ZMP
cyfip1
Ensembl ID:
ZFIN ID:
Description:
Cytoplasmic FMR1-interacting protein 1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q90YM8]
Human Orthologue:
CYFIP1
Human Description:
cytoplasmic FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:13759]
Mouse Orthologue:
Cyfip1
Mouse Description:
cytoplasmic FMR1 interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1338801]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14676 | Essential Splice Site | Available for shipment | Available now |
sa20750 | Nonsense | Available for shipment | Available now |
sa40737 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10367 | Nonsense | Available for shipment | Available now |
sa2288 | Nonsense | F2 line generated | Not yet available |
sa45259 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14676
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065127 | Essential Splice Site | 70 | 1253 | 4 | 31 |
ENSDART00000104233 | Essential Splice Site | 70 | 1257 | 3 | 31 |
ENSDART00000122199 | Essential Splice Site | 70 | 476 | 4 | 15 |
ENSDART00000124610 | Essential Splice Site | 70 | 1014 | 4 | 26 |
ENSDART00000130905 | Essential Splice Site | 70 | 511 | 4 | 15 |
The following transcripts of ENSDARG00000044345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37620275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37694033 |
GRCz11 | 6 | 37671927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGCATAAACGCRTRTAAGTGTAATGATGAACTGTTTGCTGTRCATTAC[A/T]GAATGACATGTTAGAAGAAGGTCAGCAGTATGCWGTGATGCTGTACACGT
Long Flanking Sequence:
TTTTTTAGCTTGACTTGTTCACTGATCCAAAATATTTTAAATGTTTTTCAAAATAAAATATATTGCATTCAATGGGGGGAAACGTTTTTTTTTTTTTTTTTCCCAAAACATTTAAAAAGAATATATTTTAGAACAGTATTCACAATACCGAGATACTGTGATATATTTATACAAGGTTATCTTACTGTCAAAATCTTTTACTGGCCCATGCCTAGCTGCAAAACCAGAATATCATGGAATTTTGTTAATCTTTTGGATAAATAAATAAGTAGGATTATCACTGTATATAATTATAATTACTTATATTTGTGCTGATAATTGATAATTATGCATAATTATTTGAATAGCTTAATTGAAAAATTGACAATATTAAACGTTTTTTCATTCAGTTTTTTTTTATGTGGCTTTATTTTGCACATCTTGTATGTAAAAGAAGTCTGTGTGCATTCAGTTGCATAAACGCGTATAAGTGTAATGATGAACTGTTTGCTGTGCATTAC[A/T]GAATGACATGTTAGAAGAAGGTCAGCAGTATGCTGTGATGCTGTACACGTGGAGGTGCTGTTCGAGAGCTATTCCTCAGGTAATTTAGTAAATCCCAAAGCATTTTACATTCAAACTCAAGACCACCATCATCACCAACAACCAGTCTATAGTTTTGATCCTCCTCATCATCTGTTCCTGTCACAGGTGAAGTGTAATGAACAACCCAACAGAGTGGAGATCTACGAGAAGACTGTGGAGGTGCTCGAACCCGAAGTCAACAAACTAATGAACTTCATGTACTTTCAGGTAAAGCCTAACACTATTTCCTGCATCAGAATACTGGATATTATAATGTGCATTAATACTTCTGCTTCTCTTTCAGAGGACAGCAATAGATCGCTTTTGTGGTGAAGTGCGTCGTCTCTGTCATGCAGAGCGGAGGAAAGACTTTGTGTCTGAAGCTTATCTGCTCACTCTGGGAAAGTTTATCAACATGTTTGCGGTGCTGGATGAACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20750
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 |
---|---|---|---|---|---|
ENSDART00000065127 | Nonsense | 79 | 1253 | 4 | 31 |
ENSDART00000104233 | Nonsense | 79 | 1257 | 3 | 31 |
ENSDART00000122199 | Nonsense | 79 | 476 | 4 | 15 |
ENSDART00000124610 | Nonsense | 79 | 1014 | 4 | 26 |
ENSDART00000130905 | Nonsense | 79 | 511 | 4 | 15 |
The following transcripts of ENSDARG00000044345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37620306)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37694064 |
GRCz11 | 6 | 37671958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTTTGCTGTGCATTACAGAATGACATGTTAGAAGAAGGTCAGCAGTA[T/A]GCTGTGATGCTGTACACGTGGAGGTGCTGTTCGAGAGCTATTCCTCAGGT
Long Flanking Sequence:
ATATTTTAAATGTTTTTCAAAATAAAATATATTGCATTCAATGGGGGGAAACGTTTTTTTTTTTTTTTTTCCCAAAACATTTAAAAAGAATATATTTTAGAACAGTATTCACAATACCGAGATACTGTGATATATTTATACAAGGTTATCTTACTGTCAAAATCTTTTACTGGCCCATGCCTAGCTGCAAAACCAGAATATCATGGAATTTTGTTAATCTTTTGGATAAATAAATAAGTAGGATTATCACTGTATATAATTATAATTACTTATATTTGTGCTGATAATTGATAATTATGCATAATTATTTGAATAGCTTAATTGAAAAATTGACAATATTAAACGTTTTTTCATTCAGTTTTTTTTTATGTGGCTTTATTTTGCACATCTTGTATGTAAAAGAAGTCTGTGTGCATTCAGTTGCATAAACGCGTATAAGTGTAATGATGAACTGTTTGCTGTGCATTACAGAATGACATGTTAGAAGAAGGTCAGCAGTA[T/A]GCTGTGATGCTGTACACGTGGAGGTGCTGTTCGAGAGCTATTCCTCAGGTAATTTAGTAAATCCCAAAGCATTTTACATTCAAACTCAAGACCACCATCATCACCAACAACCAGTCTATAGTTTTGATCCTCCTCATCATCTGTTCCTGTCACAGGTGAAGTGTAATGAACAACCCAACAGAGTGGAGATCTACGAGAAGACTGTGGAGGTGCTCGAACCCGAAGTCAACAAACTAATGAACTTCATGTACTTTCAGGTAAAGCCTAACACTATTTCCTGCATCAGAATACTGGATATTATAATGTGCATTAATACTTCTGCTTCTCTTTCAGAGGACAGCAATAGATCGCTTTTGTGGTGAAGTGCGTCGTCTCTGTCATGCAGAGCGGAGGAAAGACTTTGTGTCTGAAGCTTATCTGCTCACTCTGGGAAAGTTTATCAACATGTTTGCGGTGCTGGATGAACTTAAGAACATGAAGTGCAGCGTCAAAAATGACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40737
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065127 | Nonsense | 98 | 1253 | 5 | 31 |
ENSDART00000104233 | Nonsense | 98 | 1257 | 4 | 31 |
ENSDART00000122199 | Nonsense | 98 | 476 | 5 | 15 |
ENSDART00000124610 | Nonsense | 98 | 1014 | 5 | 26 |
ENSDART00000130905 | Nonsense | 98 | 511 | 5 | 15 |
The following transcripts of ENSDARG00000044345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37620470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37694228 |
GRCz11 | 6 | 37672122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTATAGTTTTGATCCTCCTCATCATCTGTTCCTGTCACAGGTGAAGTG[T/A]AATGAACAACCCAACAGAGTGGAGATCTACGAGAAGACTGTGGAGGTGCT
Long Flanking Sequence:
TTTTACTGGCCCATGCCTAGCTGCAAAACCAGAATATCATGGAATTTTGTTAATCTTTTGGATAAATAAATAAGTAGGATTATCACTGTATATAATTATAATTACTTATATTTGTGCTGATAATTGATAATTATGCATAATTATTTGAATAGCTTAATTGAAAAATTGACAATATTAAACGTTTTTTCATTCAGTTTTTTTTTATGTGGCTTTATTTTGCACATCTTGTATGTAAAAGAAGTCTGTGTGCATTCAGTTGCATAAACGCGTATAAGTGTAATGATGAACTGTTTGCTGTGCATTACAGAATGACATGTTAGAAGAAGGTCAGCAGTATGCTGTGATGCTGTACACGTGGAGGTGCTGTTCGAGAGCTATTCCTCAGGTAATTTAGTAAATCCCAAAGCATTTTACATTCAAACTCAAGACCACCATCATCACCAACAACCAGTCTATAGTTTTGATCCTCCTCATCATCTGTTCCTGTCACAGGTGAAGTG[T/A]AATGAACAACCCAACAGAGTGGAGATCTACGAGAAGACTGTGGAGGTGCTCGAACCCGAAGTCAACAAACTAATGAACTTCATGTACTTTCAGGTAAAGCCTAACACTATTTCCTGCATCAGAATACTGGATATTATAATGTGCATTAATACTTCTGCTTCTCTTTCAGAGGACAGCAATAGATCGCTTTTGTGGTGAAGTGCGTCGTCTCTGTCATGCAGAGCGGAGGAAAGACTTTGTGTCTGAAGCTTATCTGCTCACTCTGGGAAAGTTTATCAACATGTTTGCGGTGCTGGATGAACTTAAGAACATGAAGTGCAGCGTCAAAAATGACCACTCCGCCTACAAGAGGTAAACCACGCACTGCTTTCTGCATTTAGTTCTGTCTCTAATAAGAGGATTCCTCTAGATGGCAGTCATGTTACATCTGGATATTAAAGCAAACATGTTTTAGGTGCTCTGTTGACATTAAATAAACATGCAGAACTATGAAATAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10367
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 |
---|---|---|---|---|---|
ENSDART00000065127 | Nonsense | 580 | 1253 | 16 | 31 |
ENSDART00000104233 | Nonsense | 584 | 1257 | 16 | 31 |
ENSDART00000122199 | None | None | 476 | None | 15 |
ENSDART00000124610 | Nonsense | 580 | 1014 | 16 | 26 |
ENSDART00000130905 | None | None | 511 | None | 15 |
The following transcripts of ENSDARG00000044345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37645902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37719660 |
GRCz11 | 6 | 37697554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAATGCTGGAGTCTCTGGTCGCAGATAAGAGCGGATCAAAGAAGACCT[T/A]GCGCAGTAGTCTRGAGGGGCCGACCAYTCWKGACATCGAGAAGTTTCATC
Long Flanking Sequence:
TTTTTTTATAGCTACAAATACATATTTGGATAGTTGTTTCCCAAAATGCTATACTGGTCATAATTCTGCCACACTGCAGGACAGTTTGACCCAAACAATGACCTTGTAAATTTGAACACAGTACTGCGCGGACACACATTCACCCACATTTCCAGATGGAATCCAAGGACACAAATACAGACAACCCAACCTTTTTGATGCCTGTCGGAGATGTCTAGGGAAGCTTTGACACCTGTTTGCCCTCCATCAGCATGTTAATGCACTCAGAATAATGCAGAAGAGAACCCCCCCACCTGCGGCGGGATGACCAGTGCAGAATAGGAATGTGAATTTGTCTGTGTCGAGAGCTTTGATAACCATGCATATGTAAAGAACAAACTTTGCATCGGACTTGCTGTCCTTTCATCTGAGTCTTTTTTTCTGTTCCTCTATGTAGCTGTATATGGTCAGAACAATGCTGGAGTCTCTGGTCGCAGATAAGAGCGGATCAAAGAAGACCT[T/A]GCGCAGTAGTCTGGAGGGGCCGACCATTCTGGACATCGAGAAGTTTCATCGCGAATCCTTTTTCTACACTCATCTGCTCAACTTCAGTGGTAAGGAACAGGTTGAACACTTGCCCTCATCATTCTTAGATTTAATCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTACAGCTGTTAAAGATTTTTTTAGGATTAGCATATTATTGTACAACTAGACTTTTTTTTAAAATACCACTATACAATAAATGTGGCCTGAAAGTATGGACAGTTAAGCTACATTTAAATGTCACTGCTTTATGAATGGTAAACGGCATTTATTTATTTTTTGCTAATTAAAGTAGATAGAATTTTCCATACTTAAAAAAAAAGCCTAAAAAAGAATTGCAAAATTTTTTGGATATACCACTTGATTTCAAATTGTATTAATTCCAGACTGTCGGAAAAGTAAGAGAAGTCAATCCAGCAGACTCATTTCAAGCAGAATTTATTTAGACATATTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2288
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000065127 | Nonsense | 919 | 1253 | 24 | 31 |
ENSDART00000104233 | Nonsense | 923 | 1257 | 24 | 31 |
ENSDART00000122199 | None | None | 476 | None | 15 |
ENSDART00000124610 | Nonsense | 919 | 1014 | 24 | 26 |
ENSDART00000130905 | None | None | 511 | None | 15 |
The following transcripts of ENSDARG00000044345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37663785)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37737543 |
GRCz11 | 6 | 37715437 |
KASP Assay ID:
554-2555.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGCCTCTACCGCAACTTTGTGGGACCTCCACATATTAAGGCTATTTGC[A/T]GACTTCTGGGATACCAGGGAATCGCTGTGGTGATGGAGGAGCTGTTAAAA
Long Flanking Sequence:
GACACTTCTATACATCTATACAGCTTAAAGTGACATTTAAAGGGTTAACTAGGTTAATTAGGTTGAATAGGCAAGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGTTTTGTAGACTATTGGAAAAAAACTGCTTAAAGGGGCTAATCATTTTGCCCTTAAAATGGCTTTTAAAAAAATAAAAACTGATTTTATTTTGGCCGAAATTAAACAAATAAAACTTTCTCCAGAAGAAAAAATATTATCAGACATACTGTGTAAATGTCCCTGGACTGTTAAACATCATTTGGGAAATATTTAAAAAAGAAAAATAAATTCAAAGGGGGGGCTAATAATTCTGACTTTAACTGTATATGAGATTTTATATTTGTTCATAATAAACTGCTTCATTTTCTTGTTTTTCATGATTATTTAGGCCTTGAATTTGGCGTACAGCAGCATATACAGCCTCTACCGCAACTTTGTGGGACCTCCACATATTAAGGCTATTTGC[A/T]GACTTCTGGGATACCAGGGAATCGCTGTGGTGATGGAGGAGCTGTTAAAAGTTGTCAAAAGCCTGGTAAGATTTTTCATATAAATACAGACATTTGAGGATGTTTTAAAGACATGAGCATATAATCGTTTTTATCTACACCAAATTCCTTATTTCACGAATATCAAACCTGTCATTTATAAGAATCTTAACACATTATTATCGTTATTAGAACTAATTATTACACAACTAAAGTTTTCAAGAAGAAAGTCTGTCATTTTCCAGATGTACGGGCACTGGTAAACATTATTGTCTTCTTGTTCAGCTTCAAGGCACCATCCTTCAGTATGTGAAGACATTGATGGAAGTGATGCCCAAGATTTGCCGTCTGCCTCGCCATGAGTATGGCTCACCAGGTGAATAATATACTCCGAAACAATCCTTTTATTTTTTGTTGACCCAAGTGAGCAACTTGACCCTGTGCAAATACCAGCAAGTAGTAGATAAGCACTGAATTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45259
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065127 | Essential Splice Site | 1014 | 1253 | None | 31 |
ENSDART00000104233 | Essential Splice Site | 1018 | 1257 | None | 31 |
ENSDART00000122199 | None | None | 476 | None | 15 |
ENSDART00000124610 | None | 1014 | 1014 | None | 26 |
ENSDART00000130905 | None | None | 511 | None | 15 |
The following transcripts of ENSDARG00000044345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37665403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37739161 |
GRCz11 | 6 | 37717055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGTTGGAAACGCATTGCTCTTCTGCCTTCTGACTGAACAGAGCTTGG[T/A]GAGAAAACACAACATCTCCATTCACATGATTGAACTTTAAGGTGATTAAA
Long Flanking Sequence:
CGTGACTCACATTCTTTAATGATTCGTCTGAAAGCCGTCATGATGGCAAACCTTGCATAGAAGAAAGCGGTCAATTTTGACAATTAGCACTTAGTAGGATGAACTAAATTCCGGGTTTTCAAAAGTGTGTGTAGTTTTTGGTGTACAGTAGGCTATCTTTGGGACATCTACGTTGCAAAATGAACCATGTTTAGTTACTTTACTTCTTAATCAAATATTTTCTGGTGATCCTTGGCCAATAAAAGCTGCAAATGAGTTCAGATTTTGTGTTGTAAACTTGAATGTCTGACCACATCCTGATTTTAGACATTGATTTTGGAAATGCTAATCTAGGAGCAGTAAATACAATTTCTGTTTACCGGATGCAGGTATCCTGGAGTTCTTCCACCACCAGCTGAAAGACATTGTGGAGTACGCTGAGCTGAAGACTGTGTGCTTCCAGAACCTGAGGGAGGTTGGAAACGCATTGCTCTTCTGCCTTCTGACTGAACAGAGCTTGG[T/A]GAGAAAACACAACATCTCCATTCACATGATTGAACTTTAAGGTGATTAAAGTGATTGCCTTTAAAGGGGTGGTCCAGAGTGTATTTTTAAGGCTTGGTTGTGTCTATAAGATGCAAAGCAATGTGTGCTCATGCTTCACTTGTAGAAAATCAGTTTTTTCATATATCTTACTTTGATACTACACAGCTACTCTGCTAACATAGAAACGACTATCATATTCCCTAGTTCCTGCGAAAGGCCCACCCTCAAGAGGCTGTGATTGGTCAGCTAACATAATGTGCTGTGATTTGTGGATCGTCTCCATGTCACACCCCTACAAGCATGCACTTTTGCTTCGTGTAAACTGTAAGCCGTATAAGTTTGTGCCTGACTCAAACAGAACATAAAGAGCAGCATTTTCCATTGGTTACATCCTTGTTTATGTTCTCACTACAACATACCCTCAACGCTAGAAACTGTGCACGTAATTGATCAATTTTAACAAAGAAAAACACTTACAG
Associated Phenotype:
Not determined