAATTAAGTTGTCCCAAAACAAATCTCAATAATTATTATTTTTTTGTTTATTTAGCTTGTTTTAAATAAGTTTGAACAAGCCAGTTTTTTTTTCGTGTAGTAGATTAAAACATTAAACATTACATTGATTCAAATTTGTTTTATGCTTGCATGAAGTTGTATGTAAATTTATGTATTTGCTAATTATTTGTGTTCACTTTCCTGCTCTTTTAGTTTTACGTTATAGAATATGCAGCCTGTGATGCCACCCTAAATGAAATCGTCACATTAGAGAGGCTACGACCTGTGAACCCCAACAAAGCAGCAACAAAGAACACCTTTCTCAAAACCAGACTAGATGTTCCTGAAGACTTGAGACAGATG[T/A]AAGTTGGTAGCTTTTTCATTATTTTAGTGGGGATTCCTGCAGCATTGGACAATACATTGAGAAATCCAGTCATAAAAAAATCATTAACTAATGCAGGATGTCATGGAGTTTGGCCAATTTTGGATAAATAAATCAAAAGCAGAGTTTTAAACTTAATCAAACTACAAAGCAGAATAGTGTATGTGAATATTAAACTGCAATGACAAAATGTGAACTTCTCTCCAGAGCTGCTTTAAAAATCCTTTATGATAATTTTTATGGTTTAATCCAGGACCACAAAACCATAAAAGTCATAAATGTCTTTTTTTTTTTTAACTGTGATTTTATATATCTTCTTAAAGCCAAATAAGTAAACTTTTCATTGATGTGTAATTTTTTAGGTTAAGACAATATTTAGCCCAGATACAACTAATTGAAACCTGGAATCTGAGGGTTCAAAAATATCTAAATATTGAAAAAAAATGAGTTTAAACGATTGTTTAATTAATTGTTTTTAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19080
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054473 Essential Splice Site 140 493 5 15
ENSDART00000054476 Essential Splice Site 140 569 5 15
ENSDART00000123434 Essential Splice Site 140 569 5 16
ENSDART00000129431 Essential Splice Site 140 492 5 14
ENSDART00000054473 Essential Splice Site 140 493 5 15
ENSDART00000054476 Essential Splice Site 140 569 5 15
ENSDART00000123434 Essential Splice Site 140 569 5 16
ENSDART00000129431 Essential Splice Site 140 492 5 14
Genomic Location (Zv9):
Chromosome 14 (position 21161394)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 19862882
GRCz11 14 20160127
KASP Assay ID:
2260-7454.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCTTTCTCAAAACCAGACTAGATGTTCCTGAAGACTTGAGACAGATG[T/A]AAGTTGGTAGCTTTTTCATTATTTTAGTGGGGATTCCTGCAGCATTGGAC
Long Flanking Sequence:
AACAAGCAATTTTTTGAGTGTTCACTGTAAAAATGAAGGCTTCGACACTTATCAACATTTATTCATGTTTTGCCAATACAAATCGATTAAGGTAACTCTCTCTCTTTTTGGCAAATTTAAGTTGATTGAACATAAAAGAATTAAGTTGTCCCAAAACAAATCTCAATAATTATTATTTTTTTGTTTATTTAGCTTGTTTTAAATAAGTTTGAACAAGCCAGTTTTTTTTTCGTGTAGTAGATTAAAACATTAAACATTACATTGATTCAAATTTGTTTTATGCTTGCATGAAGTTGTATGTAAATTTATGTATTTGCTAATTATTTGTGTTCACTTTCCTGCTCTTTTAGTTTTACGTTATAGAATATGCAGCCTGTGATGCCACCCTAAATGAAATCGTCACATTAGAGAGGCTACGACCTGTGAACCCCAACAAAGCAGCAACAAAGAACACCTTTCTCAAAACCAGACTAGATGTTCCTGAAGACTTGAGACAGATG[T/A]AAGTTGGTAGCTTTTTCATTATTTTAGTGGGGATTCCTGCAGCATTGGACAATACATTGAGAAATCCAGTCATAAAAAAATCATTAACTAATGCAGGATGTCATGGAGTTTGGCCAATTTTGGATAAATAAATCAAAAGCAGAGTTTTAAACTTAATCAAACTACAAAGCAGAATAGTGTATGTGAATATTAAACTGCAATGACAAAATGTGAACTTCTCTCCAGAGCTGCTTTAAAAATCCTTTATGATAATTTTTATGGTTTAATCCAGGACCACAAAACCATAAAAGTCATAAATGTCTTTTTTTTTTTTAACTGTGATTTTATATATCTTCTTAAAGCCAAATAAGTAAACTTTTCATTGATGTGTAATTTTTTAGGTTAAGACAATATTTAGCCCAGATACAACTAATTGAAACCTGGAATCTGAGGGTTCAAAAATATCTAAATATTGAAAAAAAATGAGTTTAAACGATTGTTTAATTAATTGTTTTTAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
hu2898
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054473 Essential Splice Site 211 493 8 15
ENSDART00000054476 Essential Splice Site 211 569 8 15
ENSDART00000123434 Essential Splice Site 211 569 8 16
ENSDART00000129431 Essential Splice Site 211 492 8 14
Genomic Location (Zv9):
Chromosome 14 (position 21169096)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 19870584
GRCz11 14 20167829
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGAATATTAAAAACAGGTAAGATTCAAAATCTTGTTATATCTTCATC[A/G]GAGTTCTCGGCAGCTGGCCTCAAGGTTTCATGAACAGTTTGTGGTGCGGG
Long Flanking Sequence:
TAAAAACACCTCACTAATTGTTTTCAGTGTAACATGGGTTACTCTCATAATTCATGCAAAGCATCATGGGTTGTTATAAAATTTTAAAAGCAACTTCAAAAGCAGTTAAAACAAAGTAAAACATTATGCTCATATTTATTATTTCAAATCAATGCAGGTACTCAAGATAAACAATTTGCACACAAGACATTCATTTTCTAGATTGTGTTCTATAAAAGCCTACTGCAGCTGTCTCTATTAGATTGTGTAAATCCTTTTGAAAGAAGACCATAAGCATTTACAGCTTAGCAGATATCATAAAAGCACAAAAGACACACTTTATACACTAAAGAAAAAGAAAACCGTTGCAAACCTATTGTATGTATGACCTTCTCAAGCACAACAAATGTATATTGAAAACCAAAGCATACTCTATATAGATCTAAACCTAGAGATTAACAAAAGTTGAATATCAGAATATTAAAAACAGGTAAGATTCAAAATCTTGTTATATCTTCATC[A/G]GAGTTCTCGGCAGCTGGCCTCAAGGTTTCATGAACAGTTTGTGGTGCGGGACGATCTCATGGGATTGGCCATTGGCACCCATGGAGCAAACATCCAGCAAGCCAGAAAGATTTCTGGAGTTACAACCATTGATCTCGATGAAGAGACATGCACGTTTCACATCTATGGAGAGGTAAGCACTTTATCTGTGACTTTCTGCTTTACATAAATAGGACTGCAATCAGAATATGTAAGCCTGATTACGCACATCTGAGATTTTTGCGATCCTGTTTGAACTCCAGGACCAGGAGGCTGTACGGAAGGCCCGAAGCTACCTGGAATTTTCAGAAGATGTTATCAAAGTTCCTAGGAATTTAGTCGGTGAGGACAGATAAAATGAACAGCCTTCTCCTTCACATACTAGACCTGATGGTTAATAGGATTCGTTAAATTACTTTCTACAGGAAAAGTCATTGGCAAGAGTGGGAAGCTGATTCAAGAGGTTGTGGATAAATCGGGTG
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:
sa22461
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054473 Nonsense 389 493 12 15
ENSDART00000054476 Nonsense 389 569 12 15
ENSDART00000123434 Nonsense 389 569 12 16
ENSDART00000129431 Nonsense 389 492 12 14
Genomic Location (Zv9):
Chromosome 14 (position 21177110)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 19878598
GRCz11 14 20175843
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGATGAGCAGCTTAGACAGATCGGTGGAGGACCCAGAGCTTTGCCGGGA[C/T]GACCCGAGAAAGAAAAGTCTTTCATGGCTGATAATGGAATGGGACCCTCG
Long Flanking Sequence:
CTATATATTATTAAGAAAAGTTACAGAATAACACAAAGCTGTTTTTTAGCATATAATTTATGTTTGTTCAGTGTTTTACTTTGGTTAGTACCACATTTTCTTCAGAAAATGTAAATGTAGAGATATGTTCCAATTTTATGTTTACAACATGGGTCTCAAACTTAATTCCTGAAGGGCTGCAGCTCTGCACAGTTTTGCTCTAACCCTATTAAACACAGCTGATCCAAATAATCAAGGTGTTTAAGTTGTATCAGCTGTGTTTGATCAGGGTTGAAGCAAACCTGTGCAGAGCTGCAGCCCTCCAGGAATTGAGTTTGAGACCAATGGTTTACAGGGTTTTGTTAATGCTCCTTACAAAGCAGAAATTGTTAATTATACAATAATTATACAAGTTCATATTTCCTTGTATTGTTCAGGAGGTAGATCAGCTACGAATGGAGAGACTGCAGATCGATGAGCAGCTTAGACAGATCGGTGGAGGACCCAGAGCTTTGCCGGGA[C/T]GACCCGAGAAAGAAAAGTCTTTCATGGCTGATAATGGAATGGGACCCTCGCGAGGTGGAGGCAAACCTTTTGGTCGAGGAGGACGAGGAAGACGAGGCCCAACGCTGGCTTCAGGTAGAAATGGCCTCAAATTAATATTATAGCTTTTTTTATTATTTAATTGTTTATTTTGCTAGGACAGTGTACATTAATTAACATCAATAAACCAGAATTAAAAATGCCAAAATGCCACTTTATATCTGTTGTCCCTGGAAAGATGGTAAAATTGTATCCCTAAAAACAATATGAAAATTATACAATTAACAAGCAATTAAGGAGCAATAAAATGGATATAGTTTTACAAATTATGATAAATGTCAATTGTATATAGAGACAAAACAAACTAAAATACCAACAATATGTAAAGGAGACAAGAATTGTACACATACATAAACATACAATTCATCAAGATGGCAGACACAAGTTTAACCCGCAATGCGATACAGTCCTGATATTTTGCC
Associated Phenotype:
Not determined