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 |
|---|---|---|---|
| sa17889 | Nonsense | Available for shipment | Available now |
| sa32311 | Nonsense | Available for shipment | Available now |
| sa23772 | Nonsense | Available for shipment | Available now |
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