ZMP
ms4a17a.9
Ensembl ID:
ZFIN ID:
Description:
membrane-spanning 4-domains, subfamily A, member 17A.9 [Source:RefSeq peptide;Acc:NP_001013528]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33511 | Nonsense | Available for shipment | Available now |
sa8854 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33511
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064318 | Nonsense | 38 | 241 | 2 | 7 |
ENSDART00000133799 | Nonsense | 44 | 247 | 2 | 7 |
ENSDART00000141114 | Nonsense | 44 | 247 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60665105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75046230 |
GRCz11 | 4 | 76622968 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAACCAGTTCTTCTGTGCCTGTGCGCATACAGCATGCAGCAGGAGTTT[C/A]ACCTCTTCTTGGAATTCAGGCCTTTCTAAAAGGCCAACCAAAAGCCCTCG
Long Flanking Sequence:
ACTGAATGTGTGTCAGGAATATCAAAACCAACTTTACCGCGCTCATTTCTGGCGCCCCCCTGGATGTACAGCGCCCTTAGCATTTGCCTATACTGCCCATGCCGCGGGCGGGCCTTGGTAAGAACCCTGTATTCAGTCTGATACAAGTCTGAACGCAGTGTGAACGGGTATGCAGGAATTCATGCGACTTTTACAACATTTTTCACTCATCTGCTAAGGGTGAACTCTTACATTTAATATATAAACTAGCTTTATTACATATATGAAATATAGAAAGCTTCAAAAATGTAAAGTCTATCTTATTTCTAATGGTATCCTCTTTTGCTTTATTATGATTTTGTACAGGTTGGTTTTATACTCTGAAACTAAAATGTCGACTGTCGGAGCCATGAATCCTTCATCGTATGTCATCCAGCTTCAACAACCGACACAAATGGCACCGGTTGTGACTGCAACCAGTTCTTCTGTGCCTGTGCGCATACAGCATGCAGCAGGAGTTT[C/A]ACCTCTTCTTGGAATTCAGGCCTTTCTAAAAGGCCAACCAAAAGCCCTCGGGGTGAGGAAATAAAAAAACAGACAATTATTTTTGATGTCAGTATAGCACACATTAACACAGCATGTTACTCTGTTTTACTTCATGAAATACTCTTGTTCTCCTTACACTGTTCTCTCTTATTCCTAACAGACTGTGCAGATAATGATCGGTGTGGTGACTTTCCTGTTTGGAATCGTGTCTACATTATTTGCTGCCGGTGGTGTTTCTTACGTGGCATCTCTGATAGTGAGAAACAATCATACAGTTCAACATGTTGTCCTAGATAACACAAGCTACAGTGTGTAATCAGCCAGAATACATCTTACTGTCACATTTACAGACACTAAAAGAACATGTAAATGCTTTGTGCACATGTTTATTAAGTATCACGTATTGCCACTAGAGGCAGCACTGAACACACAAACAGACTCCCTGATCTGATATGGAGGACATTGGTGAACAAAGATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8854
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064318 | Essential Splice Site | 110 | 241 | 4 | 7 |
ENSDART00000133799 | Essential Splice Site | 116 | 247 | 4 | 7 |
ENSDART00000141114 | Essential Splice Site | 116 | 247 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60668120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75049245 |
GRCz11 | 4 | 76625983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTCCATTGCTGCTGAAAACAAAATTAATTCACCATCTGCTTTATGTTTGG[T/C]ATGTACACAACACTTGTTCTTTTYATNNNTTAARCAMTGGGYRCTTGTAAAAT
Long Flanking Sequence:
AACTCATTAACCGAGTGCTCACATGAAATACAACACTAAAGCACGTGACCAACATGTAAACATGGAGCCACATGCTCTACACAACACCAAGACGAGACAGAATGCATGAAAAGAGTACACAATTATTAAAACACTTATCATGCACTCGCATACATGTTACCGATCCCAGCATCAACCGAAACCAACTAGACAGAGCCACCAGGATGAGAGCCACCATTCTGAGCACAGCCAAGATGGCATTTAAACAAAAGACAAACACAGACAACGTGCGGAGAGGAGTGATCGAGCTGAGAAAACTCGAGCCGAGCACAACATACAAGACAAGACAGGACTAGTGTCTGGTTCATTACGCAGTAAAATGCACATTCTGGTTGAGTACCATGTATATACAACATAAGCTTTTAAGTGTTGCTCTTCTCTCTGTTCTCAGTACATTACTGCAGGTTCGCTCTCCATTGCTGCTGAAAACAAAATTAATTCACCATCTGCTTTATGTTTGG[T/C]ATGTACACAACACTTGTTCTTTTTATTTAAGCAATGGGCACTTGTAAAATTTGGTGTGTAAGGATTTATGCATAAATATTCTTTTTTCTGTGCTAATAGAGTATTGAACACAGACTTTCCATGTAATCACTAAAGCCCTGCTCACACTGTGAGATTTCAGCCACGATTTTGACATTTATCAATCCTAAAAGATTCCTGAAATCCCAGGCTAAAATCTGTGATCTTTGATCGTTGGTTTGACTTGTTCACAGAAGCCGATTCGTGCCCGTTGTGATCAGATTTTTCCTCTGATGAAGTTCTGGCAGTGTCAGAAGATTTCAGACACTTTCCTGCAGTGTGACAACAGCTGTGATGAGCGTCAATCCAAGAACCAATAGAAGCTCAGAATCTGATGATGCAATCCATGTGATGTTTATGTTTGCTGTGAGGGATCATTTTAGAACGCGGGATAGTGAAAGTGTCACGGGTGGATGACGTCAAACTCCGGGGGTGTTTTCTTT
Associated Phenotype:
Not determined