Busch Lab

ZMP

ankrd24

Ensembl ID:
ENSDARG00000062103
ZFIN ID:
ZDB-GENE-050208-747
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LX20]
Human Orthologue:
ANKRD24
Human Description:
ankyrin repeat domain 24 [Source:HGNC Symbol;Acc:29424]
Mouse Orthologue:
Ankrd24
Mouse Description:
ankyrin repeat domain 24 Gene [Source:MGI Symbol;Acc:MGI:1890394]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa12094 Essential Splice Site, Missense Available for shipment Available now
sa3188 Nonsense F2 line generated Not yet available
sa10909 Nonsense Available for shipment Available now
sa19294 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12094
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, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089348 Essential Splice Site 646 950 20 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 None None 77 None 3
ENSDART00000144648 Missense 77 220 1 2
Genomic Location (Zv9):
Chromosome 22 (position 21688602)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 21341850
GRCz11 22 21366828
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGGARTTGAAGGAGAGCGTCCCTCGAGGTCAGTTTGAAGAGGTTCAG[G/A]TCACTTTAGGCCTTCAGCTTAAYCAGTTAGCTCAAGAACGTGCYGAAGTG
Long Flanking Sequence:
AGAAACATCAAAAAGCACTGGAGAAAAAGTTGTCCCAAGCCCAGGCTGAGTTAGAGGAACTCAAAGAACAGATGCGTTTAGGGGTCTACTCTGTGGAGGATGCTGAAGAGAAGCCTGAAAAGAGCTCAGTGGAAGGCGGAGATTTGGAGACCCACCAGTTGAAAGCGAGGGTACAGGAGCTGGAGGCGGAGCTAGTCAGCAAAAAGACAGATGGGGAGGGGCTTAGTGAGGATGACAACAACACCATGCAACAGCTGAAAGAGAGGGTGAAGGAACTTGAGGCAGCTCTGCAAGACAGAGAGAAAGAGGGAGAGGAGAACGAGACAGTTGTAAACCTTAAAAAGCAGGTGGAAGAGCTTGGAAAAGCCCTGGAGCTAAGCAAAGCAGCAGGAAAAAAGGAGGGCGAGGGAGCACCATTGAACGGATTGCAGGCACGGGTGGAAGAACTCGAGCAGGAGTTGAAGGAGAGCGTCCCTCGAGGTCAGTTTGAAGAGGTTCAG[G/A]TCACTTTAGGCCTTCAGCTTAATCAGTTAGCTCAAGAACGTGCCGAAGTGGCTGCTCGACTCAACCAGGCCTTGCTGGAGCTGGAAAGGCTCCGACCCCCATCCCACATTGACGAGGATGAAGAGGACGATGAGCCGTCTGAGAGCTCAGAGGTCTCCATTGCATCTGGTGAGTGCACCTGTTGTCCCTCTGCGACTCTCCAAAATAACTATTTGATTCCAACGTTTAAATATAACTCTTATTTTTGACCAATCAGACCACTCTCTACATATGTCACCGGGCGGCCGGACCTTGGAGGCCATAAAAGAGGAGCTTGAGGTGGCAAGGCAAGAGGCAGCCCAAGCTCTGGACAGCCTGTGTGCTGAAAGAGAGAGCCGGGCTCAGGATGTGCTACAGCTGAGAGACGCAGTACCACTTGTTAAACACCAGGAGTCACTGTCCGCAGTAGCCCAGCAGCTAGCTCAAACAGAGAAAGAGCTGCAAGCTGAGAGGGCACTGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3188
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089348 None None 950 None 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 None None 77 None 3
ENSDART00000144648 Nonsense 96 220 1 2
ENSDART00000089348 None None 950 None 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 None None 77 None 3
ENSDART00000144648 Nonsense 96 220 1 2
Genomic Location (Zv9):
Chromosome 22 (position 21688545)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 21341793
GRCz11 22 21366771
KASP Assay ID:
554-3274.1 (used for ordering genotyping assays)
KASP Sequence:
TAGGCCTTCAGCTTAATCAGTTAGCTCAAGAACGTGCCGAAGTGGCTGCT[C/T]GACTCAACCAGGCCTTGCTGGAGCTGGAAAGGCTCCGACCCCCATCCCAC
Long Flanking Sequence:
AACTCAAAGAACAGATGCGTTTAGGGGTCTACTCTGTGGAGGATGCTGAAGAGAAGCCTGAAAAGAGCTCAGTGGAAGGCGGAGATTTGGAGACCCACCAGTTGAAAGCGAGGGTACAGGAGCTGGAGGCGGAGCTAGTCAGCAAAAAGACAGATGGGGAGGGGCTTAGTGAGGATGACAACAACACCATGCAACAGCTGAAAGAGAGGGTGAAGGAACTTGAGGCAGCTCTGCAAGACAGAGAGAAAGAGGGAGAGGAGAACGAGACAGTTGTAAACCTTAAAAAGCAGGTGGAAGAGCTTGGAAAAGCCCTGGAGCTAAGCAAAGCAGCAGGAAAAAAGGAGGGCGAGGGAGCACCATTGAACGGATTGCAGGCACGGGTGGAAGAACTCGAGCAGGAGTTGAAGGAGAGCGTCCCTCGAGGTCAGTTTGAAGAGGTTCAGGTCACTTTAGGCCTTCAGCTTAATCAGTTAGCTCAAGAACGTGCCGAAGTGGCTGCT[C/T]GACTCAACCAGGCCTTGCTGGAGCTGGAAAGGCTCCGACCCCCATCCCACATTGACGAGGATGAAGAGGACGATGAGCCGTCTGAGAGCTCAGAGGTCTCCATTGCATCTGGTGAGTGCACCTGTTGTCCCTCTGCGACTCTCCAAAATAACTATTTGATTCCAACGTTTAAATATAACTCTTATTTTTGACCAATCAGACCACTCTCTACATATGTCACCGGGCGGCCGGACCTTGGAGGCCATAAAAGAGGAGCTTGAGGTGGCAAGGCAAGAGGCAGCCCAAGCTCTGGACAGCCTGTGTGCTGAAAGAGAGAGCCGGGCTCAGGATGTGCTACAGCTGAGAGACGCAGTACCACTTGTTAAACACCAGGAGTCACTGTCCGCAGTAGCCCAGCAGCTAGCTCAAACAGAGAAAGAGCTGCAAGCTGAGAGGGCACTGCGTGAGCATGCGCAGACTGAGCTCTCCAGACTGGAAATCGAACTAAAGGCTGCGCAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10909
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089348 Nonsense 928 950 26 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 Nonsense 59 77 3 3
ENSDART00000144648 None None 220 None 2
ENSDART00000089348 Nonsense 928 950 26 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 Nonsense 59 77 3 3
ENSDART00000144648 None None 220 None 2
Genomic Location (Zv9):
Chromosome 22 (position 21681221)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 21334469
GRCz11 22 21359447
KASP Assay ID:
2261-6794.1 (used for ordering genotyping assays)
KASP Sequence:
CTGATRTCTTAAATCATGATGTCTTTTTGTCTTAATAGGGCCGTATGGAT[G/T]AAGAAGTTCAAGCGCTTTTGCTTCAAATCCTCCGTATGACACAGAAAGGT
Long Flanking Sequence:
TTTCGGTAAAATAAGCGCAATCTAGAAGACTTTGCCTTTCATACAAGCCAGTTCTGATAAGCGACAAGACTTTTGTCAGGTAGTGTATACATTTAAAAACATGATTAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACATACATATATTGTTATTATTATTTTTTTTCATATATATATATATATATATATATATATATATATGAAAAAATAGAATTATATATGAAAAATGTATTCATTTATCTTCAACTTTCTTCATTTCTCAGGACTGGGAGCGCAAACACAAGGCTGTTGTTTCAATATATCGTTCTCATCTATTAGCTGCTGTACAGGTGAGACCCATAAGCTTGACTTTTTGTCTTCAGAAACATCTGATGTCTTAAATCATGATGTCTTTTTGTCTTAATAGGGCCGTATGGAT[G/T]AAGAAGTTCAAGCGCTTTTGCTTCAAATCCTCCGTATGACACAGAAAGGTCAGAATTAGTGCATTTTTTACTGACAGCAATACACTAAGCTCAAGTGACCCCTTGAACACAAGCCTATCAGCACTGTGCACCACCAGAGAGTGAGCCATTGAAACTGTGAATGAGAAGATATAGTTTTTGGAACACGACAGAGATGATTCTATTTCCTGCTTGTGTTGATTCGTGAGGAAGAACACTGATCATTTTGTACCACGTTGCAATAAACATCGAGAAACGCTGCTGACTTGCTCTTCCTTTTTTTTGCAAGTTTGTGGTTGATAGTTTCATGCAGCTAAAGAAAGTGTATGGTAAATATTACTTTGGTGGTAAAACGAACGTCATCTTACATTTCTGTGGTGTTAAAAGATACATAGAGCAAGACTACGTCAAATCCTGTGCTCTCACATGTGTTCAACCACAATCAACCAGGCAGATCTATTAATGCAGGCTTCCTTTTCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19294
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089348 Nonsense 928 950 26 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 Nonsense 59 77 3 3
ENSDART00000144648 None None 220 None 2
ENSDART00000089348 Nonsense 928 950 26 27
ENSDART00000131476 None None 212 None 7
ENSDART00000139817 Nonsense 59 77 3 3
ENSDART00000144648 None None 220 None 2
Genomic Location (Zv9):
Chromosome 22 (position 21681221)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 21334469
GRCz11 22 21359447
KASP Assay ID:
2261-6794.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATGTCTTAAATCATGATGTCTTTTTGTCTTAATAGGGCCGTATGGAT[G/T]AAGAAGTTCAAGCGCTTTTGCTTCAAATCCTCCGTATGACACAGAAAGGT
Long Flanking Sequence:
TTTCGGTAAAATAAGCGCAATCTAGAAGACTTTGCCTTTCATACAAGCCAGTTCTGATAAGCGACAAGACTTTTGTCAGGTAGTGTATACATTTAAAAACATGATTAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACATACATATATTGTTATTATTATTTTTTTTCATATATATATATATATATATATATATATATATATGAAAAAATAGAATTATATATGAAAAATGTATTCATTTATCTTCAACTTTCTTCATTTCTCAGGACTGGGAGCGCAAACACAAGGCTGTTGTTTCAATATATCGTTCTCATCTATTAGCTGCTGTACAGGTGAGACCCATAAGCTTGACTTTTTGTCTTCAGAAACATCTGATGTCTTAAATCATGATGTCTTTTTGTCTTAATAGGGCCGTATGGAT[G/T]AAGAAGTTCAAGCGCTTTTGCTTCAAATCCTCCGTATGACACAGAAAGGTCAGAATTAGTGCATTTTTTACTGACAGCAATACACTAAGCTCAAGTGACCCCTTGAACACAAGCCTATCAGCACTGTGCACCACCAGAGAGTGAGCCATTGAAACTGTGAATGAGAAGATATAGTTTTTGGAACACGACAGAGATGATTCTATTTCCTGCTTGTGTTGATTCGTGAGGAAGAACACTGATCATTTTGTACCACGTTGCAATAAACATCGAGAAACGCTGCTGACTTGCTCTTCCTTTTTTTTGCAAGTTTGTGGTTGATAGTTTCATGCAGCTAAAGAAAGTGTATGGTAAATATTACTTTGGTGGTAAAACGAACGTCATCTTACATTTCTGTGGTGTTAAAAGATACATAGAGCAAGACTACGTCAAATCCTGTGCTCTCACATGTGTTCAACCACAATCAACCAGGCAGATCTATTAATGCAGGCTTCCTTTTCAAG
Associated Phenotype:
Not determined