Busch Lab

ZMP

hbae3

Ensembl ID:
ENSDARG00000079305
ZFIN IDs:
ZDB-GENE-990706-3, ZDB-GENE-990706-3
Description:
hemoglobin alpha embryonic-3 [Source:RefSeq peptide;Acc:NP_898889]
Human Orthologues:
HBA1, HBA2, HBQ1, HBZ
Human Descriptions:
hemoglobin, alpha 1 [Source:HGNC Symbol;Acc:4823]
hemoglobin, alpha 2 [Source:HGNC Symbol;Acc:4824]
hemoglobin, theta 1 [Source:HGNC Symbol;Acc:4833]
hemoglobin, zeta [Source:HGNC Symbol;Acc:4835]
Mouse Orthologues:
F830116E18Rik, Hba-a1, Hba-a2, Hba-x, Hbq1
Mouse Descriptions:
RIKEN cDNA F830116E18 gene Gene [Source:MGI Symbol;Acc:MGI:3613460]
hemoglobin X, alpha-like embryonic chain in Hba complex Gene [Source:MGI Symbol;Acc:MGI:96019]
hemoglobin alpha, adult chain 1 Gene [Source:MGI Symbol;Acc:MGI:96015]
hemoglobin alpha, adult chain 2 Gene [Source:MGI Symbol;Acc:MGI:96016]
hemoglobin, theta 1 Gene [Source:MGI Symbol;Acc:MGI:2685722]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa40176 Missense Mutation detected in F1 DNA Not yet available
sa33328 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40176
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109016 Missense 110 123 3 4
ENSDART00000122904 Missense 110 143 3 3
Genomic Location (Zv9):
Chromosome 3 (position 55998462)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 54892188
GRCz11 3 55146790
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTGTTTCTTCGTTTTTCTTTCAGATCATCAACCACAATCTGCTGGTG[T/A]CTCTGGCCATGATGTTCCCAGACGACTTCACTCCTGAGGTGCATGTTTCC
Long Flanking Sequence:
GTGATAAACGGAGTTTTGACTGCCGTCGGGCTGATGGATGACCTGAAGGGAGGTTTGCTGACCCTCAGCGAGCTACACGCCTTCATGCTGCGCGTGGACCCCGCAAACTTCAAGGTAGCTATATCCGTCTCTCTGCAAGCTAAACAAGCCTGTTTTTACCAAGAACTACAAAGTAACTGCGACTTCTTATTTAGATCTGACCTTTCTCTTTTTGACTACAGCTATTTTAACTTCTTGAATTTTCTTTTGTGTGGAGAAAATAGTGATTTGACTATTTTTAATTGTAGGTTTATTATACCCTTTATATTGTTTAAAATAATTAAATAAGCGTTTATGGGATATAAATATTCCCTACATGTTAACCATTGATGCTAATAAATAGTTTTTTTTTTAAACTAGGCTACATTTAGCCTATTTTGTACATTAAAGGAACAAGCTTTCCTAAATAAATTACTGTTTCTTCGTTTTTCTTTCAGATCATCAACCACAATCTGCTGGTG[T/A]CTCTGGCCATGATGTTCCCAGACGACTTCACTCCTGAGGTGCATGTTTCCGTGGACAAGTTCCTGGCCCAGGTCAGCCTGGCCCTGTCCGAGAAGTACCGCTAAAGCTGCAGCCTGCCTTCATCTCTGATGCGACACTGTATTCGCCTTAATGAGAATGAAAATAATAAATATTATTGAAATTGAATGAAATCAACAAAATTGTTTTTTTGTTTCTGTTTACAAAGCATAGCCTAACACAAATCTTCTTTGGCCGACTTCAGCCAGCACCTTCCCTTTAGCACATTGTTCACACATGTGTTAAATATCTGATAATAGAAATACAAAAAATTATCGTTTAATTTAATTAATAAAAATACTAAATAATACAAATTCTTTGAATATTTATGTCGTAAAAATAGGAAACTGTAACTTTAACTTAGAAATAGGCTAAACGACCGAAATTGTATGTAGTACATAGATATTTATTAAATTTTTTTTTGGTACGTAAAAATATTTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33328
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109016 Missense 119 123 4 4
ENSDART00000122904 Missense 139 143 3 3
Genomic Location (Zv9):
Chromosome 3 (position 55998375)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 54892101
GRCz11 3 55146703
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGCATGTTTCCGTGGACAAGTTCCTGGCCCAGGTCAGCCTGGCCCTG[T/A]CCGAGAAGTACCGCTAAAGCTGCAGCCTGCCTTCATCTCTGATGCGACAC
Long Flanking Sequence:
CTGCGCGTGGACCCCGCAAACTTCAAGGTAGCTATATCCGTCTCTCTGCAAGCTAAACAAGCCTGTTTTTACCAAGAACTACAAAGTAACTGCGACTTCTTATTTAGATCTGACCTTTCTCTTTTTGACTACAGCTATTTTAACTTCTTGAATTTTCTTTTGTGTGGAGAAAATAGTGATTTGACTATTTTTAATTGTAGGTTTATTATACCCTTTATATTGTTTAAAATAATTAAATAAGCGTTTATGGGATATAAATATTCCCTACATGTTAACCATTGATGCTAATAAATAGTTTTTTTTTTAAACTAGGCTACATTTAGCCTATTTTGTACATTAAAGGAACAAGCTTTCCTAAATAAATTACTGTTTCTTCGTTTTTCTTTCAGATCATCAACCACAATCTGCTGGTGTCTCTGGCCATGATGTTCCCAGACGACTTCACTCCTGAGGTGCATGTTTCCGTGGACAAGTTCCTGGCCCAGGTCAGCCTGGCCCTG[T/A]CCGAGAAGTACCGCTAAAGCTGCAGCCTGCCTTCATCTCTGATGCGACACTGTATTCGCCTTAATGAGAATGAAAATAATAAATATTATTGAAATTGAATGAAATCAACAAAATTGTTTTTTTGTTTCTGTTTACAAAGCATAGCCTAACACAAATCTTCTTTGGCCGACTTCAGCCAGCACCTTCCCTTTAGCACATTGTTCACACATGTGTTAAATATCTGATAATAGAAATACAAAAAATTATCGTTTAATTTAATTAATAAAAATACTAAATAATACAAATTCTTTGAATATTTATGTCGTAAAAATAGGAAACTGTAACTTTAACTTAGAAATAGGCTAAACGACCGAAATTGTATGTAGTACATAGATATTTATTAAATTTTTTTTTGGTACGTAAAAATATTTTAACCCCAAAATAGCCAACGAATCCTTGGGAAACACGTTTTGAGAGACTATTTTTGTGAGCTATTGAGAAAAACGTTAGTTAAATTTATT
Associated Phenotype:
Not determined