ZMP
si:dkey-222k23.4
Ensembl ID:
ZFIN ID:
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]
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]
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 are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23965 | Essential Splice Site | Available for shipment | Available now |
| sa23964 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23965
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa23964
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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