Busch Lab

ZMP

gnl2

Ensembl ID:
ENSDARG00000053225
ZFIN ID:
ZDB-GENE-040426-2317
Description:
guanine nucleotide binding protein-like 2 (nucleolar) [Source:RefSeq peptide;Acc:NP_998389]
Human Orthologue:
GNL2
Human Description:
guanine nucleotide binding protein-like 2 (nucleolar) [Source:HGNC Symbol;Acc:29925]
Mouse Orthologue:
Gnl2
Mouse Description:
guanine nucleotide binding protein-like 2 (nucleolar) Gene [Source:MGI Symbol;Acc:MGI:2385207]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa8829 Nonsense Available for shipment Available now
sa9463 Nonsense Available for shipment Available now
sa36199 Nonsense Mutation detected in F1 DNA Not yet available
sa36200 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa8829
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075222 Nonsense 108 726 4 16
ENSDART00000125722 Nonsense 108 725 4 16
ENSDART00000130827 None None 726 None 16
ENSDART00000134642 None None 261 None 8
ENSDART00000075222 Nonsense 108 726 4 16
ENSDART00000125722 Nonsense 108 725 4 16
ENSDART00000130827 None None 726 None 16
ENSDART00000134642 None None 261 None 8

The following transcripts of ENSDARG00000053225 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 36210384)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33951010
GRCz11 16 33905040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTGCAGAAGTTTCAGGAAGAAATGAAYGCGGTGAAGAAAGATCCATAC[C/T]GAGTGGTGATGAGACAGAGCAAACTACCAATGTCCTTGCTGCATGACCGG
Long Flanking Sequence:
TCACCTAAAATGACTGTACTTTACACATTTGCCACAGACCGAGTCAAGGGAGCTGGAGGAAACAACATGAGGGACCGAGCAACTATAAAGCGCCTGAATATGTACAGACAAAAGCAGAGATGGTAAATATTTGACCTGTCATTTACAAAAATACTAAATGTTGGAGATTGAGAATAGTAGTGAACAATTATACATTGTATCAGATTATAATGAAGTGTTTTTTTTATTCACTTACAGTAACAGTCGAGGTAAAGTCATCAAACCTTTGCAGTACCAGAACACAGTCGCTCCTGGAACTGTGGCCAGAGTTGAGCCCAACATCAAGTGGTTTGGTAAGAGGAGTACATTTTAGAGTTTGCCATCTTTTCCAGGTATGTTTAAGATCTGAATATATCAGTATTGCTTTGCTTTTCTCTTTTGCAGCCAACACAAAAGTCATCAAGCAGTCGTCCTTGCAGAAGTTTCAGGAAGAAATGAACGCGGTGAAGAAAGATCCATAC[C/T]GAGTGGTGATGAGACAGAGCAAACTACCAATGTCCTTGCTGCATGACCGGATAAAAGCACACGTGAGTATGAAAACACCTTTGTTTATTTTTATACACAGAAATCATTGTTAAATGCGTGTATAGCGCCAATGTATAGTAAATTTAGTGTTTATTTTGTTAGCTCACATTGGTTTTCATCAGGTAATCATTAAACCATTAATCCACAGGGGAAAAAAAGTTTGGTTTGGTAATCTTCATCAAAGTCTGAACATTTGTTTCTGCGTTTGGTCCTTCTCTGTTGACGTCAGTTTGACTGCTTCAGCCACATTATTCTTAACCATGCTCCTCTAATGGTTTTCTTTAAGAGAATGATGCACAAAAAGAAAGCCCTTCCTTCTATTAAAAATCCCATTTTAGTTGGAAGTACATCAGAATACTGAAATAATTCTGAAAGTCTCAGCAACTTCCAGTTTACACAGACTAGGGTTGTCAAAAGTTTCAATGTCAGTAGGGCTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9463
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075222 Nonsense 108 726 4 16
ENSDART00000125722 Nonsense 108 725 4 16
ENSDART00000130827 None None 726 None 16
ENSDART00000134642 None None 261 None 8
ENSDART00000075222 Nonsense 108 726 4 16
ENSDART00000125722 Nonsense 108 725 4 16
ENSDART00000130827 None None 726 None 16
ENSDART00000134642 None None 261 None 8

The following transcripts of ENSDARG00000053225 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 36210384)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33951010
GRCz11 16 33905040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTGCAGAAGTTTCAGGAAGAAATGAAYGCGGTGAAGAAAGATCCATAC[C/T]GAGTGGTGATGAGACAGAGCAAACTACCAATGTCCTTGCTGCATGACCGG
Long Flanking Sequence:
TCACCTAAAATGACTGTACTTTACACATTTGCCACAGACCGAGTCAAGGGAGCTGGAGGAAACAACATGAGGGACCGAGCAACTATAAAGCGCCTGAATATGTACAGACAAAAGCAGAGATGGTAAATATTTGACCTGTCATTTACAAAAATACTAAATGTTGGAGATTGAGAATAGTAGTGAACAATTATACATTGTATCAGATTATAATGAAGTGTTTTTTTTATTCACTTACAGTAACAGTCGAGGTAAAGTCATCAAACCTTTGCAGTACCAGAACACAGTCGCTCCTGGAACTGTGGCCAGAGTTGAGCCCAACATCAAGTGGTTTGGTAAGAGGAGTACATTTTAGAGTTTGCCATCTTTTCCAGGTATGTTTAAGATCTGAATATATCAGTATTGCTTTGCTTTTCTCTTTTGCAGCCAACACAAAAGTCATCAAGCAGTCGTCCTTGCAGAAGTTTCAGGAAGAAATGAACGCGGTGAAGAAAGATCCATAC[C/T]GAGTGGTGATGAGACAGAGCAAACTACCAATGTCCTTGCTGCATGACCGGATAAAAGCACACGTGAGTATGAAAACACCTTTGTTTATTTTTATACACAGAAATCATTGTTAAATGCGTGTATAGCGCCAATGTATAGTAAATTTAGTGTTTATTTTGTTAGCTCACATTGGTTTTCATCAGGTAATCATTAAACCATTAATCCACAGGGGAAAAAAAGTTTGGTTTGGTAATCTTCATCAAAGTCTGAACATTTGTTTCTGCGTTTGGTCCTTCTCTGTTGACGTCAGTTTGACTGCTTCAGCCACATTATTCTTAACCATGCTCCTCTAATGGTTTTCTTTAAGAGAATGATGCACAAAAAGAAAGCCCTTCCTTCTATTAAAAATCCCATTTTAGTTGGAAGTACATCAGAATACTGAAATAATTCTGAAAGTCTCAGCAACTTCCAGTTTACACAGACTAGGGTTGTCAAAAGTTTCAATGTCAGTAGGGCTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36199
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
ENSDART00000075222 None None 726 None 16
ENSDART00000125722 Nonsense 235 725 7 16
ENSDART00000130827 None None 726 None 16
ENSDART00000134642 None None 261 None 8

The following transcripts of ENSDARG00000053225 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 36217799)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33956210
GRCz11 16 33910240
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTAATTATCCAGGTGCTGGATGCTCGGGACCCAATGGGCACACGCTCA[C/T]AAAGCATTGAGACTTACTTGAAGAAAGAGAAGCCTTGGAAACACCTCATA
Long Flanking Sequence:
ACAAGTCTTCGTTCGTTTCAGTACTGAATAAATCAACGTTTTTGACCCAACTGCTGCATGTTTACTTGTCGCCATTAACTGTTGTGATGTTCATATTTAGTTTCTTTCAGAAAGTAATTGTACTCTTCAAAGGTTTTTAGACATAAAAAAGTTGTTTCAGATCATGTGGCTTTTTAAATAACAAGCTTAGTATGCAGCTCAGTACATCCCTATTGGAACTCTTATTGTCTAGAAAATATGTGTCATTAAATACTTCTCACCACAGGGAAGAGGCTCGTGAGGAGATCTTTAAGAAGGGGCAGTCAAAACGGATCTGGGGTGAGCTTTATAAGGTAAATCACTATTTTACATCTTCTTGCTTTTTGACAGTTTTAATAGAATCCATAGTCTTGCCAAATGATACAGCATTCTAAAATAAACCATGTTTTGCACAGGTGATCGACTCTTCGGACGTAATTATCCAGGTGCTGGATGCTCGGGACCCAATGGGCACACGCTCA[C/T]AAAGCATTGAGACTTACTTGAAGAAAGAGAAGCCTTGGAAACACCTCATATTTGTGCTCAATAAATGTGACCTCATTCCCACATGGGTAACGGTAAGAAATGAAAGCAGGGAACTGCACTCTGTGTTCTTATCCTGTTGAGCTGTCCATCTAGGCAGTATTTTAACACATGCTCCTGAAGAGAATGCTGTTCCAAAAGCTTTACAATATACCTTCGCTAGACCACACTTAATATTTAGTGCAGAATTTCCTCATTCTTGTCTAACTAAACCAAAAAATGTTCTTACCCATTATTTGTGTGTGCTGCTGTGCACACTCACTGGCCACTTTATTAGGTACACCTTATTAGCAGGCTAGACCCTCTTTTGCCTTCCGAACTGCCTTAATCCTTCAGATTCAGCAAGGTACTGGAAATATTCCTTAGAGATTTTGGTCCATATTGACATGGCATCAAGCAGTTGCTGCAGATTTTTCGGCTGCACAACCATGATGTGAATCTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36200
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075222 None None 726 None 16
ENSDART00000125722 Nonsense 240 725 7 16
ENSDART00000130827 None None 726 None 16
ENSDART00000134642 None None 261 None 8

The following transcripts of ENSDARG00000053225 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 36217816)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33956227
GRCz11 16 33910257
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGATGCTCGGGACCCAATGGGCACACGCTCACAAAGCATTGAGACTTA[C/A]TTGAAGAAAGAGAAGCCTTGGAAACACCTCATATTTGTGCTCAATAAATG
Long Flanking Sequence:
TCAGTACTGAATAAATCAACGTTTTTGACCCAACTGCTGCATGTTTACTTGTCGCCATTAACTGTTGTGATGTTCATATTTAGTTTCTTTCAGAAAGTAATTGTACTCTTCAAAGGTTTTTAGACATAAAAAAGTTGTTTCAGATCATGTGGCTTTTTAAATAACAAGCTTAGTATGCAGCTCAGTACATCCCTATTGGAACTCTTATTGTCTAGAAAATATGTGTCATTAAATACTTCTCACCACAGGGAAGAGGCTCGTGAGGAGATCTTTAAGAAGGGGCAGTCAAAACGGATCTGGGGTGAGCTTTATAAGGTAAATCACTATTTTACATCTTCTTGCTTTTTGACAGTTTTAATAGAATCCATAGTCTTGCCAAATGATACAGCATTCTAAAATAAACCATGTTTTGCACAGGTGATCGACTCTTCGGACGTAATTATCCAGGTGCTGGATGCTCGGGACCCAATGGGCACACGCTCACAAAGCATTGAGACTTA[C/A]TTGAAGAAAGAGAAGCCTTGGAAACACCTCATATTTGTGCTCAATAAATGTGACCTCATTCCCACATGGGTAACGGTAAGAAATGAAAGCAGGGAACTGCACTCTGTGTTCTTATCCTGTTGAGCTGTCCATCTAGGCAGTATTTTAACACATGCTCCTGAAGAGAATGCTGTTCCAAAAGCTTTACAATATACCTTCGCTAGACCACACTTAATATTTAGTGCAGAATTTCCTCATTCTTGTCTAACTAAACCAAAAAATGTTCTTACCCATTATTTGTGTGTGCTGCTGTGCACACTCACTGGCCACTTTATTAGGTACACCTTATTAGCAGGCTAGACCCTCTTTTGCCTTCCGAACTGCCTTAATCCTTCAGATTCAGCAAGGTACTGGAAATATTCCTTAGAGATTTTGGTCCATATTGACATGGCATCAAGCAGTTGCTGCAGATTTTTCGGCTGCACAACCATGATGTGAATCTCCCGTTTCACCACATCCCA
Associated Phenotype:
Not determined