Busch Lab

ZMP

nap1l1

Ensembl ID:
ENSDARG00000002400
ZFIN ID:
ZDB-GENE-030516-2
Description:
nucleosome assembly protein 1-like 1 [Source:RefSeq peptide;Acc:NP_958475]
Human Orthologues:
NAP1L1, NAP1L2, NAP1L3, NAP1L5, NAP1L6
Human Descriptions:
nucleosome assembly protein 1-like 1 [Source:HGNC Symbol;Acc:7637]
nucleosome assembly protein 1-like 2 [Source:HGNC Symbol;Acc:7638]
nucleosome assembly protein 1-like 3 [Source:HGNC Symbol;Acc:7639]
nucleosome assembly protein 1-like 5 [Source:HGNC Symbol;Acc:19968]
nucleosome assembly protein 1-like 6 [Source:HGNC Symbol;Acc:31706]
Mouse Orthologues:
Nap1l1, Nap1l2, Nap1l3, Nap1l5
Mouse Descriptions:
nucleosome assembly protein 1-like 1 Gene [Source:MGI Symbol;Acc:MGI:1855693]
nucleosome assembly protein 1-like 2 Gene [Source:MGI Symbol;Acc:MGI:106654]
nucleosome assembly protein 1-like 3 Gene [Source:MGI Symbol;Acc:MGI:1859565]
nucleosome assembly protein 1-like 5 Gene [Source:MGI Symbol;Acc:MGI:1923555]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa15185 Nonsense Available for shipment Available now
sa40202 Nonsense Mutation detected in F1 DNA Not yet available
sa33358 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15185
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011882 Nonsense 76 385 5 15
Genomic Location (Zv9):
Chromosome 4 (position 2231114)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 1486655
GRCz11 4 2369977
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGTGGTGAAAAGACGTGTTAATGCACTTAAGAACCTCCAGGTCAAATG[T/A]GCCCATATYGAAGCTAAATTCTATGAAGAAGTCCACGAGCTGGAGCGAAA
Long Flanking Sequence:
AATTGAGCAATACATCTTAATCAAACAAGCAAGTTTTATTCATGAACTCTAGTTACCAATATGGTTTAATTATCTTCCAGTAACATTTGTTTTCCATGTTTTTATAACTAACTGATGAGTTTATTATGGATTTTGAAACTTGTGTGTGCTTGTTTTGACGCTATTTATAATGTATGGATGAGAAATAACTCTATTTGAATTAGTTGACTGCAAGTAAATACTTTTTCCAAGTGTTTTAGTGTTTATCCCTCAAGTCTGAAATTTCATGTTTTAAAAAGTCTTAAATTTGACACTGAGCTGAAATCTGCAGAAACACTGAGCATTCAAATGTCAGGTCTTTATTGTATTTTATATATATTTATTCAGCCTTTAATCTGTTTTTGAGTCACTGATCTGTGTGATTCTTGTGCTTGTCGACCTCATTTTGTTCATTTTTTGTGCAGTTTACCAAAGGTGGTGAAAAGACGTGTTAATGCACTTAAGAACCTCCAGGTCAAATG[T/A]GCCCATATCGAAGCTAAATTCTATGAAGAAGTCCACGAGCTGGAGCGAAAATATGCAGCTCTTTATCAGCCTCTGTTCGACAAGGTGAGCTTCGAGGACCCACACGTTTCTGTCCTCCAAAAGAAAACCATGCTTTTAGTTTTCCTCCTAAATGCAGTCTCGACCATTTTAACCAGGAAAATTGTGTATAATTTTTTTGAAATATGGAAGGTTTTACAAAATTTCCCTCAATGTACTTTATTCATTTTTTTTTTTACTGTTAATTTATTTCATTTTATTTTAAATCGATGCTTTTTTTAAATTTATGAAATTCCAGTTTCCATCATTTTAATCAGGAAAATATGGGAATTTAACCTCAATATACTTATTCTTTTTTTTTTTACTATTATTTATTTTAAATGTTAATGCTTTTCATCTGAAGTTTCAAATTCCATCATTTTAATCTGGGAAAGATGTTTAGTTTTTCTAGAATAAGAATTTTTAATAAGTTCCCACTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40202
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011882 Nonsense 84 385 5 15
Genomic Location (Zv9):
Chromosome 4 (position 2231090)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 1486631
GRCz11 4 2369953
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACTTAAGAACCTCCAGGTCAAATGTGCCCATATCGAAGCTAAATTCTA[T/A]GAAGAAGTCCACGAGCTGGAGCGAAAATATGCAGCTCTTTATCAGCCTCT
Long Flanking Sequence:
ACAAGCAAGTTTTATTCATGAACTCTAGTTACCAATATGGTTTAATTATCTTCCAGTAACATTTGTTTTCCATGTTTTTATAACTAACTGATGAGTTTATTATGGATTTTGAAACTTGTGTGTGCTTGTTTTGACGCTATTTATAATGTATGGATGAGAAATAACTCTATTTGAATTAGTTGACTGCAAGTAAATACTTTTTCCAAGTGTTTTAGTGTTTATCCCTCAAGTCTGAAATTTCATGTTTTAAAAAGTCTTAAATTTGACACTGAGCTGAAATCTGCAGAAACACTGAGCATTCAAATGTCAGGTCTTTATTGTATTTTATATATATTTATTCAGCCTTTAATCTGTTTTTGAGTCACTGATCTGTGTGATTCTTGTGCTTGTCGACCTCATTTTGTTCATTTTTTGTGCAGTTTACCAAAGGTGGTGAAAAGACGTGTTAATGCACTTAAGAACCTCCAGGTCAAATGTGCCCATATCGAAGCTAAATTCTA[T/A]GAAGAAGTCCACGAGCTGGAGCGAAAATATGCAGCTCTTTATCAGCCTCTGTTCGACAAGGTGAGCTTCGAGGACCCACACGTTTCTGTCCTCCAAAAGAAAACCATGCTTTTAGTTTTCCTCCTAAATGCAGTCTCGACCATTTTAACCAGGAAAATTGTGTATAATTTTTTTGAAATATGGAAGGTTTTACAAAATTTCCCTCAATGTACTTTATTCATTTTTTTTTTTACTGTTAATTTATTTCATTTTATTTTAAATCGATGCTTTTTTTAAATTTATGAAATTCCAGTTTCCATCATTTTAATCAGGAAAATATGGGAATTTAACCTCAATATACTTATTCTTTTTTTTTTTACTATTATTTATTTTAAATGTTAATGCTTTTCATCTGAAGTTTCAAATTCCATCATTTTAATCTGGGAAAGATGTTTAGTTTTTCTAGAATAAGAATTTTTAATAAGTTCCCACTAAATATGCTATTAATATTTTTACTATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33358
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011882 Essential Splice Site 135 385 6 15
Genomic Location (Zv9):
Chromosome 4 (position 2229086)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 1484627
GRCz11 4 2367949
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTGAGTGGAAGCAGGATGAGGAGGAAGAGCTGACAGTAAGTAAGCAG[G/A]TACAGGTGATCCATACCTGCATGCTTTACAAACACTGCCACCGCCTTAAA
Long Flanking Sequence:
TAAATTCCATTAATTCCAATGAGAATTGTTATTGAATGCATAATGAGGAAGAAGAGAAAGCGTTGCTGTTCTAGAAGAGCAGTGCTGTACATTTAAACCGCTTCTATTGACCTGCTGCTTCAGCATTTCCAACTGCAGCAAACACAAACCTGCTGAAAGCCTGTGCTCAATCAAGGACACCAGAGACGAACAACACAACCTGTTTATATTCTCACCTCGGTCATAATGCTTTTACCAGATTTACTCTGCTCAAGCTAAATCTAACAAATGCATCGTTTCAGCAGGAATATTGATTCATATTGTGGTTTGTTCTGTGCATAAACTAACTTGGGAACAGTTGCTTTAGCAGTCATATATTGTGACCTTTTTGCTGTGTAGTTGGCTAAAGCATGGGTGTTTGTGTTTAGCGGAGTGAGATCGTGAGAGCGGCGTATGAACCCACAGATGAAGAGTGTGAGTGGAAGCAGGATGAGGAGGAAGAGCTGACAGTAAGTAAGCAG[G/A]TACAGGTGATCCATACCTGCATGCTTTACAAACACTGCCACCGCCTTAAAAGGACAGTTCGCCCAAAAATACTGACATCTATAGGAAAAACAAATACTGTTCAAGTCAATGGATATTGGTTTTTAGCCATTCTAAATATTTCAATGTTTGTAATTACATGAATTGAGTAATTTTGTTATATTTTTTTGGTGAACTGTTGTTTTAACTGGACGTGCTGATATACATTAATACAATATACCATAAAGAACATGCATATTATCATAGGCACTTAAACATAGTTGAATAATTATTTAAACTTTAAGTACCCTTGAATAATATTCACACACATTGTTCACTTTAATAATATTCATGCTGTAAGACTTGGTCTATTTGCAAATTTTAACAGGCCTGTTGTTTATTAAGCCCGTAATATAAGGCTTTGACATTTAACATTTAATTAACATTTAATTTCAGTATTTTTAATTAGCATTAACTTAGTAACTACAATAAAAAGCTCACTG
Associated Phenotype:
Not determined