Busch Lab

ZMP

zgc:110626

Ensembl ID:
ENSDARG00000053159
ZFIN ID:
ZDB-GENE-050417-447
Description:
hypothetical protein LOC550588 [Source:RefSeq peptide;Acc:NP_001017889]
Human Orthologues:
ARRDC2, ARRDC3, ARRDC4, TXNIP
Human Descriptions:
arrestin domain containing 2 [Source:HGNC Symbol;Acc:25225]
arrestin domain containing 3 [Source:HGNC Symbol;Acc:29263]
arrestin domain containing 4 [Source:HGNC Symbol;Acc:28087]
thioredoxin interacting protein [Source:HGNC Symbol;Acc:16952]
Mouse Orthologues:
Arrdc2, Arrdc3, Arrdc4, Txnip
Mouse Descriptions:
arrestin domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1918057]
arrestin domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2145242]
arrestin domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:1913662]
thioredoxin interacting protein Gene [Source:MGI Symbol;Acc:MGI:1889549]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa44616 Nonsense Mutation detected in F1 DNA Not yet available
sa11420 Essential Splice Site Available for shipment Available now
sa7000 Nonsense Mutation detected in F1 DNA Not yet available
sa7001 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44616
Status:
Mutation detected in F1 DNA
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
ENSDART00000045598 Nonsense 67 454 1 7
Genomic Location (Zv9):
Chromosome 5 (position 47888983)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 45677723
GRCz11 5 46277876
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCAAATGTTTGCTGGTCAGAGCGACACGGTAAAACCACTGTTCTTTA[T/A]TCGGATAAAGAGAAGTTTTATTCGGTGGAGAGGTTTTTCGTTCAGACCGA
Long Flanking Sequence:
ATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTTTTTTTACTCAGAAAGCACTTCAGTATTGCAAAAGAAACATTTGGACACATGCCCAATACTGTAATGGTCTTAAAGCACAACCTGCAATGTTTTCAGTTGTAAATTTTACAGACTGTCAGTGACAGTGTAGCCTACTACGCCACACCCACAGCTGGAAGTGCTTTACTTGCGGACTGTTTCCTGTGCATCGCTACAAAGCATTCCATTCACTTTAGATAGACGACAGAAACTGGCATAAGGAGGCACGATGTCGCTCACTGTGAAAAACATTTCTGTCATTTACAATCCTATCAATCAGAACAATACTTTCACCAGCGGGGATTATATATCTGGAAAAGTCATTCTGGAAGTGGTAAAAGACACTCAAATGCAGTCGCTGAGTGTGAAAATTAAAGGCAAAGCAAATGTTTGCTGGTCAGAGCGACACGGTAAAACCACTGTTCTTTA[T/A]TCGGATAAAGAGAAGTTTTATTCGGTGGAGAGGTTTTTCGTTCAGACCGACACAAAACATGGTAGGTGTCTGCTCGACTACTTTAGTTTTTGCAACATGAAGCCGAGTCGATTTATGTAACCAGCTTTACCCTGTGCTTGTAACTTGATCTTTTTAGCAAATGACCATGAAATGCTGAAAGATCCATCCGGGCAGCCTTGTAAGTCTTTTTTCCCTTCTTTTTCAAATGAATATTGCAGATAAATAATAAAAAAAATAAACTTTGAAAAAAATAAATATGCACATTTTAACTTTTTTTACTTTGTTTTTGATTTGTTAGACTCTTCGGTGGTGGCACCAGGGCGTCATGTTTACCCTTTCACCTTTCAGTTGCCCTTACAGTAAGTCTTTTAAGAAGACCAAATACATGATTAAATTTATAGATTAATAAAAAATCTGTGTTTGTATTCATGTTGTGTTCAGATTTGCAGAGATTGAAATGAGTAAAATAAATACATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11420
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045598 Essential Splice Site 88 454 1 7
Genomic Location (Zv9):
Chromosome 5 (position 47889046)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 45677786
GRCz11 5 46277939
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTTTTATTCGGTGGAGAGGTTTTTCGTTCAGACCGACACAAAACATGG[T/G]AGGTGTCTGCTCGACTACTTTAGTTTTTGCAACNNATGAAGCCGAGTCGATT
Long Flanking Sequence:
GAAAGCACTTCAGTATTGCAAAAGAAACATTTGGACACATGCCCAATACTGTAATGGTCTTAAAGCACAACCTGCAATGTTTTCAGTTGTAAATTTTACAGACTGTCAGTGACAGTGTAGCCTACTACGCCACACCCACAGCTGGAAGTGCTTTACTTGCGGACTGTTTCCTGTGCATCGCTACAAAGCATTCCATTCACTTTAGATAGACGACAGAAACTGGCATAAGGAGGCACGATGTCGCTCACTGTGAAAAACATTTCTGTCATTTACAATCCTATCAATCAGAACAATACTTTCACCAGCGGGGATTATATATCTGGAAAAGTCATTCTGGAAGTGGTAAAAGACACTCAAATGCAGTCGCTGAGTGTGAAAATTAAAGGCAAAGCAAATGTTTGCTGGTCAGAGCGACACGGTAAAACCACTGTTCTTTATTCGGATAAAGAGAAGTTTTATTCGGTGGAGAGGTTTTTCGTTCAGACCGACACAAAACATGG[T/G]AGGTGTCTGCTCGACTACTTTAGTTTTTGCAACATGAAGCCGAGTCGATTTATGTAACCAGCTTTACCCTGTGCTTGTAACTTGATCTTTTTAGCAAATGACCATGAAATGCTGAAAGATCCATCCGGGCAGCCTTGTAAGTCTTTTTTCCCTTCTTTTTCAAATGAATATTGCAGATAAATAATAAAAAAAATAAACTTTGAAAAAAATAAATATGCACATTTTAACTTTTTTTACTTTGTTTTTGATTTGTTAGACTCTTCGGTGGTGGCACCAGGGCGTCATGTTTACCCTTTCACCTTTCAGTTGCCCTTACAGTAAGTCTTTTAAGAAGACCAAATACATGATTAAATTTATAGATTAATAAAAAATCTGTGTTTGTATTCATGTTGTGTTCAGATTTGCAGAGATTGAAATGAGTAAAATAAATACATAAATTAATTAATTAATTAAATTATTAATTTAGAAGTGCTGAGTAAGGATTTTTCTTTCACATTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7000
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045598 Nonsense 236 454 6 7
Genomic Location (Zv9):
Chromosome 5 (position 47891773)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 45680513
GRCz11 5 46280666
KASP Assay ID:
554-5239.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCAGTCAAGCYAAAGTACTGCCTGTATGAAAAACACAGTTTTTTTGCC[A/T]GAGGAAAGMGAAAACTTCACACKCACGACATTTTTAAAGAARTGGGGGAA
Long Flanking Sequence:
CAGGCCCTGATCTTATCAGTATCTGCCTTTGGAGTCAGTATGGACCTTCTTGAGTCAGAAAGGCATGTTTTTTCATACAAACAAATGCATATGATAATTAAGCCTCTTACAACCCCCTCTGGTTTTAGAAATAGTTTACAGTTGGGGTTAAGTTTAGGCGGAGGGAATAAGTGTGGATTACATTTTCTCACAGAATTGATGTTCCATTAACACAAGCTAATCAAGGATCGCATCCACCAAAAACAGTTTACAGAACAGTCTTGATTTTTATAGCTTACTGTACGTAATTCTGAATAACTGAATGACAATTTTGTCAAAATGTCAGGCAGAAACAGTTTCCAGTGATATTTTATGTATTTATCATAAGTAATGATCTAATGACCTAATTGTTGTGTCTTTCTCTAGGAGAGGGCTTAAAATTTTTGGCTGAAGTTCAAAACAATTCCTCTCGTGCAGTCAAGCCAAAGTACTGCCTGTATGAAAAACACAGTTTTTTTGCC[A/T]GAGGAAAGAGAAAACTTCACACGCACGACATTTTTAAAGAAATGGGGGAACCCATTGAGCCAAGCTCAAAGAAAACCATCACCACGGTGCTGACCATTCCTCCCAGCCTTACAGTCTCAATCCTAAACTGTAGGATCCTCAAGGTTGAGTACAGACTGAGGGTGAGTTACAGCATCTAAAGTAGTGGTGCCCAAACTTGGTCCTGGAGGGCCGGTGTCCTGCAAAGTTTAGTCCCAACTCCAATCAGACACCTTGGCTAGCTAATCAAGCCCTTACTAAGCATTCTAGAAAGATCTGTGCAGGTGTGTTGAGGCAAGTTGGAGCTAAAATCTGCAAGACACCAGCTCTCCAGGAATGAGATTGGACACCCCTGATCTAAAGCAAATGGTGCATTCTACTTTATGCAATGGTACGCAGACCAATTAAAATATTACTTGAAGTGGTTTATGCCAGTTAAAAATTTTGCCCTTTTTGAGAAGGTGCTGACGCCACACTACTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7001
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045598 Nonsense 441 454 7 7
Genomic Location (Zv9):
Chromosome 5 (position 47896244)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 45684984
GRCz11 5 46285137
KASP Assay ID:
554-5201.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGTTCCACTTCAGTCAAGCACATCAGCTCCACCTCCATATCAGGAATA[C/A]AAGTTTTATCCACARCTGCCAGATCAGCCAGAAAAATCTTGACAAAATCW
Long Flanking Sequence:
TTGTCATTGTCCAGTCTCAATAATTGGTTTGTCATTTGTGTCTAGGTTTACTTGGATGTGAAATATGCATCAGATCCAGAGATCAAATTCCCAATAGTGATTCTTCCTGTTCAGCCTGTATCAGGTGCAAATGGTGCTAGAAATAATGACTTTGGAATTTGGAATCAGCCACCGCCAGGCATTGCAGGTCCCAACCCACCTCCTACAGCTCCATCAGCCCAACCACACAATATGGCTGGACCACCTGGTCAGTTTAGTGCTCCTGGTAATTACGGACCTCCTGTTGGTCAATTTCCATCTCCTGGTTACCCTGGACCTCCTTTGGGTCAGGGTGGTCCTCCTAGTTACACTGGACCTCCTCTGGGTCAGTTTGGGGCTCCTGCTTTTCCTGGACCTCCAGGTCAGTCCGCTCCCTCTTATTACAGTGGAGCTCCGGGCCAGTTTGGTTCTTCAGTTCCACTTCAGTCAAGCACATCAGCTCCACCTCCATATCAGGAATA[C/A]AAGTTTTATCCACAACTGCCAGATCAGCCAGAAAAATCTTGACAAAATCATTTTGGAATAACTTTCTAGGTTCCTTTTATTGTTGTGTTGTTTAAAAAGCTGCAGTTTGGGAATCATTTCTCACTTTTAATGAACCATTAACTATGACTGGCGTATTTGCTGAGCATCTGATTTGGTGTTTATTTATAATTTGGTTGTTAATAAATTTAGTCATGGGGTAGAATTACAGGATGTCAAATGTGGTCATGCAGAATAATAAGGCATCAATAAACCGACATTGTGCTAGTAATATGCAATCTAATGAACAACAAAAGTGAGAGTTGGTCCCTGAAAAAAAAAAAAAAAAAAAAACATTACTGTATCATATCTACAATGACCTATATTATTTTTGTAAGTTAGTAGTTCACTTTTAATATTTAAATAAATGAACATAGATCTATCATAGTATTATTTTTGTATGCTTAACCATCTGTGTGGTGCTAAATTCTGCATCACATACA
Associated Phenotype:
Not determined