ZMP

zgc:73225

Ensembl ID:

ENSDARG00000026875

ZFIN IDs:

ZDB-GENE-030131-2046, ZDB-GENE-030131-2046

Description:

hypothetical protein LOC323326 [Source:RefSeq peptide;Acc:NP_955931]

Human Orthologue:

FAM57B

Human Description:

family with sequence similarity 57, member B [Source:HGNC Symbol;Acc:25295]

Mouse Orthologue:

Fam57b

Mouse Description:

family with sequence similarity 57, member B Gene [Source:MGI Symbol;Acc:MGI:1916202]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa2099	Nonsense	F2 line generated	Not yet available
sa40047	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa2099

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036741	Nonsense	27	242	4	7
ENSDART00000111731	Nonsense	77	292	3	6

Genomic Location (Zv9):

Chromosome 3 (position 21140439)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	20900176
GRCz11	3	21049916

KASP Assay ID:

554-2742.1 (used for ordering genotyping assays)

KASP Sequence:

TCACTTTTTCTCTTCCATTTTCCTTCCAGGCATTGGCTCACCACCAGCTA[T/G]ATCCTCTTTGCAGTCCCCTACTTCGTTTATGACATCTATGCCATGTTCTT

Long Flanking Sequence:

ATTTTGATTTTCAGAAGTATTACAGCACTTTGTAATAGTCTATTATTACATTTGTTGAGCCTCCCCCTACTGCAGTGGTCACCAAACTTGTTCCTGGAGGGTCGGTGTCCTACAGATTTTAGCTCCAACCCTAATCAAACACACCTGAACAAGCTAATCAAGGTCTTACGAGGTATACTTGAAACATCCAGACAGGTGTGTTGAGGCAAGATGGAGCTAAACCCTGCAGGGACACCGGCCCTCCAGGACCAGGATTGGTGACCCCTGCCCTACAGTTTGATCAAGTGATTGGACCATGTAGCCACTTTGCGTGACGTCACACTTAACAAGCGGATAAAGTAAAACTATTTATTAATTGATTGACATTTAAACTATTTAAGTATTAATACATTTTATTCATAACAGTAATAACACAAACTAACCCTAAGAGCTGTGGATTTCCTCAAGTTATCACTTTTTCTCTTCCATTTTCCTTCCAGGCATTGGCTCACCACCAGCTA[T/G]ATCCTCTTTGCAGTCCCCTACTTCGTTTATGACATCTATGCCATGTTCTTGTGCTACTGGTACAAACTTCAGGTTAAAGATCACGAGGAGGAAAGCGAGACCAAACCGATGAGATCTGCCATCAGGGGATACCTGCACCGCGAGTTCCTCATGGTCCTACATCATGTGGTCATGGTCACTGTGTGCTTCCCCGTGTCTGTGGTGAGTGGACTGAGGGGCCTTCAGACATAAACGCACACCTTTACATTAGCTAACATTAGAAAGTGAATTATTGAGGCCCATCTGAGTCCGTTTGGAGTGTAGCAAACACAGCTTTGGCCTTATGACTGATGGGATTGTAATCTTGTAGTGTGCCTCAGTCCAAGTTGTCCTGTACAGGCCTGTATACTTTCACCCTGTAATTATGCTCTCCATCACTCTCCATCTGTATCCATGGAGACTGTTGCTGTCGGCAGCCATGCAGCAAGCAGCACCCTGGCATTAGCTGCACTTAAATGGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40047

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036741	Essential Splice Site	126	242	5	7
ENSDART00000111731	Essential Splice Site	176	292	4	6

Genomic Location (Zv9):

Chromosome 3 (position 21138297)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	20898034
GRCz11	3	21047774

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGCAGAACTCAGCACCCCGTCTGTCTGTCTGGGAAAAATACTCATCCAG[G/T]TACTAAACACAAACATTCTCCTCCATCTTCCTGTGTTTTTCTTTCATTGT

Long Flanking Sequence:

TTTTCTTTCTCTTGTCTTTTCCTTTTCTTCCCTTCATTTCATTTTTATTTTCTTTCCCCATTTCTTTCCCTTTCTTTCCTTCCTATTTTTATTTCTTGGCTCTAATTTTCTTTCCTTTTATTTTTTTTCCCTTTACATTCTTTACTTTCCACATACAATTCCTTCGAATTTTTTTTTCCATTTTTCTTTATCTTATTTTCCCTTTCCTCTTCTCCTTTCTTATCTTTTAATCTTCTCTCTTCTATTGATGCCTTTTCCCTGTATAAACTTAAATTTCCATTTTCTATTCAAATCCTTGTCTTCCTCCGACCTTTCATGTCCATTTACCTTTTTATTCCTTCTCCTCCCTTTCCATCTTTCTTATTGTGTCATTTCTGTTCTGTTTTCTTCTTTTTTCCCTCTAGTTCTGGAGACAGGGCAAAGGGGATTATTTCCAGGGTGTGATGTTTCTGGCAGAACTCAGCACCCCGTCTGTCTGTCTGGGAAAAATACTCATCCAG[G/T]TACTAAACACAAACATTCTCCTCCATCTTCCTGTGTTTTTCTTTCATTGTATCAGTGCATCTTTCTTTTTACTGACCTAGACATGTGGATTTTTTTGGTTTCTGCTTCTTTTCTTTTCTTGGTAGTGGATCTTAAAGCATCTGATTGATTGACAATGATTTTTCACTGACAACACTCTGTTGTACATCTCTCTCTCTCTGTCACTTCTTCAGTGTTAACATGTGTTGGGGAACATTGAATCAAGGTTGTCAGGGTTCATTGCCCTGCCTATTAATATTTTTCTATCTTTTAAACCCTCTCTCTTTCTCTACTTCCCGCTCTCTCCTTTTTTTTTGTTTGCCTCAGTACAAGCAACAGCACACTCTCCTACATAAAGTCAATGGAGCTCTTATGCTGGTCACTTTCTTCATCTGCAGAGTTGTTCTATTCCCCTACCTCTACTACGCCTATGGCAGGTACGATCACTGTTTAACACTCTTATTTCATCTAATTTCTTACCT

Associated Phenotype:

Not determined