Busch Lab

ZMP

akap9

Ensembl ID:
ENSDARG00000079610
ZFIN ID:
ZDB-GENE-030131-7276
Human Orthologues:
AC104809.3, CEP110, CEP250, CROCC, GOLGA4
Human Descriptions:
centrosomal protein 110kDa [Source:HGNC Symbol;Acc:1858]
centrosomal protein 250kDa [Source:HGNC Symbol;Acc:1859]
ciliary rootlet coiled-coil, rootletin [Source:HGNC Symbol;Acc:21299]
golgin A4 [Source:HGNC Symbol;Acc:4427]
Mouse Orthologues:
Cep110, Cep250, Crocc, Golga4
Mouse Descriptions:
centrosomal protein 110 Gene [Source:MGI Symbol;Acc:MGI:1889576]
centrosomal protein 250 Gene [Source:MGI Symbol;Acc:MGI:108084]
ciliary rootlet coiled-coil, rootletin Gene [Source:MGI Symbol;Acc:MGI:3529431]
golgi autoantigen, golgin subfamily a, 4 Gene [Source:MGI Symbol;Acc:MGI:1859646]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa25075 Nonsense Mutation detected in F1 DNA Not yet available
sa29112 Nonsense Mutation detected in F1 DNA Not yet available
sa43191 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36744 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25075
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
Founder:
SL6_12_B12
KASP Assay Location:
Project 554.49, Plate 2, Well B06
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110495 Nonsense 441 2229 5 30
Genomic Location (Zv9):
Chromosome 19 (position 539832)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 561319
GRCz11 19 561128
KASP Assay ID:
554-7390.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCAGAAGGTGGAGGAGCTGACGACTGAATGCAATTCTCTGCACCTT[C/T]AATATGAACAACTTCAGGAGGAGACGAGGGATCACGAGGACATGAAGAAG
Long Flanking Sequence:
TGGAGGAACTGACAGCTGAATCAAACGCACTACGCCTGCAATGTGAACAAGTGCAGGTGGAGACGAGAGATCCAGAGGAGATGAAGCTGAAGATGGAGGAACTGACCAATGAATCCAATACACTACAACTTCAAGATGAACAACTGCAGGGAGGGACGAGAGATCATGAGGAGGTGAAGAACATGGAGGAACTGACAACTGAATGCAATTCTCTGCGCCTTCAATGTGAACAACTGCAGGAAGAGACGAGAGATTATAAGGAGATGAAGCAGAGGGTGGAGGAACTGACCAAAGAATCCAATGCACTACGCCTTCAATATGAACAACTGCAGGAGGAGACGAGAAATCATGAGGAGATGAAGAAGAAGATGGAGGAACTGACCAATGATTCCAATGCACTACGCCTTCAATATGAACAACTGCAGGCGGAGACGAGAGATCATGAGGAGATGAAGCAGAAGGTGGAGGAGCTGACGACTGAATGCAATTCTCTGCACCTT[C/T]AATATGAACAACTTCAGGAGGAGACGAGGGATCACGAGGACATGAAGAAGAAGATAGAGGAGCTGACCAATGAATTCAATACTCTACGCCTGCAATATGACCAACTGCAGGAGGAGACCAGAGATCACGAGAAAATGAAGTTGAAGATGGAGGCGGTGACGACTGAATGCAATACGCTACGCTTACGATACGAGCAGTTGCAAGAGGAGACAAGGGATCATGAGGAGATGGGTAAGAAGATGCAGGAGGTGTCCAATGAATCCAATACACTACGCCTTCAATATGAACAACTGCAGGCAGAGATGAAAGATCACGAGGAGATGAAGCAGAAGATGGAAGGCATGACGACAGAGAGAGACTCTCTGCATCTCCAATATGAACGCCTCCATCAGGAGACTCTTCTGGAGCTGCAGGAGGCGCTGCGGGAGAAAACCGCAGCGTCTGTGGTGATGCAGGCTCAGGTGCAGGCGCTGGAGGAGAGCGCAGCCGCCAGGGTCGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29112
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
Founder:
SL4_01_B11
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110495 Nonsense 477 2229 5 30
Genomic Location (Zv9):
Chromosome 19 (position 539940)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 561427
GRCz11 19 561236
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCTGACCAATGAATTCAATACTCTACGCCTGCAATATGACCAACTG[C/T]AGGAGGAGACCAGAGATCACGAGAAAATGAAGTTGAAGATGGAGGCGGTG
Long Flanking Sequence:
ATGAATCCAATACACTACAACTTCAAGATGAACAACTGCAGGGAGGGACGAGAGATCATGAGGAGGTGAAGAACATGGAGGAACTGACAACTGAATGCAATTCTCTGCGCCTTCAATGTGAACAACTGCAGGAAGAGACGAGAGATTATAAGGAGATGAAGCAGAGGGTGGAGGAACTGACCAAAGAATCCAATGCACTACGCCTTCAATATGAACAACTGCAGGAGGAGACGAGAAATCATGAGGAGATGAAGAAGAAGATGGAGGAACTGACCAATGATTCCAATGCACTACGCCTTCAATATGAACAACTGCAGGCGGAGACGAGAGATCATGAGGAGATGAAGCAGAAGGTGGAGGAGCTGACGACTGAATGCAATTCTCTGCACCTTCAATATGAACAACTTCAGGAGGAGACGAGGGATCACGAGGACATGAAGAAGAAGATAGAGGAGCTGACCAATGAATTCAATACTCTACGCCTGCAATATGACCAACTG[C/T]AGGAGGAGACCAGAGATCACGAGAAAATGAAGTTGAAGATGGAGGCGGTGACGACTGAATGCAATACGCTACGCTTACGATACGAGCAGTTGCAAGAGGAGACAAGGGATCATGAGGAGATGGGTAAGAAGATGCAGGAGGTGTCCAATGAATCCAATACACTACGCCTTCAATATGAACAACTGCAGGCAGAGATGAAAGATCACGAGGAGATGAAGCAGAAGATGGAAGGCATGACGACAGAGAGAGACTCTCTGCATCTCCAATATGAACGCCTCCATCAGGAGACTCTTCTGGAGCTGCAGGAGGCGCTGCGGGAGAAAACCGCAGCGTCTGTGGTGATGCAGGCTCAGGTGCAGGCGCTGGAGGAGAGCGCAGCCGCCAGGGTCGACAGTCTGAGCCGGCGGGTAGAGGAGCTGCAGGAGTGTGTGGAGGAGAAGGACCGGGAGCTCCGAGCCTGCAGGATGAGGGTGGAACAAGCTCAAACTGATGCCCACGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43191
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
Founder:
SL7_05_D5
KASP Assay Location:
Unknown
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110495 Essential Splice Site 949 2229 9 30
Genomic Location (Zv9):
Chromosome 19 (position 543685)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 565172
GRCz11 19 564981
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGACAGAGAGATGAGTCTGGCTCTGCTGAAGGATCAGCTAAACCGGG[T/C]GAGTGGATATACACCTATAATCATTATAAAGTACATGCAGATACTCATAT
Long Flanking Sequence:
TGTACTTCCAACTGAAACTGAATATTGAGTAGGGGCGGGGCTTAATTTCAGTAGGTTAATGTACTTCCAACTGAAACTGAATATTGAGTAGGTGCGGGGCTTAATTTCAGTTGGTTAGTGTACTTACAACTGGAACAGAAAAATTGTGTAGAGGCGGGGCTTTCTCTAGCACATCATTCCCTTATAGCAAACTAAAGGTAAGAGAGGGTATTGATATGCAGTTGCTATGGAAACCCTCAGGGTGACATCAGCAGAAGGAGCAAATACAAACGCAGAAGCAAATGCTCAGACTTTCATTGAAGATTACCAAAATAAATACATTCCTTCAGTAAATTAACTTGCGCTGATTAATTATTCAGCTTTTGAATAACAACGTGAGCTAGCAGAATAAACAGTGTAGATTTAGATTTCAGACGGACTTTAAAACTGTGTGTGTGTGTGTGTGTGTGCGCAGGACAGAGAGATGAGTCTGGCTCTGCTGAAGGATCAGCTAAACCGGG[T/C]GAGTGGATATACACCTATAATCATTATAAAGTACATGCAGATACTCATATTGTGGACACTTACAGTAAATAATCATCAGTGTTTAGACTTGTTTTTAAGAGTGTTCAGAGTGTATTTGCAGTGGTGTTCATAACAGACCAGTTCTAGGAGATTTCATTGGTTAATTAGCTTAACAATTCAAACATCATGATGTTAATCTGAACAAATATTGACTATTGTGTGACTGTTTATAGAGCTGTTGTACATCAACACTGTGCAGTAAAGCTCCACTAGTTGACATTAAGCTGAACTAAACTCACTTTTATTCATCTTTACTGATGTGAATTTTTATTTAAAGTCTAATCATGCATTCAAGTCATAATCATAATCTGATTACCAGAGTCAGAATTGTTTTATTAAATGCATTTAATAATTAATAACATTTTTAAGTAATAAAATGAACTCATATTAAAGCAGTATATCTATTAAATCAGCTTTTCTCACTGATTTTAATGCATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36744
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
Founder:
SL6_07_C7
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110495 Nonsense 1513 2229 17 30
Genomic Location (Zv9):
Chromosome 19 (position 551126)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 572613
GRCz11 19 572422
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTGAACTGAACCACACTAAACTAGAGCTGGAGAGCGCTCTGAACACA[C/T]AACACACACACCTGAGGGAGCTTGACACACTCAGGTAACGCACACGCGCG
Long Flanking Sequence:
ACACTCATCACTGCGGTCGTCTGTTCTGGGAGTGATGTTTACTTCTGTTCTCATCAGGAATGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGTTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGTTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGTTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGATGAAGTCTGAACTGAACCACACTAAACTAGAGCTGGAGAGCGCTCTGAACACA[C/T]AACACACACACCTGAGGGAGCTTGACACACTCAGGTAACGCACACGCGCGCAATACAATACTTGCAGACATCTGAACGAGCTCAACACACTCCGATAACAAACACACACACACGTACTTGTGACATACACAAACACACACCTTAAAGAGCTGGTAACATGCACACTTTGGTAACACAGATGCAAAACACACACCTGAGGGAGCTCGACACACTCGGGTAACAGACAATAAAATGCAAAACAACACACACACACACACACTCGGATAGCACACACACACACGACACATACACTACAAACATCTGAATATAGTAACATATTCGGGTAACACAGATGCACAACACACACACACACACACTTATGTGACACACACACCTGACAGAGATTGATACACTCAGGTAATACACATATACTTCTTACAAACACACACACACACACCTAAAAGAGCTGGTAACATGCTCACTCAGGGAACACACGTGCACAACACACACACACGCACTTA
Associated Phenotype:
Not determined