ZMP
nbea
Ensembl ID:
ZFIN ID:
Description:
neurobeachin [Source:RefSeq peptide;Acc:NP_001013518]
Human Orthologue:
NBEA
Human Description:
neurobeachin [Source:HGNC Symbol;Acc:7648]
Mouse Orthologue:
Nbea
Mouse Description:
neurobeachin Gene [Source:MGI Symbol;Acc:MGI:1347075]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38806 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21772 | Nonsense | Available for shipment | Available now |
sa34946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21773 | Nonsense | Available for shipment | Available now |
sa21774 | Nonsense | Available for shipment | Available now |
sa21775 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38806
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102566 | Nonsense | 397 | 2968 | 8 | 58 |
ENSDART00000114630 | None | None | 2355 | None | 45 |
ENSDART00000144529 | Nonsense | 397 | 607 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 35616779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34645040 |
GRCz11 | 10 | 34588900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGGCAACTCGGAGCTGTGTACGTTTTCAGCGAGGCACTGAACCCCGCA[C/T]AGATCTTTGCCATTCATCAACTCGGACCGGGATATAAGGTATAGACCCTG
Long Flanking Sequence:
TGTTAGAGCCGCTAGCAAACCTTTCTCAATCTTTCCATCTCAGTCTGCCAAAAACCGTAAACTTCCAATCAACTTTATTTTCCTCAGCTTACGAAATATTGCACCTGTAGGGTGCGAACGATATGCGATTAGATAAAAGCTTGTCTCTGTGGATGAAAGCGATATAGATTAGCCGTAGCTCTTCGCTTCCTTAGGCAAACCTTTGAAGTGCATTGTGTGTAGACTATAGCTAAAGTAAATCAGAACAAGATGACCAGAAGATAGCGAGTAAACGGCTCCAGAGGGCCTTTAAAGAAAACTCTCAATCTGTTCTACTGATAGAAAGCTCCACTTTTATTTTTGGTGTTTTTTTCTTTTCTTTATCTTTATACTCTTTCTCTCTCTTCCTGCAGAGTTATGATAAATGTTTCCTGGGCTCGTCAGAGACTGCGGATGCTAACCGTGTGTTTTGTGGGCAACTCGGAGCTGTGTACGTTTTCAGCGAGGCACTGAACCCCGCA[C/T]AGATCTTTGCCATTCATCAACTCGGACCGGGATATAAGGTATAGACCCTGAAGCATTGTTTTCAGAACTCTTTAATGTGTTTTCAGAGATACAATCAACAAAGATCAGCCTGGACACACTACTATTTCAACCTGGTGTTAGTGGGAGGTCAAATGCATCTTTTGTAAGCGCTTGTGTTTGGATTTTGATGAAACAATTATTTTAGGCTTATTTTGTCGAGCCATACAGCACTTTTGTGGGAATGAAATTTAAATGAAAACAGTTGATCCTTAGAAATACTACAATTACACTGCAAAAAAGAAATATTAAGGAATTAATGGAAGTAATAAAATGTAAAAAAAAAAAAAAAAAAAACAATAAAAAAATTAAATAAAAATCTTTAAAGTTTCCTATTTACACACTTTTAGAAAACTGATGATTCCAAATGCAGCTAACAAATTATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTAAAGAAAAAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21772
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102566 | Nonsense | 947 | 2968 | 22 | 58 |
ENSDART00000114630 | Nonsense | 340 | 2355 | 10 | 45 |
ENSDART00000144529 | None | None | 607 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 35689932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34717919 |
GRCz11 | 10 | 34661779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTAGATTCACACTACAACCCTTGATCTTGACCCCTTTAGGTGACCTA[C/A]GAGGCGCATAAGGAGTACCTGGCAAAGATGTATGAGGAATATCAACGGCA
Long Flanking Sequence:
TATTGAGAAGAACAATTGCCAGTAAAGTCACTAAAGTTACCCATTCTGCTTTCTGCTGTCTTACGCTATCTGTTAAACTTTTCGTTTAATAGATTAGGACATCATAACTTTTATTAATATGTCTATTATGATTTTGGAGTATTTTCATAGCAATTTTCAAACCACCCCTTCAATATATACAACAGCAAACAAAAAGAAGGAGCTGTGAGTGCATATACTCTGGGGTAGAATGTCTGAGTGCATCACTTACATCAGGTTTCCATTTTTTCTTGTGCTTGAATGCTAAAATGTCCCTCCTATGAAATGTCAGTCACTGACATGGCCCCCACCAATTTGAGACCCCTACTTTAAAATCTTGGAAAAGTCAGGGACGTTTTGTAGTAAAATTGTGTATAACCTAAGGGCGCAGATGATAAGATGTAAAATCTGCTCGGAAAGTAGACCAAGACTAATGTAGATTCACACTACAACCCTTGATCTTGACCCCTTTAGGTGACCTA[C/A]GAGGCGCATAAGGAGTACCTGGCAAAGATGTATGAGGAATATCAACGGCAAGAAGAGGAGAACATCAAGAAGGGGAAAAAAGGCTCCGTCAGCACAATATCCGGCCTGTCTGCTCAACCCACCTCAGTCAATGGAAACCTGGAGATCCGCGAGATTGACGACACATCTCAGACACAGACACCAGAGAGCGAAGTGGACTACGGAGAGAACGCAGACTCTCGAATCCTACTAGCTGAAGCCAAAGTTCCAGAAAGCGAAGCCGAAAGTTCAGCTGCAGGGGTTCGTGTAGAAGTCCACGACCTGCTGGTGGACATAAAAGCAGAGAAGGTGGAGGCCACTGAGGTTAAATTAGATGATCTGGATCTGTCCCCGGAGGTACTCGGAGGAGGAGGAGGGATGGAGAACGGCCCCCTGGTGGAAGTAGACTCTCTTTTAGACAGCGCCTACTGTGCTGCAGTTCACAAGCTCAACGGGAGCCTTGTCCCCAAAGAGGAGGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34946
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102566 | Nonsense | 1312 | 2968 | 23 | 58 |
ENSDART00000114630 | Nonsense | 705 | 2355 | 11 | 45 |
ENSDART00000144529 | None | None | 607 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 35693117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34721104 |
GRCz11 | 10 | 34664964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGACCTGCGTGTGGATCTGGGTTTCCGGGGAATGCCTATGACTGAAGAA[C/T]AGCGGCGGCAGTTCAGCCCAGGCCCTCGCACTACCATGTTCCGTATCCCA
Long Flanking Sequence:
CTTTACTGTCTTGGTTAACATTAGGTTATGTAATAGTTGTCCCTTTACTGTTTTATTTAACATTAGGTTATATACTAGTTATCTCTTTACTGTCTTGGTTAACATACTAGTCATCTCTTTGCTGTCTTGGTTAAAACTAGATTATGTACTAGTTATATCTTTACTGCCTTGGTTAACATTAGGTTATGTACTTGTTAACCTATTGTTTACTTAAACAGTAAAGGGATATGTACTAGTTATCTCTTTACTCTCTTGGTTAACACTAGGTTATGTACTAGTTAAATCTTTACTTAAGCACTATACAAATAAACTTGAATTGAATTGCACTCAAATTCTTCAAAACATTTCGTTTCACTTAAGATTTGTAACAGCATGAAGGTGAGTAAACTAATGATTGAATTGGTGCTTTCCTGCAGGCTCTTCATGGACGTATGTCAGGTCAGATGGAGAGGGACCTGCGTGTGGATCTGGGTTTCCGGGGAATGCCTATGACTGAAGAA[C/T]AGCGGCGGCAGTTCAGCCCAGGCCCTCGCACTACCATGTTCCGTATCCCAGAATTTAAGTGGTCACCCATGCACCAGCGCCTTCTCACGGACTTATTATTCGCCCTGGAAAGCGATGTACACATGTGGAGGAGGTATGAGGCTTTGTGGCCTACAGGAATAAGGTTTAAGGTTTATTTAAACTCCTGCATAGCTATACCAATATTAAATTATAGCAGAAATTACATCAAAACAAAAATATATAAATAAACGTTTTACGTTTATATATATTCCACAAAAACTTATCATATTTATAAAACTTGCACAAATAAGCATATTTGTTTACATTAAATCATTGATATTAAACCTGCATACATCTACCCCATGATTATAATTTATTTTTTAAAATATTTTACTGATATTATTTGTTAAAAAGTCGAGTTGACTAGACCCACAGGGAATCTGTGTGTAAATATGCGTAAATATATCTATTTATTTTTATTAATACAGTAATATTATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21773
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102566 | Nonsense | 1458 | 2968 | 26 | 58 |
ENSDART00000114630 | Nonsense | 843 | 2355 | 13 | 45 |
ENSDART00000144529 | None | None | 607 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 35699235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34727222 |
GRCz11 | 10 | 34671082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGGTGGACGTGTTGGTGTTTGCCAGTTCTCTGAACTTCAGCGAGATT[G/T]AGGCTGAGAAGAACATGTCTTCAGGTGGACTGATGCGCCAGTGCCTGCGA
Long Flanking Sequence:
CCTTCTCTGTTGATGTCAGTTTGACGGTTTCACCTACAGTATTCTTAGCCACGACCCTCTCACCATTAGTTTGCAATGAGCGAATGATGTTTAACAACGAAAGTCCCGCCTCCTACTCAATATTCCGTTTCAGTTGAAAGTACATCAGCATACTAAAATAAAAGTCTCTGCAACTTCCAGTTCACACAGACTTTAAGAACGTCCACTATTTTTCGGACAACACTAATTAGCTGCTCCCTTACTTATGCAATAGTGGACTTTTTATATGGGTATATGGGGCGATCTTGGATGCAGCCTATTTTCCTGCTTTGAAAATGAATTAGGATGCTTTTCTAAACTTCTGGAGTTGGGTTATGTGTATGTGTGCATGACAGACGGAGCTTGAGAATGTGGAGGCGACTCAAGGCATGTCATCAGAGACGGCGGTCACGTTTCTCAGCAGACTGATGGCCATGGTGGACGTGTTGGTGTTTGCCAGTTCTCTGAACTTCAGCGAGATT[G/T]AGGCTGAGAAGAACATGTCTTCAGGTGGACTGATGCGCCAGTGCCTGCGATTAGGTGTGTATGAAGCATCTTTTACCGCAGAGTTATATTAGCCCTCCTGTATATCTTCCCCTAATTTCTGTTTACTGGAAAAAAGAATTTTTTTAAACAGATTTCTAAACATAATAGTTTTATTAAGTCATTTCTAATAACTGATAGGTTTTATCTTTGCCATGATGACAGTACATAATATTTTACTAGATATTTTTAAAGACACTAGTATACTTGTAACTGGGTTTATTAGGTGACTTAAGCAAATTAGGGTAATTAGGCAAGTCATTGTATAACAATGGTTTGTTTTGTAGACAATTAAAAAATATATATTGCTTAGGGGGAAAATAATATTGACAACCTGGGCTCATTGTGGAAACGTAGCCTCGCGGACGTTTCTGGGGACCGCGATTTACGTCCCGGGAGGTACGTATTCGAGCGGTTATTGTTTTCGCGGATCCGCGAGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21774
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 |
---|---|---|---|---|---|
ENSDART00000102566 | Nonsense | 2181 | 2968 | 41 | 58 |
ENSDART00000114630 | Nonsense | 1568 | 2355 | 28 | 45 |
ENSDART00000144529 | None | None | 607 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 35735111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34763098 |
GRCz11 | 10 | 34706958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGGTTTGATGTTTTCTTTCAGGTCCTGTGGTTTTGAGCACTCCGGCT[C/T]AGCTGGTTGCTCCTGTGATTGTGGCTAGAGGGACGTTGTCCATCACCACA
Long Flanking Sequence:
GTTAGCTTGTCATCCTCTGAGAAAACGGTTAATGGTCGCCTAGCAACCTACGAATTCCCCCACCCCCAGTCTGCGGTAAAATTAACAAGAGTTGACCAGTTCGCAGTGGTAAAAATGTTGGGGACCACTGGTCTACATTACATCTTACATTGTAGTATTTCTATAAAAACAAACTGGAAATGGAGGGCGTGTGACGTCATTAGCATTTTGACACGTAGCAAAGTCCATGCCACTAGTTAAAATTGGTTATATATCTTGATTTTAACATCCATTGAAACATTTGAGATAATAAAAGTACACAAGTCAGCAAAATATATAGCTTTAGATTGTTTCATATTGTGCCTTTAATTCATTCTTTAATAACTGCTCATGAAATCTCTATTATCCCTAGTGATTTTTTTATTTTCTGCTTATCTAGGGGTCTGGGAAATAAATGTTAAGCTTCTCATTCTGTGGTTTGATGTTTTCTTTCAGGTCCTGTGGTTTTGAGCACTCCGGCT[C/T]AGCTGGTTGCTCCTGTGATTGTGGCTAGAGGGACGTTGTCCATCACCACAACTGAAATCTATTTCGAGGTGGACGAGGATGATCCGACTTTCAAAAAGATCGATGCAAAGGTGAGTGCCACAGCTTTTTGTACATCGGTGTTTGTAACTTATGCTGGATAAGTTGGCGGTCCATTCTGCTGTGGCAACCCCTGATTAATAAGGGACTAAGCTGAAAATAAAATGAATGAATGAATATTGATTTAGCTTTCAACTGTATGTTAAAATATTAAGAGAAATTAGATTTTTTTTTAGTTTTTAGTCTTCTTTGCTAACTACTGTGTGTATCTGTGTGTATGTCAGGTATTGGGGTATACTGAAGGTCTGCATGGGAAATGGATGTTCAGTGAGATCAGAGCAGTTTTTTCCAGACGTTACCTGCTCCAGAATACTGGATTAGAGGTCTTCATGGCCAACAGAAGTAAGACTTCAAAAAAAAATTGCATTAAAAATAATATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21775
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102566 | Nonsense | 2274 | 2968 | 43 | 58 |
ENSDART00000114630 | Nonsense | 1661 | 2355 | 30 | 45 |
ENSDART00000144529 | None | None | 607 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 35735705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34763692 |
GRCz11 | 10 | 34707552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTCATGTTCAACTTCCCAGATCAGGCCACCGTGAAGAAAGTAGTGTA[C/A]AGTTTACCTCGGGTCGGCGTCGGAACCAGCTATGGCCTTCCACAGGCGAG
Long Flanking Sequence:
AAAAGATCGATGCAAAGGTGAGTGCCACAGCTTTTTGTACATCGGTGTTTGTAACTTATGCTGGATAAGTTGGCGGTCCATTCTGCTGTGGCAACCCCTGATTAATAAGGGACTAAGCTGAAAATAAAATGAATGAATGAATATTGATTTAGCTTTCAACTGTATGTTAAAATATTAAGAGAAATTAGATTTTTTTTTAGTTTTTAGTCTTCTTTGCTAACTACTGTGTGTATCTGTGTGTATGTCAGGTATTGGGGTATACTGAAGGTCTGCATGGGAAATGGATGTTCAGTGAGATCAGAGCAGTTTTTTCCAGACGTTACCTGCTCCAGAATACTGGATTAGAGGTCTTCATGGCCAACAGAAGTAAGACTTCAAAAAAAAATTGCATTAAAAATAATATTTATTCAGTGATTTTAAATAACGCTTTTTCATCATATCTCCACAGCATCCGTCATGTTCAACTTCCCAGATCAGGCCACCGTGAAGAAAGTAGTGTA[C/A]AGTTTACCTCGGGTCGGCGTCGGAACCAGCTATGGCCTTCCACAGGCGAGGTAAGTTTGTGGTACTGAAGAGTACTGAAAGATCATACTCAAGTAAAAGTACCATTACTTGCCTAAAAATGTAGTGCAATTGGAGTAAAAGTATCTGCTGTGAATAATCCTCAAAGTACGAGTAAAAAGCAGAGCTTTCAAAAGTACTCAATAGTAGTGAGTATTACTCTGTAAAAAGCTGATGCATTTATGTCATTTGTGGATGTGTGTAAACGTAACATTCTGTAATGCATCTAGTTGATGCCCAGCAGGCACACAACATCATAAGACATTAATATTAAGTTAGATTTAGGTTGTGATGTCAGGTGACCAAAATTCAACATCTAGCCAGTGTCTAAGGACAATGTTATTTTGATGTCCAATAATGACGCCAAATGACGTTGATTTTTGGTAGATTTTCGGTTGTTAGAAAGTGACCAAATCCAACGTCAAGCCAACATATTAAACCAA
Associated Phenotype:
Not determined