si:dkey-222k23.4

Ensembl ID:

ENSDARG00000077257

ZFIN ID:

ZDB-GENE-080303-10

Description:

hypothetical protein LOC100142639 [Source:RefSeq peptide;Acc:NP_001116089]

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]

Allele Name	Consequence	Status	Availability
sa43667	Nonsense	Mutation detected in F1 DNA	Not yet available
sa23965	Essential Splice Site	Available for shipment	Available now
sa23964	Nonsense	Available for shipment	Available now

Allele Name:

sa43667

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112420	Nonsense	129	259	2	7
ENSDART00000142598	Nonsense	129	259	2	7

The following transcripts of ENSDARG00000077257 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 21 (position 28490928)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	29059839
GRCz11	21	29096534

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGTGGACATAGAGGGCTTCTTTAATGATAAGAAGATGTCCTACACGCTA[C/T]AAGTCATGAAAGGCAAGTTTAATGATTACTTATAAAGTTGGACAGCATTT

Long Flanking Sequence:

ACCTCATAATTTGACGCAAATAAATGCAAAAAGGTCCACTTTTTGAGAAAAAAGTACCACCCCTTTTAATAGGCTGGTTAAGGGCCTGTATATATATACATATATATGGCATTTTGCTAATGCTTATTTTGCTATTTCTGATGCTAATGCTAATTTTTCATTTTCATCCTACAGCTGGCATTTCCCCCATCTTGGCATTTCATGTGACGGAGGGAAGCACAGTGATTTTATCATGTCATTATTCTGTGAAGCACCACGGTCTGAGCCACGTCTGCTGGGGTAGAGACTGCGGGACTTTTTGGTGTAACGACATCATTGTTCAGACAGATGAGTACGGCGTGATCTCCAAAGTCTCGGACAGGTACCGGCTCATCGGGGATGTGATGTTGGGACAGATGGACTTGGGGATCCAAAAGATACAGAAGTCGGACAGTGGGCCCTACTGCTGCAGAGTGGACATAGAGGGCTTCTTTAATGATAAGAAGATGTCCTACACGCTA[C/T]AAGTCATGAAAGGCAAGTTTAATGATTACTTATAAAGTTGGACAGCATTTGGAGAGATTTAAATAATTTTTTTAATTTTTTAATTTTAATTTTAGTTTTTTTTTCATGTTTTTAGCCCCAACAACTGTGGCTCCAAAAACTACTACACAAATTACAACAGAACCAATGGAAACACAGACAGGTGAGGCCAACAATTGTACAATGACTTGAGAACAGTGAACAGAGGAGTTGTTTTTAATTGACTTTCTTTTTTCTTTTTGTTTTTTTTTTGACATTACAAATATCCCAATTACTAGTTTAGGTCCTGCTAAGAAAAAAAAAAATGAAGAGTATTTAGAAATATAAACTCCGAATTGTGGCCTATAAACTCAGACAAAGGAAGGGAAAATTTATCTTTAAGTAAGAATTGTGACAAGTAATGTCACAAATCGAAAAATAAAACTTTAAAATTGCAAGACGTACTGTCATGATTATGAAAAAGGCACATGTTTTACACAGCG

Associated Phenotype:

Not determined

Allele Name:

sa23965

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112420	Essential Splice Site	155	259	None	7
ENSDART00000142598	Essential Splice Site	155	259	None	7

The following transcripts of ENSDARG00000077257 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 21 (position 28489106)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	29058017
GRCz11	21	29094712

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCTTTAGCAACAAAAAAACGATTTCCTGTGTTTCGTTCTGAATTTTGC[A/G]GCATCTCTATCAGATCCGTCCAGAGGAGGAGACTCATCACTCAATGACAT

Long Flanking Sequence:

TTTCTACAGTGTACAGTAGCAGTTACTGTCAACAGCTAAATAAAAACAAATAGATCAAAATGCTGCATATAGTGCCAATATTCTGACAGAAAACGCTTATTGAAGCAAAATAGCCAAAAACCTGAAAGACTGAAAAACCAATAGGGTTTTTTAAAGTGTGTTGCCTCAAAAAATAAATAAATAAATAAGTAAATAAAATAAAATAAATAAATAAAAAATAAAATAAATAAATAAATAAATAAATCTGCTGACTGCTATTAACAGTTAATTCCCTGCACAAACTTTTGTGTCAACTTTTTTTTTCCTACACTCTTGCTTTATCTAACAGTTCATCAGACCACCATATGCACCTCAATTATCATCATGTGTGCTTGTGCACAATCATGTCATGTCAAAAGACCACAACCCAAATGTCACAGACCCTTGTGGGCAGAGTTAACATTTCTCAGCCAGCTTTAGCAACAAAAAAACGATTTCCTGTGTTTCGTTCTGAATTTTGC[A/G]GCATCTCTATCAGATCCGTCCAGAGGAGGAGACTCATCACTCAATGACATTTCCTGGCAGAACGAAACTCATGTGCATTCAGGGGCAATGGTGAGTCATGTAAGAACATGAAAAATAAACAAACAGTGTCACCGTTAAATGCTCATGTTACATCTCTAAAGCATAATATGTATTTTAGAAAATGAAATATTTATTGTGCTTTACATGTAACTGTTTCTGCAGGAAAATGGATCACATTCATTTGGAAAGCTTATGACTCATTTTATATCTTGCAATAAAACACTGCCAGCGAGGTCTTTTATTTCTCACTAGCCACAAAGTTAAATGCCACTCAGCATTTCCACTAGCCACAGTTTGTTGTTGGGAAATTGCATATTTATATGATTCATATTCACTGTTTTGTGGTAAAACAGACTTAAATTAATTTCCATGGCTTTTTTTTTCTTTTTTGGCTTTTATAAAATGGCAAAAATAAATGTAGGAAATATAACCAACACATT

Associated Phenotype:

Not determined

Allele Name:

sa23964

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
ENSDART00000112420	Nonsense	218	259	5	7
ENSDART00000142598	Nonsense	218	259	5	7

The following transcripts of ENSDARG00000077257 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 21 (position 28486911)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	29055822
GRCz11	21	29092517

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTCTGTCTCTCAGTCTGCTTCTGGTTCTTTTGGGTGCTCTGGCCCTTT[T/A]GACCTTCAAACGTATGTATTGCCCTCAGCTATTATTCTACTGGACATTGA

Long Flanking Sequence:

TGGATTTACATGAGAACAGCGGGCACTAATGGCTGTGTCAGTTGTCATTTCTGTGTGGAGTTTGTAGGTTCTATGTTTGTGTGGGTTTCCTCCGAGTGCTCTGGTTTTCCCACACAGTCCAAAGACATGTGCTATAGGTGAATTGAAAAAGCTATATTGGCCACAGTCTATGTGTGTGAATGCGGGAGTGTATGGGTGTTTCCCAGTGTTGGGTTGTGGCTGGAAGGGCATCCGCTGCGTAAAACATTTGCATTACATAAAGTAACAAAAACTCCAACAGAAATGAAAAAATCTAAAACTGTTAATGTCTAAACTTTTATTAGTATACAAATAAAAATATGGTTTATTTTGTGAACTAACCCTAAGAGTCTTGAAATTCTTCTAAATGTGTGATTTTAAGATGGAGGAGCCGATCTCTAGGATCATGCTGCAGATTAACATCCCGGTGTTGTCTCTGTCTCTCAGTCTGCTTCTGGTTCTTTTGGGTGCTCTGGCCCTTT[T/A]GACCTTCAAACGTATGTATTGCCCTCAGCTATTATTCTACTGGACATTGAAAAAGTTCACTTCCAGAATGATTGGTCAGCATTGACATCTACTTGTTTTCCATATTCTCCCCATATATGTAAATGAATGGTAACCATAAACCTTTCGGAAACCAACATTTTTCAAATATCTTTTGTGGGTCCCACTTTATATTAGATGGCCTTAACTAATATGATTTTACACTGAAATTAATCATTTTTTTACCATGTGTTTACTGTGTAAATATTTTTTTGTTTACATTATACGTAATTGCATCTGTTAACTTCTATATTTACATTTGTAATTGACCATCCCTTACACCAGTGGTCACCAAACTTGTTCCTGGAGGGCCAGTGTCCTGCAGGTTTTAGCTCCAACTCTAATCAAACACACCTGAACAAGCCAATCAAGCTCTTACTAGGTATACTTGAAACACCCAGGCAGGTGTGTTGAGGCAAGTTGGAGCTAAACCCTGCAGGGAC

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details