ZMP
ms4a17a.4
Ensembl ID:
ZFIN IDs:
Description:
membrane-spanning 4-domains, subfamily A, member 17A.4 [Source:RefSeq peptide;Acc:NP_001096108]
Human Orthologues:
MS4A12, MS4A15, MS4A2, MS4A3, MS4A4A, MS4A8B, RP11-312N17.2
Human Descriptions:
Membrane-spanning 4-domains subfamily A member 18 [Source:UniProtKB/Swiss-Prot;Acc:Q3C1V0]
membrane-spanning 4-domains, subfamily A, member 12 [Source:HGNC Symbol;Acc:13370]
membrane-spanning 4-domains, subfamily A, member 15 [Source:HGNC Symbol;Acc:28573]
membrane-spanning 4-domains, subfamily A, member 2 (Fc fragment of IgE, high affinity I, receptor fo
membrane-spanning 4-domains, subfamily A, member 3 (hematopoietic cell-specific) [Source:HGNC Symbol
membrane-spanning 4-domains, subfamily A, member 4 [Source:HGNC Symbol;Acc:13371]
membrane-spanning 4-domains, subfamily A, member 8B [Source:HGNC Symbol;Acc:13380]
membrane-spanning 4-domains, subfamily A, member 12 [Source:HGNC Symbol;Acc:13370]
membrane-spanning 4-domains, subfamily A, member 15 [Source:HGNC Symbol;Acc:28573]
membrane-spanning 4-domains, subfamily A, member 2 (Fc fragment of IgE, high affinity I, receptor fo
membrane-spanning 4-domains, subfamily A, member 3 (hematopoietic cell-specific) [Source:HGNC Symbol
membrane-spanning 4-domains, subfamily A, member 4 [Source:HGNC Symbol;Acc:13371]
membrane-spanning 4-domains, subfamily A, member 8B [Source:HGNC Symbol;Acc:13380]
Mouse Orthologues:
AC134839.1, Ms4a15, Ms4a2, Ms4a3, Ms4a4b, Ms4a4c, Ms4a4d, Ms4a8a
Mouse Descriptions:
membrane-spanning 4-domains, subfamily A, member 15 Gene [Source:MGI Symbol;Acc:MGI:3617853]
membrane-spanning 4-domains, subfamily A, member 2 Gene [Source:MGI Symbol;Acc:MGI:95495]
membrane-spanning 4-domains, subfamily A, member 3 Gene [Source:MGI Symbol;Acc:MGI:2158468]
membrane-spanning 4-domains, subfamily A, member 4B Gene [Source:MGI Symbol;Acc:MGI:1913083]
membrane-spanning 4-domains, subfamily A, member 4C Gene [Source:MGI Symbol;Acc:MGI:1927656]
membrane-spanning 4-domains, subfamily A, member 4D Gene [Source:MGI Symbol;Acc:MGI:1913857]
membrane-spanning 4-domains, subfamily A, member 8A Gene [Source:MGI Symbol;Acc:MGI:1927657]
membrane-spanning 4-domains, subfamily A, member 2 Gene [Source:MGI Symbol;Acc:MGI:95495]
membrane-spanning 4-domains, subfamily A, member 3 Gene [Source:MGI Symbol;Acc:MGI:2158468]
membrane-spanning 4-domains, subfamily A, member 4B Gene [Source:MGI Symbol;Acc:MGI:1913083]
membrane-spanning 4-domains, subfamily A, member 4C Gene [Source:MGI Symbol;Acc:MGI:1927656]
membrane-spanning 4-domains, subfamily A, member 4D Gene [Source:MGI Symbol;Acc:MGI:1913857]
membrane-spanning 4-domains, subfamily A, member 8A Gene [Source:MGI Symbol;Acc:MGI:1927657]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14040 | Nonsense | Available for shipment | Available now |
sa20316 | Nonsense | Available for shipment | Available now |
sa16945 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14040
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 |
---|---|---|---|---|---|
ENSDART00000082121 | Nonsense | 72 | 246 | 3 | 7 |
ENSDART00000097323 | Nonsense | 72 | 246 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60797778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75178903 |
GRCz11 | 4 | 76755641 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAATGATCGGTGTGTTGACCTTGYTGTTTGGAATMGYGTCTATAGGTTA[T/A]GAAATGTTTTTCTTCWTCAACACTGGTGTTTCTTACTGGGYATCTCTGAT
Long Flanking Sequence:
AGCTGCAGCTCATGTTTTCAGACGTAAACACACATTCTGTCAAAGATAAGCTGAAGACAAAAGGTTTACCAGTGTCTATATTGTCCTGATAATGGTATCCTCTTTTGCTTTATTTTGATTTTGTACAGGTTCATTTGATACTCTGAAACTGAAATGGCGACTGTCGGAGCTATGAATCCTTCAACGATTGTCATCCAGCTTCAGCCACTGACACAAACAGCAACTGTGACCAGTTCTTCTGTGCCTGTGCGCATACAGCGTGTAGCAGGAGTTTCACCTCTTCAAGGAATTCAGGCCTTTCTGAGAGGCCAACCGAAAGCCCTCGGGGTGAGAAATCTCCCTTAAACCCAGATAACACACATTAACACACAGCATGTTATTCTGCTTTACTTCATGAAATACTCTTGTTCTTCTTACACTGTTCTCTCTTATTCCTCACAGACTGTGCAGATAATGATCGGTGTGTTGACCTTGTTGTTTGGAATCGCGTCTATAGGTTA[T/A]GAAATGTTTTTCTTCATCAACACTGGTGTTTCTTACTGGGCATCTCTGATAGTAAGAAACAATCATACAGTTTAACATGTTGTCCTAGATAACACAAGCTACAGTGGGTAATCAAGCAGAATACATCTTACTGTCACATTCACAGACACTAAAAGAACATGTAAATGCTTTGTGCACATGTTTATTAAATTATTAATTATTTTTGATCCTCCACACTGATCAAGGAGAATGCTTACACTTGCATAGTGTTTGCCAGAAGATCTGCCATCTACTAGATGAACGGTGTGTCTGTACACTCACCAGCTGATGTTCCTTCGAGCGAACTATCAGTGAGATGAATAACATCAGATGTTTACATTGACTGTGCTGTTAAAGAAGATCGCTACAGCTTTAATATCATCCCTTTGATTCCCCACTTTAATTAGTGACATTGTTTTGAATAAAACTGTGGAAAGAGAAACATCCTTGTCTACCAGTGTGGCAATGTGGCAGTGAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20316
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082121 | Nonsense | 213 | 246 | 7 | 7 |
ENSDART00000097323 | Nonsense | 213 | 246 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60803576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75184701 |
GRCz11 | 4 | 76761439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGAACAGCAACCCTTTAATTCAACACCCTCCTGCAGAAATGCCCCCA[C/T]AGTACATTCAATGTCCTCAAGAAGTCCCCGAACCATGCTTTCAACATCCT
Long Flanking Sequence:
TTTCACAAGAACCAACAAACCCAATATCTGTCTGTAATTCTTTAATCTTAAATGTCCAAACCCTTAAAGTCCATGTGAACCAGAAGTTGCTGCAGACTTTATTTAAATATGATGACTTATTTAATAATTTCACCATTTTGATTAAAGATTGCGAAGACAATTGGCTACTGAGGCGACAGTAACCGATCTCCTGCGCCATGAAAATATTGACGTAGGAGCCGATTAGGTGACCAAAGACAGAACTGAAATCTGAATTAATTAGTTTAATTCATCCTATCTCTGTTCCGTATTCACACACAAACCACATTACAACAATTTGTGAATTATTGATTTGTGAAGTAAAAATTTAATGTGTGCTGTAAACGTGTGAGGAACTGGGTAATGGAGCAATAATTGTTGAAAACTAACCAATAACTTAAGCTGACCATGTACATTTTATCCTGCAGATTCCTGTGAACAGCAACCCTTTAATTCAACACCCTCCTGCAGAAATGCCCCCA[C/T]AGTACATTCAATGTCCTCAAGAAGTCCCCGAACCATGCTTTCAACATCCTCCTGCAGAATCTCCCCCAGCGTACACTGAAGCAAATAAATGTGAATCAACATGAAAAACAGGGCAGCATATTGGTTCTGCTGCTTTGATGCTGTGACGATTCTAGTTCCCTTGTGTATCTGATCTGAATAAATCACATCATCAGATTATGTGTAAAATTATCAGTCATCAACATATCACTGTGTATTTTACATGTGTAGTTTTGCTACTATCTATGTGTATTTTTTAAATGTTGTTTGTTTGTAAATACTGATAAATTTGAAAAAAAAAAAACTGAAAAACCACACTGATAATCACTTAATCCTAAAAACCTAAGAAATCCTAAGAAAATCCTACCCTTCCTGCCTTTCTATCAGCTGGAACCAGTCTGGCCATTCTCCTCTGACTTCTGGCATCAACAAAGCATTTGCGCCCACAGAACTGCCGCTCACTAGATATTTCCTCTTTGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16945
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 |
---|---|---|---|---|---|
ENSDART00000082121 | Nonsense | 243 | 246 | 7 | 7 |
ENSDART00000097323 | Nonsense | 243 | 246 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60803668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75184793 |
GRCz11 | 4 | 76761531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACRTCCTCCTGCAGAAKCTCCCCCAGCGTACACWGAANGCAAATAAWTR[T/A]GAATCAACATGAAAAACAGGGCAGCATATTGGTTCTGCTGCTTTGATGCT
Long Flanking Sequence:
CAGACTTTATTTAAATATGATGACTTATTTAATAATTTCACCATTTTGATTAAAGATTGCGAAGACAATTGGCTACTGAGGCGACAGTAACCGATCTCCTGCGCCATGAAAATATTGACGTAGGAGCCGATTAGGTGACCAAAGACAGAACTGAAATCTGAATTAATTAGTTTAATTCATCCTATCTCTGTTCCGTATTCACACACAAACCACATTACAACAATTTGTGAATTATTGATTTGTGAAGTAAAAATTTAATGTGTGCTGTAAACGTGTGAGGAACTGGGTAATGGAGCAATAATTGTTGAAAACTAACCAATAACTTAAGCTGACCATGTACATTTTATCCTGCAGATTCCTGTGAACAGCAACCCTTTAATTCAACACCCTCCTGCAGAAATGCCCCCACAGTACATTCAATGTCCTCAAGAAGTCCCCGAACCATGCTTTCAACATCCTCCTGCAGAATCTCCCCCAGCGTACACTGAAGCAAATAAATG[T/A]GAATCAACATGAAAAACAGGGCAGCATATTGGTTCTGCTGCTTTGATGCTGTGACGATTCTAGTTCCCTTGTGTATCTGATCTGAATAAATCACATCATCAGATTATGTGTAAAATTATCAGTCATCAACATATCACTGTGTATTTTACATGTGTAGTTTTGCTACTATCTATGTGTATTTTTTAAATGTTGTTTGTTTGTAAATACTGATAAATTTGAAAAAAAAAAAACTGAAAAACCACACTGATAATCACTTAATCCTAAAAACCTAAGAAATCCTAAGAAAATCCTACCCTTCCTGCCTTTCTATCAGCTGGAACCAGTCTGGCCATTCTCCTCTGACTTCTGGCATCAACAAAGCATTTGCGCCCACAGAACTGCCGCTCACTAGATATTTCCTCTTTGTCGGAGCATTCTCTGTAAACCCAAGATATGGTTGTGCGTGAAAATCCCAGTAGATCAGCAATTTCTGAAATACTCAGACTAGCTTGTTTGGCACC
Associated Phenotype:
Not determined