Busch Lab

ZMP

HNRNPUL1 (1 of 2)

Ensembl ID:
ENSDARG00000079780
Description:
heterogeneous nuclear ribonucleoprotein U-like 1 [Source:HGNC Symbol;Acc:17011]
Human Orthologue:
HNRNPUL1
Human Description:
heterogeneous nuclear ribonucleoprotein U-like 1 [Source:HGNC Symbol;Acc:17011]
Mouse Orthologue:
Hnrnpul1
Mouse Description:
heterogeneous nuclear ribonucleoprotein U-like 1 Gene [Source:MGI Symbol;Acc:MGI:2443517]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa33744 Nonsense Mutation detected in F1 DNA Not yet available
sa10200 Essential Splice Site Available for shipment Available now
sa25316 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa26603 Nonsense Mutation detected in F1 DNA Not yet available
sa17734 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa33744
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
ENSDART00000113508 Nonsense 242 875 4 16
Genomic Location (Zv9):
Chromosome 5 (position 64864487)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 61139131
GRCz11 5 61801868
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGACCGACACAGCTCACATAGTCGTAAAAGATCCCATGATGAGAGT[C/T]GAGGATATGGCTACTACGAGCACCGTGAAGAAAGAAGGTCAGTTCTGTGT
Long Flanking Sequence:
ACCCAGACGGAAACATGAATAACATCCTCGTGAGAAAACAGCATTCTTGAAAGTGCAATGTTTACATTTTGCATTTTGTTTAGCCATATTAGTTATTTTTATGTCAAACCTGTAATCATTTGTTTTTTAAAAGTGTTTTATATTTTATTAATATTTTACATCACATATCACATGAATGATTAAATGTGTGTGTGTGTGTGTGTGTATAAGTGTGTGTGTGTGTGTATATATATATGTATGTGTGTATATATATATATATATATATATGTATGTGTTTATGTACACACATTTTAATGTAGAAAGAAATAGTTGTTCACATGTGGCCTATAACTTTTTCCTTTTCCCAACCTTTTACAGGGCGTTATGATGTGAAGTCCGAGTATAAGGCTGATGAGGATGCACCACAGCAGGCTGAGCGGTCCAGCGAGTGGGATGCACAGGCCAAATCAGAGGATGACCGACACAGCTCACATAGTCGTAAAAGATCCCATGATGAGAGT[C/T]GAGGATATGGCTACTACGAGCACCGTGAAGAAAGAAGGTCAGTTCTGTGTGCTTGGGACTACTTTTTTGTGTTGCTCAATCTGACTGTTCCTTTGGTTGTTATAGGGGAAGATCACCTCAGCCTCCAGCTGAAGAAGAAGAGGAAGACATTGATGATAATCTTGTTGTAATTGACACCTGTGAGTATAAAGAGTTTTTATTTTGTTAACTGAGCCTTCATTTGCAAAGCTGTTTTGTGTGTGTGTTAGAAATACAATTAATCCTATTCCGTACTTGTACTCTTTCTTTTTAAAAATAGCAGAGTGCTCAGTGTTTGTGTTCACACAATGAAGCATTGACTGTTGCAGAGAGAGAGCACAGTGTAAATACTTAGAGATGTCTGAGCTCTGTTTTGCACTATGTAGCAAAATCTGTTTTCATCAACCCAATCATAGGTGTAAACAGAGTTTAAGGATGTACTCACTCTAGGCATGGTTGCCTTGAACTGAGTGCACCTTTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10200
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113508 Essential Splice Site 254 875 4 16
Genomic Location (Zv9):
Chromosome 5 (position 64864526)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 61139170
GRCz11 5 61801907
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGAGAGTCGAGGATATGGYTACTACGAGCACCGTGAAGAAAGAAGG[T/G]CAGTTCTGTGTGCTTGGGAYTAYTTTTTTGTGTTGCTCAATCTGACTGTT
Long Flanking Sequence:
AGCATTCTTGAAAGTGCAATGTTTACATTTTGCATTTTGTTTAGCCATATTAGTTATTTTTATGTCAAACCTGTAATCATTTGTTTTTTAAAAGTGTTTTATATTTTATTAATATTTTACATCACATATCACATGAATGATTAAATGTGTGTGTGTGTGTGTGTGTATAAGTGTGTGTGTGTGTGTATATATATATGTATGTGTGTATATATATATATATATATATATGTATGTGTTTATGTACACACATTTTAATGTAGAAAGAAATAGTTGTTCACATGTGGCCTATAACTTTTTCCTTTTCCCAACCTTTTACAGGGCGTTATGATGTGAAGTCCGAGTATAAGGCTGATGAGGATGCACCACAGCAGGCTGAGCGGTCCAGCGAGTGGGATGCACAGGCCAAATCAGAGGATGACCGACACAGCTCACATAGTCGTAAAAGATCCCATGATGAGAGTCGAGGATATGGCTACTACGAGCACCGTGAAGAAAGAAGG[T/G]CAGTTCTGTGTGCTTGGGACTACTTTTTTGTGTTGCTCAATCTGACTGTTCCTTTGGTTGTTATAGGGGAAGATCACCTCAGCCTCCAGCTGAAGAAGAAGAGGAAGACATTGATGATAATCTTGTTGTAATTGACACCTGTGAGTATAAAGAGTTTTTATTTTGTTAACTGAGCCTTCATTTGCAAAGCTGTTTTGTGTGTGTGTTAGAAATACAATTAATCCTATTCCGTACTTGTACTCTTTCTTTTTAAAAATAGCAGAGTGCTCAGTGTTTGTGTTCACACAATGAAGCATTGACTGTTGCAGAGAGAGAGCACAGTGTAAATACTTAGAGATGTCTGAGCTCTGTTTTGCACTATGTAGCAAAATCTGTTTTCATCAACCCAATCATAGGTGTAAACAGAGTTTAAGGATGTACTCACTCTAGGCATGGTTGCCTTGAACTGAGTGCACCTTTAGTCAATATCAGGTTTGCGTAAAGTTACAATTAATTGCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25316
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
ENSDART00000113508 Essential Splice Site 526 875 10 16
Genomic Location (Zv9):
Chromosome 5 (position 64869139)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 61143783
GRCz11 5 61806520
KASP Assay ID:
554-7675.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAAGTTCAACATCCTGGGCACCAATGCTATCATGGAAAAGATGAAG[G/A]TATGGGTGTTGAATATTTCTAATATTATTATTATGTAGATATATATAATA
Long Flanking Sequence:
TTTAACACTTATGTTTATTTTATCATAAAGAGATTAGATATGTTGTTTAAATATTTATTTTTTACTGTTAAACCTATCTGCCTTTGTAATGTTGGTAAATTAAATAAAGTGGTTAAAAATCCTAATAAACCTAAATGAATTGGTAAAAAATATTCAATAGTTCTGATACCGAATGATATGAAACATGATAATGTGTTTTTTTTTTTTTTTTTTGCAATATCGCCCAGGCCTACAGTACTGTAATAATTGCATTATAACGTGTAATGTTTTGTACATGACAAACTCCAGTGTTTCGATTTACAATATGTGATCAGTAGACAGATAATGGTAGTACTTGAAAAAAATATGGTCTCTTTCTTTTTTTTTTTTACTCTCAGATCCTGATGATGGTTGGTCTGCCTGGTAGTGGAAAAACTACTTGGGCCCTAAAATATGCAAAAGAGAACCCTGAAAAGAAGTTCAACATCCTGGGCACCAATGCTATCATGGAAAAGATGAAG[G/A]TATGGGTGTTGAATATTTCTAATATTATTATTATGTAGATATATATAATATATTATTAGTGTGTTTGTGTGTGTTAAATGTATAAAAAAAATTATAAGGCCAATTTGTTGAGATTAAAAATGTATCATTGCTAATCTTTAGGCATTTAATTATAATGCAGATTTTTTTTATTGTGACAGCCCTAAATATTATAGCAACTGTGCATGGTAATGTAATAGGCATGGTATACCGCTGGTTTGGAAAAGTCAAGGTTTAAAATTTTCTGTTATACCGTTCTCAAGGTATGTGTATGATTTTTTTTTTATTTACATTTTTTTTTTTAAAACCACAGCAACTCCAGCAGAAAAGATATCCAAAGATGGCATTTTAAATTGTAAAGAAATCTGTGTTCTCCAAACATATTGCTCCAAAATATTTTAAATCTTTCACAAAATAAAATAAATTGTGTTCAAAGGAGAAAAAAAAGTTGTTGTTTTTTTACACAGACATTTAAGAAGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26603
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
ENSDART00000113508 Nonsense 579 875 12 16
Genomic Location (Zv9):
Chromosome 5 (position 64875538)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 61150182
GRCz11 5 61812919
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTCTTGTCACCATTGCTAGACAAATGTATATGGATCAGCCCAGAGA[C/T]GAAAAATGCGTCCTTTTGAAGGTTTTCAACGCAAGGCTATTGTAATTTGT
Long Flanking Sequence:
TTGATTTTAGTTTCTGTTTTACCAATTGTTTGGTTTCAGAGTAAACAGAAGGCTGTAAAACTAAGATGTCAAATCCTGAATTCATTTATTGTTTAGTGTTTTTTTTTTTTTTTTTTTTTTTTAAGACTTGCATGTTGAGTAGTGCCATGAGACAATTGTTTCTACATTAACATATCCATAAGAGACTACCTTCCTTTAAGCCATTAGTTTAGTTGAGGGAAGAAGAAAGGGTCCCCTGTACAATGTCAGTCATTTAATCTACCTTGTGTTGACCTCTTGCCTATTCACGGTAAGTCAGTTGGGGTTGTGAGAGACAACCGCTAGTTATTCCAGAGCAGTAACTATAGACATGAAAGAAAAAAAACTCTCTCACTTTCATCGTTGCAGGAATCCAATTCCCCTCCTACGGAACGCAAAGCCGTAACAAAGCAAATAATGAACAGCTTCTACTTTTTTCTTGTCACCATTGCTAGACAAATGTATATGGATCAGCCCAGAGA[C/T]GAAAAATGCGTCCTTTTGAAGGTTTTCAACGCAAGGCTATTGTAATTTGTCCCACGGATGAGGATTTAAAAGATCGAACGTTAAAGCGAACTGATGAGGAAGGGAAGGATGTTCCCGATCATGCTGTATTAGAAATGAAAGGTAGGAATGCCATGGATAAAACCAAAACAAATGTTCAAAACTACACACCAGATCTGCTTTTGCTGTTTTTATTTTGTTGTTTGTTTCTTTATTTTAAGACTTGGAAGAACCCACCCGTCCCTCCTTCTGTTAAACCTTTTTGCCAGATAAAAGAGCTATTCTCACCTTTTTTCCCCATTTCTCCCTGCCCTTTTAACCACATCTTTTGCATCGTCTGTCATGCCACTCCTCACCAACTGCAAACCAGTTCAGATAATCAGGATTGAGGAAGAGAATTGCTGTAATTGGCTCTGGCGCTACAATTCACTTCAGCAACCGAGCAGTTTGTATTGGCCGTAATGTTAAATGTTGAATAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17734
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
ENSDART00000113508 Nonsense 855 875 16 16
Genomic Location (Zv9):
Chromosome 5 (position 64881710)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 61157200
GRCz11 5 61819937
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCAGTGGCAGCAGTACTACCAGAACCAGAGCCAGTGGAACCAGTACTA[T/A]AACCAGTACGGCGGTTACGGCAACTACCAGCAGGGAGCTCAAGGCAGCCA
Long Flanking Sequence:
CAGGTACAGATGCTATAAAGGCACCAGGTTTCGGTACCCAACCCTAATTTTGGCCAGATATTTTTCTAAAACCGGGATCACCAAACTTAAAAAAAAATATCACAATGTCAGCTTTTTCCAGTATCCTGCAGCCCTAATCATGAGTAAATTTCTTCCAACCATTAAAAAATGTTCTATATAATATTAATTTAACTAAATTGAACATAGCCAATATGCAATGCATTTGTCTTGTTGACAATGTATGCATTTTCCCCTATTTAAATTCACACATTCATTATTTTGTCAATTACTCCTCTGAATGCTCAGTTGTAAGGAAAATGAAAATTCTGGGCAGAAACTAATAATTCTGCCAACTATACACCGCACACACCTGGTCAGACACTGTTCAGTATTGTGTTATCGAAGCATGTGTTTATTTACACACTGTATCTTTGCTTTCCTCAGTATGCTCAGCAGTGGCAGCAGTACTACCAGAACCAGAGCCAGTGGAACCAGTACTA[T/A]AACCAGTACGGCGGTTACGGCAACTACCAGCAGGGAGCTCAAGGCAGCCAGGGAGCCCAGGGAACACAGTAGTAGCAGCAGCATCAGCGCCGTCTCCTGCAGCCCATTCCCTAAGCAGCATTCCTCAAGCCTTTTCCCTCATCCTTCCCAGTCTTACCTTTTTCTTCGCCCGCGTAACCATTTATCCGCTCCCTATTTATGCCAACCCTAAAGATAACCACACTTCTGTGGACCTCCATTGCTCTCTTTGAGTTTTGGTGACAGGTGTCCCTTTTTTTTGCTCTTCTACTAAATATTTGTTTACATAAAGCTTTGTTTTCCCCCCTCTATGTGTACTTGTAGATGAGAGATTTTGAATTTAGTAACGTGTGGTTTAGTCGACTCCAAAACTGCTCACACACTATGATGTGCTTGAATGTTTCGAAAATAGAGCAGGAAATATTGAGGAAGCTTTGCTTGCTTGCATTTACATCTGATGTATAGAGAAAGAGGCAGGGTGT
Associated Phenotype:
Not determined