ZMP
si:dkey-31k9.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate human immunodeficiency virus type I enhancer binding protein 1 (
Human Orthologue:
HIVEP1
Human Description:
human immunodeficiency virus type I enhancer binding protein 1 [Source:HGNC Symbol;Acc:4920]
Mouse Orthologue:
Hivep1
Mouse Description:
human immunodeficiency virus type I enhancer binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:96100
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18568 | Nonsense | Available for shipment | Available now |
sa13312 | Nonsense | Available for shipment | Available now |
sa17128 | Nonsense | Available for shipment | Available now |
sa43204 | Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9898 | Nonsense | Available for shipment | Available now |
sa18511 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18568
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 |
---|---|---|---|---|---|
ENSDART00000110201 | Nonsense | 655 | 2621 | 2 | 7 |
The following transcripts of ENSDARG00000079528 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 3956962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3453535 |
GRCz11 | 19 | 3394433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGCCCARTTGTGGCAGCTGTCAKGCATGTAGCAACTATTGAAAAGCCT[C/T]GAGTTCCTTCAGGACAAATGCGTCCTCCATTGGAAACCAAAGCTCWATCT
Long Flanking Sequence:
CTCTCCCCAAAGTGGTAGTCCACCCTGTAAATGTTTCACCTCTGCGTGCGGACAGCCCTCGAGTTACAGATTCAGCACCTGAACAAGCCACAGCCCAGAGGCAGAGAGATTTCCAACCAACAAATCTAAGGTCAAATGTAACGGTTCTATCTTCGCTAAAAGAAGTGGATTGCACAAGTCCTCCACAAGATTCAGTCAGTGACGATGAAGATCAGCATTGTAAATCACCACTAGGAGGCAGCCATGCCCAGCTACAAAGGCAACAAGCAACTGATTACTCTCAACAGGCACAAGTCAAGTGCCTCCTTAGCCCTCGGAGTCTTGGGAGCACTGACTCTGGCTACTTTTCACGTTCTGAGAGTGCAGATCAAGCAATGAGTCCTCCAAGTCCTTTTGTTAAGATAACTCCACCAGGAGACACGGACATTACAAAAACCCCACACATTCCTCCTTGCCCAGTTGTGGCAGCTGTCATGCATGTAGCAACTATTGAAAAGCCT[C/T]GAGTTCCTTCAGGACAAATGCGTCCTCCATTGGAAACCAAAGCTCTATCTCTCGAGGAGCGCATTTCAAAACTGATTTCAGACAATGAGGCTGTTGTGGATGATAAACAACTAGACAGTGTCAAACCTAGACGGACTTCCCTTTCTCGGAGAGGTAGCATTGATTCCCCCAAATCCTACATATTTAAAGACTCTTTTCAGTTTGATCTCAAACCACCGGTAAGAAGATCTAGTTCTAACTCAGACATACCGAAATCTCCTTTCACTCCTACAGACAAATCCAAGCAAGTATTTCTCCTTTCTGTACCATCTCAGTATCCAGCCATGGAATGTTTACCAATAACAAGAAGTAATTCCATGCCTACCACACCTGGTCAGTCGGCTCTCTTCCCCAATGTAACAACTCAGCCACACCAACTAAGGATCTGTCAATCGTTCGATGACAAGATCAGCTCACTAAATGATGATGTATTCTCTTCTGCTCCCTCTACTCCCAACCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13312
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110201 | Nonsense | 1511 | 2621 | 2 | 7 |
The following transcripts of ENSDARG00000079528 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 3954394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3450967 |
GRCz11 | 19 | 3391865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATAACAATACCAATAGCTAATGAAATTAAAGGGTCACATTCAAATGAT[G/T]GAATGCAAAATGTCTATGTTGCACAATCAAGTTATCAGGCTGTACTCAAT
Long Flanking Sequence:
AAATGTCCTTGAAGATTGCACCAGAGCCTCAAATAGCAGTGAAACAGACTACCCCCATCCAAAGGGTCCCCTTCACCAATGAATGCTCTGGGTCCCAACCTAGATCAGTAAATCTGAACACATCCGCTCTTGCTCAGTGCTTTGCTGTGCACTCAGGAGAGGTCTCGCTACCAAAAAATGAGCAAGTGGTCCAAAGCATTAACCTTGGAGGGAAAACTGAACAACCACAAGTGCATGGCCTTCCACACCCATGGCATCAGACCTCAAGGGTTGTGGCAGGTCATGTGCAACCTCTTGTTCATATGGTAGGGGGTCAGACAGACATTAAAAAGAGTTCTGATGAGAAAAATAAAATCTTTATACCTAAATACCAAATGAACTGCCCAGTACTGAAAACAGGCCAGACATATTCTTTGGCAGGTGTGCAAGGCACACAAATCCCATTGCCAGTGATAACAATACCAATAGCTAATGAAATTAAAGGGTCACATTCAAATGAT[G/T]GAATGCAAAATGTCTATGTTGCACAATCAAGTTATCAGGCTGTACTCAATAAGCCTTCGATTGTACAGCCTTCTAATGCACAAGTTGATACAGCTTCCCATAAAGTGCCAGTATCTGCACCTGTACCACAGATTCTAATCACCCATGAGCACACCCTAGCATCTGCTTCTGCAGTTTCTAAGGTCAGCTTCCCCATTGCACCTTCTGTGAACAGAGATTCGAAGATTGGACCAGAAATTCAAGCTCAAAAGCAACCAGGCTCTGTTGCTGTACAGATGAAAAACAACATGAAAACAACTGACCAAATCCAAAACACAGAGCAAAGCATCCTTTCCCTCGGATCACTGCATTGTATGCAAAAATTGGCATCTGCAAATTTATGCCCCCAAGAATCCACTGCTTCAAGCAAGCGTATGCTCTCACCTGCTAATAGCCTAGACATTGCTATGGAAAAGACTCAGAAGCGAGCTAAAGATGAGCATGGAGCTGCATGTCTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17128
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110201 | Nonsense | 1788 | 2621 | 2 | 7 |
The following transcripts of ENSDARG00000079528 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 3953561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3450134 |
GRCz11 | 19 | 3391032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAGAGAATTCCACTTTAAAGCCACAAGAGAAACCTGAGGAGCAGCGCTG[G/A]TCTCCATCAAAATCACCTCTGAGGCCTCCATCATTTCAGGGACAAGTGAA
Long Flanking Sequence:
TCCCTCGGATCACTGCATTGTATGCAAAAATTGGCATCTGCAAATTTATGCCCCCAAGAATCCACTGCTTCAAGCAAGCGTATGCTCTCACCTGCTAATAGCCTAGACATTGCTATGGAAAAGACTCAGAAGCGAGCTAAAGATGAGCATGGAGCTGCATGTCTTACTGATGGTAGATCTCTGAACTACTTGAACTCAAAGATGTCAGAAATTACCAGACAGAGAAAGTTAATGCTGGTTAGACAGGTCTGCACCACAGAGCCAGTGGATAGCCCAATTGAGACTGATGCCCCAGAACAATTGCCTGAGACATTAGACACTGAAAAGAATACTCAGAAACCAATACCTCAGGTGACAACAACTGAGGTCAGTGAACAGGAGATGGAGAGTAGAACCCCTACAACAACACCTCCTGCACGTTCTTTACCTGGAGTTCAAGGCTACCCCATGCTAGAGAATTCCACTTTAAAGCCACAAGAGAAACCTGAGGAGCAGCGCTG[G/A]TCTCCATCAAAATCACCTCTGAGGCCTCCATCATTTCAGGGACAAGTGAAGTTAGCTTCTTCTGTGTCTGTGGTCAACACTAGAGACAGCCATCGTCTGTCTTTCCCCAGTTTGAAAACAGCTACAACTTTCACCTGGTGTTTTCTCATGAAAAGGAAACCCCTCCACGTTCAGCAGATGGATCAGAGGATCTCTGCCTATTCTGCATGGGTAGTAAACCCAAACAATCCCAATCCATTGGGGCTTCCCACGAAAGTGGTAATGTCCTTGTTTGATTCCAAACAAACATCCAAGAAAATACACTACACCCAAGCAAAAACAACTACTTTGAAATCTGACATCTTGACCTACTCTGGCAAGCTGAAGGACGTCTTGCCAAAAGTAAGAACATAATCATTCAACTGATACTGCATATTGCTTTATACATTACAAATTTTAATGGACGCTAGGATAAATAAACGATTAACAAATTCTTCTCACTTCTTTTATCGCTTCAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43204
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:
G > A
Consequence:
Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110201 | Splice Site | None | 2621 | None | 7 |
The following transcripts of ENSDARG00000079528 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 3953070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3449643 |
GRCz11 | 19 | 3390541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACGCTAGGATAAATAAACGATTAACAAATTCTTCTCACTTCTTTTATC[G/A]CTTCAGGTTTTGATACAGCAAAGATCTGTGCCAAGTGAGAATAGTGGAAA
Long Flanking Sequence:
GCAGCGCTGGTCTCCATCAAAATCACCTCTGAGGCCTCCATCATTTCAGGGACAAGTGAAGTTAGCTTCTTCTGTGTCTGTGGTCAACACTAGAGACAGCCATCGTCTGTCTTTCCCCAGTTTGAAAACAGCTACAACTTTCACCTGGTGTTTTCTCATGAAAAGGAAACCCCTCCACGTTCAGCAGATGGATCAGAGGATCTCTGCCTATTCTGCATGGGTAGTAAACCCAAACAATCCCAATCCATTGGGGCTTCCCACGAAAGTGGTAATGTCCTTGTTTGATTCCAAACAAACATCCAAGAAAATACACTACACCCAAGCAAAAACAACTACTTTGAAATCTGACATCTTGACCTACTCTGGCAAGCTGAAGGACGTCTTGCCAAAAGTAAGAACATAATCATTCAACTGATACTGCATATTGCTTTATACATTACAAATTTTAATGGACGCTAGGATAAATAAACGATTAACAAATTCTTCTCACTTCTTTTATC[G/A]CTTCAGGTTTTGATACAGCAAAGATCTGTGCCAAGTGAGAATAGTGGAAAAACAAAACCAGATACTCAACCTGTTAATCAGAAAGAGTCAGACAGAGACACTTCCAAATCGGAACCCCAGCGAGTGAAGATCTTTGATGGAGGGTTTGTAAAACTTAGAATTTATATTAACAATCTTTAAAGTTTTAAATAGGAATAGTGTTTTGATGTATTTGTTTTATGTTCAGATACAAATCAAACGAGGAGTATGTGTATGTACGGGGCCGCGGAAGAGGAAAATACATCTGTGAGGAATGTGGAATTCGCTGCAAGAAACCTAGCATGCTGCGGAAGCACATCCGTACACATTCAGATATCCGTCCATTTCACTGCACGCACTGCAACTTCTCTTTCAAAACTAAAGGTGGGTTCAGTCTCAAACACACTGATTAAAAACTGTGATGCTTACATTTTGTTTTCCTCCTCAATTAGCAAGTATTGAAAGGTTATTTTTGATGGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9898
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110201 | Nonsense | 2087 | 2621 | 6 | 7 |
The following transcripts of ENSDARG00000079528 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 3951190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3447763 |
GRCz11 | 19 | 3388661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACTCTGATGGCCCAGATGATGAAGATAATGAGGGAGAGGAGGAAGAT[G/T]AGGAGGACAGCCAGGCAGAGTCTGGCCTTTCTGCTACACCTTCYGTTTCT
Long Flanking Sequence:
TCCTTGTTAACTCTTGGTGCATGTGGGCGGCATACACAGCGTTTACTGCGAGGAAATTGCAGCATCTAATTTTAGCAAGGAAGAGAGAGAGAGAGAAGCTGTGAGCTTTCTCTGGTCTCAGTTACTGAGAGCATATTTGTTTTTCTCTCACACGGTTCCACACAAGCTGTCAGGCGCAGACTGCATTTGTGGTTCAAGGTGTTAATGTCTTCCCTATATAATGAGACGGGTGTTTCTAGAACTATCATGCCTCATTTTGCTATGAAGTATATGTGAATGCTATAACCCTGAAAGTCAAAGCTGTAATAAAACAAAAATACTACTTGAATATTAAATTTAAATATCATGTCTTTAGGATACATAATCCCATCCTGCACTTTTTTTTTTTTTGTGTCCCTAAAGGTGATCGTGGAAGAGCAGGAAGTGCTGACAGACAGGACTCCGATGGGGATGACTCTGATGGCCCAGATGATGAAGATAATGAGGGAGAGGAGGAAGAT[G/T]AGGAGGACAGCCAGGCAGAGTCTGGCCTTTCTGCTACACCTTCCGTTTCTGCAAGCCCACAGCACTTTTCTGCTAACCAGGCTGATTTGGCTCCCAGCTCTTTACTGGCTCAGATGTCCATCAGCCCAAATCCATCCCCAGCTCTGCAATCTCAGCCTCCTCCTACTTCGGACTCCCAGACATCAGATACAGAATCTGTGGCTATGACAAGCCCAGTTTCTTTGGTCAGACAGATGTCAATTTCTGCATCCTGTTCCAGCCCCGGCCCTAATCCAACCTCTTTTACATCCCACCCGACCCCTGCCTCAGAATCCCACACCTCTGATACTGACTCCGTACACATGATGAGCCCAGTGTCACCATGCAGGCAGATGTCTATCGACTACCCAGACTTTGATGTTCCCCCTAGTCCCCCAGTGTCAGGCAAGGGTGCCAAGCTCGGCCAGGTGAGACCCGTGTCCTCGCCGTCATTGTCTTTCCCGTCGTGCATCCCTTCCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18511
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 |
---|---|---|---|---|---|
ENSDART00000110201 | Nonsense | 2395 | 2621 | 7 | 7 |
The following transcripts of ENSDARG00000079528 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 3950001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3446574 |
GRCz11 | 19 | 3387472 |
KASP Assay ID:
2261-2806.1 (used for ordering genotyping assays)
KASP Sequence:
CTTGTTTCCCCCTTGGYCAAGTGGCAGGGCTTCARACACTTGGTGCTCAC[C/T]AGACCRCCCTGCAGCCTGTGGGTTTGGAGAYCTTGAGTGTTGTAGGTTTA
Long Flanking Sequence:
TGTTGTTGCTATTGTTTTAACAGGATGGAGTGTCAAGTACGATATCCCAGCCTGCAAGTGAGTGCAATGCCAATGTCGACCGTGGTACTCAGACCTCGTCTGACCCTCTTCAGGGATCCTTACACTTTCCACACGCAGGTCCGCTCCATGAACCCAGAATAGGAGCCACTACTCATCTCTTCAGCCACCTGCCCTTGCACTCCCAACAACCTCCTCGTTCCCCGTACAGCATGGTACCTGTGGGTGGCATCCAGCTTGTCCCTGCCGGTTTGGCTGCTTACTCGACATTTGTACCAATTCAAGCTGGACCAGTTCAGCTGACCATCCCAGCACTTAGTGTGATCCACAGGCAGACCGGCAGCCCCCTCTCAGCACCCAACACCTCACCCCGGCCAGATTGTTCCCCAACCCAGCCACTGGTAGTCCAGGAGCCAGTCAGCAGTGTACTGCCTTGTTTCCCCCTTGGCCAAGTGGCAGGGCTTCAGACACTTGGTGCTCAC[C/T]AGACCGCCCTGCAGCCTGTGGGTTTGGAGACCTTGAGTGTTGTAGGTTTAGCCAACTCCACCCAGCTGGTGCCTCAACAGAGTCTGCCATTAAATGCCACCCTAGGCGTGCAGGTATTGGCAGCTAGCCCTGCCCCTCAGTGCAGCACTGCCTCCCCAGCACAAATCCCTGGTCTGCAGATCCTCAACATTGCCTTACCAGCCCTCATACCGTCCCTCAGCCCACTTTCTGCCCTCAGCCCACTCCCTGCAACCCAGGACAAGCCACGTAGCCCTGAGGGTGTAGCATCTGTAACTCTACCAGCACAGGTTGCTGGATCACCACCAGCACCTCTTCCCTCAGCCAGTCCTCCAACAGCCAATCCAGGAGATGCTGCTGTCAATGCAAAGCCATGCATGGAGGTTAGGAAGGTCTCTCAAAACAACCCTAGCGTTGGATCTAGGGACACAGGGGGTGCAGAGAAGACTACAGGCATGGTGGAAAAATCAAAAGCCCCACCA
Associated Phenotype:
Not determined