ZMP
si:ch73-132m10.4
Ensembl ID:
ZFIN IDs:
Description:
membrane-spanning 4-domains, subfamily A, member 17A.17 [Source:RefSeq peptide;Acc:NP_001082925]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40337 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44595 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6954 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40337
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 |
---|---|---|---|---|---|
ENSDART00000099912 | Essential Splice Site | 98 | 293 | 3 | 8 |
ENSDART00000145536 | Essential Splice Site | 98 | 169 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 60394563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 74914132 |
GRCz11 | 4 | 76495195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCTCCATCTTCGTCTTCAGTGGCGCTCCTTACTGGGGATCTGTCCTCG[T/C]AAGAAACAATCCCACAGCAGCGTTTTGCCATGGATAACACAAGCTACAGT
Long Flanking Sequence:
TTACCTTGTCAAGGAATTAAGGCCTTTGTGAAAGGCCAACCAAAAGCCCTCGGGGTGAGAAATCTCTCTGGTATATAAAACAATTGATTTTGATGTCAGTATGAATTTTAGCACACAACATACACCATTTTAATGACCTTAATAGGTTATTATAAGTTTATTGGCTTGGTGCCTTCGCAATTGTACAGTCATCTGATAATGTTTATAATCCAGAAGATAAATTTAGATAATTACTTATTAGAATGTTTTAGGAGCAAACCACTAAAACGGCTGAAGTGCTGAGCAAATATTTACTGTCCACAAATCCATGTGTACAGTCATAGAACAGGAATTTACTGTAAAAAGAACATCTCGTCCATCTTACACTGTTCTCTCTTATTCCTCACAGACTGTCCAGATAATGATCGGTCTGTTTACTCTCCTGTTGGGAATCGCATCTACAATTGATGCAGCCTCCATCTTCGTCTTCAGTGGCGCTCCTTACTGGGGATCTGTCCTCG[T/C]AAGAAACAATCCCACAGCAGCGTTTTGCCATGGATAACACAAGCTACAGTGAATAATCAACCAGAATGCAAATTACTGTCACATTTACAGCCACTAAAGAGATATAACAACAAATAAAACACAGTCGCATGACACTCATTCGCAAAATCTAGACCGGGTGGCACGAAATGGAAAGTTAGTCAGCACTGCTTGATAATAACTCATTTAGAATTGAAAACAAAATAACGAATAACAATATTGTATTATAATACTCATTCATGATTGATTAGTCAAGAAATACATAATGTTTTGGCTAATAGACTATAGATTATTAGTGACTAATATTTGAGTTTAGTTTGGTTTAAACTTCCAGTAGTTTATGATATATGTTGTAATGGCATTAGGGGATCTACTTAAGAGACCAATCACTTCTGAGTAGTAAGAAAACAGACCTATGAATAAGACTCCATACATATGGGTTGTAATTCTGCCAGGAGAGACTACATCCTACCTAGGCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44595
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099912 | Essential Splice Site | 121 | 293 | 4 | 8 |
ENSDART00000145536 | Essential Splice Site | 121 | 169 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 60391086)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 74917609 |
GRCz11 | 4 | 76498672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCATTGATGCTGAAAACAAACGTAATTCACCAACCAATTTATGTTTG[G/A]TATGTACACAACACTTGTTCTTTTCATGGGTCTAAGCACTGGGCGCTTGC
Long Flanking Sequence:
TTAGAGTTTCACATGTTTAGTTTTACCATCTGAGTGGATCATGAAGCTTATTGGCCATTCATATTTGATCCACCTTCCCTACCTGTGTTTTCTAAGACCGTGCATTTATTAGAAAATGTAGACGCTTAAAGCTCAAATATGAAGCAGTCTATATCCAATTATTTTTAAGGACAAAAATGTCCCTGGACAGTGGGGACACATCAGATACCTCATTAGTAAATGGCCGTGTTGTGCAAAAATACGAACAATACACATAGATGAAATTCTGTGACTGTGTGACTAACTGACGTGAGACTGGATTGTAAGGATGCAAATTGCATTTAGTAGTTGAGAGAATGGTTCATGTGGCAGTAAAATGCTCATTCTGGTTGAATACCACTGGTATGTATTCCAATATAAGCTTTGATTTTTGCTCTTCTCTCTGTTCTCAGTACATTACTGCAGGCTCACTCGCCATTGATGCTGAAAACAAACGTAATTCACCAACCAATTTATGTTTG[G/A]TATGTACACAACACTTGTTCTTTTCATGGGTCTAAGCACTGGGCGCTTGCAATTGACTTGGTCTGTAAGGATATGTGCATACATTGGTGTATCGGAAACAGATATTGCTATTTGTAAGATCTAAAACTTAAAACTCCTTATATATTTAATAATAATAAAACTTATTTCAAACTCCGACTAGACTGTTGTTTAACTGAAATATAAATCCTAGAAGTTGTTCATTAATGAAAGAATTATGATGACATTGGTGAACTAAACATTCTAAAAACACACATCTTTCACAAATGTGACCTTGTGAAGGCAACACAATTCATTTTCAGCTTGACATCATTTACAGCATCATTTACAACTTGACATTTGCCAATAAAAAAATAGAATAACATATCTGTATACTAAGTCTAATGCTGTGTTCCCACCAGATGCGACAAGCGCTGATAAATCACGATATTTGCGCAATATTCAGCTTCAATCGTGGGTCAAATTCACCTCACAACAGACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6954
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 |
---|---|---|---|---|---|
ENSDART00000099912 | Nonsense | 161 | 293 | 5 | 8 |
ENSDART00000145536 | Nonsense | 161 | 169 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 60388957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 74919738 |
GRCz11 | 4 | 76500801 |
KASP Assay ID:
554-4686.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGATATGCTTACTGGACAATTCWACRRTTACTGCAGTGACTATYATTG[T/A]GCAGAAATGGAGTTGAAGTATACGGTATGTTATTTACACAATTACAGTAA
Long Flanking Sequence:
AAGATTAATCAAAGCTACCTTAAAGGGTTAATTCGCCAAAAAATGAGAATTCTGTAGTTTATTACTCACTCTAATGTCATTCCAATCTCTCGAGACGGTCATTCATAATAGCAGAATTTAGTTTTTTCATCCTAACCAGTGGATGAGATCAAGTAAACAAAGTTTTTGTCCACATTTGCAAGCGAATGCAAAGGCTATGCAAGTAAATACAACATTTATCCTGATAATGTTTTCAGTTTTAGCATGAGCCTTTAGTGCTTGGACCTTATATTTAATTTATTTGTCAATTTTTTTTTTTAATCACTTTCCATATATTCTTCCAGCACAGTGAATTAGCGTGACATGTTGCCTAACTTTTCTGTTTTTGTGCCCTTACTGTAGGTGAAAGGGTCCCTTGGAATGAACATTTTCAGTGCTATAGTTGCAGGCACCGCCATTGTTATCATTTCAATGGATATGCTTACTGGACAATTCTACGGTTACTGCAGTGACTATTATTG[T/A]GCAGAAATGGAGTTGAAGTATACGGTATGTTATTTACACAATTACAGTAAGATCATTGTGTGATCCGGTACACTTATAAAGAACTGTCTAATGGTTTTCAGCGTTAATAAGTGCTGATCATTTACACTGGGTGAAAATATTGACGTTAAAAGTGCCATTGCAGTGTTGCCAGATTGGAAATGTCAAAGTATCGCATCAGAACCTCAAAATGATCGTATTTGGAGGTAAATTATTGTACACGAGTCAAACGGAGAGTATACAGCTATTACCTAGACCAGGGGTGGCCAACCCTGTTCCTGGAGATCTACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACACCTGCCTGTAATTATCAAGTGCTGTTCAGGTCCTAATTAATTGATTCAGGTGTGTTTGATCAGGGTTTAAGCTGAACTCTTTGGCTGCGACCGAAACCGCCTATTACTCAGTAGGTACTGCATTTGAATTTAAACGTACTACTCGGCCGTTAGA
Associated Phenotype:
Not determined