ZMP

fam59b

Ensembl ID:

ENSDARG00000073933

ZFIN ID:

ZDB-GENE-081031-49

Human Orthologue:

FAM59B

Human Description:

family with sequence similarity 59, member B [Source:HGNC Symbol;Acc:27172]

Mouse Orthologue:

Fam59b

Mouse Description:

family with sequence similarity 59, member B Gene [Source:MGI Symbol;Acc:MGI:2685290]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29462	Nonsense	Mutation detected in F1 DNA	Not yet available
sa32317	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa29462

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
ENSDART00000108493	Nonsense	167	810	4	6

Genomic Location (Zv9):

Chromosome 20 (position 48680983)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	48581075
GRCz11	20	48010797

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTGACTCTTATGGGCCAAGCAGAACTGCTCTGCGTCCAATCAACTCGC[G/T]AGAAATCCCGCCTCACGGCGCTACTGCGCCGCCTGGGCAAAGCAGGAGGA

Long Flanking Sequence:

AGCCGAGAAAGGACCGGGCCCGGACATATTTTACTTTTGCTTTCAGTTTGAAGGCAGTCTCCGTGAGGAGCTGCCGTCCGTTTGTTTTGGTTTAGACGGCAGTCTCCGTGAGGAGCATGTTATAAATAAATATTTTAAAACTGAAAGCAAAAAGTAAAATATGTTCGGGCCCGGTCCTCTCTCGGCTTCCTCTGCCATCGTTTCTCCTTTTATAGTCCAGAGCTCCTTCCGTGGGACTCGAGGCAGGTGCGCAACGCAGGTGTATCCACTTACGTGGCGGCCTCATTCCATTCCCACGGATCTCGGCCATGCCCCCTCGCCACACAAGCCAATAAAAAATGGATGAATGCTAAAACATTTGTTCCTCCCTCTTTCTCTTGCTATAGGTGGTTTCCGGGGAGTTCACAGAGGACAGCGAGTTGTATAATTTCTCTCTGCAGGCGGGAGATGAACTGACTCTTATGGGCCAAGCAGAACTGCTCTGCGTCCAATCAACTCGC[G/T]AGAAATCCCGCCTCACGGCGCTACTGCGCCGCCTGGGCAAAGCAGGAGGAGCACTGGGACGTCCAGCACGCACGAAGATGCCTTGTTTAATATGCATGAACCATCGAACCAATGAGAGCGTTAGTTTGCCATTCCAATGTCGTGGTCGGTTCTGCACGCGCTCACTGCAGGAGCTTCAGATGCAGGGAGGCGAACACACCGTACGCAGCATTATTGAACGCGTGCGGCTACCGGTGAACGTTTCTGTTCCGTCACGACCTCCACGAAATCCGTACGACCTGCACGCCATCCGCGAGGGTCATCGATATAAACTTCTTAGCATCATCAGCAAAACTGTTGTTCTCTGCTGCATACTTCGCAAAGAGGAAGTGATGCCTTCTCACTTCCTGTTATTAACGGACATGCCACGGTTTACACTTCCAGAGGGTCTTTTGCGCGCTGATGCTCCCTACCAGCAGGTGGTGCTACAGTGCGCACTGCGCTGCCAAGAAAGCTTCGAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32317

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108493	Nonsense	417	810	4	6

Genomic Location (Zv9):

Chromosome 20 (position 48680233)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	48580325
GRCz11	20	48010047

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACTCGTCGACTCGCACACGCTGCCCTCTAGTGACGGCGATGGGGAAGAG[C/T]GAGAGTACGTCACGCCTGATTGGTCGACAGAGTCGCAGGAGATTCCATAC

Long Flanking Sequence:

CGTCACGACCTCCACGAAATCCGTACGACCTGCACGCCATCCGCGAGGGTCATCGATATAAACTTCTTAGCATCATCAGCAAAACTGTTGTTCTCTGCTGCATACTTCGCAAAGAGGAAGTGATGCCTTCTCACTTCCTGTTATTAACGGACATGCCACGGTTTACACTTCCAGAGGGTCTTTTGCGCGCTGATGCTCCCTACCAGCAGGTGGTGCTACAGTGCGCACTGCGCTGCCAAGAAAGCTTCGATGCGGACGATTATTCGCGTGCCGTACGTGAAGTCAAAACTGATTTCTCAGAGGAATGTCTCAGTCCGAGGCGAATTCGGGTGTGTGTTCAGGGCTACGGGCGTGACGAGTTGGGGACATCCCTGCAAAGACTGTCTCTGTGTGTGTACGGAGGCGGAGCGGTCACGCACACACACACAATCTCACACGGCTGCAGAGACTCACTCGTCGACTCGCACACGCTGCCCTCTAGTGACGGCGATGGGGAAGAG[C/T]GAGAGTACGTCACGCCTGATTGGTCGACAGAGTCGCAGGAGATTCCATACGAGGAGCTCTGGACCAATCAGACTTCTGGAAGTTTTGGAGTGACATCTGAGAGCGCAGTGAAGGCGGAGCATAACCTCATATCATTTCATTCCACTACTACGTCATTGGATGGAACGGTAGGCTCCACCCACATCGCTATGGTGCAGATGGATGCAGGAAGAGTGCCAAGGGTGTCGACCCCACCCCCTGTCCCACCAAAATCTGAAGCTGTAAGTAGATATTTTATAGATTTTCAATTAAAAATGTTTTTTTTGTTAGGATCATACTGCTTTTATAAATGATATAAACCAGGGGTCACCAACATGGTGCCCGCAAGGATCACATGAGTTGTCCACGGGCCTGTTTTGAAAAAAAAAATTAGGTCACCATAGCATCACCATTAAGATTTATCTTAAATTTTTTGTATCTATGCTTTTTAAATCACACTTGCATTGCTGTAAAACTGAAAA

Associated Phenotype:

Not determined