si:ch211-287j19.6

Ensembl ID:

ENSDARG00000001470

ZFIN IDs:

ZDB-GENE-070424-69, ZDB-GENE-070705-176

Description:

hypothetical protein LOC100038770 [Source:RefSeq peptide;Acc:NP_001083019]

Human Orthologues:

AL645933.1, AZGP1, FCGRT, HFE, MICB, MR1

Human Descriptions:

Fc fragment of IgG, receptor, transporter, alpha [Source:HGNC Symbol;Acc:3621]
MHC class I polypeptide-related sequence A isoform 2 (MICA*00801) precursor [Source:RefSeq peptide;
MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:7091]
alpha-2-glycoprotein 1, zinc-binding [Source:HGNC Symbol;Acc:910]
hemochromatosis [Source:HGNC Symbol;Acc:4886]
major histocompatibility complex, class I-related [Source:HGNC Symbol;Acc:4975]

Mouse Orthologues:

Azgp1, CR974466.3, Fcgrt, Gm11127, Gm7030, Gm8815, Gm8909, H2-Bl, H2-D1, H2-K1, H2-K2, H2-M2, H2-M3, H2-Q10, H2-Q2, H2-Q6, H2-Q7, H2-Q8, H2-T10, H2-T22, H2-T23, H2-T3, H2-gs10, Hfe, Mill1, Mill2, Mr1

Mouse Descriptions:

Fc receptor, IgG, alpha chain transporter Gene [Source:MGI Symbol;Acc:MGI:103017]
MHC I like leukocyte 1 Gene [Source:MGI Symbol;Acc:MGI:2179988]
MHC I like leukocyte 2 Gene [Source:MGI Symbol;Acc:MGI:2179989]
MHC class I like protein GS10 Gene [Source:MGI Symbol;Acc:MGI:3808875]
alpha-2-glycoprotein 1, zinc Gene [Source:MGI Symbol;Acc:MGI:103163]
hemochromatosis Gene [Source:MGI Symbol;Acc:MGI:109191]
histocompatibility 2, D region locus 1 Gene [Source:MGI Symbol;Acc:MGI:95896]
histocompatibility 2, K region locus 2 Pseudogene [Source:MGI Symbol;Acc:MGI:95906]
histocompatibility 2, K1, K region Gene [Source:MGI Symbol;Acc:MGI:95904]
histocompatibility 2, M region locus 2 Gene [Source:MGI Symbol;Acc:MGI:95914]
histocompatibility 2, M region locus 3 Gene [Source:MGI Symbol;Acc:MGI:95915]
histocompatibility 2, Q region locus 10 Gene [Source:MGI Symbol;Acc:MGI:95929]
histocompatibility 2, Q region locus 2 [Source:RefSeq peptide;Acc:NP_034522]
histocompatibility 2, Q region locus 2 Gene [Source:MGI Symbol;Acc:MGI:95931]
histocompatibility 2, Q region locus 6 Gene [Source:MGI Symbol;Acc:MGI:95935]
histocompatibility 2, Q region locus 7 Gene [Source:MGI Symbol;Acc:MGI:95936]
histocompatibility 2, Q region locus 8 Gene [Source:MGI Symbol;Acc:MGI:95937]
histocompatibility 2, T region locus 10 Gene [Source:MGI Symbol;Acc:MGI:95942]
histocompatibility 2, T region locus 22 Gene [Source:MGI Symbol;Acc:MGI:95956]
histocompatibility 2, T region locus 23 Gene [Source:MGI Symbol;Acc:MGI:95957]
histocompatibility 2, T region locus 3 Gene [Source:MGI Symbol;Acc:MGI:95959]
histocompatibility 2, blastocyst Gene [Source:MGI Symbol;Acc:MGI:892004]
major histocompatibility complex, class I-related Gene [Source:MGI Symbol;Acc:MGI:1195463]
predicted gene 11127 Gene [Source:MGI Symbol;Acc:MGI:3779381]
predicted gene 7030 Pseudogene [Source:MGI Symbol;Acc:MGI:3647514]
predicted gene 8815 Pseudogene [Source:MGI Symbol;Acc:MGI:3648635]
predicted gene 8909 Gene [Source:MGI Symbol;Acc:MGI:3704134]

Allele Name	Consequence	Status	Availability
sa19561	Nonsense	Available for shipment	Available now
sa32752	Nonsense	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa19561

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000101143	Nonsense	33	350	2	7

The following transcripts of ENSDARG00000001470 do not overlap with this mutation:

ENSDART00000048445

Genomic Location (Zv9):

Chromosome 1 (position 47618548)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	46430209
GRCz11	1	47121441

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCTCTTTTTAATACAGAAAAACACTCCCTCTACTACATATACACAGCTT[T/A]ATCCAGACCTGTCCACCTGCCGGGCATCTATGAATTCACTGCAATGGGTT

Long Flanking Sequence:

AAATACTTAAAGAAAAAATTAATCCACGTCATTGTTGTTTCTCAAGTTGCTTATTACTCTATAGCCTACTTATTTCATCGCCTAAAATTGGTATAAAATGGCTTAAGGGTTTATATGCCTGTTTATGGTGTGTGCTGGTTATGGTTATGAAGCCTCCTGCTTGTGCCGCCTTTTAGTTGTGCTTGCTCAAACTTTAAACCGTTGATCGAAACCCCCCTAGCGACTTAACTGACCTCAGCTGTGCCAAATATAAGAGCAATGAATATAACAGCTACAGATGTTGCAATACTTGGTCTATAGGTTGAAAGGAAAAGACAAAAACATCTTAAAACAATTTAACCTGATTTGTTTGTGATGGTCAGATGTCACCACTCCATCATGACGCTACTTTCATAATGTATTCTTAAAAATAATCATGTGGATCATGTGTTTTGACATCTTCATGTTTTGTTCTCTTTTTAATACAGAAAAACACTCCCTCTACTACATATACACAGCTT[T/A]ATCCAGACCTGTCCACCTGCCGGGCATCTATGAATTCACTGCAATGGGTTTGCTTGATGACAGACAGATTGACTATTACAACAGCCAAGAGCAGAAGAAGATTCCCAAACAGCACTGGATGAAAGAGAAAATGCAGGAAGATTACTGGGAAAAAGGCACCCAGTCCAGAAAGAGCAAAGAACAGTGGTTTAATGTGAATCTCAAAATTCTGATGGAACGAATGAGACACAATAATAATTCAGGTGAGGAATGGTTATCAGTTTTACCCTGCATATACACTACTGGTCAAAAGAACAGGCAAGTCAGCATATTATAGTGATGCAGGTTCACTTTTCAAATCACTAACATTTTATAAAACTACATTTTTTTAAATTCAAATAGAAAACAGCTTTTTTTAAATTACACTTTTTACACTTTTGATCAATAAATTCAGGATTGGTGAGCAGAAGAGACCTTTTTAACCATTAAAACTTTTGGCCTGTATTAATTATATTAATATA

Associated Phenotype:

Not determined

Allele Name:

sa32752

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
ENSDART00000101143	Nonsense	201	350	3	7

The following transcripts of ENSDARG00000001470 do not overlap with this mutation:

ENSDART00000048445

Genomic Location (Zv9):

Chromosome 1 (position 47617736)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	46429397
GRCz11	1	47120629

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCTACCTGGAAAAAGAGTGTGTGGACTGGCTCAACAAATTCAGAGAATA[T/A]GGAGATCAGGAGCTTAGAGAAGGCTGTGAGTTTATATACAGTACAGCATT

Long Flanking Sequence:

TATAGTGATGCAGGTTCACTTTTCAAATCACTAACATTTTATAAAACTACATTTTTTTAAATTCAAATAGAAAACAGCTTTTTTTAAATTACACTTTTTACACTTTTGATCAATAAATTCAGGATTGGTGAGCAGAAGAGACCTTTTTAACCATTAAAACTTTTGGCCTGTATTAATTATATTAATATAACGTTATGTCTGTATAATTTTTGCCTTATATTTTTGGTGTCTGTTTCAGATGTTCATGTTCTTCAGTGGAGACATGGTTGTGAAATTGACAGTCAGGGCAATGATGTCCGATTTTCTAAAGGCATTGATGAGTACAGCTATGATGGAAGAAACTTCCTGGCCTTTGATGATGCGGATTCTCAGTGGGTTGCTCCAGTGGAAGAAGCTCTTCCAACCAAGAGGAAATGGGATAATGTGCCCATCCTAAATCAGTACACCAAGGGCTACCTGGAAAAAGAGTGTGTGGACTGGCTCAACAAATTCAGAGAATA[T/A]GGAGATCAGGAGCTTAGAGAAGGCTGTGAGTTTATATACAGTACAGCATTAATTTGGTTATTGTTATAAAACTGATTGATTAAACAATGTACTTGTGATTTCAGCTCCCCCAGATGTTCATGTGTTTGCGAAGAAGATTATCAGTGGCAAAGCCAAGCTAAAACTTACCTGTATGGTCACTGGATTCTACCCCAAAGATGTGATTTTGACCATAAGGAAATACCGCACGGCACTGTCTGATAATGAGGTAGAATCTTCAGGAGTTAGACCAAACCCTGATGGGACCTTTCAGCTGAGAAAGAGCACTAACATCTATGAAAAAGCAGAATATGACTGTTATGTGGCCCACAGAACCCTCAAGGAACCAATTATCAAAAAATGGGGTAATCAAAGCATACAGAAAAAGCACCTTGTAAAAGTAAATTAAAATTGTTGATTAAAATTGAAGATGCATGTCTTTTGTATTTGTAGATGGGGAGTGCCAGGACTGCTCTTCAGGA

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details