Busch Lab

ZMP

ENSDARG00000023692

Ensembl ID:
ENSDARG00000023692
Human Orthologues:
ANKRD28, ANKRD44, ANKRD50, ANKRD52
Human Descriptions:
ankyrin repeat domain 28 [Source:HGNC Symbol;Acc:29024]
ankyrin repeat domain 44 [Source:HGNC Symbol;Acc:25259]
ankyrin repeat domain 50 [Source:HGNC Symbol;Acc:29223]
ankyrin repeat domain 52 [Source:HGNC Symbol;Acc:26614]
Mouse Orthologues:
Ankrd28, Ankrd44, Ankrd50, Ankrd52, E230028L10Rik
Mouse Descriptions:
RIKEN cDNA E230028L10 gene Gene [Source:MGI Symbol;Acc:MGI:2685285]
ankyrin repeat domain 28 Gene [Source:MGI Symbol;Acc:MGI:2145661]
ankyrin repeat domain 44 Gene [Source:MGI Symbol;Acc:MGI:3045243]
ankyrin repeat domain 50 Gene [Source:MGI Symbol;Acc:MGI:2139777]
ankyrin repeat domain 52 Gene [Source:MGI Symbol;Acc:MGI:2444029]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa16639 Nonsense Available for shipment Available now
sa23408 Nonsense Available for shipment Available now
sa36748 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16639
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 508 1404 14 28
Genomic Location (Zv9):
Chromosome 19 (position 1555025)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1047077
GRCz11 19 1463474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATAGAATGGATTTTCAGTTTGACTTGAAGCTGGCGCCGCCTGCTGRT[C/T]AAAACAGTGTAAGTGCAGTACAGTCTGGCCACGCATGTTTTCATGCAAGT
Long Flanking Sequence:
TTGTCCTCTGGATGTGAGTAAAAGTGTGAACTGTGCAGGACGGAGAGACGGCGCTTCATCTGGCAGCAGAGCTCAGGACGGATGCGCTTCATCAGCCGGAGGAGGACATTACCATCATCCAGATCCTGATGGAGCATCAGGCTGACATCACTGCAGTCACACGACAGGTCTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATAGTTATCTCAGATGCAATGTGTGACTGTGGCATTTTGAAACAGAATTAATTCGAATCTAAATTGTGTTATATTAAATGTCTTTGACTTGTGTGTGTTGTATCTAAGCATTAGAAAAAAGCTAACTCAAATTGTTATCACTTTACATCAGTATGTGTAGTATGCACATAGCAGTGGTGGCTAAATAAACGTTTAGAAAAACAATCAGTGCAAAATGATTCAGAATAGAATGGATTTTCAGTTTGACTTGAAGCTGGCGCCGCCTGCTGGT[C/T]AAAACAGTGTAAGTGCAGTACAGTCTGGCCACGCATGTTTTCATGCAAGTATCTCTTGTTAAATTAAATAGAGTTAAATAACATGTTTTTTAATTTTGTTTTGTGTTTTGTTTGTTTTTTATTTTTTTGTTTTGTTTTTTGTTTGTTTGTTTGTTTGTTTTGTTGTGTTTTATTTTGTTTTTTGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAGTAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTATAAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTAGAAATGCTGATCTAGAAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTAGAAATGCTGATCTGGGAATGCTGATCTATAAATGCTGATCTATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23408
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 868 1404 22 28
Genomic Location (Zv9):
Chromosome 19 (position 1563768)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1038334
GRCz11 19 1472217
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATATTCCTGCTC[A/T]GACGAGAGAAAAACACACTCCGGCTGCTGGACGACAAGAAGGTCAGACTC
Long Flanking Sequence:
GAACGGCAGAGTCACTCGCTGTCTTCAAGAAACCACTAAAAACTCAACTATTTAGCCTCCACTTCCCTTCCTAATCTGCAATTGCCTCTCTTGCTCCACCACTAACTGTACTACAAAAATAAAATTACTAATGTTTTGCTTCTTACACTTTACACACCTGAAACTTGCCTACAGCACTTATTCATTGTTGCTTTTATAGTTGTTTAAATTGCTTCCTTGTCCACATTTGTAAGTGGCTTTGAATAAAAGTGTCTGCTAAATGACTAAATGTAAATGTAAGGGACTCATTACATGTGTCTATATATGGTTTGTAACTTGTCCATGTGTGTGTTCAGAGTGGCTGGACAGCGCTGCATTACGCTGCTGAAGCCGGCTGTCTGGAGGTGTTGTTATTTCTGGTGGAGAGTGGAGCGTCCGCCTGTGCTGAGTGTCACGGTGGACGAACGCCGCTGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATATTCCTGCTC[A/T]GACGAGAGAAAAACACACTCCGGCTGCTGGACGACAAGAAGGTCAGACTCACTGCTGCACTCCTCAGTCTGTGTCTGTTTTAGTTTCTGTCAGCTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTATTTTTGACTGTTTGGCGCCATCTAGTGTCTGAATAATGCACAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTGGCTCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCTGCTGTTTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36748
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 1205 1404 24 28
Genomic Location (Zv9):
Chromosome 19 (position 1567717)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1034385
GRCz11 19 1476166
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTGATGTTGTTTCACACTGCATTTACACTGAGTCTCACCGCATTATG[C/A]CAGCCGCTTTATCCACAAGAACAGCACAATACCACGACAGAAGTGACCGT
Long Flanking Sequence:
ACCATCCCAATCGTGAAGTTCATGAGCCACCTGGTGTCCCACATCTTCCTGCTGACTCTGTTCATCCTGACCATCGTGTACCCGCCCGTGAGTCCTCTATCCCAGGCCCGTCTGATGCCCAGCTGGAGCGAGTGTCTGCTGCTCATCTGGCTGTGTGGGATGCTGGTCTCTGAGCTGACATTCCCCGGAGAGCGCACTGGATTAGCCTGGATCCGTCTGCTGCTTTTGGGTTTTTCTGCTGCTGCTCTGCTCTGCCACCTGCTGGCGGTGTTCACCCAATGGTGGCCGCCAACACACCTGCATTGTCTATTCGCTCGTAACGTACTGCTAGCCGTCGCCATGACTCTCGGTTTCATCCAGCTTCTGGAATTCCTCACATTTCATCATTTATTCGGGCCGTGGGCGATAATCATCAGAGACTTGATTAAAGATCTGTGCAGATTTGCTGTGATCCTGATGTTGTTTCACACTGCATTTACACTGAGTCTCACCGCATTATG[C/A]CAGCCGCTTTATCCACAAGAACAGCACAATACCACGACAGAAGTGACCGTTCCTGGGCCGTTAAATATGTCCGTGCTGCTTTTTTTTGCGTTGTTTGGTTTGACTGAGCCTGATAAAATCCCCGATGTGGATCGATCGCCTCCTGCTACGGCGGTGTTGGCTAAAATGGTGTTCGGTGTGTATCTGGTGGTGACGTTTATCGTGTTGATTAATCTGCTGATTGCGATGATGAGCGACACATATCAGCGAATACAGGCTCAGTCCGACACCGAGTGGAAGTTTGGCCGTGCTGTTTTGATTCGAGATATGAGCCGCAAATCTGGCATCCCGTCTCCGTTTAACCTGTTCACCAACCTGTTCTACTCCGTTAAAGTTGTCTGCAAACGTGCAGGTATGATCCGTTAGTCATCATCTGCATGTTTATAAACACTTTTTCTTGAAAATATTCTAAATGTACAGTTATTTTAGAGTTAAATTGTTAAGTTTTACCATTTTTGGAG
Associated Phenotype:
Not determined