ZMP
nfasca
Ensembl ID:
ZFIN IDs:
Description:
neurofascin [Source:RefSeq peptide;Acc:NP_001139239]
Human Orthologue:
NFASC
Human Description:
neurofascin [Source:HGNC Symbol;Acc:29866]
Mouse Orthologue:
Nfasc
Mouse Description:
neurofascin Gene [Source:MGI Symbol;Acc:MGI:104753]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21901 | Nonsense | Available for shipment | Available now |
sa21902 | Nonsense | Available for shipment | Available now |
sa13971 | Nonsense | Available for shipment | Available now |
sa31826 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21901
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086720 | Nonsense | 96 | 739 | 6 | 20 |
ENSDART00000112655 | Nonsense | 96 | 743 | 4 | 20 |
ENSDART00000121874 | Nonsense | 96 | 1340 | 4 | 32 |
ENSDART00000127846 | Nonsense | 96 | 1369 | 4 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 24748383)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23587682 |
GRCz11 | 11 | 23825539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAAAGTTCTTTAATGTGGGTAAGGACCCACGGGTGACCATGAGAAGT[C/T]GATCTGGAACACTAGAGATCAGAAGCAGTGGAAAACCAGAAGATTATGAA
Long Flanking Sequence:
TGGGTTGAAACCCACTTTGAGTAGGGCAAATTGAACTGGATGAATTAAATTGATGCCATGACTTGGAAAAGAGTGAGGTTTAGAGGGTGAGTGTGAAACTGTGTGTGAGGCCAACAAGGAAGAACTGGCCTGAAGATACACACTAGAATCTGATGTCTTTGACATCATTGTTAGTGTGCTCTCTTTTCATGCTGGATTAATTCAAATCCCACTCAGAGTATAGCAATTATACCTTTAGGTGTTACAACTAGAATACTGAGGGGCTGACATTTAGATCAAAATTACAAAGTTAATGTCCTTAAATTGGTTTAGCAGTCATGTTCTTTTACTCTGATGTGTATGTAAACCACCTGATTTAAAAGCTCCAAAAATGGACCTATTACATAAACAGCTTCAATGTGGCTGATTTCCTGTTTTGGCCCGGTCTGTGCAGGTTTCAGTGGAGGCGGAATGGAAAGTTCTTTAATGTGGGTAAGGACCCACGGGTGACCATGAGAAGT[C/T]GATCTGGAACACTAGAGATCAGAAGCAGTGGAAAACCAGAAGATTATGAAGGAGAATACCAGTGCTTCGCTTCCAACAACTTGGGCACAGCCATTTCCAACAAAATCCTGCTTCGAGTGTCAAGTAAGGGATGTATGATTATAACATGAAAGGATAGTTCCACCAAAAATTTAATTATGATGTTTTAAAACTGTTCTGTTGAATACAGAAAAAGCCTAAAAAGTATAACAGAACTAGTTTAATTTGAGCTATTTGCATTTTCAGTTTTCTCAAAGATTTTATTATTTTTTTTAATGTTATTGTTATCAGCCTGATATATTAAACAAGATAGATTATGCATTATATCCACTAGTACAGGGGTCACCAATCTCGTTCCTGGAGGTCCTGTGCCCTGCAAGGTTTAGCTCCAACTTGCCTCAACACACCTGCCTGCCTGGGTGTTTCAAGTATACCTAGTAGGACCTTGATTAGTTTGTTTAGGTGTGTTTGATTAGGGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21902
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 |
---|---|---|---|---|---|
ENSDART00000086720 | Nonsense | 415 | 739 | 12 | 20 |
ENSDART00000112655 | Nonsense | 415 | 743 | 10 | 20 |
ENSDART00000121874 | Nonsense | 418 | 1340 | 11 | 32 |
ENSDART00000127846 | Nonsense | 415 | 1369 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 24757988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23597287 |
GRCz11 | 11 | 23835144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGAAAGCAGTGCAGTTTACCAGTGTAACGCCTCCAATGAGCACGGTTA[T/A]CTTCTGGCAAATGCTTTCGTCAGTGTTTTGGGTATGACAGGATGAAGCGA
Long Flanking Sequence:
CCAGCAACAGAATTGGCAGCATTCGCCACACAGTTGAAGTCCAGGTCAAAGGTGAGCAATCGAGAAAAGGCAATTGATGCCCATTATGTCTGAAAAAACTGCTTCATGTATTCCACTGTCCTAAATTCCATCCACAGCTGCTCCATTTTGGCTCGAAAAGCCCATCAATCTGGTTCTTGCCCCTGATGAGAGTGGACGGTTAGTGTGCCGTGCTAACGGGAGTCCCAAACCCACTATTCAATGGCTGGTGAATGGAGAACCCATTGAAAGTCAGTCAGCTTTTGCTTGTCATGTTTGAACAGATTTAGAGTTTTAAATCATAAGCAACAAAGTGTATATTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTAACTTCAGGTTCACTCCCCAACCCCAATCGGAGAGTTCTTGATGACACGATCATATTTGAGACGGTTCAGTTTGAAAGCAGTGCAGTTTACCAGTGTAACGCCTCCAATGAGCACGGTTA[T/A]CTTCTGGCAAATGCTTTCGTCAGTGTTTTGGGTATGACAGGATGAAGCGAATTGGTGCAGAATGTCCATATAGCTCACATGGTGCGCAAATTGTGAGATGTTGGTGTTGCTGTTTTTTTCCCTAGATATGGCACCGCGGATGCTTGGCCCGAAAAACCAGCTGATCAAAGTCATTGAAAACAACAGGACCTTCCTCGAGTGTCCTTTCTTTGGCTCACCGCTCCCTTTACTTCGCTGGTAAGTTTATGTTAAATTGTTGTAAACAGTACTTGTTCACAAAGGGTAAATATTTGATCAAAATGCTGTAAAACCCACTGTAATATTGTAACATATTGTTACAATTAAAAATAAATTATTCCTATTTTGATATATTTTAAAATGTTGCTTATAGCTGTGATGAATTGATGTCAGCCTTTGCTTTTGGCTCATATTTAGGCATATTTATAACAAGAATCATTTGATAACGTTAACACTCAAATAAAGGATTATAGTGCAGACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13971
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 |
---|---|---|---|---|---|
ENSDART00000086720 | None | None | 739 | None | 20 |
ENSDART00000112655 | None | None | 743 | None | 20 |
ENSDART00000121874 | Nonsense | 800 | 1340 | 20 | 32 |
ENSDART00000127846 | Nonsense | 797 | 1369 | 19 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 24765115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23604414 |
GRCz11 | 11 | 23842271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGCCAAAACAAAAMACGTTGTCCATAATACAGACACCTACGTTCCTTA[T/A]GAGATCAAAATACAGRCTGTYAATGACTTTGGACATGGCCCAGAGTCAAA
Long Flanking Sequence:
TAACCTTCAGCTATCACCATTCGTCAACTACCAGTTCAGAGTGATTGCGATCAATGCTGTGGGTCAGAGTCAACCCAGCCACCCCTCTGCACGTTATCAGACCAGCGGAGCCTGTAAGACATTGCTTATATTGTGTATATTGACTAGTATTAGTAGTCAAAATTACCAGTTGAGACATTTACTGATATAAATTTATCTGATTTAGCTCCTGATGTTGTACCAAGTGGACTTAAAGGGTGGGGAAGCAAAAAAAACAACATGGAGATCACATGGCAGGTAAAGTGAATGGCCAATTTTAAGAAGAAAAAGGAGATAGATGTGACTTTCATTGACTTAATTTACCGTTACATGTCACAGGCCATGCAGAACACAGAGAGGAATGGGCCAAACCTGCGATATGTGCTCTCCTGGAGAAGAAAAGACACAGAAGAAGAGTGGAATAACATCACCACAGCCAAAACAAAACACGTTGTCCATAATACAGACACCTACGTTCCTTA[T/A]GAGATCAAAATACAGGCTGTCAATGACTTTGGACATGGCCCAGAGTCAAACATGGTCATCGGTTATTCTGGGGAAGACAGTAAGTACTATCATGTCATCTTTAATGACACTTGAGGCCCAAATATACTTAAAGAACACACCAGGGAAAGGCTTTACAGAAAACAAGTAGACATCTAATTGTTAGCGCTGTTTTTACGCTTTGTAAATAAACATGATGTGACTTAGCTGGAGTGTGGAATTGTAGAGATATCCACATTTCTATATCAGATGCTTTCTTAACTGCTGTTTTCTCACAGCTCAGACATTTTACCTCTAAACAATGAAAAAGAGCTTGGCTGGGAGTAAATTGGGACCTGCTTTGTCATTCACAGATATTGGTGTGTTTTTGCTGCTTCATTTGCTACTACTAATATTTTTCCCCATCAGAACCATCCGCTGCACCAACAGATCTTAGGGTGTCAAAGATCAACAGTACCAAAGTCAATATTCACTGGGAGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31826
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 |
---|---|---|---|---|---|
ENSDART00000086720 | None | None | 739 | None | 20 |
ENSDART00000112655 | None | None | 743 | None | 20 |
ENSDART00000121874 | Nonsense | 822 | 1340 | 20 | 32 |
ENSDART00000127846 | Nonsense | 819 | 1369 | 19 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 24765181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23604480 |
GRCz11 | 11 | 23842337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTCAATGACTTTGGACATGGCCCAGAGTCAAACATGGTCATCGGTTA[T/A]TCTGGGGAAGACAGTAAGTACTATCATGTCATCTTTAATGACACTTGAGG
Long Flanking Sequence:
GAGTCAACCCAGCCACCCCTCTGCACGTTATCAGACCAGCGGAGCCTGTAAGACATTGCTTATATTGTGTATATTGACTAGTATTAGTAGTCAAAATTACCAGTTGAGACATTTACTGATATAAATTTATCTGATTTAGCTCCTGATGTTGTACCAAGTGGACTTAAAGGGTGGGGAAGCAAAAAAAACAACATGGAGATCACATGGCAGGTAAAGTGAATGGCCAATTTTAAGAAGAAAAAGGAGATAGATGTGACTTTCATTGACTTAATTTACCGTTACATGTCACAGGCCATGCAGAACACAGAGAGGAATGGGCCAAACCTGCGATATGTGCTCTCCTGGAGAAGAAAAGACACAGAAGAAGAGTGGAATAACATCACCACAGCCAAAACAAAACACGTTGTCCATAATACAGACACCTACGTTCCTTATGAGATCAAAATACAGGCTGTCAATGACTTTGGACATGGCCCAGAGTCAAACATGGTCATCGGTTA[T/A]TCTGGGGAAGACAGTAAGTACTATCATGTCATCTTTAATGACACTTGAGGCCCAAATATACTTAAAGAACACACCAGGGAAAGGCTTTACAGAAAACAAGTAGACATCTAATTGTTAGCGCTGTTTTTACGCTTTGTAAATAAACATGATGTGACTTAGCTGGAGTGTGGAATTGTAGAGATATCCACATTTCTATATCAGATGCTTTCTTAACTGCTGTTTTCTCACAGCTCAGACATTTTACCTCTAAACAATGAAAAAGAGCTTGGCTGGGAGTAAATTGGGACCTGCTTTGTCATTCACAGATATTGGTGTGTTTTTGCTGCTTCATTTGCTACTACTAATATTTTTCCCCATCAGAACCATCCGCTGCACCAACAGATCTTAGGGTGTCAAAGATCAACAGTACCAAAGTCAATATTCACTGGGAGCCTGTGGAGCAGAGCAGTGTAAATGGAGAATTTAAAGAATACAAGGTGAGTGATCTTATATCTGCCAGA
Associated Phenotype:
Not determined