ZMP

hig1

Ensembl ID:

ENSDARG00000022303

ZFIN ID:

ZDB-GENE-030826-15

Description:

HIG1 domain family member 1A [Source:RefSeq peptide;Acc:NP_956394]

Human Orthologue:

HIGD1A

Human Description:

HIG1 hypoxia inducible domain family, member 1A [Source:HGNC Symbol;Acc:29527]

Mouse Orthologue:

Higd1a

Mouse Description:

HIG1 domain family, member 1A Gene [Source:MGI Symbol;Acc:MGI:1930666]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14226	Nonsense	Available for shipment	Available now
sa32823	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14226

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
Order Allele From EZRC

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029347	Nonsense	36	99	3	4

Genomic Location (Zv9):

Chromosome 2 (position 1972443)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	1827529
GRCz11	2	2170335

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AYTTTGACTGTCTTTCAAGGGATGGCTGGGTTCTTTGCCATTGTGGCGTA[C/A]AGACTGTTCAAGCTGAAGAGCCGAGGAGACACMAAGATGTCAGTGCACCT

Long Flanking Sequence:

GGAGTCTTACTGTAAATCATGTTTAAAGATGAATGTTAGTCATTTTTTGGCTCAGGAATGAATAAGAGGCTGAATTTTACTGTACGGAGAAGTTTTATTGCACGTTTTTTGATAGTTGAAGGCAAAATAATTAACCGTCTTGTGAAATTAAAAGTTTGAAATCCAAAATTAAATATATAATGCACTGTTAATGATTAATACAACATTTTAGTAGTTATTTTGCATAGGATACTAGTATTCAGATTAAAGTGCAATTTATAGGCTAACCCTAACCCTAATTAGAATAATTAGGCAAGTCATTGTACTACAGTAATTAGTTCTGTAGCCAATCAATGTTTCTAAAGGGGGGTGAATAATATTGACCGTAAAATAGTTTTACAAAATTTTAAAACTGCTTTCATTTCTTAATAAAAAACACTTTAATCGAGGTTAAAAAAACCTAATTGCTCTACTTTGACTGTCTTTCAAGGGATGGCTGGGTTCTTTGCCATTGTGGCGTA[C/A]AGACTGTTCAAGCTGAAGAGCCGAGGAGACACAAAGATGTCAGTGCACCTGATTCACATGCGTGTGGCTGCACAAGGCTTCGTGGTCGGAGCCATGACTTTAGGTGAGACAGTCTTCATCACAATACACATGCATGGTTTAAAGTACACATGAAATCCAAACTAACCATATTCATTTTGTTAGCTCACATTGCTAGTTTTTGTGGTGAACAGTTCATCCGTGCTTGTCATTAAATAAAACAATAGTTTGCCTTTGTGATCTTTAACGGAAATCTGAAATGCACTTCCTGTTTGTTTCCAGTCAAATTGTCAGATTAGGTCCGTCTGAGGTATTGGGTGTGGCTAACATGCTTAACCACGCCCCTTCAGTTGTCAGTTTTGACGATAAACAGAAATGGTGTGGAGGAGGAATCTGTTAGGTTGTAAGAACTCTCCTAAAACTCATTTACAGGGATCTTTCTAAATGAAATGCCTGTTTTACTACATCCAATCAGCTCACAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32823

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029347	Essential Splice Site	71	99	4	4

Genomic Location (Zv9):

Chromosome 2 (position 1974911)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	1829997
GRCz11	2	2172803

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAGCATTAAGACCTGTGGTATAATGTGTTGTATGTCTGTTTTTGTGTAC[A/T]GGAGTCATCTATTCGATGTACAACGAGTATATTCTGAAACCCGCCGAAGC

Long Flanking Sequence:

GTGTAGCACTAGTTTCCTCCACATCTCCACCAAAACCTTCTGATGTGATTTTTATTATATATTTTTTTCCTGTTGTAGCTGTGAAATGACTCGAATCATTCAGCGTAGTGATATAAAACTGTAAAGCACTCAAAACCTGCCGGATCTACTTCATCTGTGCGGTTAGCTGAGAATAACAGCACACCTTAGAATACTCATCAACCAGTCAGAATCAAGCATCCAACATCCACATCAGTAGTCTAAAACTGGACTCCTGGAGGGCCGCAGCATAGTTTAGCTCCTACCACCTCCAACTCGCACCTGCTTTGTAGTCTCCAGTAGTCTCGAACAACTTGATTAGTTCGATCAGCTGTGTTTGATTAGGGTTGGAAACTCTGCAGAGCCGCGGTCATCCAGGAATCCAGTTTGAGACCTATAGACTGTAATAAGGAAGAATTGGCCAATCAGAATCCAGCATTAAGACCTGTGGTATAATGTGTTGTATGTCTGTTTTTGTGTAC[A/T]GGAGTCATCTATTCGATGTACAACGAGTATATTCTGAAACCCGCCGAAGCACAGAAGGCGCTGGAGCAGAAAGCGTTGGAAAAGAAGTGAAGAGTTTTGTTGGTTTCCTGAGATATCCTTCGTACCACCTCATATTAAGGTGTCCCTTAAAGTGTATTTATAGCGAACTTTTTGTTTACTTCTTATTTCTTTACACCGTTTCCTATTTAAACCTAATAAGCCTCGGATCAGGAGGTTTGTGTGTTCATGGCACGTTTGAGGAATGACAAAATAGTTCCTATTTTGAATCTGCCAACTATTATTTATTTCTCATATCAGTAACGCGCTGATAATCACAGTATAAAATGTATTTTATTTTATTTTTGGAGTTTTTTCAAAAGTTTTGCTGCTTTTATTTTCATTTTGTGCCCTAGTTTTATGAATAAGGTGTGGCATGAAAACCTTTGTACCTTCTAATTTAGGATTTTTTTCTTGTATTATTTATATAGACTAGCAGAGCC

Associated Phenotype:

Not determined