ZMP
si:ch211-32j10
Ensembl ID:
ZFIN ID:
Human Orthologue:
NBEAL2
Human Description:
neurobeachin-like 2 [Source:HGNC Symbol;Acc:31928]
Mouse Orthologue:
Nbeal2
Mouse Description:
neurobeachin-like 2 Gene [Source:MGI Symbol;Acc:MGI:2448554]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18226 | Nonsense | Available for shipment | Available now |
sa15725 | Nonsense | Available for shipment | Available now |
sa13722 | Nonsense | Available for shipment | Available now |
sa15336 | Nonsense | Available for shipment | Available now |
sa22794 | Nonsense | Available for shipment | Available now |
sa22793 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18226
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 |
---|---|---|---|---|---|
ENSDART00000031188 | Nonsense | 254 | 2801 | 8 | 55 |
ENSDART00000135050 | Nonsense | 194 | 2647 | 6 | 51 |
The following transcripts of ENSDARG00000057508 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18519916)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16562856 |
GRCz11 | 16 | 16470833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGTCTGTGTTGCGCTCCTGGTGCCTYTGTCCTGCCTCATCCCCACAG[C/T]AGCCCAGGRACCCTCAGCTGCTCAGGATGGCCCYTCGCTGTCTGACTGTA
Long Flanking Sequence:
ATTTTGTTTTCAGTTTTGTTTTGTTTTGTTCTGTTTTGCAAATAATTTCTGTTAACAAAAGCATATCTGTGCAACTTAAGACAGAATTTGAATGAAATTTGCTTCTTGACAAAATGCATTACATATATCTGTGCCTTAAAACTTTAATGTCAGTTTTACGATTCTTGTGACTAAAAGATTAGCTATGCCTACAGAATACCTCCAAGACAGTGAACTAATCCCTGAACCACTGGTGGTGAGGCTGGTGCATCTACAGGGAGCTGTAATCAGTGGATGCAAGGTAAATTAGACCCTTAGGCCCTGTTTACACTGACATGTGTGAACGCATCAGGGGCTATGAGTGCTTTCTAAATGTACAGTATAACATTACTAAAACAGTATTGCATGCTGCCGTTCGTGTGTTTCAGAGAAATGGCCTTCTCTCCATCACCCCGCAGGCTGTGAAGGATCTCATGTCTGTGTTGCGCTCCTGGTGCCTTTGTCCTGCCTCATCCCCACAG[C/T]AGCCCAGGGACCCTCAGCTGCTCAGGATGGCCCTTCGCTGTCTGACTGTAATGATTCATCTTCTGCACTCCAGCAGTGTGAACGAGAGACAGGTGGAGATCCGGAGCGCGCTGGACGATTATTTCCAACTGCTCAACTGGAACCGTCCACCGGACAGCCAGCAGGGAGATATGCACGCCTGGGAGGATAATCTCATTACCCTTCTTGAACATATGCTTAGTAAGCTAATATTTTATTACAAAATAAAATATAAGTGAATTTATAAAAAATAAAAATAAAAAAAAGATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTGTAATGTAGCTGTGTGAACATAAACAACATCTCTGAATGTATTGAAAGACGCTCAAAGTTCAATGCAGAGGGAGACATTGGCTTTTACAGAGTTAGCTTAGCAAAGCCTACAGCGAAAAAATACATCCGGGTAATGCAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15725
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 |
---|---|---|---|---|---|
ENSDART00000031188 | Nonsense | 1075 | 2801 | 21 | 55 |
ENSDART00000135050 | Nonsense | 984 | 2647 | 18 | 51 |
The following transcripts of ENSDARG00000057508 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18476529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16519343 |
GRCz11 | 16 | 16427320 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCTGCTCTTTGACTTCCGCATCTGGAGCCGCAGCCACTTCGCTGTCTG[T/A]CTGGGTAATAAAAAATACTTTGACAAMCAKAAAACATCATTRTAGCGTTA
Long Flanking Sequence:
GGCACTTAACGGTTTTTGCATCTGAACTCTCCATATTTATCATTTCCTTCATTACACTCTATATACACTGAATTTGAATGATGCAATGTGACAATACTAAAAAAAATATGCTATATTGGTAATTTTGAGTGCACTGTGATAAATCTCCAACAGTAAACTGATGCTTATTTATGCTGTACTGACACAAAGGAAAAATGATTTTCTGTGGTCACGTCTGGTGTGGACATGGTGTTCAATCGTCAAATTATTTAATGAATTTGATTAAGCATTGCAATGAGCTGACGACTATTATGATGACAGACACTTTGTGATCTTCTCCTGTCTCATGTTGGTTTGCTCTTGCAGGTCCCCAGCAGTATGATGGACATGAGTGTACTAATGGCCTGTCAGTTCCTGCTCAAGCAGGTGTCCAATGAGGGCAACAACGCCTTGCTGTCTCAGCTGTACCAGTACCTGCTCTTTGACTTCCGCATCTGGAGCCGCAGCCACTTCGCTGTCTG[T/A]CTGGGTAATAAAAAATACTTTGACAACCATAAAACATCATTATAGCGTTAAGATATTATATTTGCATGAAATTAATGCAAATAAATTTAGATTGTTTAGCTGACTGCCATTCCAAACCATGGGCGTGAAATATTTTAGAACAAGGTTTTTGAGTTTATTTAAAAAGTAAATAAAAAAATGACATTTTCTGCTTTAACACTTGAACTACAGAGGCAGTAATTTTGTCTGTTGAACTTTGTTCAAATGAGACCCATAATTTTAACCTTACATTGGTAAAATTACAAACCTACAGTAAAAGAGTCCTGAGTATTTCTACCTTGATAGGCCAAATTAACCCCATGTATTTCACTACTTTTTCTTGCATCTTTGATTATACACTGACAATTTTATTTATATAGCACAGGTTTTTTTTAACAACTTTTGTGGCCAAAGTGCTTTCCAACAAATCAGCAGAATGCAGACAGACAACCACAAACAGACAAAAAATAATGATCATACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13722
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 |
---|---|---|---|---|---|
ENSDART00000031188 | Nonsense | 1291 | 2801 | 26 | 55 |
ENSDART00000135050 | Nonsense | 1200 | 2647 | 23 | 51 |
The following transcripts of ENSDARG00000057508 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18467126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16509940 |
GRCz11 | 16 | 16417917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACTTRTTGGCAGTGGTGTACTTATCCCATCGTGCCGATCTCAGTGCT[C/T]GACTAGAAATTGTTCGTAAGGTAAGTGATGGATTATCAAAGGATTTGTCA
Long Flanking Sequence:
TTAAAAAAAAAAACAATTCAAAGGGGAGCTAATAATTCTAACTTTATATCTAAAATTGGCTGTTTTGTTACTCCAATTATAATTACACTTTATGCTTTAAAGTATTTATAATTATATTTTATTTATACTTTATTTATACTAGTATACATACATATATACATACATATAGATTTATTTATTTATTTATTTATTTATTTGAAGTCACAAGTCATTGCATAAGCATTTCACTGCATACCGTACTGTTTATGACTTTATGTGACAACTTTTTTTTTAATTGAACTATTTTCACAACTGTAGAAGTTTTGCTGTTTGAATTTCACAATTAAATTACTGGAATTTAAAAAAAATACAATCTTTATTGCCAGTGATTGCTTTGCTCTTTAGTTCCTCATTAGTTAGTGACAGTTCTGTATTGTTGTTTACTTGTTGCAGATCCCACTCCTAGTTTTAAAGACTTGTTGGCAGTGGTGTACTTATCCCATCGTGCCGATCTCAGTGCT[C/T]GACTAGAAATTGTTCGTAAGGTAAGTGATGGATTATCAAAGGATTTGTCAACCCAAAAATCTAAATTCTGTTAATTACTTACTCTTGTGTTGTGCCAGTCCCCTGAGATTTATCATCGGAACACAAAATAAGATGTTTTAAAAGAAATCCGAGAGCTCCCTCATCCTCCATAGACAGAAAAGGTTACGAGACATTTAGAAAAGGAAGCAAAGAAGTCTTTGATATTGAGAGTTGCATCCAGCGCCAAAACATTCAAATTGTGGGCTTACCCAAACCCGACCAATGATTTTTTTACTCTCAGCTTTTGGTTGATTTCCTTGCTGCTCAAACTAGACAGACCTCACCATGGCCTCACACCTAAACCTGCACCAGATCAGAGACCGCGACTCATCATTCTAAAATATTTGTGTACTGTTGATGAAGAGATTTTGGTGACAAAAACATTGATTCACTTGTAAAATCTTGCACATTTTAAATTCTTAAAATTGAAAGTGAACCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15336
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031188 | Nonsense | 1308 | 2801 | 27 | 55 |
ENSDART00000135050 | Nonsense | 1217 | 2647 | 24 | 51 |
The following transcripts of ENSDARG00000057508 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18466492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16509306 |
GRCz11 | 16 | 16417283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTKTTTTNTCCCTGCAGCTCTTCTGCTTGATCCACTCCAACGAAGAGTA[T/G]GTGAARCAGCTGGCTCATCAATCAGGCTGGCAGGATGTTCTCACCAAACT
Long Flanking Sequence:
TGTTTTAAAAGAAATCCGAGAGCTCCCTCATCCTCCATAGACAGAAAAGGTTACGAGACATTTAGAAAAGGAAGCAAAGAAGTCTTTGATATTGAGAGTTGCATCCAGCGCCAAAACATTCAAATTGTGGGCTTACCCAAACCCGACCAATGATTTTTTTACTCTCAGCTTTTGGTTGATTTCCTTGCTGCTCAAACTAGACAGACCTCACCATGGCCTCACACCTAAACCTGCACCAGATCAGAGACCGCGACTCATCATTCTAAAATATTTGTGTACTGTTGATGAAGAGATTTTGGTGACAAAAACATTGATTCACTTGTAAAATCTTGCACATTTTAAATTCTTAAAATTGAAAGTGAACCCCATTTTTAATCCTACCGTATGTGTTGAAACATTCCTGCAATTAAATATTAATAAAACAATGAACCAATTATTTTTGTTATCTTTTTTTTTTTGTCCCTGCAGCTCTTCTGCTTGATCCACTCCAACGAAGAGTA[T/G]GTGAAGCAGCTGGCTCATCAATCAGGCTGGCAGGATGTTCTCACCAAACTCTACGTCAAAGAATCATACGAGTCTCGTGTTCGCAGTCAGTCCAATTCTTTATCCAGCCCCACTTCCTCACTGGACCCAGTCCTTTCCAGACCCGTCTTCCGTCGAGATGACAGCGTAACAGAGGATGTTCGGCAGAACGTCTATATCACCCTCGCTGCCCGCCACGAAGAAGAGTACGAAGAGGAGGAAGGAGAAACTCAGGATGCTTCTGAAGGCTTTTCTGACCTTTCCCAGTCTCCTCCGTCAACCGGGCAGCTCAAGAATGATTCCCTCCACTTTAAGCCATTTGACTCCGGAGACCAAAGCAGTCATTCGTCTACCTTGTCCAACACTGTGGACTTTCCACCATCTCGCCTGCAGGAGGAAGATGAAGCCGTGTATCAGCCCCTCTCACCATTCGGCTCACCCTTTGAGCTGGAATTAAATCACCAGAAAGGACCCCAGACCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22794
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 |
---|---|---|---|---|---|
ENSDART00000031188 | Nonsense | 1802 | 2801 | 32 | 55 |
ENSDART00000135050 | Nonsense | 1648 | 2647 | 28 | 51 |
The following transcripts of ENSDARG00000057508 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18447331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16490145 |
GRCz11 | 16 | 16398122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTTTTCCTAATGTATGCCTGCAGGTGGAGCCCACAATGCAGCAGTA[T/A]GAGCTGGACACTTTTGGGAAGAGCCACGACTTGATGTCCAACTTCTGGAA
Long Flanking Sequence:
CGCCACAGCAGAATGAACCGCCAACTTATCCGTCATATGTTTTACACAGCGAATTCCCTTTCAGCTTCAACCGATTTCTGAAAAAAAATCCATACATTCACATTCATACACTATGGACAATTTAGCTCACCCAATTTACTTGTACCACCTGTACGAAGTCTTTGGACTTTGGGTGAATCTTCACACAGAAACGCCAACTGACGCAGCCGAGGCTCGAACCAGTGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCATCGCCCTATGTTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTTTTGCCCGTTCAATAAAATTTTATTGTAAGAATATAATGTATTGTAGAAATGTAAAAAAATAATAATAATTTTAAATGTTTTTCCTAATGTATGCCTGCAGGTGGAGCCCACAATGCAGCAGTA[T/A]GAGCTGGACACTTTTGGGAAGAGCCACGACTTGATGTCCAACTTCTGGAACTCCTGCTTTGATGACCTGATGAGCACCGGTCAGAGGAGAGACAAGGAACGCTCTGATTCAAAGGCCAAATTTCAGGTGTCTCTAAAACTTATTTATTGTAAAACAAGGGTTGTTCCTGTTCTTACTGCAGTCTCTCATTACTTATCAAACACCAACCCATCAATTGACTGGTAGATCTTTATCTGGCTATCAGTAGATCCTGAGAATGACTGATGAATAAGTACAAGAAATGCATAGTGACCTCTTTTTATTTTTCTTGATCTAACTGCTGTTTTTAAATGTCAACATCCAGCTCTTCATAGGACATTCTGCACCCTATGAGGAGCCAGCCTCAAAATAATAAGGGGCCGTTTACATATCACATTTTTTTGCATGCTCAAGTTCCTTATTTCAAATGAAGATGTGCTACTTGTGCACTCCACTAAGAAACAAAGTGCACACGTTGTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22793
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 |
---|---|---|---|---|---|
ENSDART00000031188 | Nonsense | 2349 | 2801 | 44 | 55 |
ENSDART00000135050 | Nonsense | 2195 | 2647 | 40 | 51 |
The following transcripts of ENSDARG00000057508 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18428643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16471457 |
GRCz11 | 16 | 16379434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAACGGGGACCTGAAGCAGTGGAGGCTCTTAATGTCTTCTACTACTG[C/A]ACTTATGAGGGTAAGAGACCTCTTATGAGTTCACATTAGCTGTTTCCTGA
Long Flanking Sequence:
ATAATCAGTGGTTAAAGGTTTCCAGCTTTCTTCAAAACCTCTTTAGTGTTCAACCGATGAAAAAGGTGAGGGTGAGTTAACAGTGAGAACAGTTTTATTATTTATTGAATCTTTTATAACTCATAATTGTGTGGGGGAAAAGTTAGAATTGTGAGCTGTGAACTCAGAATTACTAGAAAAGGGCTGAATCACAAGTTAAAAATCTCAGAATTGTGAATGTATCTGTAAAATTGCTGTTTATATCTTGGAATTCTGATGAAAAATACTAATTGTAAAATATATATTATGTAGTCTACCAATGGAGAAAATTTTTTGGCATGGATGATATTGTTATAAATATTCTCTTGTTTTCCACCTAATAAGCACTTTTCTTGTGTATATGTATGTTTAAAGGAGAGTGAACATGTGTCTGCTCACCTGCATGAATGGATCGATCTCATATTCGGATATAAGCAACGGGGACCTGAAGCAGTGGAGGCTCTTAATGTCTTCTACTACTG[C/A]ACTTATGAGGGTAAGAGACCTCTTATGAGTTCACATTAGCTGTTTCCTGAATGGAAAATATGACTGATTGGTGTGTTTTTTGGCCGTCAGGTGCAGTCGATCTGGATGCCATTGCTAATGAGACTGAGCGCAAAGCCCTGGAAGGCATTATCAGCAACTTTGGCCAAACACCCTGTCAGCTTTTAAAGGTGAGACTTCAGACAGATGTTTCCATCTCTAGTTATCATAAGCCTCATATTACTTGAGCTCCCAAGTCTGGATAGTGATGTTTTATTGGCTTAAGAAGGTCAGAATATCTACTACTACTACTACTACTACTACTACTAAGCTTTGTTGTCATTTTCTATTTCTTGTTACAGGTACAGATTTCTTGGAACAGATTTCTTTACACTTAGCTTTCAAGTTGTCACCACAAAACATGTTTCAGACCTTCAAGACTTTGTGTGCTGATTTTATTGTAATTGATCAGATTTAGGCAATAAAAATGTCCTTTAGACTTG
Associated Phenotype:
Not determined