ZMP
si:ch211-157m21.1
Ensembl ID:
ZFIN ID:
Description:
human immunodeficiency virus type I enhancer binding protein 2 [Source:RefSeq peptide;Acc:NP_001025
Human Orthologue:
HIVEP2
Human Description:
human immunodeficiency virus type I enhancer binding protein 2 [Source:HGNC Symbol;Acc:4921]
Mouse Orthologue:
Hivep2
Mouse Description:
human immunodeficiency virus type I enhancer binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:13380
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43502 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17889 | Nonsense | Available for shipment | Available now |
| sa32311 | Nonsense | Available for shipment | Available now |
| sa23772 | Nonsense | Available for shipment | Available now |
| sa37117 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43502
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000058502 | Nonsense | 137 | 2323 | 1 | 6 |
| ENSDART00000141734 | Nonsense | 137 | 2298 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 37546767)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 37619280 |
| GRCz11 | 20 | 37522159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGGTCTTTCTCTGGTCAACTGCAATCTCTGCCACCAGATGATATGTA[T/A]CCGGTACACTCCCGCTCTCATGGAGTATTTCCTCGTCATAAGTCTCCTGC
Long Flanking Sequence:
TAACTTAATACCTTATCTGGCATGACAGCTTTCATGAATGAAATTTGACAAACAGCCATCTTAAGAAACCCTACTGGAGTACTAAGAAAAATGGAGCCACATGAACCTATTGTTGGCCAAAAATGCACCAAGGAGCAACGGGAAAAGAACCCCTTACAAAGAAAATGGGTCTCTGAGCCATCTGCTGGAACAAAAAGAAATACCTTTGCAGACCCAGATATTAAAAGACACTCACATCGTGAGCAAAGTCTAACAGGTGGTACAAACCTTACTAGTTCAACTCAAAAGTACAGTTCTGGAAACCTGATGTCATCTGCAGTGACACATTCATCACAAGAAGGTCAGTTTCAACAGATCTTTCCTCGGCCTTACCCCTACCAGCTGCCACATTCTTACCCACAGGAGCCTTTCCTTGGTGGTACAAAGCCACAACCAGGGTTAGAGGCCCATGCCTGGTCTTTCTCTGGTCAACTGCAATCTCTGCCACCAGATGATATGTA[T/A]CCGGTACACTCCCGCTCTCATGGAGTATTTCCTCGTCATAAGTCTCCTGCTGGTTTTGGCCAATTTTCCCAATCCGGACCCGAGCAGCCAGATGAAAGTCATAAGAAGGAACAAAAACCCAAGAAGCCAGGAAAGTACATATGTCACTATTGTGGTAGAGCATGTGCTAAACCCAGCGTGCTGAAAAAACACATTCGGTCCCACACAGGGGAGCGTCCTTATCCCTGTGTTCCATGTGGTTTCTCGTTCAAAACCAAGAGCAATTTGTATAAACATCGAAAATCGCATGCTCATGCCATAAAAGCAGGACTTGTTCCATTCTCTGATCTAGCAACCCGAACAGACACTGATCAAGCATCTTCAGTTGGGGAAGCAGAGGCACACTCTGATGGGGAGCAAAGCACTGACACTGATGAAGAAACAGCAGAAGGTGCAATGTTTCCTGAAAAATGTAGCCCTCAGATATCATTCGAGTCAGACAAGAGCCCGATGGAAAGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17889
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058502 | Nonsense | 219 | 2323 | 1 | 6 |
| ENSDART00000141734 | Nonsense | 219 | 2298 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 37546522)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 37619035 |
| GRCz11 | 20 | 37521914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGGTCCCACACAGGGGAGCGTCCTTATCCCTGTGTTCCATGTGGTTTCT[C/A]GTTCAAAACMAAGAGCAATTTGTATAAACATMGAAAATCGCATGCTCATG
Long Flanking Sequence:
AAGTCTAACAGGTGGTACAAACCTTACTAGTTCAACTCAAAAGTACAGTTCTGGAAACCTGATGTCATCTGCAGTGACACATTCATCACAAGAAGGTCAGTTTCAACAGATCTTTCCTCGGCCTTACCCCTACCAGCTGCCACATTCTTACCCACAGGAGCCTTTCCTTGGTGGTACAAAGCCACAACCAGGGTTAGAGGCCCATGCCTGGTCTTTCTCTGGTCAACTGCAATCTCTGCCACCAGATGATATGTATCCGGTACACTCCCGCTCTCATGGAGTATTTCCTCGTCATAAGTCTCCTGCTGGTTTTGGCCAATTTTCCCAATCCGGACCCGAGCAGCCAGATGAAAGTCATAAGAAGGAACAAAAACCCAAGAAGCCAGGAAAGTACATATGTCACTATTGTGGTAGAGCATGTGCTAAACCCAGCGTGCTGAAAAAACACATTCGGTCCCACACAGGGGAGCGTCCTTATCCCTGTGTTCCATGTGGTTTCT[C/A]GTTCAAAACCAAGAGCAATTTGTATAAACATCGAAAATCGCATGCTCATGCCATAAAAGCAGGACTTGTTCCATTCTCTGATCTAGCAACCCGAACAGACACTGATCAAGCATCTTCAGTTGGGGAAGCAGAGGCACACTCTGATGGGGAGCAAAGCACTGACACTGATGAAGAAACAGCAGAAGGTGCAATGTTTCCTGAAAAATGTAGCCCTCAGATATCATTCGAGTCAGACAAGAGCCCGATGGAAAGGGGACCAGCATATGCAGACCCAGCAGAGGAATTGTCAGTGGCATCTATGAAAGTGCCTATCTTAATTGTTCCAAAACAAGGGGTGCCATCACCTGCTACTGAGTGCCCCCAGTTTACAGACATTAAAGGTTCAGTTATTGGTGGACAGATGGGCAGAGGAGATGAGTCTCATACGGTTAAACAGAGACTTGCCTTAAGACTCACTGAGAAGAAAGACCTGGATTCAGAGCAGTCTCAAAATCTCTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32311
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058502 | Nonsense | 807 | 2323 | 1 | 6 |
| ENSDART00000141734 | Nonsense | 807 | 2298 | 1 | 7 |
| ENSDART00000058502 | Nonsense | 807 | 2323 | 1 | 6 |
| ENSDART00000141734 | Nonsense | 807 | 2298 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 37544759)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 37617272 |
| GRCz11 | 20 | 37520151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACACGCTTTATCATATGCCCCACAAACTTGTACGTCAACCAAACATT[C/T]AAGTGCCTGAGATAAGAGTTACAGAAGAGCCTGACAAACCGGAAAAAGAA
Long Flanking Sequence:
AAGACTGCCTTGGACAAGATGATGGCAGCCGTAGTGGCTCTACTGAAATGGCAGAGGAATATGACTTAAGGCAAGGAAGTCAAGATTCTTCTAAGGCTGTTCCAGCTAATAAGGGATCCATGTTTAGAGCACATAGCCCTTCAGACAGTTTTGATAGAGGTTCATGTATGACACCAGAGGATGTGGTCCATGTTCAAGATTCGGACACAAAGACTGGTGGAAATGTAATTTCTGTCATTCAACATACTAATTCGCTGAGCAGGCCAAACTCATTTGAGAAGACTGAATCAATAGAACACCCATTTTATCAGCCGGATAAGCATGCTGGACATCTTTCTGAACAATCAGACACAGAAAATATTGATGATGTTCAAAGCCCCGATTCTCATCATAGATCAGAAAGCATGGAACATCAGCAGCAGGGTGACAATGAACATGGATCTTTCTCTTCTAACACGCTTTATCATATGCCCCACAAACTTGTACGTCAACCAAACATT[C/T]AAGTGCCTGAGATAAGAGTTACAGAAGAGCCTGACAAACCGGAAAAAGAACCTGAGGTCCCAGCAAAAGAACCAGAGAAACATGTTGAAGAATTTCAGTGGCCACAACGAAGTGAAACATTGTCCCAGCTCCCTGCAGAAAAGCTACCTCCAAAGAAGAAACGTTTGCGTCTTGCAGATATGGAGCACTCTTCTGGAGAGTCCAGCTTTGAGTCCACTTGTACTAGTCTGTCAAGAAGCCCTAGTCAAGAAAGTAACTTATCTCATAGTTCAAGCTTTTCTATGTCATTTGACAGAGAGGAAAGCATCAAATCTGTATCCCCAACTAAACAAGATGAATTTGCTAAGCAGTCTGAGTTTTTAACTGTTCCAGGAAGTGGCCATTCTCTGTCAATACCAGGCCATCATCAAAGAGAAATGCGACGTTCTTCATCAGAGCAGGCACCCAGTGCTTTGCCCACTGAAGTACCAGAAATACGTAGTAAGTCATTTGACTATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23772
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058502 | Nonsense | 807 | 2323 | 1 | 6 |
| ENSDART00000141734 | Nonsense | 807 | 2298 | 1 | 7 |
| ENSDART00000058502 | Nonsense | 807 | 2323 | 1 | 6 |
| ENSDART00000141734 | Nonsense | 807 | 2298 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 37544759)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 37617272 |
| GRCz11 | 20 | 37520151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACACGCTTTATCATATGCCCCACAAACTTGTACGTCAACCAAACATT[C/T]AAGTGCCTGAGATAAGAGTTACAGAAGAGCCTGACAAACCGGAAAAAGAA
Long Flanking Sequence:
AAGACTGCCTTGGACAAGATGATGGCAGCCGTAGTGGCTCTACTGAAATGGCAGAGGAATATGACTTAAGGCAAGGAAGTCAAGATTCTTCTAAGGCTGTTCCAGCTAATAAGGGATCCATGTTTAGAGCACATAGCCCTTCAGACAGTTTTGATAGAGGTTCATGTATGACACCAGAGGATGTGGTCCATGTTCAAGATTCGGACACAAAGACTGGTGGAAATGTAATTTCTGTCATTCAACATACTAATTCGCTGAGCAGGCCAAACTCATTTGAGAAGACTGAATCAATAGAACACCCATTTTATCAGCCGGATAAGCATGCTGGACATCTTTCTGAACAATCAGACACAGAAAATATTGATGATGTTCAAAGCCCCGATTCTCATCATAGATCAGAAAGCATGGAACATCAGCAGCAGGGTGACAATGAACATGGATCTTTCTCTTCTAACACGCTTTATCATATGCCCCACAAACTTGTACGTCAACCAAACATT[C/T]AAGTGCCTGAGATAAGAGTTACAGAAGAGCCTGACAAACCGGAAAAAGAACCTGAGGTCCCAGCAAAAGAACCAGAGAAACATGTTGAAGAATTTCAGTGGCCACAACGAAGTGAAACATTGTCCCAGCTCCCTGCAGAAAAGCTACCTCCAAAGAAGAAACGTTTGCGTCTTGCAGATATGGAGCACTCTTCTGGAGAGTCCAGCTTTGAGTCCACTTGTACTAGTCTGTCAAGAAGCCCTAGTCAAGAAAGTAACTTATCTCATAGTTCAAGCTTTTCTATGTCATTTGACAGAGAGGAAAGCATCAAATCTGTATCCCCAACTAAACAAGATGAATTTGCTAAGCAGTCTGAGTTTTTAACTGTTCCAGGAAGTGGCCATTCTCTGTCAATACCAGGCCATCATCAAAGAGAAATGCGACGTTCTTCATCAGAGCAGGCACCCAGTGCTTTGCCCACTGAAGTACCAGAAATACGTAGTAAGTCATTTGACTATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37117
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058502 | Nonsense | 1772 | 2323 | 5 | 6 |
| ENSDART00000141734 | Nonsense | 1772 | 2298 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 37540730)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 37613243 |
| GRCz11 | 20 | 37516122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAATGTTTTTTTTTTCTTCTTTTCTCAGACACTACTGAGGAGGTTCAA[A/T]GAGGATCAGAGAAGAAGGGCATGTCAGAGATAATGGCAGAGCACCAGTTC
Long Flanking Sequence:
AACAACATTTTATAGTTTGAATAAAACCAAAATGTGGATATTTATTGTTGACTTCAGTAACACACTGAGGTACAGAAGATCTATGTACTGTGTAAACAGAATAAATTGAGGGTTAGAGATCATTTTTAATGCTAGTGCAAGCAATTTAAACATTTTAAAATCTCATTTCAGGAAATCTTACAAAACACATGAAGTCAAAAGCTCACATGAAAAAGTGCTTGGAGCTTGGAGTATCAGTGACTTCGGTGGATGAAACAGAGGCAGAAGAACTAGGTATGATTCAGACTCTGGTCACATTATTCTAAATGTATGCAGGCAGCTGGACTGTTGCAAGTGATACATTATTGTTTTTACATTATTTACATTAGTTTTACATTATTGTTAAAAAGTATATGTAATTTACTATTAAATAATTATTGGTTAACCTGACTTAAAGTCAAAGTCAGTTGTGAAAATGTTTTTTTTTTCTTCTTTTCTCAGACACTACTGAGGAGGTTCAA[A/T]GAGGATCAGAGAAGAAGGGCATGTCAGAGATAATGGCAGAGCACCAGTTCTCTGATGCTGATGATTCGGAGGGTGCTGAAGAGGATGGTGATGAAGTTGATGACGATGAGGATGATGATGATGATTATGAGGGTGATTCAACACCGAAGACACGCTCTCGAAGCACAAGCCCACAGCCATGTTCCATCCCCTCACTCGCTATCACTGCAATTGCCGCTTCACAGGAATCCATCCCAGAGGGTTTGGCCATCTCCAAACAGCCTATTTTCACTTACTTCACCAGTCTGCCCAGTATTCAGATCACTCAGCTCATGGCACCCAGTGAGAAAGCTGGAGAGATCCAGATGGCTGAATACCAGAAGCTCCTTCAAGGGGCTCTGGGTGAAGATCACAAAAACAGACTGGATGTGCCTAGCTCTATGGATGAAGACCTGGCTCTCTCTCCAGAACACAGCTCATCCTCCTTTGAATTCTCGTGCTCCCGGCTGTCTTCACCAGGC
Associated Phenotype:
Not determined