Busch Lab

ZMP

si:ch211-225g23.2

Ensembl ID:
ENSDARG00000038219
ZFIN ID:
ZDB-GENE-091117-6
Human Orthologue:
FNBP1
Human Description:
formin binding protein 1 [Source:HGNC Symbol;Acc:17069]
Mouse Orthologue:
Fnbp1
Mouse Description:
formin binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:109606]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa17043 Nonsense Available for shipment Available now
sa18638 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa17043
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065862 Nonsense 246 639 8 18
ENSDART00000132002 Nonsense 246 562 8 14
Genomic Location (Zv9):
Chromosome 21 (position 6294380)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 6232716
GRCz11 21 6338224
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACGTTTGCGGAGGTGGACCGACAGATTCTGCCCATCATTGGGAAATG[T/A]CTGGATGGAATGACACAAGCRGCCGAGTCCATTGAATCCAAGACTGTTAG
Long Flanking Sequence:
CTAAATCAGGTGTGTTTGGTTGAGGAGAGATGTAAAATGTGCAGAGCTGGTGGTCCGCGGTTGAGAAACACTGCCCTAAACTGTCTGTATTATACATTATAAAACAAAATGATTATGTGTGATTGAAACATAAGGGTCCCCTCAATATAAAAATACAACATAGACACACACACACACACATGCACTGAGAATGAATTATAGCTACTGATGTTATCATTTATTTGCATGCACTGCCTGCATTGTTGTAGAGTTCTTTAAAAGAATTATGCAAATGAGCTTACTGTGAAAACACGCCCCAAAATCGTGAATGATTTGCATATGCAGTAGTGTGATTCCCGATCATGCAGCTGTCTGCTCTTAAATACACACTGTAACTTTTCATGTGTGTCTGTGGAGCAGAAAATCCAGGCGATGGAAGAGAAGAGAATAGAGCGGATGGGTGAGTCTCTGAAGACGTTTGCGGAGGTGGACCGACAGATTCTGCCCATCATTGGGAAATG[T/A]CTGGATGGAATGACACAAGCAGCCGAGTCCATTGAATCCAAGACTGTTAGTAACTCACACACACACGCACTTACACTCTCACATAACATACCATGTGCATAACACACATGCATCACAGATTTACACACACTCGACACACACATACACACACACACATACAGATTTATTCACGCTAAACTCTAGCGCTCTCTTCTGTCAGAATTATCTCTCATGTTTCCATTGCACAACACATTTTCTTCTTGAACACGACTCCTAATAAATTTAAACCTGCACTAATGCTGATCTAGGATCAGTCTGCCCTGAATGGATTAGATTATTGTAAGCCGCTGATACCTGATCCTACATCTGCAGGAAGTGTCGTTTTAGCAGGAGGAAATGTGTTGTAAAATTAAATTAAACTCTACCATTCAAAAGTTGAGGGTCATAATAGATTTAATAACTAATTTCTTATAACTCATTTCTTTTGTCTTTGCCATGATGACAGTATTATCTGCTATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18638
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065862 Nonsense 331 639 10 18
ENSDART00000132002 None None 562 None 14
Genomic Location (Zv9):
Chromosome 21 (position 6305713)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 6244049
GRCz11 21 6349557
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYGCTGCTCTCTCTGTGGCTCGTGTCTTTACCGGTAGCTTATGTCCCTGT[T/A]AACGTCCCCCGTACCTCGCCAGCCCCCCCCTGACCCCCCCTCACCTTCTG
Long Flanking Sequence:
AAACAGCATAAATATCCTCCCTTGTGTTCCTCAGGAAAGTCAAAGTCACTGGCAGTGTTTGTTTTTGGTTGAACTGTCTCTTTAAGTGGTTCTGCAGTGATCTGAGCTCTGCATGCGACCCCTGATATGTATCTATATATATATAATATCCAGTTTAACGCACTAACTCTCTCGCTCAGTGATAACACCACCACAGCCACAGCGCAGTCTTTTGTTTTTTTGTTAATACTGTTTATTTACGTTTCATTTTTTGTCTTTCGGTTGCCCTTATTATTATTTTTTTTGGTTTCGTTTTTTTGTTCATTCCATTAATTGATTAATTGATTAATTCGTTGCCTTTAGTTCTGTAACATTTTTTGGGTCCTTATTTCTCTTGTTTTGTGTTCCCCTCCCTTCCTTCCTTTTGATTTTTTCCGGACCGATTTCTTTCCCCCCTCTGTCTGTCACTGGTCGCTGCTCTCTCTGTGGCTCGTGTCTTTACCGGTAGCTTATGTCCCTGT[T/A]AACGTCCCCCGTACCTCGCCAGCCCCCCCCTGACCCCCCCTCACCTTCTGCTGTGACCCCTGACCCCTGCCCCGCTCCCCAGACCCCCAAACAGTGCAAGGAGCCCCTGTCGCACCGCTTCAACGACCTCATGACCTCCAAGCCCAGAATGCAGTGCCTCAGGAGCCTGCGGCGAGGGGTGAGTATCTGCATGCTCTGCTCTGCCGGTCTGTCTGTCATCATCTGCTGCTGGACGTGTGCTGGAGGGAAAAAGGAGATGCATGAGGATTTCCTGCTGGTTTTTTGCATCGTAATGTAAATGTAAAACAACTGATAATGGCTGGCTGCTGATGTTATAGCAGAATGATTGTATTTAAACCTTAGGTCTCAAACTCAATTCCTGGAAGGCCGCAGCTCTGCACAGTTTTGTTCGAACCTTTCTTAATCCAACTAATCAAGATGATCCAAATGCTCAAGATGTTCAAGACTACTAGACACTAGTTGTCTTGAACACCTTTATT
Associated Phenotype:
Not determined