Busch Lab

ZMP

zdhhc8a

Ensembl ID:
ENSDARG00000042872
ZFIN ID:
ZDB-GENE-091118-26
Human Orthologue:
ANKLE2
Human Description:
ankyrin repeat and LEM domain containing 2 [Source:HGNC Symbol;Acc:29101]
Mouse Orthologue:
Ankle2
Mouse Description:
ankyrin repeat and LEM domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1261856]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa17483 Nonsense Available for shipment Available now
sa45384 Nonsense Mutation detected in F1 DNA Not yet available
sa21626 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21627 Essential Splice Site, Missense Available for shipment Available now

Mutation Details

Allele Name:
sa17483
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062927 Nonsense 74 682 1 12
ENSDART00000063671 None None 634 None 13
ENSDART00000135598 None None 259 None 2
ENSDART00000140715 None None 217 None 6
ENSDART00000147740 None None 239 None 6
Genomic Location (Zv9):
Chromosome 10 (position 428913)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 425686
GRCz11 10 427331
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCAAGTGGAGCACTTCCTGCGGAMGAGCCCGAGCAGCCAATCAGTGTG[C/T]AGGAGACACAGGAAGYGAGRGAGGAGAGCNNNNNNNNNTCCACTGAGGGG
Long Flanking Sequence:
TGTAGGGGAGTGCTGTGTTGGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCACTAAACTGACCGTAGTGTATGAGTGTGTGTGTGAAGGAGTGTGTATGGGTGTTTTCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATTTGCTGGAATAGTTGGTGGTTCATTCCGCTGTGGTGACCTCTTATATTGAAGTGACTGAGCTGAAGGAGAATGAATGAATGTGTGTTTCTGTGCCTGCTGTTTGGACAGATGGAGGCGGTCCTGCAGCGGCTGCAGACGCTGACCCCGGATGAGCTGAGGGTGCAGCTGAGGGCCGCTGGGCTCCAGTCGGGCCCGGTGACACACACCACCAGGAGCCTGTGGGAGAAGAGACTGGCTCGAGCGCTGCTGGAGGAACGCACAGACTCACACACACCGCATTCAAGTGGAGCACTTCCTGCGGACGAGCCCGAGCAGCCAATCAGTGTG[C/T]AGGAGACACAGGAAGCGAGGGAGGAGAGCTCAGAGACGTCCACTGAGGGGCCGAGTGTTTATTATGGGGTGTGTGCTAATCCAGATGAGCCCTCATTACTTACAGGTCTGAAGACACTTGCACAGACACACACACACACACACACACACCAAACACACACACACACACATTCATTCATTTTCCTTCGGCTTAGTTCCATATTTATCAGTGGTCACCACAGTGGAATGAACCACCAACTATTCCAGCAAATGTTTTACAAAACGGATGCCGTTTCAGCTGCAACCCAGTACTGGAAAACACCCATACACACTCATTTACACGCACACACTCATTCACTACAGCCAGTGTAGTTGATCAGTTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCACAGCTTGGGGAAAGGGGATTCTTTCTGTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45384
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062927 Nonsense 77 682 1 12
ENSDART00000063671 None None 634 None 13
ENSDART00000135598 None None 259 None 2
ENSDART00000140715 None None 217 None 6
ENSDART00000147740 None None 239 None 6
Genomic Location (Zv9):
Chromosome 10 (position 428922)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 425695
GRCz11 10 427340
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCACTTCCTGCGGACGAGCCCGAGCAGCCAATCAGTGTGCAGGAGACA[C/T]AGGAAGCGAGGGAGGAGAGCTCAGAGACGTCCACTGAGGGGCCGAGTGTT
Long Flanking Sequence:
GTGCTGTGTTGGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCACTAAACTGACCGTAGTGTATGAGTGTGTGTGTGAAGGAGTGTGTATGGGTGTTTTCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATTTGCTGGAATAGTTGGTGGTTCATTCCGCTGTGGTGACCTCTTATATTGAAGTGACTGAGCTGAAGGAGAATGAATGAATGTGTGTTTCTGTGCCTGCTGTTTGGACAGATGGAGGCGGTCCTGCAGCGGCTGCAGACGCTGACCCCGGATGAGCTGAGGGTGCAGCTGAGGGCCGCTGGGCTCCAGTCGGGCCCGGTGACACACACCACCAGGAGCCTGTGGGAGAAGAGACTGGCTCGAGCGCTGCTGGAGGAACGCACAGACTCACACACACCGCATTCAAGTGGAGCACTTCCTGCGGACGAGCCCGAGCAGCCAATCAGTGTGCAGGAGACA[C/T]AGGAAGCGAGGGAGGAGAGCTCAGAGACGTCCACTGAGGGGCCGAGTGTTTATTATGGGGTGTGTGCTAATCCAGATGAGCCCTCATTACTTACAGGTCTGAAGACACTTGCACAGACACACACACACACACACACACACCAAACACACACACACACACATTCATTCATTTTCCTTCGGCTTAGTTCCATATTTATCAGTGGTCACCACAGTGGAATGAACCACCAACTATTCCAGCAAATGTTTTACAAAACGGATGCCGTTTCAGCTGCAACCCAGTACTGGAAAACACCCATACACACTCATTTACACGCACACACTCATTCACTACAGCCAGTGTAGTTGATCAGTTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCACAGCTTGGGGAAAGGGGATTCTTTCTGTAGGTCCCCTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21626
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062927 None None 682 None 12
ENSDART00000063671 Essential Splice Site 407 634 11 13
ENSDART00000135598 None None 259 None 2
ENSDART00000140715 None None 217 None 6
ENSDART00000147740 None None 239 None 6
Genomic Location (Zv9):
Chromosome 10 (position 453150)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 449923
GRCz11 10 451568
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAACAACACTAACGCACTAGGTCTTGACACATTTTGGTTTTGTGATG[T/G]TACTATTTAAAACTATTTACCATGAGGTAAGTCATTTTACTCAGGAATGA
Long Flanking Sequence:
GAGCCAAACTCTGACGCTCAAGGTATTGCAGAATCACAGAAAAATCTCCTCATTTTACATAAGTAGTTTGAACAAGCAGCAAAAGTTATCTTTTTTTTTTGAGTTTGTCTGTGTAATGTTTCTCAGTGTTTGTTGGACGTGTGTTTGTGTCAGTGTCTAGATGAAGATGAGGATCCAGACAGTAAGCGTCTGACCACTCCTCCTCCACTACCTCCTAAACCAGATCCAGTCCTGCTCAGGAATCATCTGGCTGTGCTGGAAGGTGAATGGCAAGCGATTGGTGGGAAATGATGTTTCTGCAGGTCTGTCTTCATGATCTCTCATTGTGTTTTATTTTACAGAGAGCCTGCTTCAGTCCAGGGCGCTGCTGCCCTCAGGACACAACATGAGTCCGCTTCAGTCCTCAGAGTCGCCCACTAAAGAGCTCTATCAGCTGACTAGAGATCAGGTGAGAAACAACACTAACGCACTAGGTCTTGACACATTTTGGTTTTGTGATG[T/G]TACTATTTAAAACTATTTACCATGAGGTAAGTCATTTTACTCAGGAATGAATCACAAATACTGTAGTAGTTCCACCTGAAATCAGAGACATTACTGGCTGAAAATCAATGCTTTATAAAATATGTAATAAACATACTGATATGCAAATCTCTAATAGAATAAAACAGACTGAAATGTGCAGCTCTAATAGAACAAAACATACCACTGTGCAAATCTCTAATACAGGGGTGTCTAAACTCAGTCCTGGAGGGCTGTTGTCCTGCATTGTTTAGTTCCAGCTTCCTTCAGCACACCTGCCTGGACGTTTCTACTATACCTAGAAAGACCTCGATTAGCTGGTTCAGGTGTGTTTAGTAGGAGTTGGAACTAAACATGCAGGACACCAGCCCTCCAGGACTGAGCTTGGGCACCCCTGCTCTAATAGAATAAAACAGAACGGTATGCAAATCTCGAATAGACTAAAACAGACCGATATGCAAATCTCTAATAGAATAAAACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21627
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:
A > T
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062927 None None 682 None 12
ENSDART00000063671 Essential Splice Site 408 634 None 13
ENSDART00000135598 Missense 11 259 1 2
ENSDART00000140715 None None 217 None 6
ENSDART00000147740 None None 239 None 6
Genomic Location (Zv9):
Chromosome 10 (position 455232)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 452005
GRCz11 10 453650
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGTCTGTTGTTTATAGATGGGGATGAGGATATCTCCTCTACTCTCTC[A/T]GGAACATGCGTCTGAGCCCAGTCTGCTCCAGTCGGACAACCACATGTCTC
Long Flanking Sequence:
TAAAACAGACCGATATGCAAATCCTGAATAGAATAAAACAGACCAATATGCAAATATCGAATAGAATAAAACAGACCGATATGCAAATCACTAATAAAATAAAACAGACCGATATGCAAATCACTAATAGAATAAAACAGACTAATATGCAAATCAATAATAGAATAAAACAGACCGATATGCAAATCACTAATAGAATAAAACAGACCGATATGCAAATCAATAATAGAATAAAACAGACCGATATGCAAATCTCTAATAGATCAAAACAGACCGATATGCAAATCTCTAATAGATCAAAACAGACCGATATGCAAATCTCTAATAGATCAAAACAGACCGATATGCAAATCTCTAATAGATCAAAACAGACCGATATGCAAATCTCTAATAGATCGAAACAGACCGATATGTGAATTGTAAAGTTCATACAACAACAAAAACCCTCAAGTTTGTCTGTTGTTTATAGATGGGGATGAGGATATCTCCTCTACTCTCTC[A/T]GGAACATGCGTCTGAGCCCAGTCTGCTCCAGTCGGACAACCACATGTCTCTTCAGCCCATAAACTCTCTGACGCTGAACTCCTGCTCTCTGAGCCTGAAACACTCGGCCCGCCGAGGCTCACAGCGGGCAGAAACTCAGGCTCCACAAACCATCCCTACACCCAGCGCCCTCAGCAGCCGCTCCGGGAGTCTTTCCTACGACAGTCTACTGCGTCCAGCGGGACACCAGATGCAGTTCAGACCCACAGATACAAGTAGGTATCACTGCAGCCCGATAATAAAACACAACAGGTTACCGTGAGGTTGGGTTTAGTGTTAGGGTAGGTGTAGACATTCATAAAACACAATAGGTTGGACTGTACAAGACTGTACACTGTGTCATGTACAAGACATTTAATAAATGAACACCAGGAGGTTTGCACAGCCCACTTGGAGCTCGAGTCCCACCCACTTACCTTCGTTTATGCCCTTGTCTCCACAGATCTGTCCCGTGGACCAGT
Associated Phenotype:
Not determined