Busch Lab

ZMP

si:dkey-18h14.3

Ensembl ID:
ENSDARG00000037154
ZFIN ID:
ZDB-GENE-100922-42
Human Orthologue:
HIVEP3
Human Description:
human immunodeficiency virus type I enhancer binding protein 3 [Source:HGNC Symbol;Acc:13561]
Mouse Orthologue:
Hivep3
Mouse Description:
human immunodeficiency virus type I enhancer binding protein 3 Gene [Source:MGI Symbol;Acc:MGI:10658

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa28701 Nonsense Mutation detected in F1 DNA Not yet available
sa36204 Nonsense Mutation detected in F1 DNA Not yet available
sa39118 Nonsense Mutation detected in F1 DNA Not yet available
sa42776 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36203 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42775 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa28701
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
ENSDART00000054020 Nonsense 91 1439 1 7
ENSDART00000110258 None None 580 None 9
ENSDART00000142223 None None 694 None 6
Genomic Location (Zv9):
Chromosome 16 (position 36759101)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 34387722
GRCz11 16 34341752
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGGAAACAAGTTTTATTGGGCCAGAAGGTGCAGTCTTGGGTGAAGAA[C/T]AAGAAGAGGGTACGGAGGGAGAGAGTACAGGTTCTGAGGATGAGACAGGG
Long Flanking Sequence:
ATGGATCACATGGCCGCCTTCAACACAGGCAGCCGAAACGCTGTGAAATGCTCCAAAGGCAGAAGCAGCGACATCAGTCACAGGCGAGTGGGTCATCTTGGCAGCTCTCAGAAATACCTGGTCCTTCAAGAGGCAGCTGTTCTGCCCTGGGAGATCCATCTCCCCAATCTCACAATGTCCATCAAACTCAATCTATGCCCAATGTCGAAGTACAGGAAGGCACCCCATGTAGACAAGAGCGCAAACCCCAAAAACCAGGGAAATATGTGTGCACATACTGCGGCCGACCTTGTGCAAAACCTAGCGTCCTGCAAAAACATATCCGATCCCACACAGGAGAGAGGCCCTATCCATGTGTCCCATGTGGCTTTTCCTTCAAGACCAAAAGCAACCTGTACAAACATCGCAAATCTCATGCACACCGAATAAAAGCAGGCATGGCTTCAAGTCGTGAGGAAACAAGTTTTATTGGGCCAGAAGGTGCAGTCTTGGGTGAAGAA[C/T]AAGAAGAGGGTACGGAGGGAGAGAGTACAGGTTCTGAGGATGAGACAGGGCAGCACCAACCATCTACCTCACAAGGCAGACCAACTCTGAAAAAAAGCTGCAAAGTGGAATTGTCATTCATAGAGGAGGGACCCCAAACTGAGGATTCACAGGCAGTCAAGCAAAGGTTAGCAATGAGGCTAAGTGAGAGAAAACGTGCGCCCAGAACATCTTCAGATGATACACGATCCTCATTGGGTCCTGGCAGTAAGGGGAGCACAGAATCCGGATATTTTTCCAGTTCTGGGAGTGCTGAGCTCTCCCAAGTGAGCCCACCAAATGCCAGTGCTAAAACATATGCTGAGATAATTCTAGGAAAGTATGGACGACTAGGACAACAGCAACGAATTCCACATCAACAACTGCAGTTATCATCATCATCTTCAGGTCAACAAGAAAAATCAATCCCTTTCACCGTTCCCAAGACACAAGTCATTGAGCATATAACAAAGTTAATCACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36204
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
ENSDART00000054020 Nonsense 559 1439 3 7
ENSDART00000110258 None None 580 None 9
ENSDART00000142223 None None 694 None 6
Genomic Location (Zv9):
Chromosome 16 (position 36757618)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 34386239
GRCz11 16 34340269
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGAACATGAGCCATCACAGGAGCCAAAACCAACCTCTACTTCCCGGT[T/A]AATTCGTCAATCCAACATTCAAGTTCCAGAAATTCTTGTTACAGAGGAGC
Long Flanking Sequence:
ACCAGGAATAAAGCGAGAAAGGGAAATTTTCTTATATGAGTGTGAAATGTGTGGAAGTCATTTAAAGAATCAAGACTCTTTTGCTGCACACAGACTAGCATGCATGAGTAAATCTTTACATAGTTTTCAAAGTGAAGAAGGAAGTGCTTTAATTGAAAACCAGCCACAGATCATGAGCTACAAGTTCAAAGCTATGGCCATGGCTGTTCGCAAGCGTAAAAAGAAAGAGGAGAGTCTTGAGGAAGACCCCCCCAGTCCAGGTCCAACCGCTGTGTCATTCTGCTCTAAGCCTCTGTCTATGCCAGGTTGTAGTGATAATCAGGGTGCATCTTGTGGCCTTTCACCAAGTGAGCTAGAAAGAAGGGGTTCCTGTAAAGAAATTTCTGTCATCCAACATACCAGATCATTTGAAAAACAGGAAAGCATCCCTATGACAAACCAGGAAGAAGAGCCAGAACATGAGCCATCACAGGAGCCAAAACCAACCTCTACTTCCCGGT[T/A]AATTCGTCAATCCAACATTCAAGTTCCAGAAATTCTTGTTACAGAGGAGCCAGATTCAGAGATGTTATCTCAACCAGTAAGCACCTCTCTAGAATCTGAGAAAGTGGAGGAATTCCAGTGGCCTCAGCGTAGCCAAAGTCTGTCTCAGCTCCCTGCAGAGAAGCTACCGCCAAAGAAAAAGCGTCTCCGTTTGGCTGAGGCAACCCAATCATCAGGAGAATCTAGCTTTGAGTCAGTATCGCTGCCACACAGCCCAAGCCAAGAGAGCAATGTTTCCCATGCCTCCAGCCGATCTGCATCCTTTGAGGAAATGGGAAGGCCAGACTCTGAAATGCAAAGTGCTACTAGGAGCTCCCAAGTTTCTCACATGCTCACCGTCCCATCAAGTGTCTATCAATACCATCAGTCTCAAAGAGAGATGCGGCGCTCAACCTCTGAACAGGCATCTGCAAGTCCGGCTTACCCAGCACATGTAGAAGAAACAAGAAGCAAGTCATTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39118
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
ENSDART00000054020 Nonsense 870 1439 3 7
ENSDART00000110258 None None 580 None 9
ENSDART00000142223 None None 694 None 6
Genomic Location (Zv9):
Chromosome 16 (position 36756684)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 34385305
GRCz11 16 34339335
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTACCTTCACAGTGAGACACCTCCGGTAAATCAAAGACCCACAGAGTA[T/A]GTAGAACGCCTGCCCCTTCAGCCACTCGCAACTTTATTCCCGCTACAATC
Long Flanking Sequence:
TCTGAACAGGCATCTGCAAGTCCGGCTTACCCAGCACATGTAGAAGAAACAAGAAGCAAGTCATTTGACTATGGCTCCCTATCTCTAGAGCGTACTTCTGTTACTTGGAAGGAGAGGAGGAAATGTCTCTTGGTGAAACACGGAACTCTTGGTGAACCTGACCATGAGGAGCCATCTTCTAAACATGGCTTCTTAGCTGTTTGCCAGTCCTACCCAGCTCATCCTCCTTTCACAATCACAGAGAACAGAGAGGGAAACAGGACCTCTAGGTTTAGCTCAGAGAATATAGGCAAGACCTTGCAACTGTTCCACTCCCCTCTTGGCCTCCCACCAGCAGTTTTCCCTATACATCAAGCAAATCCTGATTTTTATTCCTCAAGTCAGCTAACTAGATTCGTCCCAGTCACTACAGGAATCTCAGCAGTCATTTCACCGCAAATGTTTCACCAAGGCTACCTTCACAGTGAGACACCTCCGGTAAATCAAAGACCCACAGAGTA[T/A]GTAGAACGCCTGCCCCTTCAGCCACTCGCAACTTTATTCCCGCTACAATCAAGTGATGTTGCTCAGGCGGTTTGCTTTCCCATGCCAGGAGGTCTGACTATTCAGGTCCCCTCTGGGCCTCTTTTCAGGGAGTTTAGGTCATCACCATCCTCTTTGCCTAGTCCTGTTCATTCACAACAGCAGCTAGTAGTTCGCCACAGTCCCCATCCTGTGATTGCTCCTTGCCTTCAACAGCTTGTGCCAGTGGTGTCCCTTGTAGTGCCTGTGCGCTTACAGACTCACATTCCTACCTATGCTAGTGCCATGTATACAACCATCTCACAAATTTTAGCCACAACACAACATCCAATCTGTTGTACAGCTATGGTCATCATGGGTAAACTGGAGGAAGACAAGATTCAGAGATCTTACCTTAGGCTGCCCTCGCCAAGCCCTAAGAGCTATATTCCCTTGCCGCTGCCTCTCGAACATGGAGCAGGAACTTCATCTGATGACAGCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42776
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054020 Essential Splice Site 1361 1439 5 7
ENSDART00000110258 Essential Splice Site 201 580 3 9
ENSDART00000142223 Essential Splice Site 226 694 3 6
Genomic Location (Zv9):
Chromosome 16 (position 36748682)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 34377303
GRCz11 16 34331333
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCGTCCGTATGTCTGCAAGTACTGCAACTTCGCCTTTAAAACCAAAGG[T/C]AGACATACATTCAAACTCATCCTATCATCTCTTTAAAGGCTCACGTTTCG
Long Flanking Sequence:
AAGAAGCTTATGGATTTTATTGGCCACTTTTAGCTCTCTGTCCTTAAGTGGAATTGTCTCGCCAGCAAAAAATACAATCTTTGAGCCAAAGTGTGGATTCTTTGAGACTATCTTCATAGTGACAAGTGCTGAAAATATATAGCGGAACCCGGAGCTCTTATAATGAGAGATTCAGTGTTTGGGGAGTTCACATGAGGGTCCTGCCAAAGTGAAGATCTTTGCATTATTACTCTTCATGAATGTGATAACCTTATATATTAGATAGATTAAAAAATAGATTTTTTATGAACACCTCTATCTATCTGTCTGTCTTACCTGAACAGGTATAAGTCAAACGAGGATTATGTGTATGTTCGTGGAAGGGGAAGAGGCAAGTACGTGTGTGGTGAATGTGGGATTCGCTGTAAGAAGCCCAGCATGTTAAAAAAGCACATTCGCACTCATACAGATCTGCGTCCGTATGTCTGCAAGTACTGCAACTTCGCCTTTAAAACCAAAGG[T/C]AGACATACATTCAAACTCATCCTATCATCTCTTTAAAGGCTCACGTTTCGGTACTGTGTTGATGTTGAGACTTGTCTTTTTCTTCAAGGGAACCTTACCAAACACATGAAGTCTAAGGCTCATGGTAAGAAATGCCTGGAGATGGGAGCATCCGAGTCCTCTGAGCTGGACCCTGAGGAAGCAGGTAATGTTAACAAAAAGATTGTACGTAAAGTTGAAAAAAAATAATAATAATAAATAAATAAATAAAGTTGAGAAAAAAAAAAAAAAAATATATATATATATATATATATATAAATATATATATATATATATATATATATATTTATATATATATATATATATATATGTTTTTTTTTGCCTTCCAGAGAAAGTCGTATTTGTTTTATTTTTGCTAGAATAAAAGCTGTTATAAATTTTTTAAACCCATTTTATAGTCAATATCATTAGCCCTCTTTAGCATACTGTTTACAGAACAATCATTATAGAATGACTTGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36203
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054020 Essential Splice Site 1393 1439 6 7
ENSDART00000110258 Essential Splice Site 233 580 4 9
ENSDART00000142223 Essential Splice Site 258 694 4 6
Genomic Location (Zv9):
Chromosome 16 (position 36748496)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 34377117
GRCz11 16 34331147
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGATGGGAGCATCCGAGTCCTCTGAGCTGGACCCTGAGGAAGCAGG[T/A]AATGTTAACAAAAAGATTGTACGTAAAGTTGAAAAAAAATAATAATAATA
Long Flanking Sequence:
TTCACATGAGGGTCCTGCCAAAGTGAAGATCTTTGCATTATTACTCTTCATGAATGTGATAACCTTATATATTAGATAGATTAAAAAATAGATTTTTTATGAACACCTCTATCTATCTGTCTGTCTTACCTGAACAGGTATAAGTCAAACGAGGATTATGTGTATGTTCGTGGAAGGGGAAGAGGCAAGTACGTGTGTGGTGAATGTGGGATTCGCTGTAAGAAGCCCAGCATGTTAAAAAAGCACATTCGCACTCATACAGATCTGCGTCCGTATGTCTGCAAGTACTGCAACTTCGCCTTTAAAACCAAAGGTAGACATACATTCAAACTCATCCTATCATCTCTTTAAAGGCTCACGTTTCGGTACTGTGTTGATGTTGAGACTTGTCTTTTTCTTCAAGGGAACCTTACCAAACACATGAAGTCTAAGGCTCATGGTAAGAAATGCCTGGAGATGGGAGCATCCGAGTCCTCTGAGCTGGACCCTGAGGAAGCAGG[T/A]AATGTTAACAAAAAGATTGTACGTAAAGTTGAAAAAAAATAATAATAATAAATAAATAAATAAAGTTGAGAAAAAAAAAAAAAAAATATATATATATATATATATATATAAATATATATATATATATATATATATATATTTATATATATATATATATATATATGTTTTTTTTTGCCTTCCAGAGAAAGTCGTATTTGTTTTATTTTTGCTAGAATAAAAGCTGTTATAAATTTTTTAAACCCATTTTATAGTCAATATCATTAGCCCTCTTTAGCATACTGTTTACAGAACAATCATTATAGAATGACTTGCAAAATGTCAATGCTATGCTTATTACCCTAATGCTTAATTAACCTAGTTAAGCTATTAAATTGCACTTTAAGCTTAGTAGTGTCTTGAAACATATCTAGTAAAATATTACGTACTGTCATCATGGCAAAGATAAATGAATCAGTTATTATAAATGAGTTATTAAAACTATTTAGAAAAATCTTCTTTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42775
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054020 None None 1439 None 7
ENSDART00000110258 Essential Splice Site 437 580 5 9
ENSDART00000142223 Essential Splice Site 462 694 5 6
Genomic Location (Zv9):
Chromosome 16 (position 36742523)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 34371144
GRCz11 16 34325174
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGGCCTCCACTGGGAGCCCAGCAAACCAGCTACTAACACTCAAAAGG[T/C]AGGCAATGTAACAATTTAAAGGGGTCTTGTTATGCTGGGTTTTTACGAGA
Long Flanking Sequence:
TGATGAGCCATCTTCAGCCTGCTCTACTGACACCCGTCAGTCTACAGGTGACCTTTCTGAAAGTGGCCACGGCTCACAGACTGAGCCCTCTGACCCTACAGCAAGGGAGGAATACTCTTCACCTCATAGGCCTTGGCCTGGCATACGAGCCATGTCTCCAGGAGGCAAGAGGGCGTCTTTCTCTCGGAAGGGCTGGGAGGTTTCCCCGAGGAACTTCTCCCCAAGCAGCGAGGGCTCTCCTCTCAGAAGCCTGTCTCCAAGGGTTGAATTGTCCTCACCCAGTCGTCATCTCTCTCCATCTCCAGAGAGAGGCCCGTCACCCATCAGAGCTTTGTCTCCTCTCAGACCTCTCTCTCCTCTGAGACCCGTGTCACCCGCTAGATACAGGAGTGCCAGAGCTCTATCCTCCCCTACGCCTTTAAAGCCTCAGCATCGCCCGCACAGCTCTCCCGCAGGCCTCCACTGGGAGCCCAGCAAACCAGCTACTAACACTCAAAAGG[T/C]AGGCAATGTAACAATTTAAAGGGGTCTTGTTATGCTGGGTTTTTACGAGATGTTATTTTCCAGAATGCTTCTGTGGAAAAATGCTTGACAGATTATTACTATGCCCTGCTGCTAATGAGACTTTTTGGATAAAAGCAAAAACACTGCAAAAACTAAACATGTAAATGAGCTGCATGTCCCTGCCCAATTACAGCTCATGCTTTTCTCCAGTAGCTAAATGTCAGTAAACTCCTGATATTTGGTTCTGAACGCACAGCCAAATAGTATCAGTATATTAGACCTGTGAAAATGAACCTGAACCACACTGTTCCAGTTACTATGACCAATTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTGAATTGAATTGAATTGAAAATGTCTCTTGGACATGACGACAACCAGGGATGGGCGGTATTTATGATACATGTATTTCAAATACGTATTTTAAATACAAAATAGTCATTGTAT
Associated Phenotype:
Not determined