Busch Lab

ZMP

ch1073-321c8.1

Ensembl ID:
ENSDARG00000090656
ZFIN IDs:
ZDB-GENE-040426-1976, ZDB-GENE-081028-53
Description:
translocase of outer mitochondrial membrane 20 homolog a [Source:RefSeq peptide;Acc:NP_998201]
Human Orthologue:
ARID4B
Human Description:
AT rich interactive domain 4B (RBP1-like) [Source:HGNC Symbol;Acc:15550]
Mouse Orthologue:
Arid4b
Mouse Description:
AT rich interactive domain 4B (RBP1-like) Gene [Source:MGI Symbol;Acc:MGI:2137512]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa16991 Essential Splice Site Available for shipment Available now
sa22385 Nonsense Available for shipment Available now
sa11972 Essential Splice Site Available for shipment Available now
sa11502 Essential Splice Site Available for shipment Available now
sa13629 Essential Splice Site Available for shipment Available now
sa35597 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa16991
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028457 None None 145 None 5
ENSDART00000128415 Essential Splice Site 150 1249 6 28
ENSDART00000148083 Essential Splice Site 148 387 5 12
Genomic Location (Zv9):
Chromosome 13 (position 50653193)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49364981
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTCATCGGCAARAAGRGAAACCGCGGCGGWCGRCGCTCCAACCCCAT[G/A]TGAGTGCCTGTGYGATTGTGTGTGTGTGTGTGTKTGTGTGTGTGTGTGTG
Long Flanking Sequence:
CAGTGTTTGATGACGGTGATGAGAAGACTCTGCGCCGCTCGTCCCTCTGTCTGAAAGGAGCGAGACACTTTGCTGAGAGTGAGGTTAGTGTCTGTCCTCTTCACATCATCACTGTAAATCTCCTGTACAACACAACACAACACAACACATCCTGCTCACTGTAAAAGCGCACACAAATAACACTTTCTCACCTCAGTATTAGTATTTTTGATTACTATAAGTGGCTCTGTGTTGATTCATTTCTTCATCCGAATATGCATGTGTACAGTTGAAGTCAGAATTATTAGCCCCCGTTTATTTTTTTCTCTCTATGTTTGTATGAATCTATTAGTTTAGTCCTCTGGGCTGGTGATGTTGTTGTTATAGTTGTGTCAGTGCTGAATCTGAGCTCTGCTTCTCCTGCAGACTCTGGACAGGCTTCCTCTGACCAACCCTGAACACTTCGGCACTCCTGTCATCGGCAAGAAGGGAAACCGCGGCGGACGGCGCTCCAACCCCAT[G/A]TGAGTGCCTGTGCGATTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGTGTGTGTGTTTGCGATTGTGAGTGTGTGTGCACATATTTGTGACTGTGTGAGTTTGTGACTGAGTGTGTTTGTGTATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTATTTGACACTGTTTGTTATTCTGTGTATGGATGTGTCTTTGTGACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTATATGACACTGTGTTAGTTATTCTGTTTATGGGTATGTGTTTGTAACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATTGTGAGTGTGTTAATGTGCACACATTTGTGACTGTGTGAGTTTGTGACTGAGTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22385
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
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028457 None None 145 None 5
ENSDART00000128415 Nonsense 225 1249 9 28
ENSDART00000148083 Nonsense 223 387 8 12
Genomic Location (Zv9):
Chromosome 13 (position 50646284)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49358072
GRCz11 13 49648750
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGATGGTATGATTTAATGCATACCGTGTTGTGTTATGTCCTACAGTTA[T/A]ACAGTTTTACGGAAAGATATTCGAGAGTTGGATGAAGATAAAGCTCCCAA
Long Flanking Sequence:
TGTATTGTAGTATATTATACTATATGGTTGAAAAACTACAGTGTAGGGTTATTTGTTTATATTTTGTGTTACCTTAGCAGTTGTATAATTAATTCTAATGCTTAAAAAACTCTATAGCATTGGCTGTAAATTACTATAGTACTTATTGACGTGGCTATGTCTGAGGAACAGCCTGTTTGGTTGCATATTTTGTGATCATGTTTGCCTCGTTTAGTTTTTATTATTATGGTGCTGATTTGTTTGTGATTTTGTTTATAATAAGTGCTTGAAATATCACTGTAAACACAATATTTTCAAGCACACAATTATTAAAAAAAATTTGACTAATGTATAATATAAGTAAACTAACAAAAATAATTAAAAAATTTTAAGTCAAAGTGCAGACTCAGGTTGTTAAATTATGATCATGACTTGTTTGTTTTAGTTTGTTGTTGTTTATTATTGGTTATTTCAGATGGTATGATTTAATGCATACCGTGTTGTGTTATGTCCTACAGTTA[T/A]ACAGTTTTACGGAAAGATATTCGAGAGTTGGATGAAGATAAAGCTCCCAAAGCAGATGCAGGACTCAAACCAGGTAAGAGGACATGTCTTTATTATTACATAAAACTAAACATTATTTTTATACTATTTTAATTTTGTTTCATATATTTATTTTAACTAATGGCATTTCATATTTTATATATAATTTTTATTTTTATTTAGATTATTTCTTCACATTACAGAACAATAATTTAACAGGATTTTTAATTATATATGACAACATATATCATTACATATATACACATATCAATATGCACATACAAATGTTAATTATATACATAGAAATAATACTATTCGCTTATTGCAAATATTTGCAGCTTAAAAAATAATTAAAAAAAACGTGTCACATTTTATTATTACTCTCGGACATCATGAAAAATTTTCATATTTAAAATTTGGGGCAGCAATGAGGCTCAGTGGTTAGCACTGTGGCCTCGCAGTATGAAGTTGCACAAAGTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11972
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028457 None None 145 None 5
ENSDART00000128415 Essential Splice Site 355 1249 12 28
ENSDART00000148083 Essential Splice Site 353 387 11 12
Genomic Location (Zv9):
Chromosome 13 (position 50638484)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49350272
GRCz11 13 49640950
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTGTTCAAGCTCTACAGGCTGGTGCATAAGCTGGGAGGATTCGACAAT[G/T]WGAGTGAAACACGGTCTCAATCATTNNNNGGAAAATAAAGATTTAAATTG
Long Flanking Sequence:
CAGCGTGGGAGGAAGTTGCCGTGGGCCTTGGTGCAGATGAAAAGTAAAAATAAAAAGTATATTTATATAGACAGATAGGTAACTAGATACAATAGACAGGGATAGATCGGCACAAAAAAATTGTCAGCCCAGCCGGAAACTACCCGCTCTGCCAGATGGCCAGTCCGCCCCTGCCTATGTCTCACTTGCCAGTCAGAACAGTTAAATGGACCTAATTGTATAGCTATGTCATCACATAAAAAGGAAAAATATTGGATTATTATTATGTATGATTTTTTTTTTTTATTTAACTTTTTTTTTTTTTTTTTTACATTTGCAAACTTTTTAATTTGAACTTTCTGTAAACTTAGATTTCACTTACACCTTAAACCCACTTTAAACTATCTTCTTGACTCTTCTGCTCAGGAACCCCCATCAACAAGCGGCCGGTGCTGGGCTACAAGAATCTGAATCTGTTCAAGCTCTACAGGCTGGTGCATAAGCTGGGAGGATTCGACAAT[G/T]TGAGTGAAACACGGTCTCAATCATTTTCAGGAAAATAAAGATTTAAATTGTTTTATAAAATTAGCTTGACAGATTTTCACAACTAGTTCAACATTAAGTATGTAATGACTGAAGTGATGAAATGAGGACTTAGGGTGCTTTCACATCTGTAGTTCGCTTCATTTGGTCCGGACCAAGGGTAGTAAATGATACATTGTTGCATTTTCTGCCGTCTTTGGGTCGTTTTCACACCACACTGCTGGCTTTGGTCCGAACCAGTTGAAACGAACCAAAATGCAGTCATCTGACAAAATGCACATCTCTCATTGGCCAGATGTTGTTGAACAAATTTCCTAAACTGCTTATCGATTGGTCAGAATTCACGTGCGGGAAAATGCCAATGAACTCCCGCAGGTAAACAAAACCGGCAGACACAAAATGTCGCTTTTTACTATGAAGGGACGACTGCGCTGACTGATTGTATGGCTGCTTTAAACAAACTATACATTTCGAGAATGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11502
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028457 None None 145 None 5
ENSDART00000128415 Essential Splice Site 355 1249 12 28
ENSDART00000148083 Essential Splice Site 353 387 11 12
Genomic Location (Zv9):
Chromosome 13 (position 50638483)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49350271
GRCz11 13 49640949
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTTCAAGCTCTACAGGCTGGTGCATAAGCTGGGAGGATTCGACAATK[T/A]GAGTGAAACACGGTCTCAATCATTNNNNGGAAAATAAAGATTTAAATTGT
Long Flanking Sequence:
AGCGTGGGAGGAAGTTGCCGTGGGCCTTGGTGCAGATGAAAAGTAAAAATAAAAAGTATATTTATATAGACAGATAGGTAACTAGATACAATAGACAGGGATAGATCGGCACAAAAAAATTGTCAGCCCAGCCGGAAACTACCCGCTCTGCCAGATGGCCAGTCCGCCCCTGCCTATGTCTCACTTGCCAGTCAGAACAGTTAAATGGACCTAATTGTATAGCTATGTCATCACATAAAAAGGAAAAATATTGGATTATTATTATGTATGATTTTTTTTTTTTATTTAACTTTTTTTTTTTTTTTTTTACATTTGCAAACTTTTTAATTTGAACTTTCTGTAAACTTAGATTTCACTTACACCTTAAACCCACTTTAAACTATCTTCTTGACTCTTCTGCTCAGGAACCCCCATCAACAAGCGGCCGGTGCTGGGCTACAAGAATCTGAATCTGTTCAAGCTCTACAGGCTGGTGCATAAGCTGGGAGGATTCGACAATG[T/A]GAGTGAAACACGGTCTCAATCATTTTCAGGAAAATAAAGATTTAAATTGTTTTATAAAATTAGCTTGACAGATTTTCACAACTAGTTCAACATTAAGTATGTAATGACTGAAGTGATGAAATGAGGACTTAGGGTGCTTTCACATCTGTAGTTCGCTTCATTTGGTCCGGACCAAGGGTAGTAAATGATACATTGTTGCATTTTCTGCCGTCTTTGGGTCGTTTTCACACCACACTGCTGGCTTTGGTCCGAACCAGTTGAAACGAACCAAAATGCAGTCATCTGACAAAATGCACATCTCTCATTGGCCAGATGTTGTTGAACAAATTTCCTAAACTGCTTATCGATTGGTCAGAATTCACGTGCGGGAAAATGCCAATGAACTCCCGCAGGTAAACAAAACCGGCAGACACAAAATGTCGCTTTTTACTATGAAGGGACGACTGCGCTGACTGATTGTATGGCTGCTTTAAACAAACTATACATTTCGAGAATGAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13629
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028457 None None 145 None 5
ENSDART00000128415 Essential Splice Site 355 1249 12 28
ENSDART00000148083 Essential Splice Site 353 387 11 12
Genomic Location (Zv9):
Chromosome 13 (position 50638483)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49350271
GRCz11 13 49640949
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTTCAAGCTCTACAGGCTGGTGCATAAGCTGGGAGGATTCGACAATK[T/A]GAGTGAAACACGGTCTCAATCATTNNNNGGAAAATAAAGATTTAAATTGT
Long Flanking Sequence:
AGCGTGGGAGGAAGTTGCCGTGGGCCTTGGTGCAGATGAAAAGTAAAAATAAAAAGTATATTTATATAGACAGATAGGTAACTAGATACAATAGACAGGGATAGATCGGCACAAAAAAATTGTCAGCCCAGCCGGAAACTACCCGCTCTGCCAGATGGCCAGTCCGCCCCTGCCTATGTCTCACTTGCCAGTCAGAACAGTTAAATGGACCTAATTGTATAGCTATGTCATCACATAAAAAGGAAAAATATTGGATTATTATTATGTATGATTTTTTTTTTTTATTTAACTTTTTTTTTTTTTTTTTTACATTTGCAAACTTTTTAATTTGAACTTTCTGTAAACTTAGATTTCACTTACACCTTAAACCCACTTTAAACTATCTTCTTGACTCTTCTGCTCAGGAACCCCCATCAACAAGCGGCCGGTGCTGGGCTACAAGAATCTGAATCTGTTCAAGCTCTACAGGCTGGTGCATAAGCTGGGAGGATTCGACAATG[T/A]GAGTGAAACACGGTCTCAATCATTTTCAGGAAAATAAAGATTTAAATTGTTTTATAAAATTAGCTTGACAGATTTTCACAACTAGTTCAACATTAAGTATGTAATGACTGAAGTGATGAAATGAGGACTTAGGGTGCTTTCACATCTGTAGTTCGCTTCATTTGGTCCGGACCAAGGGTAGTAAATGATACATTGTTGCATTTTCTGCCGTCTTTGGGTCGTTTTCACACCACACTGCTGGCTTTGGTCCGAACCAGTTGAAACGAACCAAAATGCAGTCATCTGACAAAATGCACATCTCTCATTGGCCAGATGTTGTTGAACAAATTTCCTAAACTGCTTATCGATTGGTCAGAATTCACGTGCGGGAAAATGCCAATGAACTCCCGCAGGTAAACAAAACCGGCAGACACAAAATGTCGCTTTTTACTATGAAGGGACGACTGCGCTGACTGATTGTATGGCTGCTTTAAACAAACTATACATTTCGAGAATGAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35597
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028457 None None 145 None 5
ENSDART00000128415 Nonsense 861 1249 19 28
ENSDART00000148083 None None 387 None 12
Genomic Location (Zv9):
Chromosome 13 (position 50606452)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49318240
GRCz11 13 49608918
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAGGAGCGGTCGCCCGGCTGTCGCACCAAAGGACAGAAGGACGTTTG[G/A]TCGAGTATTCAGGTTCAGTGGCCCAAGAAAACTCTTAAAGAGCTGTTTTC
Long Flanking Sequence:
GCTGATCATGATGAAGATGATGATCATCCAGGAGCACATAAAGCAGATCCTCCTCAATCACAGCACTGGGAGAAAAACAGCAGCCCGCCTGAAGCCCCCAAAACCCCTGCAGATGCGGAGCAGGAGCCCACCCTGCAGGACAGCACAGAAGCACCCAAGAGGAAGGAGCTGGACACGGACGCTTCTGCTGGCAGGAGGAAAAAAGCAGAAAACACCTCGAAAAGCCCAGCGAAAGGCAAAACCAGAAACAGCAGAGGAGGCGAATGGCTGCAGAGTGGCTCGCCGAAGAAGCTGGAGGATCGAGGAGAAAGCAGCTCTGAGGATGAACCGAAAGGACACCCTAAAAATAAATCCTCGCCTTCAAAGAAATACAACGGTGTTAAAGAGAAGAGTAAGAGCCGTGGGGCGTTTTGGGAAATCCCCGAGAAGAGAGCTAAGGTATCGGCAGGGATTGAGGAGCGGTCGCCCGGCTGTCGCACCAAAGGACAGAAGGACGTTTG[G/A]TCGAGTATTCAGGTTCAGTGGCCCAAGAAAACTCTTAAAGAGCTGTTTTCGGACTCGGACACGGAGGCGGCCAACTCTCCTCCGCCTGCAGGACCCGAAGCGTGCTCTGAATCCGCACGGGATGAAGAAGAGGAGGAGGAAGAGGAGGAGAAACTGCAGGAGCATCCCAGCAGCGGGACCAATTCAGTGCTCAACACGCCGCCCACCACGCCAGAGTCGCCCGCTGCAGCTGAAGGTATGCCCATAGCAATGCTAAACACAAATGCACTGCTTTCAGTTCTGTTCCAGGGTGTCTGCAGATCCTTAGGGTGCTTTCACATCTGTAGTTCGCTTCATTTGGTCCGCACCAAGGGTAGTAAATGATACATTGTTGCATTTTCTGCCGTCTTTGGGTCGTTTTCACACCACACTGCTGGCTTTGGTCCGAACCAGTTGAAACAAACAAAAATGCAGTCATCTGACAAAATCCACATCTCTCATTGGCCAGATGTTGTTGAACA
Associated Phenotype:
Not determined