Busch Lab

ZMP

fndc3bb

Ensembl ID:
ENSDARG00000062023
ZFIN ID:
ZDB-GENE-070510-2
Human Orthologue:
FNDC3B
Human Description:
fibronectin type III domain containing 3B [Source:HGNC Symbol;Acc:24670]
Mouse Orthologue:
Fndc3b
Mouse Description:
fibronectin type III domain containing 3B Gene [Source:MGI Symbol;Acc:MGI:1919257]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa17966 Essential Splice Site Available for shipment Available now
sa30112 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25214 Nonsense Mutation detected in F1 DNA Not yet available
sa37907 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa7520 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17966
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087991 Essential Splice Site 62 1194 2 25
ENSDART00000147788 None None 1134 None 23
Genomic Location (Zv9):
Chromosome 24 (position 27651677)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 26711853
GRCz11 24 26853660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACGTTCACCATCCGCATGGAGGACGGGGCTTTGCAGTGCATCCAAGG[T/C]TTGAACAATTCTGTGTTTTGTTTWGTTTWGTTTTTTCCTCTAAGTTAATC
Long Flanking Sequence:
TTGATTTGTGTTTGCGGATGGAGGATCTGTTTTAGTCGTCTTCATCGTTTCATCACACAGTCCCATTTAATATTACTTTAATAAAAAGTGTGCATCTCTTTCAGGCTGTCGCCGGGAGGGCTCCATGAATGTTCGTCACCATGATGATGACGGACCAAATGCTGGACCTCCCGCCTCCATTGAGCAACGAGCTTCCCATGATGCACCACATGATCAATGGCGATGCATCACAGCAGGTCAGCTCTTCATTTCAATTCTCCCTAAAATCATTGTGATTATACTTTTCTTTTATTGGATGTTGACTTGTTGTTTTTATAGTCCTCACTATTATACATTGGTTGTTATGAGGCAGATACGCTTTAGCTCTCTGATATAAACAAAAGTTGTGATGAGCGAATGTGTAAATGTTTAATGTTTTTACAGATGATCTTGGTCCAGGTGAACCCAGGTGAGACGTTCACCATCCGCATGGAGGACGGGGCTTTGCAGTGCATCCAAGG[T/C]TTGAACAATTCTGTGTTTTGTTTTGTTTTGTTTTTTCCTCTAAGTTAATCTCACCTGTTTTGAAATCAATCAAGGCTCTTTTATAGAAGTGTTAGGTGCCGTTTGATTTATTTTTGTTTATTTTCTTGGTTAATGTGAATGCTGTTTTCTTGTAAATGTTGTGAACACATATCGTGGTTTTTGTCTGGACAATAATTTGGATGGTTGGCAATTAGTGGAAATACACCTTTGAAGGCAAATTTGCAAAGCTTATGATCGTGAGAATGAAGTATAATGAGCTTGTTTTAATGGATGCCACTTTTAAAAATATCTAAAAAAAAATATCTTAAAAATATCTTTTATTTGGCTTTGTTCTTGGGATGCAGGATGATTGTTTTTTGTTTTGATGTAATCACATAATTTTACCAAATTGTTGAATTATAAAACATTTTAAGGGTAATATTTAATATCAGTGGTTTTCAAACTGTGGTACGTGTACCACTAGAGGTACGTGGGCTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30112
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087991 Essential Splice Site 62 1194 None 25
ENSDART00000147788 None 1 1134 1 23
Genomic Location (Zv9):
Chromosome 24 (position 27617379)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 26678891
GRCz11 24 26820698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGTGTTTCTCTTTGATTGACGCCATTCTTCTCTTTTTTTTCTGCCTT[A/T]GGGCCTGCTGAGGTTCCCATGATGTCACCAAACGGCTCCATTCCACCAAT
Long Flanking Sequence:
GGCATAAGTACAAAATGGGACCAAAAGTACAGCCCCTCGTATATCAAATATTTAATTTTTTTTATGAACAATCCACTGTAAACTCTCAGTAGATCAGCATTTTCTGAAATTCGAGTTAGCCATCTCATAATCAAAGATTCCCAATTTGCCTTCTCCCCATCCAGGTGCTCAGTTTAATCTTTACCAGATTGTCTTGACCACGTCTGCAACATTTGATTGGCTGATTAGGTAATGAGTGTTAGTGGATTGTATAAGTTAGACATACTATATACCAAGCTTTAAATATGCTTTGGGTGGTAATGCAGTTCACCTATTGTGATGCTACAATGATTATCTATTGTACATGCCATATAACTAACGCATTCCTGTTTCTCTACCGTTTTCTTGTAGTCCCTGGAATTTTCTTTGCTCAGCCCTGCATTACGTGATGGAATGAGGGGGTGGAGTCAGCTTTGTGTTTCTCTTTGATTGACGCCATTCTTCTCTTTTTTTTCTGCCTT[A/T]GGGCCTGCTGAGGTTCCCATGATGTCACCAAACGGCTCCATTCCACCAATCCACGTTCCTCCTGGCTACGTCTCTCAGGTAACCAGCAGGAATGGGCCAGTCCTGTGCATCTGGGTGGCAAAAGCTCTCTTTTTACAATGAGAATGCGATTGCAGCCCTGACAGGAGAAATTTCCCTTTCTGAGAAACACACTCACAGAGTATACAACCAAACAAACAACTGAGCCACAAGCAGCAAACTCCCAAGTTGTCCGTCTTTACTGAACAGTGTCAAGCTAAAGTTTACTAAAGGTCAGCTGCGGTGACATTTCAGTAGAAAGGTCAAAAAACTTCAGCGGAGAGGGCAGGAGAAAGAGTTTGATTTGTGGGTGTAATAAATCAGTGGGGGGTTATAATGGCACAAAGGTCACTTGTGTAAATATGATCTATTAGTGCATTCCACCCGAATGTGAGGGGCAGGACCGGTCCATGTTTGGTGGGCCGCCCGTTTCTTTGTCTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25214
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087991 Nonsense 576 1194 14 25
ENSDART00000147788 Nonsense 516 1134 12 23
Genomic Location (Zv9):
Chromosome 24 (position 27584947)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 26646459
GRCz11 24 26788266
KASP Assay ID:
554-7657.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGAGACCCGGACCCCCTGTGAATCCTGCAGTTAACACACTAACATA[T/A]CACAGCTTCTGCGTGACGTGGGGTAGGAAAAACTTTTATCTTTTAAGCAT
Long Flanking Sequence:
TTTAAATGTAAATCCTTTCACAATTGTACAATTTTTATTAAAAATAAACCTTAAAAACGGCTCTAGATTTTCTTAAATATTATTATTATTATTATTATGTATTTTATCTCACATATTATTTATTGCTGTTGATGACTTTTTATTGTTCAAATATTTTCATAATTATAGAAGAGTGATATTTATAAAATCTGGTAAACCTAATGTTTTTTGTTTTTTTTTGCCATGACATAGCCAGAGAAGCTAATATGGCAATAAACTCCAAACTGTATCTTTTATGAATAAAAGCAGTGATTTCTTCTGAAAAACACACACTAAATACATAATGCAGAAATAATATATGCTTCTGTTCACGTGATTCTCTAAAATCTCTCCAATTGCCTCCTATAGCTCATCACATGTAGTGGCGAGTGGCGTAGCGCACCGAGTTCTCTGCTTGTGTGTAAGACGACCGCAGAGAGACCCGGACCCCCTGTGAATCCTGCAGTTAACACACTAACATA[T/A]CACAGCTTCTGCGTGACGTGGGGTAGGAAAAACTTTTATCTTTTAAGCATTTTATCTTTTAGATTCTTTTCTGTACATTTTAATAACACTTCCACCCTTTCCCCTTCTCTCTGTTTTTATATGATGAAATCAGAACCTCCAGAAGATGATGGTGGCTCTGGAGACTTGACGTACATCCTGGAGATTTCAGAAAGTAATAATAATGAAGGTATTATTAAAGGTTTCCCTTTTTATTCCAATACTACTAACTCATTTAAATAATCTTATTTATTTAAAGGAATAGTTGGCGCAAAAATAAAAATTTAATTTTTTACTCACCCTATACCAAGACTTTATGACTTTCTTTTTTCTGTCAATCAAAAAATTTGCTAATTTGAAGAATGTTTGTAGTTTAGTTCCGCTTTGGGGCAATTCATTTGGAGATGGTGGTGCTTCAAATGACAAGAATGACACACTTAACACAATAAACACCAACGCTTAACATACCTGTCAACATATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37907
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087991 Essential Splice Site 927 1194 21 25
ENSDART00000147788 Essential Splice Site 867 1134 19 23
Genomic Location (Zv9):
Chromosome 24 (position 27569067)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 26630579
GRCz11 24 26772386
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAAACCAGCACATTATCAGAGACCTGCTGCCGGACAGCGAGTACAGG[T/C]GAGCGCACATGCTGTTCAACACTTCAGATCCTTTTTTACCTTCATCCTCT
Long Flanking Sequence:
ACACTTGCAGATATTTACATCTATTAAACAAGGAACACTTTTAGCTGTCATTTGTAGCAATTGAATTGAACAATAGAACATATTCTATATTACTAATGTAACTTATGATCTAAATATTTGTTAAATTCAACAACAGATTCTCAAATGTCTGAATTTAAATTAATATATTGTTGTTTTTCCTCTCTCTCTGTCTCTCTTTATCTGGTTTACAGGCAGTTAACCAGGCTGGGGCGGGCCCCTACAGTGATCTGGTGACATGTCGAACCCCTGCCGCAGCCCCTGATCTCATATCCGGATTTCACCAACTCAACCTCCCTCTGAACCCAGCAGAAAGTGAATCCTTCTCCCTCTCCACCTGTCTGGCCCTCACCTGGGACGAGCCGAACTGTAATGGTGCCCAAATCATCTCCTACAACATCCAGATCGGGGACCGAATCATTTCCACTGAAAACACAAACCAGCACATTATCAGAGACCTGCTGCCGGACAGCGAGTACAGG[T/C]GAGCGCACATGCTGTTCAACACTTCAGATCCTTTTTTACCTTCATCCTCTCCATCAGCAGCTCTTTGCTGCTGAAGGTCACTGATACTGCATTAGTGCTGACCAGAGACCTTATTTCCTCATTATTTTGGTTCCAATAATATAGGGACGAGTACTGGTAAATCCCTGATAGAGCGTGTCGGTGTTATTAGCTCTACAAATGGACCCCTCTTACATCTGGCTCAAGATGTAATCAGCTAAATGCTGTATTCTGGGTAGATGTTGGACTTTGTGTGTTGCTTTATTGGTAGCAGGGTATATTTGATGCTTGTTTTTTTGGTTAGATGGTACAGTGATGGATCAAGTGGTAAAACTATGGTATTTTTGAAAGGGTTAAACATAAATTAAATGACTTAGTATTATGAGATATATAACACTTGAAAATGTATGGAATATGATACAAGTAAAGTCTAAAGAATAAAATCTAGAATGTGCATAACAAAAAAATGCTTTTCTTACTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7520
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087991 Missense 1022 1194 23 25
ENSDART00000147788 Missense 962 1134 21 23
Genomic Location (Zv9):
Chromosome 24 (position 27560475)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 26621987
GRCz11 24 26763794
KASP Assay ID:
554-4385.1 (used for ordering genotyping assays)
KASP Sequence:
CGAGCCACACTTTTAAGTTGCAGAGACTGAATGAATCCAGCAGGTACCGT[T/A]TCCGGATCCAGGCGGTGAGCGWAGCTGGYGAAGGGCCKTTTTCTGAGACC
Long Flanking Sequence:
ACGTCTGTTTGAGCTTTCAGCCTCGGGTCTACTTCTGAAAATTTGTAACCGTATAAGCAGTAATGGCGAATGGATCTAATGAAGGCCGGCTTCTACCTGCCTGTCTTTTCTTCATTCAGGATATTAATTAAAGCCATCAGAAAGTGACAGAGTTCAGATATAGGATCTCAAGCAATGGATTTACGTTATTTGCACTTGAGAGTTTTAATAAATGACAAAGTTATATGTTATTTTATATAATGCTCTTAAATTTTTTTGCATTCAGACTATCTATTAATGTGATGCGAGTTCACTTATATGATCTCAAGCATCACGTTTTTGCACTTAACACTGTACAAAAATTATTACGCTATCAGATAATAAAGAATATCGTTAAAAAGCTGTACCTAATTTTTTTTTTTTGTGTATGTTTGTAATGTTTTGTTAGGTTTGTGGTGGTTTATCGAGGTCCGAGCCACACTTTTAAGTTGCAGAGACTGAATGAATCCAGCAGGTACCGT[T/A]TCCGGATCCAGGCGGTGAGCGAAGCTGGCGAAGGGCCTTTTTCTGAGACCTACACCTTCAGCACAACCAAATCTCTGCCACCAACGCTGAAAGGTACCATATTTATATACACATTACTTACTTACTTTATTTCCAGCTGTTCAAGATCATTTTTTTTTTATTTTAAATAGTTTTTTTTTTCTTTCTTCATTTGGTCAAATTCTTTTTTTATTTCTTCATTGTTATTTTTTTTAAATGTGACAGGAAGGGCTGCCAAATGGTGTAATATTTTTCAGTATTACCGCAAACTGTATATTTTGTGTTCATTTTTATTTTGCAAATATGCATTATATTATTTACAAATGACAGCAAGTATATACACTACTGGTTAAAAGTTTGGGTTCAGTTTTTTTAATGAATTTTATTTAATAATTTAAATAAATTCATTCTGTTCATCAAGGCGGCATTTATTAAATGTAAAAAAAAATGTTAAATTGTTTAATACTTATTTATTGAATATT
Associated Phenotype:
Not determined