ZMP

si:ch211-197g15.10

Ensembl ID:

ENSDARG00000071361

ZFIN ID:

ZDB-GENE-050208-617

Description:

hypothetical protein LOC555357 [Source:RefSeq peptide;Acc:NP_001122156]

Human Orthologues:

IFI44, IFI44L

Human Descriptions:

interferon-induced protein 44 [Source:HGNC Symbol;Acc:16938]
interferon-induced protein 44-like [Source:HGNC Symbol;Acc:17817]

Mouse Orthologues:

H28, Ifi44

Mouse Descriptions:

histocompatibility 28 Gene [Source:MGI Symbol;Acc:MGI:95975]
interferon-induced protein 44 Gene [Source:MGI Symbol;Acc:MGI:2443016]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37487	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43808	Nonsense	Mutation detected in F1 DNA	Not yet available
sa29754	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37487

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105458	Nonsense	181	483	2	8
ENSDART00000105459	Nonsense	167	469	4	10
ENSDART00000142267	Nonsense	190	492	2	8

Genomic Location (Zv9):

Chromosome 22 (position 17681649)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	17432584
GRCz11	22	17457562

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGACTGTTTGGAAATGTTAGCGCAATGAATGCATTCAATTTTAATTCTT[C/A]AACACTATATGGAAACGACTGTGCCCTGACTGAATGTGAGGTGTACAAAG

Long Flanking Sequence:

CAGTACACCTATAGGTGGATTTACCTTCGGTGGGTCTGTCAGAGTCAGTCAAGCTCCACTCACTTTATCAGATGAGCAGAAAGATCAGCTCTGTGCATCAATTGGCGATGTGGATCTGACTCTTCTCTATAAAGCTTCAGTTCATGGATATAAAGCTTCTGCCTTTCATCAGAAATGTGACAATCAGGGTCCCACTTTACTAGTAGCCTACAATCGTTCAGGCTACATCTTCGGTGGATACACTAGTGTAGATTATACTCAAAGTGGCCAGGAAATTAGGGATGAGGCAGCGTTTCTGTTTAGCTTTCAAGGCAATACCAGCCTTTTCATCAAGGCTAACAGCGGATGTTATGCACGATATGATGGCGATGAAGGACCCAACTTTGGCAACAAGTTGTACTTCTGCAACAACAACCAACCAGTTGTGTCTAATCGAGGAGCATCCCAAGGTGGACTGTTTGGAAATGTTAGCGCAATGAATGCATTCAATTTTAATTCTT[C/A]AACACTATATGGAAACGACTGTGCCCTGACTGAATGTGAGGTGTACAAAGTAAAGCAGAGTAAGTCAATCGTCAGAAAATAGCCATAGACAGTAAATAACCTCCAGTTTCTATAAGTAAACATTTACAAGTGTATCAATAAATTAATTGTTGGCATTACTTCAGCTGAAAGCCCTCTGTCAGACTATCTGAAGCCATGGAGGAATGTTCTGTGGACAGCCGAGTAAGTTTTCCCCTTGCTATATTTATTAACATTGGTAATAAGTTAGTTAAAATGTTATTAAATTAAGTTTTGATCTGTCACAGACAAAAAGCAGAGCTCATGGAAATGATCAGGAATTATAAACCCCTGACATCTTCTGTCAGCCATATTCGAATCCTGATGATTGGTCCTGTTGGTGCTGGAAAATCCAGTTTCTTCAACTCTATAAACTCCATCTTTATGGGTCGCATAACCAGCAAAGCCATGTCAGGATCTGCAGACACCAGTCTGACCACACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43808

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105458	Nonsense	233	483	4	8
ENSDART00000105459	Nonsense	219	469	6	10
ENSDART00000142267	Nonsense	242	492	4	8

Genomic Location (Zv9):

Chromosome 22 (position 17681306)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	17432241
GRCz11	22	17457219

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGATCTGTCACAGACAAAAAGCAGAGCTCATGGAAATGATCAGGAATTAT[A/T]AACCCCTGACATCTTCTGTCAGCCATATTCGAATCCTGATGATTGGTCCT

Long Flanking Sequence:

GGATGTTATGCACGATATGATGGCGATGAAGGACCCAACTTTGGCAACAAGTTGTACTTCTGCAACAACAACCAACCAGTTGTGTCTAATCGAGGAGCATCCCAAGGTGGACTGTTTGGAAATGTTAGCGCAATGAATGCATTCAATTTTAATTCTTCAACACTATATGGAAACGACTGTGCCCTGACTGAATGTGAGGTGTACAAAGTAAAGCAGAGTAAGTCAATCGTCAGAAAATAGCCATAGACAGTAAATAACCTCCAGTTTCTATAAGTAAACATTTACAAGTGTATCAATAAATTAATTGTTGGCATTACTTCAGCTGAAAGCCCTCTGTCAGACTATCTGAAGCCATGGAGGAATGTTCTGTGGACAGCCGAGTAAGTTTTCCCCTTGCTATATTTATTAACATTGGTAATAAGTTAGTTAAAATGTTATTAAATTAAGTTTTGATCTGTCACAGACAAAAAGCAGAGCTCATGGAAATGATCAGGAATTAT[A/T]AACCCCTGACATCTTCTGTCAGCCATATTCGAATCCTGATGATTGGTCCTGTTGGTGCTGGAAAATCCAGTTTCTTCAACTCTATAAACTCCATCTTTATGGGTCGCATAACCAGCAAAGCCATGTCAGGATCTGCAGACACCAGTCTGACCACACAGGTACAGATTCAGCAGAGTTTTCCACAGACGACTCCTGAGTCTCTGATACGTTTCTCTTCTTGGTTGACAGTTTCGAACTTACCCAATTAAAGATGGTCGTGAAGGAAAGCCATTGCCGTTTGTGTTGTGTGACACCATGGGCCTCGAGGAGCAATCAGGAGCAGGACTGGACATTGAGGACATCAGCAGCATTCTTCAAGGACAAATACCAGACCGCTATAAAGTAAGAGCACTTACTGAATCTCCAAAATGAATGAAGACTGAAGTGTGAATGCTAAAATATAAATCCTGCTGATTCAGTTCAATCCAGTCACACCATTTCAACCTGATGAGCAAAAGTCC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29754

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105458	Essential Splice Site	336	483	5	8
ENSDART00000105459	Essential Splice Site	322	469	7	10
ENSDART00000142267	Essential Splice Site	345	492	5	8

Genomic Location (Zv9):

Chromosome 22 (position 17680924)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	17431859
GRCz11	22	17456837

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGAGGACATCAGCAGCATTCTTCAAGGACAAATACCAGACCGCTATAAA[G/A]TAAGAGCACTTACTGAATCTCCAAAATGAATGAAGACTGAAGTGTGAATG

Long Flanking Sequence:

AAGTTTTCCCCTTGCTATATTTATTAACATTGGTAATAAGTTAGTTAAAATGTTATTAAATTAAGTTTTGATCTGTCACAGACAAAAAGCAGAGCTCATGGAAATGATCAGGAATTATAAACCCCTGACATCTTCTGTCAGCCATATTCGAATCCTGATGATTGGTCCTGTTGGTGCTGGAAAATCCAGTTTCTTCAACTCTATAAACTCCATCTTTATGGGTCGCATAACCAGCAAAGCCATGTCAGGATCTGCAGACACCAGTCTGACCACACAGGTACAGATTCAGCAGAGTTTTCCACAGACGACTCCTGAGTCTCTGATACGTTTCTCTTCTTGGTTGACAGTTTCGAACTTACCCAATTAAAGATGGTCGTGAAGGAAAGCCATTGCCGTTTGTGTTGTGTGACACCATGGGCCTCGAGGAGCAATCAGGAGCAGGACTGGACATTGAGGACATCAGCAGCATTCTTCAAGGACAAATACCAGACCGCTATAAA[G/A]TAAGAGCACTTACTGAATCTCCAAAATGAATGAAGACTGAAGTGTGAATGCTAAAATATAAATCCTGCTGATTCAGTTCAATCCAGTCACACCATTTCAACCTGATGAGCAAAAGTCCTCCAGATCTGCGTCTCTACAGGAGAAGATCCACTGTGTGGTGTACGTGATCGACGCCACCAAAATCTCCCTCATGTCTGAGAAACTAGAGGAAAAACTGTCTGCCATACGCAGAAAAGTCAACTCACTGGGTTAGTGAACATTTATGCATATCTTGTGACCAATCAAAGGTAAATTGAAGTAATTAATATACATAAGTCAACATACCTCAAACTATTTCAGGCATTGCTCAGATTGTCTTGATGACAAAAGTAGATGAAGCTTGTCCACTAGTGCAGGAAGACCTTCAAAACCTTTATCTCAGTTCCTACATCAAGACGAAGGTGAGACATCATGATCACATGAACTGTTCTTATTTCTGTACAAGCACTTTCCAGAACCTT

Associated Phenotype:

Not determined