ZMP

fetub

Ensembl ID:

ENSDARG00000053973

ZFIN ID:

ZDB-GENE-050208-4

Human Orthologue:

FETUB

Human Description:

fetuin B [Source:HGNC Symbol;Acc:3658]

Mouse Orthologue:

Fetub

Mouse Description:

fetuin beta Gene [Source:MGI Symbol;Acc:MGI:1890221]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37572	Nonsense	Mutation detected in F1 DNA	Not yet available
sa24222	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa37572

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
ENSDART00000076082	Nonsense	199	499	5	7

Genomic Location (Zv9):

Chromosome 22 (position 40854387)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	37940501
GRCz11	22	37894239

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATACAATCTTTTTCTTTTTATTTTGTAGCTTCACTTAGGAAGATTCTA[T/A]ACTGCGGAGTTCACCATCCAGGAAACCGTCTGCTCCTCCAAAACTAAAGA

Long Flanking Sequence:

CATTAGTTAATGTTGAACTATGATCAATAAATGCAAGATTATTCATACCTAAGTAAGGTTTGTAATTGCATTAACTATTCATTCACTCATTCATTTTCTTTTCGGCTCAGTCCCTTTATTAATCTGGGGTCGCCACAGCGAAATGAACCGCCAACTTATCCAGCACGTTTTTTTACGCCTAGATTAACTAATATACAATTAAGAAGTGTAACACTGTAAAATGCTGGGCTCCACATAATGGATTTGTGTTGGGGCATCATGAAATAATTAAGTTAACTTAATAGTTTTTTTTTCTTCAAATTTAAGTTTTAGAATATAAAACAATCAGTTTCAGCTCATTTTAAACAAGTAGTTCGAGCAAACAACAAAGGTAATGTTATTGAGTGTACCACTGATCCTTCAAGCATGAAAAATAATGCAATTCCTGCACTGAAGGATGACATTAAATATGTATACAATCTTTTTCTTTTTATTTTGTAGCTTCACTTAGGAAGATTCTA[T/A]ACTGCGGAGTTCACCATCCAGGAAACCGTCTGCTCCTCCAAAACTAAAGATGTTGATGTCTCGAAATGTGAGCTGATGGCGTGTGAATTTGCGGTGAGTGTTGAGACTTTTCAGTATAGCAGATGCACAGAAATACAGTCCTCAAATACAGTCGAAGACACAACAATCATTATTTATTTATTTTCCAAATATTTCCCAAATGATGTTGAACAGATTCAGGAATTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCTGCTAGAATTAAAGCAGTTTTTAATTGTTTTAAACTCATTTTAAGGTCAATATTATTAGCGCCCTTAAGTTATATTTATTTTGGATAGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCGAGATAAGCCTTTAAATGTCACTTTTAGCTAAATACTAGTGTCTTGAAGAATATCTAGTCTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24222

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076082	Essential Splice Site	230	499	5	7

Genomic Location (Zv9):

Chromosome 22 (position 40854482)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	37940596
GRCz11	22	37894334

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAAAGATGTTGATGTCTCGAAATGTGAGCTGATGGCGTGTGAATTTGCGG[T/A]GAGTGTTGAGACTTTTCAGTATAGCAGATGCACAGAAATACAGTCCTCAA

Long Flanking Sequence:

TTCTTTTCGGCTCAGTCCCTTTATTAATCTGGGGTCGCCACAGCGAAATGAACCGCCAACTTATCCAGCACGTTTTTTTACGCCTAGATTAACTAATATACAATTAAGAAGTGTAACACTGTAAAATGCTGGGCTCCACATAATGGATTTGTGTTGGGGCATCATGAAATAATTAAGTTAACTTAATAGTTTTTTTTTCTTCAAATTTAAGTTTTAGAATATAAAACAATCAGTTTCAGCTCATTTTAAACAAGTAGTTCGAGCAAACAACAAAGGTAATGTTATTGAGTGTACCACTGATCCTTCAAGCATGAAAAATAATGCAATTCCTGCACTGAAGGATGACATTAAATATGTATACAATCTTTTTCTTTTTATTTTGTAGCTTCACTTAGGAAGATTCTATACTGCGGAGTTCACCATCCAGGAAACCGTCTGCTCCTCCAAAACTAAAGATGTTGATGTCTCGAAATGTGAGCTGATGGCGTGTGAATTTGCGG[T/A]GAGTGTTGAGACTTTTCAGTATAGCAGATGCACAGAAATACAGTCCTCAAATACAGTCGAAGACACAACAATCATTATTTATTTATTTTCCAAATATTTCCCAAATGATGTTGAACAGATTCAGGAATTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCTGCTAGAATTAAAGCAGTTTTTAATTGTTTTAAACTCATTTTAAGGTCAATATTATTAGCGCCCTTAAGTTATATTTATTTTGGATAGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCGAGATAAGCCTTTAAATGTCACTTTTAGCTAAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAACACTATTATATTTAGAAATGTGTTAAAAAAAAATC

Associated Phenotype:

Not determined