ZMP
arid2
Ensembl ID:
ZFIN ID:
Description:
AT-rich interactive domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001071231]
Human Orthologue:
ARID2
Human Description:
AT rich interactive domain 2 (ARID, RFX-like) [Source:HGNC Symbol;Acc:18037]
Mouse Orthologue:
Arid2
Mouse Description:
AT rich interactive domain 2 (ARID, RFX-like) Gene [Source:MGI Symbol;Acc:MGI:1924294]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40197 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20174 | Nonsense | Available for shipment | Available now |
sa6926 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40197
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019144 | Essential Splice Site | 140 | 1565 | 5 | 21 |
ENSDART00000113360 | Essential Splice Site | 140 | 1573 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 1530165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1821797 |
GRCz11 | 4 | 1671110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATGTACACATTGTGTGAATCTCTAAACCCCCTTTTCTTCTATTGGAC[A/G]GACTATCTCCGCCAAAGCTATGGGCTATCGACGGATTTTATCCCTCCATC
Long Flanking Sequence:
ATCTATATGAGTTCACCCCTCACAAATCTCTCGTTTATATTAATATTTTCTATAGCAAGCTTTACAATATTTTATTTGCGCATATACATTTAGATGAGCAAAATCTGGGGATAATCTAACAAAATAACTTATGATAACGGTCCAAATTTATGTCAGGAGAAAATATTAAAAGAATTTAAAAAAAAAAAGTAAAGTAGCAGAATTTAAGAGAAACAAAAAAATGTATAAAATTTGTCATTTTTTATTTGTTGTTCTAATATTTTACTTCAAATGTATGATTTTTCTCATTCTAAAGATGATCAGTGACTAAAATATTATTTTAATAAATATCTGTTTAATAAATCTGTTTTGTTCACATGCACCAAAATATATGACCCATATTCACTGAGAAATAACAAAACAAAAAAAAAGTTGGGGTGTACTCCTTTATGTTGAGCATTGTGTGTGGTCGGCATGTACACATTGTGTGAATCTCTAAACCCCCTTTTCTTCTATTGGAC[A/G]GACTATCTCCGCCAAAGCTATGGGCTATCGACGGATTTTATCCCTCCATCCGATTACAACAAACTGGTGCTGTCCCTCTTATCTGGGCTCCCGAATGAGGTGGACTTCGCCATTAACGTGTGCACGCTGCTGTCCAACGAGAGCAAGCACGCCATGCAGCTAGAAAAAGAGCCCAAACTCGTCACACTGCTGCTGGCACACGCCGGAGTATTCGACGACTGTATGTTTGCATTTCTGATTTAATACTGCACTTAGTGTTTGCACTTTAGATAGTATATATGCATTTTAACTTTACATGCATTTTTATTTTAGCATTAGGCAGCTTTTCTGCTGTATTCGGGACAGACTGGCAGGAGAAAACGTCACGAGATTTTGTGAGGGTAAGAAAATGAGCATGTCGACTTGATTTGTATGGAGGCTTATGAGTTGCTAAATCAGTTTTTAAGTGTAATATGCAAAACTGGCAATGCAATGTTACATGACGATGTATTTCTGTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20174
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 |
---|---|---|---|---|---|
ENSDART00000019144 | Nonsense | 424 | 1565 | 10 | 21 |
ENSDART00000113360 | Nonsense | 424 | 1573 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 1520812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1812444 |
GRCz11 | 4 | 1661757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACGCTGCCGGACGTCATGCTGGTCATCTCTGCGCTGGAGGTCCTGTA[T/A]CAGCTGGCTGAGCTCGGAGAGATAACCTGCTCCAAAATCTCCTCCGTGGA
Long Flanking Sequence:
AGTTTCTAAAGTTATAAAACATTATTAGTGTGGTATTTGAGCTGACACATAAGACTCTCTAGGGACATCAGAGACTTACTTTACATTTTGTAAAAAGGGACATAACAGAAGAAACACATGAAGATATTCTGATGAAACTAGAAATCTGTAACCATTGACATCTATAGTGTTTGTTTTTCTTACTATGGATGTCAATGGTTACAAGTTTCCATCATTCATCAATATAAATAATTTGTGTTCAGCAGAATAAAGAAACACCTAAGGTTTATAACCACTTGAGGGAGATTAAATAGTGATTACAACTTCATTTTTGAGTGAACTATCCCTTTAAGATGTTCATTGCATCCTACAGCCATGGAAATCCTGGGGAACCTGAGCAAAGTGGAGGATAACGGTGTGCTGATCTGCGAGTATGTGGATCAGGAGTCATACCGAGAAATCATTGCTCTTCTGACGCTGCCGGACGTCATGCTGGTCATCTCTGCGCTGGAGGTCCTGTA[T/A]CAGCTGGCTGAGCTCGGAGAGATAACCTGCTCCAAAATCTCCTCCGTGGAGAGAAGCATAGGTTTGTGTTCAGCTAAAAAATTCAGTCTGCCGCTAGCTGCGTTTCCATCCACCTATTTTTATGCACATTTTGGAATATGGGAAATAAAATGCCAAGATGCACATAAATTGTCAAAATGTGCATAAAAAACTATGTATATTATATCATAATATATTAAATAAGATTAAATCAGATTAAAATATATTATATTATTTTAAATTATATTATTATATTATATTAAATTATATTATTTTAAATTATATTATTATTATCATTATTATATTATATTAAATTATATAAAACTATATTATAATAAATTATATTATTATTATATTTAATTATATTATTATATAAAATTATATTAAATTAAATTATATTAAAGTATTTCATATTATATTAAATTACATTATAAATTATATTTAAATTATATTATTATTATATTTAATTATATTATATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6926
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 |
---|---|---|---|---|---|
ENSDART00000019144 | Nonsense | 1381 | 1565 | 16 | 21 |
ENSDART00000113360 | Nonsense | 1382 | 1573 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 1515418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1807050 |
GRCz11 | 4 | 1656363 |
KASP Assay ID:
554-5063.1 (used for ordering genotyping assays)
KASP Sequence:
CCCGCCCTCTCTCCAGAGCAAACRCGGAAACCTGGACAGAACTTTAAGTG[T/A]CTGTGGCAAGCATGCAAACGGTAAGAAAGCAYGCTTTACRGATGTWCTTC
Long Flanking Sequence:
ACACTGAGTTAATCGTCAGCAGCAATTTACAGTTTACTTAACATGCATATAATGTATAATACTGTGTGTATTGCAGTTTTTCATGGTCGACTACAAATGTTTACTAAACATAATATTATGACAAAATATTAAATACAGCACCACAAGGGTACTGACAGCTATTGAAGATGACAAATGCAACACTTGAAACTATGTTTGACTTGACCAGTGCACCTACAAATTAATTTGTGCAAGGGATAATGTTTTCTTTCTTGTGTACATTTATATTGTGCTTTCCATTTAATATCATTATCATGTAGGACCCATTGATTTTATTTAGATTGAATGAAGTTTTCCCTTAAGCCTTCTTTAAAATTAAATAACTGTTCGTGTGTGCAGCAGCCTGTGTCAGTGCAGACTCCGCCTCCTGTGGATCCGGCTGCACAGGGAACCAATCAGAGTTCTCCAGCACCCGCCCTCTCTCCAGAGCAAACACGGAAACCTGGACAGAACTTTAAGTG[T/A]CTGTGGCAAGCATGCAAACGGTAAGAAAGCATGCTTTACGGATGTACTTCGCAATGTGAATAATAGCCGTATTATAGTTCTTTTTTAATGTTAGTTTTAACAAAAAAGTAGTAATTGGCTACAATTAATTAAATTTGTTGATTGAATAAAATCTTTTGGTTTTAAGGGTTGTTTTACTGGCATAAACTAAGAAATGAATATTAGCTAAGATAAGAAATGTTGGCTTCAGTATAACTGATTTTATTTCTGTGACTGTTTCAGGTGGTTTGACACGCCATCACAGGTGTTTTACCATGCAGCGACCCTTCATGGCAGTAAAGACTCATACCCAGGGCAGTGCCAATGGGAGGGATGTGAACCTTTTCCTCGCCAGAGATTATCCTTCATCACACACCTACAGGCAAGATCCTGACCCTCTGTTGTAGTGATAATAATGACATATATTTTTCCATAGTTAAAGGCCCTTGAAATTAAAATAAAAGTAATAAGATGTCTTAAGG
Associated Phenotype:
Not determined