ZMP
nipblb
Ensembl ID:
ZFIN ID:
Description:
nipped-B-like protein [Source:RefSeq peptide;Acc:NP_001154919]
Human Orthologue:
NIPBL
Human Description:
Nipped-B homolog (Drosophila) [Source:HGNC Symbol;Acc:28862]
Mouse Orthologue:
Nipbl
Mouse Description:
Nipped-B homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1913976]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17819 | Nonsense | Available for shipment | Available now |
sa34952 | Essential Splice Site, Missense | Available for shipment | Available now |
sa10463 | Nonsense | Available for shipment | Available now |
sa31792 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17819
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 |
---|---|---|---|---|---|
ENSDART00000086653 | Nonsense | 1484 | 2856 | 21 | 48 |
ENSDART00000086861 | Nonsense | 1510 | 2882 | 20 | 47 |
ENSDART00000108484 | Nonsense | 1510 | 2876 | 19 | 46 |
The following transcripts of ENSDARG00000061052 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37757187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36569348 |
GRCz11 | 10 | 36513106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGGAGATCTTCACCTCTCTAGCCAGACTGCCAACCAGCAAGAGGAACT[T/A]GAGGAATTACAGGTACTNGCCCAGTCTAGAGATAGTCTTGCAMATGTATT
Long Flanking Sequence:
ACAATTTGCCCACAGTGTATTGAGTTTTTGAAATATTCCGAAGCATTTTCCCAAAATAGATGACCAAGATGAGGTTTGTCTCCAAAAATCATTCAATTTGCTAAAACACAGAGAAACTTGTGGCCAAATTAAGACTCAAAATCCCCCCAGAGTGGATGAAAACATCCTCAACAGCACGCAAGGGTTAAACTTTTGTCAAGTAGTTTAAATATATTCGTTTTTTAAATCCAATCTTGTTCTTTTTGCAGATTTCATCTCTAGGTATCACTCCATTTTTTGTGGAGAACGTGAGCGAGCTGCAGCTCTGTGCCATTAAACTAGTGACTGCTGTAAGTACCAGTGTGTTCCAGTCTACTCCACACTCCTCTGTTGCTCAACTATGTCTGACGTGCTGATCTTGTGCGTTTTCTAGGTATTTTCTCGATATGAGAAGCACAGACAGCTGATCCTGGAGGAGATCTTCACCTCTCTAGCCAGACTGCCAACCAGCAAGAGGAACT[T/A]GAGGAATTACAGGTACTCGCCCAGTCTAGAGATAGTCTTGCACATGTATTAAATACTCCGATGTCCTGATTTGATTTGATTCTCAATTTGTTTCAGTGAATACAGAATTGATACAAATGCTGACACTGATTTAGCAGTTTTTTTTTTCAAAGTTAAAGACTGGGGAAGTTTGTATATACAGTTGAAGTCTGAATTATTCGCCCTCCTATGAATTTTGTTTTTCTTTTTTAAATATTTCCCAAATGATGTTTAACAGAGCAAGGATTTTTTACAGGATTTTTTCTTCCTAAGTAAGTCTTATTTGTTTTGTTTCATCTAAAATAAAAACAGTTCTTAATTTTTATATTATTCAATATTATTCAAAATATATTGCTAATTCAATATTATCAATATTATTAACCCCCTTAAGCGATACTTTATTTCGAATGTCTACAGAACAAACCACTGTAATACAACAACGTGCCTAATTACCCTAACTTGCCTAATTAACCTAGTTAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34952
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086653 | Missense | 1654 | 2856 | 25 | 48 |
ENSDART00000086861 | Missense | 1680 | 2882 | 24 | 47 |
ENSDART00000108484 | Essential Splice Site | 1677 | 2876 | 23 | 46 |
The following transcripts of ENSDARG00000061052 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37750105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36562266 |
GRCz11 | 10 | 36506024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCACCAGCAAAATGGACCAGCGCTCCATCAACCGCATCCTCGGAGAG[G/A]TAAACAACAGAGTCTGTGTCATCACATGTGGGGCCAAATCAAATTGTTTT
Long Flanking Sequence:
AAACTCTAAGCCATCTGTATATAAGCAATGTCTTTCTAGAATCAATAAGACTTTGTCTAAATAGTGCGGCTATTAGATGAATGTGGAATGATGTCAATAAACGTAATTATTTAACATTATTTGTTTATTTTTCAATCTAAGGTGTGGTAGTAAGCAGGGTGAAGACGACTACAGGCCGCTCTTTGAGAACTTTGTTCAGGATCTCCTTTCTACGGTTAACAAACCTGATTGGCCGGCTGCAGAGCTACTGCTGAGCCTTCTGGGAAGGCTGCTGGTGAGTTCCGATTGATATTCACAGGTTGATTGCTGGGACACACACTTGAAAGCTGACATTATGCCCTGACTCCTCTCTGTAGGTTCATCAGTTCAGTAATAAGCAGACGGAGATGGCTCTGAGAGTGGCTTCTTTGGATTATCTGGGCACAGTGGCTGCGCGACTTCGCAAAGATGCCGTCACCAGCAAAATGGACCAGCGCTCCATCAACCGCATCCTCGGAGAG[G/A]TAAACAACAGAGTCTGTGTCATCACATGTGGGGCCAAATCAAATTGTTTTATTAGTTTTTAGTAGGGCTGCTTGATATTAGAAAAATCTGACATTGCATATTTAGTTTTGGTGCGATTAAATATTATTTACAATTTCACCGGTTAACTTGAAAACTGTTGGAAAAGAATGGAAAGAATGTATTCATTTAGAATGATTGGGATGATTTTGTAGAGGTGTAAATCATGCATAAAATTTAGTAATTGCAAGCAAGGTCAGCAAAGCAAAGATAAAAGTGAATTCAAGAGTGTTTTATGATTTCGGGGCAGTCAAGTAGCATTCAGGAAAAGACGGGGCCGGAATACGCCGGATCAGGCACCTCTGAAATCTGATCTGGCACCTCATTTTTCCGATCCCCTTCCTCAACAGCCCTCATTCCCCGTCTGCTCTTTACTTTCACTTTCTTTCGCGACTTCCCAACCCCTTCACTTTCATCTGCGACAGCCCTCCATCATGTACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10463
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 |
---|---|---|---|---|---|
ENSDART00000086653 | Nonsense | 2381 | 2856 | 43 | 48 |
ENSDART00000086861 | Nonsense | 2407 | 2882 | 42 | 47 |
ENSDART00000108484 | Nonsense | 2401 | 2876 | 41 | 46 |
The following transcripts of ENSDARG00000061052 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37731716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36543877 |
GRCz11 | 10 | 36487635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTGTCGTCCAATTAGATGAAGGCWGTGGCGGGGATGAAGATGTCATA[T/A]CAGGTGCAGCAGGCCATYGTGGGCTCGAAGGACACTGTGATCAGGGGTTT
Long Flanking Sequence:
TCATTGAACATGTACACATGGACATCACCCATATACCATGTAACTGCAGGTTAACTGTGTTTATATATATATATATATATATATATATATATATATATATACATACATGGATATATATATATGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTACACACGTACACACACACACACACACACACACACACACATATATATATATATATATATACACATATATACATATATATATATATATATATATATATATATATACATATAATAACTTCAACTGTTAAAAGCTATTAGTTACTAGTTAATTAATGAAAGATTTACTTATGGTATCTAATAGCCTTATTTTGATTGTAATGCAATAATGTCCACCTTTTGTTAAGCTGCATTGAAACAATAATTAATGTGAAAAGTGCTATACAATTACAATTGAATTGAATGATGGTGTCGTCCAATTAGATGAAGGCAGTGGCGGGGATGAAGATGTCATA[T/A]CAGGTGCAGCAGGCCATTGTGGGCTCGAAGGACACTGTGATCAGGGGTTTCCGGCTGGACGAGAGCAGCACAGCTCTGTGTTCACATCTGTACACGATGGTGCGCGGAAACAGGCAACACCGCAGGGCTTTCCTCATCTCACTGCTCAACCTGTTCGACGACAACACGGTTAGTTTTTTCTTTCATAACCTCTGTGTAATTAATACATGTGTCAATTTCTACAAATTCCCGTGATCATTAATCCTTAACCTTAATGCAGAGTTTGTAAGGGTTCTGGAAATCCAGGAAAATGCTTGAATCTAGTGTTTTAAGGTTTGGAAAGGAGAAATTTAGGAGAAAAAAAGTGCTTGTAACTGCTTGGATGTGCAATCCTTACTTTCATAATAATTTATTTTGCTGAATAGTTTTCTATTTAAACAAAATACTGTAACCCAAACACAGCGCACACATAGCAACACAACAAAACAAGATGCAACAACACACTATAAACCACACAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31792
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 |
---|---|---|---|---|---|
ENSDART00000086653 | Essential Splice Site | 2618 | 2856 | 46 | 48 |
ENSDART00000086861 | Essential Splice Site | 2644 | 2882 | 45 | 47 |
ENSDART00000108484 | Essential Splice Site | 2638 | 2876 | 44 | 46 |
The following transcripts of ENSDARG00000061052 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37726121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36538282 |
GRCz11 | 10 | 36482040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAACTTTATGAATGGTTTCATTACAAACGCCTCTTTGTCTGTCCCTGCA[G/A]TAAAATTCAGAAGTACTCGCCTACAGAATCTGCAAAGATTTATGACAAGG
Long Flanking Sequence:
GCTGCCAGACAACCCAGAACCCCTGCTGGACTTCGCCAACGCGTCTCAGGGCATCCTCCTGCTCTTGATGCTCAAACAGCACCTCAAAAACCTCTATGGCTTCTCTGACAGGTGAAACACTAATGTTCTGGTGCAATCAGCTTTGACATGCACCGAGCTTGATTTATTTCATGCCCATTTTTAGACTTTTCTTTTCTTTTCAGCTAGAAACCAGAAAACCATCTAACCAACAAAAATGACTCTGGCAAATAGATTAGCCCTCCTGTGATGATTTTATTAAATATTAAATATACAGGAGGATTAATAAATTTGACTTGCTCTGTACATGATCTTGGGCAGGTAGTGTTTTAAATCAGATTGTGTAATTTAACAAATATGACTTGTAGTGACATAAAACGTGCTTCTGGTTTCTAGCCGATCCATCTTTGTATGTGCAATTCTGCTCTCACTATAACTTTATGAATGGTTTCATTACAAACGCCTCTTTGTCTGTCCCTGCA[G/A]TAAAATTCAGAAGTACTCGCCTACAGAATCTGCAAAGATTTATGACAAGGCTGTAAACAGGAAAGCCAACGTGCATTTCAACCCACGGCAGACGCTAGACTACCTGACCAACAGTCTGTCCAATTCAGATCTCAGCAACGATGTCAAGAGGAGAGTCGTCAGACAGTATTTAGATGTAAGCTTTGCCTTTTGTCTTAGCAATTTGCCATATAATAAGGCACAGTTCAGTAGGGATGGATGAATGAAAAGGATTTGAACATTTTCAGTTTTTTGTATTTATTATTGTAACTAAACTTAACTGTATTGATGAAAAATGATGTTTTCAGTTATTATTAGTCATTTCTGTTAGTTTAATATGTATTTTTTTATATTTATAACATAAGTTATATATTTAACAATTTATAAATTTATAAGTTATAAGTTTAACAATTTTTAAACGTATAAAACTAGTGATTGTTTTTCAACTTTCAACTTATTGATTTTAATCATATTACAAAACT
Associated Phenotype:
Not determined