ZMP
hiat1a
Ensembl ID:
ZFIN ID:
Description:
hippocampus abundant transcript 1a [Source:RefSeq peptide;Acc:NP_955878]
Human Orthologues:
HIATL1, HIATL2
Human Descriptions:
hippocampus abundant transcript-like 1 [Source:HGNC Symbol;Acc:23376]
hippocampus abundant transcript-like 2 [Source:HGNC Symbol;Acc:23672]
hippocampus abundant transcript-like 2 [Source:HGNC Symbol;Acc:23672]
Mouse Orthologue:
Hiatl1
Mouse Description:
hippocampus abundant transcript-like 1 Gene [Source:MGI Symbol;Acc:MGI:1913881]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19820 | Nonsense | Available for shipment | Available now |
sa25862 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19820
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012191 | Nonsense | 180 | 493 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 37390373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37687083 |
GRCz11 | 2 | 37669540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCCACATTCGCAGCCAGTCTGGTCACCAGTCCGGCGATCGGGGCGTA[T/A]CTGTCTGAGGTGTACGGAGACACTCTAGTGGTGATCCTCGCCACGGCTAT
Long Flanking Sequence:
ACTCTCATATTTCATATGTTTGTTTTAAAGTTTTTTTTTTTTTTTTTTGCTTATCTCAATCATTCTGAATGCTTTACTGTAACCTTAGTCTGATGTTTTCCATCTACTCATTCTCTCTGTCTAATCCTGCAGGTGGTATTTTGCAGTTATCTCCATGTCTGGAGTGTTTGCGGTCACATTCTCTGTGATCTTCGCGTATGTGGCTGATATCACGCAGGAGCATGAGAGGAGCACAGCGTATGGCCTGGTGAGCAGAAGCATGTCGAAACTCTGAATTATACAACAGCTGTAGGTGCAAGAACAATTTCTCTATTCGTAGTACATTGGTTTCCTGTTATTTTGACAGCCATCTGCAGTTTCCTCTATTGCTCTTCAAATTAGAAATGGTGTTAATTACGTCAATGAATGTTTTCTTCGTGGTCTGAAGATTCTGATCTTCTTTCACAGGTATCAGCCACATTCGCAGCCAGTCTGGTCACCAGTCCGGCGATCGGGGCGTA[T/A]CTGTCTGAGGTGTACGGAGACACTCTAGTGGTGATCCTCGCCACGGCTATTGCTCTGCTGGACATCTGCTTCATCCTGGTGGCGGTTCCGGAGTCTCTGCCTGAGAAGATGAGACCAGCCTCTTGGGGAGCTCCTATTTCCTGGGAGCAGGCAGATCCATTCGCTGTGAGTCTATGATGCCTGTGAAGATGCAGTCATTATGATAAGATGACCTTGTCGTATTTTGTCACATCATCAGACTGAGTGCTCCTGATTGGTGGTCCAGCTTAATTTAATGATTGGTGATTGATTAACTGATTAATTAGTTATTTTAGGTTTGCTTTAATATATATAATATACATCATTCAGAAAGATTAAGTTAGTTTTGTTTGTTTTTTCAGATTTGACTTCCTGAAAAAAAAAAAACATATTAAGCACAGTTTTGAGTATTGATCTTAACCATTGACCAAATCCAGCAAATATAATTAAGTACATTCCATAAAAACCTGAGGATTAATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25862
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012191 | Essential Splice Site | 423 | 493 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 37380327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37677037 |
GRCz11 | 2 | 37659494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCCAGAAAAGGGTGTCAAACCCAACATGGCCAATCCCACAGATGAGG[T/C]GAGGAATGTCATGCAGTTAGGAGTGCTAAAAATAAGATCAGGTCAACAGA
Long Flanking Sequence:
GTATTTGTATATGTTTTAATAATGTTTAAAAATATATCGTGATGCATATTGAAAAGAGCTGTGCTTGTGATTCTGTTTTATAATTTTTTGCAATTACAGTTGTTCTAATAAAAAATTAAATAGATCTTAAATGGATGTAAAAAAACAAAACTTTTTGTAACAATTATTTGCTGTCATTTTTAATCCGTTTAAAGAATCCTTTCTGAATAAAAGTTTTTACCCCAAAAAAACTTTTAAATGATGGTTATTAATAAATGATAATATTAAGTAGTAATGTTTACCCTTGTCAATATATGATGGCAAAAAAGCATATGTCTCTGTGTCTGGGTCAGGTGTGGTTCAGGGGATGATCACAGGAATCAGAGGACTGTGCAATGGTCTCGGTCCAGCGCTCTATGGCTTCGTCTTCTACCTGTTTCACGTGGAGCTCAGTGAAATGGACCCTGCAGAGAGTCCAGAAAAGGGTGTCAAACCCAACATGGCCAATCCCACAGATGAGG[T/C]GAGGAATGTCATGCAGTTAGGAGTGCTAAAAATAAGATCAGGTCAACAGATCATTCTTTGTATATTAATGAATATTTGCCTGTATTGTGATTGAAGTTCATGTTAATGGAGTTATTTAGCTGTGTTTACTGACAGTCACTAGTCTAGCATGAGCAGCAGCCTCTTCAAGTCCCAATGCCCACTATATAAAACAATGGATTTAAAATACAAAAAAATATATACTATGGAAAAGAAAGTTTGCCGGTTTCCAGCTTTCTTCAAAAAACAAAAAGTTTTTTCAACCACAGAAAAGTCAACCGGTTTGAAACAATTAAAGGGTTAGTAAATGATGACGAAATTTTCATTTTTGGTTAAACTGTCCCTTTACTTTCAGACCTTCATGTTTGTGTCAACAATTACTGATTATAAAAAAATAAATATAAAGGTTTGCTCATTCGTTCGCTCGTTTGTATGTTTGTACATTCGCTTGTTCGTTTGTTTGCTTGCTAGGGCAAAGTATC
Associated Phenotype:
Not determined