Busch Lab

ZMP

fndc3ba

Ensembl ID:
ENSDARG00000078179
ZFIN ID:
ZDB-GENE-070510-1
Description:
fibronectin type III domain-containing protein 3B [Source:RefSeq peptide;Acc:NP_001153304]
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
sa19762 Essential Splice Site Available for shipment Available now
sa18483 Nonsense Available for shipment Available now
sa11399 Essential Splice Site Available for shipment Available now
sa16307 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa19762
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089108 Essential Splice Site 168 1202 4 25

The following transcripts of ENSDARG00000078179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 25603403)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 25799599
GRCz11 2 25455233
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCCACACCAGTACTACCAGCACCACCTCCCGCCCATGTACAATGAAG[G/A]TAAGAGTGTGTGTGTTTGTGTGTGTGATCAAGACTTTTATTAAGCTTTTC
Long Flanking Sequence:
ATCCCGAGACTTATGTTAATAAATGCATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATATTTATTATTCATAACATTGTATTAACATTTTAGATCTTTGCATCAATGTTTTCTATTTTAAATTGTTCATAAAAATAAATTCTTACAGGCAAAGGTAAGCAGGAGATGTCAGTGAAAGTTGAAGTACTCATTTCAAGCTACAGAAAATTAATTCAGATGAGTAAAACCATTTATGCTATCCTTACAGGTGCTGGAAGACAACACAGGGGTCCGGAGGGTGGTGGTCACCCCTCAGTCTCCAGAGTGTTATCCTCCCAGCTATTCCCCTGCTATCTCTCCAACTCATCACTTACCTCCATACATGGCTCCACCACCTTTCATCCCTAACTCACACACCGCCTTTTACCCACCCGTCAGTCCCGGAGACATTCCTCCACACCAGTACTACCAGCACCACCTCCCGCCCATGTACAATGAAG[G/A]TAAGAGTGTGTGTGTTTGTGTGTGTGATCAAGACTTTTATTAAGCTTTTCTTTTTTTTAATTTACTGAGCGTTGCAAATTTCAAGTGAAATGTGGTGATTCCTCAAACCTATGCCAATATCACACCCTGCACATTTATTGTACACACTCACTGGACACAATGTTGAAAATGGTAAATAACCAATTTAACTAACTGTAATTAAACAAAGTTTTGTTGAGTTTTGATTTTGTGTCTTCTTTGTTGGTTAAGGCTTGTTATGAGAAAATAAATATAACACTTAAACCACCAGTATGTGGCTTATTAGATTATCTTCAACATTATTGTTATGACACATGTACAAGTAAAATTATAGAAAAACTATGGGTAATATTTACAGATGGGTGTACTAGGAACATTATATACAGGTTGTAACTATAAACAGATTTACAATAAATCAATAAGGGTACAGGTTGTTGTTAATAATCAGAGTTTTGCAGATAGATAGGAACATAATTACAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18483
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
ENSDART00000089108 Nonsense 313 1202 7 25

The following transcripts of ENSDARG00000078179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 25628411)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 25824607
GRCz11 2 25480241
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCAGAACAGAGAGAGGCAYAGTAACGGACACCCRTTTACCWGCAGCTA[T/A]GAGGTCGCTCTCTCAGACAAGGGTCGGAACGGCCAGTACCGCATCATCTA
Long Flanking Sequence:
TGAAGATTGTAGTTGAATCATTTAAATTATTATTATTATTTTATCAGAATTCATGCAATGGTAAGGTGCTTATGAGTTTGAAGTGACATACAACAAATCACAATTAGGAAACCCTTCTATGTGTGTGTACGTATATACTATTATTATATAACTATCTATATAACTTTATTTGGCATCACTTTATTTTGATGGTCCCTTTAATGCGTAATGTTGAATTTGAGAGTTGGAATTAATGAGAATTAATTTGCATGTAGTTGCAATGCAACTTTTATTCATCAAAATGTGCAATAGAGACCATCTAAATAAAGTCTTACCCTTTATTCATCCTTTATATTGATAAGTCTAATACTATTGCTTTAGTTTTTATATGCTGATTATTTTGAATGTCCTCCACAGGTTTTAAATATTCAGTCCCGTACAGCTCGACTGACCTGGGCTCCACCAGCAGGCCTCCAGAACAGAGAGAGGCACAGTAACGGACACCCATTTACCTGCAGCTA[T/A]GAGGTCGCTCTCTCAGACAAGGGTCGGAACGGCCAGTACCGCATCATCTATAGGTAAGACACAGAGGAGCTGTTTTGACCATGCAAAAATCCTTGAAGTCTTGATGTACTCATGATTTTAACAGCGCTCTCCACAAGGGAGCGGATTATGTATGATTACATCATCCTTTGAGTAAAAAAGCAAAAAGAATCATTGGATGCAGCCTTTTCTCCCATCAGGATGTGCATGATTCAATTTCCAGAGAGCGGAGACGAAAGATAATCAGACCTTCAAACCATGTTATCGCCCCTGTGAAGCATGAGGCTCAAAGCCCAAAGATGCAGACTGACTTATGAGAGATGTGCTGCTGCTTTAATTATATTTATTAAATATTACTGTTCAAAAGAGGATCTTCACCTGATAAATCTTTTTTAAAAAGTGTGTTCACCTTTTTCACTTTCTGGGTCTGTTTGCATATACCAGCAAGACCTAATTGAGTAAACATGGAAAAATTATTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11399
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
ENSDART00000089108 Essential Splice Site 331 1202 7 25

The following transcripts of ENSDARG00000078179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 25628466)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 25824662
GRCz11 2 25480296
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGCTCTCTCAGACAAGGGTCGGAACGGCCAGTACCGCATCATCTATAGG[T/C]AAGACACAGAGGAGCTGTTTTGACCATGCAAAAATCCTTGAAGTCTTGAT
Long Flanking Sequence:
CAATGGTAAGGTGCTTATGAGTTTGAAGTGACATACAACAAATCACAATTAGGAAACCCTTCTATGTGTGTGTACGTATATACTATTATTATATAACTATCTATATAACTTTATTTGGCATCACTTTATTTTGATGGTCCCTTTAATGCGTAATGTTGAATTTGAGAGTTGGAATTAATGAGAATTAATTTGCATGTAGTTGCAATGCAACTTTTATTCATCAAAATGTGCAATAGAGACCATCTAAATAAAGTCTTACCCTTTATTCATCCTTTATATTGATAAGTCTAATACTATTGCTTTAGTTTTTATATGCTGATTATTTTGAATGTCCTCCACAGGTTTTAAATATTCAGTCCCGTACAGCTCGACTGACCTGGGCTCCACCAGCAGGCCTCCAGAACAGAGAGAGGCACAGTAACGGACACCCATTTACCTGCAGCTATGAGGTCGCTCTCTCAGACAAGGGTCGGAACGGCCAGTACCGCATCATCTATAGG[T/C]AAGACACAGAGGAGCTGTTTTGACCATGCAAAAATCCTTGAAGTCTTGATGTACTCATGATTTTAACAGCGCTCTCCACAAGGGAGCGGATTATGTATGATTACATCATCCTTTGAGTAAAAAAGCAAAAAGAATCATTGGATGCAGCCTTTTCTCCCATCAGGATGTGCATGATTCAATTTCCAGAGAGCGGAGACGAAAGATAATCAGACCTTCAAACCATGTTATCGCCCCTGTGAAGCATGAGGCTCAAAGCCCAAAGATGCAGACTGACTTATGAGAGATGTGCTGCTGCTTTAATTATATTTATTAAATATTACTGTTCAAAAGAGGATCTTCACCTGATAAATCTTTTTTAAAAAGTGTGTTCACCTTTTTCACTTTCTGGGTCTGTTTGCATATACCAGCAAGACCTAATTGAGTAAACATGGAAAAATTATTTTTTGCTTGTACTAGATTTATATGTTGCTGTTTTACCATGTTATTACTGCATTAATCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16307
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
ENSDART00000089108 Nonsense 705 1202 18 25

The following transcripts of ENSDARG00000078179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 25651321)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 25847517
GRCz11 2 25503151
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGACTGTCCTTCCKCTGAAGGGGCATGCGAGGTGAGCGAGTACAGTT[T/A]GGAAATGAGGGAGGGAGTGATGGAGCCAGCTGAGGTCTATCACGGTTCAG
Long Flanking Sequence:
CAGTTGTTGTATCAAGATACAGTGTTGATCTTAGCCTAAAAATCTAAATTTTCCCCTTATTTTCTCCATTTTCTTCAAAATGTCATTCTCAAATCACAACTTGCACATATAGTCTAGTTTTAGACTGTAATGATGCTTTTAAAGTGCGCTTTGCACAGTGAGTTCCTGTGCCAGAGCTATTGGTTGGAAGTTAAAGACTGAACACCTTTAGCACTTACAGTAAACACCCTGTTTCTGATCCATTGGAGCATCATTGTAGACCTGCTGATTCAAGAGTTTTTAGCCTAACACTGGATATTCAGGCCTTCGGTCAGAAAGCAGAAGTTGTAAAGCTGCAATTTTCTCTGCTTGAAAAGAACCTAAAATCCTTTGCTTTCGTCTAAAAGATGAAATGAGGCTGTAATTTTTGGTGCTGGACTGAAGTGCTTTATGTGTGTGTGTGTGTGTTATTTCAGACTGTCCTTCCTCTGAAGGGGCATGCGAGGTGAGCGAGTACAGTT[T/A]GGAAATGAGGGAGGGAGTGATGGAGCCAGCTGAGGTCTATCACGGTTCAGATCTGGAGTGCACTGTGGGTAGTTTGCTCCCCGGCGCCACCTACAGCTTCCGCCTTCGTGCTGCCAATGAGGCAGGGGTGAGTGAGGCTTGAGAGTTTGTCATGCAAAATATATCATGAAGTCTAGTCCCAGACTAAAAGTGCTATAGGTCTGAGCTATTTTAGCTGAAAGTTGCGTTGCTTTTGTTTTGTCTCAAGAGGGACACCAGTAATGTTTTAAGCACATTTTGTAAGAATTACTTGCGTGTTCTGATTGACTATGAACTATGGCCTAATCCTGGCTGAAATTGTTTTACGCTGAGTACTTCTTCAGTATTTCTTTTCACTAGCCCATAGTTAAAAATACACAAAACTAATAATATTTTGGTATTTGACAAGTCACTGAAATTATTAATGCTCATCATTATTAATCATCTAAACTAGCCAATCATTATTTTAATCTGTCTGGAAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25811
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089108 Essential Splice Site 1099 1202 24 25

The following transcripts of ENSDARG00000078179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 25676944)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 25873140
GRCz11 2 25528774
KASP Assay ID:
2259-2035.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTACATCCTGCAGGTGCTGGTGGGCCGAGAGTCTGACTACAAACAGG[T/C]AAGCATTCTATTTCTTAAATCACAAAAGAGTAGATTAGCACTATCGATTT
Long Flanking Sequence:
CAAAAAAAAAAAAACTCTGTAGACTGATGGCAGTATTAATTGTACGCAGTTAAAGTAAATGTGTACGGTTTGTGTGTTTCAGGTTTGTCACAATCTACAGGGGGCCAAGCCACACATATAAGGTACAGAGACTAAGTGAATCAAGCAGCTACTGTCTCAGGATTCAGGCTGTGAGTGAAGCAGGAGAAGGGCTTTTTTCTGAAGTTTACACCTTCAGCACCACCAAATCTGTTCCTCCAGCTCTCAAGGGTAAACCATTGCTTTATAATCCACACACAGTTCCTGTTTTATGTACTTGTTTGATTTCTCCATGTATGATCGTCATTATTATTATTATTATTATTATTATTATTATTTATACATTTGTTTAGCTCCCAAAGTGGTACAGATGGAAGGGAATGTGTGTGAGGTGAGCTGGGAGAGCATCTCACCAATGAGAGGAGACCCCATCATCTACATCCTGCAGGTGCTGGTGGGCCGAGAGTCTGACTACAAACAGG[T/C]AAGCATTCTATTTCTTAAATCACAAAAGAGTAGATTAGCACTATCGATTTACCTGTGAACAATCTCACAAGTTAAACAAATTTACTATAGAAGATAAATTGATATAAATACTTAACTTATTTATTAGTTCTAAGACACGGAAGAGACAATGGAGTACTGTAGTGGACAGTCACTTTTCTCTAGGGTTTCAGTACAGTGTACTTGATACTACGTCATCGGGTGGGCGTGGCCTATTTGTGAATTAGCATAGGTCATGGATCATACTCGCATTGTGAAAGCAGCCATTTGTTTCAGATACCTGTACGCGATCGCAGGAGTTTCGAGTCCAATGCCTTTTATATGCAGTACTTTGAAAAAGCTGATTACAAGTCTTTCATGTGCAGCTAGTGTATTTTATATTAAACAAAATACCTTAAGATACCTGTCAGATTACTTTAATACAGTAATATTCTTCAGATACCTGTCCTGATCCCAGGTGTTTCGTGTCTTATTACTTTTGT
Associated Phenotype:
Not determined