ZMP

si:busm1-118j2.5

Ensembl ID:

ENSDARG00000090689

ZFIN IDs:

ZDB-GENE-030131-7722, ZDB-GENE-090501-3

Description:

hypothetical protein LOC793447 [Source:RefSeq peptide;Acc:NP_001096600]

Human Orthologues:

HBB, HBD, HBE1, HBG1, HBG2

Human Descriptions:

hemoglobin, beta [Source:HGNC Symbol;Acc:4827]
hemoglobin, delta [Source:HGNC Symbol;Acc:4829]
hemoglobin, epsilon 1 [Source:HGNC Symbol;Acc:4830]
hemoglobin, gamma A [Source:HGNC Symbol;Acc:4831]
hemoglobin, gamma G [Source:HGNC Symbol;Acc:4832]

Mouse Orthologues:

Gm5736, Hbb-b1, Hbb-b2, Hbb-bh1, Hbb-y

Mouse Descriptions:

hemoglobin Y, beta-like embryonic chain Gene [Source:MGI Symbol;Acc:MGI:96027]
hemoglobin Z, beta-like embryonic chain Gene [Source:MGI Symbol;Acc:MGI:96024]
hemoglobin beta, bh2 Gene [Source:MGI Symbol;Acc:MGI:96025]
hemoglobin, beta adult major chain Gene [Source:MGI Symbol;Acc:MGI:96021]
hemoglobin, beta adult minor chain Gene [Source:MGI Symbol;Acc:MGI:96022]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa26160	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa26160

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128380	Essential Splice Site	31	147	None	3

The following transcripts of ENSDARG00000090689 do not overlap with this mutation:

ENSDART00000138051

Genomic Location (Zv9):

Chromosome 3 (position 55974484)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	54859645
GRCz10	3	54868210
GRCz11	3	55114247
GRCz11	3	55122812

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTCGCCAAGGCTGACTACGACGTCATCGGTCCTCAGGCTCTGGCAAGG[T/G]AATGAGTCTTGGAGCTTATATTAACTTATATTTATAACATTACATAAGGC

Long Flanking Sequence:

ACAGTGTGACAAAGGGATCTGTGTAGTGTAAATAGAGTGCAAAATATATTCTTTAATTTATGCTTTATTATTTGGCTCACATTTGCAAATGATTTAATCTTGGTTAACAAACAAATTGACATAAATTCATAATCATTTTATGTATGTGTTATTTATTACTAAATTGCATTTCAGCAAATATTGCTAAATTTAACAGTCTTGGTAGATATTACTTGAGAAAATAAGCTGGTTGAGATATGCATCTTTTGGGTGTATGTGCTTGAACCATCCCACAAACCCATCACCCAATAGCCTGTAAAGGGGTGTGGTGGTGAACCTTGTTTAAAAGTTCCACAGTGAACTCTGTCTTCACAGCACTCTTCAGCTTCTGTTTAAGACACTTAGTCTGAACATCTAAAGTCGAAAACATGGTTGTGTGGACAGACTTCGAGAAGGCCACCATTCAAGATATCTTCGCCAAGGCTGACTACGACGTCATCGGTCCTCAGGCTCTGGCAAGG[T/G]AATGAGTCTTGGAGCTTATATTAACTTATATTTATAACATTACATAAGGCAGGAGACTGGTTTCGAGACAGCTGCTCTAATAAAATTTGTTTTCATCAGGTGTCTTATCGTGTACCCCTGGACCCAGCGGTACTTCGCCAAGTTTGGAAACCTCTACAATGCCGCTGCCATCCTGGGAAACCCAATGGTTGCTGCCCACGGTAAAACTGTGCTCAAGGGTCTGGAGCTGGCTGTAAAGAACATGGACAACATCAAGGCCACCTATGCTGATTTAAGTGTGCTGCACTCCGAGAAGCTCCACGTAGATCCCGACAACTTCAGGGTAAGCTGACATCCAGATTACGGATGTTTTTAAGAAAGTCTTTGGTTATTCATGATATGTGTCGATATAACCCTACTCTTGTGTCCTCTCACAGCTTTTGGCTGATTGCTTGACCATCGTTGTTGCTGCTCAGATGGGTGCTGGATTCACACCTGAAGTTCAGGCCGCTTTCCAGAAA

Associated Phenotype:

Not determined