ZMP

si:dkey-222k23.2

Ensembl ID:

ZFIN ID:

Human Orthologues:

HAVCR1, HAVCR2, TIMD4

Human Descriptions:

T-cell immunoglobulin and mucin domain containing 4 [Source:HGNC Symbol;Acc:25132]
hepatitis A virus cellular receptor 1 [Source:HGNC Symbol;Acc:17866]
hepatitis A virus cellular receptor 2 [Source:HGNC Symbol;Acc:18437]

Mouse Orthologues:

BC053393, Gm12169, Havcr1, Havcr2, Timd2, Timd4

Mouse Descriptions:

T-cell immunoglobulin and mucin domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2159681]
T-cell immunoglobulin and mucin domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:2445125]
cDNA sequence BC053393 Gene [Source:MGI Symbol;Acc:MGI:3039605]
hepatitis A virus cellular receptor 1 Gene [Source:MGI Symbol;Acc:MGI:2159680]
hepatitis A virus cellular receptor 2 Gene [Source:MGI Symbol;Acc:MGI:2159682]
predicted gene 12169 Gene [Source:MGI Symbol;Acc:MGI:3650838]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa37337	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37337

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124327	Essential Splice Site	152	231	None	7
ENSDART00000147367	Essential Splice Site	53	127	None	5

Genomic Location (Zv9):

Chromosome 21 (position 28510936)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	29079847
GRCz11	21	29116542

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTCCGAAACACAATTGGCCCCTACAACAGCAAAGCAGGAAAAACAAGG[T/C]ACGAAAATTGTTCAGTGTTTTTGCAAAAATGTAATCCAGCACTAGCTATT

Long Flanking Sequence:

TATAGCCTGCAGCGAATCATCAAAGTTGGTGATTGGACTGGTTGGAGACACAGTTACTCTACCATGTAAATATGACATTAACACCAATGGCCCATTGGGCGTTTGTTGGGGCCGACACCAGTCATTGTTCAGCTGTGAAAACACTGTTATCTCCATTGATGGCTTACAACTGAACTACAGAGAGTCCCACAGATTCAGCTTGGACAGTGGACTCGACCGAGGAGATGTTTCACTCACCATAAGAGCTGTTCAGAAGAGTGATGCTGGGATGTACGTCTGCCGTATCGAGATCCCGGGTCTTTTCAATGACATCAGTTACAACGTTTATCTTTTTATCCGCAGTGGTGAGTAACAGCTCAATTTAGTCTCTTGGTCAGTGTTGTAGCGCTCAGATGTTGTGATGGACAGTTTTTCTGCTTATCCATAAAAGGACTGGATCCAAAGAGAGTTGTCTCCGAAACACAATTGGCCCCTACAACAGCAAAGCAGGAAAAACAAGG[T/C]ACGAAAATTGTTCAGTGTTTTTGCAAAAATGTAATCCAGCACTAGCTATTTCAGTTTACCATTTAAATGAACATGCTACTGAACTGTTTTTTTGTTGTAGATGACAGCTAGTAATTTAGAAAGAAAATATATTAAGCCACAGTTTTTACTGTTGACAATAATCAGACATTTAACTTGATTTTGGCTAACATTATTAACAACTGGCATGTTTATATGATCATTGTTAGCATGCTTCTAGCATAAACTAACATGTTGGTTACATGTTTCTAGTACTATTAGCATATTGTTACAATGAAGCCACGTTGCTTTCACTGTTGACAATAATAAGACATTTAACTTGATGTTGGCTAACATTAGCAATAATTGGCATGTTTATATGATCATTGTTAGCGTGTTTTTAGCATAAATTAACATGTTATTTACATGTTTGCAGCATTATTAGCATATTGTTACAATGAAGCCATGCTGTTTTCTTTGTTGACATTAAAAAGACATTTTAC

Associated Phenotype:

Not determined