Busch Lab

ZMP

hnrnpl2

Ensembl ID:
ENSDARG00000059303
ZFIN ID:
ZDB-GENE-040426-2707
Description:
heterogeneous nuclear ribonucleoprotein L2 [Source:RefSeq peptide;Acc:NP_998548]
Human Orthologues:
AC027139.1, HNRNPL
Human Description:
heterogeneous nuclear ribonucleoprotein L [Source:HGNC Symbol;Acc:5045]
Mouse Orthologue:
Hnrnpl
Mouse Description:
heterogeneous nuclear ribonucleoprotein L Gene [Source:MGI Symbol;Acc:MGI:104816]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa22584 Essential Splice Site Available for shipment Available now
sa8434 Nonsense Mutation detected in F1 DNA Not yet available
sa28401 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22584
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
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051180 Essential Splice Site 234 481 None 13
ENSDART00000102471 Essential Splice Site 234 499 None 12
ENSDART00000142334 Essential Splice Site 234 522 None 13

The following transcripts of ENSDARG00000059303 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 5689153)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 5807490
GRCz11 15 5795341
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGACCAGGACACATGGGACTACACCAATCCGAGCCTGGGCACTCAAGG[T/G]ACTGTTAACCTTACTTCTGCTTTAGCATTTGTCAGCGCCCTTACTGCCAC
Long Flanking Sequence:
ATGCTCAGCAAAGTCTAATGTGAGATTACATTACTTTTGGTCAAGTGAAAAAGATAGTTTGAGAGTTTTAATTTAAGCTGTGTATTTAAAAAAAAAACCTCTGGATTTAAAATGTTTTATTTTAGCTTTGTGCATTTTTTTAATCAATTTGAAAATGGGTAAATATATAGTTAAGAAAACACATTTCGTAATTTTTCCTAGAAGTAGATACATTTGGACAGTAAGTGTCATATTCAGAAGTGTGATGGCTGTAATTATGGCTTGCCAGAATCTTCTCTCAGTGATTCAATGAATCATTACTTTGTGTAATAAATGAAAGTGTCTGCTGGGGAAAGATTTCAAATAATTTGGCAACAAACAAATAATATCTGCTGGTTATGTCAGTAATTAAAAATCTAAATAAAACTGTTTGTTTTGTGATTTAAGCCAACACGCCTTAATGTGTTCAAGAATGACCAGGACACATGGGACTACACCAATCCGAGCCTGGGCACTCAAGG[T/G]ACTGTTAACCTTACTTCTGCTTTAGCATTTGTCAGCGCCCTTACTGCCACTGTGACGGAAATAAGCGGGTGGGCTTGGGGAATCCTAGAACCGCATTAATAAATCCGCTGTTTCACCTCCCCTGTGCTGAGTGTTAGGCATACCAGCATCTACACAACATGTTGTGCTTGTTCTCGTGACTCTTAAGGGGAGGTCAAATCGTAACACTCTGATCAAACTAAGGCTTCCTCAATGTTATCCTGCTGATATCTTACAGACTTCTTTTTCCAGCAAAGCCTGTCACATGAAGTGTGAGGGGCAAGTGGCTTTTTGGGAAAGCACCATAAACGTGGCCTTATCCATGGACAACCCTGATATCTTTTGATATCAAGAGACTTGATTTAGTCTTTCTGGGTTTATTGGAGCAGAAGGTCTTTAAACAATTAGAGTCGTAAGGTGTGGTGTATTGTTCTATGGAATAACATGAATTGTTTGCCAGAAGTATCCAATTAAAAGTACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8434
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051180 Nonsense 250 481 7 13
ENSDART00000102471 Nonsense 250 499 7 12
ENSDART00000142334 Nonsense 273 522 8 13

The following transcripts of ENSDARG00000059303 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 5684705)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 5803042
GRCz11 15 5790893
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGTGGTTATCCCGGGTACCCAGATGAGAGCTATGGCTATGAGGGYCGA[C/T]GAATGGGACCTCCTATGAGTGCTCCAAGGCGAGGTGGAGCCAGCCAGCGC
Long Flanking Sequence:
TTTCTGATATTCTGTGTGTCCCCTTTTTGCTGATCTTTAAACAAAGTCAGTGTCCTGGCCTGTCATCTCTTAGCAAACTCATCTATCACCTTCTCTGCCCCCCCTCTCTCTCTTTTACCCCGTCCCCCTTTCTTTTCTTGACCTTCTTTCTTTCTTCACCTCTTAGATATGAACGCCAACCCCAACAAGCGCCAGAGGCAGCCGGCTCTGCTGGGAGACCACCCTCCAGAGTATGGTAAGGCTTGCGGGGGCACACGCGCTAACACATTTGCCTCATTTGCTCGCAAATCAGGGGAGTGAATGTTAAAGCGACAACAAGTTGGGGTGTACTTATCACAGTGGCAGCAAGATGGTGCTGTGTTGATGTTAAAACTTAACGTGTAGTGTAAAATGTGTTTGCCCACCTGCAGCAACTCACCCCATGTGTTCTGTTTTTTCGTTTGTGAAATTCAGGTGGTTATCCCGGGTACCCAGATGAGAGCTATGGCTATGAGGGTCGA[C/T]GAATGGGACCTCCTATGAGTGCTCCAAGGCGAGGTGGAGCCAGCCAGCGCTACAGCGCACAGTATGGTGGTCCTCCACCACCACCTCCGGGGGAGTATGGCGCACATGCAGACTCACCTGTGATCATGGTGTACGGTCTGGATCCCGTAAAAATAAACGCTGACAGGGTCTTCAACATCTTCTGCCTTTATGGCAATGTGGAACGGGTATGTAATACTTTTTTTGTTTCCAGCAATTCTGTCGGACCATTATTGCAGGATGTTCTGCTTTATGGGATTTGAGATTAGCTCAGAAATTGATAATGATCATTAACCATTTTCTTTTAGGATACATGTTGACTAAGGGTGTCACGATTTCAATTTTAAATTGAAATCGATCGAAATTTATGCTCAATTTCGATTATCGAATCAAAAAATAGAATTGTCGATGCTGCCACGCCCCCATGTCACGTCAGCTTGGCTTGCCAAGCGGTAAAAAAACAGGCTTGTTGAAGTGCTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28401
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051180 Splice Site None 481 None 13
ENSDART00000102471 Nonsense 260 499 7 12
ENSDART00000142334 Nonsense 283 522 8 13

The following transcripts of ENSDARG00000059303 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 5684675)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 5803012
GRCz11 15 5790863
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTATGGCTATGAGGGTCGACGAATGGGACCTCCTATGAGTGCTCCAAGG[C/T]GAGGTGGAGCCAGCCAGCGCTACAGCGCACAGTATGGTGGTCCTCCACCA
Long Flanking Sequence:
TGATCTTTAAACAAAGTCAGTGTCCTGGCCTGTCATCTCTTAGCAAACTCATCTATCACCTTCTCTGCCCCCCCTCTCTCTCTTTTACCCCGTCCCCCTTTCTTTTCTTGACCTTCTTTCTTTCTTCACCTCTTAGATATGAACGCCAACCCCAACAAGCGCCAGAGGCAGCCGGCTCTGCTGGGAGACCACCCTCCAGAGTATGGTAAGGCTTGCGGGGGCACACGCGCTAACACATTTGCCTCATTTGCTCGCAAATCAGGGGAGTGAATGTTAAAGCGACAACAAGTTGGGGTGTACTTATCACAGTGGCAGCAAGATGGTGCTGTGTTGATGTTAAAACTTAACGTGTAGTGTAAAATGTGTTTGCCCACCTGCAGCAACTCACCCCATGTGTTCTGTTTTTTCGTTTGTGAAATTCAGGTGGTTATCCCGGGTACCCAGATGAGAGCTATGGCTATGAGGGTCGACGAATGGGACCTCCTATGAGTGCTCCAAGG[C/T]GAGGTGGAGCCAGCCAGCGCTACAGCGCACAGTATGGTGGTCCTCCACCACCACCTCCGGGGGAGTATGGCGCACATGCAGACTCACCTGTGATCATGGTGTACGGTCTGGATCCCGTAAAAATAAACGCTGACAGGGTCTTCAACATCTTCTGCCTTTATGGCAATGTGGAACGGGTATGTAATACTTTTTTTGTTTCCAGCAATTCTGTCGGACCATTATTGCAGGATGTTCTGCTTTATGGGATTTGAGATTAGCTCAGAAATTGATAATGATCATTAACCATTTTCTTTTAGGATACATGTTGACTAAGGGTGTCACGATTTCAATTTTAAATTGAAATCGATCGAAATTTATGCTCAATTTCGATTATCGAATCAAAAAATAGAATTGTCGATGCTGCCACGCCCCCATGTCACGTCAGCTTGGCTTGCCAAGCGGTAAAAAAACAGGCTTGTTGAAGTGCTTGTTAAACTGCAGAAGCAGGAGACCCGTCGACA
Associated Phenotype:
Not determined