ZMP
arr3l
Ensembl ID:
ZFIN ID:
Description:
arrestin 3, retinal (X-arrestin), like [Source:RefSeq peptide;Acc:NP_001002405]
Human Orthologue:
ARR3
Human Description:
arrestin 3, retinal (X-arrestin) [Source:HGNC Symbol;Acc:710]
Mouse Orthologue:
Arr3
Mouse Description:
arrestin 3, retinal Gene [Source:MGI Symbol;Acc:MGI:2159617]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38804 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34922 | Essential Splice Site | Available for shipment | Available now |
sa17404 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38804
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078996 | Essential Splice Site | 114 | 357 | 6 | 16 |
ENSDART00000105733 | Essential Splice Site | 113 | 356 | 8 | 18 |
ENSDART00000105734 | Essential Splice Site | 113 | 372 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 27441063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26843857 |
GRCz11 | 10 | 26805570 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTCTCCTGAAGAAAGCTGGAGAGCAGGGCCATCCCTTCACTTTCAAT[G/A]TAAGTCATCTGCCATCATTTTACTTTTCCTTTTAAGTCTTTTTTAATCTT
Long Flanking Sequence:
CAGTGTTTTCTTTCTAATTAAAATAATTGAATAGTTAATTGATAAAAGTTTATCAGTTCTCAGTATTACTTTCTTCCTAATTTTAAAGAGTAATGATTAATTAATGTACGCATTCAACTTGATTCCATTTTTTTGATATTGTAACTGTGAATCCAATAGTTTTATTGATTGATCGATCGATTCATTCATTCGTTCCCAAAGAAAGGGTCAAAATGACTTCAAGACAGCTAATGAAAACAGTTTAATTTAAAAAAGATTGATGTATAAAACTGACTTTAAATTTAAACATTACTTTGCTTCATCTAGTTTGGGTTCAGCTGGCCTGTGCTTTCCGCTATGGCCGTGAAGACCTGGACGTGATTGGACTTTCCTTCAGAAAAGACATCTGGATTCAGCACATACAGCTCTACCCTGAAGCAGGACACAAACCCACCCTGACCGAGATGCACAACACTCTCCTGAAGAAAGCTGGAGAGCAGGGCCATCCCTTCACTTTCAAT[G/A]TAAGTCATCTGCCATCATTTTACTTTTCCTTTTAAGTCTTTTTTAATCTTTCTATCATTTGACCCAAACAATACTGCACAGAACTAAGACATACATTTAAAACGAGCTGTTCTGTTTGTCTTTCAGATTCCTACCAACCTTCCCTGCTCTGTTACACTTCAGCCTGGGCCAGACGACAAAGGAAAAGTGAGTTAAAATCAGCTGAAATTAGTTGAAATGTACTGAATGGACATCTTCATGGCTCTGTTCTTCACAGGCTTGCGGCGTTGACTTCGAGGTTAAAGCCTACGTGGCCAAATCAGCCGATGACCCCGATGAGAAAGTTGACAAGAAGTAAGAGTGTTACTGATTACTCTGCACATTTATTTCTGTTTTTAAATTTTTTTATAATTGTTTTTTTTTATTATTTCTATCGTCTCTCTCTAAAGGGATACCTGCCGACTTGTCATTCGTAAAATCCAGTTTGCACCTGATAACACAGGATCTGGACAGAAAGCCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34922
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078996 | Essential Splice Site | 258 | 357 | 11 | 16 |
ENSDART00000105733 | Essential Splice Site | 257 | 356 | 13 | 18 |
ENSDART00000105734 | Essential Splice Site | 257 | 372 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 27442920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26845714 |
GRCz11 | 10 | 26807427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTACTCAGCTGACAAATACACCAAAAATGTGCTGACTGAAGAGTTCGG[G/A]TGAGTGTTGTTCTATTTGATAGTGATGTTTGTCAGCCATAAAATCCGTCT
Long Flanking Sequence:
GATATTTATGCAATATATGCAAATGACATATAAAACAAATTCATGTTTGGATTTCACCTATATAAAATATGTCTTATGTGCAAAGGACATATAAAACAAGTTCATTTTTGGATTTCACATATATAAATTATGTGTTTTGGCTGTTAATTGTAATGGCATATATTTTTTATCAACCATTTGAAATACAAATATGTAAATAAGTTCAATGTATATGATCCTACATGGCCATATATCATATTTCCATACAGGCAACAGCAAAACTTGTTTAATTATCATTATCAAAAAAATAATAATCCTAAAATATGTTGCTTAAATATAATTCCTTTAGCAGCAGAATGCTGTAATTTGCATATCCAAATCAAGTATTACATCAGTGGTAATGCAATATATTCAACCTGACTAATTTTAGTGTCTGTTATTTTCATAGTTGACCAAACCACAGACGTCGTCCTGTACTCAGCTGACAAATACACCAAAAATGTGCTGACTGAAGAGTTCGG[G/A]TGAGTGTTGTTCTATTTGATAGTGATGTTTGTCAGCCATAAAATCCGTCTAAATTATTTGATTTAATTGTTCTTTACAGAGAAACTGTAGAAGCCAATTCGTCTTTTGAAAAGTCCCTTGATATTACTCCTTTACTGGCAAACAACAAGGAGAAACGTGGCCTGGCGCTGGACGGCAGGCTTAAAGATGAAGACACCAATCTGGCCTCAACCACTATGTGAGTGTTTGGTTCTGTTTTAACGGAACACAAAACTTTTTTTGGAAATAAACGCCCTAAAGTTTGACTAATCTCCAGATCTGGCGGGAGCACTTTTAGCTTATCTTAGCATAGATCATTGAATCGGATTAGACCATTAGCATCTCACTCAAAAATGTAAAAATGAGTTTGAATAATTTTCTTATTTTAGGCTTGACTCTTCTGTAGTTACATTGTGCACTAAGACAGATGGAAAATTATATTTTCTAGCAGCATATAACTAGGAACGATACTCTCATTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17404
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078996 | Essential Splice Site | 304 | 357 | 12 | 16 |
ENSDART00000105733 | Essential Splice Site | 303 | 356 | 14 | 18 |
ENSDART00000105734 | Essential Splice Site | 303 | 372 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 27443139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26845933 |
GRCz11 | 10 | 26807646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACGGCAGGCTTAAAGATGAAGACACCAATCTGGCCTCAACCACTATG[T/C]GAGTGTTTGGTTCTGTTTTAACGGAAMACAAAACTTTTTTTGGAAATAAA
Long Flanking Sequence:
ACATGGCCATATATCATATTTCCATACAGGCAACAGCAAAACTTGTTTAATTATCATTATCAAAAAAATAATAATCCTAAAATATGTTGCTTAAATATAATTCCTTTAGCAGCAGAATGCTGTAATTTGCATATCCAAATCAAGTATTACATCAGTGGTAATGCAATATATTCAACCTGACTAATTTTAGTGTCTGTTATTTTCATAGTTGACCAAACCACAGACGTCGTCCTGTACTCAGCTGACAAATACACCAAAAATGTGCTGACTGAAGAGTTCGGGTGAGTGTTGTTCTATTTGATAGTGATGTTTGTCAGCCATAAAATCCGTCTAAATTATTTGATTTAATTGTTCTTTACAGAGAAACTGTAGAAGCCAATTCGTCTTTTGAAAAGTCCCTTGATATTACTCCTTTACTGGCAAACAACAAGGAGAAACGTGGCCTGGCGCTGGACGGCAGGCTTAAAGATGAAGACACCAATCTGGCCTCAACCACTATG[T/C]GAGTGTTTGGTTCTGTTTTAACGGAACACAAAACTTTTTTTGGAAATAAACGCCCTAAAGTTTGACTAATCTCCAGATCTGGCGGGAGCACTTTTAGCTTATCTTAGCATAGATCATTGAATCGGATTAGACCATTAGCATCTCACTCAAAAATGTAAAAATGAGTTTGAATAATTTTCTTATTTTAGGCTTGACTCTTCTGTAGTTACATTGTGCACTAAGACAGATGGAAAATTATATTTTCTAGCAGCATATAACTAGGAACGATACTCTCATTATCATAAACTCTCATCGTAATAATCAAGGAAATTAGCTGCTGTACCATTAATATGGCAAGTGCAATGATATTATGCAGTGCTTTTATCTAGTTACCTAACTGTGCTTGATGCAACTATGGTGGTAAAACTCAATAATAGTAACTGTAGTAATAATAGTAATAGTAACTCAACTGGTGACTTGTAAAATTTCCAAATGCAAAAACCTATTTCACACCATAGAAA
Associated Phenotype:
Not determined