ZMP
ms4a17a.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC798290 [Source:RefSeq peptide;Acc:NP_001093531]
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 |
---|---|---|---|
sa31408 | Essential Splice Site | Available for shipment | Available now |
sa33512 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14285 | Essential Splice Site | Available for shipment | Available now |
sa20315 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31408
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005585 | Essential Splice Site | 58 | 247 | 2 | 7 |
The following transcripts of ENSDARG00000093546 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 60717485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75098610 |
GRCz11 | 4 | 76675348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTCAAGGAATTCAGGCCTTTCTTAAAGGCCAACCGAAAGCCCTCGGGG[T/C]GAGAAATCTCCCTTAAACCCAGATAACACACATTAACACACAGCATGTTA
Long Flanking Sequence:
CAGTGTTTATATCTGAGCCATAAAATGTTATTCCAGTACTTCTGTGACTATTTGATTGTACCTCAAAGACTAAAGAACGAAGCTCCCAGAGAATAGTGAGATCGAAGCATTAATAAACGAATACAAATCAGACGACTGTCATTCATTATTGTCTTTTTATTGTCACTTGTGATACCTTGTCTGATTGTCAATGTGATGTATATTATAGTTCAGATAATATTTATACAAATGTAGTTATAATATTTATCTATATTTTACTGATAATGGTATCCTCTTTTGCTTTATTTTGATTTTGTACAGGTTCATTTGATACTCTGAAACTGAAATGGCGACTGTCAGAGCCATGAATCCTTCAACGATTGTCATCCAGCTTCAGCCACTGACACAAACAGCAACTGGGACCAGTTCTTCTGTGCCTGTGCGCATACAGCATGTAGCAGGAGTTTCACCTCGTCAAGGAATTCAGGCCTTTCTTAAAGGCCAACCGAAAGCCCTCGGGG[T/C]GAGAAATCTCCCTTAAACCCAGATAACACACATTAACACACAGCATGTTAGTCTGCTTTACTTCATGAAATACTCTCATCCTTACACTGTTCTCTCTTATTCCTCACAGACTGTCCAGATAATGATCGGTGTGTTGACCTTCCTGTTGGGAATCTTGTGTACAATTTATGGAAATTATATCTTCTTCTTCACTGGTGTTTCTTACGTGGCATCTCTGATAGTAAGAAACAATCATACAGTTTAACATGTTGTCCTAGATAACACAAGCTACAGTGTGTAATCAACCAGAATACATCTTACTGTCACATTTACAGACACTAAAAGAACATGTAAATGCTTTGTGCACATGTTTATTAAGTATCTCGTATTGCCACTAGAGGCAGCACTGAACACACAAACAGACTCCCTGATCTGATATGGAGGACATTGGTGAACAAAGATGCTTTAACTTTATTTTGGCACACAAAAGTGTTCCTGGAGCTTCATATGATTACTATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33512
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005585 | Nonsense | 158 | 247 | 5 | 7 |
The following transcripts of ENSDARG00000093546 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 60719978)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75101103 |
GRCz11 | 4 | 76677841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGTTTGGCTGTTGGACCCACCAACCGTTACTGCAGAGACTTTTATTG[T/A]TATAATTATACGGTAAGTCATCAACTCTTAAATTTATATCATTTTTGTAT
Long Flanking Sequence:
GTTTGCTGTGAGGAATCATTTCAGAACGCGGGATAGTGAAAGTGTCACGGGTGGATGATGTCAAACTCCGGGGGCGTTTTCTTTCGTGTTTGTCGCGTCTTCATTGTCGTTCAGTCTGACTTTATGACAGCTGAGATCTTACAGTGTGACATGAGCACCATGTTCGTGCAGTCTGACATGCTACAATCGTTCAGGATTATAAACAATCCCACTGTGTGAGCCGGCCTTTACTCATACACGAGTCTTTGGTGCTTAGATCCTGTATTGTATTCATTTATCAATTCATTTAGATCACTTTCCATATAATCTATCATCTGCTTAACCACAGTGTGTTAACACAACATGATACAAAACCTTTCTATTTCTGTGTGTCTACTGTAGGTGAGAGCTTCCCTCGGGATGAACATTTTCAGTGCTATAGCTGCGGTCTTTTCCATTATTATGCTTTCACTGGGTTTGGCTGTTGGACCCACCAACCGTTACTGCAGAGACTTTTATTG[T/A]TATAATTATACGGTAAGTCATCAACTCTTAAATTTATATCATTTTTGTATTGTGTTATTTTATAATTACAGTAAGATCACTGTGTGACCGGTGCACTTGTGAAAATCAAGTGTAATCTGCACTCATCTGTCCAATGCTGTCCAGAACTTGACACAATATTTCTGTTCATTTACACTGGACACAAATATTGTAATTAAAGGTGCCACAGATTGCACTGATACATTGTTTAAATTGTTCATTAATATCTACATATATATGGGGCTTAGGTACGTGCAAAAATGTAAAATTTTTAAGGCCGTGAAGGAGCAGTCGGATGCGATGGGCAAAGTCATCTATCGGCGGGGCCGTAAGCCCGCTCCATCCCCGGCCGAGCCATCCACCTCCGCTGCTCCTCGCCGAGGGCGCCCGCCAACGGCCGATGCCCCGCCTCCGCCTCCGTCGAGCACGCCGAAAGCCGGTAGCCCCTCCTGCCCAGGGCGCCACTAAGTCCGGTAAACGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14285
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005585 | Essential Splice Site | 162 | 247 | 5 | 7 |
The following transcripts of ENSDARG00000093546 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 60719992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75101117 |
GRCz11 | 4 | 76677855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACCCACCAACCGTTACTGCAGAGACTTTTATTGTTATAATTATACGG[T/A]AAGTCATCAACTCTTAAATTKATAKCATTTTTGTATTRTKTTATTTTATA
Long Flanking Sequence:
ATCATTTCAGAACGCGGGATAGTGAAAGTGTCACGGGTGGATGATGTCAAACTCCGGGGGCGTTTTCTTTCGTGTTTGTCGCGTCTTCATTGTCGTTCAGTCTGACTTTATGACAGCTGAGATCTTACAGTGTGACATGAGCACCATGTTCGTGCAGTCTGACATGCTACAATCGTTCAGGATTATAAACAATCCCACTGTGTGAGCCGGCCTTTACTCATACACGAGTCTTTGGTGCTTAGATCCTGTATTGTATTCATTTATCAATTCATTTAGATCACTTTCCATATAATCTATCATCTGCTTAACCACAGTGTGTTAACACAACATGATACAAAACCTTTCTATTTCTGTGTGTCTACTGTAGGTGAGAGCTTCCCTCGGGATGAACATTTTCAGTGCTATAGCTGCGGTCTTTTCCATTATTATGCTTTCACTGGGTTTGGCTGTTGGACCCACCAACCGTTACTGCAGAGACTTTTATTGTTATAATTATACGG[T/A]AAGTCATCAACTCTTAAATTTATATCATTTTTGTATTGTGTTATTTTATAATTACAGTAAGATCACTGTGTGACCGGTGCACTTGTGAAAATCAAGTGTAATCTGCACTCATCTGTCCAATGCTGTCCAGAACTTGACACAATATTTCTGTTCATTTACACTGGACACAAATATTGTAATTAAAGGTGCCACAGATTGCACTGATACATTGTTTAAATTGTTCATTAATATCTACATATATATGGGGCTTAGGTACGTGCAAAAATGTAAAATTTTTAAGGCCGTGAAGGAGCAGTCGGATGCGATGGGCAAAGTCATCTATCGGCGGGGCCGTAAGCCCGCTCCATCCCCGGCCGAGCCATCCACCTCCGCTGCTCCTCGCCGAGGGCGCCCGCCAACGGCCGATGCCCCGCCTCCGCCTCCGTCGAGCACGCCGAAAGCCGGTAGCCCCTCCTGCCCAGGGCGCCACTAAGTCCGGTAAACGGACCGTGAAGCGTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20315
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 |
---|---|---|---|---|---|
ENSDART00000005585 | Nonsense | 243 | 247 | 7 | 7 |
The following transcripts of ENSDARG00000093546 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 60730983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75112108 |
GRCz11 | 4 | 76688846 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCCTGAACCATGCTTTCAACATCCTCCTGCAGAAACTCCCCCAGCGTA[C/A]ACTGAAGGCAAATAAATGTGAATCAACATGAAAAACGGGGCAGAGCGGTG
Long Flanking Sequence:
TGACTTATTTATTAAATTCACCCTTGTCATTAAATAATGCGAAGACAATTGTCTGTTGAGGCGACAGCAACCGATCTCTTTCACCATGTAGTTAATGATGTCGGAGTAGTTAATGATCAATCAGCCTGTGATGATGACAGAATTGAAATCTGGATTTGATGCAGACCAGACAGAAACCAATTACATGTTTTTTTTTGTTTTGTTTAATTCATCCAATCTCTGTTCTACAAACCACATTACAACAATTTGTGATGTAAAAATCCACAAAACCTTTAATGTGTGCTGTAAACGTGTGAGGAACTAGGTAATGGAGCAATAATTGTTAAACACTGACCAATAACTTAAGCTGACCATGTTCATTTTATCCTGCAGATTCATGTGAGCAGCAACCCTTTAATTCAACGCCCTCCTGCAGAAACGCCCCAACAGTACAGTCAATGTCCTCAAGAAGTCCCTGAACCATGCTTTCAACATCCTCCTGCAGAAACTCCCCCAGCGTA[C/A]ACTGAAGGCAAATAAATGTGAATCAACATGAAAAACGGGGCAGAGCGGTGGATCTGCTGCTTTGATGCTGTGACTGTTCTAGTTTCCTTGTGTATCTGATCTGAATAAAGCACATCATCAGATTGTGTCAAATGGTTATTATAGTCATCAACATAGATACCGCTGTGCATTTTACATTTACCTATGTGTATTTCTCAAATGTTATTTGTTTGTATACTGATAAATTGGATTTGTTTTATGACTAGCACTGCCTGTGTCTTTCTCTGACTCAACACGAGTAACTGCAGGAAAGCAGATTGTGTTTAGCCGGTGATCACACCGGTGTGATTGTAGGAGTCAAAGGGTTAAATGTGTTTTTAACATTTTTTTTCTATGAGTCCTCTGCATACCACTAGAAGAAGCCTGTGTACCACTAGCAGTACATATACCACACTTTGAGAAATAAATCCTGTACATCCTAAAAACCTGAAAGAAAATCCCAACCCTTAATACAGAGGTGA
Associated Phenotype:
Not determined