ZMP

chaf1b

Ensembl ID:

ENSDARG00000056473

ZFIN ID:

ZDB-GENE-040426-1947

Description:

chromatin assembly factor 1 subunit B [Source:RefSeq peptide;Acc:NP_998177]

Human Orthologue:

CHAF1B

Human Description:

chromatin assembly factor 1, subunit B (p60) [Source:HGNC Symbol;Acc:1911]

Mouse Orthologue:

Chaf1b

Mouse Description:

chromatin assembly factor 1, subunit B (p60) Gene [Source:MGI Symbol;Acc:MGI:1314881]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21510	Nonsense	Available for shipment	Available now
sa34675	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21510

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
ENSDART00000078965	Nonsense	64	237	3	10
ENSDART00000079222	Nonsense	64	613	3	14
ENSDART00000122052	Nonsense	64	613	2	13

Genomic Location (Zv9):

Chromosome 9 (position 31587062)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	30743008
GRCz11	9	30553754

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATAAAGGGCCTGATGGGAAAGCGGTCGTTGAGTTTTTGTCTAACTTGGCA[C/T]GACACACGAAAGCAGTGAATGTAGTGCGTTTCTCACCCACTGCTGAAGTG

Long Flanking Sequence:

TTTTGTTCTGTTTAGCGCTCCTCAGCATGTTTAGTAGGAGAGAGGGAGAGGGATCAAATCACATATACAGTTCTTCCACTCACCTTCATCTTCCATCGATTCAAATATACTTTCCCAGCATCCCTCAAAGCTATCCTGACTCTGCGCCTACTTACGCTTTCCTTTTTTTGCTGAGGATTTGTCTTTTAATGTTTGAAGCTGACATGACAGCTTGGGTCATCTTCGTTCTTAGACATCTTCTTAAAAGACAACGTTTTTTTTACTCGTGAAGCTATTTTAACATTTAAAATGGAGACTGTGGCTGCAAACTTTCTGTATGCAAAGTTCACACATACAATTAATGTCACATGGTTATCTCATTTTTATTTTTTCTGGACTTGTACTGATGTTCATCGCACGCACTCATATAGTAAGATGAGATCTGCTCTCATTTTCAGATGTGGCGTGTGGATAAAGGGCCTGATGGGAAAGCGGTCGTTGAGTTTTTGTCTAACTTGGCA[C/T]GACACACGAAAGCAGTGAATGTAGTGCGTTTCTCACCCACTGCTGAAGTGTTGGCTTCTGGGGGAGATGGTGAGCTAAAAGTCATTCCAATACTTGGCTGAAATTGTGTATGGAGGCTGTAAAAAGTTAAATGTAGTGTCTTATTCTTAAGATGCGGCCATCTTGCTTTGGAAGCTGAATGACAATAAGGAGCCTGAACAAACTCCGACCTTTCAGGAAGAGGAAGATGCTCAACTTAATAAAGAGAGCTGGAGTGTGGTCAAGACTCTAAGGTTTGATTTTAGACCTTTTTTATTACCTCTTGATTGTCTTTTACATTTAAATCAGCATGAAATGAATATTTGACTAATGTGTCCTCTTAATGCAAGCTTTGATGTTATTGGAGCCTGTAACTTTTTTTTTAAGTTCAAAATTTTTTCTGATAGTGATTATGTGAAGAACGTTGTGAAATTCATTTAGTTCCTTTAACAGGCATTAAATATCAGTATATTCTGGAATCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34675

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078965	Essential Splice Site	87	237	3	10
ENSDART00000079222	Essential Splice Site	87	613	3	14
ENSDART00000122052	Essential Splice Site	87	613	2	13

Genomic Location (Zv9):

Chromosome 9 (position 31586991)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	30742937
GRCz11	9	30553683

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTAGTGCGTTTCTCACCCACTGCTGAAGTGTTGGCTTCTGGGGGAGATGG[T/A]GAGCTAAAAGTCATTCCAATACTTGGCTGAAATTGTGTATGGAGGCTGTA

Long Flanking Sequence:

TCTTCCACTCACCTTCATCTTCCATCGATTCAAATATACTTTCCCAGCATCCCTCAAAGCTATCCTGACTCTGCGCCTACTTACGCTTTCCTTTTTTTGCTGAGGATTTGTCTTTTAATGTTTGAAGCTGACATGACAGCTTGGGTCATCTTCGTTCTTAGACATCTTCTTAAAAGACAACGTTTTTTTTACTCGTGAAGCTATTTTAACATTTAAAATGGAGACTGTGGCTGCAAACTTTCTGTATGCAAAGTTCACACATACAATTAATGTCACATGGTTATCTCATTTTTATTTTTTCTGGACTTGTACTGATGTTCATCGCACGCACTCATATAGTAAGATGAGATCTGCTCTCATTTTCAGATGTGGCGTGTGGATAAAGGGCCTGATGGGAAAGCGGTCGTTGAGTTTTTGTCTAACTTGGCACGACACACGAAAGCAGTGAATGTAGTGCGTTTCTCACCCACTGCTGAAGTGTTGGCTTCTGGGGGAGATGG[T/A]GAGCTAAAAGTCATTCCAATACTTGGCTGAAATTGTGTATGGAGGCTGTAAAAAGTTAAATGTAGTGTCTTATTCTTAAGATGCGGCCATCTTGCTTTGGAAGCTGAATGACAATAAGGAGCCTGAACAAACTCCGACCTTTCAGGAAGAGGAAGATGCTCAACTTAATAAAGAGAGCTGGAGTGTGGTCAAGACTCTAAGGTTTGATTTTAGACCTTTTTTATTACCTCTTGATTGTCTTTTACATTTAAATCAGCATGAAATGAATATTTGACTAATGTGTCCTCTTAATGCAAGCTTTGATGTTATTGGAGCCTGTAACTTTTTTTTTAAGTTCAAAATTTTTTCTGATAGTGATTATGTGAAGAACGTTGTGAAATTCATTTAGTTCCTTTAACAGGCATTAAATATCAGTATATTCTGGAATCTATAAATATTTCCTTTGGTGTGGAATATGTGCATGTCAGCAACCTGGAAAATTACAAAGCGCAAAAGCATAC

Associated Phenotype:

Not determined