ZMP

FAM81B

Ensembl ID:

ENSDARG00000035193

Description:

family with sequence similarity 81, member B [Source:HGNC Symbol;Acc:26335]

Human Orthologue:

FAM81B

Human Description:

family with sequence similarity 81, member B [Source:HGNC Symbol;Acc:26335]

Mouse Orthologue:

Fam81b

Mouse Description:

family with sequence similarity 81, member B Gene [Source:MGI Symbol;Acc:MGI:2685122]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8861	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa10724	Essential Splice Site	Available for shipment	Available now
sa17631	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa8861

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050979	Essential Splice Site	152	341	4	8

Genomic Location (Zv9):

Chromosome 5 (position 52487992)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	50155188
GRCz11	5	50801781

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTAAACAATGTGCAGAAATGACTGTTGCTTCGTAATGTATTGTCATTTTC[A/G]GCTGTCTCGGGACGTAGGAAAACTGGAGACRTCCCTGTCAGAGAAGCTGA

Long Flanking Sequence:

CAGGTACTTGACTGGCCTGCCTGCAGTCCTGACCTGTCTCCAATAAAGAACGTGTGGTGCATTTTGAAGCTTTTGAAAACCCTGTACCATTGCCTGACTTAAAACTTGTTTGCAGGAACAATGGGACAAAATTACACCTGAAACACTTCATCACTTGGTGTCTTTAGTCACTAAACGTCTTTTAACTGTTGTGAAAAGGAATGACAACATTACAAAGTAGTAAATGTTTCAACTTTTTTTGTAAATGTGTTGCAAGAATCAAGTGTTTATTAAAAAACGAACAAACAAACAAATAATGAGGAACACGTTAAAATGTTTGCTGTATTGTCTGTAATAAAATACAAGTCGAAGTAAATTTAAAAATCTTTTTTTTTTCTTTTTTGTGTTTTCCATACTGTCCCAGATTTTTCTAATTTGAGGTTGTATTTCCAATCGATATAGAAGAACAATGTAAACAATGTGCAGAAATGACTGTTGCTTCGTAATGTATTGTCATTTTC[A/G]GCTGTCTCGGGACGTAGGAAAACTGGAGACATCCCTGTCAGAGAAGCTGATCTCTCAGAGAAACACCATTGCAGATTTACACAAGGAAATTCAACTACTGGATGTAAAGTAAGAGCAACTGAGAACAATTGCATAAACTGCTGAGAAAAACATGCTGAAAAATTTTTTTTCCAGCAAACCAGCAGTCATTTGTCAAAACGTACCATTCGTCAAAATCTAGCATATGCTAGCGGTGGTTTTCAACATGGGTAGTCTTAAGAAAGCTACCTTTCTTCAAGGCTGGGCATAACTCATTTAAGGTCTAAATTCCAATTTAAATCTAAAAAGCAGAGCTTGGTTAACTGAGAGAGTCTCAGCATTGTCTATGCAACTCTCCTTCTTAAAAAAAACTAATTTGTAGCTAATAAATATTTTGAAGGTTTATGAAAATTCATCTTTAATATAGTAAAAATGTTTCTTAGCATATTCATTATTTAGTATGTTGGCATATAGGCTATTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa10724

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050979	Essential Splice Site	232	341	5	8

Genomic Location (Zv9):

Chromosome 5 (position 52497791)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	50164987
GRCz11	5	50811580

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACACACACAGAACAGCCAGCAGCTGCAGACACTACTGCAGGACAGACTGG[T/A]AAACACATACAAACACATTNTGTGTNNNNNNNCAATTCCCRGTAAATGTAA

Long Flanking Sequence:

TTAGGGGTGGGGTTGGGTGCCACGCCTCCTTTTTAAAATCGTACATTTTCGTAATTCGAACTCATACGAATTAGCCACTAAAATGACAAAAAGTAAAATACTTACGTTTCCTCGTGAGATCAGGCTGAAATATGACCTTTTTTAATGTATAATAGGGGCTGTTTAACTAAAGAACCCTTATAGTAAAGTGTGACCAAAATATGATGCTTGAATTGTATCTTATATATTGTTTAACACCTTCATATTATAGCTTTTTTCATAAGACCAATAGCAAAGTCAATTCATGCACAATAAATATAATAATACCTTAATGAAGGCAGGTATTATAATGTGTAGTGTGCGTATTTGTGTATTTTTCTACAGGAGCTCTAGTGGTGTAAAGGAGGTAGAGGAGCAGACTGTGAGATTGAGGAAGTGGTTTGAGGAGCAGATGAAAACCGCACTCCAGTCACACACACAGAACAGCCAGCAGCTGCAGACACTACTGCAGGACAGACTGG[T/A]AAACACATACAAACACATTTGTGTCAATGCACAATTCCCAGTAAATGTAACAAGTGAGCAATGAATAATACGACACAGGAATAACAGTTGTGGTCTCTAACTCAAACTGAAGACAAATGAGAGTACAAATACTTACATGAAGTTAATTATAGTCGAGATCAAAATTAGAGAATAGCCAACAACAATTCTATAGTAATATCTGAATATAGAAGGGTTCTGTTTATTACAGTGCCAAAGCATTTCCAGCGCAGGAAAATGTTGAGAATCCCAGTGGGCAATCGGGTAAACTCTGTGACGAAGATTTTTATTTACTAAACCTATATGAAGACACATTTGATTGGGTGATTGGAGGGCCCTATGCATCTGCCATTATATGTCTTTGAAAACAGGTGACAGGTTAAGGCAAAGGGGTCATAAAAGAGCGACTTGGGGACACAATGAAAACCAACTGTGTCAGAAAAGCATGAAATGTATACAAAATATTCTCAGCGCACTCAGAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17631

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050979	Nonsense	293	341	6	8

Genomic Location (Zv9):

Chromosome 5 (position 52499194)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	50166390
GRCz11	5	50812983

KASP Assay ID:

2259-6480.1 (used for ordering genotyping assays)

KASP Sequence:

AGATGAACATTCTRGAGAACAGCTTCAGAGAWGASCTAGAGCAGAWGAGA[A/T]RRGAATACCAGTCAGGTGAATCGAGCATATAAGCATCTCAATTATTAAAA

Long Flanking Sequence:

CTGTACTAAACCTGACTGAAACTTTCTGGAAAAACCTTATATCAAAGTTATAAACCAACTCAGTGGGACTGAAGAAGAGTGGATCGAGATGATTATAAAGTGTGAAAGAGTAGTGTTGCAATTTTATTTTATTTATCTTATTTCTCTTATTTTCATCACTGTGATAGTTGTTTCTTGAAGTGCTTTTATGGAAAAAATAATAAGAAGAAGAAACTAAATTCCTACAAATTTTAAACAAAGAAGATTATTTGTCTATGTTGAATTTCTCTCATCTATATCCACATTCAAACTGTTATGATTTCTATATATATGGGGCATAGGTGGAAATGGAAGGCAAGCAGAAAGAGAACATGGTTATTCTCTCTGGTCACCTGGAGAGGTTTGAGGCAGCGCTGGAGAAGGTGCGATCAGCTGACAGGATCAAGCGCTCGGAGAGCAAAATCTACAACAAGATGAACATTCTGGAGAACAGCTTCAGAGAAGACCTAGAGCAGATGAGA[A/T]GAGAATACCAGTCAGGTGAATCGAGCATATAAGCATCTCAATTATTAAAAACATCCTTGATTATACTACAGTTATGTTGACAAGTTTGGCTCAGTATTGGTAAATGTGGTTTAAAATACATGTATTTAATCACAAATATAAAACAAACTGTAATAATTGTGAAATAGCATTATATTTATATGTAGCTGTCCTCTGCTTAGATCGTTTTTATTGTGGAAAGATGCACTTTACCATTATTCTGAGTGTCAATGAATTTTCTGATATATTTCTAATATGCAAATTTGATGCTCAAGACAAGTTTATTTAATCATTTGCCATATATTTATGTTTTGTAATTGCATTACGGGACCTTCAACTTTGCTCCATCAACTGTTGATGTTGAAAATTTAACTGCAGTTTAACAGTGTTTTTATTGGCATTGATTTAAATACAATGTTTAACAAATTATATATATATATATATATATATATATATATATATATATATATATATATATACAA

Associated Phenotype:

Not determined