ZMP

fam102bb

Ensembl ID:

ENSDARG00000002333

ZFIN ID:

ZDB-GENE-041014-330

Description:

hypothetical protein LOC557909 [Source:RefSeq peptide;Acc:NP_001038309]

Human Orthologue:

FAM102B

Human Description:

family with sequence similarity 102, member B [Source:HGNC Symbol;Acc:27637]

Mouse Orthologue:

Fam102b

Mouse Description:

family with sequence similarity 102, member B Gene [Source:MGI Symbol;Acc:MGI:3036259]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43483	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa16607	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa43483

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000020183	Essential Splice Site	45	367	1	11

Genomic Location (Zv9):

Chromosome 20 (position 33814177)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	33886690
GRCz11	20	33789569

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGTAAAGTCCGACTGCTCGACGGCGGATTCTCAGAAGAATCTTCGCGG[T/C]AAGAAACCTGTCAGATCTTCAGTGGATTAGTATGATTGGTTTAGATGAAA

Long Flanking Sequence:

GCGCGCTCCCGCTACTACACGACAACACAATACAACAGCAGCAGCACAACACAAGCTGTCGCGGAGCGAGACAGTCTATCACCTACTGCCTGCACATCCACTGACCAGCATATTTCCTTTTAATGCCTTTATCAACCGTAACGATGTAGTTAATGACAGAAGAATCCGACAAGACTGTGTTTCATCATCATCGTCGTTAGCTTAGCTTTTCATTTCAGGCAGTGGCGGATTCCAGCAGTGGCTAACGGCTATCAGCTCCAACAACAGAAGCAACCGAAGATGAGCAAATAAAAGTGATGCTTGTCCACCGCGTATGACCAAAGCTACCGTCAAGGCTTACAGGACTGCTTAGAATTGACGCCAAGATGATGAAGAAAAAGAAGTTTAAGTTCAGAGTGGATTTTGAGCTGGACGAGCTGTCCTCTGTTCCGTTCGTGAACGGAGTTCTGTTCTGTAAAGTCCGACTGCTCGACGGCGGATTCTCAGAAGAATCTTCGCGG[T/C]AAGAAACCTGTCAGATCTTCAGTGGATTAGTATGATTGGTTTAGATGAAAAATGAGCTGGTGTCATTCTACAGTTTTATTCCCAATAGAGCATAACCCAAACAGAGTATATTATGGTCCATCTTTTCACAGAATTGGTAACATTAGCTAGTTAGTGTGTCTTAAAGAATGTTTAGTCCTGTAAGGTGTATATGCTCTTGTAAAAAGTCAAGACACTGCAGGCGAACGGGGTAAATATTTAACTTATTGATCGCCATACTTCCCTAGTTGATTGACTCTATTAAGTATTGCAAACATTTTTGTAGTGCAGATTTGTAAAAATGTTTGCATGAAAACTGCATGAAGTCATGTCCAAATTTCTTGTCGTTTCTTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCCTCTTCTTCTTCTACTTCTTCTTTTTTTTTTTTTTTTTTTTAGAAAAAAACAACAACTGTATAATCAAACATATAGTGCAAAACTGAAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16607

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000020183	Nonsense	121	367	4	11

Genomic Location (Zv9):

Chromosome 20 (position 33796162)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	33868675
GRCz11	20	33771554

KASP Assay ID:

2261-4592.1 (used for ordering genotyping assays)

KASP Sequence:

GAGTTTGCWGGATCGGGTAGCACCAYACGCAGGTGTCTGTTGGAGGGTTA[C/A]GACAYCAAAAACACTAGACAGGACAACTCCATCCTTAAGGTATGAAGACA

Long Flanking Sequence:

AAATGATAATTGTGTTATATATAATATATTATTTTATTATGTCAGCTGCAAAAAAAAAAAAAAATTAAATTGGTGCTAAAAACAAAAGAATTTTAATATTAATTAATCATCTAAAATCCTCATGGTGAACACAAATGAACAATTTCACTTTCATGAATGGAAACTAACACAGGCCATTGCTAATTCATCAAATAGACAGTTCTGTAGAGGATTATAAAATATTGATAGCAAAGGCACAGCTGAAAATAGATCACACCGGAACATTGTGTTTGTTTGTAATACTGTTTGTGCTTGAGCTGGGCACTTCTGTTCATAAAAGCATTAACCTCTTTACTTTGTTTTAACTCAAAAGCTCTAGTACCTTTTAAATGATTTAAAGTGAATGTCTAAACTTAACGTGTGCTGTTTTGGCTCTTCGCATAGCTGGGTTTTGCTGATCTCAACCTGGCTGAGTTTGCAGGATCGGGTAGCACCACACGCAGGTGTCTGTTGGAGGGTTA[C/A]GACACCAAAAACACTAGACAGGACAACTCCATCCTTAAGGTATGAAGACAATCAAGTTTCCTCATATGATCTTTTCAGCTAAATCCATTCATGCTTGTGTTTATTAAACTTGTGTTTCTTAAGATAGTAGTGGTGCTCGCTGCTAAAGTGGTGATGCTATTTATTACTTTTAGGTGGCCCAAACTAATTTCTCAACTTTAGATTTGTGTACATGTTTTAAGGAATTAAGAGTTAAGGCTGATTTATACTTCTGTGTCAAACGCCGGCGTATGCTACGTCGCTGACGCATAGCCCTTCGCCGTGGCCGTCACTGACGTGCACCTCTCAAAAAATGTAACTACACGTCGCAACGATGCGTAGCGTAAGCTCTGTGATTGGTCGGCTTGGTAGCGCTGACGAGTCTGGGCGGGACCGAGAGCCGCACGAATGGCGCGAGCGATTGTTTACAAGTGTGGAGTCCCGTGAAGGAGCTCCGGATAGAAAGTTTTGTTTTGTGTTTA

Associated Phenotype:

Not determined