ZMP
fndc3ba
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
---|---|---|---|---|---|
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
---|---|---|---|---|---|
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