ZMP

zgc:171674

Ensembl ID:

ENSDARG00000074507

ZFIN ID:

ZDB-GENE-070928-17

Description:

regulator of microtubule dynamics protein 1 [Source:RefSeq peptide;Acc:NP_001098576]

Human Orthologue:

FAM82B

Human Description:

family with sequence similarity 82, member B [Source:HGNC Symbol;Acc:24285]

Mouse Orthologue:

Fam82b

Mouse Description:

family with sequence similarity 82, member B Gene [Source:MGI Symbol;Acc:MGI:1913552]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44208	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37971	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa13552	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa44208

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112680	Nonsense	63	295	2	10

Genomic Location (Zv9):

Chromosome 24 (position 43916383)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	42226045
GRCz11	24	42147778

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTCTGTCATACCTGATCTACCAGAGAGTGTCTCGTCTCGCTCCGGTGTG[T/A]GCGCTGAACTCAGGTCAGTTCTTCATCATCATCATCATCATCATCATCAT

Long Flanking Sequence:

ATCTGGAACATCTCACACACACTCACACTCACACACTCTGTCTCACACACACCTGCTCTGATGGCGAACGCGGCTTTATTCGGAGCTTTCAGGCGCTTTATGAGCAGAAATGTGAAGATCTGGAGAAGCAATGAGCGCGTCTGGGCGGAGAGAGTCCGAGCTTCAGTAAGACACACACACATACACACACACACACACATAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGTCATGATTGCTGTATTACCTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGTCATGATTGCTGTATTACCTCTGTGTGTGTGTGTGTGTGTTCAGAGCAGGAAGGGTGTAGTGCTGTTGGCTGTAACTCCTCTGTCATACCTGATCTACCAGAGAGTGTCTCGTCTCGCTCCGGTGTG[T/A]GCGCTGAACTCAGGTCAGTTCTTCATCATCATCATCATCATCATCATCATCATCATCATCTACCTGTCAATAACACTGTGATTAACTCTACCTGAGATTACCACTGCTGCTGGGTTATTGACTGACTGCATCTTCTGTCCAGCTGAAGAGATTCTAGAACAAGCAGATTACCTGTACAGCTGCGGAGAAACACAGAAGCTGCACCAACTGCTGGACAAACACAGAGACAGGTAAACCACTGACCACACACAGGTAAACCACTGACCAAACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCAAACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCACACACAGGTAAACCACTGACCAAACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37971

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112680	Essential Splice Site	97	295	4	10

Genomic Location (Zv9):

Chromosome 24 (position 43915467)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	42225129
GRCz11	24	42146862

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATGTGTGTGAGTCAGTAACTCTGTGTGTGTGTGTGTGTGTGTGTGCACA[G/A]TGGTGACGCAGAGTTCCTGTGGCGTCTGGCGCGTGTGTGTCGTGATCTGG

Long Flanking Sequence:

CACACACAACTGACCACACACAGGTAAACCACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCAAACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCACACACAGGTAAACCACTGACCAAACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAGGTAAACCACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAGGTAAAACTGATGAATGATGAACACTTCTGGGTTAGGGTTAGTGCATGTGTGTGAGTCAGTAACTCTGTGTGTGTGTGTGTGTGTGTGTGCACA[G/A]TGGTGACGCAGAGTTCCTGTGGCGTCTGGCGCGTGTGTGTCGTGATCTGGCTCTCCTGTCATCCGCGGAAGAGAAGCGGCGTCTGACGTACGAAGCGTTTCAGTACGCCACCGCCGCGCTGCAGAGAGACGAGCAGTGCTACGCTGCGCACAAAGTACAGCACCATCATCTACCTGTGTGTGTGTGTGTGTGTGTGAACTGCAGTGTGTGTGACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGCAGTGGTTCGCCATCTGCCTCAGTGATGTGGGCGATTATGAGGGCATCAAAGTGAAGATTGGAAACTCCTACATCATCAGAGAACACCTGGAGGTAAGAGTCACGGCCACAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCTGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa13552

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
ENSDART00000112680	Nonsense	161	295	5	10

Genomic Location (Zv9):

Chromosome 24 (position 43915178)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	42224840
GRCz11	24	42146573

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTNNNNCTGCAGTGGTTCGCCATCTGCCTCAGTGAWGTGGGCGATTAT[G/T]AGGGCATCAAAGTGAAGATTGGAAACTCCTACATCATCAGAGAACACCTG

Long Flanking Sequence:

GACCACACACAACTGACCACACACAGGTAAACCACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAACTGACCACACACAGGTAAAACTGATGAATGATGAACACTTCTGGGTTAGGGTTAGTGCATGTGTGTGAGTCAGTAACTCTGTGTGTGTGTGTGTGTGTGTGTGCACAGTGGTGACGCAGAGTTCCTGTGGCGTCTGGCGCGTGTGTGTCGTGATCTGGCTCTCCTGTCATCCGCGGAAGAGAAGCGGCGTCTGACGTACGAAGCGTTTCAGTACGCCACCGCCGCGCTGCAGAGAGACGAGCAGTGCTACGCTGCGCACAAAGTACAGCACCATCATCTACCTGTGTGTGTGTGTGTGTGTGTGAACTGCAGTGTGTGTGACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGCAGTGGTTCGCCATCTGCCTCAGTGATGTGGGCGATTAT[G/T]AGGGCATCAAAGTGAAGATTGGAAACTCCTACATCATCAGAGAACACCTGGAGGTAAGAGTCACGGCCACAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATACAGTGCAGTAAATAACCCATCAGTGCTGTAAATAACCCATCAGTGCAGTAAATACAGTGCTGTAA

Associated Phenotype:

Not determined