Busch Lab

ZMP

ggnbp2

Ensembl ID:
ENSDARG00000055086
ZFIN ID:
ZDB-GENE-060929-52
Description:
gametogenetin-binding protein 2 [Source:RefSeq peptide;Acc:NP_001073430]
Human Orthologue:
GGNBP2
Human Description:
gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:19357]
Mouse Orthologue:
Ggnbp2
Mouse Description:
gametogenetin binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2387356]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa9478 Nonsense Available for shipment Available now
sa18795 Nonsense Mutation detected in F1 DNA Not yet available
sa17293 Missense, Splice Site, Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9478
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
ENSDART00000077399 Nonsense 72 681 4 14
ENSDART00000105832 None None 350 None 11
ENSDART00000112134 Nonsense 72 679 3 15
ENSDART00000113627 None None 354 None 11
ENSDART00000121415 Nonsense 105 708 4 13
ENSDART00000077399 Nonsense 72 681 4 14
ENSDART00000105832 None None 350 None 11
ENSDART00000112134 Nonsense 72 679 3 15
ENSDART00000113627 None None 354 None 11
ENSDART00000121415 Nonsense 105 708 4 13

The following transcripts of ENSDARG00000055086 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 4032029)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 3691698
GRCz11 5 4024733
KASP Assay ID:
2259-5359.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTCTCCAGCATCACAGCATGCTAAAGCAGCAGGACCTGAACATGGCGT[T/A]GATGGTGATGTCRCGYGAAGTGTTCAACGCTCTGTCTCAGTCGGTGCCGT
Long Flanking Sequence:
TTTTCCACAGATTTTCCAGAAACTTTTAGCCTATCATTAATTCTGTTTATTTACTTGAGTAAATATGTGTAAATCTATATTTATTCAGTTTTGAAAATATTTACAGTAATATTATTGAATAATATGAAAATATTCATATGATTTATTTACAATGCAGTTTGTAAAGTAATATTTTCTGTCTTTTAGTTGATATGTTATATGAGAGACTTGCTTTGTTTACCAAGGAAAGTGGACATAAAGAACACTTTCTGAACACTGGAGGATTCTTGGAGTGAACCTATAAGAAAGTGCCTTGGCAGTTGTTGTGTACAGTTTAACCACAGCTACTCTCAAAGCATCATGGGGCATAGCAATAAAGTAGATTTGAGAGAGAGTTTTTATTTTTCAATTTTTTTAATTAATTAATTAATTTTTTTTAAAGTTTCCATCTTGACTGTACCCGCTGTGTTTTGTTCTCCAGCATCACAGCATGCTAAAGCAGCAGGACCTGAACATGGCGT[T/A]GATGGTGATGTCACGCGAAGTGTTCAACGCTCTGTCTCAGTCGGTGCCGTGTGTGGGCTGTCGGCGCAGCGTGGAGCGGCTCTTCTCTCAGCTCACAGACTCTGGCTATTTTGCGCTGGAACCGCTCACTGTGGGATCATCTGGAGTGCTTTCAGTCACACGCGCATGCATCACAGACCCCAGGAAGCTCTACACACTCTTTTATGTTCATGGGTAAGTGGTACAGACTCTGTTTAGGGTCCAGATGAAGTCAATCTAAAATCATTATTTAGAAAAACTTGTATTTTATCAATGCAAATTATTTAAAGGGATAGTAAAAGGGATAATTTTTTTTCTATTATACCAAAAAAAAGTCAAAGGCTCAAAATCATACAATTTTTAAGTGCATGAAAACTTTTTTTGCCTGCAGTGCCTTTCCTTCAAGAAATTATTTTAAGCTATTATTCATCATCATGTCCTCACTGGGCAATAAAATGCTATTATTCATAGTCGAAGCCTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18795
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
ENSDART00000077399 Nonsense 72 681 4 14
ENSDART00000105832 None None 350 None 11
ENSDART00000112134 Nonsense 72 679 3 15
ENSDART00000113627 None None 354 None 11
ENSDART00000121415 Nonsense 105 708 4 13
ENSDART00000077399 Nonsense 72 681 4 14
ENSDART00000105832 None None 350 None 11
ENSDART00000112134 Nonsense 72 679 3 15
ENSDART00000113627 None None 354 None 11
ENSDART00000121415 Nonsense 105 708 4 13

The following transcripts of ENSDARG00000055086 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 4032029)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 3691698
GRCz11 5 4024733
KASP Assay ID:
2259-5359.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCTCCAGCATCACAGCATGCTAAAGCAGCAGGACCTGAACATGGCGT[T/A]GATGGTGATGTCACGCGAAGTGTTCAACGCTCTGTCTCAGTCGGTGCCGT
Long Flanking Sequence:
TTTTCCACAGATTTTCCAGAAACTTTTAGCCTATCATTAATTCTGTTTATTTACTTGAGTAAATATGTGTAAATCTATATTTATTCAGTTTTGAAAATATTTACAGTAATATTATTGAATAATATGAAAATATTCATATGATTTATTTACAATGCAGTTTGTAAAGTAATATTTTCTGTCTTTTAGTTGATATGTTATATGAGAGACTTGCTTTGTTTACCAAGGAAAGTGGACATAAAGAACACTTTCTGAACACTGGAGGATTCTTGGAGTGAACCTATAAGAAAGTGCCTTGGCAGTTGTTGTGTACAGTTTAACCACAGCTACTCTCAAAGCATCATGGGGCATAGCAATAAAGTAGATTTGAGAGAGAGTTTTTATTTTTCAATTTTTTTAATTAATTAATTAATTTTTTTTAAAGTTTCCATCTTGACTGTACCCGCTGTGTTTTGTTCTCCAGCATCACAGCATGCTAAAGCAGCAGGACCTGAACATGGCGT[T/A]GATGGTGATGTCACGCGAAGTGTTCAACGCTCTGTCTCAGTCGGTGCCGTGTGTGGGCTGTCGGCGCAGCGTGGAGCGGCTCTTCTCTCAGCTCACAGACTCTGGCTATTTTGCGCTGGAACCGCTCACTGTGGGATCATCTGGAGTGCTTTCAGTCACACGCGCATGCATCACAGACCCCAGGAAGCTCTACACACTCTTTTATGTTCATGGGTAAGTGGTACAGACTCTGTTTAGGGTCCAGATGAAGTCAATCTAAAATCATTATTTAGAAAAACTTGTATTTTATCAATGCAAATTATTTAAAGGGATAGTAAAAGGGATAATTTTTTTTCTATTATACCAAAAAAAAGTCAAAGGCTCAAAATCATACAATTTTTAAGTGCATGAAAACTTTTTTTGCCTGCAGTGCCTTTCCTTCAAGAAATTATTTTAAGCTATTATTCATCATCATGTCCTCACTGGGCAATAAAATGCTATTATTCATAGTCGAAGCCTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17293
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:
Missense, Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077399 None 537 681 12 14
ENSDART00000105832 Missense 321 350 9 11
ENSDART00000112134 Splice Site, Nonsense 528 679 12 15
ENSDART00000113627 None 210 354 9 11
ENSDART00000121415 None 570 708 12 13

The following transcripts of ENSDARG00000055086 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 4054329)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 3713998
GRCz11 5 4047033
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCTGAAGACAGCACAAAGGGCAAAAACAAAAAGAAGAAAAGAAAAAA[C/T]AAGGGCACACTTTGCAGAAAYGAGATCGTGAGTTGTTNNTNNNNTGTNNNTTTT
Long Flanking Sequence:
AAGTCATTCTCTATTTTCTAATAATCAATAAAGAAACATTCATTTAATAATAAAAAGGAATAAGCCATTCAAATAAAGAGCTCAGTCAGCAGATGGCGGGCGGGTGCGGTTTTAAAAATTGGTCAATGTTAGTGCGGATGGATGGCGGACGGATGATGAGTTTTGTGATGCGGTTGCGGATGAAATAATAGCCCATCCGCGCATCTCTATTACAAACACCTCGCTTAAGCAGTAAGATGCTGATGAGTGTTAAACGCATCATAACAGTCTTGTGAAAAGGGGCCAATATAATTATTACTGTTTTAAACCGAGGATTCCTTTGATTGATTGATTGATTGATGCTGATGATGATGATGCTAATGTCTGTCTCCAGGTGAATTCTCCTGCATTCACCGCTGCTCAGAGGAGAAGGAGGAGGACGCTGTGGACAGCTGTGTGGAGTGCTGGGCCAACTCTGAAGACAGCACAAAGGGCAAAAACAAAAAGAAGAAAAGAAAAAA[C/T]AAGGGCACACTTTGCAGAAACGAGATCGTGAGTTGTTGTTTGTTTGTTTTTTTGTCCCATTTTTTTTGGATACAAAAATACATATTGACAATCGGTCATAAACTAAAATTCTAGTCTTTAGTGACGAGCCAGCACTGGCAATTTAAAAATGCTTTTCATCCAGTCAAAGTGACTAGTGTGTGCGGCTGTCTAACCTGCCACAACTGAAATCTTCACACATTTAATGGGTTGGCGGGTGTTAATGTCAAGCCCTGGGGCCTGTTTCAGAAAGGAGGTTAACTGAAAACTCAGAGTATTTTAACCCTGAAATGAGAGAAATTCTGGGTTTTGCGTTTCAAAATGGCAGGTTTGTTAAACTCGAGAAAGCAGGGTAAGTCAAGCCAGGTTTTATTCTCTAAACTCAGAGTTTCTGTCGGTCTCCTCCCCTTTTTTAAAGACGAAGCGGTATTTCTCGCCTTAGCCTTACGTTTCATTTTGGATACGTGCATAAAAACGATTGA
Associated Phenotype:
Not determined